Patent Application
20180134741
The present invention relates to preparations comprising arabinoxylo-oligosaccharides, which are particularly useful as food or beverage ingredients or as nutritional supplements as well as to methods for producing such preparations. Further the invention also relates to the improved generation of arabinoxylo-oligosaccharides in established prebiotic formulations comprising mixtures between xylo-oligosaccharides and arabinoxylo-oligosaccharides.
Xylan hemicelluloses are the second most abundant biopolymers in the plant kingdom after cellulose. A common feature for all xylans in higher plants are their backbone of β-(1→4)-linked D-xylopyranosyl (Xylp) residues. Xylans containing other sugars than xylose are called heteroxylans and can be divided into glucuronoxylans (GX), found in secondary cell walls of dicot plants, or arabinoxylan (AX), found in the primary cell walls of cereals. AX content and composition in cereals varies with botanical source, cultivar and tissue. Most AX is found in the outer bran tissues (outer- and inner pericarp, testa, nucellar epidermis and associated aleurone layer), although the starchy endosperm also contains a considerable amount. AX can be classified as water extractable (WE-AX) or water-unextractable (WU-AX). Solubility in water is limited by covalent and/or non-covalent linkages to other cell wall components. While easily soluble, AX is weakly bound at the surface.
Generally four main structural elements are present in cereal AX, I) un-substituted Xylp units (uXyl), II) α-(1→2)-linked L-arabinofuranosyl (Araf) linked to a Xylp unit (mXyl2), III) α-(1→3)-linked Araf linked to a Xylp unit (mXyl3) and IV) double α-(1→2) and α-(1→3)-linked Araf linked to a Xylp unit (dXyl). In addition, galactose and glucuronic acids can be present in AX from the outer grain tissues. Hydroxycinnamic acid derivatives, mainly ferulic acid (FA), can be ester-linked to position O-5 on a few Araf substituents causing oxidative gelation in water (crosslinking of dihydrodiferulic acids) and antioxidant properties. The molar ratio of arabinose and xylose (A/X) in AX is an important characteristic when it comes to enzymatic hydrolysis, solubility and fermentative properties in the gastrointestinal tract (GIT).
Oligosaccharides, which are short saccharide polymers, can be derived by partial hydrolysis of the AX backbone using either thermo/chemical or enzymatic methods. Considering only AX from cereals, two main groups of oligosaccharides can be obtained from enzymatic hydrolysis: xylo-oligosaccharides (XOS) and arabinoxylo-oligosaccharides (AXOS). XOS are xylose oligomers, which are linked by β-(1→4) linkages with the general molecular formula C5nH8n+2O4n+1, where n is the number of xylose units 2-10. The XOS are X2: xylobiose, X3: xylotriose, X4: xylotetraose, X5: xylopentaose, X6: xylohexaose, X7: xyloheptaose, X8: xylooctaose, X9: xyloenneaose and X10: xylodecaose. AXOS on the other hand have a XOS as a backbone with at least one Araf group attached as a side chain to one of the xylose units. Depending on how many Araf groups are attached, to which residue, and on the chemical linkage type (1→2) and/or (1→3), many different combinations of AXOS are possible. Arabinoxylan-oligosaccharides (A)XOS comprises a mixture of both xylo-oligosaccharides (XOS) and arabinoxylo-oligosaccharides (AXOS) and is obtained after enzymatic hydrolysis with commercial xylanases.
Xylanases are used for example, in pulp and paper processing, biofuels production, the baking, and the brewing industries and in processing of animal feed. These enzymes are able to hydrolyze the β-(1→4)-xylosidic linkages found in xylan and xylan derived oligosaccharides. Depending on the xylanase used different size of XOS and structures of AXOS can be generated. Family 10 xylanases are known to produce small end products. This is consistent with the production of xylose and X2 as the main hydrolysis products from AX. The smallest AXOS produced by family 10 xylanases is a tri-saccharide (A3X). Family 11 xylanases have the same catalytic mechanism as does family 10, but activity is generally higher on polymeric substrates than oligomeric and they have higher activity against insoluble substrates compared with family 10. The main hydrolysis products by family 11 xylanases are xylose, X2 and X3 while the smallest AXOS is a tetra-saccharide (A3XX).
