Suppr超能文献

丁香假单胞菌对紫外线的抗性:质粒编码的rulAB基因的序列和功能分析

Resistance to ultraviolet light in Pseudomonas syringae: sequence and functional analysis of the plasmid-encoded rulAB genes.

作者信息

Sundin G W, Kidambi S P, Ullrich M, Bender C L

机构信息

Department of Microbiology and Immunology, University of Illinois-Chicago 60612, USA.

出版信息

Gene. 1996 Oct 24;177(1-2):77-81. doi: 10.1016/0378-1119(96)00273-9.

Abstract

The indigenous plasmids, pPSR1 and pPSR5, were each shown to confer resistance to ultraviolet light (UV) in Pseudomonas syringae (Ps) pv. syringae FF5. The UV-resistance (UVR) determinant was subcloned from a cosmid library of pPSR1, and sequence analysis revealed the presence of two ORFs, designated rulAB which are homologous to the Escherichia coli umuDC mutagenic DNA repair systems and other plasmid-encoded UVR operons. Amino acid (aa) alignments indicated that RulAB are most closely related to the RumAB proteins from plasmid R391, sharing 40.5% and 48.6% aa identity with RumA and RumB, respectively. UV sensitivity assays with the cloned rulAB genes indicated that the expression of UVR in Ps required a functional recA gene.

摘要

研究表明,本地质粒pPSR1和pPSR5可使丁香假单胞菌丁香致病变种FF5对紫外线(UV)产生抗性。从pPSR1的黏粒文库中对紫外线抗性(UVR)决定簇进行亚克隆,序列分析显示存在两个开放阅读框(ORF),命名为rulAB,它们与大肠杆菌umuDC诱变DNA修复系统及其他质粒编码的UVR操纵子同源。氨基酸(aa)序列比对表明,RulAB与质粒R391的RumAB蛋白关系最为密切,分别与RumA和RumB共享40.5%和48.6%的氨基酸序列一致性。对克隆的rulAB基因进行的紫外线敏感性测定表明,丁香假单胞菌中UVR的表达需要一个功能性recA基因。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验