Inactivation of rsmA leads to overproduction of extracellular pectinases, cellulases, and proteases in Erwinia carotovora subsp. carotovora in the absence of the starvation/cell density-sensing signal, N-(3-oxohexanoyl)-L-homoserine lactone
The soft-rotting bacterium, Erwinia carotovora subsp. carotovora 71, produces extracellular enzymes such as pectate lyase isozymes (Pels), cellulase (Cel), polygalacturonase (Peh), and protease (Prt). While the extracellular levels of these enzymes are extremely low when the bacterium is grown in sa...
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description | The soft-rotting bacterium, Erwinia carotovora subsp. carotovora 71, produces extracellular enzymes such as pectate lyase isozymes (Pels), cellulase (Cel), polygalacturonase (Peh), and protease (Prt). While the extracellular levels of these enzymes are extremely low when the bacterium is grown in salts-yeast extract-glycerol (SYG) medium, the enzymatic activities are highly induced in SYG medium supplemented with celery extract. By transposon (mini-TnS) mutagenesis, we isolated a RsmA-mutant, AC5070, which overproduces extracellular enzymes; the basal levels of Pel, Peh, and Cel in AC5070 are higher than the induced levels in the RsmA+ parent, AC5047. While Peh production is mostly constitutive in AC5070, Pel, Cel, and Prt production is still inducible with celery extract. The high basal levels of pel-1, pel-3, and peh-1 mRNAs in AC5070 demonstrate that overproduction of the pectolytic enzymes is due to the stimulation of transcription. Using chromosomal DNA flanking mini-TnS as a probe, we cloned the wild-type rsmA+ allele, which suppresses Pel, Peh, Cel, and Prt production in both RsmA+ and RsmA- strains. The RsmA-mutant, like its parent, produces N-(3-oxohexanoyl)-L-homoserine lactone (HSL), a starvation/cell density-sensing signal required for extracellular enzyme production. To examine the role of HSL, we constructed HSL-deficient strains by replacing hslI, a locus required for HSL production, with hslI::Tn3HoHo1-Spc. While the basal levels of Pel, Peh, Cel, and Prt are comparable in the RsmA- mutant and its HSL- derivative, these enzymes are barely detectable in the Hsl-derivative of the RsmA+ parent strain. The Hsl- RsmA+ strain fails to elicit soft rot, whereas the Hsl-RsmA-strain, like its Hsl+ RsmA- parent, remains hypervirulent. These findings demonstrate that the RsmA-mutant produces extracellular enzymes and macerates plant tissue in the absence of HSL |
doi_str_mv | 10.1128/aem.61.5.1959-1967.1995 |
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(University of Missouri, Columbia, MO.) ; Cui, Y ; Liu, Y ; Korsi Dumenyo, C ; Chatterjee, A.K</creator><creatorcontrib>Chatterjee, A. (University of Missouri, Columbia, MO.) ; Cui, Y ; Liu, Y ; Korsi Dumenyo, C ; Chatterjee, A.K</creatorcontrib><description>The soft-rotting bacterium, Erwinia carotovora subsp. carotovora 71, produces extracellular enzymes such as pectate lyase isozymes (Pels), cellulase (Cel), polygalacturonase (Peh), and protease (Prt). While the extracellular levels of these enzymes are extremely low when the bacterium is grown in salts-yeast extract-glycerol (SYG) medium, the enzymatic activities are highly induced in SYG medium supplemented with celery extract. By transposon (mini-TnS) mutagenesis, we isolated a RsmA-mutant, AC5070, which overproduces extracellular enzymes; the basal levels of Pel, Peh, and Cel in AC5070 are higher than the induced levels in the RsmA+ parent, AC5047. While Peh production is mostly constitutive in AC5070, Pel, Cel, and Prt production is still inducible