Title of Invention	"A FOOD OR BEVERAGE PRODUCT"
Abstract	The present invention relates to a nutritional additive comprising arabinoxylans, which beneficially modulates the human intestinal flora. Furthermore, several food and beverage products comprising the additive are provided as well as methods to prepare the said additive.

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PREBIOTIC PREPARATION FIELD OF THE INVENTION The present invention relates to arabinoxylan preparations for use as prebiotic nutritional additives and to methods of improving gastro-intestinal health of human beings through the supplementation of their diets with the said additives. In a preferred embodiment, the arabinoxylan preparations are derived from natural sources, such as plant material and more preferably from cereals. BACKGROUND OF THE INVENTION The invention relates to the positive effect on gastro-intestinal health, and more particularly on the gut mlcrobiota, of food with given non-starch polysaccharides (NSP). NSP Include a range of compounds possessing different physicochemical properties. Arabinoxylans, also called pentosans, are an important group of cereal NSP and consist of a main chain of p-1,4-linked D-xylopyranosyl units to which O-2 and/or 0-3 a-L-arabino-furanosyl units are linked. In a typical arabinoxylan, unsubstituted, monosubstituted and disubstituted xylose residues occur (see Figure 1). Arabinoxylans are either water-extractable or water-unextractable. The latter can be partially solubilised under alkaline conditions or by using enzymes and bind large amounts of water. The water-extractable arabinoxylans have an extraordinary viscosity forming potential. In general, their molecular masses are very high (up to 800,000 Dalton) depending on the source and extraction method. Despite the fact that they are only minor constituents, they are Important for the functionality of cereals in biotechnological processes such as the production of wheat starch, pasta and beer, breadmaking and other food applications. Some types of oligosaccharides derived from arabinoxylan or xylan (an unsubstituted polymer of p-1,4-linked D-xylopyranosyl units) have been shown to exert prebiotic properties. Prebiotlcs are compounds, usually non-glucosidic oligosaccharides, that can not be digested by enzymes of the upper gastro-intestinal tract but are fermented selectively by some types of intestinal bacteria in the large intestine (Gibson and Roherfroid, 1995; Roberfroid. 1988; Van Loo, 2004). Presence of prebiotics in the diet causes a shift in the composition of the intestinal bacterial population, typically characterised by a relative increase in Lactobacillus and Bifidobacterium species. This shift in the microbiota of the intestine is associated with improved overall health, reduced gut infections, increased levels of intestinal short chain fatty acids, better absorption of minerals, and suppression of colon cancer initiation (Van Loo, 2004). Preparations of xylo-oligosaccharides (XOS, oligosaccharides consisting of p-1,4-!inked D-xylopyranosyl units) with predominance of oligosaccharides with a degree of polymerisation (DP) of 2-3 (xylobiose and xyiotriose), have been shown to cause a significant increase in the level of Bifidobacteria in the faeces and caecum of rats (EP 0265970B1; Campbell et al., 1997; Hsu et al., 2004), and the colon of humans (Okazaki et al., 1990). Such xylobiose-rich XOS preparations also suppress early symptoms of chemical-induced colon carcinogenesis in rats (Hsu et al., 2004) and enhance the absorption of calcium (Toyoda et al., 1993). A preparation consisting predominantly of arabinoxylo-oligosaccharides (AXOS) with a DP of 3-5 (arabinosylxylobiose, arabinosylxylotriose, arabinosylxylotetraose, and diarabinosylxylotetraose) has also been shown to increase the levels of Bifidobacteria in the intestines of rats and mice (Yamada et al., 1993). One major drawback of current commercial XOS preparations, which severely limits their commercial potential, is their very high price level compared to other oligosaccharides, indicating that current manufacturing processes are not cost-effective. A method has been described for the manufacturing of prebiotic preparations with predominance of XOS with DP 2-3, involving chemical extraction of xylan from plant-based products (hardwood, com cobs, cottonseed hull, wheat bran, or brewery spent grain) using NaCIO solutions and highly concentrated KOH solutions, followed by enzymic hydrolysis of the extracted xylan by endoxylanase enzymes (EP 0265970B1). A similar method has been used to make a prebiotic AXOS preparation (preparation of AXOS with DP 3-5) involving chemical extraction of arabinoxylan using a concentrated alkaline solution followed by removal of the salts, enzymic hydrolysis with endoxylanase, and chromatography on a carbon column (Yamada et al., 1993). The main drawback of these methods is that the chemical extraction of xylan or arabinoxylan Is environment-unfriendly, and requires costly removal of the chemicals by extensive dialysis or ultrafiltration before enzymic hydrolysis can be performed. Another method to produce XOS or AXOS involves hydrothermal autohydrolysis of hardwood or brewery spent grain. In this method a suspension of plant material is heated in a special reactor at 150-190°C for 20-60 min (EP 0265970B1; Kabel et al., 2002; Carvalheiro et al., 2004). The drawback of this method is that, due to the high reaction temperature, side products are produced that are undesirable for food purposes, such as furfural, hydroxymethylfurfural and levulinic acid (Carvalheiro et al., 2004). The currently described prebiotic preparations of XOS and AXOS have an average degree of polymerisation that is either 2 (EP 0265970B1) or 4 (Yamada et al., 1993). For particular applications in the food sector these preparations have some drawbacks. First, the preparations are rich in xylose, which has a sweet taste that is about 60% as sweet as sucrose (Suntory, xylo-oligosaccharide, brochure and product sheet, 2001). Sweetness can be desired for some applications, but for other applications a more neutral taste is more desired. The xylo-oligosaccharides with a low average degree of polymerisation also have a sweet taste that is about 40% that of sucrose (Suntory, xylo-oligosaccharide, brochure and product sheet, 2001). Second, the preparations with a low average degree of polymerisation have an energy level that is not desired in low-calorie food ingredients. For the calculation of the energy value of xylo-oligosaccharides, the metabolisable energy value of xylose is considered 4 calories per g, 2 calories per g for xylobiose and xylotriose,' and 0 cal per gram for xylo-arabino-oligosaccharides with a DP > 4 (Suntory, xylo-oligosaccharide, brochure and product sheet, 2001). SUMMARY OF THE INVENTION The present invention relates to a nutritional additives comprising arabinoxylans, which beneficially modulates the human intestinal flora. Furthermore, several food and beverage products comprising the additives are provided as well as methods to prepare the said additives. DETAILED DESCRIPTION List of figures Figure 1: Structural elements of arabinoxylans. A: unsubstituted (3-D-xylopyranosyl residue. B: p-D-xylopyranosyl residue substituted at O-2 with an a-L-arabinofuranosyl moiety. C: J3-D-xylopyranosyl residue substituted at O-3 with an a-L-arabinofuranosyl moiety. D: J3-D-xylopyranose residue substituted at O-2 and O3 with cc-L-arabino-furanosyl moieties. Structure C shows the linkage of ferulic acid to O-5 of an a-L-arabinofuranosyl residue. Figure 2: HPSEC molecular mass profiles of different AXOS preparations. The column was a Shodex SB-806 HQ (300 x 8 mm, Showa, Denko K.K., Tokyo, Japan). Elution volumes of pullulan standards with molecular mass of 78.8 x 1Q4, 40.4 x io4, 21.2 x 104, 11.2 x 104, 4.73 x 104, 2.28 x 104,1.18 x 104, 0.59 x 104 Da and of glucose (180 Da) are indicated by an "x" symbol from left to right. Figure 3: Percentage degradation of constituent monosaccharides of AXOS-15-0.27 (A), Xylooligo-95P (B), and Fructo-oligosaccharides (C) for different incubation times at 100°C at pH2, 3, 7 and 11. Figure 4: Percentage hydrolysis of AXOS-15-0.27 (A), Xylooligo-95P (B), and Fructo-oligosaccharides (C) for different incubation times at 100°C at pH 2, 3, and 7. Figure 5: Percentage hydrolysis of xylose linkages (A) and arabinose linkages (B) in AXOS-15-0.27 for different incubation times at 100°C at pH 2, 3, and 7. Figure 6: Sweetness of AXOS-15-0.27, Xylooligo-95P and sucrose. The curves show the cumulative percentage of the subjects (n = 20) recognizing sweet taste plotted against the concentration of the compound in g/l. Figure 7: HPSEC molecular mass profiles of oligosaccharide fractions obtained after ultrafiltration of AXOS produced by endoxylanase treatment of squeegee WU-AX. The membranes used had a MMCO of 5 kDa (panel A), 10 kDa (panel B) and 30 kDa (panel C). The column was a Shodex SB-802.5 HQ (300 x 8 mm, Showa, Denko K.K., Tokyo, Japan). Molecular mass markers were Shodex standard P-82 pullulans with a molecular mass of 11.2 x 104, 4.73 x 104, 2.28 x 104, 1.18 x 104 and 0.59 x 104 Da, xylo-oligosaccharide standards with a molecular mass of 810 (DP6), 678 (DPS), 546 (DP4), 414 (DP3) and 282 Da (DP2) and glucose with a molecular mass of 180 Da, and their respective elutlon volume is indicated by an "x" symbol from left to right. Figure 8: HPSEC molecular mass profiles of oligosaccharide fractions obtained after ultrafiltration by consecutive passing through membranes with MMCO of 10 kDa and 30 kDa of AXOS produced by endoxylanase treatment of squeegee WU-AX. Fractions analysed are either the retentate after passing through a 30 kDa MMCO of the retentate of a 10 kDa membrane (RETiokoa+aokDa), the permeate after passing through a 30 kDa MMCO of the retentate of a 10 kDa membrane (PERiokoa+aokDa). or the permeate after passing through a 10 kDa membrane (PERiokDa). The column was a Shodex SB-802.5 HQ (300 x 8 mm, Showa, Denko K.K., Tokyo, Japan). Molecular mass markers were Shodex standard P-82 pullulans with a molecular mass of 11.2 x 104, 4.73 x 104, 2.28 x 104, 1.18 x 104 and 0.59 x 104 Da, xylo-oligosaccharide standards with a molecular mass of 810 (DP6), 678 (DPS), 546 (DP4), 414 (DPS) and 282 Da (DP2) and glucose with a molecular mass of 180 Da, and their respective elution volume is Indicated by an "x" symbol from left to right. Figure 9: Effects of the addition to chicken feed of AXOS-7-0.34, AXOS-122-0.66 or XyiooIigo-95P on the microbiota in the caecum of chickens. The composition of the caecal microbiota was determined 1 and 2 weeks, respectively, after the start of the experiment by plate counting for enterobacteriaciae and bifidobacteriaceae. Bars represent averages of the measurements and error bars indicate the standard deviation. For a given time point the values marked with a different letter are significantly different from each other according to Tukey's test at p Figure 10: Effects of the addition to chicken feed of AXOS-15-0.27 at 0.1% or at 0.25%, Fructo-oligosaccharides (FOS) at 0.25% or 1%, or endoxylanase on the number of bifidobacteria in the caecum of chickens after 14 days. Bacteria belonging to the genus Bifidobacterium were measured by quantitative PCR. The values marked with a different letter are significantly different from each other according to the least significance difference test (p Figure 11: Effects of the addition to rat diets of 0.25% of AXOS-8-0.27, AXOS-15-0.27, AXOS-16-0.78 or AXOS-122-0.66 on the level of acetate (top panel), propionate (middle panel) and butyrate (bottom panel) in faeces of rats after 13 days of feeding. The values marked with a different letter are significantly different from each other according to the least significance difference test (p Figure 12: Effects of the addition to rat diets of 4% AXOS-15-0.27 or Xyiooligo-9GP on the level of acetate in the proximal colon (A), acetate in the distal colon (B), propionate in the distal colon (C) and butyrate in the distal colon (D) of rats after 14 days of feeding. Bars represent averages of the measurements and error bars indicate the standard deviation. Figure 13: Effects of the addition to rat diets of 4% AXOS-15-0.27 or Xylooligo-95P on the level of bifidobacteria in the caecum after 14 days of feeding. Bacteria belonging to the genus Bifidobacterium were measured by quantitative PCR. The values indicated with a different letter are significantly different from each other according to the least significance difference test (p Figure 14: Effect of the ingestion of 4.88 g/day of AXOS-15-0.27 or 4.81 g/day of WPC