Physiological response of Corynebacterium glutamicum to oxidative stress induced by deletion of the transcriptional repressor McbR

1 Biochemical Engineering Institute, Saarland University, Saarbrücken, Germany 2 BASF SE, Ludwigshafen, Germany Correspondence Christoph Wittmann c.wittmann{at}tu-bs.de In the present work the metabolic response of Corynebacterium glutamicum to deletion of the global transcriptional regulator McbR,...

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Veröffentlicht in:Microbiology (Society for General Microbiology) 2008-12, Vol.154 (12), p.3917-3930
Hauptverfasser: Kromer, Jens O, Bolten, Christoph J, Heinzle, Elmar, Schroder, Hartwig, Wittmann, Christoph
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container_issue 12
container_start_page 3917
container_title Microbiology (Society for General Microbiology)
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creator Kromer, Jens O
Bolten, Christoph J
Heinzle, Elmar
Schroder, Hartwig
Wittmann, Christoph
description 1 Biochemical Engineering Institute, Saarland University, Saarbrücken, Germany 2 BASF SE, Ludwigshafen, Germany Correspondence Christoph Wittmann c.wittmann{at}tu-bs.de In the present work the metabolic response of Corynebacterium glutamicum to deletion of the global transcriptional regulator McbR, which controls, e.g. the expression of enzymes of L -methionine and L -cysteine biosynthesis and sulfur assimilation, was studied. Several oxidative stress proteins were significantly upregulated among about 40 proteins in response to deletion of McbR. Linked to this oxidative stress, the mutant exhibited a 50 % reduced growth rate, a 30 % reduced glucose uptake rate and a 30 % reduced biomass yield. It also showed metabolic flux rerouting in response to the deletion. NADPH metabolism was strongly altered. In contrast to the wild-type, the deletion strain supplied significantly more NADPH than required for anabolism, indicating the activity of additional NADPH-consuming reactions. These involved enzymes of oxidative stress protection. Through redirection of metabolic carbon flux in the central catabolism, including a 40 % increased tricarboxylic acid (TCA) cycle flux, the mutant revealed an enhanced NADPH supply to provide redox power for the antioxidant systems. This, however, was not sufficient to compensate for the oxidative stress, as indicated by the drastically disturbed redox equilibrium. The NADPH/NADP + ratio in C. glutamicum mcbR was only 0.29, and thus much lower than that of the wild-type (2.35). Similarly, the NADH/NAD + ratio was substantially reduced from 0.18 in the wild-type to 0.08 in the mutant. Deletion of McbR is regarded as a key step towards biotechnological L -methionine overproduction in C. glutamicum . C. glutamicum mcbR , however, did not overproduce L -methionine; this was very likely linked to the low availability of NADPH. Since oxidative stress is often observed in industrial production processes, engineering of NADPH metabolism could be a general strategy for improvement of production strains. Unlike the wild-type, C. glutamicum mcbR contained large granules with high phosphorus content. The storage of these energy-rich polyphosphates is probably the result of a large excess of formation of ATP, as revealed by estimation of the underlying fluxes linked to energy metabolism. Abbreviations: CDM, cell dry mass; EDX, energy dispersive X-ray; PPP, pentose phosphate pathway; TCA cycle, tricarboxylic acid cycle Present address: Australia
doi_str_mv 10.1099/mic.0.2008/021204-0
