Biodegradation of lignocellulose in Bermuda grass by white rot fungi analyzed by solid-state 13C nuclear magnetic resonance.
Identifieur interne : 000D67 ( Main/Exploration ); précédent : 000D66; suivant : 000D68Biodegradation of lignocellulose in Bermuda grass by white rot fungi analyzed by solid-state 13C nuclear magnetic resonance.
Auteurs : G R Gamble ; A. Sethuraman ; D E Akin ; K E ErikssonSource :
- Applied and environmental microbiology [ 0099-2240 ] ; 1994.
Descripteurs français
- KwdFr :
- MESH :
- microbiologie : Poaceae.
- métabolisme : Basidiomycota, Cellulose, Lignine, Poaceae.
- Aliment pour animaux, Cinétique, Dépollution biologique de l'environnement, Fermentation, Spectroscopie par résonance magnétique.
English descriptors
- KwdEn :
- MESH :
- chemical , metabolism : Cellulose, Lignin.
- metabolism : Basidiomycota, Poaceae.
- microbiology : Poaceae.
- Animal Feed, Biodegradation, Environmental, Fermentation, Kinetics, Magnetic Resonance Spectroscopy.
Abstract
Following the solid-state fermentation of Bermuda grass by two lignin-degrading white rot fungi, compositional changes have been observed in situ by utilization of cross-polarization and magic angle spinning 13C nuclear magnetic resonance difference spectra and interrupted decoupling spectra. Intensity differences in the 13C resonances assigned to specific components of the cell wall were used to observe these changes. Bermuda grass treated with Phanerochaete chrysosporium K-3 exhibited losses primarily in the polysaccharide components, with a smaller proportion of phenolic components also being degraded. In contrast, Ceriporiopsis subvermispora FP 90031-sp removed a proportionate amount of phenolic components compared with polysaccharide components. The results also indicated that C. subvermispora preferentially removes guaiacyl phenolic components relative to syringyl phenolic components, while P. chrysosporium was nonspecific in its attack on phenolic components.
DOI: 10.1128/AEM.60.9.3138-3144.1994
PubMed: 7944358
PubMed Central: PMC201781
Affiliations:
Links toward previous steps (curation, corpus...)
Le document en format XML
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Sethuraman</name></author><author><name sortKey="Akin, D E" sort="Akin, D E" uniqKey="Akin D" first="D E" last="Akin">D E Akin</name></author><author><name sortKey="Eriksson, K E" sort="Eriksson, K E" uniqKey="Eriksson K" first="K E" last="Eriksson">K E Eriksson</name></author></titleStmt><publicationStmt><idno type="wicri:source">PubMed</idno><date when="1994">1994</date><idno type="RBID">pubmed:7944358</idno><idno type="pmid">7944358</idno><idno type="pmc">PMC201781</idno><idno type="doi">10.1128/AEM.60.9.3138-3144.1994</idno><idno type="wicri:Area/Main/Corpus">000D38</idno><idno type="wicri:explorRef" wicri:stream="Main" wicri:step="Corpus" wicri:corpus="PubMed">000D38</idno><idno type="wicri:Area/Main/Curation">000D38</idno><idno type="wicri:explorRef" wicri:stream="Main" wicri:step="Curation">000D38</idno><idno type="wicri:Area/Main/Exploration">000D38</idno></publicationStmt><sourceDesc><biblStruct><analytic><title xml:lang="en">Biodegradation of lignocellulose in Bermuda grass by white rot fungi analyzed by solid-state 13C nuclear magnetic resonance.</title><author><name sortKey="Gamble, G R" sort="Gamble, G R" uniqKey="Gamble G" first="G R" last="Gamble">G R Gamble</name><affiliation><nlm:affiliation>Department of Biochemistry, University of Georgia, Athens 30602.