Glucosamine as carbon source for amino acid-producing Corynebacterium glutamicum
Corynebacterium glutamicum grows with a variety of carbohydrates and carbohydrate derivatives as sole carbon sources; however, growth with glucosamine has not yet been reported. We isolated a spontaneous mutant (M4) which is able to grow as fast with glucosamine as with glucose as sole carbon source...
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creator | Uhde, Andreas Youn, Jung-Won Maeda, Tomoya Clermont, Lina Matano, Christian Krämer, Reinhard Wendisch, Volker F. Seibold, Gerd M. Marin, Kay |
description | Corynebacterium glutamicum
grows with a variety of carbohydrates and carbohydrate derivatives as sole carbon sources; however, growth with glucosamine has not yet been reported. We isolated a spontaneous mutant (M4) which is able to grow as fast with glucosamine as with glucose as sole carbon source. Glucosamine also served as a combined source of carbon, energy and nitrogen for the mutant strain. Characterisation of the M4 mutant revealed a significantly increased expression of the
nagB
gene encoding the glucosamine-6P deaminase NagB involved in degradation of glucosamine, as a consequence of a single mutation in the promoter region of the
nagAB-scrB
operon. Ectopic
nagB
overexpression verified that the activity of the NagB enzyme is in fact the growth limiting factor under these conditions. In addition, glucosamine uptake was studied, which proved to be unchanged in the wild-type and M4 mutant strains. Using specific deletion strains, we identified the PTS
Glc
transport system to be responsible for glucosamine uptake in
C. glutamicum
. The affinity of this uptake system for glucosamine was about 40-fold lower than that for its major substrate glucose. Because of this difference in affinity, glucosamine is efficiently taken up only if external glucose is absent or present at low concentrations.
C. glutamicum
was also examined for its suitability to use glucosamine as substrate for biotechnological purposes. Upon overexpression of the
nagB
gene in suitable
C. glutamicum
producer strains, efficient production of both the amino acid
l
-lysine and the diamine putrescine from glucosamine was demonstrated. |
doi_str_mv | 10.1007/s00253-012-4313-8 |
format | Article |
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grows with a variety of carbohydrates and carbohydrate derivatives as sole carbon sources; however, growth with glucosamine has not yet been reported. We isolated a spontaneous mutant (M4) which is able to grow as fast with glucosamine as with glucose as sole carbon source. Glucosamine also served as a combined source of carbon, energy and nitrogen for the mutant strain. Characterisation of the M4 mutant revealed a significantly increased expression of the
nagB
gene encoding the glucosamine-6P deaminase NagB involved in degradation of glucosamine, as a consequence of a single mutation in the promoter region of the
nagAB-scrB
operon. Ectopic
nagB
overexpression verified that the activity of the NagB enzyme is in fact the growth limiting factor under these conditions. In addition, glucosamine uptake was studied, which proved to be unchanged in the wild-type and M4 mutant strains. Using specific deletion strains, we identified the PTS
Glc
transport system to be responsible for glucosamine uptake in
C. glutamicum
. The affinity of this uptake system for glucosamine was about 40-fold lower than that for its major substrate glucose. Because of this difference in affinity, glucosamine is efficiently taken up only if external glucose is absent or present at low concentrations.
