Literature DB >> 1864360

Osmoregulation in Saccharomyces cerevisiae. Studies on the osmotic induction of glycerol production and glycerol-3-phosphate dehydrogenase (NAD+)

L André1, A Hemming, L Adler.   

Abstract

Production of glycerol and a key enzyme in glycerol production, glycerol 3-phosphate dehydrogenase (NAD+) (GPD), was studied in Saccharomyces cerevisiae cultured in basal media or media of high salinity, with glucose, raffinose or ethanol as the sole carbon source. At high salinity, glycerol production was stimulated with all carbon sources and glycerol was accumulated to high intracellular concentration in cells grown on glucose and raffinose. Cells grown on ethanol accumulated glycerol to a lower level but showed an increased content of trehalose at high salinity. However, the trehalose concentration corresponded only to about 20% of the glycerol level, and did not compensate for the shortfall in intracellular osmolyte content. Immunoblot analysis demonstrated an increased production of GPD at high salinity. This increase was osmotically mediated but was lower when glycerol was substituted for NaCl or sorbitol as the stress-solute. The enzyme also appeared to be subject to glucose repression; the specific activity of GPD was significantly lower in cells grown on glucose, than on raffinose or ethanol.

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Year:  1991        PMID: 1864360     DOI: 10.1016/0014-5793(91)80930-2

Source DB:  PubMed          Journal:  FEBS Lett        ISSN: 0014-5793            Impact factor:   4.124


  23 in total

1.  Evolutionary differences in food preference rely on Gr64e, a receptor for glycerol.

Authors:  Zev Wisotsky; Adriana Medina; Erica Freeman; Anupama Dahanukar
Journal:  Nat Neurosci       Date:  2011-11-06       Impact factor: 24.884

2.  Generation of an evolved Saccharomyces cerevisiae strain with a high freeze tolerance and an improved ability to grow on glycerol.

Authors:  Annamaria Merico; Enrico Ragni; Silvia Galafassi; Laura Popolo; Concetta Compagno
Journal:  J Ind Microbiol Biotechnol       Date:  2010-09-29       Impact factor: 3.346

3.  Application of C Nuclear Magnetic Resonance To Elucidate the Unexpected Biosynthesis of Erythritol by Leuconostoc oenos.

Authors:  M Veiga-Da-Cunha; P Firme; M V Romão; H Santos
Journal:  Appl Environ Microbiol       Date:  1992-07       Impact factor: 4.792

4.  A halotolerant mutant of Saccharomyces cerevisiae.

Authors:  R Gaxiola; M Corona; S Zinker
Journal:  J Bacteriol       Date:  1996-05       Impact factor: 3.490

5.  Signaling of chloroquine-induced stress in the yeast Saccharomyces cerevisiae requires the Hog1 and Slt2 mitogen-activated protein kinase pathways.

Authors:  Shivani Baranwal; Gajendra Kumar Azad; Vikash Singh; Raghuvir S Tomar
Journal:  Antimicrob Agents Chemother       Date:  2014-07-14       Impact factor: 5.191

6.  Heterologous expression of glycerol 3-phosphate dehydrogenase gene [DhGPD1] from the osmotolerant yeast Debaryomyces hansenii in Saccharomyces cerevisiae.

Authors:  Patricia E Thomé
Journal:  Curr Microbiol       Date:  2005-07-12       Impact factor: 2.188

7.  Cloning, sequence, and disruption of the Saccharomyces diastaticus DAR1 gene encoding a glycerol-3-phosphate dehydrogenase.

Authors:  H T Wang; P Rahaim; P Robbins; R R Yocum
Journal:  J Bacteriol       Date:  1994-11       Impact factor: 3.490

8.  Regulation of mannitol biosynthesis and degradation by Cryptococcus neoformans.

Authors:  W G Niehaus; T Flynn
Journal:  J Bacteriol       Date:  1994-02       Impact factor: 3.490

9.  GPD1, which encodes glycerol-3-phosphate dehydrogenase, is essential for growth under osmotic stress in Saccharomyces cerevisiae, and its expression is regulated by the high-osmolarity glycerol response pathway.

Authors:  J Albertyn; S Hohmann; J M Thevelein; B A Prior
Journal:  Mol Cell Biol       Date:  1994-06       Impact factor: 4.272

10.  Characterization of the osmotic-stress response in Saccharomyces cerevisiae: osmotic stress and glucose repression regulate glycerol-3-phosphate dehydrogenase independently.

Authors:  J Albertyn; S Hohmann; B A Prior
Journal:  Curr Genet       Date:  1994-01       Impact factor: 3.886

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