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假单胞菌科中外膜蛋白OprF基因的保守性:丁香假单胞菌oprF基因序列

Conservation of the gene for outer membrane protein OprF in the family Pseudomonadaceae: sequence of the Pseudomonas syringae oprF gene.

作者信息

Ullstrom C A, Siehnel R, Woodruff W, Steinbach S, Hancock R E

机构信息

Department of Microbiology, University of British Columbia, Vancouver, Canada.

出版信息

J Bacteriol. 1991 Jan;173(2):768-75. doi: 10.1128/jb.173.2.768-775.1991.

DOI:10.1128/jb.173.2.768-775.1991
PMID:1898935
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC207070/
Abstract

The conservation of the oprF gene for the major outer membrane protein OprF was determined by restriction mapping and Southern blot hybridization with the Pseudomonas aeruginosa oprF gene as a probe. The restriction map was highly conserved among 16 of the 17 serotype strains and 42 clinical isolates of P. aeruginosa. Only the serotype 12 isolate and one clinical isolate showed small differences in restriction pattern. Southern probing of PstI chromosomal digests of 14 species from the family Pseudomonadaceae revealed that only the nine members of rRNA homology group I hybridized with the oprF gene. To reveal the actual extent of homology, the oprF gene and its product were characterized in Pseudomonas syringae. Nine strains of P. syringae from seven different pathovars hybridized with the P. aeruginosa gene to produce five different but related restriction maps. All produced an OprF protein in their outer membranes with the same apparent molecular weight as that of P.aeruginosa OprF. In each case the protein reacted with monoclonal antibody MA4-10 and was similarly heat and 2-mercaptoethanol modifiable. The purified OprF protein of the type strain P. syringae pv. syringae ATCC 19310 reconstituted small channels in lipid bilayer membranes. The oprF gene from this latter strain was cloned and sequenced. Despite the low level of DNA hybridization between P. aeruginosa and P. syringae DNA, the OprF gene was highly conserved between the species with 72% DNA sequence identity and 68% amino acid sequence identity overall. The carboxy terminus-encoding region of P. syringae oprF showed 85 and 33% identity, respectively, with the same regions of the P. aeruginosa oprF and Escherichia coli ompA genes.

摘要

通过限制性酶切图谱分析以及以铜绿假单胞菌oprF基因作为探针进行Southern杂交,确定了主要外膜蛋白OprF的oprF基因的保守性。在17个血清型菌株中的16个以及42株铜绿假单胞菌临床分离株中,限制性酶切图谱高度保守。只有血清型12分离株和1株临床分离株在限制性图谱上显示出微小差异。对假单胞菌科14个物种的PstI染色体消化产物进行Southern杂交检测发现,只有rRNA同源组I的9个成员与oprF基因杂交。为了揭示同源性的实际程度,对丁香假单胞菌中的oprF基因及其产物进行了特性分析。来自7个不同致病型的9株丁香假单胞菌与铜绿假单胞菌基因杂交,产生了5种不同但相关的限制性图谱。所有菌株在外膜中都产生了一种OprF蛋白,其表观分子量与铜绿假单胞菌的OprF相同。在每种情况下,该蛋白都能与单克隆抗体MA4-10发生反应,并且对热和2-巯基乙醇的修饰作用相似。丁香假单胞菌丁香致病变种ATCC 19310的纯化OprF蛋白在脂质双分子层膜中重建了小通道。克隆并测序了后一株菌株的oprF基因。尽管铜绿假单胞菌和丁香假单胞菌的DNA之间的杂交水平较低,但oprF基因在这两个物种之间高度保守,总体DNA序列同一性为72%,氨基酸序列同一性为68%。丁香假单胞菌oprF的羧基末端编码区分别与铜绿假单胞菌oprF和大肠杆菌ompA基因的相同区域显示出85%和33%的同一性。

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