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Open AccessJournal ArticleDOI

p-Cymene pathway in Pseudomonas putida: selective enrichment of defective mutants by using halogenated substrate analogs.

G J Wigmore, +1 more
- 01 Aug 1980 - 
- Vol. 143, Iss: 2, pp 816-824
TLDR
It is suggested that the defective mutants are enriched because of the genetic alterations they possess, which confer immunity to a lethal synthesis performed by transformation of the analogs in clones possessing an intact p-cymene pathway.
Abstract
Several classes of mutants of Pseudomonas putida (JT810) defective in the utilization of p-cymene as sole carbon source have been isolated. Selective enrichment of the mutants and for strains putatively cured of a degradative plasmid was achieved by incubation of cells in minimal growth media containing p-cymene (or p-cumate) and various halogenated analogs of the growth substrates or pathway intermediates. Analogs which led to successful enrichments included: p-chlorotoluene, p-bromotoluene, alpha-chloro-p-xylene, and p-iodobenzoate. A mutant strain, PpJT811, constitutive for the p-cymene pathway gave significantly greater enrichments of defective mutants than the wild-type parent PpJT810 after incubation with the halogenated analogs. It is suggested that the defective mutants are enriched because of the genetic alterations they possess, which confer immunity to a lethal synthesis performed by transformation of the analogs in clones possessing an intact p-cymene pathway. A nomenclature for the genetic organization of p-cymene pathway is described.

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Journal ArticleDOI

Suicide Inactivation of Catechol 2,3-Dioxygenase from Pseudomonas putida mt-2 by 3-Halocatechols

TL;DR: Rates of inactivation by 3-fluorocatechol were reduced in the presence of superoxide dismutase, catalase, formate, and mannitol, which implies that superoxide anion, hydrogen peroxide, and hydroxyl radical exhibit additional inactivation.

Transposon Mutagenesis andCloning Analysis ofthePathways for Degradation of2,4-Dichlorophenoxyacetic Acidand 3-Chlorobenzoate inAlcaligenes eutrophus JMP134(pJP4)

TL;DR: Inactivation of genes tfdC, tfdD, and tfdE, which encode the transformation of dichlorocatechol to chloromaleylacetic acid, prevented host strain JMP134 from degrading both 3-chlorobenzoate and 2,4-dichlorophenoxyacetic Acid, which indicates that the pathways for these two substrates utilize common enzymes for the dissimilation of chlorocatechols.
Journal ArticleDOI

Transposon mutagenesis and cloning analysis of the pathways for degradation of 2,4-dichlorophenoxyacetic acid and 3-chlorobenzoate in Alcaligenes eutrophus JMP134(pJP4).

TL;DR: Pemberton et al. as mentioned in this paper showed that inactivation of genes tfdC, tfdD, and tfdE, which encode the transformation of dichlorocatechol to chloromaleylacetic acid, prevented host strain JMP134 from degrading both 3-chlorobenzoate and 2,4-dichlorophenoxyacetic acids, which indicates that the pathways for these two substrates utilize common enzymes for the dissimilation of chlorocatechols.
Journal ArticleDOI

Inhibition of catechol 2,3-dioxygenase from Pseudomonas putida by 3-chlorocatechol.

TL;DR: Kinetic analyses revealed that 2,3-dioxygenase preparations from toluene-grown cells of Pseudomonas putida catalyzed the stoichiometric oxidation of 3-methylcatechol to 2-hydroxy-6-oxohepta-2,4-dienoate and 3-chlorocatechol were noncompetitive or mixed-type inhibitors of the enzyme.
Journal ArticleDOI

P450BM-3 and other Inducible Bacterial P450 Cytochromes: Biochemistry and Regulation

TL;DR: The catalytically self-sufficient P450BM-3 is currently the only single-component P450-dependent monooxygenase known but additional examples of this arrangement may well be found in other bacteria.
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Journal ArticleDOI

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Journal ArticleDOI

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Journal ArticleDOI

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Journal ArticleDOI

Isolation of the lac repressor

TL;DR: An assay is developed for the lactose repressor, the product of the control gene (i gene) ofThe lactose operon, which detects and quantitates this repressor by measuring its binding to an inducer, as seen by equilibrium dialysis against radioactive IPTG (isopropyl-thio-galactoside).
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