</nlm:affiliation><wicri:noCountry code="subField">Athens 30602</wicri:noCountry></affiliation></author><author><name sortKey="Sethuraman, A" sort="Sethuraman, A" uniqKey="Sethuraman A" first="A" last="Sethuraman">A. Sethuraman</name></author><author><name sortKey="Akin, D E" sort="Akin, D E" uniqKey="Akin D" first="D E" last="Akin">D E Akin</name></author><author><name sortKey="Eriksson, K E" sort="Eriksson, K E" uniqKey="Eriksson K" first="K E" last="Eriksson">K E Eriksson</name></author></analytic><series><title level="j">Applied and environmental microbiology</title><idno type="ISSN">0099-2240</idno><imprint><date when="1994" type="published">1994</date></imprint></series></biblStruct></sourceDesc></fileDesc><profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Animal Feed (MeSH)</term><term>Basidiomycota (metabolism)</term><term>Biodegradation, Environmental (MeSH)</term><term>Cellulose (metabolism)</term><term>Fermentation (MeSH)</term><term>Kinetics (MeSH)</term><term>Lignin (metabolism)</term><term>Magnetic Resonance Spectroscopy (MeSH)</term><term>Poaceae (metabolism)</term><term>Poaceae (microbiology)</term></keywords><keywords scheme="KwdFr" xml:lang="fr"><term>Aliment pour animaux (MeSH)</term><term>Basidiomycota (métabolisme)</term><term>Cellulose (métabolisme)</term><term>Cinétique (MeSH)</term><term>Dépollution biologique de l'environnement (MeSH)</term><term>Fermentation (MeSH)</term><term>Lignine (métabolisme)</term><term>Poaceae (microbiologie)</term><term>Poaceae (métabolisme)</term><term>Spectroscopie par résonance magnétique (MeSH)</term></keywords><keywords scheme="MESH" type="chemical" qualifier="metabolism" xml:lang="en"><term>Cellulose</term><term>Lignin</term></keywords><keywords scheme="MESH" qualifier="metabolism" xml:lang="en"><term>Basidiomycota</term><term>Poaceae</term></keywords><keywords scheme="MESH" qualifier="microbiologie" xml:lang="fr"><term>Poaceae</term></keywords><keywords scheme="MESH" qualifier="microbiology" xml:lang="en"><term>Poaceae</term></keywords><keywords scheme="MESH" qualifier="métabolisme" xml:lang="fr"><term>Basidiomycota</term><term>Cellulose</term><term>Lignine</term><term>Poaceae</term></keywords><keywords scheme="MESH" xml:lang="en"><term>Animal Feed</term><term>Biodegradation, Environmental</term><term>Fermentation</term><term>Kinetics</term><term>Magnetic Resonance Spectroscopy</term></keywords><keywords scheme="MESH" xml:lang="fr"><term>Aliment pour animaux</term><term>Cinétique</term><term>Dépollution biologique de l'environnement</term><term>Fermentation</term><term>Spectroscopie par résonance magnétique</term></keywords></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en">Following the solid-state fermentation of Bermuda grass by two lignin-degrading white rot fungi, compositional changes have been observed in situ by utilization of cross-polarization and magic angle spinning 13C nuclear magnetic resonance difference spectra and interrupted decoupling spectra. Intensity differences in the 13C resonances assigned to specific components of the cell wall were used to observe these changes. Bermuda grass treated with Phanerochaete chrysosporium K-3 exhibited losses primarily in the polysaccharide components, with a smaller proportion of phenolic components also being degraded. In contrast, Ceriporiopsis subvermispora FP 90031-sp removed a proportionate amount of phenolic components compared with polysaccharide components. The results also indicated that C. subvermispora preferentially removes guaiacyl phenolic components relative to syringyl phenolic components, while P. chrysosporium was nonspecific in its attack on phenolic components.</div></front></TEI><pubmed><MedlineCitation Status="MEDLINE" Owner="NLM"><PMID Version="1">7944358</PMID><DateCompleted><Year>1994</Year><Month>11</Month><Day>18</Day></DateCompleted><DateRevised><Year>2020</Year><Month>07</Month><Day>24</Day></DateRevised><Article PubModel="Print"><Journal><ISSN IssnType="Print">0099-2240</ISSN><JournalIssue CitedMedium="Print"><Volume>60</Volume><Issue>9</Issue><PubDate><Year>1994</Year><Month>Sep</Month></PubDate></JournalIssue><Title>Applied and environmental microbiology</Title><ISOAbbreviation>Appl Environ Microbiol</ISOAbbreviation></Journal><ArticleTitle>Biodegradation of lignocellulose in Bermuda grass by white rot fungi analyzed by solid-state 13C nuclear magnetic resonance.