Functional analysis of the ALD gene family of Saccharomyces cerevisiae during anaerobic growth on glucose: the NADP+-dependent Ald6p and Ald5p isoforms play a major role in acetate formation

UMR Sciences pour l' nologie, Microbiologie et Technologie des Fermentations, INRA, 2 Place Viala, F-34060 Montpellier Cedex 1, France Correspondence Sylvie Dequin dequin{at}ensam.inra.fr In Saccharomyces cerevisiae , acetate is formed by acetaldehyde dehydrogenase (ACDH), a key enzyme of the p...

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Veröffentlicht in:Microbiology (Society for General Microbiology) 2004-07, Vol.150 (7), p.2209-2220
Hauptverfasser: Saint-Prix, Florence, Bonquist, Linda, Dequin, Sylvie
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description UMR Sciences pour l' nologie, Microbiologie et Technologie des Fermentations, INRA, 2 Place Viala, F-34060 Montpellier Cedex 1, France Correspondence Sylvie Dequin dequin{at}ensam.inra.fr In Saccharomyces cerevisiae , acetate is formed by acetaldehyde dehydrogenase (ACDH), a key enzyme of the pyruvate dehydrogenase (PDH) bypass, which fulfils the essential task of generating acetyl-CoA in the cytosol. The role of the five members of the ACDH family ( ALD genes) was investigated during anaerobic growth on glucose. Single and multiple ald mutants were generated in the wine-yeast-derived V5 and laboratory CEN.PK strains and analysed under standard (YPD 5 % glucose) and wine (MS 20 % glucose) fermentation conditions. The deletion of ALD6 and ALD5 decreased acetate formation in both strains, demonstrating for the first time that the mitochondrial Ald5p isoform is involved in the biosynthesis of acetate during anaerobic growth on glucose. Acetate production of the ald4 mutant was slightly decreased in the CEN.PK strain during growth on YPD only. In contrast, the deletion of ALD2 or ALD3 had no effect on acetate production. The absence of Ald6p was compensated by the mitochondrial isoforms and this involves the transcriptional activation of ALD4 . Consistent with this, growth retardation was observed in ald6 ald4 , and this effect was amplified by the additional deletion of ALD5 . A ald null mutant, devoid of ACDH activity, was viable and produced similar levels of acetate to the ald6 ald4 ald5 strain, excluding a role of Ald2p and Ald3p. Thus, acetate is mainly produced by the cytosolic PDH bypass via Ald6p and by a mitochondrial route involving Ald5p. An unknown alternative pathway can compensate for the loss of Ald6p, Ald4p and Ald5p. Abbreviations: ACDH, acetaldehyde dehydrogenase; HA, haemagglutinin; PDC, pyruvate decarboxylase; PDH, pyruvate dehydrogenase
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The role of the five members of the ACDH family ( ALD genes) was investigated during anaerobic growth on glucose. Single and multiple ald mutants were generated in the wine-yeast-derived V5 and laboratory CEN.PK strains and analysed under standard (YPD 5 % glucose) and wine (MS 20 % glucose) fermentation conditions. The deletion of ALD6 and ALD5 decreased acetate formation in both strains, demonstrating for the first time that the mitochondrial Ald5p isoform is involved in the biosynthesis of acetate during anaerobic growth on glucose. Acetate production of the ald4 mutant was slightly decreased in the CEN.PK strain during growth on YPD only. In contrast, the deletion of ALD2 or ALD3 had no effect on acetate production. The absence of Ald6p was compensated by the mitochondrial isoforms and this involves the transcriptional activation of ALD4 . Consistent with this, growth retardation was observed in ald6 ald4 , and this effect was amplified by the additional deletion of ALD5 . 