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- W2056643056 abstract "The action of β‐xylosidase from Trichoderma reesei against different substituted xylo‐oligosaccharides was studied. The enzyme cleaved off all unsubstituted xylose units from the non‐reducing end of 1,2‐linked uronic acid substituted xylo‐oligosaccharides. Surprisingly, an l ‐arabinofuranosyl group linked α‐1,3 to the xylopyranosyl ring was found to protect the β‐1,4‐xylosidic linkage before the substituted xylose unit from being cleaved by the β‐xylosidase. Most probably the 1,3‐linked substituent sterically hinders the hydrolysis. According to the results of the present work, β‐xylosidase of T. reesei is not able to remove all unsubstituted xylose units from the non‐reducing end of substituted xylo‐oligosaccharides, as had been believed previously." @default.
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- W2056643056 title "Effect of side groups on the action of β‐xylosidase from <i>Trichoderma reesei</i> against substituted xylo‐oligosaccharides" @default.
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- W2056643056 doi "https://doi.org/10.1016/s0014-5793(96)01313-0" @default.
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