Serveur d'exploration sur le phanerochaete

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Phanerochaete chrysosporium Multienzyme Catabolic System for in Vivo Modification of Synthetic Lignin to Succinic Acid.

Identifieur interne : 000155 ( Main/Exploration ); précédent : 000154; suivant : 000156

Phanerochaete chrysosporium Multienzyme Catabolic System for in Vivo Modification of Synthetic Lignin to Succinic Acid.

Auteurs : Chang-Young Hong [Corée du Sud] ; Sun-Hwa Ryu [Corée du Sud] ; Hanseob Jeong [Corée du Sud] ; Sung-Suk Lee [Corée du Sud] ; Myungkil Kim [Corée du Sud] ; In-Gyu Choi [Corée du Sud]

Source :

RBID : pubmed:28463479

Descripteurs français

English descriptors

Abstract

Whole cells of the basidiomycete fungus Phanerochaete chrysosporium (ATCC 20696) were applied to induce the biomodification of lignin in an in vivo system. Our results indicated that P. chrysosporium has a catabolic system that induces characteristic biomodifications of synthetic lignin through a series of redox reactions, leading not only to the degradation of lignin but also to its polymerization. The reducing agents ascorbic acid and α-tocopherol were used to stabilize the free radicals generated from the ligninolytic process. The application of P. chrysosporium in combination with reducing agents produced aromatic compounds and succinic acid as well as degraded lignin polymers. P. chrysosporium selectively catalyzed the conversion of lignin to succinic acid, which has an economic value. A transcriptomic analysis of P. chrysosporium suggested that the bond cleavage of synthetic lignin was caused by numerous enzymes, including extracellular enzymes such as lignin peroxidase and manganese peroxidase, and that the aromatic compounds released were metabolized in both the short-cut and classical tricarboxylic acid cycles of P. chrysosporium. In conclusion, P. chrysosporium is suitable as a biocatalyst for lignin degradation to produce a value-added product.

