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一些作为抑菌和抗生素作用靶点的细菌膜巯基的鉴定与表征。

Identification and characterization of some bacterial membrane sulfhydryl groups which are targets of bacteriostatic and antibiotic action.

作者信息

Morris S L, Walsh R C, Hansen J N

出版信息

J Biol Chem. 1984 Nov 10;259(21):13590-4.

PMID:6436249
Abstract

Covalent modification of sulfhydryl groups which become sensitive toward sulfhydryl agents during germination of Bacillus cereus spores exerts a profound bacteriostatic effect, resulting in outgrowth inhibition. The modified spore components are membrane species of 13,000, 28,000, and 29,000 daltons. Detergent disruption of the membrane inactivated the sulfhydryl groups. A highly sigmoid inhibition curve (n = 11.8) with diamide suggested the participation of closely neighboring sulfhydryl groups. Substate and substrate analogs of the lactose and dicarboxylic acid permeases protected the sulfhydryl groups against modification. Nisin, a 34-residue peptide antibiotic, inhibited spore outgrowth and sulfhydryl modification at a concentration of about 0.1 microM. Since these sulfhydryl groups have been implicated as involved with the bacteriostatic action of nitrite, substances directed toward them may be a useful new class of bacteriostatic agents and antibiotics.

摘要

在蜡样芽孢杆菌孢子萌发过程中,巯基会发生共价修饰,修饰后的巯基对巯基试剂变得敏感,这会产生显著的抑菌作用,导致芽孢生长受到抑制。被修饰的孢子成分是分子量为13,000、28,000和29,000道尔顿的膜蛋白。用去污剂破坏细胞膜会使巯基失活。二酰胺的高度S形抑制曲线(n = 11.8)表明相邻紧密的巯基参与其中。乳糖和二羧酸通透酶的底物及底物类似物可保护巯基不被修饰。乳链菌肽是一种由34个氨基酸残基组成的肽抗生素,在浓度约为0.1微摩尔时可抑制芽孢生长和巯基修饰。由于这些巯基被认为与亚硝酸盐的抑菌作用有关,针对它们的物质可能是一类有用的新型抑菌剂和抗生素。

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