during 14 days on the number of bifidobacteria in the faeces of healthy human volunteers. Bacteria belonging to the genus Bifidobacterium were measured by quantitative PCR. Bars represent averages of the measurements and error bars indicate the standard deviation. Bars with a star show a significant difference from the basal level according to the Wilcoxon Signed Ranks test (p Figure 15: Effect of the ingestion of once-off doses of AXOS-15-0.27 (0.24, 0.73, 2.21 or 4.88 g) on urinary (A) and faecal (B) excretion of nitrogen, and on oro-caecal transit time (C). Nitrogen excretion is expressed as the percentage of the administered 15N-labeled nitrogen recovered in either the urine or faeces samples collected during 0-48h and 0-72h after ingestion of the test meal, respectively. Oro-caecal transit time is expressed as the percentage of the administered 3H-labelled PEG in faecal samples collected during 0-72h. Bars represent averages of the measurements and error bars indicate the standard deviation. Bars with one star or two stars show a significant difference from the control treatment according to the to the Wilcoxon Signed Ranks test at p Figure 16: Effect of 1he ingestion of once-off doses of AXOS-15-0.27 (0.24, 0.73, 2.21 or 4.88 g) on urinary p-cresol (A) and phenol (B) excretion. p-Cresol and phenol excretion are expressed as the total p-cresol and phenol content (mg) recovered in urine samples collected over 0-24h after ingestion of the test meal. Bars represent averages of the measurements and error bars indicate the standard deviation. Bars with one star or two stars show a significant difference from the control treatment according to the to the Wilcoxon Signed Ranks test at p Description The prebiotic effect of supplementing feed or food products with particular arabinoxylan preparations has been described previously. More particularly the prior art provides examples of the bifidogenic effects of on the one hand xylo-arabino-oligosaccharides having an average degree of polymerisation (DP) lower than 4 and on the other hand of arabinoxylan preparations comprising long chain naturally occurring arabinoxylans. The available xylo-arabino-oligosaccharide preparations are produced under drastic and uncontrolled depolymerisation conditions resulting in the presence of relatively high levels of xylose and short xylo-oligosaccharides, which have a sweet taste. The sweetness of these preparations limits their use to specific food products. Furthermore, xylo-arabino-oligosaccharide molecules with a DP lower than 4 have a metabolical energy content, which is undesired in low-calorie foods. The physicochemical characteristics of naturally occurring arabinoxylans, such as high viscosity and high water retention, make them unsuited for use in a wide range of food products. Partial depolymerisation of natural arabinoxylans improves their physicochemical characteristics and preparations comprising arabinoxylan molecules having an average DP of about 58 have been described. However, the prebiotic action in humans of these partially depolymerised arabinoxylans has only been demonstrated at relatively high doses (> 6 g per day; Grasten et al. 2003). The present invention is based on the finding that arabinoxylan preparations comprising arabinoxylans having an average DP between 5 and 50 are potent prebiotic agents when adminstered to human beings and test animals serving as models for humans. Moreover, such preparations have none of the physicochemical or organoleptic inconveniences of the preparations comprising either natural arabinoxylans or short-chain xylo-arabino-oligosaccharides. It was also found that in both humans, rats and chickens the arabinoxylan preparations of the present invention had a stronger bifidogenic effect than preparations comprising partially depolymerised arabinoxylans having an average DP of 58 or more. In addition it was observed that the arabinoxylan preparations of the present invention mainly exert their prebiotic action in the distal part of the colon, while short-chain xylo-oligosaccharides were more active in the proximal part of the colon. This finding is particularly important as their appears to be a relation between the composition of the flora in the distal colon and the development of colon disease and more particularly colon cancer. Next to the prebiotic effect per se also other beneficial effects of the use of the arabinoxylan preparations of the present invention were seen such as a reduction of urinary nitrogen excretion and concomitant Increase of faecal N-excretion, as well as a reduction of the urinary excretion of cresol and phenol. Therefore, in a first object the present Invention provides arabinoxylan preparations to be used as a food additive or as a basis for a nutritional supplement product. The arabinoxylan preparations being characterised In that the arabinoxylan molecules comprised in said preparations have an average DP varying between 5 and 50. In a preferred embodiment the arabinoxylan preparation comprises at least 15% of said arabinoxylan molecules. In a more preferred embodiment the preparations comprises more than 30% of said arabinoxylans, for instance more than 60%. In an even more preferred embodiment the arabinoxylans comprised in preparations according to the present invention have an average DP between 7 and 40 DP, even more preferably between 7 and 20 DP. Preferably, 90% of the arabinoxylans comprised in the preparations of the present invention have a DP between 2 and 650 as determined using High Performance Size Exclusion Chromatography (HPSEC), more preferably between 2 and 130. In a preferred embodiment, the arabinoxylan preparations of the present invention are obtainable from natural sources, such as plant material and more preferably from cereals. They can be selected fractions of said natural arabinoxylans or can be obtained by depolymerisation or fragmentation of said natural arabinoxylans or they can be structural analogues produced by chemical, enzymic and/or physical processes. In a preferred embodiment the arabinoxylan preparations are derived from a side-stream of the gluten-starch separation process, such as WPC (Pfeifer & Langen). In another preferred embodiment the arabinoxylan preparations are derived from cereal bran. Prebiotic effects of the arabinoxylan preparations of the present invention when administered via the food were observed at a dose of 0.25 g per serving. So in a second object the present invention provides a food or beverage product comprising an arabinoxylan preparation according to the present invention. In a preferred embodiment the food or beverage product comprises between 0.1 and 5 g of an arabinoxylan preparation according to the present Invention per serving. In a more preferred embodiment the food or beverage product comprises between 0.25 and 5 g of an arabinoxylan preparation according to the present invention per serving. In an even more preferred embodiment the food or beverage product comprises between 1 and 3 g of an arabinoxylan preparation according to the present invention per serving, in another preferred embodiment the food or beverage product comprises between 0.1 and 5 g of arabinoxylans having an average DP between 5 and 50 per serving. In a more preferred embodiment the food or beverage product comprises between 0.25 and 5 g of arabinoxylans having an average DP between 5 and 50 per serving. In an even more preferred embodiment the food or beverage product comprises between 1 and 3 g of arabinoxylans having an average DP between 5 and 50 per serving. As indicated above arabinoxylan preparations according to the present invention are particularly suited as a beneficial additive to low calorie foods. In a particular embodiment the food product is a dairy product such as yoghurt or fresh cheese. Preferably said dairy product comprises between 0.25 and 5 g, more preferably between 1 and 3 g, of arabinoxylans having an average DP between 5 and 50 per 100 g per serving of 125 g. Optionally said dairy product comprises living bacteria of the genus Bifidobacterium or Lactobacillus, which are capable of fermenting arabinoxylans. In another particular embodiment the beverages of the present invention are so called non-alcoholic functional soft drinks. Preferably such functional soft drinks comprise between 0.25 and 5 g, more preferably between 1 and 3 g, of arabinoxylans having an average DP between 5 and 50 per 100 ml. Alternatively said functional soft drink comprises the desired amount of such arabinoxylans in 250 ml. In a particular embodiment said functional soft drinks comprise living bacteria of the genus Bifidobacterium or Lactobacillus, which are capable of fermenting arabinoxylans. In general, food products having cereals or cereal derived material as an ingredient contain arabinoxylans. However, the arabinoxylans comprised in these food products are either long-chain natural arabinoxylans with a DP of over 6000 or partially depolymerised arabinoxylans having a DP of at least 200 to 300. Therefore, the enrichment of said food products with arabinoxylans according to present invention also improves their nutritional value. Preferably, such enrichment is obtained by adding a given amount of an arabinoxylan preparation of the present invention as an ingredient during the preparation of cereal-containing food products. It is clear that such enrichment results in a cereal-containing food product comprising arabinoxylans having a DP of 200 and higher next to a population of arabinoxylans having a DP below 200, said population being characterised by an average DP between 5 and 50. The person skilled in the art will understand that the enrichment of the cereal-containing food products with the said population of arabinoxylans having a DP below 200 can at least in part be obtained by using xylanolitic enzymes under appropriate conditions during the preparation of these food products. In a particular embodiment said food product is a bakery product such as bread. Preferably said bread is enriched with between 0.25 and 5 g, more preferably between 1 and 3 g, of arabinoxylans having an average DP between 5 and 50 per 100 g. In another embodiment the food product is a pastry product, such as cake. Preferably said pastry product is enriched with between 0.25 and 5 g, more preferably between 1 and 3 g, of arabinoxylans having an average DP between 5 and 50 per 100 g. In yet another embodiment the food product is a pasta product. Preferably said pasta product is enriched with between 0.25 and 5 g, more preferably between 1 and 3 g, of arabinoxylans having an average DP between 5 and '50 per 80 g. In yet another embodiment the food product is a breakfast cereal. Preferably said breakfast cereal is enriched with between 0.25 and 5 g, more preferably between 1 and 3 g, of arabinoxylans having an average DP between 5 and 50 per 30 g. In yet another embodiment the food product is a biscuit, for instance dry breakfast biscuit. Preferably said biscuit is enriched with between 0.25 and 5 g, more preferably between and 3 g, of arabinoxylans having an average DP between 5 and 50 per 125 g. Other food products that can beneficially be supplemented with the arabinoxylan preparations of the present invention are for example, but without limitation, ground meat products, chocolates, cookies, bars, and desserts such as dessert puddings. In a third object the present invention provides a food supplement product comprising an arabinoxylan preparation according to the present invention. In a preferred embodiment the food supplement product is a capsule, tablet, powder or the like. In a more preferred embodiment the food supplement product is formulated such that it allows a daily administration of 0.1 and 5 g of arabinoxylans having an average DP between 5 and 50, more preferably between 0.25 and 5 g, for instance between 1 and 3 g. in a fifth object the present invention provides a method to prepare an arabinoxyian preparation according to the present invention. In a first embodiment the method comprises the steps of: i. isolating the water unextractable arabinoxyian fraction from an arabinoxylan-rich material such as bran, wheat flour or wheat squeegee by destarchification and deproteinisation of said arabinoxyian rich material, preferably using amylolytic and proteolytic enzymes, respectively ii. depolymerising the water unextractable arabinoxyian fraction using one or more xylanolitic enzymes In a second embodiment the method comprises the steps of: i. obtaining a partially depolymerised water extractable arabinoxylan-containing preparation, such as a preparation obtained out of a side stream of the starch-gluten