中国科学院机构知识库网格
Chinese Academy of Sciences Institutional Repositories Grid
Culture and characteristics of recombinant protein production of an Escherichia coli strain expressing carboxylesterase B1

文献类型:会议论文

作者Qiao, C. L. ; Shen, B. C. ; Xing, J. M. ; Huang, J. ; Zhang, J. L. ; Zhao, D. X. ; Yang, B.
出版日期2006
关键词high-density culture E coli carboxylesterase B1 recombinant gene expression HIGH-CELL-DENSITY FED-BATCH CULTURES GROWTH CULTIVATION POLLUTANTS GLUCOSE
期号2
页码77-81
其他题名Int. Biodeterior. Biodegrad.
中文摘要High-density culture was achieved through controlling specific growth rate by limiting glucose concentration to < 0.2gL(-1). Carboxylesterase B I capable of hydrolyzing organophosphate esters was purified from Escherichia coli strain BL21 carrying a cloned esterase B I gene from mosquito. The recombinant strain BL21 carrying pET-ESTB1 was used for the fermentation. Product formation was induced by either a temperature shift from 30 to 42 degrees C or by feeding a mixture of glucose and lactose. Cell growth and production of detoxifying enzyme were affected by oxygen availability. The maximum biomass of E. coli BL21 (pET-ESTB1) increased from 14.9 to 31.5 g dry cell weight l(-1). Using the host strain E. coli BL21 (DE3), detoxifying enzyme was over-expressed at a biomass level of up to 31.5 g dry weight l(-1). The enzyme had a molecular mass of 64 kDa, its optimum temperature was approx. 37 degrees C; at pH 7 the relative activity after 3 h was 85.9% at 28 degrees C, 64.9% at 34 degrees C, and 4.5% at 40 degrees C. The enzyme activity of cells grown at lower temperatures was much higher; at 18 degrees C it almost twice than at 20 or 22 degrees C. degrees 2006 Elsevier Ltd. All rights reserved.
会议网址://WOS:000242779600005
会议录International Biodeterioration & Biodegradation
语种英语
源URL[http://ir.ipe.ac.cn/handle/122111/11205]  
专题过程工程研究所_研究所(批量导入)
推荐引用方式
GB/T 7714
Qiao, C. L.,Shen, B. C.,Xing, J. M.,et al. Culture and characteristics of recombinant protein production of an Escherichia coli strain expressing carboxylesterase B1[C]. 见:.://WOS:000242779600005.

入库方式: OAI收割

来源:过程工程研究所

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