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维生素B6的生源论解剖学。大肠杆菌中吡哆醇生物合成的13C核磁共振研究。

The biogenetic anatomy of vitamin B6. A 13C NMR investigation of the biosynthesis of pyridoxol in Escherichia coli.

作者信息

Hill R E, Himmeldirk K, Kennedy I A, Pauloski R M, Sayer B G, Wolf E, Spenser I D

机构信息

Department of Pathology, McMaster University, Hamilton, Ontario L8S 4M1, Canada.

出版信息

J Biol Chem. 1996 Nov 29;271(48):30426-35. doi: 10.1074/jbc.271.48.30426.

DOI:10.1074/jbc.271.48.30426
PMID:8940007
Abstract

It is shown by incorporation experiments with 13C bond-labeled substrates, followed by analysis by means of 13C NMR spectroscopy, that two compounds, 1-deoxy-D-xylulose (12) and 4-hydroxy-L-threonine (), serve as precursors of pyridoxol (vitamin B6) (1) in Escherichia coli. Together, these two compounds account for the entire C8N skeleton of the vitamin. 1-Deoxy-D-xylulose supplies the intact C5 unit, C-2',2,3,4,4' of pyridoxol. 4-Hydroxy-L-threonine undergoes decarboxylation in supplying the intact C3N unit, N-1,C-6,5,5'. Both precursors are ultimately derived from glucose. The C5 unit of pyridoxol that is derived from 1-deoxy-D-xylulose originates by union of a triose phosphate (yielding C-3,4,4') with pyruvic acid (which decarboxylates to yield C-2',2). D-Erythroate (11) enters the C3 unit, C-6,5,5', and is therefore an intermediate on the route from glucose into 4-hydroxy-L-threonine.

摘要

通过用(^{13}C)键标记的底物进行掺入实验,随后借助(^{13}C)核磁共振光谱进行分析表明,两种化合物,1-脱氧-D-木酮糖(12)和4-羟基-L-苏氨酸(),是大肠杆菌中吡哆醇(维生素B6)(1)的前体。这两种化合物共同构成了维生素的整个C8N骨架。1-脱氧-D-木酮糖提供了完整的C5单元,即吡哆醇的C-2',2,3,4,4'。4-羟基-L-苏氨酸在提供完整的C3N单元N-1,C-6,5,5'时发生脱羧反应。两种前体最终都来源于葡萄糖。吡哆醇中源自1-脱氧-D-木酮糖的C5单元是由磷酸丙糖(产生C-3,4,4')与丙酮酸(脱羧产生C-2',2)结合而成。D-赤藓糖(11)进入C3单元C-6,5,5',因此是从葡萄糖到4-羟基-L-苏氨酸途径中的中间体。

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