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鱼类病原菌杀鲑气单胞菌DNA促旋酶gyrA基因的克隆与核苷酸序列分析

Cloning and nucleotide sequence of the DNA gyrase gyrA gene from the fish pathogen Aeromonas salmonicida.

作者信息

Oppegaard H, Sørum H

机构信息

Department of Pharmacology, Microbiology and Food Hygiene, Norwegian College of Veterinary Medicine, Oslo, Norway.

出版信息

Antimicrob Agents Chemother. 1996 May;40(5):1126-33. doi: 10.1128/AAC.40.5.1126.

Abstract

The DNA gyrase gyrA gene from the fish pathogen Aeromonas salmonicida 2148/89 was cloned, and the nucleotide sequence was determined. An open reading frame of 2,766 nucleotides was identified and was found to encode a protein of 922 amino acids with a calculated molecular mass of 101.1 kDa. The derived amino acid sequence shared a high degree of identity with other DNA gyrase A proteins, in particular, with other gram-negative GyrA sequences. When the amino acid sequence of A. salmonicida GyrA was compared with that of Escherichia coli GyrA, a number of conserved residues were present at identical coordinates, including the catalytic Tyr residue at position 122 (Tyr-122) and residues whose substitution confers quinolone resistance, notably, Ser-83, Ala-67, Gly-81, Asp-87, Ala-84, and Gln-106. An intragenic region corresponding to 48 amino acids, which is not present in E. coli or other bacteria, was identified in the C-terminal part of A. salmonicida GyrA. This intragenic region shared sequence identity with various DNA-binding proteins of both prokaryotic and eukaryotic origins.

摘要

对鱼类病原菌杀鲑气单胞菌2148/89的DNA促旋酶gyrA基因进行了克隆,并测定了其核苷酸序列。确定了一个2766个核苷酸的开放阅读框,发现它编码一个由922个氨基酸组成的蛋白质,计算分子量为101.1 kDa。推导的氨基酸序列与其他DNA促旋酶A蛋白具有高度同源性,特别是与其他革兰氏阴性菌的GyrA序列。当将杀鲑气单胞菌GyrA的氨基酸序列与大肠杆菌GyrA的氨基酸序列进行比较时,在相同位置存在许多保守残基,包括位于第122位的催化性酪氨酸残基(Tyr-122)以及其取代会赋予喹诺酮抗性的残基,特别是Ser-83、Ala-67、Gly-81、Asp-87、Ala-84和Gln-106。在杀鲑气单胞菌GyrA的C末端部分鉴定出一个对应于48个氨基酸的基因内区域,该区域在大肠杆菌或其他细菌中不存在。该基因内区域与原核和真核来源的各种DNA结合蛋白具有序列同源性。

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