There is a commercial interest in XOS and AXOS as emerging prebiotics, defined as “a selectively fermented ingredient that results in specific changes in the composition and/or activity of the GI microbiota, thus conferring benefit(s) upon host health”. Considerable proofs of these compounds' prebiotic properties are now available based on in vitro and in vivo trials which demonstrated that they fulfill all the criteria for a prebiotic. XOS and AXOS are fermented by the faecal microbiota producing health promoting short chain fatty acids acetate, lactate, propionate and butyrate. Depending on the size of the oligosaccharides, different metabolic acids are produced. The prebiotic effect of XOS and AXOS is tightly linked to the size of the oligosaccharides and the arabinose substitution; a small size is required for most bifidobacteria in order for them to be utilized as a carbon source. The Araf group(s) attached to the AXOS are therefore an important characteristic when it comes to the fermentative properties in the gastrointestinal tract (GIT) since not all XOS utilizing bacteria can utilize AXOS.
Bifidobacteria is considered one of the most important groups of beneficial bacteria due their ability to stimulate immune system development, produce vitamins, inhibit pathogens, reduce ammonia and cholesterol in the blood and help to restore a healthy gut after antibiotic treatment. The ability among bifidobacteria to use XOS and/or AXOS is strain-dependent, meaning that strains can be grouped based on their carbohydrate preference. Bifidobacteria can be clustered into five different groups (I-V) based on their ability to ferment arabinose, xylose, XOS or AXOS. In cluster I, the strains can not use XOS or AXOS. In cluster II strains are able to ferment the arabinose substituents present on AXOS. Cluster III contains strains that are able to ferment the XOS backbone up to xylotetraose, but have a more limited consumption of AXOS. In cluster IV and V the strains have a broad degradation of both XOS and AXOS.
State of the art preparation of prebiotics from AX include (A)XOS products comprising a mixture of both XOS and AXOS obtained by xylanase hydrolysis of AX or AX containing material. In EP 2 265 127, prebiotic (A)XOS preparations are prepared from wheat bran using a family 10 and/or family 11 xylanase. This application is based on a method by Swennen et al. (2006) where the final preparation is a mixture between XOS and AXOS (Swennen et al., 2006,
The current invention describes how prebiotic AXOS can be generated from AX using an arabinoxylanase without creating xylose and XOS. The preparations are special in their composition of arabinose containing oligosaccharides without xylose and XOS. Their ability to specifically stimulate certain strains of bifidobacteria make them useful as a more selective prebiotic. In one embodiment the present invention relates to an AXOS composition comprising at least one arabinose unit linked to one of the xylose units of the backbone, per molecule, wherein the at least one arabinose unit is an α-L-arabinofuranosyl, wherein said composition has an XOS backbone with a degree of polymerization of 1-10. In another embodiment the AXOS composition has an average degree of arabinose substitution of 0.3-0.6. In yet another embodiment the AXOS composition has an average degree of arabinose substitution of 0.2-0.7. The application of the pure AXOS is to selectively stimulate certain groups of bifidobacteria. Such preparations can be used in food or beverage ingredients or as nutritional supplements with or without added bifidobacteria. In one embodiment the AXOS composition selectively is adapted to stimulate the growth of Bifidobacterium spp. In another embodiment the Bifidobacterium spp belong to strains adapted to ferment AXOS or the arabinose substituents on the oligosaccharides. In yet another embodiment the Bifidobacterium spp is selected from the group consisting of Bifidobacterium adolescentis, Bifidobacterium longum, Bifidobacterium catenulatum, Bifidobacterium animalis, Bifidobacterium pseudolongum, Bifidobacterium gallicum Bifidobacterium lactis, Bifidobacterium infantis, Bifidobacterium bifidum, Bifidobacterium angulatum or Bifidobacterium breve. Further the invention also relates to the improved generation of AXOS in established prebiotic (A)XOS formulations comprising mixtures between XOS and AXOS. In one embodiment the present invention is a synbiotic preparation comprising an AXOS composition, further comprising a Bifidobacterium spp. In another embodiment the synbiotic preparation is for the treatment of improving gastrointestinal problems. In yet another embodiment the synbiotic preparation is for use as an ingredient in a product selected from the group consisting of food, feed, beverages or nutritional supplements. In yet another embodiment the present invention is an AXOS composition or a synbiotic preparation comprising AXOS composition, for use in the treatment of improving gastrointestinal problems.
