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氨曲南及相关单环β-内酰胺类药物与革兰氏阴性菌β-内酰胺酶的相互作用。

Interaction of azthreonam and related monobactams with beta-lactamases from gram-negative bacteria.

作者信息

Bush K, Freudenberger J S, Sykes R B

出版信息

Antimicrob Agents Chemother. 1982 Sep;22(3):414-20. doi: 10.1128/AAC.22.3.414.

Abstract

Monobactams containing 3 beta-aminothiazolyl oxime side chains (SQ 81,377, SQ 81,402, azthreonam, and SQ 26,917) have poor affinities for the broad-spectrum beta-lactamases TEM-2 and K1. Addition of a 4-methyl substituent significantly increased stability to hydrolysis by these enzymes. P99 cephalosporinase from Enterobacter cloacae was strongly inhibited by the monobactams. Interaction of azthreonam with the P99 enzyme in equimolar concentrations resulted in a single covalent complex which retained less than 3% catalytic activity. On incubation, enzymatic activity was slowly regained. Chromatographic studies of the incubation mixtures revealed the presence of a single ring-opened product. It is concluded that monobactams act as poor substrates for broad-spectrum beta-lactamases and tight-binding competitive substrates for the P99 beta-lactamase.

摘要

含有3-β-氨基噻唑肟侧链的单环β-内酰胺类抗生素(SQ 81,377、SQ 81,402、氨曲南和SQ 26,917)对广谱β-内酰胺酶TEM-2和K1的亲和力较差。添加4-甲基取代基可显著提高这些酶对水解的稳定性。阴沟肠杆菌的P99头孢菌素酶受到单环β-内酰胺类抗生素的强烈抑制。等摩尔浓度的氨曲南与P99酶相互作用产生单一的共价复合物,其催化活性保留不到3%。孵育后,酶活性缓慢恢复。对孵育混合物的色谱研究显示存在单一的开环产物。结论是,单环β-内酰胺类抗生素是广谱β-内酰胺酶的不良底物,是P99β-内酰胺酶的紧密结合竞争性底物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ce84/183759/08d34168b0a6/aac00210-0075-a.jpg

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