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温和型乳酸乳球菌噬菌体TP901-1的位点特异性整合需要一种类解离酶蛋白。

A resolvase-like protein is required for the site-specific integration of the temperate lactococcal bacteriophage TP901-1.

作者信息

Christiansen B, Brøndsted L, Vogensen F K, Hammer K

机构信息

Department of Microbiology, Technical University of Denmark, Lyngby, Denmark.

出版信息

J Bacteriol. 1996 Sep;178(17):5164-73. doi: 10.1128/jb.178.17.5164-5173.1996.

Abstract

The integration system of the temperate lactococcal phage TP901-1 was characterized in Lactococcus lactis subsp. cremoris LM0230 and MG1363 with the use of deletion derivatives of the integration vector pBC143 (B. Christiansen, M. G. Johnsen, E. Stenby, F. K. Vogensen, and K. Hammer, J. Bacteriol. 176:1069-1076, 1994). The phage-encoded elements necessary for integration were localized on a 2.8-kb NsiI-EcoRI fragment including the phage attachment site, attP. This fragment was DNA sequenced, and sequence analysis revealed three putatively expressed open reading frames, Orf1, Orf2, and Orf3 By the introduction of mutations within the orf1, orf2, and orf3 genes, it was shown that only Orf1 was necessary for the integration process. Furthermore, it was found that Orf1, attP, and a 425-bp region upstream of the orf1 gene are sufficient for integration. Orf1 contains 485 amino acids and is located just upstream of attP. The N-terminal 150 to 180 amino acids of Orf1 showed 38 to 44% similarity to the resolvase group of site-specific integrases, while no similarity to known proteins was found in the C-terminal end. Bacteriophage TP901-1 therefore contains a unique integration system that does not resemble the Int class of site-specific integrases usually found in temperate bacteriophages. The constructed integration vector, pBC170, integrates into the chromosomal attachment site very efficiently and forms stable transformants with a frequency corresponding to 20% of the transformation efficiency.

摘要

利用整合载体pBC143的缺失衍生物(B. 克里斯蒂安森、M. G. 约翰森、E. 斯滕比、F. K. 沃根森和K. 哈默,《细菌学杂志》176:1069 - 1076, 1994年),对温和型乳酸乳球菌噬菌体TP901 - 1的整合系统在乳酸乳球菌乳脂亚种LM0230和MG1363中进行了表征。整合所需的噬菌体编码元件定位在一个2.8 kb的NsiI - EcoRI片段上,该片段包括噬菌体附着位点attP。对该片段进行了DNA测序,序列分析揭示了三个推测表达的开放阅读框,即Orf1、Orf2和Orf3。通过在orf1、orf2和orf3基因内引入突变,结果表明只有Orf1是整合过程所必需的。此外,还发现Orf1、attP和orf1基因上游的一个425 bp区域足以实现整合。Orf1包含485个氨基酸,位于attP的上游。Orf1的N端150至180个氨基酸与位点特异性整合酶的解离酶组显示出38%至44%的相似性,而在C端未发现与已知蛋白质的相似性。因此,噬菌体TP901 - 1包含一个独特的整合系统,该系统与通常在温和噬菌体中发现的Int类位点特异性整合酶不同。构建的整合载体pBC170能非常高效地整合到染色体附着位点,并形成稳定的转化体,其频率相当于转化效率的20%。

相似文献

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Resolvase-like recombination performed by the TP901-1 integrase.由TP901-1整合酶进行的类解离酶重组。
Microbiology (Reading). 2001 Aug;147(Pt 8):2051-2063. doi: 10.1099/00221287-147-8-2051.

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