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[对大环内酯类药物的耐药性]

[Resistance to macrolides].

作者信息

Endou K, Nakajima Y

机构信息

Division of Microbiology, Hokkaido College of Pharmacy.

出版信息

Nihon Rinsho. 1997 May;55(5):1238-44.

PMID:9155181
Abstract

Resistance mechanisms to macrolide antibiotics involving lincosamide and streptogramin type B antibiotics were described in bacteria. Phenotype in the resistant microorganism is generally observed as one of two characteristics, i.e., decrease of intracellular macrolide-accumulation and inactivation of the drugs. The former phenotypic resistance results from one of three mechanisms: (1) mono- or di- methylation of a specific adenine residue in 23 S ribosomal RNA and (2) impaired uptake and (3) enhanced efflux of the antibiotics. The latter is caused by one of two mechanisms: (1) degradation of the drugs by a hydrolytic enzyme such as an esterase and (2) drug modification by one of enzymes such as nucleotidyl- and phospho- transferases.

摘要

细菌中涉及林可酰胺类和B型链阳菌素类抗生素的大环内酯类抗生素耐药机制已被描述。耐药微生物的表型通常表现为两种特征之一,即细胞内大环内酯类药物积累减少和药物失活。前一种表型耐药是由三种机制之一引起的:(1)23S核糖体RNA中特定腺嘌呤残基的单甲基化或二甲基化,(2)摄取受损,(3)抗生素外排增强。后一种是由两种机制之一引起的:(1)由水解酶如酯酶降解药物,(2)由核苷酸转移酶和磷酸转移酶等酶之一对药物进行修饰。

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