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在商业制备的培养基中,胸腺嘧啶核苷可逆转甲氧苄啶的抗菌活性。

Reversal of the antimicrobial activity of trimethoprim by thymidine in commercially prepared media.

作者信息

Koch A E, Burchall J J

出版信息

Appl Microbiol. 1971 Nov;22(5):812-7. doi: 10.1128/am.22.5.812-817.1971.

Abstract

The ability of a potent dihydrofolate reductase inhibitor, trimethoprim, to inhibit the growth of Escherichia coli B in vitro is dependent on the composition of the medium in which the cells are grown. The inhibition observed in minimal broth could be partially reversed by the addition of thymidine, ribonucleosides, amino acids, and vitamins. No reversal occurred in the absence of thymidine. In a number of commercially prepared media, the inhibitory activity of trimethoprim correlated inversely with the amount of thymidine found to be present by microbiological assay. The significance of these findings for the routine testing of new, synthetic antibacterial agents is discussed.

摘要

强效二氢叶酸还原酶抑制剂甲氧苄啶在体外抑制大肠杆菌B生长的能力取决于培养细胞所用培养基的成分。在基本肉汤中观察到的抑制作用可通过添加胸苷、核糖核苷、氨基酸和维生素而部分逆转。在没有胸苷的情况下则不会发生逆转。在许多商业制备的培养基中,甲氧苄啶的抑制活性与通过微生物测定法发现的胸苷含量呈负相关。本文讨论了这些发现对新型合成抗菌剂常规测试的意义。

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Initiation of E. coli proteins.大肠杆菌蛋白质的起始
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