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谷氨酸棒状杆菌gdh基因在黄色短杆菌C-11中的克隆及表达
引用本文:王宁,包慧芳,杨慧,王炜.谷氨酸棒状杆菌gdh基因在黄色短杆菌C-11中的克隆及表达[J].新疆农业科学,2011(9):1711-1715.
作者姓名:王宁  包慧芳  杨慧  王炜
作者单位:新疆农业科学院微生物应用研究所;
基金项目:新疆维吾尔自治区高技术研究发展计划(200910102); 新疆维吾尔自治区重大专项(200740147-2); 新疆维吾尔自治区科技支疆项目(201091227); 新疆维吾尔自治区科技基础条件平台建设项目(PT0807)
摘    要:【目的】研究谷氨酸脱氢酶的表达对L-丝氨酸产率及发酵效率的影响。【方法】从谷氨酸棒杆菌模式菌株C.glutamicum ATCC39135中克隆出gdh基因,以大肠杆菌-黄色短杆菌穿梭表达载体pEC7为基础,构建重组质粒pEC7G,并转化黄色短杆菌B.flavum C-11,获得重组菌株C-11G。【结果】重组菌株C-11G的GDH酶活力提高32.7%,产酸率为15.28 g/L,比原宿主菌提高了33.80%。【结论】成功构建重组菌株C-11G,所克隆的gdh基因有较高表达活性,并对L-丝氨酸产量的提高有促进作用。

关 键 词:谷氨酸脱氢酶  pEC7  穿梭表达  电击转化

The Cloning and Expression of gdh Gene from Corynebacterium glutamicum in Brevibacterium flavum C-11
WANG Ning,BAO Hui -Fang,WANG Wei.The Cloning and Expression of gdh Gene from Corynebacterium glutamicum in Brevibacterium flavum C-11[J].Xinjiang Agricultural Sciences,2011(9):1711-1715.
Authors:WANG Ning  BAO Hui -Fang  WANG Wei
Institution:WANG Ning,BAO Hui -Fang,WANG Wei (Research Institute of Applied Microbiology,Xinjiang Academy of Agricultural Sciences,Urumqi 830091,China )
Abstract:Objective]The purpose of this project was to study L - serine production rate and the fermentation efficiency affected by the expression of GDH.Method]The gdh(glutamate dehydrogenase) gene was cloned from Corynebacterium glutamicum ATCC39135 and amplified by PCR.The gdh gene was inserted into E.coli - Brevibacterium flavum shuttle expression vector pEC7 to construct a recombinant plasmid pEC7G, which was subsequently transformed into B.Jlavum C - 11,producing a genetic engineering strain C - 11G. Result]...
Keywords:glutamate dehydrogenase  pEC7  shuttle expression  electroporation  
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