In one embodiment, the present invention comprise selective prebiotics for certain groups of intestinal bacteria belonging to the group of bifidobacteria adapted to ferment AXOS or the arabinose substituents attached to the AXOS molecule(s). In one embodiment obtained AXOS, according to the present invention can be used to selectively stimulate the growth of bifidobacteria over other groups of intestinal bacteria that normally can use XOS. In another embodiment strains from a cluster selected from the group consisting of II, III, IV and V are selectively stimulated with preparations containing only AXOS. In another more specific embodiment the strains of bifidobacteria are selected from the group consisting of Bifidobacterium longum subsp. longum DSMZ 20219 (Cluster 2), Bifidobacterium adolescentis DSMZ 20083 (Cluster 3), Bifidobacterium longum subsp. longum CCUG 15137 (Cluster 4) or Bifidobacterium catenulatum DSMZ 16992 (Cluster 5).
The present invention implies that various starting points and hence various starting material may be used in a process for producing an AXOS composition according to the present invention. In one embodiment endosperm AX is used as starting material. In another embodiment bran is used as a starting material. Various kinds of flour fractions or bran are thinkable and the present invention is not to be seen as limited by the selection of starting material. In one embodiment the starting material is selected from the group consisting of endosperm AX, bran, husk or straw. In another more specific embodiment the bran starting material is selected from the group of cereals such as rye, maize, millets, rice, barley, oat or wheat but not limited to these. Other possible starting materials are pseudocereals such as, but not limited to, quinoa, amaranth or buckwheat. Preferably the starting material is flour or bran from any of the above plants. In one embodiment the starting material is flour comprising endosperm AX.
Therefore, another aspect of the present invention relates to a process for producing an AXOS composition from flour comprising the steps of:
In one embodiment the A/X ratio is in the interval of 0.2-0.7 preferably 0.28-0.65, preferably 0.35-0.5, preferably 0.38-0.45 preferably 0.4. In another embodiment the A/X ratio is 0.4. In yet another embodiment the invention is a process for producing an AXOS composition, wherein the AXOS composition is produced using an arabinoxylan specific endoxylanase. In another, more specific embodiment the invention is a process for producing an AXOS composition, wherein the arabinoxylan specific endoxylanase is arabinoxylanase.
Further, in another embodiment, the invention is a process for producing an AXOS composition wherein the step C′ includes an optional treatment with arabinofuranosidases to increase the yield of AXOS of 10-100%, more preferred of 50-100%, even more preferred of 70-100%, yet even more preferred of 85-100% and most preferred 100%. In one embodiment the increased yield is of 95-99%.
When preparing an AXOS composition from bran AX additional steps are possible. In one embodiment, the invention relates to a process for producing an AXOS composition, wherein the step A′ includes removal of starch and proteins with amylases and proteases respectively. In another embodiment the invention relates to a process for producing an AXOS composition, wherein the step C′ includes extraction with alkali and peroxide, with optionally using other means of extraction. Various means of heat treatment are possible in step C′. In one embodiment the step C′ includes steam treatment to increase the water soluble AX content. In another embodiment the step C′ includes preasurised water treatment. In yet another embodiment the invention relates to a process for producing an AXOS composition, wherein the step E includes an optional treatment to increase the yield of AXOS. In one embodiment the step E includes an optional treatment with arabinofuranosidases. In another embodiment step E includes an optional treatment with a weak acid solution, such as, but not limited to, inorganic acids, preferably hydrochloric acid, preferably sulfuric acid, preferably phosphoric acid or preferably nitric acid.
Another aspect of the present invention relates to use of an arabinoxylanase to improve the generation of AXOS in XOS and AXOS containing preparations. In one embodiment the invention relates to use of an arabinoxylanase to improve the generation of AXOS in (A)XOS, wherein the preparation of XOS and AXOS is prepared using a family 10 or 11 xylanase. One aspect of the present invention relates to an arabinoxylo-oligosaccharide composition comprising at least one arabinose unit linked to one of the xylose units of the backbone, per molecule, wherein the at least one arabinose unit is an α-L-arabinofuranosyl, wherein said composition has a xylo-oligosaccharide backbone with a degree of polymerization of 1-10, wherein the composition comprise at most 10% monosaccharides and/or at most 10% xylooligosaccharides.