with celery extract. The high basal levels of pel-1, pel-3, and peh-1 mRNAs in AC5070 demonstrate that overproduction of the pectolytic enzymes is due to the stimulation of transcription. Using chromosomal DNA flanking mini-TnS as a probe, we cloned the wild-type rsmA+ allele, which suppresses Pel, Peh, Cel, and Prt production in both RsmA+ and RsmA- strains. The RsmA-mutant, like its parent, produces N-(3-oxohexanoyl)-L-homoserine lactone (HSL), a starvation/cell density-sensing signal required for extracellular enzyme production. To examine the role of HSL, we constructed HSL-deficient strains by replacing hslI, a locus required for HSL production, with hslI::Tn3HoHo1-Spc. While the basal levels of Pel, Peh, Cel, and Prt are comparable in the RsmA- mutant and its HSL- derivative, these enzymes are barely detectable in the Hsl-derivative of the RsmA+ parent strain. The Hsl- RsmA+ strain fails to elicit soft rot, whereas the Hsl-RsmA-strain, like its Hsl+ RsmA- parent, remains hypervirulent. These findings demonstrate that the RsmA-mutant produces extracellular enzymes and macerates plant tissue in the absence of HSL</description><identifier>ISSN: 0099-2240</identifier><identifier>EISSN: 1098-5336</identifier><identifier>DOI: 10.1128/aem.61.5.1959-1967.1995</identifier><identifier>PMID: 7646031</identifier><identifier>CODEN: AEMIDF</identifier><language>eng</language><publisher>Washington, DC: American Society for Microbiology</publisher><subject>4-Butyrolactone - analogs & derivatives ; 4-Butyrolactone - genetics ; 4-Butyrolactone - physiology ; Amino Acid Sequence ; ARN MENSAJERO ; ARN MESSAGER ; Bacteria ; Bacterial plant pathogens ; Biological and medical sciences ; Biology ; BIOSINTESIS ; BIOSYNTHESE ; CELLULASE ; Cellulase - biosynthesis ; Cellulase - genetics ; CELULASA ; Culture Media - pharmacology ; Disease ; Enzyme Induction - drug effects ; ERWINIA CAROTOVORA ; EXPRESION GENICA ; EXPRESSION DES GENES ; Flowers & plants ; Fundamental and applied biological sciences. Psychology ; GENE ; Gene Expression Regulation, Bacterial - drug effects ; GENES ; Genes, Bacterial ; Isoenzymes - biosynthesis ; Isoenzymes - genetics ; LACTONAS ; LACTONE ; LIASAS ; LOCI ; LOCUS ; LYASE ; Molecular Sequence Data ; MUTACION ; Mutagenesis, Insertional ; MUTANT ; MUTANTES ; MUTATION ; Pectobacterium carotovorum - drug effects ; Pectobacterium carotovorum - enzymology ; Pectobacterium carotovorum - genetics ; Pectobacterium carotovorum - pathogenicity ; Phytopathology. Animal pests. Plant and forest protection ; Plant Extracts - pharmacology ; POLIGALACTURONASA ; POLYGALACTURONASE ; Polygalacturonase - biosynthesis ; Polygalacturonase - genetics ; Polysaccharide-Lyases - biosynthesis ; Polysaccharide-Lyases - genetics ; PROTEASAS ; PROTEASE ; Recombinant Fusion Proteins - metabolism ; Repressor Proteins - genetics ; Repressor Proteins - physiology ; SECUENCIA NUCLEICA ; Sequence Alignment ; Sequence Homology, Amino Acid ; SEQUENCE NUCLEIQUE ; Systematics. Structure, properties and multiplication. Genetics ; Virulence</subject><ispartof>Applied and Environmental Microbiology, 1995-05, Vol.61 (5), p.1959-1967</ispartof><rights>1995 INIST-CNRS</rights><rights>Copyright American Society for Microbiology May 1995</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c609t-3b697e8051909ec6eda2870072cb221d234c0a7d70bdce7217b4b8f914585a1d3</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC167458/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC167458/$$EHTML$$P50$$Gpubmedcentral$$H</linktohtml><link.rule.ids>230,315,728,781,785,886,3189,3190,27925,27926,53792,53794</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=3512392$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/7646031$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Chatterjee, A. (University of Missouri, Columbia, MO.)