| Literature DB >> 10753941 |
M Tazoe1, K Ichikawa, T Hoshino.
Abstract
The biosynthetic pathway of pyridoxol (vitamin B(6)) in Rhizobium was clarified by studies on the incorporation of (13)C- or (15)N-labeled precursors into pyridoxol or its biosynthetic intermediates. Pyridoxol was formed by ring closure of two compounds, 1-deoxy-D-xylulose and 4-hydroxy-L-threonine. The former was formed from D-glyceraldehyde and pyruvate through decarboxylation of pyruvate, and the latter from glycine and glycolaldehyde.Entities:
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Year: 2000 PMID： 10753941 DOI： 10.1074/jbc.275.15.11300
Source DB: PubMed Journal: J Biol Chem ISSN： 0021-9258 Impact factor: 5.157