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Construction of vectors for inducible gene expression in Lactobacillus sakei and L. plantarum

机译:在日本乳杆菌和植物乳杆菌中可诱导基因表达的载体的构建

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摘要

We have constructed vectors for inducible expression of genes in Lactobacillus sakei and Lactobacillus plantarum. The key elements of these vectors are a regulatable promoter involved in the production of the bacteriocins sakacin A and sakacin P and the genes encoding the cognate histidine protein kinase and response regulator that are necessary to activate this promoter upon induction by a peptide pheromone. The vectors are built up of cassettes that permit easy exchange of all parts through restriction enzyme digestion and ligation. Using beta-glucuronidase as a reporter enzyme, variants of these vectors were compared with each other, and with a corresponding system based on genes involved in the production of nisin. Several of the new vectors permitted tightly controlled and efficient expression of beta-glucuronidase in both L. sakei and L. plantarum. (C) 2003 Federation of European Microbiological Societies. Published by Elsevier B.V. All rights reserved. [References: 33]
机译:我们已经构建了用于在日本乳杆菌和植物乳杆菌中诱导表达基因的载体。这些载体的关键元件是参与细菌素sakacin A和sakacin P的产生的可调节启动子,以及编码同源组氨酸蛋白激酶和应答调节剂的基因,它们是在肽信息素诱导后激活该启动子所必需的。载体由盒组成,该盒允许通过限制酶消化和连接容易地交换所有部分。使用β-葡萄糖醛酸苷酶作为报告酶,将这些载体的变体相互比较,并与基于涉及乳链菌肽产生的基因的相应系统进行了比较。几种新的载体允许在酿酒酵母和植物乳杆菌中严格控制和有效表达β-葡萄糖醛酸苷酶。 (C)2003年欧洲微生物学会联合会。由Elsevier B.V.发布。保留所有权利。 [参考:33]

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