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导入脂肪酶基因提高荧光假单胞菌26-2的产酶效率
引用本文:张搏,王青艳. 导入脂肪酶基因提高荧光假单胞菌26-2的产酶效率[J]. 广西科学, 2009, 16(2): 185-187
作者姓名:张搏  王青艳
作者单位:广西科学院,广西南宁,530007;广西科学院,广西南宁,530007
摘    要:采用导入脂肪酶基因的方法对荧光假单胞菌(Pseudomonas fluorescence)26—2的产酶效率进行实验。实验以质粒ppic9k—lipA为模板,通过PCR的方式在26—2脂肪酶基因的两端引入BamHl和EcoR1的酶切位点,并将该基因与大肠杆菌荧光假单胞菌穿梭质粒pDSK 519连接,获得重组质粒pDSK519-lipA,再将重组质粒转入荧光假单胞菌26—2,获得工程菌株P.fluorescence 26—2—1。在相同的发酵条件下,工程菌株的发酵液酶活力比原始菌株的发酵液酶活力提高2倍,实现了荧光假单胞菌脂肪酶基因的同源性表达。

关 键 词:荧光假单胞菌  同源性表达  脂肪酶基因
收稿时间:2008-11-17

Improving the Lipase Production of Pseudomonas fluorescence 26-2 through Transform Its Lipase Gene into the Originally Strain
ZHANG Bo and WANG Qing-yan. Improving the Lipase Production of Pseudomonas fluorescence 26-2 through Transform Its Lipase Gene into the Originally Strain[J]. Guangxi Sciences, 2009, 16(2): 185-187
Authors:ZHANG Bo and WANG Qing-yan
Affiliation:Guangxi Academy of Science;Nanning;Guangxi;530007;China
Abstract:A Pseudomonas fluorescence lipase gene lipA was subcloned from ppic9k-lipA and inserted into vector pDSK519 to construct a new plasmid,pDSK519-lipA,which was transformed into its original strain P.fluorescence 26-2.The recombinant strain 26-2-1 was confirmed by restriction digestion.Compared with wild type 26-2 in pot experiment and ferment experiment,the lipase production of 26-2-1 is 2 times more than its original strain
Keywords:P.fluorescence  homologous expression  lipase gene  
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