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Plant and forest protection</topic><topic>Saccharomyces cerevisiae - enzymology</topic><topic>Saccharomyces cerevisiae - genetics</topic><topic>Saccharomyces cerevisiae - growth &amp; development</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Saint-Prix, Florence</creatorcontrib><creatorcontrib>Bonquist, Linda</creatorcontrib><creatorcontrib>Dequin, Sylvie</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>Hyper Article en Ligne (HAL)</collection><jtitle>Microbiology (Society for General Microbiology)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Saint-Prix, Florence</au><au>Bonquist, Linda</au><au>Dequin, Sylvie</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Functional analysis of the ALD gene family of Saccharomyces cerevisiae during anaerobic growth on glucose: the NADP+-dependent Ald6p and Ald5p isoforms play a major role in acetate formation</atitle><jtitle>Microbiology (Society for General Microbiology)</jtitle><addtitle>Microbiology</addtitle><date>2004-07-01</date><risdate>2004</risdate><volume>150</volume><issue>7</issue><spage>2209</spage><epage>2220</epage><pages>2209-2220</pages><issn>1350-0872</issn><eissn>1465-2080</eissn><abstract>UMR Sciences pour l' nologie, Microbiologie et Technologie des Fermentations, INRA, 2 Place Viala, F-34060 Montpellier Cedex 1, France Correspondence Sylvie Dequin dequin{at}ensam.inra.fr In Saccharomyces cerevisiae , acetate is formed by acetaldehyde dehydrogenase (ACDH), a key enzyme of the pyruvate dehydrogenase (PDH) bypass, which fulfils the essential task of generating acetyl-CoA in the cytosol. The role of the five members of the ACDH family ( ALD genes) was investigated during anaerobic growth on glucose. Single and multiple ald mutants were generated in the wine-yeast-derived V5 and laboratory CEN.PK strains and analysed under standard (YPD 5 % glucose) and wine (MS 20 % glucose) fermentation conditions. The deletion of ALD6 and ALD5 decreased acetate formation in both strains, demonstrating for the first time that the mitochondrial Ald5p isoform is involved in the biosynthesis of acetate during anaerobic growth on glucose. Acetate production of the ald4 mutant was slightly decreased in the CEN.PK strain during growth on YPD only. In contrast, the deletion of ALD2 or ALD3 had no effect on acetate production. The absence of Ald6p was compensated by the mitochondrial isoforms and this involves the transcriptional activation of ALD4 . Consistent with this, growth retardation was observed in ald6 ald4 , and this effect was amplified by the additional deletion of ALD5 . A ald null mutant, devoid of ACDH activity, was viable and produced similar levels of acetate to the ald6 ald4 ald5 strain, excluding a role of Ald2p and Ald3p. Thus, acetate is mainly produced by the cytosolic PDH bypass via Ald6p and by a mitochondrial route involving Ald5p. An unknown alternative pathway can compensate for the loss of Ald6p, Ald4p and Ald5p. Abbreviations: ACDH, acetaldehyde dehydrogenase; HA, haemagglutinin; PDC, pyruvate decarboxylase; PDH, pyruvate dehydrogenase</abstract><cop>Reading</cop><pub>Soc General Microbiol</pub><pmid>15256563</pmid><doi>10.1099/mic.0.26999-0</doi><tpages>12</tpages><orcidid>https://orcid.org/0000-0002-9114-2324</orcidid><oa>free_for_read</oa></addata></record>
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subjects Acetates - metabolism
Aldehyde Oxidoreductases - genetics
Aldehyde Oxidoreductases - metabolism
Anaerobiosis
Biological and medical sciences
Culture Media
Fermentation
Fundamental and applied biological sciences. Psychology
Fungal plant pathogens
Gene Deletion
Gene Expression Regulation, Fungal
Genes, Fungal
Glucose - metabolism
Isoenzymes - metabolism
Life Sciences
Microbiology
Microbiology and Parasitology
Miscellaneous
Multigene Family
Mycological methods and techniques used in mycology
Mycology
NADP - metabolism
Phytopathology. Animal pests. Plant and forest protection
Saccharomyces cerevisiae - enzymology
Saccharomyces cerevisiae - genetics
Saccharomyces cerevisiae - growth & development
title Functional analysis of the ALD gene family of Saccharomyces cerevisiae during anaerobic growth on glucose: the NADP+-dependent Ald6p and Ald5p isoforms play a major role in acetate formation
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