4.7 Article

Enzymatically derived aldouronic acids from Cryptomeria japonica arabinoglucuronoxylan

期刊

CARBOHYDRATE POLYMERS
卷 87, 期 2, 页码 1425-1432

出版社

ELSEVIER SCI LTD
DOI: 10.1016/j.carbpol.2011.09.033

关键词

Arabinoglucuronoxylan; Aldouronic acids; NMR spectroscopy; Xylanase; Enzymatic hydrolysis; Ion exchange chromatography; Softwood

资金

  1. Ministry of Education, Culture, Sports, Science and Technology of Japan

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An arabinoglucuronoxylan was extracted from the holocellulose of sugi (Cryptomeria japonica) wood with 10% KOH and subjected to hydrolysis by partially purified xylanase fraction from a commercial cellulase preparation Meicelase. Neutral sugars liberated were analyzed by size exclusion chromatography showing the presence of xylooligosaccharides up to xylohexaose. Aldouronic acids liberated were purified by preparative anion exchange chromatography. Their structures were identified by monosaccharide analysis, comparison of their volume distribution coefficients (Dvs) with those of the authentic samples in anion exchange chromatography and H-1 and C-13 NMR spectroscopy. resulting in the characterization of eight aldouronic acids including acids consisting of two 4-O-Me-alpha-D-GlcAp residues and 3-5 D-Xyl residues. 1. Fr. 1-S1: (aldohexaouronic acid, MeGlcA(3)Xyl(5)), O-beta-Xylp-(1 -> 4)-O-beta-D-Xylp-(1 -> 4)-[O-(4-O-Me-alpha-D-GlcAp)-(1 -> 2)]-O-beta-Xylp-(1 -> 4)-O-beta-D-Xylp-(1 -> 4)-O-beta-D-Xyl 2. Fr. 1-S2: (aldopentaouronic acid, MeGIcA(3)Xyl(4)),O-beta-Xylp-(1 -> 4)-[O-(4-O-Me-alpha-D-GlCAp)-(1 -> 2)]-O-beta-D-Xylp-(1 -> 4)-O-beta-Xylp-(1 -> 4)-D-Xyl 3. Fr. 2-S1: (aldotetraouronic acid, MeGIcA(3)Xyl(3)),O-(4-O-Me-alpha-D-GlcAp)-(1 -> 2)-O-beta-D-Xylp-(1 -> 4)-O-beta-D-Xylp-(1 -> 4)-D-Xyl 4. Fr. 3-S1: (aldotetraouronic acid, GIcA(3)Xyl(3)), O-(alpha-D-GlcAp)-(1 -> 2)-O-beta-D-Xylp-(1 -> 4)-O-beta-Xylp-(1 -> 4)-D-Xyl, 5. Fr. 4-S1: (aldotriouronic acid, GlcA(2)Xyl(2)), O-(4-O-Me-alpha-D-GlcAp)-(1 -> 2)-O-beta-D-Xylp-(1 -> 4)-D-Xyl 6. Fr. 4-S2: (MeGlc(4)MeGlcA(3)Xyl(5)), O-beta-D-xylp-(1 -> 4)-[O-(4-O-Me-alpha-D-GlcAp)]-(1 -> 2)-O-beta-D-Xylp-(1 -> 4)-[O-(4-O-Me-alpha-D-GlcAp)]-(1 -> 2)-O-beta-D-Xylp-(1 -> 4)-O-beta-D-Xylp-(1 -> 4)-D-Xyl 7. Fr. 6-S1: (MeGlcA(4)MeGlcA(3)Xyl(4)), O-(4-O-Me-alpha-D-GlcAp)-(1 -> 2)-O-beta-D-Xylp-(1 -> 4)-O-[(4-O-Me-alpha-D-GlcAp)]-(1 -> 2)-O-beta-D-Xylp-(1 -> 4)-O-beta-D-Xylp-(1 -> 4)-D-Xyl 8. Fr. 7-51 : (MeGlcA(3)MeGlc(2)Xyl(3)), O-(4-O-Me-alpha-D-GlcAp)-(1 -> 2)-O-beta-D-Xylp-(1 -> 4)-O-[(4-O-Me-alpha-D-GlcAp)]-(1 -> 2)-O-beta-D-Xylp-(1 -> 4)-D-Xyl Fr. 4-S2 was a new acidic oligosaccharide. The distribution pattern of these vicinal uronic acid units along the D-xylan chain was discussed. (C) 2011 Elsevier Ltd. All rights reserved.

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