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[康宁木霉和绿色木霉纤维素酶影响下转糖基化反应的检测]

[Detection of transglycosylation reactions under the influence of Trichoderma koningii and Trichoderma viride cellulase].

作者信息

Maksimov V I

出版信息

Prikl Biokhim Mikrobiol. 1981 Jul-Aug;17(4):563-8.

PMID:7197022
Abstract

The transglycosylation reactions catalyzed by the low molecular weight endo-beta-1,4-glucanase from the cellulase complex of Trichoderma koningii as well as unseparated complexes from Tr. koningii and Tr. viride were investigated. The products obtained from the mixture of cellodextrine (donor, 0.5%) and p-nitrophenyl-beta-D-glucopyranoside (acceptor, 0.4%) with the aid of the above enzymes were analyzed. Transglycosylation products were separated by Sephadex G-15 gel-filtration. In all the three cases the highest molecular weight p-nitrophenyl glycosides of oligosaccharides (with a molecular weight of over 1500) were first synthesized and then hydrolyzed. At the beginning of the reaction the amount of p-nitrophenyl glycosides of oligosaccharides synthesized was greater than that of the reducing groups measured according to Nelson. Addition of p-nitrophenyl-beta-D-glucopyranoside to cellodextrine did not influence the rate with which the latter was hydrolyzed by endoglucanase.

摘要

研究了康宁木霉纤维素酶复合物中的低分子量内切-β-1,4-葡聚糖酶以及康宁木霉和绿色木霉未分离的复合物所催化的转糖基化反应。分析了在上述酶的作用下,从纤维糊精(供体,0.5%)和对硝基苯基-β-D-吡喃葡萄糖苷(受体,0.4%)的混合物中获得的产物。转糖基化产物通过葡聚糖G-15凝胶过滤进行分离。在所有三种情况下,首先合成了分子量最高的低聚糖对硝基苯基糖苷(分子量超过1500),然后进行水解。在反应开始时,合成的低聚糖对硝基苯基糖苷的量大于根据尼尔森法测定的还原基团的量。向纤维糊精中添加对硝基苯基-β-D-吡喃葡萄糖苷不会影响内切葡聚糖酶对后者的水解速率。

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