| Autor: |
Tazoe, Masaaki, Ichikawa, Keiko, Hoshino, Tatsuo |
| Zdroj: |
Journal of Biological Chemistry; April 2000, Vol. 275 Issue: 15 p11300-11305, 6p |
| Abstrakt: |
The biosynthetic pathway of pyridoxol (vitamin B6) in Rhizobiumwas clarified by studies on the incorporation of 13C- or 15N-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. |
| Databáze: |
Supplemental Index |
| Externí odkaz: |
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