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一种中温淀粉酶在解淀粉芽孢杆菌LT的重组表达
引用本文:邓鑫,刘潇逸,汤尼,王瑞璇,孙俊松,纪明华.一种中温淀粉酶在解淀粉芽孢杆菌LT的重组表达[J].食品工业科技,2018,39(23):117-122.
作者姓名:邓鑫  刘潇逸  汤尼  王瑞璇  孙俊松  纪明华
作者单位:1. 中国科学院上海高等研究院, 绿色化学工程技术研究中心, 上海 201210;2. 中国科学院大学, 北京 100049;3. 上海科技大学生命科学学院, 上海 201210
基金项目:福建省STS合作项目(2018T3021)。
摘    要:解淀粉芽孢杆菌可用作多种食品工业酶的生产菌株,但其极低的转化效率影响了这类工业菌株的重组改造及优化。通过对1398解淀粉芽孢杆菌和一种地衣芽孢杆菌Jbac基因组的数据分析,发现这些微生物存在IV型DNA限制修饰系统。对这些微生物转化经甲基化和未经甲基化的质粒,证实外源DNA甲基化修饰会降低DNA的转化效率;利用将外源质粒进行相同类型甲基化的这种新转化策略,表达质粒pMK4E-dx被转入解淀粉芽孢杆菌LT中,发酵结果显示,其中重组菌株LT-J1/pMK4-dx和LT-J2/pMK4-dx分泌的中温淀粉酶活达到145.9和153.6 U/mL,分别为原菌株发酵淀粉酶活的3.65和3.84倍。

关 键 词:感受态    芽孢杆菌    甲基化    中温淀粉酶
收稿时间:2018-03-09

Recombinant Expression of a Medium-temperature Amylase Production in Bacillus amyloliquefaciens LT
DENG Xin,LIU Xiao-yi,TANG Ni,WANG Rui-xuan,SUN Jun-song,JI Ming-hua.Recombinant Expression of a Medium-temperature Amylase Production in Bacillus amyloliquefaciens LT[J].Science and Technology of Food Industry,2018,39(23):117-122.
Authors:DENG Xin  LIU Xiao-yi  TANG Ni  WANG Rui-xuan  SUN Jun-song  JI Ming-hua
Affiliation:1. Center of Green Chemistry Technology and Enginerring, Shanghai Advanced Research Institute, Chinese Academy of Sciences, Shanghai 201210, China;2. University of Chinese Academy of Science, Beijing 100049, China;3. School of Life Science, Shanghai Tech University, Shanghai 201210, China
Abstract:Bacillus amyloliquefaciens is one of best host cells for production of a wide spectrum of enzymes applied in food industry. However,studies for strain optimization are always difficult due to the low efficiency in transforming foreign DNA into those industrial strains. A novel type IV DNA methylation/restriction system was identified in B. amyloliquefaciens and other close species that was not found in model bacillus strain through genomic data mining,such as B. subtilis 164 or 168. It was confirmed that transformation efficiency of non-methylated DNA was much higher than DNAs purified from E. coli strain with methylation activity. With the optimized vector preparation and transformation protocols,two recombinant B. amyloliquefaciens LT transformants expressing its native medium-temperature amylase were obtained,namely LT-J1 and LT-J2,they produced the enzyme up to 145.9 U/mL and 153.6 U/mL,respectively,more than two times higher than the original strain that does not harbor the expression vector pMK4E-dx.
Keywords:
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