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博来霉素对枯草芽孢杆菌中噬菌体PBS2复制的抑制作用。

Inhibition of bacteriophage PBS2 replication in Bacillus subtilis by phleomycin.

作者信息

Post L, Price A R

出版信息

J Virol. 1975 Feb;15(2):363-71. doi: 10.1128/JVI.15.2.363-371.1975.

Abstract

Phleomycin is an effective inhibitor of the replication of Bacillus subtilis bacteriophage PBS2, whose DNA contains uracil instead of thymine. Phleomycin does not affect the induction of the known phage enzymes involved in deoxyribonucleotide metabolism. But phage DNA synthesis is severely inhibited by phleomycin, and late virion protein synthesis is eliminated. These effects appear to result from a phleomycin-induced degradation of the parental phage DNA. Similar inhibitory and degradative effects on DNA are seen in phleomyinc-treated, uninfected cells. This system is unaffected by the related antibiotic, bleomycin.

摘要

博来霉素是枯草芽孢杆菌噬菌体PBS2复制的有效抑制剂,该噬菌体的DNA含有尿嘧啶而非胸腺嘧啶。博来霉素不影响参与脱氧核糖核苷酸代谢的已知噬菌体酶的诱导。但博来霉素会严重抑制噬菌体DNA合成,并消除晚期病毒粒子蛋白合成。这些效应似乎是由博来霉素诱导的亲本噬菌体DNA降解所致。在经博来霉素处理的未感染细胞中也观察到对DNA的类似抑制和降解作用。该系统不受相关抗生素争光霉素的影响。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/32e9/354461/1f159fd074c2/jvirol00230-0158-a.jpg

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