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Several oxidative stress proteins were significantly upregulated among about 40 proteins in response to deletion of McbR. Linked to this oxidative stress, the mutant exhibited a 50 % reduced growth rate, a 30 % reduced glucose uptake rate and a 30 % reduced biomass yield. It also showed metabolic flux rerouting in response to the deletion. NADPH metabolism was strongly altered. In contrast to the wild-type, the deletion strain supplied significantly more NADPH than required for anabolism, indicating the activity of additional NADPH-consuming reactions. These involved enzymes of oxidative stress protection. Through redirection of metabolic carbon flux in the central catabolism, including a 40 % increased tricarboxylic acid (TCA) cycle flux, the mutant revealed an enhanced NADPH supply to provide redox power for the antioxidant systems. This, however, was not sufficient to compensate for the oxidative stress, as indicated by the drastically disturbed redox equilibrium. The NADPH/NADP + ratio in C. glutamicum mcbR was only 0.29, and thus much lower than that of the wild-type (2.35). Similarly, the NADH/NAD + ratio was substantially reduced from 0.18 in the wild-type to 0.08 in the mutant. Deletion of McbR is regarded as a key step towards biotechnological L -methionine overproduction in C. glutamicum . C. glutamicum mcbR , however, did not overproduce L -methionine; this was very likely linked to the low availability of NADPH. Since oxidative stress is often observed in industrial production processes, engineering of NADPH metabolism could be a general strategy for improvement of production strains. Unlike the wild-type, C. glutamicum mcbR contained large granules with high phosphorus content. The storage of these energy-rich polyphosphates is probably the result of a large excess of formation of ATP, as revealed by estimation of the underlying fluxes linked to energy metabolism. Abbreviations: CDM, cell dry mass; EDX, energy dispersive X-ray; PPP, pentose phosphate pathway; TCA cycle, tricarboxylic acid cycle Present address: Australian Institute for Bioengineering and Nanotechnology, University of Queensland, Brisbane, Australia. 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Several oxidative stress proteins were significantly upregulated among about 40 proteins in response to deletion of McbR. Linked to this oxidative stress, the mutant exhibited a 50 % reduced growth rate, a 30 % reduced glucose uptake rate and a 30 % reduced biomass yield. It also showed metabolic flux rerouting in response to the deletion. NADPH metabolism was strongly altered. In contrast to the wild-type, the deletion strain supplied significantly more NADPH than required for anabolism, indicating the activity of additional NADPH-consuming reactions. These involved enzymes of oxidative stress protection. Through redirection of metabolic carbon flux in the central catabolism, including a 40 % increased tricarboxylic acid (TCA) cycle flux, the mutant revealed an enhanced NADPH supply to provide redox power for the antioxidant systems. This, however, was not sufficient to compensate for the oxidative stress, as indicated by the drastically disturbed redox equilibrium. The NADPH/NADP + ratio in C. glutamicum mcbR was only 0.29, and thus much lower than that of the wild-type (2.35). Similarly, the NADH/NAD + ratio was substantially reduced from 0.18 in the wild-type to 0.08 in the mutant. Deletion of McbR is regarded as a key step towards biotechnological L -methionine overproduction in C. glutamicum . C. glutamicum mcbR , however, did not overproduce L -methionine; this was very likely linked to the low availability of NADPH. Since oxidative stress is often observed in industrial production processes, engineering of NADPH metabolism could be a general strategy for improvement of production strains. Unlike the wild-type, C. glutamicum mcbR contained large granules with high phosphorus content. The storage of these energy-rich polyphosphates is probably the result of a large excess of formation of ATP, as revealed by estimation of the underlying fluxes linked to energy metabolism. Abbreviations: CDM, cell dry mass; EDX, energy dispersive X-ray; PPP, pentose phosphate pathway; TCA cycle, tricarboxylic acid cycle Present address: Australian Institute for Bioengineering and Nanotechnology, University of Queensland, Brisbane, Australia. Present address: Biochemical Engineering Institute, Technische Universität Braunschweig, Gaussstrasse 17, 38106 Braunschweig, Germany.