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离子螯合剂对大肠杆菌K-12的短暂生长抑制:核糖核酸合成的“体内”抑制

Transient growth inhibition of Escherichia coli K-12 by ion chelators: "in vivo" inhibition of ribonucleic acid synthesis.

作者信息

Collins J J, Alder C R, Fernandez-Pol J A, Court D, Johnson G S

出版信息

J Bacteriol. 1979 Jun;138(3):923-32. doi: 10.1128/jb.138.3.923-932.1979.

Abstract

The ion chelators picolinic acid, quinaldic acid, 1,10-phenanthroline, and 8-hydroxyquinoline, but not ethylenediaminetetraacetate, ethyleneglycol-bis-(beta-aminoethyl ether)-N,N-tetraacetate, or dipicolinic acid, rapidly but transiently arrest growth of Escherichia coli K-12. Cells adapt and become resistant to growth inhibition by these agents, a process which requires protein synthesis. Mn2+, at low concentrations, decreases the time required for resumption of growth. Proteins synthesized during the lag are quantitatively and qualitatively different from those synthesized during normal growth. Inhibition of growth can explained by an effect on RNA polymerase, a known metalloenzyme.

摘要

离子螯合剂吡啶甲酸、喹哪啶酸、1,10-菲咯啉和8-羟基喹啉能迅速但短暂地抑制大肠杆菌K-12的生长,而乙二胺四乙酸、乙二醇双(β-氨基乙醚)-N,N-四乙酸或二吡啶甲酸则不能。细胞会适应并对这些试剂产生生长抑制抗性,这一过程需要蛋白质合成。低浓度的Mn2+会缩短恢复生长所需的时间。停滞期合成的蛋白质在数量和质量上与正常生长期间合成的蛋白质不同。生长抑制可以通过对RNA聚合酶(一种已知的金属酶)的作用来解释。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/89bc/218123/6a183bb9d8c5/jbacter00283-0282-a.jpg

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