DOI: 10.1021/acschembio.7b00046
PubMed: 28463479


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Le document en format XML

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<term>Ascorbic Acid (chemistry)</term>
<term>Free Radicals (MeSH)</term>
<term>Lignin (chemistry)</term>
<term>Lignin (metabolism)</term>
<term>Molecular Weight (MeSH)</term>
<term>Multienzyme Complexes (chemistry)</term>
<term>Nitrobenzenes (chemistry)</term>
<term>Oxidation-Reduction (MeSH)</term>
<term>Phanerochaete (enzymology)</term>
<term>Phanerochaete (metabolism)</term>
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<term>Acide succinique (synthèse chimique)</term>
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<term>Lignine (composition chimique)</term>
<term>Lignine (métabolisme)</term>
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<term>Phanerochaete (métabolisme)</term>
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<term>Multienzyme Complexes</term>
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<div type="abstract" xml:lang="en">Whole cells of the basidiomycete fungus Phanerochaete chrysosporium (ATCC 20696) were applied to induce the biomodification of lignin in an in vivo system. Our results indicated that P. chrysosporium has a catabolic system that induces characteristic biomodifications of synthetic lignin through a series of redox reactions, leading not only to the degradation of lignin but also to its polymerization. The reducing agents ascorbic acid and α-tocopherol were used to stabilize the free radicals generated from the ligninolytic process. The application of P. chrysosporium in combination with reducing agents produced aromatic compounds and succinic acid as well as degraded lignin polymers. P. chrysosporium selectively catalyzed the conversion of lignin to succinic acid, which has an economic value. A transcriptomic analysis of P. chrysosporium suggested that the bond cleavage of synthetic lignin was caused by numerous enzymes, including extracellular enzymes such as lignin peroxidase and manganese peroxidase, and that the aromatic compounds released were metabolized in both the short-cut and classical tricarboxylic acid cycles of P. chrysosporium. In conclusion, P. chrysosporium is suitable as a biocatalyst for lignin degradation to produce a value-added product.</div>
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<DescriptorName UI="D020075" MajorTopicYN="N">Phanerochaete</DescriptorName>
<QualifierName UI="Q000201" MajorTopicYN="Y">enzymology</QualifierName>
<QualifierName UI="Q000378" MajorTopicYN="N">metabolism</QualifierName>
</MeshHeading>
<MeshHeading>
<DescriptorName UI="D019802" MajorTopicYN="N">Succinic Acid</DescriptorName>
<QualifierName UI="Q000138" MajorTopicYN="Y">chemical synthesis</QualifierName>
<QualifierName UI="Q000737" MajorTopicYN="N">chemistry</QualifierName>
<QualifierName UI="Q000378" MajorTopicYN="N">metabolism</QualifierName>
</MeshHeading>
<MeshHeading>
<DescriptorName UI="D024505" MajorTopicYN="N">Tocopherols</DescriptorName>
<QualifierName UI="Q000737" MajorTopicYN="N">chemistry</QualifierName>
</MeshHeading>
</MeshHeadingList>
</MedlineCitation>
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<History>
<PubMedPubDate PubStatus="pubmed">
<Year>2017</Year>
<Month>5</Month>
<Day>4</Day>
<Hour>6</Hour>
<Minute>0</Minute>
</PubMedPubDate>
<PubMedPubDate PubStatus="medline">
<Year>2018</Year>
<Month>2</Month>
<Day>8</Day>
<Hour>6</Hour>
<Minute>0</Minute>
</PubMedPubDate>
<PubMedPubDate PubStatus="entrez">
<Year>2017</Year>
<Month>5</Month>
<Day>3</Day>
<Hour>6</Hour>
<Minute>0</Minute>
</PubMedPubDate>
</History>
<PublicationStatus>ppublish</PublicationStatus>
<ArticleIdList>
<ArticleId IdType="pubmed">28463479</ArticleId>
<ArticleId IdType="doi">10.1021/acschembio.7b00046</ArticleId>
</ArticleIdList>
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</pubmed>
<affiliations>
<list>
<country>
<li>Corée du Sud</li>
</country>
<region>
<li>Région capitale de Séoul</li>
</region>
<settlement>
<li>Séoul</li>
</settlement>
</list>
<tree>
<country name="Corée du Sud">
<region name="Région capitale de Séoul">
<name sortKey="Hong, Chang Young" sort="Hong, Chang Young" uniqKey="Hong C" first="Chang-Young" last="Hong">Chang-Young Hong</name>
</region>
<name sortKey="Choi, In Gyu" sort="Choi, In Gyu" uniqKey="Choi I" first="In-Gyu" last="Choi">In-Gyu Choi</name>
<name sortKey="Choi, In Gyu" sort="Choi, In Gyu" uniqKey="Choi I" first="In-Gyu" last="Choi">In-Gyu Choi</name>
<name sortKey="Choi, In Gyu" sort="Choi, In Gyu" uniqKey="Choi I" first="In-Gyu" last="Choi">In-Gyu Choi</name>
<name sortKey="Jeong, Hanseob" sort="Jeong, Hanseob" uniqKey="Jeong H" first="Hanseob" last="Jeong">Hanseob Jeong</name>
<name sortKey="Kim, Myungkil" sort="Kim, Myungkil" uniqKey="Kim M" first="Myungkil" last="Kim">Myungkil Kim</name>
<name sortKey="Lee, Sung Suk" sort="Lee, Sung Suk" uniqKey="Lee S" first="Sung-Suk" last="Lee">Sung-Suk Lee</name>
<name sortKey="Ryu, Sun Hwa" sort="Ryu, Sun Hwa" uniqKey="Ryu S" first="Sun-Hwa" last="Ryu">Sun-Hwa Ryu</name>
</country>
</tree>
</affiliations>
</record>

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