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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

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【作者】 殷丽霞崔春生简子健谭慧林包慧芳

【Author】 YIN Li-xia~1,CUI Chun-sheng~2,JIAN Zi-jian~1,TAN Hui-lin~2,BAO Hui-fang~2(1.College of Animal Medicine,Xinjiang Agricultural University,Urumqi 830052,China;2.Insitute of Microbiology,Xinjiang Academy of Agricultural Science,Urumqi 830000,China)

【机构】 新疆农业大学动物医学学院新疆农科院微生物所新疆农科院微生物所 新疆乌鲁木齐830052新疆乌鲁木齐830000新疆乌鲁木齐830052

【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.

【关键词】 磷酸丝氨酸转氨酶克隆表达
【Key words】 Phosphoserine aminotransferasecloningexpression
【基金】 国家“十五”重点攻关项目(2004BA713B07-04)
  • 【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
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