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Mannanase man23 mutant library construction based on a novel cell-free protein expression system

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成果类型:
期刊论文
作者:
Zhou, Haiyan;Yong, Jie;Gao, Han;Li, Tong;Xiao, Hongshi;...
通讯作者:
Wu, Yongyao
作者机构:
[Zhou, Haiyan; Li, Tong; Wu, Yongyao; Gao, Han; Xiao, Hongshi; Yong, Jie] Hunan Agr Univ, Coll Biosci & Biotechnol, Changsha 410128, Hunan, Peoples R China.
通讯机构:
[Wu, Yongyao] H
Hunan Agr Univ, Coll Biosci & Biotechnol, Changsha 410128, Hunan, Peoples R China.
语种:
英文
关键词:
bacterial protein;beta mannosidase;Bacillus subtilis;chemistry;enzyme stability;enzymology;gene expression;gene library;genetics;kinetics;metabolism;molecular cloning;pH;temperature;Bacillus subtilis;Bacterial Proteins;beta-Mannosidase;Cloning, Molecular;Enzyme Stability;Gene Expression;Gene Library;Hydrogen-Ion Concentration;Kinetics;Temperature
期刊:
Journal of the Science of Food and Agriculture
ISSN:
0022-5142
年:
2017
卷:
97
期:
7
页码:
2199-2204
基金类别:
This work was supported by the Natural Science Foundation of China (31401637) and Science Funding of The Education Department of Hunan Province (15K062). The funders had no role in the study design, data collection and analysis, decision to publish or preparation of the manuscript.
机构署名:
本校为第一且通讯机构
院系归属:
生物科学技术学院
摘要:
BACKGROUND: Mannanases are important enzymes which are widely used as a tool in agriculture and food industries. To improve the performance of mannanase Man23, a mutant library was created with rational design, and mutations were introduced on loops around the catalytic region. The Brevibacillus brevis B16 cell-free system which was created in this experiment provided the ability to express the mutant library efficiently. The activities of mutants were measured with a multi-volume spectrophotometer. RESULTS: The mutant Man1606 gained from this ...

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