separation process ii. if necessary eliminating the starch and proteins from said arabinoxylan-containing preparation, preferably using amylolytic and proteolytic enzymes, respectively, iii. depolymerising the arabinoxylans contained in said preparation using one or more xylanolitic enzymes In a particular embodiment the preparation is subjected to ultrafiltration after the treatment with the xylanolitic enzymes in order to reduce the amount of monosaccharides and oligosaccharides having a OP of 4 or less from the preparation.. In a final object the present invention provides a method for the analysis of the concentration and average DP of a population of arabinoxylans with a DP smaller than 200 in a cereal containing-food product. Said method comprising the steps of: i. grinding a sample of the cereal-containing food product, preferably after having dried or freeze-dried said sample; ii. extracting the ground sample in distilled water; iii. treating the extract with amylolytic enzymes at appropriate conditions in order to transform all starch into glucose, for Instance using an amylase treatment followed by an amyloglucosidase treatment; iv. eliminating the glucose from the sample obtained in (iii), for instance by metabolising the glucose using yeast; v. determining the molecular mass profile of the arabinoxylans comprised in the sample obtained in (iv), preferably using High Performance Liquid Chromatography (HPLC); vi. calculating the relative amount and average DP of the arabinoxyian fraction smaller than DP 200, for instance by analysis of the surface under the HPLC curve. The invention is further illustrated by way of the illustrative embodiments described below. Illustrative embodiment EXAMPLES EXAMPLE 1: Preparation of XOS/AXOS with average DP >4 Materials and methods Xylooligo-95P. The commercial xylo-oligosaccharide preparation Xyiooligo-95P, consisting predominantly of xylobiose, xylotriose, and xylotetraose, was obtained from Suntory Ltd. (Tokyo, Japan). Preparation of water-unextractable arabinoxylan from wheat bran. For the preparation of bran water-unexfractable arabinoxylan (WU-AX), commercial wheat bran (Meneba Meei BV, Rotterdam, The Netherlands) was used as starting material. Non-arabinoxylan material was partially removed from the bran by enzymic treatment according to the method described in Maes et al. (2004). A suspension of wheat bran in water (1:7 w/v) was first treated with a thermostable or-amylase (Termamyl 120LS, Novozymes, Bagsvaerd, Denmark; 1 ul/g wheat bran) for 90 mln at 90°C to hydrolyse the starch. After cooling to 50°C, the pH of the suspension was adjusted to 6.0 using concentrated HCI and the suspension was incubated with a protease (Neutrase 0.8L, Novozymes, Bagsvaerd. Denmark; 150 ul/g wheat bran) for 24 h at 50°C to hydrolyse residual proteins. Thereafter, the suspension was boiled and filtered and the filtrate discarded. The residue, referred to as "bran WU-AX", was washed with water and air-dried. Preparation of water-unextractable arabinoxylan from wheat flour or wheat squeegee starch. Wheat flour can be fractionated in 4 different fractions using standard methods (McRitchie, 1985): A-starch (prime starch), B-starch (squeegee starch or tailings), gluten and a water soluble fraction. The WU-AX is concentrated in the squeegee starch fraction. Non-arabinoxylan material was partially removed from the squeegee fraction by enzymic treatment. A suspension of squeegee starch in water (1:6 w/v) was first treated with a thermostable cr-amylase (Termamyl 120LS, Novozymes, Bagsvaerd, Denmark, 30 ul/g squeegee starch) for 60 min at 90°C and amyloglucosidase (Megazyme, Bray, Ireland, 20 ul/g squeegee starch) for 16 h at 60°C to hydrolyse the starch. After boiling for 30 minutes and centrifugation, the residue was incubated with a protease (Neutrase 0.8L, Novozymes, Bagsvaerd, Denmark, 20 ul/g squeegee starch) for 20 h at 50°C to hydrolyse residual proteins. Thereafter, the suspension was boiled again (30 min), filtered and the filtrate discarded. The residue, referred to as "flour WU-AX", was washed with water, ethanol (95% v/v) and air-dried. Rather than extracting WU-AX from wheat starch, WU-AX can also be directly isolated from wheat squeegee starch. In this case, Meritena 233 (Tate & Lyle, Aalst, Belgium), a commercially available side-stream of the industrial starch-gluten separation process, was used as starting material. A suspension of Meritena 233 in water (1:5 w/v) was subsequently treated with a thermostable cr-amylase (Temnamyl 120LS, Novozymes, Bagsvaerd, Denmark; 30 ul/g Meritena 233) for 60 min at 90°C and amyloglucosidase (Megazyme, Bray, Ireland; 20 p!/g Meritena 233) for 16 h at 60eC to hydrolyse the starch. After boiling for 30 minutes and oentrifugation, the residue was incubated with a protease (Neutrase 0.8L, Novozymes, Bagsvaerd, Denmark; 20 ul/g Meritena 233) for 20 h at 50°C to hydrolyse residual proteins. Thereafter, the suspension was boiled again (30 min), filtered and the filtrate discarded. The residue, referred to as "squeegee WU-AX", was washed with water, ethanol (95% v/v) and air-dried. Wheat Pentosan Concentrate (WPC). Wheat Pentosan Concentrate (WPC, Pfeifer & Langen, Dormagen, Germany) is derived from wheat flour and its chemical composition has been described in detail by Courtin and Delcour (1998). WPC is rich in water extractable arabinoxylan (ca. 43%) and protein material (ca. 30%). The remaining part mainfy consists of arabinogalactan peptide (ca. 14%) and to a lesser extent, polymeric glucose (6%). Preparation ofAXOS with avDP of 122 and A/Xratio of 0.66 (AXOS-122-0.66). The starting material for the preparation of AXOS-122-0.66 was the commercial product Wheat Pentosan Concentrate (WPC, Pfeifer & Langen, Dormagen, Germany). The WPC was solubillsed in deionised water (1:10 w/v) and silica was added as an aqueous suspension (20% w/v) until a silica/protein ration of 7:1. De pH of the mixture was adjusted to 4.8 using 0.1 M HCI in order to obtain a maximal adsorption of the proteins to the silica. After 30 min stirring the suspension was BQchner filtered. The residue comprising the silica/protein was discarded, while the filtrate was subjected to an ethanol precipitation. Ethanol (95% v/v) was added under continuous stirring to a final concentration of 65% (v/v) and after stirring for an additional 30 min, settling (24 h, 4eC) and filtration, the obtained residue, was solvent-dried (ethanol, acetone and diethyl ether) and air-dried. The obtained material was homogenised and sieved through 250 urn sieve. Preparation ofAXOS with avDP of 16 and A/Xratio of 0.78 (AXOS-16-0.78). AXOS-16-0.78 was prepared starting from the commercial product Wheat Pentosan Concentrate (WPC, Pfeifer & Langen, Dormagen, Germany). WPC was treated with silica to remove proteins as described for the preparation of AXOS-122-0.66. The recovered filtrate was further incubated at 30°C during 24 h with an XAA, an endoxylanase from Aspergillus aculeatus (Shearzyme 500L, Novozymes, Bagsvaerd, Denmark) at 29 units per g Wheat Pentosan Concentrate. After inactivation of the enzyme by boiling (30 min), the obtained solution was cooled and subjected to an ethanol precipitation. Ethanol (95% v/v) was added under continuous stirring to a final concentration of 80% (v/v) and after stirring for an additional 30 min, settling (24 h, 4°C) and filtration, the obtained residue was dissolved in deionised water and again subjected to an ethanol precipitation. Ethanol (95% v/v) was added under continuous stirring to a final concentration of 65% (v/v) and after stirring for an additional 30 min, settling (24 h, 4°C) and filtration, the precipitated material was removed. The remaining supernatant was subjected to rotary evaporation, to remove ethanol, dissolved in deionised water and lyophilised. The obtained material was homogenised and sieved through a 250 urn sieve. Preparation ofAXOS with avDP of 7 and A/X ratio of 0.34 (AXOS-7-0.34). The starting material for the preparation of AXOS-7-0.34 was bran WU-AX that was isolated as described above. Bran WU-AX was subsequently incubated at 30°C during 24 h with an endoxylanase XBS (Grindamyl H640, Danisco, Denmark) at 80 units per g dry isolated bran WU-AX. After filtration and inactivation of the enzyme by boiling (30 min), the filtrate was lyophilised and the obtained material was homogenised and sieved through a 250 urn sieve. Preparation ofAXOS with avDP of 15 and A/X ratio of 0.27 (AXOS-15-0.27). Commercial wheat bran (Dossche Mills & Bakery, Delnze, Belgium) was used as starting material for the preparation of AXOS-15-0.27. A suspension of wheat bran in water (1:7 w/v) was first treated with a thermostable o-amylase (Termamyl 120LS, Novozymes, Bagsvaerd, Denmark; 1 ul/g wheat bran) for 90 min at 90CC to hydrolyse the starch. After cooling to 50°C, the pH of the suspension was adjusted to 6.0 using concentrated HCI and the suspension was incubated with a protease (Neutrase 0.8L, Novozymes, Bagsvaerd, Denmark; 40 ul/g wheat bran) for 4 h at 50°C to hydrolyse residual proteins. Thereafter, the suspension was boiled during 20 min, filtered and the filtrate discarded. The residue was washed with water, and resuspended in deionised water (1:14 w/v). The suspension was incubated under continuous stirring for 10 h at 50°C with endoxylanase XBS (Grindamyl H640, Danisco, Denmark) at 1.4 units per g destarched and deproteinised wheat bran, and for another 10 h at 50°C after addition of a second dose of endoxylanase XBS at 1.1 units per g destarched and deproteinised wheat bran. After inactivation of the enzyme by boiling (30 min), the solution was concentrated till 20% dry matter in a falling film evaporator and finally dried in a spray-drier. Preparation of AXOS with avDP of 8 and A/X ratio of 0.27 (AXOS-8-0.27). AXOS-8-0.27 was prepared by incubating a solution (1:10 w/v) of AXOS-15-0.27 at 30°C during 1 h with XAA, an endoxylanase from Aspergillus aculeatus (Shearzyme 500L, Novozymes, Bagsvaerd, Denmark) at 125 units per g AXOS-15-0.27. After inactivation of the enzyme by boiling (30 min), the solution was lyophilised and the obtained material was homogenised and sieved through a 250 urn sieve. Preparation of AXOS with avDP of 39 and A/X ratio of 0.22 (AXOS-39-0.22). AXOS-39-0.22 was prepared from wheat squeegee WU-AX that was isolated from Meritena 233 B-starch as described above. Squeegee WU-AX, which had an average A/X ratio of 0.63, was suspended at 3 g/l in 25 mM sodium acetate buffer (pH 4.7) and incubated under continuous stirring for 2 h at 30°C with endoxylanase XBS (Grindamyl H640, Danisco, Denmark) at 3.3 units per g squeegee WU-AX After centrifugation (10,000 g, 15 min, 18°C) the supernatant was boiled for 30 min, to inactivate the enzyme, while the residue was washed with the earlier mentioned sodium acetate buffer (1/4 of the initial volume). The wash water was inactivated (30 min, 100°C) and combined with the supernatant. After filtration, the obtained solution was lyophilised to yield AXOS with an avDPoc of 262 and an A/X ratio of 0.50. The enzyme-solubilised material was further dissolved in deionised water (1:20 w/v) and the pH of the solution brought to 2.8 by addition of HCI (1M). The solution was incubated for 24 h at 90°C to remove a large fraction of the a-1,2- and a-1,3-linked arabinose substituents, which appear to be more prone to acid hydrolysis than the (3-1,4-linked xylose subunits of AXOS. After cooling to room temperature, the solution was neutralised by addition of 1 M NaOH and centrifuged (10,000 g, 20 min, 18°C). Ethanol (95% v/v) was added to the obtained supernatant under continuous stirring to a final ethanol concentration of 80% (v/v). The mixture was stirred for an additional 30 min and kept overnight at 4°C. Precipitated AXOS compounds were recovered by centrifugation (10,000 g, 20 min, 4°C), dissolved in deionised water, lyophilised and the obtained material was homogenised and sieved through a 250 urn sieve. Preparation of AXOS with avDP of 13 and A/X ratio of 0.21 (AXOS-13-0.21). AXOS-13-0.21 was prepared by incubating a solution of AXOS-39-0.22 (3 g/l) at 30°C during 2 h with XAA, an endoxylanase from Aspergillus aculeatus (Shearzyme 500L, Novozymes, Bagsvaerd, Denmark), at 27.7 units per g AXOS-39-0.22. After inactivation of the enzyme by boiling (30 min), the solution was lyophilised and the obtained material was homogenised and sieved through a 250 urn sieve. Characterisation of the isolated preparations. Different techniques were used to characterise the oligosaccharide preparations. The total and reducing end sugar content was determined by gas-iiquid chromatographic analysis