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β-内酰胺类抗生素渗入大肠杆菌、铜绿假单胞菌及其他革兰氏阴性菌的情况。

Permeation of beta-lactam antibiotics into Escherichia coli, Pseudomonas aeruginosa, and other gram-negative bacteria.

作者信息

Livermore D M

机构信息

Department of Medical Microbiology, London Hospital Medical College, United Kingdom.

出版信息

Rev Infect Dis. 1988 Jul-Aug;10(4):691-8. doi: 10.1093/clinids/10.4.691.

Abstract

Cell wall impermeability is a major determinant of the susceptibility of gram-negative bacilli to beta-lactam antibiotics. The outer membrane, which beta-lactam agents cross via pores composed of porin proteins, is the major individual barrier in the wall structure but does not of itself exclude these antibiotics. Rather, it slows their influx to a level that the periplasmic clearance mechanisms may manage to contain. The clearance mechanisms include hydrolysis and perhaps covalent binding by beta-lactamases and nonessential penicillin-binding proteins. The balance between uptake and clearance determines the fate of the cell, rather than one or the other factor alone. It is possible to represent this interplay mathematically for Escherichia coli, but Pseudomonas aeruginosa presents a more ambivalent picture. Moreover, the relations among porin quantity, permeability, and resistance are much better established for E. coli than for P. aeruginosa, and the possible existence of additional barrier layers--besides the outer membrane--in the latter species cannot be excluded.

摘要

细胞壁的不透性是革兰氏阴性杆菌对β-内酰胺类抗生素敏感性的主要决定因素。β-内酰胺类药物通过由孔蛋白构成的孔道穿过外膜,外膜是细胞壁结构中的主要个体屏障,但它本身并不排斥这些抗生素。相反,它会减缓抗生素的流入速度,使周质清除机制能够设法控制其浓度。清除机制包括β-内酰胺酶和非必需青霉素结合蛋白的水解作用,或许还有共价结合作用。摄取和清除之间的平衡决定了细胞的命运,而不是单一因素。对于大肠杆菌,可以用数学方法表示这种相互作用,但铜绿假单胞菌的情况则更为复杂。此外,与铜绿假单胞菌相比,大肠杆菌中孔蛋白数量、通透性和耐药性之间的关系更为明确,并且不能排除后者除了外膜之外还存在其他屏障层的可能性。

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