Literature DB >> 11208791

p-Hydroxyphenylacetic Acid Metabolism in Pseudomonas putida F6.

K E O'Connor1, B Witholt, W Duetz.   

Abstract

Pseudomonas putida F6 was found to metabolize p-hydroxyphenylacetic acid through 3,4-dihydroxyphenylacetic acid, 3,4-dihydroxymandelic acid, and 3,4-dihydroxybenzaldehyde. Cell extracts of P. putida F6 catalyze the NAD(P)H-independent hydroxylation of p-hydroxyphenylacetic acid to 3,4-dihydroxyphenylacetic acid which is further oxidized to 3,4-dihydroxymandelic acid. Oxidation and decarboxylation of the latter yields 3,4-dihydroxybenzaldehyde. A red-brown color accompanies all of the above enzyme activities and is probably due to the polymerization of quinone-like compounds. 3,4-Dihydroxybenzaldehyde is further metabolized through extradiol ring cleavage.

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Year:  2001        PMID: 11208791      PMCID: PMC94960          DOI: 10.1128/JB.183.3.928-933.2001

Source DB:  PubMed          Journal:  J Bacteriol        ISSN: 0021-9193            Impact factor:   3.490


  28 in total

1.  p-Hydroxyphenylacetate-3-hydroxylase. A two-protein component enzyme.

Authors:  U Arunachalam; V Massey; C S Vaidyanathan
Journal:  J Biol Chem       Date:  1992-12-25       Impact factor: 5.157

2.  Metabolism of p-Cresol by the Fungus Aspergillus fumigatus.

Authors:  K H Jones; P W Trudgill; D J Hopper
Journal:  Appl Environ Microbiol       Date:  1993-04       Impact factor: 4.792

3.  Purification and properties of 4-hydroxyphenylacetic acid 3-hydroxylase from Pseudomonas putida.

Authors:  S G Raju; A V Kamath; C S Vaidyanathan
Journal:  Biochem Biophys Res Commun       Date:  1988-07-29       Impact factor: 3.575

4.  Metabolism of mandelate and related compounds by bacterium NCIB 8250.

Authors:  S I Kennedy; C A Fewson
Journal:  J Gen Microbiol       Date:  1968-09

5.  Mammalian monophenol monooxygenase (tyrosinase): purification, properties, and reactions catalyzed.

Authors:  V J Hearing
Journal:  Methods Enzymol       Date:  1987       Impact factor: 1.600

6.  Metabolic function and properties of 4-hydroxyphenylacetic acid 1-hydroxylase from Pseudomonas acidovorans.

Authors:  W A Hareland; R L Crawford; P J Chapman; S Dagley
Journal:  J Bacteriol       Date:  1975-01       Impact factor: 3.490

7.  Facile oxidative decarboxylation of 3,4-dihydroxyphenylacetic acid catalyzed by copper and manganese ions.

Authors:  I N Mefford; L Kincl; K H Dykstra; J T Simpson; S P Markey; S Dietz; R M Wightman
Journal:  Biochim Biophys Acta       Date:  1996-08-13

8.  Identification of a novel positive regulator of the 4-hydroxyphenylacetate catabolic pathway of Escherichia coli.

Authors:  M A Prieto; J L García
Journal:  Biochem Biophys Res Commun       Date:  1997-03-27       Impact factor: 3.575

9.  Degradation of (+/-)-synephrine by Arthrobacter synephrinum. Oxidation of 3,4-dihydroxyphenylacetate to 2-hydroxy-5-carboxymethyl-muconate semialdehyde.

Authors:  R K Kutty; N A Devi; M Veeraswamy; S Ramesh; P V Rao
Journal:  Biochem J       Date:  1977-10-01       Impact factor: 3.857

10.  Catabolism of aromatic biogenic amines by Pseudomonas aeruginosa PAO1 via meta cleavage of homoprotocatechuic acid.

Authors:  S M Cuskey; R H Olsen
Journal:  J Bacteriol       Date:  1988-01       Impact factor: 3.490

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  1 in total

1.  Furan, phenolic, and heptelidic acid derivatives produced by Aspergillus oryzae.

Authors:  Minji Lee; Jeong-Yong Cho; Yu Geon Lee; Hyoung Jae Lee; Seong-Il Lim; So-Young Lee; Young-Do Nam; Jae-Hak Moon
Journal:  Food Sci Biotechnol       Date:  2016-10-31       Impact factor: 2.391

  1 in total

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