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通过基因融合在耐甲氧西林金黄色葡萄球菌中诱导型青霉素靶蛋白的进化

Evolution of an inducible penicillin-target protein in methicillin-resistant Staphylococcus aureus by gene fusion.

作者信息

Song M D, Wachi M, Doi M, Ishino F, Matsuhashi M

出版信息

FEBS Lett. 1987 Aug 31;221(1):167-71. doi: 10.1016/0014-5793(87)80373-3.

Abstract

A new beta-lactam-inducible penicillin-binding protein (PBP) that has extremely low affinity to penicillin and most other beta-lactam antibiotics has been widely found in highly beta-lactam(methicillin)-resistant Staphylococcus aureus (MRSA). The gene for this protein was sequenced and the nucleotide sequence in its promoter and close upstream area was found to show close similarity with that of staphylococcal penicillinase, while the amino acid sequence over a wide range of the molecule was found to be similar to those of two PBPs of Escherichia coli, the shape-determining protein (PBP 2) and septum-forming one (PBP 3). Probably the MRSA PBP (Mr 76462) evolved by recombination of two genes: an inducible type I penicillinase gene and a PBP gene of a bacterium, causing the formation of a beta-lactam-inducible MRSA PBP.

摘要

一种对青霉素及大多数其他β-内酰胺类抗生素亲和力极低的新型β-内酰胺诱导型青霉素结合蛋白(PBP),已在高度耐β-内酰胺(耐甲氧西林)的金黄色葡萄球菌(MRSA)中广泛发现。对该蛋白的基因进行了测序,发现其启动子及紧邻上游区域的核苷酸序列与葡萄球菌青霉素酶的核苷酸序列极为相似,而在该分子的广泛区域内,氨基酸序列与大肠杆菌的两种PBP相似,即决定形状的蛋白(PBP 2)和形成隔膜的蛋白(PBP 3)。MRSA的PBP(分子量76462)可能是由两个基因重组进化而来:一个诱导型I型青霉素酶基因和一种细菌的PBP基因,从而导致形成β-内酰胺诱导型MRSA PBP。

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