Literature DB >> 8572717

Degradation of cocaine by a mixed culture of Pseudomonas fluorescens MBER and Comamonas acidovorans MBLF.

D L Lister1, R F Sproulé, A J Britt, C R Lowe, N C Bruce.   

Abstract

A mixed culture that could utilize cocaine as the sole source of carbon and energy for growth was isolated by selective enrichment. The individual microorganisms within this mixed culture were identified as Pseudomonas fluorescens (termed MBER) and Comamonas acidovorans (termed MBLF). Each microorganism was shown to be unable to grow to any appreciable extent on 10 mM cocaine in the absence of the other. C. acidovorans MBLF was found to possess an inducible cocaine esterase which catalyzed the hydrolysis of cocaine to ecgonine methyl ester and benzoate. C. acidovorans was capable of growth on benzoate at concentrations below 5 mM but was unable to metabolize ecgonine methyl ester. P. fluorescens MBER was capable of growth on either benzoate as the sole source of carbon or ecgonine methyl ester as the sole source of carbon and nitrogen. P. fluorescens MBER was found to initiate the degradation of ecgonine methyl ester via ecgonine, pseudoecgonine, and pseudoecgonyl-coenzyme A. Subcellular studies resulted in the identification of an ecgonine methyl esterase, an ecgonine epimerase, and a pseudoecgonyl-coenzyme A synthetase which were induced by growth on ecgonine methyl ester or ecgonine. Further metabolism of the ecgonine moiety is postulated to involve nitrogen debridging, with the production of carbonyl-containing intermediates.

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Year:  1996        PMID: 8572717      PMCID: PMC167777          DOI: 10.1128/aem.62.1.94-99.1996

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


  9 in total

1.  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

2.  Separation of cocaine, some of its metabolites and congeners on glass fibre sheets.

Authors:  A L Misra; R B Pontani; S J Mulé
Journal:  J Chromatogr       Date:  1973-06-27

3.  Fatty acid degradation in Escherichia coli. An inducible acyl-CoA synthetase, the mapping of old-mutations, and the isolation of regulatory mutants.

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Journal:  Eur J Biochem       Date:  1969-02

4.  The isolation and identification of 6-hydroxycyclohepta-1,4-dione as a novel intermediate in the bacterial degradation of atropine.

Authors:  B A Bartholomew; M J Smith; M T Long; P J Darcy; P W Trudgill; D J Hopper
Journal:  Biochem J       Date:  1993-07-01       Impact factor: 3.857

5.  Identification of a cocaine esterase in a strain of Pseudomonas maltophilia.

Authors:  A J Britt; N C Bruce; C R Lowe
Journal:  J Bacteriol       Date:  1992-04       Impact factor: 3.490

6.  The microbial degradation of cyclohexanecarboxylic acid by a beta-oxidation pathway with simultaneous induction to the utilization of benzoate.

Authors:  E R Blakley
Journal:  Can J Microbiol       Date:  1978-07       Impact factor: 2.419

7.  Cocaine as a naturally occurring insecticide.

Authors:  J A Nathanson; E J Hunnicutt; L Kantham; C Scavone
Journal:  Proc Natl Acad Sci U S A       Date:  1993-10-15       Impact factor: 11.205

8.  Tropine dehydrogenase: purification, some properties and an evaluation of its role in the bacterial metabolism of tropine.

Authors:  B A Bartholomew; M J Smith; M T Long; P J Darcy; P W Trudgill; D J Hopper
Journal:  Biochem J       Date:  1995-04-15       Impact factor: 3.857

9.  Estimation of the molecular weights of proteins by Sephadex gel-filtration.

Authors:  P Andrews
Journal:  Biochem J       Date:  1964-05       Impact factor: 3.766

  9 in total
  1 in total

1.  Gene cloning and nucleotide sequencing and properties of a cocaine esterase from Rhodococcus sp. strain MB1.

Authors:  M M Bresler; S J Rosser; A Basran; N C Bruce
Journal:  Appl Environ Microbiol       Date:  2000-03       Impact factor: 4.792

  1 in total

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