as described by Courtin et al. (2000). The arabinoxylan (AX) content of samples was expressed as 0.88 x (% arabinose + % xylose). The average degree of polymerisation of AXOS as determined by gas-liquid chromatography (avDPGc) was calculated as the sum of the total xylose and arabinose content divided by the reducing end xylose content. The protein content (N x 5.7) of samples was determined by the Dumas combustion method, an adaptation of the AOAC Official Method (1995). Profiling of the constituting oligosaccharides in the preparations was done by High Performance Anion Exchange Chromatography with Pulsed Amperometric Detection (HPAEC-PAD) using a Dlonex DX-500 chromatographic system (Sunnyvale, CA, USA) equipped with an ED-40 electrochemical detector, a GP-50 gradient pump and an AS-3500 autosampler. Samples (10 mg) were solubilised in purified delonised water (2 ml, specific resistance 18 mQ-cm), filtered and injected (25 ul) on a Carbopac PA-100 guard column (4 x 25 -mm) attached to a Carbopac PA-100 anion exchange column (4 x 250 mm). Elutlon (1.0 rhl/min) was with a linear gradient of 0 to 250 mM sodium acetate in 100 mM NaOH during 30 minutes, followed by a linear gradient of 250 to 400 mM sodium acetate in 100 mM NaOH during 15 minutes. After the gradient, the column was eluted during 5 minutes with 100 mM NaOH. The elution was monitored using the ED-40 detector in the pulsed amperometric detection mode with following settings for potentials and time periods: E1f + 0,05 V fa = 400 ms); E2, + 0,75 V (t2 = 200 ms); E3, - 0,15 V (U = 400 ms). Arabinose (A), xylose (X^, xyloblose (X2) and XOS with DP of 3 to 6 (X3 to XB) were used as references. High Performance Size Exclusion Chromatography (HPSEC) was performed on a HPLC system (Kontron Instruments, 325 pump systems, Kontron, Milan, Italy) equipped with autoinjection. All preparations were dissolved in 0.3% sodium chloride (1 .5 ml), filtered and injected (20 pi) on a Shodex SB-800P guard column (Showa, Denko K.K., Tokyo, Japan, 50 x 6 mm) attached to a Shodex SB-806 HQ HPSEC column (300 x 8 mm, separation range: 1 x 102 - 20 x 108 Da). Elution was with 0.3% sodium chloride (0.5 ml/min; 30°C) and monitored with a refractive index detector (VDS Optilab, Berlin, Germany). Molecular mass markers were Shodex standard P-82 pullulans (2.0 mg/ml) with a molecular mass of 78.8 x 104, 40.4 x 104, 21.2 x 104, 11.2 x 104, 4.73 x 104, 2.28 * 104, 1.18 x 104 and 0.59 x 104 Da, and glucose with a molecular mass of 180 Da. The average degree of polymerisation (avDP) of oligosaccharides as determined by High Performance Size Exclusion Chromatography (avDPHpsec) was calculated as MMHPSEc/132. Determination of the activity of the xylanolytic enzymes. The activity of the xylanolytic enzymes was measured colorimetric using xylazyme (Megazyme, Bray, Ireland) as an insoluble substrate according to manufacturer's instructions for the assay. One unit-was defined as the amount of enzyme required to yield a change in extinction at 590 nm of 1.0 under the assay conditions. Results and discussion Different types of AXOS were prepared from either wheat bran, wheat flour or wheat squeegee starch as described in the Materials and Methods. The properties of the different preparations in terms of arabinoxylan content, average degree of substitution (arabinose to xylose ratio), and average degree of polymerisation are shown in Table 1, where they are compared to those of Xylooligo-95P, a commercial XOS preparation with known prebiotic properties (Campbell et al., 1997; Hsu et al., 2004). According to the nomenclature used in Table 1 and also hereinafter, AXOS preparations are referred to as AXOS-x-y, whereby x is the average degree of polymerisation as determined by gas-liquid Chromatography and y is the ratio of arabinose to xylose. The different preparations had average degrees of polymerisation ranging from 7 to 122 (compared to 2 for Xylooligo-95P), and the degrees of substitution ranged from 0.21 to 0.78 (compared to 0.09 for XylooIigo-9.5P). The preparations derived from wheat bran (AXOS-7-0.34, AXOS-16-0.27, AXOS-8-0.27) had a lower degree of substitution than the preparations derived from wheat flour (AXOS-122-0.66, AXOST16-0.78). We have also shown that the degree of substitution of AXOS compounds can be reduced by acid treatment. Indeed, AXOS-39-U.22 is prepared from squeegee WU-AX by different steps including acid treatment (see Materials and Methods) and this reduces the average degree of substitution from 0.63 in squeegee WU-AX to 0.22 in AXOS-39-0.22. Figure 2 shows the molecular mass distribution of the different AXOS preparations as determined by HPSEC. All AXOS preparations were polydlsperse and consisted of molecular entities with a peak situated close to the avDP as determined by gas-liquid Chromatography. The range of degrees of polymerisation within which 90% of the oligosaccharides fall, as determined from the HPSEC elution profiles, is provided in Table 1 for the different AXOS preparations. EXAMPLE 2: Physicochemical and sensory properties of XOS/AXOS preparations Materials and methods Oligosaccharide preparations. Xylooligo-95P, AXOS-15-0.27, AXOS-39-0.22, and AXOS-13-0.21 were obtained as described in the Materials and Methods of example 1. The Fructo-oligosaccharide (FOS) preparation was the commercial product Raftilose (Orafti, Tienen, Belgium). The AXOS-15-0.27 used for sensory analysis was first dissolved in water (1:25 w/v) and treated with active carbon to remove possible off-flavours resulting from the production process. The suspension of AXOS-15-0.27 and active carbon (0.75 g/g AXOS-15-0.27) was stirred for 1 h at 18°C, and after decantation, the active carbon was removed by centrifugation (10000 g, 30 min, 18°C). Stability measurements. Stability measurements were carried out on the water-extractable part of Oligosaccharide preparations, which was obtained by suspension of the preparations in deionised water (1:10 w/v) followed by shaking (2 h, 18eC), centrifugation (10,000 g, 20 min, 18°C) and filtration. After lyophilisation of the filtrate, water-extractable samples were dissolved in an universal buffer with pH values of 2, 3, 7 and 11 to obtain solutions having Oligosaccharide concentrations of 0.15% (w/v). The universal buffer was prepared from a stock solution of 6.0 g citric acid, 3.9 g potassium dihydrogen phosphate, 1.8 g boric acid and 5.8 g diethylbarbituric acid in water (1.01) (Britton and Weiford, 1937). Aliquots (20 ml) of this stock solution were either adjusted with 2.0 M HCI or 2.0 M NaOH to obtain the desired pH. Each of the Oligosaccharide solutions was kept in boiling water for different time periods (0, 5, 10, 15, 20, 30 and 60 min). Thereafter, the solution was cooled and total monosaccharide and the reducing end sugar content were measured by gas-liquid chromatography as described In the Materials and Methods of example 1. The percentage degradation of FOS was calculated with formula (1), whereas the percentage degradation of XylooIigo-95P and AXOS-15-0.27 were calculated with formula (2). The percentage hydrolysis of FOS and of Xylooligo-95P and AXOS-15-0.27 were calculated with formulae (3) and (4), respectively. (total glucose + mannose cone, at time 0 and pH7) - (total glucose + mannose cone.) (1) % degradation = (total glucose + mannose cone at time 0 and pH7) (2) % degradation = • (total xylose + arabinose cone, at time 0 and pH7) - (total xylose + arabinose cone.) (total xylose + arabinose cone at time 0 and pH7) (3) % hydrolysis (reducing glucose + mannose cone.) - (reducing glucose + mannose cone, at time 0 and pH7) (4) % hydrolysis = - (maximum amount of reducing glucose + mannose that can go in solution) (reducing xylose + arablnose cone.) - (reducing xylose + arabinose cone, at time 0 and pH7) (maximum amount of reducing xylose + arabinose that can go in solution) The percentage of hydrolysed xylose and arabinose linkages in AXOS-15-0.27 was calculated by formulae (5) and (6), respectively. (reducing xylose cone.) - (reducing xylose cone, at time 0 and pH7) (5) % xylose hydrolysis = - (maximum amount of reducing xylose that can go In solution) (reducing arabinose cone.) - (reducing arabinose cone, at time 0 and pH7) (6) % arabinose hydrolysis « (maximum amount of reducing arabinose that can go in solution) Sensory analyses. Sensory analyses were conducted in a quiet room in sessions involving maximally 10 volunteers at once. The subjects were asked to refrain from eating and drinking for at least 1 h prior to the session. The subjects were first familiarised with the procedures and subsequently asked to taste coded samples with different concentrations of Xylooligo-95P, AXOS-15^0.27, sucrose (reference sweet stimulus), sodium chloride (reference salty stimulus), and ascorbic acid (reference sour stimulus) prepared in purified deionised water (specific resistance 18 mn-cm). The solution with the highest concentration of each compound was numbered 8 and the lowest concentration was numbered 1 (Table 2). The subjects were asked to taste consecutively the full range of concentrations of one compound in order of increasing concentrations, yet the order by which the different compounds were presented to each Individual was random. Before tasting the concentration series of a compound, the mouth was first rinsed twice with purified deionised water (specific resistance 18 rrvQ-cm). and then 5 ml of each test solution was brought in the subject's mouth by means of a disposable syringe, swirled around for 5 seconds and then swallowed. The participants were asked to indicate the lowest concentration at which the taste of the compound could be recognized as sweet, salty or sour (individual recognition threshold). The average taste recognition threshold, determined as the concentration at which half of the subjects recognised the correct taste quality of a particular compound, was calculated with data on individual recognition thresholds obtained from 20 persons in total. Viscosity measurements. Viscosity measurements were carried out on the water-extractable part of oligosaccharide preparations, which was obtained by suspension of the preparations in water (1:10 w/v) followed by shaking (2 h, 18°C), centrifugation (10,000 g, 20 min, 18°C) and filtration. After lyophilisation of the filtrate, the viscosity of a 5.0% (w/v) solution was measured with an Ostwald type viscosimeter (Capillary Viscosimeter, Schott Gerate, Type 50904) at 30°C according to Vinkx et al. (1991). Solution viscosity measurements were done in triplicates and expressed relative (rirei) to that of deionised water by dividing the flow times of each of the oligosaccharide solutions by the flow times of deionised water under the same experimental conditions. After calculation of the specific viscosity (t|sp = TVSI -1), the apparent intrinsic viscosity ([tiappL dl/g) was determined using the Morris equation (Morris, 1984) as indicated in formula (7), where c (expressed as mg/ml) represents the oligosaccharide concentration, assuming that only oligosaccharides contribute to the viscous properties of the solutions. After each analysis, the viscosimeter was rinsed twice with deionised water,.twice with 95% ethanol, once with acetone and once with diethyl ether and subsequently dried with compressed air. [2 [t^-lnto™.)]]" * 1000 Results and discussion The pH stability of AXOS-15-0.27 was compared to that of established prebiotic compounds, fructc-oligosaccharides (FOS, commercial product Raftilose) and xylo-oligosaccharides (XOS, commercial product Xyloollgo-95P). The different oiigosaccha-rides were kept at different pH values (pH 2, 3, 7 and 11) at 100°C for different time periods. The percentage degradation was determined by measuring the decrease in content of the constituent monosaccharides, and the percentage hydrolysis was determined by measuring the Increase in amount of reducing constituent monosaccha-rides. As shown in Figure 3, none of the oligosaccharides underwent substantial degradation at low or neutral pH (pH 2, 3 or 7). On the other hand, degradation was observed at alkaline pH (pH 11) for all three oligosaccharides tested. This effect was most outspoken for Xylooligo-95P, of which 73% was degraded after 60 minutes. The most alkaline-stable oligosaccharide was AXOS-15-0.27 (Figure 3). The observed degradation at alkaline pH is known as alkali peeling, a reaction that occurs at elevated temperatures (60-100 °C) and progresses from the reducing end of the oligosaccharide (Whistler and BeMiller, 1958; Santori et al., 2003). Of the three oligosaccharides tested, FOS was clearly the most sensitive to hydrolysis at low pH (Figure 4). At