Literature DB >> 342501

Utilization of arginine by Klebsiella aerogenes.

B Friedrich, B Magasanik.   

Abstract

Klebsiella aerogenes utilized arginine as the sole source of carbon or nitrogen for growth. Arginine was degraded to 2-ketoglutarate and not to succinate, since a citrate synthaseless mutant grows on arginine as the only nitrogen source. When glucose was the energy source, all four nitrogen atoms of arginine were utilized. Three of them apparently did not pass through ammonia but were transferred by transamination, since a mutant unable to produce glutamate by glutamate synthase or glutamate dehydrogenase utilized three of four nitrogen atoms of arginine. Urea was not involved as intermediate, since a unreaseless mutant did not accumulate urea and grew on arginine as efficiently as the wild-type strain. Ornithine appeared to be an intermediate, because cells grown either on glucose and arginine or arginine alone could convert arginine in the presence of hydroxylamine to ornithine. This indicates that an amidinotransferase is the initiating enzyme of arginine breakdown. In addition, the cells contained a transaminase specific for ornithine. In contrast to the hydroxylamine-dependent reaction, this activity could be demonstrated in extracts. The arginine-utilizing system (aut) is apparently controlled like the enzymes responsible for the degradation of histidine (hut) through induction, catabolite repression, and activation by glutamine synthetase.

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Year:  1978        PMID: 342501      PMCID: PMC222075          DOI: 10.1128/jb.133.2.680-685.1978

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


  18 in total

1.  Behavior of purified arginine desiminase from S. faecalis.

Authors:  B PETRACK; L SULLIVAN; S RATNER
Journal:  Arch Biochem Biophys       Date:  1957-07       Impact factor: 4.013

2.  An improved method for the microdetermination of arginine by use of 8-hydroxyquinoline.

Authors:  G CERIOTTI; L SPANDRIO
Journal:  Biochem J       Date:  1957-08       Impact factor: 3.857

3.  Enzymology of mycobacteria. VII. Degradation of guanidine derivatives.

Authors:  E A ZELLER; L S VAN ORDEN; W VOGTLI
Journal:  J Biol Chem       Date:  1954-07       Impact factor: 5.157

4.  Protein measurement with the Folin phenol reagent.

Authors:  O H LOWRY; N J ROSEBROUGH; A L FARR; R J RANDALL
Journal:  J Biol Chem       Date:  1951-11       Impact factor: 5.157

5.  Catabolic N2-acetylornithine 5-aminotransferase of Klebsiella aerogenes: control of synthesis by induction, catabolite repression, and activation by glutamine synthetase.

Authors:  B Friedrich; C G Friedrich; B Magasanik
Journal:  J Bacteriol       Date:  1978-02       Impact factor: 3.490

6.  Resistance to catabolite repression of histidase and proline oxidase during nitrogen-limited growth of Klebsiella aerogenes.

Authors:  M J Prival; B Magasanik
Journal:  J Biol Chem       Date:  1971-10-25       Impact factor: 5.157

7.  Glutamine synthetase and the regulation of histidase formation in Klebsiella aerogenes.

Authors:  M J Prival; J E Brenchley; B Magasanik
Journal:  J Biol Chem       Date:  1973-06-25       Impact factor: 5.157

8.  Regulation of the synthesis of enzymes responsible for glutamate formation in Klebsiella aerogenes.

Authors:  J E Brenchley; M J Prival; B Magasanik
Journal:  J Biol Chem       Date:  1973-09-10       Impact factor: 5.157

9.  Absence of involvement of glutamine synthetase and of NAD-linked glutamate dehydrogenase in the nitrogen catabolite repression of arginase and other enzymes in Saccharomyces cerevisiae.

Authors:  E L Dubois; M Grenson
Journal:  Biochem Biophys Res Commun       Date:  1974-09-09       Impact factor: 3.575

10.  Urease of Klebsiella aerogenes: control of its synthesis by glutamine synthetase.

Authors:  B Friedrich; B Magasanik
Journal:  J Bacteriol       Date:  1977-08       Impact factor: 3.490

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  17 in total

1.  Genetic regulation of nitrate assimilation in Klebsiella pneumoniae M5al.

Authors:  B M Cali; J L Micca; V Stewart
Journal:  J Bacteriol       Date:  1989-05       Impact factor: 3.490

2.  Amino acid transport and metabolism in mycobacteria: cloning, interruption, and characterization of an L-Arginine/gamma-aminobutyric acid permease in Mycobacterium bovis BCG.

Authors:  A Seth; N D Connell
Journal:  J Bacteriol       Date:  2000-02       Impact factor: 3.490

3.  Catabolic N2-acetylornithine 5-aminotransferase of Klebsiella aerogenes: control of synthesis by induction, catabolite repression, and activation by glutamine synthetase.

Authors:  B Friedrich; C G Friedrich; B Magasanik
Journal:  J Bacteriol       Date:  1978-02       Impact factor: 3.490

4.  Purification and properties of agmatine ureohydrolyase, a putrescine biosynthetic enzyme in Escherichia coli.

Authors:  C Satishchandran; S M Boyle
Journal:  J Bacteriol       Date:  1986-03       Impact factor: 3.490

Review 5.  Biosynthesis and metabolism of arginine in bacteria.

Authors:  R Cunin; N Glansdorff; A Piérard; V Stalon
Journal:  Microbiol Rev       Date:  1986-09

6.  Characterization of mutations that lie in the promoter-regulatory region for glnA, the structural gene encoding glutamine synthetase.

Authors:  L McCarter; K Krajewska-Grynkiewicz; D Trinh; G Wei; S Kustu
Journal:  Mol Gen Genet       Date:  1984

7.  Metabolic pathway for the utilization of L-arginine, L-ornithine, agmatine, and putrescine as nitrogen sources in Escherichia coli K-12.

Authors:  E Shaibe; E Metzer; Y S Halpern
Journal:  J Bacteriol       Date:  1985-09       Impact factor: 3.490

8.  Control of utilization of L-arginine, L-ornithine, agmatine, and putrescine as nitrogen sources in Escherichia coli K-12.

Authors:  E Shaibe; E Metzer; Y S Halpern
Journal:  J Bacteriol       Date:  1985-09       Impact factor: 3.490

9.  Arginine degradation in Pseudomonas aeruginosa mutants blocked in two arginine catabolic pathways.

Authors:  D Haas; H Matsumoto; P Moretti; V Stalon; A Mercenier
Journal:  Mol Gen Genet       Date:  1984

10.  Regulation of nitrogen catabolic enzymes in Bacillus spp.

Authors:  H J Schreier; T M Smith; R W Bernlohr
Journal:  J Bacteriol       Date:  1982-08       Impact factor: 3.490

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