Literature DB >> 2268147

Reductive dehalogenation of carbon tetrachloride by Escherichia coli K-12.

C S Criddle1, J T DeWitt, P L McCarty.   

Abstract

The formation of radicals from carbon tetrachloride (CT) is often invoked to explain the product distribution resulting from its transformation. Radicals formed by reduction of CT presumably react with constituents of the surrounding milieu to give the observed product distribution. The patterns of transformation observed in this work were consistent with such a hypothesis. In cultures of Escherichia coli K-12, the pathways and rates of CT transformation were dependent on the electron acceptor condition of the media. Use of oxygen and nitrate as electron acceptors generally prevented CT metabolism. At low oxygen levels (approximately 1%), however, transformation of [14C]CT to 14CO2 and attachment to cell material did occur, in accord with reports of CT fate in mammalian cell cultures. Under fumarate-respiring conditions, [14C]CT was recovered as 14CO2, chloroform, and a nonvolatile fraction. In contrast, fermenting conditions resulted in more chloroform, more cell-bound 14C, and almost no 14CO2. Rates of transformation of CT were faster under fermenting conditions than under fumarate-respiring conditions. Transformation rates also decreased over time, suggesting the gradual exhaustion of transformation activity. This loss was modeled with a simple exponential decay term.

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Year:  1990        PMID: 2268147      PMCID: PMC184937          DOI: 10.1128/aem.56.11.3247-3254.1990

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


  14 in total

Review 1.  Bacterial respiration.

Authors:  B A Haddock; C W Jones
Journal:  Bacteriol Rev       Date:  1977-03

2.  Transformation of carbon tetrachloride by Pseudomonas sp. strain KC under denitrification conditions.

Authors:  C S Criddle; J T DeWitt; D Grbić-Galić; P L McCarty
Journal:  Appl Environ Microbiol       Date:  1990-11       Impact factor: 4.792

3.  A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding.

Authors:  M M Bradford
Journal:  Anal Biochem       Date:  1976-05-07       Impact factor: 3.365

4.  Energy conservation in chemotrophic anaerobic bacteria.

Authors:  R K Thauer; K Jungermann; K Decker
Journal:  Bacteriol Rev       Date:  1977-03

5.  Isolation and initial characterization of glutathione-deficient mutants of Escherichia coli K 12.

Authors:  P Apontoweil; W Berends
Journal:  Biochim Biophys Acta       Date:  1975-07-14

6.  Determination of highly volatile organic contaminants in water by the closed-loop gaseous stripping technique followed by thermal desorption of the activated carbon filters.

Authors:  J W Graydon; K Grob; F Zuercher; W Giger
Journal:  J Chromatogr       Date:  1984-03-02

Review 7.  The respiratory chains of Escherichia coli.

Authors:  W J Ingledew; R K Poole
Journal:  Microbiol Rev       Date:  1984-09

8.  Kinetics of biotransformation of 1,1,1-trichloroethane by Clostridium sp. strain TCAIIB.

Authors:  R Gälli; P L McCarty
Journal:  Appl Environ Microbiol       Date:  1989-04       Impact factor: 4.792

9.  Effect of O2 tension on the bioactivation and metabolism of aliphatic halides by primary rat-hepatocyte cultures.

Authors:  A B DiRenzo; A J Gandolfi; I G Sipes; K Brendel; J L Byard
Journal:  Xenobiotica       Date:  1984-07       Impact factor: 1.908

10.  Occurrence of glutathione in bacteria.

Authors:  R C Fahey; W C Brown; W B Adams; M B Worsham
Journal:  J Bacteriol       Date:  1978-03       Impact factor: 3.490

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  13 in total

Review 1.  Microbial reductive dehalogenation.

Authors:  W W Mohn; J M Tiedje
Journal:  Microbiol Rev       Date:  1992-09

2.  Transformation of carbon tetrachloride by Pseudomonas sp. strain KC under denitrification conditions.

Authors:  C S Criddle; J T DeWitt; D Grbić-Galić; P L McCarty
Journal:  Appl Environ Microbiol       Date:  1990-11       Impact factor: 4.792

3.  Enhanced biotransformation of carbon tetrachloride by Acetobacterium woodii upon addition of hydroxocobalamin and fructose.

Authors:  S A Hashsham; D L Freedman
Journal:  Appl Environ Microbiol       Date:  1999-10       Impact factor: 4.792

Review 4.  Reductive dehalogenation as a respiratory process.

Authors:  C Holliger; W Schumacher
Journal:  Antonie Van Leeuwenhoek       Date:  1994       Impact factor: 2.271

5.  Methyl-coenzyme M reductase of Methanobacterium thermoautotrophicum delta H catalyzes the reductive dechlorination of 1,2-dichloroethane to ethylene and chloroethane.

Authors:  C Holliger; S W Kengen; G Schraa; A J Stams; A J Zehnder
Journal:  J Bacteriol       Date:  1992-07       Impact factor: 3.490

6.  Isolation and Characterization of a Facultatively Aerobic Bacterium That Reductively Dehalogenates Tetrachloroethene to cis-1,2-Dichloroethene.

Authors:  P K Sharma; P L McCarty
Journal:  Appl Environ Microbiol       Date:  1996-03       Impact factor: 4.792

7.  Effects of medium and trace metals on kinetics of carbon tetrachloride transformation by Pseudomonas sp. strain KC.

Authors:  G M Tatara; M J Dybas; C S Criddle
Journal:  Appl Environ Microbiol       Date:  1993-07       Impact factor: 4.792

Review 8.  Bacterial dehalogenases: biochemistry, genetics, and biotechnological applications.

Authors:  S Fetzner; F Lingens
Journal:  Microbiol Rev       Date:  1994-12

9.  Reductive dechlorination of Tri- and tetrachloroethylenes depends on transition from aerobic to anaerobic conditions.

Authors:  M Kästner
Journal:  Appl Environ Microbiol       Date:  1991-07       Impact factor: 4.792

10.  Involvement of cytochromes in the anaerobic biotransformation of tetrachloromethane by Shewanella putrefaciens 200.

Authors:  F W Picardal; R G Arnold; H Couch; A M Little; M E Smith
Journal:  Appl Environ Microbiol       Date:  1993-11       Impact factor: 4.792

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