In one embodiment, the composition according to the present invention may comprise monosaccharides present in an amount of at most 20%, at most 15%, at most 10%, at most 8%, at most 5%. at most 4%, at most 3%, at most 2%, at most 1.6%, at most 1%, at most 0.1%, or at most 0.01%. In one embodiment the composition according to the present invention may comprise monosaccharides present in an amount of 0.01-20%, 0.05-10%, 0.01-5%, 0.05-5%, 0.05-2%, 0.01-0.1%, 0.01-1%, 0.05-1.8% or 0.05-1.5%.
In one embodiment, the composition according to the present invention may comprise xylooligosaccharides present in an amount of at most 20%, at most 15%, at most 10%, at most 8%, at most 5%. at most 4%, at most 3%, at most 2%, at most 1.6%, at most 1% at most 0.1%, or at most 0.01%. In one embodiment the composition according to the present invention may comprise xylooligosaccharides present in an amount of 0.01-20%, 0.05-10%, 0.01-5%, 0.05-5%, 0.05-2%, 0.01-0.1%, 0.01-1%, 0.05-1.8%, or 0.05-1.5%. In one embodiment the monosaccharides may comprise arabinose. In one embodiment the monosaccharides may comprise xylose. In one embodiment the amount of monosacharides and/or xylooligosaccharides herein is based on the dry weight % of the preparation.
Yet another aspect relates to use of an arabinoxylanase to improve the generation of arabinoxylo-oligosaccharides in xylo-oligosaccharides and arabinoxylo-oligosaccharides comprising preparations. In one embodiment the preparation of xylo-oligosaccharides and arabinoxylo-oligosaccharides is prepared using a family 11 xylanase. In another the arabinoxylanase is a xylanase beloning to glycoside hydrolase family 5. In another embodiment the arabinoxylo-oligosaccharides are generated from a cereal fiber. In another embodiment, use of an arabinoxylanase according to the present invention comprises the steps of:
Arabinoxylanases are unique in their specificity for AX since they do not attack unsubstituted xylans. The oligosaccharides generated by these enzymes contain at least one (1→3) Araf group linked to a reducing end Xylp unit. This group of enzymes have not previously been used or considered in the production of prebiotic AXOS from AX or AX containing materials. In the present invention an arabinoxylanase is used to produce AXOS from AX containing materials. These AXOS preparations obtained by the arabinoxylanase are unique prebiotics in their AXOS composition and lack of xylose and XOS. Comparison with state of the art xylanases used to make prebiotics from AX clearly show the difference in hydrolysis products obtained (
In the first example AXOS are generated from endosperm (flour) AX from but not limited to wheat and rye. The endosperm AX is optionally enzymatically treated with arabinofuranosidases to remove a fraction of the Araf groups in order to improve the yield of AXOS. Pure AXOS generated from endosperm AX is shown in
Further was the impact of the arabinose content in the AX substrate determined for the generation of AXOS by an arabinoxylanase. The highest yield of AXOS obtained from AX was achieved using an A/X of 0.43 (
Another application of the technology is demonstrated in improved generation of AXOS in mixtures containing both XOS and AXOS. By adding an arabinoxylanse to an (A)XOS mixture from a family 11 xylanase new AXOS are formed by degrading poly- and oligosaccharides not hydrolysed by the family 11 xylanase (
In the second example wheat bran is used as a substrate to make different fractions of AX suitable for making AXOS by an arabinoxylanase. The fractions are isolated from bran material by first removing starch and proteins followed by an extraction of the AX components from the bran material. The AX is then subsequently treated enzymatically with an arabinofuranosidase, or acid treated to obtain fractions with different A/X ratios (Table 3) that could be used to make different AXOS compositions using an arabinoxylanase.
