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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Veröffentlicht in:Applied and Environmental Microbiology 1995-05, Vol.61 (5), p.1959-1967
Hauptverfasser: Chatterjee, A. (University of Missouri, Columbia, MO.), Cui, Y, Liu, Y, Korsi Dumenyo, C, Chatterjee, A.K
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container_end_page 1967
container_issue 5
container_start_page 1959
container_title Applied and Environmental Microbiology
container_volume 61
creator Chatterjee, A. (University of Missouri, Columbia, MO.)
Cui, Y
Liu, Y
Korsi Dumenyo, C
Chatterjee, A.K
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 &amp; 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 &amp; 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&amp;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 &amp; 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 &amp; 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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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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identifier ISSN: 0099-2240
ispartof Applied and Environmental Microbiology, 1995-05, Vol.61 (5), p.1959-1967
issn 0099-2240
1098-5336
language eng
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
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-18T15%3A03%3A54IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_highw&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Inactivation%20of%20rsmA%20leads%20to%20overproduction%20of%20extracellular%20pectinases,%20cellulases,%20and%20proteases%20in%20Erwinia%20carotovora%20subsp.%20carotovora%20in%20the%20absence%20of%20the%20starvation/cell%20density-sensing%20signal,%20N-(3-oxohexanoyl)-L-homoserine%20lactone&rft.jtitle=Applied%20and%20Environmental%20Microbiology&rft.au=Chatterjee,%20A.%20(University%20of%20Missouri,%20Columbia,%20MO.)&rft.date=1995-05-01&rft.volume=61&rft.issue=5&rft.spage=1959&rft.epage=1967&rft.pages=1959-1967&rft.issn=0099-2240&rft.eissn=1098-5336&rft.coden=AEMIDF&rft_id=info:doi/10.1128/aem.61.5.1959-1967.1995&rft_dat=%3Cproquest_highw%3E4487955%3C/proquest_highw%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=205934539&rft_id=info:pmid/7646031&rfr_iscdi=true