2,4,5-三氨基-6-羟基嘧啶在核黄素生物合成途径中作为中间体的可能性。

Acta vitaminologica et enzymologica Pub Date : 1985-01-01
K Nakajima, Y Yamada, H Mitsuda
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引用次数: 0

摘要

用高黄酮类发酵剂灰石霉静息细胞研究了2,4,5-三氨基-6-羟基嘧啶(THP)是否为核黄素生物合成早期途径的中间体。少量THP强烈抑制静息细胞中核黄素的形成,但这种抑制作用被添加嘌呤(腺嘌呤除外)有效逆转。放射性示踪实验表明,[2-14C]THP在核黄素中的放射性掺入可以忽略不计。结果表明,THP不是核黄素形成的中间体,而是一种刚性抑制剂,因此THP在静息细胞中核黄素的生物合成途径中存在非补救性途径。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Possibility of 2,4,5-triamino-6-hydroxypyrimidine as an intermediate in the pathway of riboflavin biosynthesis.

It was studied with resting cells of a high flavinogenic mold, Eremothecium ashbyii, whether or not 2,4,5-triamino-6-hydroxypyrimidine (THP) is an intermediate in the early pathway of riboflavin biosynthesis. A small amounts of THP strongly inhibited riboflavin formation in the resting cells, but the inhibition was effectively reversed by the added purines, except for adenine. Radioactive tracer experiments showed that the incorporation of the radioactivity from [2-14C]THP into riboflavin was negligible. The results obtained strongly suggest that THP is not an intermediate but a rigid inhibitor for riboflavin formation, and thus there is non salvage pathway of THP for the pathway of riboflavin biosynthesis in resting cells of E. ashbyii.

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