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青霉素结合蛋白2和RodA蛋白过量产生导致大肠杆菌细胞膜中肽聚糖合成活性增强。

Peptidoglycan synthetic activities in membranes of Escherichia coli caused by overproduction of penicillin-binding protein 2 and rodA protein.

作者信息

Ishino F, Park W, Tomioka S, Tamaki S, Takase I, Kunugita K, Matsuzawa H, Asoh S, Ohta T, Spratt B G

出版信息

J Biol Chem. 1986 May 25;261(15):7024-31.

PMID:3009484
Abstract

Penicillin-binding protein (PBP)-2 and the RodA protein are known to function in determining the rod shape of Escherichia coli cells. Peptidoglycan biosynthetic reactions that required these two proteins were demonstrated in the membrane fraction prepared from an E. coli strain that overproduced both of these two proteins and which lacked PBP-1B activity (the major peptidoglycan synthetase activity in the normal E. coli membranes). The cross-linked peptidoglycan was synthesized from UDP-N-acetylmuramylpentapeptide and UDP-N-acetylglucosamine in the presence of a high concentration of cefmetazole that inhibited all of PBPs except PBP-2. The peptidoglycan was synthesized via a lipid intermediate and showed up to 30% cross-linking. The cross-linking reaction was strongly inhibited by the amidinopenicillin, mecillinam, and by other beta-lactam antibiotics that have a high affinity for PBP-2, but not by beta-lactams that had very low affinity for PBP-2. The formation of peptidoglycan required the presence of high levels of both PBP-2 and the RodA protein in the membranes, but it is unclear which of the two proteins was primarily responsible for the extension of the glycan chains (transglycosylation). However, the sensitivity of the cross-linking reaction to specific beta-lactam antibiotics strongly suggested that it was catalyzed by PBP-2. The transglycosylase activity of the membranes was sensitive to enramycin and vancomycin and was unusual in being stimulated greatly by a high concentration of a chelating agent.

摘要

已知青霉素结合蛋白(PBP)-2和RodA蛋白在决定大肠杆菌细胞的杆状形态中发挥作用。在从一种大肠杆菌菌株制备的膜组分中证实了需要这两种蛋白的肽聚糖生物合成反应,该菌株过量产生这两种蛋白且缺乏PBP-1B活性(正常大肠杆菌膜中的主要肽聚糖合成酶活性)。在高浓度头孢美唑存在下,交联的肽聚糖由UDP-N-乙酰胞壁酰五肽和UDP-N-乙酰葡糖胺合成,头孢美唑抑制除PBP-2之外的所有青霉素结合蛋白。肽聚糖通过脂质中间体合成,交联率高达30%。交联反应受到脒基青霉素、美西林以及其他对PBP-2具有高亲和力的β-内酰胺抗生素的强烈抑制,但不受对PBP-2亲和力非常低的β-内酰胺的抑制。肽聚糖的形成需要膜中高水平的PBP-2和RodA蛋白,但尚不清楚这两种蛋白中哪一种主要负责聚糖链的延伸(转糖基化)。然而,交联反应对特定β-内酰胺抗生素的敏感性强烈表明它是由PBP-2催化的。膜的转糖基酶活性对恩拉霉素和万古霉素敏感,并且其不同寻常之处在于受到高浓度螯合剂的极大刺激。

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