Literature DB >> 10640599

The role of ammonia metabolism in nitrogen catabolite repression in Saccharomyces cerevisiae.

E G ter Schure1, N A van Riel, C T Verrips.   

Abstract

Saccharomyces cerevisiae is able to use a wide variety of nitrogen sources for growth. Not all nitrogen sources support growth equally well. In order to select the best out of a large diversity of available nitrogen sources, the yeast has developed molecular mechanisms. These mechanisms consist of a sensing mechanism and a regulatory mechanism which includes induction of needed systems, and repression of systems that are not beneficial. The first step in use of most nitrogen sources is its uptake via more or less specific permeases. Hence the first level of regulation is encountered at this level. The next step is the degradation of the nitrogen source to useful building blocks via the nitrogen metabolic pathways. These pathways can be divided into routes that lead to the degradation of the nitrogen source to ammonia and glutamate, and routes that lead to the synthesis of nitrogen containing compounds in which glutamate and glutamine are used as nitrogen donor. Glutamine is synthesized out of ammonia and glutamate. The expression of the specific degradation routes is also regulated depending on the availability of a particular nitrogen source. Ammonia plays a central role as intermediate between degradative and biosynthetic pathways. It not only functions as a metabolite in metabolic reactions but is also involved in regulation of metabolic pathways at several levels. This review describes the central role of ammonia in nitrogen metabolism. This role is illustrated at the level of enzyme activity, translation and transcription.

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Year:  2000        PMID: 10640599     DOI: 10.1111/j.1574-6976.2000.tb00533.x

Source DB:  PubMed          Journal:  FEMS Microbiol Rev        ISSN: 0168-6445            Impact factor:   16.408


  70 in total

1.  Saccharomyces cerevisiae GATA sequences function as TATA elements during nitrogen catabolite repression and when Gln3p is excluded from the nucleus by overproduction of Ure2p.

Authors:  K H Cox; R Rai; M Distler; J R Daugherty; J A Coffman; T G Cooper
Journal:  J Biol Chem       Date:  2000-06-09       Impact factor: 5.157

2.  Gln3p nuclear localization and interaction with Ure2p in Saccharomyces cerevisiae.

Authors:  A A Kulkarni; A T Abul-Hamd; R Rai; H El Berry; T G Cooper
Journal:  J Biol Chem       Date:  2001-06-14       Impact factor: 5.157

3.  Ammonia regulates VID30 expression and Vid30p function shifts nitrogen metabolism toward glutamate formation especially when Saccharomyces cerevisiae is grown in low concentrations of ammonia.

Authors:  G K van der Merwe; T G Cooper; H J van Vuuren
Journal:  J Biol Chem       Date:  2001-05-16       Impact factor: 5.157

4.  Evidence for control of nitrogen metabolism by a START-dependent mechanism in Saccharomyces cerevisiae.

Authors:  B A Bryan; E McGrew; Y Lu; M Polymenis
Journal:  Mol Genet Genomics       Date:  2003-11-27       Impact factor: 3.291

Review 5.  Transmitting the signal of excess nitrogen in Saccharomyces cerevisiae from the Tor proteins to the GATA factors: connecting the dots.

Authors:  Terrance G Cooper
Journal:  FEMS Microbiol Rev       Date:  2002-08       Impact factor: 16.408

6.  Cytoplasmic compartmentation of Gln3 during nitrogen catabolite repression and the mechanism of its nuclear localization during carbon starvation in Saccharomyces cerevisiae.

Authors:  Kathleen H Cox; Jennifer J Tate; Terrance G Cooper
Journal:  J Biol Chem       Date:  2002-07-24       Impact factor: 5.157

7.  Assessment of bacterial and fungal growth on natural substrates: consequences for preserving caves with prehistoric paintings.

Authors:  Francesca Stomeo; Maria C Portillo; Juan M Gonzalez
Journal:  Curr Microbiol       Date:  2009-06-18       Impact factor: 2.188

8.  Green fluorescent protein-Dal80p illuminates up to 16 distinct foci that colocalize with and exhibit the same behavior as chromosomal DNA proceeding through the cell cycle of Saccharomyces cerevisiae.

Authors:  M Distler; A Kulkarni; R Rai; T G Cooper
Journal:  J Bacteriol       Date:  2001-08       Impact factor: 3.490

9.  GLN3 encodes a global regulator of nitrogen metabolism and virulence of C. albicans.

Authors:  Wei-Li Liao; Ana M Ramón; William A Fonzi
Journal:  Fungal Genet Biol       Date:  2007-09-07       Impact factor: 3.495

10.  Actin cytoskeleton is required for nuclear accumulation of Gln3 in response to nitrogen limitation but not rapamycin treatment in Saccharomyces cerevisiae.

Authors:  Kathleen H Cox; Jennifer J Tate; Terrance G Cooper
Journal:  J Biol Chem       Date:  2004-02-16       Impact factor: 5.157

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