文章基本信息

标题：Diversity in fosfomycin resistance proteins
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作者：Matthew K. Thompson ; Matthew K. Thompson ; Mary E. Keithly 等
期刊名称：Perspectives in Science
印刷版ISSN：2213-0209
电子版ISSN：2213-0209
出版年度：2015
卷号：4
页码：17-23
DOI：10.1016/j.pisc.2014.12.004
语种：English
出版社：Elsevier
摘要：AbstractCertain strains of the soil microorganismStreptomycesproduce an antibiotic, fosfomycin [(1 R,2 S)-epoxypropylphosphonic acid], which is effective against both Gram-positive and Gram-negative pathogens by inhibiting the first committed step in cell-wall biosynthesis. Fosfomycin resistance proteins are metallo-enzymes that are known to inactivate the antibiotic by the addition of nucleophiles such as water, glutathione (GSH),l-cysteine and bacillithiol (BSH) to the oxirane ring of the molecule. Progress in the characterisation of FosB-type fosfomycin resistance proteins found in many Gram-positive organisms has been slow. This paper provides a brief description of the diversity of fosfomycin resistance proteins in general and, more specifically, new data characterising the substrate selectivity, structure, mechanism and metal-ion dependence of FosB enzymes from pathogenic strains ofStaphylococcusandBacillus. These new findings include the high-resolution X-ray diffraction structures of FosB enzymes fromStaphylococcus aureusandBacillus cereusin various liganded states and kinetic data that suggest that Mn(II) and BSH are the preferred divalent cation and thiol substrate for the reaction, respectively. The discovery of the inhibition of the enzyme by Zn(II) led to the determination of a ternary structure of the FosB·Zn(II)·fosfomycin·l-Cys complex which reveals both substrates present in a pose prior to reaction.
关键词：Antibiotic;Fosfomycin resistance;Phosphonate metabolism;Bacillithiol-S-transferase;Diversification of function