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嗜冷黄杆菌β-甘露聚糖酶生产的优化

Optimization for beta-mannanase production of a psychrophilic bacterium, Flavobacterium sp.

作者信息

Zakaria M M, Ashiuchi M, Yamamoto S, Yagi T

机构信息

Department of Bioresources Science, Faculty of Agriculture, Kochi University, Japan.

出版信息

Biosci Biotechnol Biochem. 1998 Apr;62(4):655-60. doi: 10.1271/bbb.62.655.

Abstract

We found that a psychrophilic bacterium, Flavobacterium sp., characterized in this study, has a beta-mannanase (EC 3.2.1.78) activity in the culture medium. The mannanase activity was the highest in the culture medium, containing 1.0% (w/v) guar gum (as a carbon source), 0.3% (NH4)2SO4 (as a nitrogen source), and 0.06% (w/v) yeast extract, of five-days cultivation at 4 degrees C. No mannanase activity was found in the medium containing a monosaccharide or a disaccharide as a carbon source, although the psychrophile could use them. The enzyme activity was found only when the bacterium was cultured in the medium containing a polysaccharide. The enzyme preparation showed a single activity band on a washed gel of SDS-PAGE. The optimal temperature for the enzyme activity was 35 degrees C. When the reaction was done at 10 degrees C, the enzyme showed 25% of the optimal activity. The beta-mannanase preparation efficiently hydrolyzed guar gum, locust bean gum, and glucomannan as well as beta-mannan.

摘要

我们发现,本研究中鉴定的嗜冷细菌——黄杆菌属(Flavobacterium sp.)在培养基中具有β-甘露聚糖酶(EC 3.2.1.78)活性。在4℃下培养五天的培养基中,甘露聚糖酶活性最高,该培养基含有1.0%(w/v)瓜尔豆胶(作为碳源)、0.3%硫酸铵(作为氮源)和0.06%(w/v)酵母提取物。尽管该嗜冷菌可以利用单糖或双糖作为碳源,但在以单糖或双糖作为碳源的培养基中未发现甘露聚糖酶活性。只有当该细菌在含有多糖的培养基中培养时,才会发现酶活性。该酶制剂在SDS-PAGE洗涤凝胶上显示出单一活性条带。酶活性的最佳温度为35℃。当反应在10℃下进行时,该酶显示出最佳活性的25%。β-甘露聚糖酶制剂能有效水解瓜尔豆胶、刺槐豆胶、葡甘露聚糖以及β-甘露聚糖。

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