Identification and disruption of the gene encoding the K+-activated acetaldehyde dehydrogenase of Saccharomyces cerevisiae

The identity of the gene encoding the mitochondrial K+-activated acetaldehyde dehydrogenase (K+-ACDH) of Saccharomyces cerevisiae has been confirmed. The gene is situated on the right arm of chromosome XV, bears the systematic name YOR374w and the deduced product shows significant homology to other...

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Veröffentlicht in:FEMS microbiology letters 1998-07, Vol.164 (1), p.29-34
Hauptverfasser: Tessier, W.D, Meaden, P.G, Dickinson, F.M, Midgley, M
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creator Tessier, W.D
Meaden, P.G
Dickinson, F.M
Midgley, M
description The identity of the gene encoding the mitochondrial K+-activated acetaldehyde dehydrogenase (K+-ACDH) of Saccharomyces cerevisiae has been confirmed. The gene is situated on the right arm of chromosome XV, bears the systematic name YOR374w and the deduced product shows significant homology to other members of the S. cerevisiae aldehyde dehydrogenase (ALDH) family. YOR374w has now been assigned the gene name ALD7. The N-terminal amino acid sequences of K+-ACDHs purified from several diverse strains of S. cerevisiae were determined, and found to have 81-100% identity in alignments with the product of ALD7. Haploid mutants containing a deletion of ALD7 were constructed and, in these strains, the K+-ACDH was not detectable under any growth conditions examined. The activity of the Mg2+-activated acetaldehyde dehydrogenase (Mg2+-ACDH), encoded by ALD6, remained at wild-type levels in the mutants. Growth on glucose was not affected in the mutants lacking ALD7 (in contrast to the behaviour of ald6 mutants), whereas growth on ethanol was severely impaired. This observation, together with previous work by our group, shows that both the Mg2+- and K+-ACDHs are required for growth on ethanol, whilst only the former plays a role during growth on glucose.
doi_str_mv 10.1111/j.1574-6968.1998.tb13063.x
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The gene is situated on the right arm of chromosome XV, bears the systematic name YOR374w and the deduced product shows significant homology to other members of the S. cerevisiae aldehyde dehydrogenase (ALDH) family. YOR374w has now been assigned the gene name ALD7. The N-terminal amino acid sequences of K+-ACDHs purified from several diverse strains of S. cerevisiae were determined, and found to have 81-100% identity in alignments with the product of ALD7. Haploid mutants containing a deletion of ALD7 were constructed and, in these strains, the K+-ACDH was not detectable under any growth conditions examined. The activity of the Mg2+-activated acetaldehyde dehydrogenase (Mg2+-ACDH), encoded by ALD6, remained at wild-type levels in the mutants. Growth on glucose was not affected in the mutants lacking ALD7 (in contrast to the behaviour of ald6 mutants), whereas growth on ethanol was severely impaired. 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Psychology ; Fungi ; Gene sequencing ; Genes, Fungal - genetics ; Glucose ; Growth conditions ; Growth, nutrition, metabolism, transports, enzymes. Molecular biology ; Homology ; Magnesium ; Microbiology ; Mitochondria ; Mitochondria - enzymology ; Mitochondria - genetics ; Molecular Sequence Data ; Mutants ; Mycology ; Potassium ; Protein purification ; Saccharomyces cerevisiae ; Saccharomyces cerevisiae - enzymology ; Saccharomyces cerevisiae - genetics ; Sequence Alignment ; Yeast</subject><ispartof>FEMS microbiology letters, 1998-07, Vol.164 (1), p.29-34</ispartof><rights>1998 Federation of European Microbiological Societies. Published by Elsevier Science B.V. All rights reserved. 1998</rights><rights>1998 INIST-CNRS</rights><rights>1998 Federation of European Microbiological Societies. Published by Elsevier Science B.V. 