In the third example it is demonstrated that the obtained AXOS can be used to selectively stimulate the growth of bifidobacteria over other groups of intestinal bacteria that normally can use xylose or XOS (
Representative strains from cluster II-V are but not limited to the following strains of bifidobacteria:
Especially strains belonging to cluster 4 and 5, are able to efficiently utilize the entire AXOS and are of special interest to combine with the obtained AXOS. However, all bifidobacteria, able to cleave the arabinose substituents present on AXOS or utilize the entire AXOS, are possible to stimulate.
Arabinoxylanase from Clostridium thermocellum (CtXyl5A) was purchased from Nzytech (Lisboa, Portugal). A family 10 xylanase from Rhodothermus marinus (RmXyn10A) was prepared as described in Falck et al. (2013). Pentopan mono bg, a commercial family 11 xylanase was obtained from Novozymes (Bagsvaerd, Denmark). High purity recombinant α-L-arabinofuranosidase (E-ABFCJ) from Cellvibrio japonicus was purchased from Megazyme (Wicklow Ireland). Endosperm AX extracted by alkali from wheat (P-WAXYM, P-EDWAX30, P-ADWAX26, P-ADWAX22) and rye (P-RAXY) were purchase from Megazyme. AX substrates were dissolved 10 g/L according to manufactures instructions in 50 mL MQ water and the pH was adjusted to 7 with 8M HCl. Arabinoxylanase from family 5 and xylanases from family 10 and 11 were added at an enzyme to substrate ratio of 1:1000 on a mass basis. In the arabinoxylanase reactions 2 mM CaCl2 was used to stabilize the enzyme. All reactions were performed at 50° C. for 24 h using either a thermoblock or water bath. Enzymes were inactivated by incubating the sample at 95° C. for 30 minutes.
The comparison between the arabinoxylanase and family 10 and 11 xylanases (
The relation between arabinose content and the yield of arabinoxylanase generated AXOS was determined using wheat endosperm with different arabinose content. P-WAXYM, P-EDWAX30, P-ADWAX26 and P-ADWAX22 with an arabinose content of 38%, 30%, 26% and 22% percent respectively or based on A/X 0.61, 0.43, 0.35 and 0.28 respectively (
Analysis of the obtained AXOS fractions and XOS backbones was done by High-Performance Anion-Exchange Chromatography Coupled with Pulsed Electrochemical Detection (HPAEC-PAD) using (ICS-5000) using a CarboPac PA200 column (250 mm×3 mm, 5.5 μm) and a guard column (50 mm×3 mm) of the same material and a mobile phase of 100 mM NaOH at 0.5 mL/min and a linear gradient (0-30 min) of 0-120 mM of sodium acetate (Sigma). Monosaccharide and xylooligosaccharide standards used were as follows: arabinose and xylose (Sigma), xylobiose, xylotriose, xylotetraose, xylopentaose and xylohexaose (Megazyme). All samples were filtered through a 0.22 μm filter and diluted to a final concentration of 0.2 g/L before analysis.
Commercial wheat bran (Lantmännen Mill Malmö, Sweden) was used as starting material for the preparation of AX with different arabinose content defined as A/X. A suspension (1:9 w/v) of 250 g wheat bran in 2.5 L DI water was adjusted to pH 6.0 with HCl 8 M and treated with a thermostable α-amylase 0.12 U/g (Thermamyl, SIGMA-ALDRICH) for 90 min at 90° C. to hydrolyse the starch. The bran was then rinsed with hot tap water to remove solubles until a clear permeate was obtained. A new suspension in water (1:9 w/v) was prepared to remove proteins by incubating with a protease 0.035 U/g (Neutralse 0.8 L, SIGMA-ALDRICH) for 4 h at 50° C. Thereafter the bran was rinsed with hot tap water, then with DI water and then vacuum dried. Destarched and deproteinised wheat bran was extracted with a dilute alkaline solution (NaOH) of hydrogen peroxide containing 2% hydrogen peroxide at pH 11.5 for 4 h at 60° C. under 200 rpm stirring to obtain soluble AX. Antifoam TRITON X-100 was added to reduce foaming. After the extraction solids were removed by filtration and the solution was centrifuged (SIGMA) 6000 g for 20 min. The supernatant was neutralized with 8 M HCl and horseradish peroxidase was added to remove remaining hydrogen peroxide. The extract was centrifuged again at 6000 g for 20 minutes. The supernatant was divided and 50 mL was adjusted to pH 6 with 8 M HCl and treated with 5 U of an arabinofuranosidase from Bifidobacterium adolescentis (Megazyme, E-AFAM2) by incubating the sample at 37° C. for 24 h. Supernatant was also acid debranched by a weak HCl acid at pH 2.5 at 90° C. on a magnetic plate stirrer at 200 rpm. Samples (50 mL) were removed and neutralized with 1 M NaOH after 3.4, 5.1, 6.8, and 8.6 h. All fractions were desalted by dialysis bags (SpectrumLab, USA) using a 3500 Da Mw cut off. Dialysis was performed in 5 L DI water twice and then all samples were freeze dried.