</description><subject>Bacterial Proteins - genetics</subject><subject>Bacterial Proteins - metabolism</subject><subject>Bacteriology</subject><subject>Biological and medical sciences</subject><subject>Corynebacterium glutamicum</subject><subject>Corynebacterium glutamicum - genetics</subject><subject>Corynebacterium glutamicum - growth &amp; development</subject><subject>Corynebacterium glutamicum - metabolism</subject><subject>Corynebacterium glutamicum - physiology</subject><subject>Culture Media</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Gene Deletion</subject><subject>Gene Expression Profiling</subject><subject>Gene Expression Regulation, Bacterial</subject><subject>Genetics</subject><subject>Growth, nutrition, cell differenciation</subject><subject>Microbiology</subject><subject>Oxidative Stress</subject><subject>Proteome</subject><subject>Repressor Proteins - genetics</subject><subject>Repressor Proteins - metabolism</subject><issn>1350-0872</issn><issn>1465-2080</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2008</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkU9v1DAQxSMEon_gEyAhX-BQKduxHSf2Ea1Ki9QKhOBsOc5k1yiJg-0Ae-0nx2FXcOQ0o_HvvSf5FcUrChsKSl2Pzm5gwwDkNTDKoCrhSXFOq1qUDCQ8zTsXUIJs2FlxEeM3gPwI9HlxRhVUTSPkefH4aX-Izg9-56wZSMA4-yki8T3Z-nCYsDU2YXDLSHbDkkwOzWvyxP9ynUnuB5KYsioSN3WLxY60B9LhgMn5aXVJeyQpmCna4Ob1-CdlXiU-kAfbfn5RPOvNEPHlaV4WX9_ffNnelfcfbz9s392XVlBIpQWqVMsrJTuFveSmN5ZWlkrBKZVMcqGk6nqUQjJVMaUMr4FDC72sa24YvyzeHn3n4L8vGJMeXbQ4DGZCv0Rdq2wllfgvSFXDqKxVBvkRtMHHGLDXc3CjCQdNQa8dZaHVoNeO9LEjDVn1-mS_tCN2_zSnUjLw5gSYmEvp8-9ZF_9yDFTT1LLJ3NWR27vd_qcLqHc45cTgW-fXaCoqTZnmijb8N7dIqv4</recordid><startdate>20081201</startdate><enddate>20081201</enddate><creator>Kromer, Jens O</creator><creator>Bolten, Christoph J</creator><creator>Heinzle, Elmar</creator><creator>Schroder, Hartwig</creator><creator>Wittmann, Christoph</creator><general>Soc General Microbiol</general><general>Society for General Microbiology</general><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>7QL</scope><scope>7TM</scope><scope>C1K</scope><scope>7X8</scope></search><sort><creationdate>20081201</creationdate><title>Physiological response of Corynebacterium glutamicum to oxidative stress induced by deletion of the transcriptional repressor McbR</title><author>Kromer, Jens O ; Bolten, Christoph J ; Heinzle, Elmar ; Schroder, Hartwig ; Wittmann, Christoph</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c510t-c0199b3498d9ef83afac14c18531182835989dfe858294299a36030b0f8663a23</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2008</creationdate><topic>Bacterial Proteins - genetics</topic><topic>Bacterial Proteins - metabolism</topic><topic>Bacteriology</topic><topic>Biological and medical sciences</topic><topic>Corynebacterium glutamicum</topic><topic>Corynebacterium glutamicum - genetics</topic><topic>Corynebacterium glutamicum - growth &amp; development</topic><topic>Corynebacterium glutamicum - metabolism</topic><topic>Corynebacterium glutamicum - physiology</topic><topic>Culture Media</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Gene Deletion</topic><topic>Gene Expression Profiling</topic><topic>Gene Expression Regulation, Bacterial</topic><topic>Genetics</topic><topic>Growth, nutrition, cell differenciation</topic><topic>Microbiology</topic><topic>Oxidative Stress</topic><topic>Proteome</topic><topic>Repressor Proteins - genetics</topic><topic>Repressor Proteins - metabolism</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kromer, Jens O</creatorcontrib><creatorcontrib>Bolten, Christoph J</creatorcontrib><creatorcontrib>Heinzle, Elmar</creatorcontrib><creatorcontrib>Schroder, Hartwig</creatorcontrib><creatorcontrib>Wittmann, Christoph</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>Bacteriology Abstracts (Microbiology B)</collection><collection>Nucleic Acids Abstracts</collection><collection>Environmental Sciences and Pollution Management</collection><collection>MEDLINE - Academic</collection><jtitle>Microbiology (Society for General Microbiology)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kromer, Jens O</au><au>Bolten, Christoph J</au><au>Heinzle, Elmar</au><au>Schroder, Hartwig</au><au>Wittmann, Christoph</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Physiological response of Corynebacterium glutamicum