</ArticleTitle><Pagination><MedlinePgn>3138-44</MedlinePgn></Pagination><Abstract><AbstractText>Following the solid-state fermentation of Bermuda grass by two lignin-degrading white rot fungi, compositional changes have been observed in situ by utilization of cross-polarization and magic angle spinning 13C nuclear magnetic resonance difference spectra and interrupted decoupling spectra. Intensity differences in the 13C resonances assigned to specific components of the cell wall were used to observe these changes. Bermuda grass treated with Phanerochaete chrysosporium K-3 exhibited losses primarily in the polysaccharide components, with a smaller proportion of phenolic components also being degraded. In contrast, Ceriporiopsis subvermispora FP 90031-sp removed a proportionate amount of phenolic components compared with polysaccharide components. The results also indicated that C. subvermispora preferentially removes guaiacyl phenolic components relative to syringyl phenolic components, while P. chrysosporium was nonspecific in its attack on phenolic components.</AbstractText></Abstract><AuthorList CompleteYN="Y"><Author ValidYN="Y"><LastName>Gamble</LastName><ForeName>G R</ForeName><Initials>GR</Initials><AffiliationInfo><Affiliation>Department of Biochemistry, University of Georgia, Athens 30602.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Sethuraman</LastName><ForeName>A</ForeName><Initials>A</Initials></Author><Author ValidYN="Y"><LastName>Akin</LastName><ForeName>D E</ForeName><Initials>DE</Initials></Author><Author ValidYN="Y"><LastName>Eriksson</LastName><ForeName>K E</ForeName><Initials>KE</Initials></Author></AuthorList><Language>eng</Language><PublicationTypeList><PublicationType UI="D016428">Journal Article</PublicationType></PublicationTypeList></Article><MedlineJournalInfo><Country>United 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Environmental</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D002482" MajorTopicYN="N">Cellulose</DescriptorName><QualifierName UI="Q000378" MajorTopicYN="Y">metabolism</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D005285" MajorTopicYN="N">Fermentation</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D007700" MajorTopicYN="N">Kinetics</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D008031" MajorTopicYN="N">Lignin</DescriptorName><QualifierName UI="Q000378" MajorTopicYN="Y">metabolism</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D009682" MajorTopicYN="N">Magnetic Resonance Spectroscopy</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D006109" MajorTopicYN="N">Poaceae</DescriptorName><QualifierName UI="Q000378" MajorTopicYN="N">metabolism</QualifierName><QualifierName UI="Q000382" MajorTopicYN="N">microbiology</QualifierName></MeshHeading></MeshHeadingList></MedlineCitation><PubmedData><History><PubMedPubDate PubStatus="pubmed"><Year>1994</Year><Month>9</Month><Day>1</Day></PubMedPubDate><PubMedPubDate PubStatus="medline"><Year>1994</Year><Month>9</Month><Day>1</Day><Hour>0</Hour><Minute>1</Minute></PubMedPubDate><PubMedPubDate PubStatus="entrez"><Year>1994</Year><Month>9</Month><Day>1</Day><Hour>0</Hour><Minute>0</Minute></PubMedPubDate></History><PublicationStatus>ppublish</PublicationStatus><ArticleIdList><ArticleId IdType="pubmed">7944358</ArticleId><ArticleId IdType="pmc">PMC201781</ArticleId><ArticleId IdType="doi">10.1128/AEM.60.9.3138-3144.1994</ArticleId></ArticleIdList><ReferenceList><Reference><Citation>Appl Environ Microbiol. 1993 Jun;59(6):1792-7</Citation><ArticleIdList><ArticleId IdType="pubmed">16348955</ArticleId></ArticleIdList></Reference><Reference><Citation>Appl Environ Microbiol. 1993 Dec;59(12):4017-23</Citation><ArticleIdList><ArticleId 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Eriksson</name><name sortKey="Gamble, G R" sort="Gamble, G R" uniqKey="Gamble G" first="G R" last="Gamble">G R Gamble</name><name sortKey="Sethuraman, A" sort="Sethuraman, A" uniqKey="Sethuraman A" first="A" last="Sethuraman">A. 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