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展青霉素在大肠杆菌中的DNA损伤活性。

DNA-damaging activity of patulin in Escherichia coli.

作者信息

Lee K S, Röschenthaler R J

出版信息

Appl Environ Microbiol. 1986 Nov;52(5):1046-54. doi: 10.1128/aem.52.5.1046-1054.1986.

Abstract

At a concentration of 10 micrograms/ml, patulin caused single-strand DNA breaks in living cells of Escherichia coli. At 50 micrograms/ml, double-strand breaks were observed also. Single-strand breaks were repaired in the presence of 10 micrograms of patulin per ml within 90 min when the cells were incubated at 37 degrees C in M9-salts solution without a carbon source. The same concentration also induced temperature-sensitive lambda prophage and a prophage of Bacillus megaterium. When an in vitro system with permeabilized Escherichia coli cells was used, patulin at 10 micrograms/ml induced DNA repair synthesis and inhibited DNA replication. The in vivo occurrence of DNA strand breaks and DNA repair correlated with the in vitro induction of repair synthesis. In vitro the RNA synthesis was less affected, and overall protein synthesis was not inhibited at 10 micrograms/ml. Only at higher concentrations (250 to 500 micrograms/ml) was inhibition of in vitro protein synthesis observed. Thus, patulin must be regarded as a mycotoxin with selective DNA-damaging activity.

摘要

展青霉素在浓度为10微克/毫升时,可导致大肠杆菌活细胞中的单链DNA断裂。在50微克/毫升时,也可观察到双链断裂。当细胞在不含碳源的M9盐溶液中于37℃孵育时,每毫升含10微克展青霉素的情况下,单链断裂在90分钟内得到修复。相同浓度还诱导了温度敏感型λ原噬菌体和巨大芽孢杆菌的一种原噬菌体。当使用通透化大肠杆菌细胞的体外系统时,10微克/毫升的展青霉素诱导DNA修复合成并抑制DNA复制。体内DNA链断裂和DNA修复的发生与体外修复合成的诱导相关。在体外,RNA合成受影响较小,在10微克/毫升时总体蛋白质合成未受抑制。仅在较高浓度(250至500微克/毫升)时才观察到体外蛋白质合成受到抑制。因此,展青霉素必须被视为具有选择性DNA损伤活性的霉菌毒素。

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DNA-damaging activity of patulin in Escherichia coli.展青霉素在大肠杆菌中的DNA损伤活性。
Appl Environ Microbiol. 1986 Nov;52(5):1046-54. doi: 10.1128/aem.52.5.1046-1054.1986.
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