MOYED H S
J Bacteriol. 1964 Oct;88(4):1024-9. doi: 10.1128/jb.88.4.1024-1029.1964.
Moyed, H. S. (Harvard Medical School, Boston, Mass.). Inhibition of the biosynthesis of the pyrimidine portion of thiamine by adenosine. J. Bacteriol. 88:1024-1029. 1964.-The bacteriostatic effects of adenosine and several other purines on Aerobacter aerogenes can be overcome by either thiamine or the pyrimidine portion of thiamine. Adenosine causes almost complete cessation of the synthesis of the pyrimidine and consequently also of thiamine. However, synthesis of deoxyribonucleic acid, ribonucleic acid, and protein persists in the absence of thiamine synthesis until a three-or fourfold increase has occurred, indicating that A. aerogenes has a surplus supply of either thiamine or the pyrimidine. The failure of cells to continue production of the thiazole portion of thiamine when the synthesis of the pyrimidine is blocked indicates that control over the thiazole is exerted by the thiazole itself rather than by the intact thiamine molecule. Bacteria blocked in the synthesis of the pyrimidine either as the result of mutation or because of inhibition by adenosine excrete an intensely fluorescent, but as yet unidentified, compound. The fluorescent compound bears the nutritional relationship to the pyrimidine characteristic of that between an intermediate and an end product: an excess of the pyrimidine prevents its formation, whereas a deficiency of the pyrimidine greatly stimulates its formation. Adenosine inhibition of the synthesis of the pyrimidine is partially relieved by histidine or succinate. It is suggested that these compounds either bypass the blocked reaction or participate in the detoxification of adenosine.
莫耶德,H. S.(哈佛医学院,马萨诸塞州波士顿)。腺苷对硫胺素嘧啶部分生物合成的抑制作用。《细菌学杂志》88:1024 - 1029。1964年。——腺苷和其他几种嘌呤对产气气杆菌的抑菌作用可被硫胺素或硫胺素的嘧啶部分克服。腺苷几乎完全停止嘧啶的合成,因而也停止硫胺素的合成。然而,在没有硫胺素合成的情况下,脱氧核糖核酸、核糖核酸和蛋白质的合成仍持续进行,直到增加了三到四倍,这表明产气气杆菌有过量的硫胺素或嘧啶供应。当嘧啶合成受阻时,细胞无法继续产生硫胺素的噻唑部分,这表明对噻唑的控制是由噻唑本身而非完整的硫胺素分子施加的。由于突变或腺苷抑制而在嘧啶合成中受阻的细菌会分泌一种强烈荧光但尚未鉴定的化合物。这种荧光化合物与嘧啶的营养关系具有中间体与终产物之间的特征:过量的嘧啶会阻止其形成,而嘧啶缺乏则会极大地刺激其形成。组氨酸或琥珀酸盐可部分缓解腺苷对嘧啶合成的抑制作用。有人认为这些化合物要么绕过受阻反应,要么参与腺苷的解毒过程。