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The gene is situated on the right arm of chromosome XV, bears the systematic name YOR374w and the deduced product shows significant homology to other members of the S. cerevisiae aldehyde dehydrogenase (ALDH) family. YOR374w has now been assigned the gene name ALD7. The N-terminal amino acid sequences of K+-ACDHs purified from several diverse strains of S. cerevisiae were determined, and found to have 81-100% identity in alignments with the product of ALD7. Haploid mutants containing a deletion of ALD7 were constructed and, in these strains, the K+-ACDH was not detectable under any growth conditions examined. The activity of the Mg2+-activated acetaldehyde dehydrogenase (Mg2+-ACDH), encoded by ALD6, remained at wild-type levels in the mutants. Growth on glucose was not affected in the mutants lacking ALD7 (in contrast to the behaviour of ald6 mutants), whereas growth on ethanol was severely impaired. This observation, together with previous work by our group, shows that both the Mg2+- and K+-ACDHs are required for growth on ethanol, whilst only the former plays a role during growth on glucose.</description><subject>Acetaldehyde</subject><subject>Acetaldehyde dehydrogenase</subject><subject>Aldehyde dehydrogenase</subject><subject>Aldehyde dehydrogenase family</subject><subject>Aldehyde Oxidoreductases - genetics</subject><subject>Aldehyde Oxidoreductases - isolation &amp; purification</subject><subject>Aldehydes</subject><subject>Amino Acid Sequence</subject><subject>Amino acids</subject><subject>Biological and medical sciences</subject><subject>cations</subject><subject>Chromosomes</subject><subject>Dehydrogenase</subject><subject>Dehydrogenases</subject><subject>Disruption</subject><subject>Ethanol</subject><subject>Ethanol metabolism</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Fungi</subject><subject>Gene sequencing</subject><subject>Genes, Fungal - genetics</subject><subject>Glucose</subject><subject>Growth conditions</subject><subject>Growth, nutrition, metabolism, transports, enzymes. Molecular biology</subject><subject>Homology</subject><subject>Magnesium</subject><subject>Microbiology</subject><subject>Mitochondria</subject><subject>Mitochondria - enzymology</subject><subject>Mitochondria - genetics</subject><subject>Molecular Sequence Data</subject><subject>Mutants</subject><subject>Mycology</subject><subject>Potassium</subject><subject>Protein purification</subject><subject>Saccharomyces cerevisiae</subject><subject>Saccharomyces cerevisiae - enzymology</subject><subject>Saccharomyces cerevisiae - genetics</subject><subject>Sequence Alignment</subject><subject>Yeast</subject><issn>0378-1097</issn><issn>1574-6968</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1998</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><recordid>eNqVkc2O0zAUhSMEGsrAIyAiQGxQiv8Sx0gs0IiBEUUshllbN_ZN6yqNO3YyTHl6nLbqAsECbyz7fOf6yCfLXlIyp2m9W89pKUVRqaqeU6Xq-dBQTio-v3-QzU7Sw2xGuKwLSpR8nD2JcU0IEYxUZ9mZqmRZCznLfl1Z7AfXOgOD830Ovc2ti2Hc7o--zYcV5kvsMcfeeOv65f7m69sCzODuYECbg8EBOourncV8vwWfLBBxGnANxqwg-M3OYMwNBrxz0QE-zR610EV8dtzPs5vLTz8uvhSL75-vLj4uCsMFU4VpJMpSgG2pJLQ1pSWIdcMVUK4YV7ZVsmaWSGoNNKRtRMNLIaisSfqVivPz7M1h7jb42xHjoDcuGuw66NGPUdeEMCJKksBXf4BrP4Y-ZdOMcyoqQVSVqPcHygQfY8BWb4PbQNhpSvRUj17rqQM9daCnevSxHn2fzM-PT4zNBu3Jeuwj6a-POkQDXRugNy6eMMZLpUqVsA8H7KfrcPcfAfTltwWb_OXB78ftP9zF3-O_OPha8BqWIUW7uWYkyaxWlFWM_wZDJMaU</recordid><startdate>199807</startdate><enddate>199807</enddate><creator>Tessier, W.D</creator><creator>Meaden, P.G</creator><creator>Dickinson, F.M</creator><creator>Midgley, M</creator><general>Blackwell Publishing Ltd</general><general>Blackwell</general><general>Oxford University