functional analysis of Kluyveromyces lactis glutathione reductase
Glutathione reductase (GLR) null mutants of the yeast Kluyveromyces lactis, a model eukaryotic respiratory cell, were created and phenotypically analysed. We found that cells lacking GLR show decreased resistance to oxidative stress and higher levels of reactive oxygen species and catalase activity...
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Veröffentlicht in: | Yeast (Chichester, England) England), 2010-07, Vol.27 (7), p.431-441 |
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description | Glutathione reductase (GLR) null mutants of the yeast Kluyveromyces lactis, a model eukaryotic respiratory cell, were created and phenotypically analysed. We found that cells lacking GLR show decreased resistance to oxidative stress and higher levels of reactive oxygen species and catalase activity than the wild-type strain. However, glutathione redox levels (GSH : GSSG ratio) were similar in the ΔKlglr1 mutant and wild-type strains. The thioredoxin-thioredoxin reductase system is proposed as an alternative system for maintaining the GSH : GSSG ratio in the ΔKlglr1 mutant. The involvement of GLR in glucose metabolism in K. lactis is suggested by the improved growth on glucose caused by the ΔKlglr1 mutation and by the increased GLR activity in the ΔKlgcr1 strain, KlGcr1 being a transcriptional activator of glycolytic genes. We also studied the subcellular location of GLR in K. lactis, showing that it is present in mitochondria; however, the ΔKlglr1 mutation does not affect mitochondrial morphology. Genomic DNA integrity and life span are also unaffected by the ΔKlglr1 mutation, at least under the conditions tested in this study. Copyright © 2010 John Wiley & Sons, Ltd. |
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We found that cells lacking GLR show decreased resistance to oxidative stress and higher levels of reactive oxygen species and catalase activity than the wild-type strain. However, glutathione redox levels (GSH : GSSG ratio) were similar in the ΔKlglr1 mutant and wild-type strains. The thioredoxin-thioredoxin reductase system is proposed as an alternative system for maintaining the GSH : GSSG ratio in the ΔKlglr1 mutant. The involvement of GLR in glucose metabolism in K. lactis is suggested by the improved growth on glucose caused by the ΔKlglr1 mutation and by the increased GLR activity in the ΔKlgcr1 strain, KlGcr1 being a transcriptional activator of glycolytic genes. We also studied the subcellular location of GLR in K. lactis, showing that it is present in mitochondria; however, the ΔKlglr1 mutation does not affect mitochondrial morphology. Genomic DNA integrity and life span are also unaffected by the ΔKlglr1 mutation, at least under the conditions tested in this study. 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We found that cells lacking GLR show decreased resistance to oxidative stress and higher levels of reactive oxygen species and catalase activity than the wild-type strain. However, glutathione redox levels (GSH : GSSG ratio) were similar in the ΔKlglr1 mutant and wild-type strains. The thioredoxin-thioredoxin reductase system is proposed as an alternative system for maintaining the GSH : GSSG ratio in the ΔKlglr1 mutant. The involvement of GLR in glucose metabolism in K. lactis is suggested by the improved growth on glucose caused by the ΔKlglr1 mutation and by the increased GLR activity in the ΔKlgcr1 strain, KlGcr1 being a transcriptional activator of glycolytic genes. We also studied the subcellular location of GLR in K. lactis, showing that it is present in mitochondria; however, the ΔKlglr1 mutation does not affect mitochondrial morphology. Genomic DNA integrity and life span are also unaffected by the ΔKlglr1 mutation, at least under the conditions tested in this study. Copyright © 2010 John Wiley & Sons, Ltd.</description><subject>Catalase - metabolism</subject><subject>Fungal Proteins - genetics</subject><subject>Fungal Proteins - metabolism</subject><subject>Gene Deletion</subject><subject>Glucose - metabolism</subject><subject>glutathione reductase</subject><subject>Glutathione Reductase - genetics</subject><subject>Glutathione Reductase - metabolism</subject><subject>Kluyveromyces</subject><subject>Kluyveromyces - drug effects</subject><subject>Kluyveromyces - enzymology</subject><subject>Kluyveromyces - metabolism</subject><subject>Kluyveromyces lactis</subject><subject>Oxidative Stress</subject><subject>Oxidoreductases - genetics</subject><subject>Reactive Oxygen Species - metabolism</subject><subject>yeast</subject><issn>0749-503X</issn><issn>1097-0061</issn><issn>1097-0061</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2010</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqF0b1OwzAUhmELgWgpSFwBZIMl5Ti2Y2esqvIjKjFAJZgsJzkuQUlT4gSUu8dVCxvqYi-P3uF8hJxTGFOA6KZHM6YyhgMypJDIECCmh2QIkiehAPY6ICfOfQBQKiJ1TAYRUK6YkkMysd0qa4t6ZcrA-Kd3hQtqGzyWXf-FTV31GbqgNN64YFl2rWnfvcagwbzLWuPwlBxZUzo82_0jsridvUzvw_nT3cN0Mg8zziMIk8wIiTQXKYXUMogVz5WKjBRGxSIX0iLQWFobcWUilaNAatPUSAuY2gTYiFxtu-um_uzQtboqXIZlaVZYd04rxYAxxuP9UkaUccWTvVIylsRcSOXl9VZmTe1cg1avm6IyTa8p6M0G2m-gNxt4erGLdmmF-R_8PboH4RZ8FyX2_4b022yyC15uvTW1NsumcHrx7GsMqD9dLCn7AVXBmTY</recordid><startdate>201007</startdate><enddate>201007</enddate><creator>García-Leiro, A</creator><creator>Cerdán, M.E</creator><creator>González-Siso, M.I</creator><general>John Wiley & Sons, Ltd</general><scope>FBQ</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>7X8</scope><scope>M7N</scope></search><sort><creationdate>201007</creationdate><title>functional analysis of Kluyveromyces lactis glutathione reductase</title><author>García-Leiro, A ; Cerdán, M.E ; González-Siso, M.I</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4420-9ca57e1d5b10bf30684d882a75a865d57fe0167ff248a28de5e1fbba7f0ebf903</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2010</creationdate><topic>Catalase - metabolism</topic><topic>Fungal Proteins - genetics</topic><topic>Fungal Proteins - metabolism</topic><topic>Gene Deletion</topic><topic>Glucose - metabolism</topic><topic>glutathione reductase</topic><topic>Glutathione Reductase - genetics</topic><topic>Glutathione Reductase - metabolism</topic><topic>Kluyveromyces</topic><topic>Kluyveromyces - drug effects</topic><topic>Kluyveromyces - enzymology</topic><topic>Kluyveromyces - metabolism</topic><topic>Kluyveromyces lactis</topic><topic>Oxidative Stress</topic><topic>Oxidoreductases - genetics</topic><topic>Reactive Oxygen Species - metabolism</topic><topic>yeast</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>García-Leiro, A</creatorcontrib><creatorcontrib>Cerdán, M.E</creatorcontrib><creatorcontrib>González-Siso, M.I</creatorcontrib><collection>AGRIS</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>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><jtitle>Yeast (Chichester, England)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>García-Leiro, A</au><au>Cerdán, M.E</au><au>González-Siso, M.I</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>functional analysis of Kluyveromyces lactis glutathione reductase</atitle><jtitle>Yeast (Chichester, England)</jtitle><addtitle>Yeast</addtitle><date>2010-07</date><risdate>2010</risdate><volume>27</volume><issue>7</issue><spage>431</spage><epage>441</epage><pages>431-441</pages><issn>0749-503X</issn><issn>1097-0061</issn><eissn>1097-0061</eissn><abstract>Glutathione reductase (GLR) null mutants of the yeast Kluyveromyces lactis, a model eukaryotic respiratory cell, were created and phenotypically analysed. We found that cells lacking GLR show decreased resistance to oxidative stress and higher levels of reactive oxygen species and catalase activity than the wild-type strain. However, glutathione redox levels (GSH : GSSG ratio) were similar in the ΔKlglr1 mutant and wild-type strains. The thioredoxin-thioredoxin reductase system is proposed as an alternative system for maintaining the GSH : GSSG ratio in the ΔKlglr1 mutant. The involvement of GLR in glucose metabolism in K. lactis is suggested by the improved growth on glucose caused by the ΔKlglr1 mutation and by the increased GLR activity in the ΔKlgcr1 strain, KlGcr1 being a transcriptional activator of glycolytic genes. We also studied the subcellular location of GLR in K. lactis, showing that it is present in mitochondria; however, the ΔKlglr1 mutation does not affect mitochondrial morphology. Genomic DNA integrity and life span are also unaffected by the ΔKlglr1 mutation, at least under the conditions tested in this study. Copyright © 2010 John Wiley & Sons, Ltd.</abstract><cop>Chichester, UK</cop><pub>John Wiley & Sons, Ltd</pub><pmid>20148387</pmid><doi>10.1002/yea.1760</doi><tpages>11</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Catalase - metabolism Fungal Proteins - genetics Fungal Proteins - metabolism Gene Deletion Glucose - metabolism glutathione reductase Glutathione Reductase - genetics Glutathione Reductase - metabolism Kluyveromyces Kluyveromyces - drug effects Kluyveromyces - enzymology Kluyveromyces - metabolism Kluyveromyces lactis Oxidative Stress Oxidoreductases - genetics Reactive Oxygen Species - metabolism yeast |
title | functional analysis of Kluyveromyces lactis glutathione reductase |
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