pH 2 and 3, 58% and 53% of FOS was hydrolysed after 60 minutes. Xylooligo-95P and AXOS-15-0.27 showed an equal level of hydrolysis at pH 2. However, AXOS-15-0.27 was more stable at pH 3 than Xylooligo-95P, with only 2% hydrolysis for AXOS-15-0.27 versus 6% for Xylooligo-95P (Figure 4). Further investigation of the hydrolysis of AXOS-15-0.27 at low pH revealed that the arabinose linkages are more susceptible to acidic hydrolysis than the xylose linkages. Indeed, incubation of AXOS-15-0.27 at pH 2, 100°C for 60 min caused hydrolysis of 54% of all arabinose linkages, whereas only 4% of the xylose linkages were hydrolyzed under these conditions (Figure 5). Xylooligosaccharides with low DP such as Xylooligo-95P have been reported to taste sweet, with a sweetness being about 40% that of sucrose (Suntory, xylo-oligosaccharide, brochure and product sheet, 2001). Nothing is known so far about the taste properties of arabinoxylo-oligosaccharides with a larger degree of polymerisation. With a taste panel consisting of 20 persons we have determined the taste recognition threshold of AXOS-15-0.27 and Xylooligo-95P. The test samples also included sucrose, sodium chloride and ascorbic acid as representatives of sweet salty and sour taste, respectively. The subjects were asked to indicate the concentration at which they recognised a taste as being sweet, salty or sour, for the concentration series of each of the test compounds. Only 15% of the taste panel noted a sweet taste for AXOS-15-0.27 at the highest concentration tested (71.5 g/l), and none of the subjects indicated a salty or sour taste. The average taste recognition threshold for sweetness of sucrose and Xylooligo-95P was 7 and 24 g/L, respectively, whereas that of AXOS-15-0.27 is higher than 71.5 g/L. AXOS-15-0.27 is therefore more than 10 times less sweet than sucrose and more than 3-fold less sweet than Xylooligo-95P, which by itself is about three times less sweet than sucrose. The viscosity was determined for AXOS-15-27, AXOS-39-0.22 and AXOS-13-0.21, and compared to that of fructo-oligosaccharides (FOS, commercial product Raftilose) and xylo-oligosaccharides (XOS, commercial product Xylooligo-95P). As shown in Table 3, the different AXOS preparations have a higher apparent intrinsic viscosity that is 3 to 10 times higher relative to FOS and Xylooligo-95P. EXAMPLE 3: Fractionation of AXOS preparations by ultrafiltration Materials and methods Preparation of AXOS. Squeegee WU-AX was prepared as described in the Materials and Methods of example 1. Squeegee WU-AX was suspended in sodium acetate buffer (25 mM, pH 4.7) at 3 g/l and incubated with XAA, an endoxylanase from Aspergillus aculeatus (Shearzyme 500L, Novozymes, Bagsvaerd, Denmark), at 18.4 U per g squeegee WU-AX for 4 h at 30°C . After inactivation of the enzymes by boiling for 30 min and subsequent filtration of the suspension, AXOS was recovered in the filtrate. Separation ofAXOS by ultrafiltration. AXOS were fractionated in a dead-end 'HP4750 stirred cell' ultrafiltration device (Sterlitech Corporation, Kent, USA). The ultrafiltration membranes used had a molecular mass cut off (MMCO) of either 5 kDa (P005F, Celgard, Wiesbaden, Germany), 10 kDa (PES-10, Synder Filtration, Vacaville, CA, USA), or 30 kDa (PES-030H, Celgard). Concentration polarization at the membrane surface was minimized by a Teflon-coated magnetic stir bar mechanism which was centrally positioned in the cell and had a stirring rate of 700 rpm. The pressure source was a compressed nitrogen gas cylinder. The pressure was controlled by a pressure regulator and all filtration experiments were carried out at a constant pressure of 4 bar at room temperature. The dead-end ultrafiltration cell was filled with 300 ml of the solution to be fractionated and filtration was stopped when a total volume of approximately 200 ml of permeate was collected. Characterisation of the isolated preparations. See Materials and Methods In example 1. High Performance Size Exclusion Chromatography (HPSEC) was performed as described in the Materials and Methods in example 1, except that a Shodex SB-802.5 HQ HPSEC column (Showa, Denko K.K., Tokyo, Japan, 300.x 8 mm, separation range: IxlO^-lxlO4 Da) was used. Molecular mass markers were Shodex standard P-82 pullulans (2.0 mg/ml) with a molecular mass of 11.2 x 104, 4.73 x 104, 2.28 x 104, 1.18 x 104 and 0.59 x 103 Da, xylo-oligosaccharide standards with a molecular mass of 810 (DP6), 678 (DPS), 546 (DP4), 414 (DPS) and 282 Da (DP2) and glucose with a molecular mass of 180 Da. Results and discussion The presence of sweet-tasting and metabolisable low molecular mass oligosaccharides in AXOS preparations can be undesired for particular applications as food component, whereas for other applications it is desired to use sweet-tasting AXOS preparations consisting mainly of low molecular mass oligosaccharides. For this reason it is useful to develop a method that allows fractionating AXOS preparations such that AXOS/XOS with DP2-3 are separated from AXOS with a higher DP. Fractionation of arabinoxylans has previously always been carried out by precipitation-with alcoholic solutions of different concentrations (Courtin and Delcour, 1998). However, applying alcohol precipitation at an industrial scale is technically and economically unattractive. Therefore, the feasibility to further fractionate enzymically produced AXOS by ultrafiltration was investigated. As an example, AXOS prepared by incubation of squeegee WU-AX with XAA (18.4 U/g) for 4 h at 30°C was subjected to ultrafiltration using membranes with a molecular mass cut-off (MMCO) of either 5 kDa, 10 kDa, or 30 kDa. When the 5 kDa membrane is used, the HPSEC profile of the permeate fraction (PER5kDa) (Figure 7a) mainly shows oligosaccharides corresponding in size to xylobiose (DP2) and xylotriose (DPS). The retentate fraction (RET5kDa), which contains 86% of the soluble arabinoxylan in the AXOS stock solution (Table 4), shows basically the same molecular mass profile as the AXOS preparation before ultrafiltration, except that the amount of oligosaccharides with DP2 and DPS is reduced by about half (Figure 7a). The incomplete removal of oligosaccharides with low DP in the RET6kDa fraction might result from their retention as a result of reduced permeate fluxes caused by the presence of high molecular mass components. Through ultrafiltration using the 10 kDa membrane, 34% of the arabinoxylan content was recovered in the permeate fraction, while 65% was retained in the permeate fraction (Table 4). The permeate fraction (PER10koa) contained mainly oligosaccharides with DP2 to DP6. The retentate fraction (RET10kDa) had a low level of small-sized oligosaccharides with DP 2-4, and consisted mainly of oligosaccharides with a molecular mass ranging from 700 to >110,000 Da (DPS to DP>850) (Figure 7b). Compared to the PER10kDa fraction, the permeate obtained with tiie 30 kDa membrane (PERgokDa) had a higher content in oligosaccharides'frr'the 1000 to 10,000 Da range. Correspondingly the retentate fraction of the 30 kDa membrane (RETsokoa) had a lower content of oligosaccharides in the 1000 to 10,000 Da range in comparison to RETi^a, yet surprisingly the content of DP2 and DPS oligosaccharides was higher in RETaokoa than in RET10kDa- From Table 4 it is dear that ultrafiltration influences the A/X ratio of the obtained AXOS fractions. The permeate fractions (PERe^a, PERiokoa and PERaokOa) were enriched for oligosaccharides with a relatively low A/X ratio, while the retentate fractions (RET^a, RETiokoa and RETaokDa) contained components with a higher A/X ratio. To assess the possibility of further fractionation of AXOS by ultrafiltration, the RET10kDa fraction was subjected to a second ultrafiltration process in which a membrane with MMCO of 30kDa was used. The HPSEC profiles of the permeate fraction (PER10kDa+30kDa) and retentate fraction (RET10kDa+30kDa) obtained after ultrafiltration of the RET10kDa fraction through a membrane with MMCO of 30 kDa are, together with the PER10koa fraction, shown in figure 8. The RET10kDa«30kDa fraction contains mainly high molecular mass components (> 20,000 Da) which appear in the void volume of the Shodex SB-802.5 HQ column.. The PER10kDa+30kDa fraction, which represents approximately 25% of the arabinoxylans in the AXOS stock solution (Table 5), consists mainly of medium-sized oligosaccharides with a molecular mass ranging from 700 to 10,000 Da (DP 5 to 75) (figure 8). These results indicate that ultrafiltration, preferably using a membrane with a MMCO of 10 kDa can be used as a method to make AXOS preparations with either a high content of oligosaccharides with DP2-6, by taking the permeate of the ultrafiltration, or a high content of oligosaccharides with DP>4 and a low content of DP2-4, by taking the retentate of the ultrafiltration. Consecutive ultrafiltration, preferably using the retentate of a 10 kDa membrane and passing that over a 30 kDa membrane, can be used to obtain an AXOS fraction that is enriched in AXOS ranging from DP 5-75. EXAMPLE 4: Effect of AXOS preparations on chicken intestines Materials and methods Oligosaccharide preparations. See Materials and Methods in example 1. Microbiological analyses by plate counting. The caeca! content of chickens was weighed, diluted 1:10 in sterile peptone physiological salt solution (PPSS; 0.1% bacto peptone, 0.85% NaCI), homogenized in a stomacher, and further diluted in PPSS according to a tenfold dilution scheme. Appropriate dilutions were then plated using the pour plate technique on Violet Red Bile Glucose agar (VRBG; Oxoid CM0485B, Basingstoke, U.K) for the Enterobacteriaceae count, and on Wilkins-Chalgren anaerobe agar (Oxoid CMS 19) modified by addition of glacial acetic acid (1 ml/I) and mupirocin (100 mg/l) for the bifidobacteria. The latter modifications enhance the selectivity of Wilkins-Chalgren agar for bifidobacteria, and modified Wilkins-Chalgren agar showed particularly suitable for the one step determination of the bifidobacteria! count in chicken caeca (Rada et al., 1999; Rada and Petr, 2000). Colonies were counted after 1 day of aerobic incubation at 37°C for Enterobacteriaceae, and after 4 days of anaerobic incubation (in anaerobic jars with Oxoid anaerogen system AN0025A) at 37°C for the bifidobacteria. Counts were expressed per g of caecal content. Several precautions were taken to minimize exposure of bifidobacteria to oxygen during sample preparation: (i) caecal content was only removed from the caeca just before the start of the sample preparation; (ii) diluents and agars were autoclaved or boiled just before use to remove dissolved oxygen; (iii) plates for bifidobacteria! counts were placed under anaerobic atmosphere within 2 h from the start of sample preparation. Microbiological analyses by quantitative PCR. Extraction of DMA was performed as described by Van de Wiele et al (2004) on caeca samples diluted 1:5 in PPSS. Amplification wac performed in 25 ul reactions mixtures by using buffers supplied with the SYBR® Green PCR Core Reagents as described by the suppliers (PE Applied Biosystems, Nieuwerkerk a/d Ijssel. The Netherlands) in MicroAmp Optical 96-well reaction plates with optical caps (PE Applied Biosystems). Forward and reverse primers, BIF164f and BIF163r respectively (Satokari et al., 2001), were used at a concentration of 1 uM for detection of copies of the 16S ribosomal RNA genes from bacteria of the genus Bifidobacterium. The PCR temperature program was as follows: 50°C for 2 min, 95°C for 10 min, followed by 40 cycles of 94°C for 1 min, 62°C for 1 min, and 60°C for 1 min. The template DNA was amplified in triplicate reaction mixtures and monitored with an ABI Prism SDS7000 instrument (PE Applied Biosystems). Standard curves were constructed based on real-time PCR amplification in quadruplicate reactions on four different dilutions of DNA extracted from a culture of Bifidobacterium breve (strain LMG11042). Real-time PCR data from the experimental samples were plotted against the standard curve and corrected for efficiency of DNA extraction using a factor consisting of the DNA concentration in the experimental sample with the highest DNA concentration divided by the DNA concentration of each individual experimental sample. Statistical analyses. The effect of different diets on body mass, feed intake or the microbial composition of the intestines of animals was analysed by 1-factor variance analysis at the 95% confidence level using the Analyse-it software, version 1.71. In case a statistically significant effect was observed for the factor diet, differences between the diets were analysed either by the least significant difference (LSD) test