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通过阻断合成修饰氨基酸的突变株生产与 A54145 相关的新型脂肽类抗生素及 lptJ、lptK 和 lptL 基因功能的确定。

Production of novel lipopeptide antibiotics related to A54145 by Streptomyces fradiae mutants blocked in biosynthesis of modified amino acids and assignment of lptJ, lptK and lptL gene functions.

机构信息

Cubist Pharmaceuticals, Lexington, MA 02421, USA.

出版信息

J Antibiot (Tokyo). 2011 Jan;64(1):79-87. doi: 10.1038/ja.2010.138. Epub 2010 Nov 24.

Abstract

A54145 is a complex of lipopeptide antibiotics produced by Streptomyces fradiae. A54145 factors are structurally related to daptomycin, with four modified amino acids, only one of which is present in daptomycin. We generated three mutants defective in lptJ, lptK or lptL, whose gene products are involved in the formation of hydroxy-Asn(3) (hAsn(3)) and methoxy-Asp(9) (moAsp(9)). Each of the mutants produced novel lipopeptides related to A54145 and the profiles allowed assignment of functions for those genes. We constructed strains carrying different combinations of these genes coupled with a mutation in the lptI gene involved in the biosynthesis of 3-methyl-Glu(12) (3mGlu(12)), and all recombinants produced novel lipopeptides. One of the compounds displayed very good antibacterial activity in the presence of bovine surfactant, which interacts with daptomycin or A54145E to inhibit their antibacterial activities.

摘要

A54145 是由链霉菌 fradiae 产生的脂肽类抗生素复合物。A54145 因子与达托霉素在结构上相关,有四个修饰的氨基酸,而达托霉素中只存在一个。我们生成了三个突变体,它们在 lptJ、lptK 或 lptL 基因产物缺失,这些基因产物参与形成羟基-Asn(3) (hAsn(3))和甲氧基-Asp(9) (moAsp(9))。每个突变体都产生了与 A54145 相关的新型脂肽,这些特征图谱可以确定这些基因的功能。我们构建了携带这些基因不同组合的菌株,并与参与 3-甲基-Glu(12) (3mGlu(12))生物合成的 lptI 基因突变体相连,所有重组体都产生了新型脂肽。其中一种化合物在存在牛表面活性剂的情况下显示出非常好的抗菌活性,牛表面活性剂与达托霉素或 A54145E 相互作用抑制它们的抗菌活性。

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