to oxidative stress induced by deletion of the transcriptional repressor McbR</atitle><jtitle>Microbiology (Society for General Microbiology)</jtitle><addtitle>Microbiology</addtitle><date>2008-12-01</date><risdate>2008</risdate><volume>154</volume><issue>12</issue><spage>3917</spage><epage>3930</epage><pages>3917-3930</pages><issn>1350-0872</issn><eissn>1465-2080</eissn><abstract>1 Biochemical Engineering Institute, Saarland University, Saarbrücken, Germany 2 BASF SE, Ludwigshafen, Germany Correspondence Christoph Wittmann c.wittmann{at}tu-bs.de In the present work the metabolic response of Corynebacterium glutamicum to deletion of the global transcriptional regulator McbR, which controls, e.g. the expression of enzymes of L -methionine and L -cysteine biosynthesis and sulfur assimilation, was studied. Several oxidative stress proteins were significantly upregulated among about 40 proteins in response to deletion of McbR. Linked to this oxidative stress, the mutant exhibited a 50 % reduced growth rate, a 30 % reduced glucose uptake rate and a 30 % reduced biomass yield. It also showed metabolic flux rerouting in response to the deletion. NADPH metabolism was strongly altered. In contrast to the wild-type, the deletion strain supplied significantly more NADPH than required for anabolism, indicating the activity of additional NADPH-consuming reactions. These involved enzymes of oxidative stress protection. Through redirection of metabolic carbon flux in the central catabolism, including a 40 % increased tricarboxylic acid (TCA) cycle flux, the mutant revealed an enhanced NADPH supply to provide redox power for the antioxidant systems. This, however, was not sufficient to compensate for the oxidative stress, as indicated by the drastically disturbed redox equilibrium. The NADPH/NADP + ratio in C. glutamicum mcbR was only 0.29, and thus much lower than that of the wild-type (2.35). Similarly, the NADH/NAD + ratio was substantially reduced from 0.18 in the wild-type to 0.08 in the mutant. Deletion of McbR is regarded as a key step towards biotechnological L -methionine overproduction in C. glutamicum . C. glutamicum mcbR , however, did not overproduce L -methionine; this was very likely linked to the low availability of NADPH. Since oxidative stress is often observed in industrial production processes, engineering of NADPH metabolism could be a general strategy for improvement of production strains. Unlike the wild-type, C. glutamicum mcbR contained large granules with high phosphorus content. The storage of these energy-rich polyphosphates is probably the result of a large excess of formation of ATP, as revealed by estimation of the underlying fluxes linked to energy metabolism. Abbreviations: CDM, cell dry mass; EDX, energy dispersive X-ray; PPP, pentose phosphate pathway; TCA cycle, tricarboxylic acid cycle Present address: Australian Institute for Bioengineering and Nanotechnology, University of Queensland, Brisbane, Australia. Present address: Biochemical Engineering Institute, Technische Universität Braunschweig, Gaussstrasse 17, 38106 Braunschweig, Germany.</abstract><cop>Reading</cop><pub>Soc General Microbiol</pub><pmid>19047758</pmid><doi>10.1099/mic.0.2008/021204-0</doi><tpages>14</tpages><oa>free_for_read</oa></addata></record>
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subjects Bacterial Proteins - genetics
Bacterial Proteins - metabolism
Bacteriology
Biological and medical sciences
Corynebacterium glutamicum
Corynebacterium glutamicum - genetics
Corynebacterium glutamicum - growth & development
Corynebacterium glutamicum - metabolism
Corynebacterium glutamicum - physiology
Culture Media
Fundamental and applied biological sciences. Psychology
Gene Deletion
Gene Expression Profiling
Gene Expression Regulation, Bacterial
Genetics
Growth, nutrition, cell differenciation
Microbiology
Oxidative Stress
Proteome
Repressor Proteins - genetics
Repressor Proteins - metabolism
title Physiological response of Corynebacterium glutamicum to oxidative stress induced by deletion of the transcriptional repressor McbR
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