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Open AccessJournal ArticleDOI

Metabolism of toluene and xylenes by Pseudomonas (putida (arvilla) mt-2: evidence for a new function of the TOL plasmid.

M J Worsey, +1 more
- 01 Oct 1975 - 
- Vol. 124, Iss: 1, pp 7-13
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TLDR
Pseudomonas putida (arvilla) mt-2 carries genes for the catabolism of toluene, m- xylene, and p-xylene on a transmissible plasmid, TOL, suggesting that a single set of nonspecific enzymes is responsible for the dissimilation of the breakdown products of toLUene and m- and p -xylene.
Abstract
Pseudomonas putida (arvilla) mt-2 carries genes for the catabolism of toluene, m-xylene, and p-xylene on a transmissible plasmid, TOL. These compounds are degraded by oxidation of one of the methyl substituents via the corresponding alcohols and aldehydes to benzoate and m- and p-toluates, respectively, which are then further metabolised by the meta pathway, also coded for by the TOL plasmid. The specificities of the benzyl alcohol dehydrogenase and the benzaldehyde dehydrogenase for their three respective substrates are independent of the carbon source used for growth, suggesting that a single set of nonspecific enzymes is responsible for the dissimilation of the breakdown products of toluene and m- and p-xylene. Benzyl alcohol dehydrogenase and benzaldehyde dehydrogenase are coincidently and possible coordinately induced by toluene and the xylenes, and by the corresponding alcohols and aldehydes. They are not induced in cells grown on m-toluate but catechol 2,3-oxygenase can be induced by m-xylene.

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Citations
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A sensitive, viable-colony staining method using Nile red for direct screening of bacteria that accumulate polyhydroxyalkanoic acids and other lipid storage compounds.

TL;DR: The oxazine dye Nile blue A and its fluorescent oxazone form, Nile red, were used to develop a simple and highly sensitive staining method to detect poly(3-hydroxybutyric acid) and other polyhydroxyalkanoic acids (PHAs) directly in growing bacterial colonies.
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Interposon mutagenesis of soil and water bacteria : a family of DNA fragments designed for in vitro insertional mutagenesis of gram-negative bacteria

TL;DR: A series of derivatives of the omega interposon that can be used for in vitro insertional mutagenesis are constructed and insertion of these interposons in the plasmid between the promoter and the catechol 2,3-dioxygenase (C23O) gene dramatically reduced the expression of this enzyme in Escherichia coli.
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Microbial metabolism of polycyclic aromatic hydrocarbons.

TL;DR: Studies on PAH metabolism are entering a new era; biochemical genetic techniques such as gene cloning and transposon mutagenesis will provide new insight into the biochemistry and regulation of PAH degradative pathways.
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Metabolism of sulfur amino acids in Saccharomyces cerevisiae.

TL;DR: The AdoMet-mediated control of the sulfur amino acid pathway illustrates the molecular strategies used by eucaryotic cells to couple gene expression to metabolic changes.
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Molecular and functional analysis of the TOL plasmid pWWO from Pseudomonas putida and cloning of genes for the entire regulated aromatic ring meta cleavage pathway

TL;DR: Evidence is presented that suggests the promoter operator of the meta pathway gene functions less effectively with the RNA polymerase or xylS product of E. coli than with the enzyme or product of P. putida.
References
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Journal ArticleDOI

The Aerobic Pseudomonads a Taxonomic Study

TL;DR: A collection of 267 strains, representing many of the principal biotypes among aerobic pseudomonads, has been subjected to detailed study, with particular emphasis on biochemical, physiological and nutritional characters.
Journal ArticleDOI

Metabolism of benzoate and the methylbenzoates by Pseudomonas putida (arvilla) mt-2: evidence for the existence of a TOL plasmid.

TL;DR: Preliminary results from mutant strains of Pseudomonas putida mt-2 and from a mutant defective in the regulation of the plasmid-carried pathway suggest that the wild type contains two benzoate oxidase systems, one on thePlasmid which is nonspecific in both its catalysis and its induction and one in the chromosome which is more specific to benzoates as substrate and is specifically induced by benzosate.
Journal ArticleDOI

Transmissible Plasmid Coding Early Enzymes of Naphthalene Oxidation in Pseudomonas putida

TL;DR: The capacity of Pseudomonas putida PpG7 to grow on naphthalene, phenotype Nah(+), is lost spontaneously, and the frequency is increased by treatment with mitomycin C, and this character can be transferred to cured or heterologous fluorescent pseudomonads lacking this capacity by conjugation.
Journal ArticleDOI

The meta Cleavage of Catechol by Azotobacter Species

TL;DR: Catechol was metabolized through 2-hydroxymuconic semialdehyde by cell-free extracts of benzoate-grown Azotobacter Strains and the findings described here are discussed in connection with the two previously reported meta cleavage pathways for the oxidation of catechol in Pseudomonas strains.
Journal ArticleDOI

The Conversion of Catechol and Protocatechuate to β-Ketoadipate by Pseudomonas putida IV. REGULATION

TL;DR: Moraxella lwoffii, which degrades protocatechuate and catechol through identical step-reactions, regulates the synthesis of the enzymes mediating these conversions by a different mechanism.
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