</creatorcontrib><creatorcontrib>Cui, Y</creatorcontrib><creatorcontrib>Liu, Y</creatorcontrib><creatorcontrib>Korsi Dumenyo, C</creatorcontrib><creatorcontrib>Chatterjee, A.K</creatorcontrib><title>Inactivation of rsmA leads to overproduction of extracellular pectinases, cellulases, and proteases in Erwinia carotovora subsp. carotovora in the absence of the starvation/cell density-sensing signal, N-(3-oxohexanoyl)-L-homoserine lactone</title><title>Applied and Environmental Microbiology</title><addtitle>Appl Environ Microbiol</addtitle><description>The soft-rotting bacterium, Erwinia carotovora subsp. carotovora 71, produces extracellular enzymes such as pectate lyase isozymes (Pels), cellulase (Cel), polygalacturonase (Peh), and protease (Prt). While the extracellular levels of these enzymes are extremely low when the bacterium is grown in salts-yeast extract-glycerol (SYG) medium, the enzymatic activities are highly induced in SYG medium supplemented with celery extract. By transposon (mini-TnS) mutagenesis, we isolated a RsmA-mutant, AC5070, which overproduces extracellular enzymes; the basal levels of Pel, Peh, and Cel in AC5070 are higher than the induced levels in the RsmA+ parent, AC5047. While Peh production is mostly constitutive in AC5070, Pel, Cel, and Prt production is still inducible with celery extract. The high basal levels of pel-1, pel-3, and peh-1 mRNAs in AC5070 demonstrate that overproduction of the pectolytic enzymes is due to the stimulation of transcription. Using chromosomal DNA flanking mini-TnS as a probe, we cloned the wild-type rsmA+ allele, which suppresses Pel, Peh, Cel, and Prt production in both RsmA+ and RsmA- strains. The RsmA-mutant, like its parent, produces N-(3-oxohexanoyl)-L-homoserine lactone (HSL), a starvation/cell density-sensing signal required for extracellular enzyme production. To examine the role of HSL, we constructed HSL-deficient strains by replacing hslI, a locus required for HSL production, with hslI::Tn3HoHo1-Spc. While the basal levels of Pel, Peh, Cel, and Prt are comparable in the RsmA- mutant and its HSL- derivative, these enzymes are barely detectable in the Hsl-derivative of the RsmA+ parent strain. The Hsl- RsmA+ strain fails to elicit soft rot, whereas the Hsl-RsmA-strain, like its Hsl+ RsmA- parent, remains hypervirulent. These findings demonstrate that the RsmA-mutant produces extracellular enzymes and macerates plant tissue in the absence of HSL</description><subject>4-Butyrolactone - analogs & derivatives</subject><subject>4-Butyrolactone - genetics</subject><subject>4-Butyrolactone - physiology</subject><subject>Amino Acid Sequence</subject><subject>ARN MENSAJERO</subject><subject>ARN MESSAGER</subject><subject>Bacteria</subject><subject>Bacterial plant pathogens</subject><subject>Biological and medical sciences</subject><subject>Biology</subject><subject>BIOSINTESIS</subject><subject>BIOSYNTHESE</subject><subject>CELLULASE</subject><subject>Cellulase - biosynthesis</subject><subject>Cellulase - genetics</subject><subject>CELULASA</subject><subject>Culture Media - pharmacology</subject><subject>Disease</subject><subject>Enzyme Induction - drug effects</subject><subject>ERWINIA CAROTOVORA</subject><subject>EXPRESION GENICA</subject><subject>EXPRESSION DES GENES</subject><subject>Flowers & plants</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>GENE</subject><subject>Gene Expression