Literature DB >> 1245464

Properties of an inducible uptake system for beta-ketoadipate in Pseudomonas putida.

L N Ornston, D Parke.   

Abstract

Wild-type strains of Pseudomonas putida form an inducible uptake system that appears to act on beta-ketoadipate under normal physiological conditions. The system is induced by beta-ketoadipate and is represented by catabolites derived from it. Adipate is metabolized very slowly by wild-type P. putida cultures; [14C]adipate was used as an analogue of beta-ketoadipate to measure the transport activity in wild-type cells and in cells that constitutively produced the uptake system. Constitutive cells that contained high levels of the uptake system concentrated adipate to a level up to 200-fold above the concentration in the external medium. The process was energy dependent. The activity of the system with radioactive adipate was inhibited by beta-ketoadipate, by beta-ketoadipate analogues, and by some compounds (e.g., acetate, glucose) that are structurally unrelated to beta-ketoadipate; it is not known if the inhibitory effects are exerted directly by the compounds themselves or indirectly by catabolites derived from the compounds. The discovery of the beta-ketoadipate uptake system is surprising in view of earlier studies that had indicated that beta-ketoadipate does not permeate the membrane of wild-type P. putida cells. Contradictions between the former investigations and the present analysis are due primarily to the relatively high concentrations of substrate used in the earlier experiments. The existence of the beta-ketoadipate uptake system indicates that beta-ketoadipate may exist as a selective nutrient in the natural niche of P. putida and may play a determinative role in the evolution of induction mechanisms that are characteristic of fluorescent pseudomonads.

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Year:  1976        PMID: 1245464      PMCID: PMC236106          DOI: 10.1128/jb.125.2.475-488.1976

Source DB:  PubMed          Journal:  J Bacteriol        ISSN: 0021-9193            Impact factor:   3.490


  24 in total

1.  The regulation and properties of the galactose transport system in Escherichia coli K12.

Authors:  D B Wilson
Journal:  J Biol Chem       Date:  1974-01-25       Impact factor: 5.157

2.  Relationships among enzymes of the beta-ketoadipate pathway. II. Properties of crystalline beta-carboxy-cis,cis-muconate-lactonizing enzyme from Pseudomonas putida.

Authors:  R N Patel; R B Meagher; L N Ornston
Journal:  Biochemistry       Date:  1973-08-28       Impact factor: 3.162

3.  Inhibition of beta-galactoside transport by substrates of the glucose transport system in Escherichia coli.

Authors:  H H Winkler; T H Wilson
Journal:  Biochim Biophys Acta       Date:  1967

4.  Evidence for induced synthesis of an active transport factor for mandelate in Pseudomonas putida.

Authors:  S J Higgins; J Mandelstam
Journal:  Biochem J       Date:  1972-02       Impact factor: 3.857

5.  Regulation of the enzymes of the beta-ketoadipate pathway in Moraxella calcoacetica. 2. The role of protocatechuate as inducer.

Authors:  J L Cánovas; M L Wheelis; R Y Stanier
Journal:  Eur J Biochem       Date:  1968-01

6.  Evolutionary significance of metabolic control systems. The beta-ketoadipate pathway provides a case history in bacteria.

Authors:  J L Cánovas; L N Ornston; R Y Stanier
Journal:  Science       Date:  1967-06-30       Impact factor: 47.728

7.  Genetic control of enzyme induction in the -ketoadipate pathway of Pseudomonas putida: deletion mapping of cat mutations.

Authors:  M L Wheelis; L N Ornston
Journal:  J Bacteriol       Date:  1972-02       Impact factor: 3.490

8.  Regulation of the enzymes of the beta-ketoadipate pathway in Moraxella calcoacetica. 1. General aspects.

Authors:  J L Cánovas; R Y Stanier
Journal:  Eur J Biochem       Date:  1967-05

9.  Inducible uptake system for -carboxy-cis, cis-muconate in a permeability mutant of Pseudomonas putida.

Authors:  R B Meagher; G M McCorkle; M K Ornston; L N Ornston
Journal:  J Bacteriol       Date:  1972-08       Impact factor: 3.490

10.  Malate utilization by a group D Streptococcus: regulation of malic enzyme synthesis by an inducible malate permease.

Authors:  J London; E Y Meyer
Journal:  J Bacteriol       Date:  1970-04       Impact factor: 3.490

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  21 in total

Review 1.  Bacteria are not what they eat: that is why they are so diverse.

Authors:  D Parke; D A D'Argenio; L N Ornston
Journal:  J Bacteriol       Date:  2000-01       Impact factor: 3.490

2.  Application of p-Toluidine in Chromogenic Detection of Catechol and Protocatechuate, Diphenolic Intermediates in Catabolism of Aromatic Compounds.

Authors:  D Parke
Journal:  Appl Environ Microbiol       Date:  1992-08       Impact factor: 4.792

3.  Constitutive synthesis of enzymes of the protocatechuate pathway and of the beta-ketoadipate uptake system in mutant strains of Pseudomonas putida.

Authors:  D Parke; L N Ornston
Journal:  J Bacteriol       Date:  1976-04       Impact factor: 3.490

4.  Conservation of PcaQ, a transcriptional activator of pca genes for catabolism of phenolic compounds, in Agrobacterium tumefaciens and Rhizobium species.

Authors:  D Parke
Journal:  J Bacteriol       Date:  1996-06       Impact factor: 3.490

5.  Energy-dependent uptake of 4-chlorobenzoate in the coryneform bacterium NTB-1.

Authors:  P E Groenewegen; A J Driessen; W N Konings; J A de Bont
Journal:  J Bacteriol       Date:  1990-01       Impact factor: 3.490

6.  Nucleotide sequence of the gyrB gene of Pseudomonas putida.

Authors:  R E Parales; C S Harwood
Journal:  Nucleic Acids Res       Date:  1990-10-11       Impact factor: 16.971

7.  Regulation of the pcaIJ genes for aromatic acid degradation in Pseudomonas putida.

Authors:  R E Parales; C S Harwood
Journal:  J Bacteriol       Date:  1993-09       Impact factor: 3.490

8.  Identification of the pcaRKF gene cluster from Pseudomonas putida: involvement in chemotaxis, biodegradation, and transport of 4-hydroxybenzoate.

Authors:  C S Harwood; N N Nichols; M K Kim; J L Ditty; R E Parales
Journal:  J Bacteriol       Date:  1994-11       Impact factor: 3.490

9.  Characterization of the pcaR regulatory gene from Pseudomonas putida, which is required for the complete degradation of p-hydroxybenzoate.

Authors:  S Romero-Steiner; R E Parales; C S Harwood; J E Houghton
Journal:  J Bacteriol       Date:  1994-09       Impact factor: 3.490

10.  Repression of 4-hydroxybenzoate transport and degradation by benzoate: a new layer of regulatory control in the Pseudomonas putida beta-ketoadipate pathway.

Authors:  N N Nichols; C S Harwood
Journal:  J Bacteriol       Date:  1995-12       Impact factor: 3.490

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