Literature DB >> 8611153

Identification of a multienzyme complex of the tricarboxylic acid cycle enzymes containing citrate synthase isoenzymes from Pseudomonas aeruginosa.

C G Mitchell1.   

Abstract

A multienzyme complex of tricarboxylic acid cycle enzymes, catalysing the consecutive reactions from fumarate to 2-oxoglutarate, has been identified in extracts of Pseudomonas aeruginosa prepared by gentle osmotic lysis of the cells. The individual enzyme activities of fumarase, malate dehydrogenase, citrate synthase, aconitase and isocitrate dehydrogenase can be used to reconstitute the complex. The citrate synthase isoenzymes, CSI and CSII, from this organism can be used either together or as the individual activities to reconstitute the complex. No complex can be reformed in the absence of CSI or CSII. Which CS isoenzyme predominates in the complex depends on the phase of growth at which the cells were harvested and the extract prepared. More CSI was found in the complex during exponential growth, whereas CSII predominated during the stationary phase. The results support the idea of a 'metabolon' in this organism, with the composition of the CS component varying during the growth cycle.

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Year:  1996        PMID: 8611153      PMCID: PMC1216976          DOI: 10.1042/bj3130769

Source DB:  PubMed          Journal:  Biochem J        ISSN: 0264-6021            Impact factor:   3.857


  28 in total

1.  Organization of citric acid cycle enzymes into a multienzyme cluster.

Authors:  S J Barnes; P D Weitzman
Journal:  FEBS Lett       Date:  1986-06-09       Impact factor: 4.124

2.  Molecular size diversity of citrate synthases from Pseudomonas species.

Authors:  C G Mitchell; P D Weitzman
Journal:  J Gen Microbiol       Date:  1986-03

Review 3.  The role of isozymes in metabolism: a model of metabolic pathways as the basis for the biological role of isozymes.

Authors:  T Ureta
Journal:  Curr Top Cell Regul       Date:  1978

4.  Association between the alpha-ketoglutarate dehydrogenase complex and succinate thiokinase.

Authors:  Z Porpáczy; B Sümegi; I Alkonyi
Journal:  Biochim Biophys Acta       Date:  1983-12-12

Review 5.  Unity and diversity in some bacterial citric acid-cycle enzymes.

Authors:  P D Weitzman
Journal:  Adv Microb Physiol       Date:  1981       Impact factor: 3.517

6.  Interaction between the pyruvate dehydrogenase complex and citrate synthase.

Authors:  B Sümegi; L Gyócsi; I Alkonyi
Journal:  Biochim Biophys Acta       Date:  1980-12-04

7.  Saccharomyces cerevisiae contains two functional citrate synthase genes.

Authors:  K S Kim; M S Rosenkrantz; L Guarente
Journal:  Mol Cell Biol       Date:  1986-06       Impact factor: 4.272

8.  Metabolic studies on citrate synthase mutants of yeast. A change in phenotype following transformation with an inactive enzyme.

Authors:  G Kispal; C T Evans; C Malloy; P A Srere
Journal:  J Biol Chem       Date:  1989-07-05       Impact factor: 5.157

9.  Mitochondrial and nonmitochondrial citrate synthases in Saccharomyces cerevisiae are encoded by distinct homologous genes.

Authors:  M Rosenkrantz; T Alam; K S Kim; B J Clark; P A Srere; L P Guarente
Journal:  Mol Cell Biol       Date:  1986-12       Impact factor: 4.272

10.  A study on the physical interaction between the pyruvate dehydrogenase complex and citrate synthase.

Authors:  B Sümegi; I Alkonyi
Journal:  Biochim Biophys Acta       Date:  1983-12-12
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4.  Independent evolutionary origins of functional polyamine biosynthetic enzyme fusions catalysing de novo diamine to triamine formation.

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Journal:  Mol Microbiol       Date:  2011-07-18       Impact factor: 3.501

5.  Elements of the cellular metabolic structure.

Authors:  Ildefonso M De la Fuente
Journal:  Front Mol Biosci       Date:  2015-04-28

6.  First evidence for a multienzyme complex of lipid biosynthesis pathway enzymes in Cunninghamella bainieri.

Authors:  Shuwahida Shuib; Izyanti Ibrahim; Mukram Mohamed Mackeen; Colin Ratledge; Aidil Abdul Hamid
Journal:  Sci Rep       Date:  2018-02-15       Impact factor: 4.379

  6 in total

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