2,3-Dihydroxybenzoate pathway in Pseudomonas putida. 1H n.m.r. study on the ring-cleavage site
- 15 February 1981
- journal article
- research article
- Published by Portland Press Ltd. in Biochemical Journal
- Vol. 194 (2) , 607-610
- https://doi.org/10.1042/bj1940607
Abstract
Ring cleavage of 2,3-dihydroxybenzoate by cell-free extracts of P. putida leads to 2-hydroxy-6-oxo-(2Z,4E)-hexa-2,4-dienoic acid and CO2. The 1H NMR spectrum of the ring-fission product obtained in a 2H2O solution suggests that the extra-diol cleavage occurs between C-3 and C-4.This publication has 5 references indexed in Scilit:
- 2,3-Dihydroxybenzoate 3,4-oxygenase from Pseudomonas fluorescens—Oxidation of a substrate analogArchives of Biochemistry and Biophysics, 1970
- Formation of 2-hydroxy-6-oxo-2,trans-4,trans-heptadienoic acid from 3-methylcatechol by aPseudomonasCellular and Molecular Life Sciences, 1968
- Metapyrocatechase: a New Catechol-cleaving EnzymeJournal of Biological Chemistry, 1961
- n-Alkane utilization and lipid formation by a Nocardia.1960
- New Pathways in the Oxidative Metabolism of Aromatic Compounds by Micro-OrganismsNature, 1960