or by Tukey's test at the 95% confidence level. Results and discussion The effect of the addition of different (arabino)xylan derived preparations was tested on the microbial composition of the lower intestines of chickens. For a first experiment, 64 one-day-old male chickens (Ross roosters) were purchased from a commercial hatchery (Avibel, Tielt, Belgium) and distributed over 4 pens (16 chickens per pen). In each pen a drinking basin and a feed container of 1 m was present. The temperature of the stable was 35°C at the arrival of the birds and was subsequently decreased with 1° C every 2 days. The animals were kept at a photoperiod of 23 hours light and 1 hour darkness. The feeds (1 feed per pen) and drinking water were administered ad libitum. The duration of the experiment was 14 days. The following experimental feeds were tested: • Control feed • Control feed + 0.25% AXOS-7-0.34 preparation (0.17% pure AX) • Control feed + 0.25% AXO3-122-O.GG preparation (0.10% pure AX) • Control feed + 0.25% Xylooligo-95P (0.22% pure AX) The concentrations indicated between brackets were corrected for their purity as calculated by their AX content. The control feed consisted of a commercial starter feed (Krix 0, Hendrix UTD, Boxmeer, The Netherlands) that contained a xylanase and glucanase enzyme mix (Roxazyme) as an additive. At the age of seven days all animals were weighed and 8 animals per group were randomly selected and sacrificed by decapitation. Thereafter, the animals were dissected to collect the caeca. Caeca were emptied and the contents were pooled in two groups per treatment (four caeca each). This protocol was repeated when the remaining animals reached the age of fourteen days, except that the caeca were pooled in three groups per treatment (from three, three, and two animals each). For the animals in the AXOS-7-0.34 group, no significant differences in mean body weight were observed relative to the control group. The animals in the AXOS-122-0.66 and Xyloollgo-95P groups had a significantly lower body weight than the control group after seven days, but the animals caught up after 14 days and the difference with the control became non-significant. In the case of the AXOS-122-0.66 group, the relatively lower body weight after 7 days might have been due to a significantly lower weight of the chickens in this group at hatching. Analysis of the caecal microbiota of the chickens indicated high levels of enterobacteriaceae (about 10B-109/g caecal content), both after 7 days and 14 days of feeding, and no significant differences were observed for any of the treatments. The levels of bifidobacteria after 7 days were low in all treatment groups (about 102-103/g caecal content) (Figure 9), except for the animals in the Xylooligo-95P group for which the level of bifidobacteria was much higher (about 108/g caecal content). After 14 days the number of bifidobacteria in the caecum stayed low for the control group. In contrast, a clear increase in the number of bifidobacten'a (by a factor of about 106) was observed in the caecal content of the AXOS-7-0.34 group. In the Xyiooligo-95P group, the level of bifidobacteria was somewhat lower relative to the level after 7 days, yet after 14 days It was still significantly higher than for the control group. In the AXOS-122-0.66 group a moderate increase of the number of bifidobacteria in the caecal content occurred after 14 days, however this increase was not significant relative to the control group. For a second experiment on chickens, 54 one-day-old male chickens (Ross roosters) were purchased from a commercial hatchery (Avibel, Tielt, Belgium) and distributed over 6 pens (9 chickens per pen). Pen conditions were as described for the first experiment (see above). The duration of the experiment was 14 days. Following experimental feeds were tested: • Control feed » Control feed + 0.141% AXOS-15-0.27 preparation (0.1 % pure AX) • Control feed + 0.352% AXOS-15-0.27 preparation (0.25% pure AX) • Control feed + 0.263% FOS preparation (0.25% pure FOS) • Control feed + 1.053% FOS preparation (1% pure FOS) • Control feed + 0.01% Xylanase preparation The concentrations indicated between brackets were corrected for their purity as calculated by their AX or FOS content. The FOS preparation was the commercial product Raftilose (Orafti, Tienen, Belgium). The xylanase preparation was the commercial product Belfeed (Beldem, Groot-Bijgaarden, Belgium). The composition of the control feed is given in Table 6. At the age of 14 days all animals were weighed and sacrificed by decapitation. Thereafter, the animals were dissected to collect the caeca, and the contents of the caeca were pooled per 3 animals belonging to the same treatment group. The number of bifidobacteria in the pooled caecum samples was measured by quantitative PCR. After two weeks of feeding the respective diets, no significant differences in body weight could be observed between the different treatments. With respect to the number of bifidobacteria in the caecum of the chickens after 2 weeks, only the chickens fed the diet containing 0.25% AXOS-15-0.27 differed significantly from the control treatment (Figure 10). The number of tffittobacteria in chickens fed with 0.25% AXOS-15-0.27 was 22-fold higher than in the chickens fed the control diet. It should be noted that fructo-oligosaccharides (FOS), a well documented prebiotic compound which was included for comparative purposes, did not cause an increase In the number of bifidobacteria in chicken caeca, even at a dose 4 times higher than that at which AXOS-15-0.27 is effective. This indicates that AXOS-15-0.27 Is a surprisingly potent blfldogenic compound. Bifidobacteria have been positively associated with animal and human health and are components of many probiotic compounds. There has been an increasing Interest In selectively enriching these bacterial populations within the gastro-intestinal tract, in addition to directly feeding microbial preparations, to promote or maintain a positive health status in animals and humans, including a suppressive effect on colorectal cancer (Van Loo et al., 2004). The results of the feeding trials with chickens indicate that all arabinoxylan containing feeds stimulated the presence of bifidobacteria in the caeca of the chickens. The AXOS preparation with high degree of polymerisation, AXOS-122-0.66, caused only a moderate non-significant increase in bifidobacterial population in the caecum of chickens. On the other hand, the preparations with low to intermediate degree of polymerisation, Xylooligo-95P, AXOS-7-0.34 and AXOS-15-0.27, triggered a strong and significant increase in bifidobacteria without causing a reduction of the body weight of the animals. The response to Xylooligo-95P could be observed already after 7 days, whereas AXOS-7-0.34 and AXOS-15-0.27 only caused a bifidogenic response after 14 days. This indicates that Xylooligo-95P is fermented faster by Bifidobacteria than the AXOS-7-0.34 and AXOS-15-0.27 preparations which have a higher average degree of polymerisation and a higher degree average degree of substitution. Slow fermentation by selected beneficial bacteria is a desired property of a prebiotic compound for application in humans and other animals with long bowels. Slow fermentation by intestinal bacteria increases the fraction of the prebiotic compound that is not fully consumed after passage through the proximal parts of the colon and thus can be used as a substrate for fermentation by the appropriate bacteria in the distal parts of the colon. In humans the incidence of cancer in the distal and rectal parts of the colon, taken together, are higher than that of the proximal parts of the colon (http^/www.state.ni.us/health/cancer/a/subsites.htm). and it is therefore important that prebiotic compounds can stimulate the beneficial microbiota of the distal colon and rectum. EXAMPLE 5: Effect of AXOS preparations on rat intestines Materials and methods XOS/AXQS preparations. See Materials and Methods in example 1. Microbiological analyses by quantitative PCR. See Materials and Methods in example 4. Short chain fatty acid analysis. Intestinal samples were extracted with 5 volumes of water/phosphoric acid/formic acid (98/1.8/0.2, v/v/v) and clarified by centrifugation (22,000 g, 10 min). Short chain fatty adds (SCFAs) were analysed by gas-liquid chromatography (Shimadzu, GC 14A) on a column packed with Chromosorb W (mesh size 60/30; Supelco, Bellefonte, USA) and detected by flame lonization. Concentrations of SCFAs were calculated based on standards with known concentrations of the different acids. Capronic acid was used as an internal standard. Statistical analyses. The effect of different diets on body mass, feed intake, SCFA or the microbial composition of the intestines of animals was analysed by 1-factor variance analysis at the 95% confidence level using the Analyse-it software, version 1.71. In case a statistically significant effect was observed for the factor diet, differences between the diets were analysed by the least significant difference (LSD) test at the 95% confidence level. Results and discussion For a first experiment on rats, 40 6-week-old male rats (Wistar) were purchased from Elevage Janvier (Le Genest-St-lsle, France) and housed in stainless steel wire-bottom cages (2 rats per cage) in an environmentally controlled room (22DC) with a 14-10 h light-dark cycle. Rats were given free access to water and to pellets (10 mm) of a 'basic humanised diet' during 7 days. The composition of the 'basic humanised diet' is given in Table 7. After 7 days of adaptation on the basic humanised diet, the rats were randomly assigned to one of 5 different treatment groups (8 rats/group), and the groups were each given free access to pellets (10 mm) of one of the following diets during 13 days: • Basic humanised diet • Basic humanised diet + 0.70% AXOS-122-0.66 preparation (0.5% pure AX) • Basic humanised diet + 0.69% AXOS-16-0.78 preparation (0.5% pure AX) • Basic humanised diet + 0.73% AXOS-15-0.27 preparation (0.5% pure AX) • Basic humanised diet + 0.72% AXOS-8-0.27 preparation (0.5% pure AX) The concentrations indicated between brackets were corrected for their purity as calculated by their AX content For the AXOS containing diets, the starch in the basic humanised diet was replaced with the appropriate amount of AXOS. Animals were weighed and feed intake was measured 3 times per week. After 13 days of treatment, all animals were weighed and euthanized with an overdose of Nembutal. Thereafter, the animals were dissected to collect the faeces. The faeces were collected as pellets from the distal colon to the anus. The faeces were pooled per 2 animals belonging to the same treatment group and analyzed for SCFA content Feed intake during the treatment period ranged from 18.9 to 27.7 g/day with an average of 22.7 g/d. Initial body weights of the rats at the start of the treatment were on average 262.0 g, and final body weights after 13 days of treatment were on average 375.3 g. No significant differences in body weight or feed intake could be observed between the different treatments. As increased intestinal SCFA levels are the hallmark of shifts in the intestinal microflora induced by intake of prebiotic compounds (Van Loo, 2004), we have measured the SCFA content of faeces for the different treatment groups. As shown in Figure 11, the propionate level in the faeces of rats fed AXOS-8-0.27, AXOS-15-0.27 and AXOS-16-0.78 were significantly higher than that in the control group or the AXOS-122-0.66 group. There was also a trend for increased levels of acetate and butyrate in the faeces of the AXOS-8-0.27, AXOS-15-0.27 and AXOS-16-0.78 groups. SCFAs such as acetate, propionate and but/rate are produced as electron sinks of respiration by bacteria in the anaerobic environment of the gut. Prebiotic compounds are known to increase SFCA levels in the lower gastro-intestinal tract. High levels of SCFAs are desirable because they reduce the pH of the gut content and thereby limit the growth of potentially pathogenic putrefactive bacteria. The lowering of the intestinal pH also entails an increase in the solubility and bio-availability of the minerals calcium and magnesium (Teitelbaum and Walker, 2002). Short chain fatty acids, especially butyrate, moreover stimulate colon epithelial cells, thereby increasing the absorptive capacity of the epithelium (Topping and Clifton, 2001). The fact that no significant differences were observed among the rats treated with AXOS-15-0.27 or AXOS-16-0.78, two preparations with approximately the same average degree of polymerisation but with a different A/X ratio, indicates that the