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植物乳杆菌隐秘质粒 pD403 的特性及其复制子为基础的穿梭载体的构建。

Characterization of a cryptic plasmid pD403 from Lactobacillus plantarum and construction of shuttle vectors based on its replicon.

机构信息

State Key Laboratory of Microbial Technology, Shandong University, Jinan, China.

出版信息

Mol Biotechnol. 2010 May;45(1):24-33. doi: 10.1007/s12033-010-9242-0.

Abstract

A cryptic plasmid pD403 was isolated from Lactobacillus plantarum D403 derived from fermented dairy products. It was 2,791 bp in size with a G+C content of 37%. Nucleotide sequence analysis revealed two open reading frames, orf1 and orf2. ORF1 (318 amino acids) was identified as a replication protein (RepA). ORF2 (137 amino acids) shared 31% similarity with the transcriptional regulator of Ralstonia pickettii 12D. Functional investigation indicated that ORF2 (Tra) had the ability of improving the transformation efficiency. The origin of replication was predicted, suggesting that pD403 was a rolling-circle-replication (RCR) plasmid. An Escherichia coli/Lactobacillus shuttle vector pCD4032 was constructed based on the pD403 replicon, and proved to be successfully transformed into various lactobacilli including Lactobacillus casei, Lactobacillus plantarum, Lactobacillus fermentum, and Lactobacillus brevis. The transformation efficiencies were ranged from 1.3 x 10(2) to 7 x 10(4) transformants per microgram DNA. Furthermore, an expression vector pCD4033 was developed with the promoter of the lactate dehydrogenase from Lactobacillus delbrueckii 11842. The green fluorescent protein (gfp) as a reporter was expressed successfully in various lactobacilli tested, suggesting that the expression vector pCD4033 had the potential to be used as a molecular tool for heterologous gene cloning and expression in lactobacilli.

摘要

从发酵乳制品中分离出植物乳杆菌 D403 的隐秘质粒 pD403。它长 2791bp,G+C 含量为 37%。核苷酸序列分析揭示了两个开放阅读框,orf1 和 orf2。ORF1(318 个氨基酸)被鉴定为复制蛋白(RepA)。ORF2(137 个氨基酸)与 Ralstonia pickettii 12D 的转录调节因子具有 31%的相似性。功能研究表明,ORF2(Tra)具有提高转化效率的能力。复制起点被预测,表明 pD403 是一种滚环复制(RCR)质粒。基于 pD403 复制子构建了大肠杆菌/乳杆菌穿梭载体 pCD4032,并成功证明其转化到包括干酪乳杆菌、植物乳杆菌、发酵乳杆菌和短乳杆菌在内的各种乳杆菌中。转化效率范围为每微克 DNA 1.3 x 10(2)到 7 x 10(4)个转化体。此外,开发了一种带有 Lactobacillus delbrueckii 11842 乳酸脱氢酶启动子的表达载体 pCD4033。绿色荧光蛋白(gfp)作为报告基因在测试的各种乳杆菌中成功表达,表明表达载体 pCD4033 有可能成为在乳杆菌中进行异源基因克隆和表达的分子工具。

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