Regulation, Bacterial - drug effects</subject><subject>GENES</subject><subject>Genes, Bacterial</subject><subject>Isoenzymes - biosynthesis</subject><subject>Isoenzymes - genetics</subject><subject>LACTONAS</subject><subject>LACTONE</subject><subject>LIASAS</subject><subject>LOCI</subject><subject>LOCUS</subject><subject>LYASE</subject><subject>Molecular Sequence Data</subject><subject>MUTACION</subject><subject>Mutagenesis, Insertional</subject><subject>MUTANT</subject><subject>MUTANTES</subject><subject>MUTATION</subject><subject>Pectobacterium carotovorum - drug effects</subject><subject>Pectobacterium carotovorum - enzymology</subject><subject>Pectobacterium carotovorum - genetics</subject><subject>Pectobacterium carotovorum - pathogenicity</subject><subject>Phytopathology. Animal pests. Plant and forest protection</subject><subject>Plant Extracts - pharmacology</subject><subject>POLIGALACTURONASA</subject><subject>POLYGALACTURONASE</subject><subject>Polygalacturonase - biosynthesis</subject><subject>Polygalacturonase - genetics</subject><subject>Polysaccharide-Lyases - biosynthesis</subject><subject>Polysaccharide-Lyases - genetics</subject><subject>PROTEASAS</subject><subject>PROTEASE</subject><subject>Recombinant Fusion Proteins - metabolism</subject><subject>Repressor Proteins - genetics</subject><subject>Repressor Proteins - physiology</subject><subject>SECUENCIA NUCLEICA</subject><subject>Sequence Alignment</subject><subject>Sequence Homology, Amino Acid</subject><subject>SEQUENCE NUCLEIQUE</subject><subject>Systematics. Structure, properties and multiplication. 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(University of Missouri, Columbia, MO.)</creator><creator>Cui, Y</creator><creator>Liu, Y</creator><creator>Korsi Dumenyo, C</creator><creator>Chatterjee, A.K</creator><general>American Society for Microbiology</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>7QL</scope><scope>7QO</scope><scope>7SN</scope><scope>7SS</scope><scope>7ST</scope><scope>7T7</scope><scope>7TM</scope><scope>7U9</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>H94</scope><scope>M7N</scope><scope>P64</scope><scope>RC3</scope><scope>SOI</scope><scope>5PM</scope></search><sort><creationdate>19950501</creationdate><title>Inactivation of rsmA leads to overproduction of extracellular pectinases, cellulases, and proteases in Erwinia carotovora subsp. carotovora in the absence of the starvation/cell density-sensing signal, N-(3-oxohexanoyl)-L-homoserine lactone</title><author>Chatterjee, A. (University of Missouri, Columbia, MO.) ; Cui, Y ; Liu, Y ; Korsi Dumenyo, C ; Chatterjee, A.K</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c609t-3b697e8051909ec6eda2870072cb221d234c0a7d70bdce7217b4b8f914585a1d3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1995</creationdate><topic>4-Butyrolactone - analogs & derivatives</topic><topic>4-Butyrolactone - genetics</topic><topic>4-Butyrolactone - physiology</topic><topic>Amino Acid Sequence</topic><topic>ARN MENSAJERO</topic><topic>ARN MESSAGER</topic><topic>Bacteria</topic><topic>Bacterial plant pathogens</topic><topic>Biological and medical sciences</topic><topic>Biology</topic><topic>BIOSINTESIS</topic><topic>BIOSYNTHESE</topic><topic>CELLULASE</topic><topic>Cellulase - biosynthesis</topic><topic>Cellulase - genetics</topic><topic>CELULASA</topic><topic>Culture Media - pharmacology</topic><topic>Disease</topic><topic>Enzyme Induction - drug effects</topic><topic>ERWINIA CAROTOVORA</topic><topic>EXPRESION GENICA</topic><topic>EXPRESSION DES GENES</topic><topic>Flowers & plants</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>GENE</topic><topic>Gene