C. glutamicum
was also examined for its suitability to use glucosamine as substrate for biotechnological purposes. Upon overexpression of the
nagB
gene in suitable
C. glutamicum
producer strains, efficient production of both the amino acid
l
-lysine and the diamine putrescine from glucosamine was demonstrated.</description><identifier>ISSN: 0175-7598</identifier><identifier>EISSN: 1432-0614</identifier><identifier>DOI: 10.1007/s00253-012-4313-8</identifier><identifier>PMID: 22854894</identifier><language>eng</language><publisher>Berlin/Heidelberg: Springer-Verlag</publisher><subject>Aldose-Ketose Isomerases - genetics ; Aldose-Ketose Isomerases - metabolism ; Amino acids ; Amino Acids - biosynthesis ; Applied Microbial and Cell Physiology ; Bacteria ; Bacterial Proteins - genetics ; Bacterial Proteins - metabolism ; Biomedical and Life Sciences ; Biotechnology ; Carbohydrates ; Carbon ; Carbon - metabolism ; Carbon sources ; Cloning ; Corynebacteria ; Corynebacterium glutamicum ; Corynebacterium glutamicum - enzymology ; Corynebacterium glutamicum - genetics ; Corynebacterium glutamicum - growth & development ; Corynebacterium glutamicum - metabolism ; E coli ; Genes ; Glucosamine ; Glucosamine - metabolism ; Glucose ; Glucose metabolism ; Life Sciences ; Metabolism ; Microbial Genetics and Genomics ; Microbiological research ; Microbiology ; Mutants ; Mutation ; Nitrogen ; Physiological aspects ; Plasmids ; Point Mutation ; Prokaryotes ; Promoter Regions, Genetic ; Studies</subject><ispartof>Applied microbiology and biotechnology, 2013-02, Vol.97 (4), p.1679-1687</ispartof><rights>Springer-Verlag 2012</rights><rights>COPYRIGHT 2013 Springer</rights><rights>Springer-Verlag 2013</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c657t-6b269ab3323551b596069059d3605cbd081aa88bb7f38ab558809347ec827ac03</citedby><cites>FETCH-LOGICAL-c657t-6b269ab3323551b596069059d3605cbd081aa88bb7f38ab558809347ec827ac03</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1007/s00253-012-4313-8$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s00253-012-4313-8$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>314,777,781,27905,27906,41469,42538,51300</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/22854894$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Uhde, Andreas</creatorcontrib><creatorcontrib>Youn, Jung-Won</creatorcontrib><creatorcontrib>Maeda, Tomoya</creatorcontrib><creatorcontrib>Clermont, Lina</creatorcontrib><creatorcontrib>Matano, Christian</creatorcontrib><creatorcontrib>Krämer, Reinhard</creatorcontrib><creatorcontrib>Wendisch, Volker F.</creatorcontrib><creatorcontrib>Seibold, Gerd M.</creatorcontrib><creatorcontrib>Marin, Kay</creatorcontrib><title>Glucosamine as carbon source for amino acid-producing Corynebacterium glutamicum</title><title>Applied microbiology and biotechnology</title><addtitle>Appl Microbiol Biotechnol</addtitle><addtitle>Appl Microbiol Biotechnol</addtitle><description>Corynebacterium glutamicum
grows with a variety of carbohydrates and carbohydrate derivatives as sole carbon sources; however, growth with glucosamine has not yet been reported. We isolated a spontaneous mutant (M4) which is able to grow as fast with glucosamine as with glucose as sole carbon source. Glucosamine also served as a combined source of carbon, energy and nitrogen for the mutant strain. Characterisation of the M4 mutant revealed a significantly increased expression of the
nagB
gene encoding the glucosamine-6P deaminase NagB involved in degradation of glucosamine, as a consequence of a single mutation in the promoter region of the
nagAB-scrB
operon. Ectopic
nagB
overexpression verified that the activity of the NagB enzyme is in fact the growth limiting factor under these conditions. In addition, glucosamine uptake was studied, which proved to be unchanged in the wild-type and M4 mutant strains. Using specific deletion strains, we identified the PTS
Glc
transport system to be responsible for glucosamine uptake in
C. glutamicum
. The affinity of this uptake system for glucosamine was about 40-fold lower than that for its major substrate glucose. Because of this difference in affinity, glucosamine is efficiently taken up only if external glucose is absent or present at low concentrations.