degree of substitution does not have a large impact on the ability of AXOS to stimulate bacterial fermentation in the colon. On the other hand, when comparing the effects of AXOS-16-0.78 and AXOS-122-0.66, two preparations with approximately the same degree of substitution but with a different degree of polymerisation, it is clear that AXOS preparations with a high degree of polymerisation such as AXOS-122-0.66 are less potent prebiotic compounds than preparations with a lower average degree of polymerisation. Therefore, AXOS preparations with an average degree of polymerisation below 120 are preferred prebiotic compounds. In case slow fermentation is preferred, in order to increase availability of AXOS in the distal colon and rectum, AXOS preparations with an average degree of polymerisation ranging from above 4 are preferred. For a second experiment on rats, 24 6-week-old male rats (Wistar) were purchased from Elevage Janvier (Le Genest-St-lsle, France) and housed in stainless steel wire-bottom cages (2 rats per cage) in an environmentally controlled room (22°C) with a 14-10 h light-dark cycle. Rats were given free access to water and to pellets (10 mm) of a 'basic humanised diet' during 6 days. The composition of the 'basic humanised diet' is given in Table 7. After 6 days on the basic humanised diet, the rats were randomly assigned to one of 3 different treatment groups (8 rats/group), and the groups were each given free access to pellets (10 mm) of one of the following diets: • Basic humanised diet • Basic humanised diet + 5.87 % AXOS-15-0.27 preparation (4 % pure AX) » Basic humanised diet + 5.26 % Xylooligo-95P (4 % pure AX) The concentrations indicated between brackets were corrected for their purity as calculated by their AX content. For the diets containing AXOS-15-0.27 or Xylooligo-95P, the starch in the basic humanised diet was replaced with the appropriate amount of AXOS. Animals were weighed and feed intake was measured 3 times per week. After 14 days of treatment, all animals were weighed, euthanized with an overdose of Nembutal, and dissected to collect the proximal colon, the caecum, and the distal colon. The contents of the caecum were pooled per 2 animals belonging to the same treatment group and analyzed for the amount of bifidobacteria by quantitative PCR. The contents of the proximal colon and the distal colon were pooled per 2 animals belonging to the same treatment group and analyzed for SCFA content. In the proximal colon, SCFA levels were much lower than in the distal colon, and only acetate was above the detection threshold in proximal colon samples. Hence, data could only be obtained for acetate in the proximal colon and for acetate, propionate and butyrate in the distal colon. None of the treatments resulted in a significant effect on SCFA levels at a 95% probability level. However, clear trends could be observed from the data. As shown in Figure 12, the AXbS-15-0.27 and Xylooligo-95P groups had higher levels of acetate and butyrate, but not propionate, compared to the control group. The most striking effect was observed for butyrate in the distal colon, for which the increase relative to the control group was 58% in the AXOS-15-0.27 group and 34% in the Xylooligo-95P group. The stronger effect of AXOS-15-0.27 relative to Xylooligo-95P was observed for all SCFAs in the distal colon. Interestingly, Xylooligo-95P caused the strongest acetate Increase in proximal colon, whereas AXOS-15-0.27 resulted in the strongest acetate boost in the distal colon, the amount of bifidobacteria was significantly increased In the caeca of rats fed either AXOS-15-0.27 or XylooIigo-95P compared to rats that received the control diet. The highest increase in caecal bifidobacteria was observed in the AXOS-15-0.27 group. (1.08 log units or 12 times higher versus the control group, Figure 13). These results indicate that AXOS-15-0.27 is a more potent prebiotic compound than Xylooligo-95P. The data also indicate that AXOS-15-0.27 Is fermented more slowly than Xylooligo-95P since the Xylooligo-95P causes a stronger SCFA effect in the proximal colon while AXOS-15-0.27 caused a stronger effect in the distal colon. The slower fermentation of AXOS-15-0.27 versus Xylooligo-95P was also observed in the experiments on chickens presented in example 5. The slow fermentation properties of AXOS-15-0.27 are desired since it results in more prebiotic compound reaching the distal colon, where it can exert its beneficial and presumed carcinogenesis-suppressing effects. EXAMPLE 6: Effect of AXOS preparations on human intestines Materials and methods AXOS-1 5-0.27 and WPC preparations. See Materials and Methods of example 1. Microbiological analyses by quantitative PCR. See Materials and Methods in example 4. Subjects. None of the volunteers participating in the experiments had a history of gastrointestinal or metabolic disease or previous surgery. The subjects were free of antibiotics or any other medical treatment influencing gut transit or intestinal flora for at least 3 months before the start of the study. None of the women were pregnant during the experiments. No standard diets were imposed on the volunteers. However, they were asked to maintain a regular eating pattern until the end of the study period and to avoid excessive intake of fermented milk products and food components containing high quantities of fermentable carbohydrates. The Ethical Committee of the University of Leuven approved the experiments and aH subjects gave informed consent. Labelled substrates. Lactose-[15N,16N]-ureide was synthesized according to the method of Schoori as modified by Hofmann (1931) with [16N,15N]urea obtained from Euriso-top (Saint-Aubin, France). 3H-labelled polythyleneglycol (3H-PEG) was obtained from New England Nuclear Life Science Products (Boston, MA, USA). . Determination of urinary and fecal A^ and 1BN. Total N content and 16N enrichment of urine and faeces were measured by using an elemental analyzer (ANCA-SL; PDZ, Cheshire, UK) coupled with both a thermal conductor detector (TCD; PDZ) and a stable isotope ratio mass spectrometer (IRMS; PDZ). A known volume of urine (15 pi) or a known mass of faeces (about 5-7 mg of freeze-dried stool) was oxidized in the presence of oxygen at 1,000°C. The combustion products thereafter passed through a second furnace containing copper at 600°C where excess oxygen was absorbed and nitrogen oxides were reduced to elemental nitrogen. Total nitrogen content was measured by means of a TCD detector, whereas the 15N enrichment was determined by means of an IRMS detector, coupled to the combustion unit of the elemental analyzer. The 15N to 14N isotope ratio of N2 was measured with reference to a calibrated laboratory standard (i.e. a standard ammonium sulfate solution). The percentage of administered dose of 16N recovered was calculated as follows (Evenepoel et a/., 1999): % dose "N- 100 x mg N administered AP — AP where mg excess ISN, = —'• — x Ntot and APt: the measured 15N enrichment of a specified urine sample, expressed in atom percent (AP) APbas: the 15N enrichment of a basal urine sample (expressed in AP) MM: the total nitrogen content in a specified urine sample For urine samples, the percentage of administered 15N dose was cumulated for the period of 0-48h after the test meal, whereas for faecal samples the percentage of administered 15N dose was cumulated for the period of 0-72h after the test meal. A correction for interindividual oro-faecal transit time differences was performed for the faecal samples. This was done by dividing the cumulative percentage of administered dose 16N recovered over 72 h by the cumulative percentage of administered dose of 3H-PEG recovered over 72 h. The 3H-PEG content in stool was measured by liquid-scintillation counting (Tricarb liquid scintillation spectrometer, model 3375; Packard Instruments, Downers Grove, IL, USA) after oxidation to 3H-H2O (Packard sample oxidizer, model 307). Determination of urinary phenolic compounds. Total p-cresol and phenol content were measured by Gas-liquid Chromatography - Mass Spectrometry (GC-MS) technology. The pH of 950 mi urine was adjusted to pH 1 with concentrated HzSO*. This solution was heated for 30 mln at 90°C to deproteinise and hydrolyse the conjugated phenols. After cooling down to room temperature, 50 ml 2,6-dimethylphenol (20 mg/100 ml) was added as an internal standard. The phenols ware extracted with 1ml ethyl acetate. The ethyl acetate layer was dried with NajsSO* and 0.5 ml of this solution was analysed on a GO-MS (Trace GC-MS, Thermo Finnlgan, San Jose, CA, USA). The analytical column was a 30 m x u.32 mm internal diameter, 1um AT5-MS (Alltech Associates, Deerfield, IL, USA). Helium gas, GC grade, was used as a carrier at a constant flow rate of 1.3 ml/min. The oven temperature was programmed from 75°C (isothermal for 5 min), and increased by 10°C/min to 160°C and by 20°C/min to 280°C. Mass spectrometrlc detection was performed in electron impact full scan mode from m/z 59 to m/z 590 at two scans/s. Results for p-cresol and phenol were expressed as total content (mg) recovered in 0-24 h collections. Statistical analysis. The statistical analysis was performed with SPSS software, version 12.0. Statistical evaluation of the data was performed by applying a Wilcoxon Signed Ranks test at the 95% confidence level. Results and discussion A first experiment on humans was performed on 10 healthy volunteers (5 men and 5 women, age range 23-37 years). The 10 volunteers were randomly allocated to either of two groups of 5 persons. The first group, received for 2 weeks per day 7 g (4.88 g) of AXOS-15-0.27 suspended in water, whereas the second group received daily 11.6 g (4.82 g) of WPC suspended in water. The weight values between brackets are corrected weights for AXOS on the basis of AX content and moisture content of'the preparation. For each of the volunteers faecal samples were collected during the day prior to the start of the experiment, and during the 15th day. Each time the first stool voiding of the day was collected, weighed, and stored at -20°C until microbial analysis by quantitative PCR. As shown in Figure 14, the subjects receiving 4.88 g/day of AXOS-15-0.27 during 14 days had a level of faecal bifidobacteria that was 1.55 log units (= 35 times) higher relative to the basal level (p = 0.043). In contrast, the level of bifidobacteria was slightly reduced after 2 weeks in the subjects administered 4.82 g/day WPC, although the difference relative to the basal level was not significant (p=0.715). These data indicate that AXOS compounds with an intermediate average degree of polymerisation such as AXOS-15-0.27 (avDP = 15, Table 1) exert a stronger prebiotic effect than compounds with a high average degree of polymerisation such as WPC (avDP = 58, Table 1). The same conclusion could already be drawn from tests on bifidogenic effects in chickens (see example 4) and on the increase of SCFAs in rats (see example 5). In a second experiment the effect of different once-off doses of AXOS-15-0.27 was assessed on the metabolism of NH3, p-cresol and phenol in the human colon. NH3, phenol and p-cresol are toxic and potentially carcinogenic metabolites that are produced by bacteria in the colon upon fermentation of proteins. NH3 metabolism was assessed using lactose-[15N,15N]-ureide as a biomarker. On oral administration, lactose-ureide reaches the colon unmodified, because the molecular bond between the carbohydrate moiety and urea in lactose-ureide resists enzymatic degradation in the human gastrointestinal tract. When lactose-[15N,16N]-ureide reaches the colon, it is degraded to [15N,15N]-labeled urea by selected bacteria. The labeled urea undergoes fast hydrolysis with production of 15NH3 (Wutzke et al. 1997). The labeled NH3 is mixed with the ammonia present in the colon, and as a consequence, the variations observed in the 15N-labeled measurement reflect the fate of total colonic NH3. In addition to monitoring colonic NH3 metabolism, the presence of phenol and p-cresol were measured in the urine as hallmarks of bacterial fermentation of proteins in the colon. Based on literature data (Evenepoel et al. 1999), it is assumed that in physiological circumstances about 3 to 6% of the proteins ingested remains undigested. When the non-digested proteins reach the colon, they are fermented by the colonic flora. Bacterial fermentation of the amino add tyrosine results in the production of phenol and p-cresol. These compounds are largely absorbed from the colon, detoxified in the mucosa and in the liver (by glucuronide- and sulphate- conjugation) and finally excreted in the urine. Since phenol and p-cresol