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用美西林对大肠杆菌和铜绿假单胞菌进行的体外研究。

In vitro studies with mecillinam on Escherichia coli and Pseudomonas aeruginosa.

作者信息

Richmond M H

出版信息

J Antimicrob Chemother. 1977 Jul;3 Suppl B:29-39. doi: 10.1093/jac/3.suppl_b.29.

Abstract

The ability of a beta-lactam antibiotic to inhibit the growth of Gram-negative bacteria depends on three main properties: ting sites in the bacterial cell; the ability to penetrate through the outer layers of the bacterial envelope to these sites; and the ability to resist destruction by beta-lactamases that may be encountered on the way to the target. This article describes the properties of mecillinam with respect to the last two of these properties. Although able to hydrolyse mecillinam under some conditions, the beta-lactamases present in many Gram-negative species are unlikely to be very effective at protecting the bacteria in vivo because of their relatively low affinity for this penicillin and the good penetrative properties of the antibiotic.

摘要

β-内酰胺类抗生素抑制革兰氏阴性菌生长的能力取决于三个主要特性:在细菌细胞中的作用位点;穿透细菌包膜外层到达这些位点的能力;以及抵抗在到达靶点途中可能遇到的β-内酰胺酶破坏的能力。本文描述了美西林在上述后两个特性方面的性质。尽管许多革兰氏阴性菌中存在的β-内酰胺酶在某些条件下能够水解美西林,但由于它们对这种青霉素的亲和力相对较低以及该抗生素具有良好的穿透特性,因此在体内不太可能非常有效地保护细菌。

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