C. glutamicum
was also examined for its suitability to use glucosamine as substrate for biotechnological purposes. Upon overexpression of the
nagB
gene in suitable
C. glutamicum
producer strains, efficient production of both the amino acid
l
-lysine and the diamine putrescine from glucosamine was demonstrated.</description><subject>Aldose-Ketose Isomerases - genetics</subject><subject>Aldose-Ketose Isomerases - metabolism</subject><subject>Amino acids</subject><subject>Amino Acids - biosynthesis</subject><subject>Applied Microbial and Cell Physiology</subject><subject>Bacteria</subject><subject>Bacterial Proteins - genetics</subject><subject>Bacterial Proteins - metabolism</subject><subject>Biomedical and Life Sciences</subject><subject>Biotechnology</subject><subject>Carbohydrates</subject><subject>Carbon</subject><subject>Carbon - metabolism</subject><subject>Carbon sources</subject><subject>Cloning</subject><subject>Corynebacteria</subject><subject>Corynebacterium glutamicum</subject><subject>Corynebacterium glutamicum - enzymology</subject><subject>Corynebacterium glutamicum - genetics</subject><subject>Corynebacterium glutamicum - growth & development</subject><subject>Corynebacterium glutamicum - metabolism</subject><subject>E coli</subject><subject>Genes</subject><subject>Glucosamine</subject><subject>Glucosamine - metabolism</subject><subject>Glucose</subject><subject>Glucose metabolism</subject><subject>Life Sciences</subject><subject>Metabolism</subject><subject>Microbial Genetics and Genomics</subject><subject>Microbiological research</subject><subject>Microbiology</subject><subject>Mutants</subject><subject>Mutation</subject><subject>Nitrogen</subject><subject>Physiological aspects</subject><subject>Plasmids</subject><subject>Point Mutation</subject><subject>Prokaryotes</subject><subject>Promoter Regions, 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as carbon source for amino acid-producing Corynebacterium glutamicum</title><author>Uhde, Andreas ; Youn, Jung-Won ; Maeda, Tomoya ; Clermont, Lina ; Matano, Christian ; Krämer, Reinhard ; Wendisch, Volker F. ; Seibold, Gerd M. ; Marin, Kay</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c657t-6b269ab3323551b596069059d3605cbd081aa88bb7f38ab558809347ec827ac03</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2013</creationdate><topic>Aldose-Ketose Isomerases - genetics</topic><topic>Aldose-Ketose Isomerases - metabolism</topic><topic>Amino acids</topic><topic>Amino Acids - biosynthesis</topic><topic>Applied Microbial and Cell Physiology</topic><topic>Bacteria</topic><topic>Bacterial Proteins - genetics</topic><topic>Bacterial Proteins - metabolism</topic><topic>Biomedical and Life Sciences</topic><topic>Biotechnology</topic><topic>Carbohydrates</topic><topic>Carbon</topic><topic>Carbon - metabolism</topic><topic>Carbon sources</topic><topic>Cloning</topic><topic>Corynebacteria</topic><topic>Corynebacterium glutamicum</topic><topic>Corynebacterium glutamicum - enzymology</topic><topic>Corynebacterium glutamicum - genetics</topic><topic>Corynebacterium glutamicum - growth & development</topic><topic>Corynebacterium glutamicum - metabolism</topic><topic>E coli</topic><topic>Genes</topic><topic>Glucosamine</topic><topic>Glucosamine - metabolism</topic><topic>Glucose</topic><topic>Glucose metabolism</topic><topic>Life Sciences</topic><topic>Metabolism</topic><topic>Microbial Genetics and Genomics</topic><topic>Microbiological research</topic><topic>Microbiology</topic><topic>Mutants</topic><topic>Mutation</topic><topic>Nitrogen</topic><topic>Physiological aspects</topic><topic>Plasmids</topic><topic>Point Mutation</topic><topic>Prokaryotes</topic><topic>Promoter Regions, Genetic</topic><topic>Studies</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Uhde, Andreas</creatorcontrib><creatorcontrib>Youn, Jung-Won</creatorcontrib><creatorcontrib>Maeda, Tomoya</creatorcontrib><creatorcontrib>Clermont, Lina</creatorcontrib><creatorcontrib>Matano, Christian</creatorcontrib><creatorcontrib>Krämer, Reinhard</creatorcontrib><creatorcontrib>Wendisch, Volker F.</creatorcontrib><creatorcontrib>Seibold, Gerd M.