originate exclusively from bacterial metabolism and not from human metabolism, the urinary output of phenol and p-cresol reflects the bacterial production of these compounds in the colon (Smith and Macfarlane, 1996). As a consequence, any influence of prebiotic compounds on the colonic protein fermentation should be reflected in the urinary concentration of phenol and p-cresol. The second experiment on humans was performed on 9 healthy volunteers (3 men and 6 women, age range 19-26 years). Each volunteer received 5 different test meals containing different doses of AXOS-15-0.27 with an interval of 1 week between each test. meal. The different AXOS-15-0.27 doses per day were either 0, 0.35 g (0.24g), 1.05 g (0.73 g), 3.17 g (2.21 g) and 7 g (4.88 g), with the weight values between brackets being corrected weights for AXOS on- the basis of AX content and moisture content of the preparation. The order by which the volunteers received the different test meals was random. The test meal consisted of a pancake (15,8 g proteins, 11,6 g fat and 21,1 g carbohydrates; 255 Real) containing 75 mg of the stable isotope labelled substrate lactose-[16N,15N]-ureidef 185 kBq of tritium-labelled polyethylene glycol (3H-PEG), and AXOS-15-0.27 at the appropriate dose. 3H-PEG was used as a biomarker for oro-faecai transit time (Geboes et al 2005). Urine was collected in recipients to which 1 gram of neomycin was added for prevention of bacterial growth. A basal urine sample was collected before consumption of the test meal. After intake of each test meal, a 48 h urine collection was performed in 3 different fractions: 0-6 h, 6-24h and 24-48 h. After measurement of the urine volume, samples were taken and stored at-20°C until analysis. Stools were collected over 72 h after the test meal. The stools were frozen immediately after voiding, weighed, and then stored at -20°C. Ail stools collected on the same day were combined and homogenized before further analysis. Samples of known weight were removed and freeze-dried. The dried material was weighed again, and aliquots were taken for analysis of nitrogen and radioactivity. As shown in Figure 15A, a consistently lower urinal excretion rate of 15N-Iabelfed nitrogen was noted after intake of the test meal containing AXOS-15-0.27 as compared to the control meal lacking AXOS-15-0.27. 44.5 % of the administered 16N dose was retrieved in urine samples after consumption of the control meal. This fraction was lowered to 40.4% (-9% relative to control), 43.7% (-2% relative to control), 33.1% (-26% relative to control) and 33.6% (-25% relative to control) after ingestion of 0.24, 0.73, 2.21 and 4.88 g AXOS-15-0.27, respectively. The decrease in urinary 15N excretion was significant at p Conversely, AXOS-15-0.27 supplementation to the test meals caused a consistent increase in 15N excretion via the faeces (Figure 15 B). In the control test meal group, 15.1 % of the administered 15N dose was recovered in the faeces. This fraction was increased to 16.4% (+8% relative to control), 18.8% (+24% relative to control), 25.3% (+67% relative to control) and 26.1% (+72 % relative to control) after ingestion of 0.24, 0.73, 2.21 and 4.88 g, respectively. The increase in faecal 15N excretion was significant at p Reduction of urinary excretion of nitrogen and concomitant increase of faecal N-excretion has previously been observed in humans that were administered known prebiotic compounds such as inulin and lactulose (De Preter et al. 2004; Geboes et al. 2005). Stimulated excretion of ammonia via the faeces is desired since ammonia has been shown to reduce the life span of colonlc epithelial cells, to increase their turnover, and to make them more susceptible to chemical carclnogenesis (Visek 1978). Ammonia in the lumen of the colon is mainly derived from bacterial fermentation of non-digested proteins (Smith & Macfariane, 1996; Fooks et al., 1999). Slowly fermentable prebiotic carbohydrates, such as AXOS with intermediate degrees of polymerisation, stimulate saccharolytlc bacteria and saccharolytic pathways in bacteria present in the colon. 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(1999b) Simultaneous application of phytase and xylanase to broiler feeds based on wheat: feeding experiment with growing broilers. J. Sci. Food Agric. 79: 1841 -184$ Zyla , K., Gogal, D.; Koreleski, J.; Swiatkiewicz, S. and Ledoux, D.R. (1999a) Simultaneous application of phyatee arid xyianasa to broiler feeds based on wheat: in vitro measurements of phosphorus and pentose release from wheat and wheat-based feeds. J. Sci. Food Agric., 79:1832-1840. TABLES Table 1: Properties of different (arablno)xyian preparations. AX: arabinoxylan content expressed as % of dry matter; A/X: the arabinose to xylose ratio; avDPoc: average degree of polymerisation as determined by gas-liquid chromatographv; avDPnpsec: average degree of polymerisation as determined by high performance size exclusion chromatography. DP 90% range: range of degrees of polymerisation within which 90% of the oligosaccharides fail. (Table Remove) Table 4: Ultraflltration of AXOS preparation by passing through a single membrane with a MMCO of either 5 kDa, 10 kDa, or 30 kDa. Recovery is expressed as % of the arabinoxylan content of the starting material. The analyses include the arabinose to xylose ratfo (A/X), and the average degree of polymerisation as determined by gas-liquid chromatography (avDPGc). (Table Remove) Table 5: Ultrafiltration of AXOS preparation by passing consecutively through membranes of 10 and 30 kDa. .Recovery is expressed as % of the arabinoxylan content of the starting material. The analyses include the arabinose to xylose ratio (A/X), and the average degree of polymerisation as determined by gas-liquid chromatography (avDPGC). Fraction Recovery A/X avDPGC AXOS before Ultraflltration 100% 0.50 8 AXOS after passing through 10kDa 34.2% 0.33 5 membrane (permeate) AXOS after passing consecutively 25.2% 0.50 7 throughlOkDa membrane (retentate) and SOkDa membrane (permeate) AXOS after passing consecutively 36.6% 0.65 18 throughlOkDa membrane (retentate) and SOkDa membrane (retentate) • Table 6: Feedstuffs and compositional analysis of the chicken feed diet used in the second chicken experiment. (Table Remove) CLAIMS 1. A food or beverage product modulating the human Intestinal flora comprising between 0.25 and 5 g of arabinoxyians per serving of said food or beverage product wherein said arabtnoxylans have an average degree of polymerisation (DP) between 5 and 50. 2. The food or beverage product according to claim 1 comprising between 1 and 3 g of said arabinoxyians per serving of said food or beverage product 3. The food or beverage product according to claims 1 or 2 wherein said arablnoxyfens have an average DP between 7 and 40. 4. The food or beverage product according to claims 1 or 2 wherein said arabinoxyians have an average DP between 7 and 20. 5. The food or beverage product according to claims 1 to 4 wherein the arabinoxylana are derived from arablnoxylan-contalning plant material. 6. The food or beverage product according to claim 5 wherein the arabinoxyfen-contalning material is cereal derived material. 7. The food or beverage product according to claim 6 wherein the cereal is derived from the group constating of wheat, barley, rye, oats, com, sorghum and rice. 8. The food or beverage product according to claims 6 or 7 wherein the cereal material is bran, flour or squeegee. 9. The food or beverage product according to claims 6 or 7 wherein the arabinoxyians are derived from a side-stream of the gluten-starch or protein-starch separation process. 10. The food product according to claims 1 to 9 wherein the food product is a meat product 11. The food product according to claims 1 to 9 wherein the food product is a dairy product 12. The beverage according to claims 1 to 9 wherein the beverage is a non-alcoholic beverage. 13. The beverage according to daim 12 wherein the beverage is a functional soft drink. 14. The beverage or food product according to claims 1 to 13 wherein said food product comprises living bacteria of the genus Bifidobacterium or Lactobacillus. 15. The food or beverage product according to any of the claims 1 to 14 wherein said food product Is a non-cereal based food product 16. The food product according to claim 1 wherein said food product is a cereal-based food product comprising between 0.25 and 5 g of arablnoxylans having a DP below 200 per serving of said product and wherein said population of arablnoxylans has an average DP between 6 and 60. 17. The cereal-based food product according to daim 16 comprising between 1 and 3 g of arablnoxylans having a DP below 200 per serving of said product end wherein said population of erabfnoxyians has an average DP between 5 and 50. 18. The c«»al-based food product according to daim 16 comprising between 0.25 and 5 g of arablnoxyfans haying a DP below 200 per serving of aaid product and wherein said population of arablnoxylans has an average DP between 7 and 40. 19. The cereal-based food product according to claim 16 comprising between 1 and 3 g of arabinoxylarts having a DP below 200 per serving of said product and wherein said population of arabinoxyians has an average DP between 7 and 40. 20. The cereal-based food product according to daim 16 comprising between 0.25 and 6 g of arabinoxyians having a DP below 200 per serving of said product and wherein said population of arablnoxylans has an average DP between 7 and 20. 21. The cereal-based food product according to claim 16 comprising between 1 and 3 g of arabinoxyians having a DP below 200 per serving of said product and wherein said population of arablnoxylans has an average DP between 7 and 20. 22. The food product according to any of the daims 16 to 21 wherein the food product is bakery product. 23. The food product according to any of the claims 16 to 21 wherein the food product Is a pastry product 24. The food product according to any of the daims 1C to 21 wherein the food product Is a breakfast cereal. 25. The food product according to any of the daims 16 to 21 wherein the food product Is a biscuit 26. The food product according to any of the claims 18 to 21 wherein the food product is a pasta product. 27. The food product according to any of the claims 1 to 26 wherein the food product is an industrially prepared dessert product 28. The food or beverage product according to any of the claims 1 to 27 wherein the food or beverage product Is a low calorie product. 29. A method for the preparation of a nutritional additive to be used as an additive In the preparation of a food product according to any of the claims 1 to 28 comprising the steps of: i. Isolating the water unextractable arablnoxylan fraction from an arabinoxylan-rich material such as seed bran, veed flour or seed squeegee by destarchtficatton and deproteinisation of said arabinoxylan rich material, preferably using amyforytic and proteotytic enzymes, respectively ii. depolymerising the water unextractable arablnoxylan fraction using one or more xylanolftic enzymes 30. A method for the preparation of a nutritional additive to be used as an additive In the preparation of a food product according to any of the claims 1 to 28 comprising the steps of: i. obtaining a partially depolymerised water extractable arabinoxylan-containing preparation, such as a preparation obtained out of a side stream of the starch-gluten separation process ii. if necessary eliminating the starch and proteins from said arabinoxylan-containing preparation, preferably using amylolytJc and proteolytlc enzymes, respectively: iii.depolymerising the arabinoxylans contained in said preparation using one or more xylanolWc enzymes 31, The method according to the claims 30 or 31 wherein the preparation Is subjected to membrane filtration, such as ultrafittration, after the treatment with the xylanolytio enzymes in order to remove low molecular weight compounds. 32. A nutritional additive to be used as an additive in the preparation of a food product according to any of the claims 1 to 28 wherein said additive comprises at least 15% arablnoxyJans having an average DP between 7 and 20. 33. The nutritional additive according to claim 32 comprising more than 30% arablnoxytans. 34. The nutritional additive according to claims 32 or 33 comprising more than 60 % arabinoxylane. 35. The nutritional additive according to any of the claims 32 to 34 wherein 00% of the arabtnoxylans have a DP between 2 and 650. 36. The nutritional additive according to any of the claim 32 to 35 wherein 90% of the arabinoxylans have a OP between 2 and 130.

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