Literature DB >> 10194857

Investigation of the impact of MIG1 and MIG2 on the physiology of Saccharomyces cerevisiae.

C J Klein1, J J Rasmussen, B Rønnow, L Olsson, J Nielsen.   

Abstract

The gene functions of MIG1 and MIG2 are well known for their role in glucose control in Saccharomyces cerevisiae. A prototrophic mig1 disruptant (T468) and mig1mig2 double disruptant (T475) as well as their congenic wild-type strain (CEN.PK 113-7D) were analysed for changes in their peripheral metabolism (batch cultivations on sugar mixtures) and central metabolism (batch and continuous cultivations as well as acceleratostats). Sucrose metabolism was alleviated of glucose control in the mig1 disruptant, and even more so in the mig1mig2 disruptant compared with their wild-type strain. The lag phase in a batch cultivation grown on a glucose-galactose mixture was reduced by 50% in either disruptant, i.e. additional disruption of MIG2 in a mig1 background did not further alleviate galactose metabolism from glucose control. In contrast, both disruptants exhibited a more stringent glucose control of maltose metabolism compared with the wild-type strain. Growing on glucose, the mig1mig2 double disruptant exhibited a 12% higher specific growth rate than the wild-type strain, as well as a significantly higher respiratory capacity.

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Year:  1999        PMID: 10194857     DOI: 10.1016/s0168-1656(98)00205-3

Source DB:  PubMed          Journal:  J Biotechnol        ISSN: 0168-1656            Impact factor:   3.307


  22 in total

1.  The Snf1 kinase controls glucose repression in yeast by modulating interactions between the Mig1 repressor and the Cyc8-Tup1 co-repressor.

Authors:  Manolis Papamichos-Chronakis; Thomas Gligoris; Dimitris Tzamarias
Journal:  EMBO Rep       Date:  2004-03-12       Impact factor: 8.807

2.  Evaluation of gene modification strategies for the development of low-alcohol-wine yeasts.

Authors:  C Varela; D R Kutyna; M R Solomon; C A Black; A Borneman; P A Henschke; I S Pretorius; P J Chambers
Journal:  Appl Environ Microbiol       Date:  2012-06-22       Impact factor: 4.792

Review 3.  Metabolic engineering of Saccharomyces cerevisiae.

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

4.  Network identification and flux quantification in the central metabolism of Saccharomyces cerevisiae under different conditions of glucose repression.

Authors:  A K Gombert; M Moreira dos Santos ; B Christensen; J Nielsen
Journal:  J Bacteriol       Date:  2001-02       Impact factor: 3.490

5.  Inactivation of the transcription factor mig1 (YGL035C) in Saccharomyces cerevisiae improves tolerance towards monocarboxylic weak acids: acetic, formic and levulinic acid.

Authors:  Victor E Balderas-Hernández; Kevin Correia; Radhakrishnan Mahadevan
Journal:  J Ind Microbiol Biotechnol       Date:  2018-06-06       Impact factor: 3.346

6.  Redirection of the respiro-fermentative flux distribution in Saccharomyces cerevisiae by overexpression of the transcription factor Hap4p.

Authors:  J Blom; M J De Mattos; L A Grivell
Journal:  Appl Environ Microbiol       Date:  2000-05       Impact factor: 4.792

7.  Hxt-carrier-mediated glucose efflux upon exposure of Saccharomyces cerevisiae to excess maltose.

Authors:  Mickel L A Jansen; Johannes H De Winde; Jack T Pronk
Journal:  Appl Environ Microbiol       Date:  2002-09       Impact factor: 4.792

8.  Isocitrate lyase of the yeast Kluyveromyces lactis is subject to glucose repression but not to catabolite inactivation.

Authors:  M Luz López; Begoña Redruello; Eva Valdés; Fernando Moreno; Jürgen J Heinisch; Rosaura Rodicio
Journal:  Curr Genet       Date:  2003-10-21       Impact factor: 3.886

9.  Construction of lactose-consuming Saccharomyces cerevisiae for lactose fermentation into ethanol fuel.

Authors:  Jing Zou; Xuewu Guo; Tong Shen; Jian Dong; Cuiying Zhang; Dongguang Xiao
Journal:  J Ind Microbiol Biotechnol       Date:  2013-01-24       Impact factor: 3.346

10.  Directed evolution of pyruvate decarboxylase-negative Saccharomyces cerevisiae, yielding a C2-independent, glucose-tolerant, and pyruvate-hyperproducing yeast.

Authors:  Antonius J A van Maris; Jan-Maarten A Geertman; Alexander Vermeulen; Matthijs K Groothuizen; Aaron A Winkler; Matthew D W Piper; Johannes P van Dijken; Jack T Pronk
Journal:  Appl Environ Microbiol       Date:  2004-01       Impact factor: 4.792

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