2-Naphthoate catabolic pathway in Burkholderia strain JT 1500

被引:18
作者
Morawski, B
Eaton, RW
Rossiter, JT
Sun, GP
Griengl, H
Ribbons, DW
机构
[1] GRAZ TECH UNIV, INST ORGAN CHEM, SFB BIOCATALYSIS, A-8010 GRAZ, AUSTRIA
[2] US EPA, PENSACOLA, FL 32561 USA
[3] UNIV MIAMI, SCH MED, DEPT BIOCHEM, MIAMI, FL 33133 USA
[4] UNIV MIAMI, SCH MED, DEPT MICROBIOL, MIAMI, FL 33133 USA
[5] UNIV LONDON IMPERIAL COLL SCI TECHNOL & MED, CTR BIOTECHNOL, LONDON SW 2AZ, ENGLAND
关键词
D O I
10.1128/jb.179.1.115-121.1997
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
A Burkholderia strain (JT 1500), able to use 2-naphthoate as the sole source of carbon, was isolated from soil. On the basis of growth characteristics, oxygen uptake experiments, enzyme assays, and detection of intermediates, a degradation pathway of 2-naphthoate is proposed. The features of this pathway are convergent with those for phenanthrene. We propose a pathway for the conversion of 2-naphthoate to 1 mol (each) of pyruvate, succinate, and acetyl coenzyme A and 2 mol of CO2. During growth in the presence of 2-naphthoate, six metabolites were detected by thin-layer chromatography, high-performance liquid chromatography, and spectroscopy, 1-Hydroxy-2-naphthoate accumulated in the culture broth during growth on 2-naphthoate. Also, the formation of 2'-carboxybenzalpyruvate, phthalaldehydate, phthalate, protocatechuate, and beta-carboxy-cis,cis-muconic acid was demonstrated. (LR,2S)-cis-1,2-Dihydro-1,2-dihydroxy-2-naphthoate was thus considered an intermediate between 2-naphthoate and 1-hydroxy-2-naphthoate, but it was not transformed by whole cells or their extracts. We conclude that this diol is not responsible for the formation of 1-hydroxy-2-naphthoate from 2-naphthoate but that one of the other three diastereomers is not eliminated as a potential intermediate fora dehydration reaction.
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页码:115 / 121
页数:7
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