</creatorcontrib><creatorcontrib>Marin, Kay</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Gale In Context: Science</collection><collection>ProQuest Central (Corporate)</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Industrial and Applied Microbiology Abstracts 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Basic</collection><collection>MEDLINE - Academic</collection><collection>Biotechnology Research Abstracts</collection><jtitle>Applied microbiology and biotechnology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Uhde, Andreas</au><au>Youn, Jung-Won</au><au>Maeda, Tomoya</au><au>Clermont, Lina</au><au>Matano, Christian</au><au>Krämer, Reinhard</au><au>Wendisch, Volker F.</au><au>Seibold, Gerd M.</au><au>Marin, Kay</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Glucosamine as carbon source for amino acid-producing Corynebacterium glutamicum</atitle><jtitle>Applied microbiology and biotechnology</jtitle><stitle>Appl Microbiol Biotechnol</stitle><addtitle>Appl Microbiol Biotechnol</addtitle><date>2013-02-01</date><risdate>2013</risdate><volume>97</volume><issue>4</issue><spage>1679</spage><epage>1687</epage><pages>1679-1687</pages><issn>0175-7598</issn><eissn>1432-0614</eissn><abstract>Corynebacterium glutamicum
grows with a variety of carbohydrates and carbohydrate derivatives as sole carbon sources; however, growth with glucosamine has not yet been reported. We isolated a spontaneous mutant (M4) which is able to grow as fast with glucosamine as with glucose as sole carbon source. Glucosamine also served as a combined source of carbon, energy and nitrogen for the mutant strain. Characterisation of the M4 mutant revealed a significantly increased expression of the
nagB
gene encoding the glucosamine-6P deaminase NagB involved in degradation of glucosamine, as a consequence of a single mutation in the promoter region of the
nagAB-scrB
operon. Ectopic
nagB
overexpression verified that the activity of the NagB enzyme is in fact the growth limiting factor under these conditions. In addition, glucosamine uptake was studied, which proved to be unchanged in the wild-type and M4 mutant strains. Using specific deletion strains, we identified the PTS
Glc
transport system to be responsible for glucosamine uptake in
C. glutamicum
. The affinity of this uptake system for glucosamine was about 40-fold lower than that for its major substrate glucose. Because of this difference in affinity, glucosamine is efficiently taken up only if external glucose is absent or present at low concentrations.
C. glutamicum
was also examined for its suitability to use glucosamine as substrate for biotechnological purposes. Upon overexpression of the
nagB
gene in suitable
C. glutamicum
producer strains, efficient production of both the amino acid
l
-lysine and the diamine putrescine from glucosamine was demonstrated.</abstract><cop>Berlin/Heidelberg</cop><pub>Springer-Verlag</pub><pmid>22854894</pmid><doi>10.1007/s00253-012-4313-8</doi><tpages>9</tpages></addata></record> |
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source | MEDLINE; SpringerLink Journals |
subjects | Aldose-Ketose Isomerases - genetics Aldose-Ketose Isomerases - metabolism Amino acids Amino Acids - biosynthesis Applied Microbial and Cell Physiology Bacteria Bacterial Proteins - genetics Bacterial Proteins - metabolism Biomedical and Life Sciences Biotechnology Carbohydrates Carbon Carbon - metabolism Carbon sources Cloning Corynebacteria Corynebacterium glutamicum Corynebacterium glutamicum - enzymology Corynebacterium glutamicum - genetics Corynebacterium glutamicum - growth & development Corynebacterium glutamicum - metabolism E coli Genes Glucosamine Glucosamine - metabolism Glucose Glucose metabolism Life Sciences Metabolism Microbial Genetics and Genomics Microbiological research Microbiology Mutants Mutation Nitrogen Physiological aspects Plasmids Point Mutation Prokaryotes Promoter Regions, Genetic Studies |
title | Glucosamine as carbon source for amino acid-producing Corynebacterium glutamicum |
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