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硫胺素生物合成的调控机制:一个用于研究汇聚途径调控的模型。

The control mechanism of thiamine biosynthesis a model for the study of control of converging pathways.

作者信息

Newell P C, Tucker R G

出版信息

Biochem J. 1966 Aug;100(2):517-24. doi: 10.1042/bj1000517.

Abstract
  1. Thiamine or the pyrimidine moiety of thiamine added in excess to a growing culture of Salmonella typhimurium LT2 repressed subsequent thiamine synthesis in non-growing organisms. 2. A mutant unable to convert added pyrimidine moiety into thiamine was not repressible by the pyrimidine, showing that thiamine, not the pyrimidine, was the repressor. 3. Thiamine repression occurred at 40mmug. of thiamine/mg. dry wt. or above and de-repression occurred at 30mmug. of thiamine/mg. dry wt. or below. 4. Thiamine controlled the pyrimidine and thiazole pathways at the same concentration and to the same extent. 5. Biosynthesis of the thiazole moiety had, in contrast with biosynthesis of the pyrimidine moiety, an additional feedback inhibition control that allowed utilization of the exogenous thiazole. 6. The enzymes joining the pyrimidine and thiazole moieties were repressible by high concentrations of thiamine. 7. Thiamine was rapidly converted into thiamine pyrophosphate and this appeared to be the active repressor. 8. Theoretical aspects of control of converging pathways are discussed.
摘要
  1. 向鼠伤寒沙门氏菌LT2的生长培养物中过量添加硫胺素或硫胺素的嘧啶部分,会抑制非生长状态生物体中后续的硫胺素合成。2. 一个无法将添加的嘧啶部分转化为硫胺素的突变体不受嘧啶的抑制,这表明是硫胺素而非嘧啶是抑制剂。3. 硫胺素抑制在硫胺素含量为40微克/毫克干重及以上时发生,去抑制在硫胺素含量为30微克/毫克干重及以下时发生。4. 硫胺素在相同浓度下以相同程度控制嘧啶和噻唑途径。5. 与嘧啶部分的生物合成相反,噻唑部分的生物合成有额外的反馈抑制控制,使得能够利用外源性噻唑。6. 将嘧啶和噻唑部分连接起来的酶可被高浓度的硫胺素抑制。7. 硫胺素迅速转化为硫胺素焦磷酸,这似乎是活性抑制剂。8. 讨论了汇聚途径控制的理论方面。

相似文献

4
Precursors of the pyrimidine moiety of thiamine.硫胺素嘧啶部分的前体。
Biochem J. 1968 Jan;106(1):271-7. doi: 10.1042/bj1060271.

引用本文的文献

10
Precursors of the pyrimidine moiety of thiamine.硫胺素嘧啶部分的前体。
Biochem J. 1968 Jan;106(1):271-7. doi: 10.1042/bj1060271.

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