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紫霉素对二氢链霉素与细菌核糖体结合的影响。

Effect of viomycin on dihydrostreptomycin binding to bacterial ribosomes.

作者信息

Masuda K, Yamada T

出版信息

Biochim Biophys Acta. 1976 Jul 16;435(4):333-9. doi: 10.1016/0005-2787(76)90199-4.

Abstract

Viomycin, a peptide antibiotic, reduced the amounts of dihydrostreptomycin bound to ribosomes of Myobacterium smegmatis and Escherichia coli, although they have different modes of action. The [3H]dihydrostreptomycin binding to ribosomes could not exchanged with streptomycin or dihydrostreptomycin, but not with unrelated antibiotics, namely, kanamycin, neomycin, spectinomycin, capreomycin, tuberactinomycin-N, chloramphenicol and erythromycin. We suggest that there is a significant interaction between the binding sites of viomycin and streptomycin on ribosomes.

摘要

紫霉素是一种肽类抗生素,尽管其作用方式不同,但它能减少与耻垢分枝杆菌和大肠杆菌核糖体结合的二氢链霉素的量。与核糖体结合的[3H]二氢链霉素不能被链霉素或二氢链霉素置换,但不能被无关抗生素(即卡那霉素、新霉素、壮观霉素、卷曲霉素、结核放线菌素 -N、氯霉素和红霉素)置换。我们认为紫霉素和链霉素在核糖体上的结合位点之间存在显著相互作用。

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