Literature DB >> 7476212

Cloning and characterization of GPD2, a second gene encoding sn-glycerol 3-phosphate dehydrogenase (NAD+) in Saccharomyces cerevisiae, and its comparison with GPD1.

P Eriksson1, L André, R Ansell, A Blomberg, L Adler.   

Abstract

We have cloned and characterized a homologue of the previously isolated GPD1 gene, encoding sn-glycerol 3-phosphate dehydrogenase (NAD+) in Saccharomyces cerevisiae. This second gene, called GPD2, encodes a protein of 384 amino acids that shares 69% sequence identity with GPD1. Like GPD1 it has an amino-terminal extension of unknown function. GPD2 is located on chromosome VII and cross-hybridizes with GPD1 at chromosome IV as well as with an unknown homologue at chromosome XV. Disruption of the GPD2 gene did not reveal any observable phenotypic effects, whereas overexpression resulted in a slight, but significant, increase of GPD enzyme activity in wild-type cells. Analysis of gene transcription by a CAT-reporter gene fused to the GPD promoters revealed decreased transcriptional activity of the GPD2 promoter in cells grown on nonfermentable as opposed to fermentable carbon sources, and no induction in cells exposed to high osmolarity or heat shock. Similar analysis of GPD1 demonstrated an 8-17-fold higher basal level of transcription compared to GPD2. Furthermore, such analysis revealed that the GPD1 promoter was induced by increased osmolarity essentially independent of the type of stress solute used, the level of GPD1 transcription being increased about sevenfold in cells growing at 1.4 M NaCl.

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Year:  1995        PMID: 7476212     DOI: 10.1111/j.1365-2958.1995.mmi_17010095.x

Source DB:  PubMed          Journal:  Mol Microbiol        ISSN: 0950-382X            Impact factor:   3.501


  33 in total

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Authors:  Sandra C Dos Santos; Nuno P Mira; Ana S Moreira; Isabel Sá-Correia
Journal:  OMICS       Date:  2012-07-09

Review 2.  Metabolic engineering of Saccharomyces cerevisiae.

Authors:  S Ostergaard; L Olsson; J Nielsen
Journal:  Microbiol Mol Biol Rev       Date:  2000-03       Impact factor: 11.056

3.  A MAPK gene from Dead Sea fungus confers stress tolerance to lithium salt and freezing-thawing: Prospects for saline agriculture.

Authors:  Yan Jin; Song Weining; Eviatar Nevo
Journal:  Proc Natl Acad Sci U S A       Date:  2005-12-19       Impact factor: 11.205

4.  A glycerol-3-phosphate dehydrogenase-deficient mutant of Saccharomyces cerevisiae expressing the heterologous XYL1 gene.

Authors:  G Lidén; M Walfridsson; R Ansell; M Anderlund; L Adler; B Hahn-Hägerdal
Journal:  Appl Environ Microbiol       Date:  1996-10       Impact factor: 4.792

5.  Expression of heterologous aquaporins for functional analysis in Saccharomyces cerevisiae.

Authors:  Nina Pettersson; Johan Hagström; Roslyn M Bill; Stefan Hohmann
Journal:  Curr Genet       Date:  2006-08-18       Impact factor: 3.886

6.  The malate-aspartate NADH shuttle components are novel metabolic longevity regulators required for calorie restriction-mediated life span extension in yeast.

Authors:  Erin Easlon; Felicia Tsang; Craig Skinner; Chen Wang; Su-Ju Lin
Journal:  Genes Dev       Date:  2008-04-01       Impact factor: 11.361

7.  Quantitative evaluation of yeast's requirement for glycerol formation in very high ethanol performance fed-batch process.

Authors:  Julien Pagliardini; Georg Hubmann; Carine Bideaux; Sandrine Alfenore; Elke Nevoigt; Stéphane E Guillouet
Journal:  Microb Cell Fact       Date:  2010-05-21       Impact factor: 5.328

8.  The mitogen-activated protein kinase homolog HOG1 gene controls glycerol accumulation in the pathogenic fungus Candida albicans.

Authors:  C San José; R A Monge; R Pérez-Díaz; J Pla; C Nombela
Journal:  J Bacteriol       Date:  1996-10       Impact factor: 3.490

Review 9.  MAP kinase pathways in the yeast Saccharomyces cerevisiae.

Authors:  M C Gustin; J Albertyn; M Alexander; K Davenport
Journal:  Microbiol Mol Biol Rev       Date:  1998-12       Impact factor: 11.056

10.  Regulation of cell cycle progression by Swe1p and Hog1p following hypertonic stress.

Authors:  M R Alexander; M Tyers; M Perret; B M Craig; K S Fang; M C Gustin
Journal:  Mol Biol Cell       Date:  2001-01       Impact factor: 4.138

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