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. 1981 Feb 15;194(2):607–610. doi: 10.1042/bj1940607

2,3-Dihydroxybenzoate pathway in Pseudomonas putida. 1H n.m.r. study on the ring-cleavage site.

V Andreoni, L Canonica, E Galli, C Gennari, V Treccani
PMCID: PMC1162785  PMID: 7306005

Abstract

1. Ring cleavage of 2,3-dihydroxybenzoate by cell-free extracts of Pseudomonas putida leads to 2-hydroxy-6-oxo-(2Z,4E)-hexa-2,4-dienoic acid and CO2. 2. The 1H n.m.r. spectrum of the ring-fission product obtained in a 2H2O solution suggests that the extra-diol cleavage occurs between C-3 and C-4.

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Selected References

These references are in PubMed. This may not be the complete list of references from this article.

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