Expression Regulation, Bacterial - drug effects</topic><topic>GENES</topic><topic>Genes, Bacterial</topic><topic>Isoenzymes - biosynthesis</topic><topic>Isoenzymes - genetics</topic><topic>LACTONAS</topic><topic>LACTONE</topic><topic>LIASAS</topic><topic>LOCI</topic><topic>LOCUS</topic><topic>LYASE</topic><topic>Molecular Sequence Data</topic><topic>MUTACION</topic><topic>Mutagenesis, Insertional</topic><topic>MUTANT</topic><topic>MUTANTES</topic><topic>MUTATION</topic><topic>Pectobacterium carotovorum - drug effects</topic><topic>Pectobacterium carotovorum - enzymology</topic><topic>Pectobacterium carotovorum - genetics</topic><topic>Pectobacterium carotovorum - pathogenicity</topic><topic>Phytopathology. Animal pests. Plant and forest protection</topic><topic>Plant Extracts - pharmacology</topic><topic>POLIGALACTURONASA</topic><topic>POLYGALACTURONASE</topic><topic>Polygalacturonase - biosynthesis</topic><topic>Polygalacturonase - genetics</topic><topic>Polysaccharide-Lyases - biosynthesis</topic><topic>Polysaccharide-Lyases - genetics</topic><topic>PROTEASAS</topic><topic>PROTEASE</topic><topic>Recombinant Fusion Proteins - metabolism</topic><topic>Repressor Proteins - genetics</topic><topic>Repressor Proteins - physiology</topic><topic>SECUENCIA NUCLEICA</topic><topic>Sequence Alignment</topic><topic>Sequence Homology, Amino Acid</topic><topic>SEQUENCE NUCLEIQUE</topic><topic>Systematics. Structure, properties and multiplication. Genetics</topic><topic>Virulence</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Chatterjee, A. (University of Missouri, Columbia, MO.)</creatorcontrib><creatorcontrib>Cui, Y</creatorcontrib><creatorcontrib>Liu, Y</creatorcontrib><creatorcontrib>Korsi Dumenyo, C</creatorcontrib><creatorcontrib>Chatterjee, A.K</creatorcontrib><collection>AGRIS</collection><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>Biotechnology Research Abstracts</collection><collection>Ecology Abstracts</collection><collection>Entomology Abstracts (Full archive)</collection><collection>Environment Abstracts</collection><collection>Industrial and Applied Microbiology Abstracts (Microbiology A)</collection><collection>Nucleic Acids Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><collection>Environment Abstracts</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Applied and Environmental Microbiology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Chatterjee, A. (University of Missouri, Columbia, MO.)</au><au>Cui, Y</au><au>Liu, Y</au><au>Korsi Dumenyo, C</au><au>Chatterjee, A.K</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Inactivation of rsmA leads to overproduction of extracellular pectinases, cellulases, and proteases in Erwinia carotovora subsp. carotovora in the absence of the starvation/cell density-sensing signal, N-(3-oxohexanoyl)-L-homoserine lactone</atitle><jtitle>Applied and Environmental Microbiology</jtitle><addtitle>Appl Environ Microbiol</addtitle><date>1995-05-01</date><risdate>1995</risdate><volume>61</volume><issue>5</issue><spage>1959</spage><epage>1967</epage><pages>1959-1967</pages><issn>0099-2240</issn><eissn>1098-5336</eissn><coden>AEMIDF</coden><abstract>The soft-rotting bacterium, Erwinia carotovora subsp. carotovora 71, produces extracellular enzymes such as pectate lyase isozymes (Pels), cellulase (Cel), polygalacturonase (Peh), and protease (Prt). While the extracellular levels of these enzymes are extremely low when the bacterium is grown in salts-yeast extract-glycerol (SYG) medium, the enzymatic activities are highly induced in SYG medium supplemented with celery extract. By