The monosaccharide composition of the AX fractions were analysed by HPAEC-PAD after hydrolysing the samples with 2 M TFA for 60 min at 110° C. Total arabinoxylan content in the samples were calculated as 0.88 times (% arabinose+% xylose) after subtracting any free arabinose. Analysis of the obtained monosaccharides was done by HPAEC-PAD using a CarboPac PA20 column (250 mm×3 mm, 5.5 μm) and a guard column (30 mm×3 mm) of the same material and a mobile phase of 0.75 mM NaOH at 0.5 mL/min with a post column addition of base of 100 mM at 0.15 mL/min. Monosaccharide (SIGMA) were as follows: arabinose, galactose, glucose and xylose. The resulting A/X fractions obtained are listed in Table 3.
The bacterial strains used to test the fermentability of the obtained AXOS from rye endosperm AX were Bifidobacteria adolescentis (B. adolescentis) ATCC 15703 and Lactobacillus brevis (L. brevis) DSMZ 1269. B. adolescentis, L. brevis, were all pre-cultivated twice using 5 g/L glucose as carbon source. B. adolescentis was inoculated in Bifidobacterium medium at 37° C. and pH 6.8. The medium contained 12.5 g of casein peptone, tryptic digest, 6.25 g of yeast extract, 6.25 g of meat extract, 6.25 g of bacto soytone, 2.5 g of K2PO4, 0.25 g of MgSO4.7 H2O, 0.0625 g of MnSO4.H2O, 6.25 g of NaCl, and 1.25 mL of Tween 80 per litre, respectively. To this solution was added 5 mL of solution with resazurin (25 mg/100 mL) together with 50 mL of salt solution containing 0.25 g of CaCl2.H2O, 0.5 g of MgSO4.7 H2O, 1 g of K2HPO4, 1 g of KH2PO4, 10 g of NaHCO3, and 2 g of NaCl per litre, respectively. The medium was subsequently boiled followed by cooling under N2 gas. Cysteine was added to a concentration of 0.625 g/L and adjusted to pH 6.8 using NaOH. L. brevis was grown anaerobically in MRS broth at pH 6.5 under anaerobic condition at 37° C. All media for the cultivation experiments, broth as well as agar, were autoclaved at 121° C. for 15 min. All cultivation media used for anaerobic growth were deaerated by replacing the oxygen in the anaerobic tubes with nitrogen gas. Then, all tubes were closed with metal caps and autoclaved at 121° C. for 15 min. The respective carbon sources glucose and AXOS were filter sterilized through a 0.45 μm filter and added to the media at a final concentration of 5 g/L and a total volume of 5 mL. The fermentation experiment started from the second pre-culture using 2% vol./vol. inoculum and samples were withdrawn after 24 and 48 h. Optical density and pH was measured after 0, 24 and 48 h, while consumption of oligosaccharides was analysed after 48 hours using HPAEC-PAD with the same conditions as described for the oligosaccharide analysis. B. adolescentis could grow on the arabinoxylanase AXOS produced from rye endosperm AX while L. brevis could not due to the fact that the preparation does not contain any xylose or XOS molecules (
B. adolescentis
L. brevis
| Number | Date | Country | Kind |
|---|---|---|---|
| 1550542-3 | Apr 2015 | SE | national |
| Filing Document | Filing Date | Country | Kind |
|---|---|---|---|
| PCT/SE2016/050377 | 4/29/2016 | WO | 00 |