Press</general><scope>FBQ</scope><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7QL</scope><scope>7T7</scope><scope>7TK</scope><scope>7TM</scope><scope>7U9</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8C1</scope><scope>8FD</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AEUYN</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>C1K</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>H94</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M7N</scope><scope>M7P</scope><scope>P64</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>RC3</scope><scope>7X8</scope></search><sort><creationdate>199807</creationdate><title>Identification and disruption of the gene encoding the K+-activated acetaldehyde dehydrogenase of Saccharomyces cerevisiae</title><author>Tessier, W.D ; Meaden, P.G ; Dickinson, F.M ; Midgley, M</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3429-cb7e754adf1701fc5d0ee8b39a139239df9782d071dcab0fb4b35441780b13633</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1998</creationdate><topic>Acetaldehyde</topic><topic>Acetaldehyde dehydrogenase</topic><topic>Aldehyde dehydrogenase</topic><topic>Aldehyde dehydrogenase family</topic><topic>Aldehyde Oxidoreductases - genetics</topic><topic>Aldehyde Oxidoreductases - isolation &amp; purification</topic><topic>Aldehydes</topic><topic>Amino Acid Sequence</topic><topic>Amino acids</topic><topic>Biological and medical sciences</topic><topic>cations</topic><topic>Chromosomes</topic><topic>Dehydrogenase</topic><topic>Dehydrogenases</topic><topic>Disruption</topic><topic>Ethanol</topic><topic>Ethanol metabolism</topic><topic>Fundamental and applied biological sciences. 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The gene is situated on the right arm of chromosome XV, bears the systematic name YOR374w and the deduced product shows significant homology to other members of the S. cerevisiae aldehyde dehydrogenase (ALDH) family. YOR374w has now been assigned the gene name ALD7. The N-terminal amino acid sequences of K+-ACDHs purified from several diverse strains of S. cerevisiae were determined, and found to have 81-100% identity in alignments with the product of ALD7. Haploid mutants containing a deletion of ALD7 were constructed and, in these strains, the K+-ACDH was not detectable under any growth conditions examined. The activity of the Mg2+-activated acetaldehyde dehydrogenase (Mg2+-ACDH), encoded by ALD6, remained at wild-type levels in the mutants. Growth on glucose was not affected in the mutants lacking ALD7 (in contrast to the behaviour of ald6 mutants), whereas growth on ethanol was severely impaired. This observation, together with previous work by our group, shows that both the Mg2+- and K+-ACDHs are required for growth on ethanol, whilst only the former plays a role during growth on glucose.</abstract><cop>Oxford, UK</cop><pub>Blackwell Publishing Ltd</pub><pmid>9675847</pmid><doi>10.1111/j.1574-6968.1998.tb13063.x</doi><tpages>6</tpages></addata></record>
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subjects Acetaldehyde
Acetaldehyde dehydrogenase
Aldehyde dehydrogenase
Aldehyde dehydrogenase family
Aldehyde Oxidoreductases - genetics
Aldehyde Oxidoreductases - isolation & purification
Aldehydes
Amino Acid Sequence
Amino acids
Biological and medical sciences
cations
Chromosomes
Dehydrogenase
Dehydrogenases
Disruption
Ethanol
Ethanol metabolism
Fundamental and applied biological sciences. Psychology
Fungi
Gene sequencing
Genes, Fungal - genetics
Glucose
Growth conditions
Growth, nutrition, metabolism, transports, enzymes. Molecular biology
Homology
Magnesium
Microbiology
Mitochondria
Mitochondria - enzymology
Mitochondria - genetics
Molecular Sequence Data
Mutants
Mycology
Potassium
Protein purification
Saccharomyces cerevisiae
Saccharomyces cerevisiae - enzymology
Saccharomyces cerevisiae - genetics
Sequence Alignment
Yeast
title Identification and disruption of the gene encoding the K+-activated acetaldehyde dehydrogenase of Saccharomyces cerevisiae
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