transposon (mini-TnS) mutagenesis, we isolated a RsmA-mutant, AC5070, which overproduces extracellular enzymes; the basal levels of Pel, Peh, and Cel in AC5070 are higher than the induced levels in the RsmA+ parent, AC5047. While Peh production is mostly constitutive in AC5070, Pel, Cel, and Prt production is still inducible with celery extract. The high basal levels of pel-1, pel-3, and peh-1 mRNAs in AC5070 demonstrate that overproduction of the pectolytic enzymes is due to the stimulation of transcription. Using chromosomal DNA flanking mini-TnS as a probe, we cloned the wild-type rsmA+ allele, which suppresses Pel, Peh, Cel, and Prt production in both RsmA+ and RsmA- strains. The RsmA-mutant, like its parent, produces N-(3-oxohexanoyl)-L-homoserine lactone (HSL), a starvation/cell density-sensing signal required for extracellular enzyme production. To examine the role of HSL, we constructed HSL-deficient strains by replacing hslI, a locus required for HSL production, with hslI::Tn3HoHo1-Spc. While the basal levels of Pel, Peh, Cel, and Prt are comparable in the RsmA- mutant and its HSL- derivative, these enzymes are barely detectable in the Hsl-derivative of the RsmA+ parent strain. The Hsl- RsmA+ strain fails to elicit soft rot, whereas the Hsl-RsmA-strain, like its Hsl+ RsmA- parent, remains hypervirulent. These findings demonstrate that the RsmA-mutant produces extracellular enzymes and macerates plant tissue in the absence of HSL</abstract><cop>Washington, DC</cop><pub>American Society for Microbiology</pub><pmid>7646031</pmid><doi>10.1128/aem.61.5.1959-1967.1995</doi><tpages>9</tpages><oa>free_for_read</oa></addata></record> |
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recordid | cdi_proquest_miscellaneous_16771623 |
source | American Society for Microbiology; MEDLINE; PubMed Central; Alma/SFX Local Collection |
subjects | 4-Butyrolactone - analogs & derivatives 4-Butyrolactone - genetics 4-Butyrolactone - physiology Amino Acid Sequence ARN MENSAJERO ARN MESSAGER Bacteria Bacterial plant pathogens Biological and medical sciences Biology BIOSINTESIS BIOSYNTHESE CELLULASE Cellulase - biosynthesis Cellulase - genetics CELULASA Culture Media - pharmacology Disease Enzyme Induction - drug effects ERWINIA CAROTOVORA EXPRESION GENICA EXPRESSION DES GENES Flowers & plants Fundamental and applied biological sciences. Psychology GENE Gene Expression Regulation, Bacterial - drug effects GENES Genes, Bacterial Isoenzymes - biosynthesis Isoenzymes - genetics LACTONAS LACTONE LIASAS LOCI LOCUS LYASE Molecular Sequence Data MUTACION Mutagenesis, Insertional MUTANT MUTANTES MUTATION Pectobacterium carotovorum - drug effects Pectobacterium carotovorum - enzymology Pectobacterium carotovorum - genetics Pectobacterium carotovorum - pathogenicity Phytopathology. Animal pests. Plant and forest protection Plant Extracts - pharmacology POLIGALACTURONASA POLYGALACTURONASE Polygalacturonase - biosynthesis Polygalacturonase - genetics Polysaccharide-Lyases - biosynthesis Polysaccharide-Lyases - genetics PROTEASAS PROTEASE Recombinant Fusion Proteins - metabolism Repressor Proteins - genetics Repressor Proteins - physiology SECUENCIA NUCLEICA Sequence Alignment Sequence Homology, Amino Acid SEQUENCE NUCLEIQUE Systematics. Structure, properties and multiplication. Genetics Virulence |
title | Inactivation of rsmA leads to overproduction of extracellular pectinases, cellulases, and proteases in Erwinia carotovora subsp. carotovora in the absence of the starvation/cell density-sensing signal, N-(3-oxohexanoyl)-L-homoserine lactone |
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