首页> 外文期刊>Journal of Bioscience and Bioengineering >Heterologous Expression of a Gene Encoding Cholesterol Oxidase in Probiotic Strains of Lactobacillus plantarum and Propionibacterium freudenreichii under the Control of Native Promoters
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Heterologous Expression of a Gene Encoding Cholesterol Oxidase in Probiotic Strains of Lactobacillus plantarum and Propionibacterium freudenreichii under the Control of Native Promoters

机译:天然启动子控制下的植物乳杆菌和费氏丙酸杆菌益生菌中胆固醇氧化酶编码基因的异源表达

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摘要

To develop systems for the expression of heterologous genes in probiotic strains of Lactobacillus and Propionibacterium, we used Lactobacillus plantarum and Propionibacterium freudenreichii and a modified gene encoding cholesterol oxidase (choA) from Streptomyces sp. to generate working models. The acetyl coenzyme A carboxylase (acc) promoter derived from the acc operon of L. plantarum L137 and a previously constructed shuttle vector, pRN14, were used to construct vectors for the expression of heterologous genes in lactic acid bacteria. The concentration of cholesterol oxidase in recombinant L. plantarum carrying choA fused to the NH_2-terminal region of the first open reading frame of the acc operon was 3.6 mU/mg of protein. Using the promoters from Propionibacterium, namely, P4, P8, and P138, which enabled high-level expression of choA in Escherichia coli, and a previously constructed shuttle vector pPK705, we constructed expression vectors for Propionibacterium. In recombinant P. freudenreichii subsp. shermanii IFO12426, the activities of cholesterol oxidase generated under the control of promoters P4, P8, and P138 were 1.6, 4.3, and 7.2 U/mg of protein, respectively. The expression of heterologous genes may facilitate the production of useful proteins in these economically important bacteria.
机译:为了开发在乳杆菌和丙酸杆菌益生菌菌株中表达异源基因的系统,我们使用了植物乳杆菌和弗氏丙酸杆菌以及来自链霉菌属的编码胆固醇氧化酶(choA)的修饰基因。生成工作模型。来源于植物乳杆菌L137的acc操纵子的乙酰辅酶A羧化酶(acc)启动子和先前构建的穿梭载体pRN14被用于构建用于在乳酸菌中表达异源基因的载体。携带choA融合到acc操纵子第一个开放阅读框的NH_2末端区域的重组植物乳杆菌中胆固醇氧化酶的浓度为3.6 mU / mg蛋白质。使用丙酸杆菌的启动子,即能够在大肠杆菌中高效表达choA的P4,P8和P138,以及先前构建的穿梭载体pPK705,我们构建了丙酸杆菌的表达载体。在重组弗氏疟原虫亚种中。 shermanii IFO12426,在启动子P4,P8和P138的控制下产生的胆固醇氧化酶的活性分别为1.6、4.3和7.2 U / mg蛋白质。异源基因的表达可以促进这些经济上重要的细菌中有用蛋白质的产生。

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