Literature DB >> 991

Tricarboxylic acid-cycle and related enzymes in restricted facultative methylotrophs.

J Colby, L J Zatman.   

Abstract

The isolation is described of pure cultures of three non-methane-utilizing methylotrophic bacteria which, together with the previously described Bacillus PM6, have a very limited range of growth substrates; these organisms are designated "restricted facultative' methylotrophs. Two of these isolates, W6A and W3A1, grow only on glucose out of 50 non-C1 compounds tested, whereas the third isolate S2A1 and Bacillus PM6 grow on betaine, glucose, gluconate, alanine, glutamate, citrate and nutrient agar, but not on any of a further 56 non-C1 compounds. Crude sonic extracts of trimethylamine-grown and glucose-grown W6A and W3A1 isolates, and of trimethylamine-grown C2A1 (an obligate methylotroph) contain (i) no detectable 2-oxogltarate dehydrogenase activity, (ii) very low or zero specific activities of succinate dehydrogenase and succinyl-CoA synthetase and (iii) NAD+-dependent isocitrate dehydrogenase activity. Extracts of trimethylamine-grown PM6 and S2A1 methylotrophs have (i) very low 2-oxoglutarate dehydrogenase specific activities, (ii) comparatively high specific activities of succinate dehydrogenase, malate dehydrogenase and succinyl-CoA synthetase and (iii) NADP+-dependent isocitrate dehydrogenase activity but no NAD+-dependent isocitrate dehydrogenase activity. The activities of most of these enzymes are increased during growth on glucose, alanine, glutamate or citrate, but only very low 2-oxoglutarate dehydrogenase activities are present under all growth conditions. The restricted facultative methylotrophs grow on certain non-C1 compounds in the absence of 2-oxoglutarate dehydrogenase and, in some cases, of other enzymes of the tricarboxylic acid cycle; these lesions cannot therefore be the sole cause of obligate methylotrophy.

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Year:  1975        PMID: 991      PMCID: PMC1165569          DOI: 10.1042/bj1480505

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


  14 in total

1.  BIOLOGY OF BUDDING BACTERIA. II. GROWTH AND NUTRITION OF HYPHOMICROBIUM SPP.

Authors:  P HIRSCH; S F CONTI
Journal:  Arch Mikrobiol       Date:  1964-06-26

2.  RESOLUTION AND RECONSTITUTION OF THE ESCHERICHIA COLI ALPHA-KETOGLUTARATE DEHYDROGENASE COMPLEX.

Authors:  B B MUKHERJEE; J MATTHEWS; D L HORNEY; L J REED
Journal:  J Biol Chem       Date:  1965-05       Impact factor: 5.157

3.  ENZYMATIC PROPERTIES OF ALANINE DEHYDROGENASE OF BACILLUS SUBTILIS.

Authors:  A YOSHIDA; E FREESE
Journal:  Biochim Biophys Acta       Date:  1965-02-22

4.  Microbial growth on C1 compounds. I. Isolation and characterization of Pseudomonas AM 1.

Authors:  D PEEL; J R QUAYLE
Journal:  Biochem J       Date:  1961-12       Impact factor: 3.857

Review 5.  Autotrophy: concepts of lithotrophic bacteria and their organic metabolism.

Authors:  D P Kelly
Journal:  Annu Rev Microbiol       Date:  1971       Impact factor: 15.500

6.  The distribution in the methylobacteria of some key enzymes concerned with intermediary metabolism.

Authors:  J F Davey; R Whittenbury; J F Wilkinson
Journal:  Arch Mikrobiol       Date:  1972

7.  New obligate methylotroph.

Authors:  J S Dahl; R J Mehta; D S Hoare
Journal:  J Bacteriol       Date:  1972-02       Impact factor: 3.490

8.  Hexose phosphate synthese and tricarboxylic acid-cycle enzymes in bacterium 4B6, an obligate methylotroph.

Authors:  J Colby; L J Zatman
Journal:  Biochem J       Date:  1972-08       Impact factor: 3.857

9.  Enzymological aspects of the pathways for trimethylamine oxidation and C1 assimilation of obligate methylotrophs and restricted facultative methylotrophs.

Authors:  J Colby; L J Zatman
Journal:  Biochem J       Date:  1975-06       Impact factor: 3.857

10.  Trimethylamine metabolism in obligate and facultative methylotrophs.

Authors:  J Colby; L J Zatman
Journal:  Biochem J       Date:  1973-01       Impact factor: 3.857

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  13 in total

1.  Participation of the iron-sulphur cluster and of the covalently bound coenzyme of trimethylamine dehydrogenase in catalysis.

Authors:  D J Steenkamp; T P Singer
Journal:  Biochem J       Date:  1978-02-01       Impact factor: 3.857

2.  L-lysine production at 50 degrees C by mutants of a newly isolated and characterized methylotrophic Bacillus sp.

Authors:  F J Schendel; C E Bremmon; M C Flickinger; M Guettler; R S Hanson
Journal:  Appl Environ Microbiol       Date:  1990-04       Impact factor: 4.792

Review 3.  Evolutionary aspects of autotrophy.

Authors:  J R Quayle; T Ferenci
Journal:  Microbiol Rev       Date:  1978-06

Review 4.  Specialist phototrophs, lithotrophs, and methylotrophs: a unity among a diversity of procaryotes?

Authors:  A J Smith; D S Hoare
Journal:  Bacteriol Rev       Date:  1977-06

5.  Regulation by carbon source of enzyme expression and slime production in bacterium W3A1.

Authors:  V L Davidson
Journal:  J Bacteriol       Date:  1985-11       Impact factor: 3.490

6.  A biochemical study of the intermediary carbon metabolism of Shewanella putrefaciens.

Authors:  J H Scott; K H Nealson
Journal:  J Bacteriol       Date:  1994-06       Impact factor: 3.490

7.  Biodegradation and utilization of quaternary alkylammonium compounds by specialized methylotrophs.

Authors:  O Ghisalba; M Küenzi
Journal:  Experientia       Date:  1983-11-15

8.  Factors affecting the production of pyrroloquinoline quinone by the methylotrophic bacterium W3A1.

Authors:  W S McIntire; W Weyler
Journal:  Appl Environ Microbiol       Date:  1987-09       Impact factor: 4.792

9.  Regulation of citrate synthase activity in methylotrophs by reduced nicotinamide-adenine dinucleotide, adenine nucleotides and 2-oxoglutarate.

Authors:  J Colby; L J Zatman
Journal:  Biochem J       Date:  1975-07       Impact factor: 3.857

10.  Enzymological aspects of the pathways for trimethylamine oxidation and C1 assimilation of obligate methylotrophs and restricted facultative methylotrophs.

Authors:  J Colby; L J Zatman
Journal:  Biochem J       Date:  1975-06       Impact factor: 3.857

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