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1
The control mechanism of thiamine biosynthesis a model for the study of control of converging pathways.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。
Biochem J. 1966 Aug;100(2):517-24. doi: 10.1042/bj1000517.
2
The de-repression of thiamine biosynthesis by adenosine a tool for investigating this biosynthetic pathway.腺苷对硫胺素生物合成的去抑制作用——一种研究该生物合成途径的工具。
Biochem J. 1966 Aug;100(2):512-6. doi: 10.1042/bj1000512.
3
Biosynthesis of the pyrimidine moiety of thiamine. A new route of pyrimidine biosynthesis involving purine intermediates.硫胺素嘧啶部分的生物合成。一种涉及嘌呤中间体的嘧啶生物合成新途径。
Biochem J. 1968 Jan;106(1):279-87. doi: 10.1042/bj1060279.
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.
5
Thiamine pyrophosphate (TPP) negatively regulates transcription of some thi genes of Salmonella typhimurium.硫胺素焦磷酸(TPP)对鼠伤寒沙门氏菌的一些硫基因转录起负调控作用。
J Bacteriol. 1996 May;178(9):2533-8. doi: 10.1128/jb.178.9.2533-2538.1996.
6
The biosynthesis of the thiazole moiety of thiamine in Salmonella Typhimurium.鼠伤寒沙门氏菌中硫胺素噻唑部分的生物合成。
Biochim Biophys Acta. 1976 Jun 23;437(1):229-37. doi: 10.1016/0304-4165(76)90364-0.
7
Biosynthesis of thiamine: origin of the methyl carbon atom of the pyrimidine moiety in Salmonella typhimurium.硫胺素的生物合成:鼠伤寒沙门氏菌中嘧啶部分甲基碳原子的来源。
Biochem Biophys Res Commun. 1986 Feb 13;134(3):1136-41. doi: 10.1016/0006-291x(86)90369-4.
8
Evidence for a new, oxygen-regulated biosynthetic pathway for the pyrimidine moiety of thiamine in Salmonella typhimurium.鼠伤寒沙门氏菌中硫胺素嘧啶部分新的氧调节生物合成途径的证据。
J Bacteriol. 1992 Mar;174(5):1515-21. doi: 10.1128/jb.174.5.1515-1521.1992.
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The apbE gene encodes a lipoprotein involved in thiamine synthesis in Salmonella typhimurium.apbE基因编码一种参与鼠伤寒沙门氏菌硫胺素合成的脂蛋白。
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The rhodanese domain of ThiI is both necessary and sufficient for synthesis of the thiazole moiety of thiamine in Salmonella enterica.硫辛酰胺域的 ThiI 是合成沙门氏菌硫胺素噻唑部分所必需且充分的。
J Bacteriol. 2011 Sep;193(18):4582-7. doi: 10.1128/JB.05325-11. Epub 2011 Jul 1.

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Alternatives to vitamin B1 uptake revealed with discovery of riboswitches in multiple marine eukaryotic lineages.发现多个海洋真核生物谱系中的核糖开关可作为维生素 B1 摄取的替代物。
ISME J. 2014 Dec;8(12):2517-29. doi: 10.1038/ismej.2014.146. Epub 2014 Aug 29.
2
Metabolic flux in both the purine mononucleotide and histidine biosynthetic pathways can influence synthesis of the hydroxymethyl pyrimidine moiety of thiamine in Salmonella enterica.在肠炎沙门氏菌中,嘌呤单核苷酸和组氨酸生物合成途径中的代谢通量都可能影响硫胺素羟甲基嘧啶部分的合成。
J Bacteriol. 2002 Nov;184(22):6130-7. doi: 10.1128/JB.184.22.6130-6137.2002.
3
Identification and characterization of an operon in Salmonella typhimurium involved in thiamine biosynthesis.鼠伤寒沙门氏菌中参与硫胺素生物合成的一个操纵子的鉴定与表征。
J Bacteriol. 1997 Aug;179(15):4894-900. doi: 10.1128/jb.179.15.4894-4900.1997.
4
Characterization of thiI, a new gene involved in thiazole biosynthesis in Salmonella typhimurium.硫胺素合成酶基因thiI的特性研究,thiI是鼠伤寒沙门氏菌中参与噻唑生物合成的一个新基因。
J Bacteriol. 1997 Jul;179(13):4399-402. doi: 10.1128/jb.179.13.4399-4402.1997.
5
Cytokinin activation of de novo thiamine biosynthesis in tobacco callus cultures.细胞分裂素对烟草愈伤组织培养物中硫胺素从头生物合成的激活作用。
Plant Physiol. 1969 Jun;44(6):866-70. doi: 10.1104/pp.44.6.866.
6
Biosynthesis of thiamine. Incorporation experiments with 14C-labelled substrates and with (15N)glycine in Saccharomyces cerevisiae.硫胺素的生物合成。在酿酒酵母中用14C标记的底物和(15N)甘氨酸进行掺入实验。
Biochem J. 1968 Sep;109(2):161-8. doi: 10.1042/bj1090161.
7
The de-repression of thiamine biosynthesis by adenosine a tool for investigating this biosynthetic pathway.腺苷对硫胺素生物合成的去抑制作用——一种研究该生物合成途径的工具。
Biochem J. 1966 Aug;100(2):512-6. doi: 10.1042/bj1000512.
8
Inhibition by phenylalanine of thiazole biosynthesis in Escherichia coli.苯丙氨酸对大肠杆菌中噻唑生物合成的抑制作用。
J Bacteriol. 1970 Nov;104(2):1014-6. doi: 10.1128/jb.104.2.1014-1016.1970.
9
Biosynthesis of the pyrimidine moiety of thiamine. A new route of pyrimidine biosynthesis involving purine intermediates.硫胺素嘧啶部分的生物合成。一种涉及嘌呤中间体的嘧啶生物合成新途径。
Biochem J. 1968 Jan;106(1):279-87. doi: 10.1042/bj1060279.
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.

本文引用的文献

1
INHIBITION OF THE BIOSYNTHESIS OF THE PYRIMIDINE PORTION OF THIAMINE BY ADENOSINE.腺苷对硫胺素嘧啶部分生物合成的抑制作用。
J Bacteriol. 1964 Oct;88(4):1024-9. doi: 10.1128/jb.88.4.1024-1029.1964.
2
Tetrazolium bioautography.四氮唑生物自显影法。
Appl Microbiol. 1954 Jan;2(1):29-33. doi: 10.1128/am.2.1.29-33.1954.
3
The de-repression of thiamine biosynthesis by adenosine a tool for investigating this biosynthetic pathway.腺苷对硫胺素生物合成的去抑制作用——一种研究该生物合成途径的工具。
Biochem J. 1966 Aug;100(2):512-6. doi: 10.1042/bj1000512.

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.

DOI:10.1042/bj1000517
PMID:5338808
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1265166/
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。