Literature DB >> 1892382

Degradation of 2,4,6-trichlorophenol by Azotobacter sp. strain GP1.

D Y Li1, J Eberspächer, B Wagner, J Kuntzer, F Lingens.   

Abstract

A bacterium which utilizes 2,4,6-trichlorophenol (TCP) as a sole source of carbon and energy was isolated from soil. The bacterium, designated strain GP1, was identified as an Azotobacter sp. TCP was the only chlorinated phenol which supported the growth of the bacterium. Resting cells transformed monochlorophenols, 2,6-dichlorophenol, and 2,3,6-trichlorophenol. Phenol and a number of phenolic compounds, including 4-methylphenol, all of the monohydroxybenzoates, and several dihydroxybenzoates, were very good carbon sources for Azotobacter sp. strain GP1. The organism utilized up to 800 mg of TCP per liter; the lag phase and time for degradation, however, were severely prolonged at TCP concentrations above 500 mg/liter. Repeated additions of 200 mg of TCP per liter led to accelerated degradation, with an optimum value of 100 mg of TCP per liter per h. TCP degradation was significantly faster in shaken than in nonshaken cultures. The optimum temperature for degradation was 25 to 30 degrees C. Induction studies, including treatment of the cells with chloramphenicol prior to TCP or phenol addition, revealed that TCP induced TCP degradation but not phenol degradation and that phenol induced only its own utilization. Per mol of TCP, 3 mol of Cl- was released. 2,6-Dichloro-p-benzoquinone was detected in the resting-cell medium of Azotobacter sp. strain GP1. By chemical mutagenesis, mutants blocked in either TCP degradation or phenol degradation were obtained. No mutant defective in the degradation of both phenols was found, indicating separate pathways for the dissimilation of the compounds. In some of the phenol-deficient mutants, pyrocatechol was found to accumulate, and in some of the TCP-deficient mutants, 2,6-dichlorohydroquinone was found to accumulate.

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Year:  1991        PMID: 1892382      PMCID: PMC183500          DOI: 10.1128/aem.57.7.1920-1928.1991

Source DB:  PubMed          Journal:  Appl Environ Microbiol        ISSN: 0099-2240            Impact factor:   4.792


  13 in total

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Authors:  J M Sala-Trepat; W C Evans
Journal:  Eur J Biochem       Date:  1971-06-11

3.  Dissimilation of 2,4-dichlorophenoxyacetic acid by Azotobacter chroococcum.

Authors:  S Balajee; A Mahadevan
Journal:  Xenobiotica       Date:  1990-06       Impact factor: 1.908

4.  Degradation of the chlorinated phenoxyacetate herbicides 2,4-dichlorophenoxyacetic acid and 2,4,5-trichlorophenoxyacetic acid by pure and mixed bacterial cultures.

Authors:  R A Haugland; D J Schlemm; R P Lyons; P R Sferra; A M Chakrabarty
Journal:  Appl Environ Microbiol       Date:  1990-05       Impact factor: 4.792

5.  Utilization and cooxidation of chlorinated phenols by Pseudomonas sp. B 13.

Authors:  H J Knackmuss; M Hellwig
Journal:  Arch Microbiol       Date:  1978-04-27       Impact factor: 2.552

6.  Dechlorination and para-hydroxylation of polychlorinated phenols by Rhodococcus chlorophenolicus.

Authors:  J H Apajalahti; M S Salkinoja-Salonen
Journal:  J Bacteriol       Date:  1987-02       Impact factor: 3.490

7.  Catabolism of pentachlorophenol by a Flavobacterium sp.

Authors:  J G Steiert; R L Crawford
Journal:  Biochem Biophys Res Commun       Date:  1986-12-15       Impact factor: 3.575

8.  Complete dechlorination of tetrachlorohydroquinone by cell extracts of pentachlorophenol-induced Rhodococcus chlorophenolicus.

Authors:  J H Apajalahti; M S Salkinoja-Salonen
Journal:  J Bacteriol       Date:  1987-11       Impact factor: 3.490

9.  Degradation of chlorinated phenols by a pentachlorophenol-degrading bacterium.

Authors:  J G Steiert; J J Pignatello; R L Crawford
Journal:  Appl Environ Microbiol       Date:  1987-05       Impact factor: 4.792

10.  Enzymatic dehalogenation of pentachlorophenol by extracts from Arthrobacter sp. strain ATCC 33790.

Authors:  T Schenk; R Müller; F Mörsberger; M K Otto; F Lingens
Journal:  J Bacteriol       Date:  1989-10       Impact factor: 3.490

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  26 in total

1.  Autoradiographic method for isolation of diverse microbial species with unique catabolic traits.

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Journal:  Appl Environ Microbiol       Date:  1996-11       Impact factor: 4.792

2.  Purification and characterization of 2,6-dichloro-p-hydroquinone chlorohydrolase from Flavobacterium sp. strain ATCC 39723.

Authors:  J Y Lee; L Xun
Journal:  J Bacteriol       Date:  1997-03       Impact factor: 3.490

3.  Purification of hydroxyquinol 1,2-dioxygenase and maleylacetate reductase: the lower pathway of 2,4,5-trichlorophenoxyacetic acid metabolism by Burkholderia cepacia AC1100.

Authors:  D L Daubaras; K Saido; A M Chakrabarty
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4.  Isolation of Pseudomonas pickettii strains that degrade 2,4,6-trichlorophenol and their dechlorination of chlorophenols.

Authors:  H Kiyohara; T Hatta; Y Ogawa; T Kakuda; H Yokoyama; N Takizawa
Journal:  Appl Environ Microbiol       Date:  1992-04       Impact factor: 4.792

5.  A previously unexposed forest soil microbial community degrades high levels of the pollutant 2,4,6-trichlorophenol.

Authors:  M A Sánchez; M Vásquez; B González
Journal:  Appl Environ Microbiol       Date:  2004-12       Impact factor: 4.792

6.  Novel pathway for conversion of chlorohydroxyquinol to maleylacetate in Burkholderia cepacia AC1100.

Authors:  O Zaborina; D L Daubaras; A Zago; L Xun; K Saido; T Klem; D Nikolic; A M Chakrabarty
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7.  Straw compost and bioremediated soil as inocula for the bioremediation of chlorophenol-contaminated soil.

Authors:  M M Laine; K S Jorgensen
Journal:  Appl Environ Microbiol       Date:  1996-05       Impact factor: 4.792

8.  Purification and Characterization of Hydroxyquinol 1,2-Dioxygenase from Azotobacter sp. Strain GP1.

Authors:  M Latus; H Seitz; J Eberspacher; F Lingens
Journal:  Appl Environ Microbiol       Date:  1995-07       Impact factor: 4.792

9.  Monitoring of an Alkaline 2,4,6-Trichlorophenol-Degrading Enrichment Culture by DNA Fingerprinting Methods and Isolation of the Responsible Organism, Haloalkaliphilic Nocardioides sp. Strain M6.

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Journal:  Appl Environ Microbiol       Date:  1997-11       Impact factor: 4.792

10.  Efficient degradation of 2,4,6-Trichlorophenol requires a set of catabolic genes related to tcp genes from Ralstonia eutropha JMP134(pJP4).

Authors:  V Matus; M A Sánchez; M Martínez; B González
Journal:  Appl Environ Microbiol       Date:  2003-12       Impact factor: 4.792

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