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大肠杆菌SerB基因的克隆及其在黄色短杆菌中的表达
Cloning of Phosphoserine Aminotransferase (SerB) Gene of Escherichia coli and Expression in Brevibacterium flavum
【摘要】 磷酸丝氨酸转氨酶(Phosphoserine aminotransferase,SerB)是L-丝氨酸生物合成中的关键酶,应用PCR技术从大肠杆菌JM109(E.ColiJM109)中扩增出磷酸丝氨酸转氨酶基因,将其与表达载体pEC 7连接。通过电转化方法,将重组质粒转入黄色短杆菌(Brevibacterium flavumC-11,BfC-11)中,经酶活检测和摇瓶发酵培养,含有重组表达质粒的BfC-11B的磷酸丝氨酸转氨酶的活力和L-丝氨酸产率均比原宿主菌BfC-11有所提高,为构建L-丝氨酸高产基因工程菌的研究奠定了基础。
【Abstract】 Phosphoserine aminotransferase(SerB) is a key enzyme in biosynthesis of L-serine.The SerB gene is obtained from E.coli JM109 by PCR. This gene was inserted into pEC7 and the recombinant plasmids with SerB gene were transformed into Brevibacterium flavum C-11(BfC-11)by the method of electrotransformation and by detecting enzyme activity and the fermentation culture of BfC-11 and BfC-11B.The results showed that the activity of SerB and the yield of L-serine in BfC11B are higher than those in BfC-11.It lays foundations for the research of construction of high L-serine produced gene-engineering strain.
- 【文献出处】 新疆农业科学 ,Xinjiang Agricultural Sciences , 编辑部邮箱 ,2006年02期
- 【分类号】Q78
- 【被引频次】11
- 【下载频次】158