Suppr超能文献

反硝化微球菌中硫胺素焦磷酸的合成途径。

Pathway of thiamine pyrophosphate synthesis in Micrococcus denitrificans.

作者信息

Sanemori H, Egi Y, Kawasaki T

出版信息

J Bacteriol. 1976 Jun;126(3):1030-6. doi: 10.1128/jb.126.3.1030-1036.1976.

Abstract

The pathway of thiamine pyrophosphate (TPP) biosynthesis, which is formed either from exogeneously added thiamine or from the pyrimidine and thiazole moieties of thiamine, in Micrococcus denitrificans was investigated. The following indirect evidence shows that thiamine pyrophosphokinase (EC 2.7.6.2) catalyzes the synthesis of TPP from thiamine: (i) [35S]thiamine incubated with cells of this microorganism was detected in the form of [35S]thiamine; (ii) thiamine gave a much faster rate of TPP synthesis than thiamine monophosphate (TMP) when determined with the extracts; and (iii) a partially purified preparation of the extracts can use thiamine, but not TMP, as the substrate. The activities of the four enzymes involved in TMP synthesis from pyrimidine and thiazole moieties of thiamine were detected in the extracts of M. denitrificans. The extracts contained a high activity of the phosphatase, probably specific for TMP. After M. denitrificans cells were grown on a minimal medium containing 3 mM adenosine, which causes derepression of de novo thiamine biosynthesis in Escherichia coli, the activities of the four enzymes involved with TMP synthesis, the TMP phosphatase, and the thiamine pyrophosphokinase were enhanced two- to threefold. These results indicate that TPP is synthesized directly from thiamine without forming TMP as an intermediate and that de novo synthesis of TPP from the pyrimidine and thiazole moieties involves the formation of TMP, followed by hydrolysis to thiamine, which is then converted to TPP directly. Thus, the pathway of TPP synthesis from TMP synthesized de novo in M. denitrificans is different from that found in E. coli, in which TMP synthesized de novo is converted directly to TPP without producing thiamine.

摘要

研究了反硝化微球菌中硫胺素焦磷酸(TPP)的生物合成途径,该途径可由外源添加的硫胺素或硫胺素的嘧啶和噻唑部分形成。以下间接证据表明硫胺素焦磷酸激酶(EC 2.7.6.2)催化从硫胺素合成TPP:(i)与该微生物细胞一起孵育的[35S]硫胺素以[35S]硫胺素的形式被检测到;(ii)用提取物测定时,硫胺素合成TPP的速率比硫胺素单磷酸(TMP)快得多;(iii)提取物的部分纯化制剂可以使用硫胺素而非TMP作为底物。在反硝化微球菌的提取物中检测到了从硫胺素的嘧啶和噻唑部分合成TMP所涉及的四种酶的活性。提取物中含有高活性的磷酸酶,可能对TMP具有特异性。在反硝化微球菌细胞在含有3 mM腺苷的基本培养基上生长后,这会导致大肠杆菌中硫胺素从头生物合成的去阻遏,参与TMP合成的四种酶、TMP磷酸酶和硫胺素焦磷酸激酶的活性提高了两到三倍。这些结果表明,TPP直接由硫胺素合成,不形成TMP作为中间体,并且从嘧啶和噻唑部分从头合成TPP涉及TMP的形成,随后水解为硫胺素,然后硫胺素直接转化为TPP。因此,反硝化微球菌中从头合成的TMP合成TPP的途径与大肠杆菌中发现的途径不同,在大肠杆菌中,从头合成的TMP直接转化为TPP而不产生硫胺素。

相似文献

2
Enzymic formation of thiamine pyrophosphate in plants.植物中硫胺素焦磷酸的酶促形成。
J Nutr Sci Vitaminol (Tokyo). 1975;21(1):19-26. doi: 10.3177/jnsv.21.19.

本文引用的文献

2
Partial purification and properties of thiaminokinase from yeast.酵母硫胺素激酶的部分纯化及性质
Biochim Biophys Acta. 1952 Mar;8(3):310-24. doi: 10.1016/0006-3002(52)90046-2.
5
The enzymatic synthesis of thiamine monophosphate.
J Biol Chem. 1961 Nov;236:3066-71.
6
Enzymic synthesis of thiamine.硫胺素的酶促合成
Biochim Biophys Acta. 1959 Jul;34:277-9. doi: 10.1016/0006-3002(59)90270-7.

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验