Transcription of ligninase H8 by Phanerochaete chrysosporium under nutrient nitrogen sufficient conditions.
Identifieur interne : 000D21 ( Main/Exploration ); précédent : 000D20; suivant : 000D22Transcription of ligninase H8 by Phanerochaete chrysosporium under nutrient nitrogen sufficient conditions.
Auteurs : C G Johnston ; S D AustSource :
- Biochemical and biophysical research communications [ 0006-291X ] ; 1994.
Descripteurs français
- KwdFr :
- ARN messager (analyse), ARN messager (biosynthèse), Agaricales (croissance et développement), Agaricales (enzymologie), Agaricales (génétique), Introns (MeSH), Milieux de culture (MeSH), Oxygénases (biosynthèse), Oxygénases (génétique), Oxygénases (isolement et purification), Peroxidases (biosynthèse), Peroxidases (génétique), Peroxidases (isolement et purification), Réaction de polymérisation en chaîne (MeSH), Transcription génétique (MeSH).
- MESH :
- analyse : ARN messager.
- biosynthèse : ARN messager, Oxygénases, Peroxidases.
- croissance et développement : Agaricales.
- enzymologie : Agaricales.
- génétique : Agaricales, Oxygénases, Peroxidases.
- isolement et purification : Oxygénases, Peroxidases.
- Introns, Milieux de culture, Réaction de polymérisation en chaîne, Transcription génétique.
English descriptors
- KwdEn :
- Agaricales (enzymology), Agaricales (genetics), Agaricales (growth & development), Culture Media (MeSH), Introns (MeSH), Oxygenases (biosynthesis), Oxygenases (genetics), Oxygenases (isolation & purification), Peroxidases (biosynthesis), Peroxidases (genetics), Peroxidases (isolation & purification), Polymerase Chain Reaction (MeSH), RNA, Messenger (analysis), RNA, Messenger (biosynthesis), Transcription, Genetic (MeSH).
- MESH :
- chemical , analysis : RNA, Messenger.
- chemical , biosynthesis : Oxygenases, Peroxidases, RNA, Messenger.
- chemical , genetics : Oxygenases, Peroxidases.
- chemical , isolation & purification : Oxygenases, Peroxidases.
- chemical : Culture Media.
- enzymology : Agaricales.
- genetics : Agaricales.
- growth & development : Agaricales.
- Introns, Polymerase Chain Reaction, Transcription, Genetic.
Abstract
Dot blot analyses showed that more ligninase H8 mRNA was present in ammonium sufficient cultures of Phanerochaete chrysosporium than in ammonium limited cultures. Reverse transcription followed by polymerase chain reaction and DNA sequencing verified that H8 mRNA was present under both conditions. Fast protein liquid chromatography profiles indicated that H8 was present but lacked heme in ammonium sufficient cultures. These data indicated that H8 was transcribed and translated by day 5 under ammonium sufficient conditions, but was inactive due to lack of heme.
DOI: 10.1006/bbrc.1994.1421
PubMed: 8166678
Affiliations:
Links toward previous steps (curation, corpus...)
Le document en format XML
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(MeSH)</term><term>Milieux de culture (MeSH)</term><term>Oxygénases (biosynthèse)</term><term>Oxygénases (génétique)</term><term>Oxygénases (isolement et purification)</term><term>Peroxidases (biosynthèse)</term><term>Peroxidases (génétique)</term><term>Peroxidases (isolement et purification)</term><term>Réaction de polymérisation en chaîne (MeSH)</term><term>Transcription génétique (MeSH)</term></keywords><keywords scheme="MESH" type="chemical" qualifier="analysis" xml:lang="en"><term>RNA, Messenger</term></keywords><keywords scheme="MESH" type="chemical" qualifier="biosynthesis" xml:lang="en"><term>Oxygenases</term><term>Peroxidases</term><term>RNA, Messenger</term></keywords><keywords scheme="MESH" type="chemical" qualifier="genetics" xml:lang="en"><term>Oxygenases</term><term>Peroxidases</term></keywords><keywords scheme="MESH" type="chemical" qualifier="isolation & purification" xml:lang="en"><term>Oxygenases</term><term>Peroxidases</term></keywords><keywords scheme="MESH" type="chemical" xml:lang="en"><term>Culture Media</term></keywords><keywords scheme="MESH" qualifier="analyse" xml:lang="fr"><term>ARN messager</term></keywords><keywords scheme="MESH" qualifier="biosynthèse" xml:lang="fr"><term>ARN messager</term><term>Oxygénases</term><term>Peroxidases</term></keywords><keywords scheme="MESH" qualifier="croissance et développement" xml:lang="fr"><term>Agaricales</term></keywords><keywords scheme="MESH" qualifier="enzymologie" xml:lang="fr"><term>Agaricales</term></keywords><keywords scheme="MESH" qualifier="enzymology" xml:lang="en"><term>Agaricales</term></keywords><keywords scheme="MESH" qualifier="genetics" xml:lang="en"><term>Agaricales</term></keywords><keywords scheme="MESH" qualifier="growth & development" xml:lang="en"><term>Agaricales</term></keywords><keywords scheme="MESH" qualifier="génétique" xml:lang="fr"><term>Agaricales</term><term>Oxygénases</term><term>Peroxidases</term></keywords><keywords scheme="MESH" qualifier="isolement et purification" xml:lang="fr"><term>Oxygénases</term><term>Peroxidases</term></keywords><keywords scheme="MESH" xml:lang="en"><term>Introns</term><term>Polymerase Chain Reaction</term><term>Transcription, Genetic</term></keywords><keywords scheme="MESH" xml:lang="fr"><term>Introns</term><term>Milieux de culture</term><term>Réaction de polymérisation en chaîne</term><term>Transcription génétique</term></keywords></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en">Dot blot analyses showed that more ligninase H8 mRNA was present in ammonium sufficient cultures of Phanerochaete chrysosporium than in ammonium limited cultures. Reverse transcription followed by polymerase chain reaction and DNA sequencing verified that H8 mRNA was present under both conditions. Fast protein liquid chromatography profiles indicated that H8 was present but lacked heme in ammonium sufficient cultures. These data indicated that H8 was transcribed and translated by day 5 under ammonium sufficient conditions, but was inactive due to lack of heme.</div></front></TEI><pubmed><MedlineCitation Status="MEDLINE" Owner="NLM"><PMID Version="1">8166678</PMID><DateCompleted><Year>1994</Year><Month>05</Month><Day>23</Day></DateCompleted><DateRevised><Year>2019</Year><Month>06</Month><Day>12</Day></DateRevised><Article PubModel="Print"><Journal><ISSN IssnType="Print">0006-291X</ISSN><JournalIssue CitedMedium="Print"><Volume>200</Volume><Issue>1</Issue><PubDate><Year>1994</Year><Month>Apr</Month><Day>15</Day></PubDate></JournalIssue><Title>Biochemical and biophysical research communications</Title><ISOAbbreviation>Biochem Biophys Res Commun</ISOAbbreviation></Journal><ArticleTitle>Transcription of ligninase H8 by Phanerochaete chrysosporium under nutrient nitrogen sufficient conditions.</ArticleTitle><Pagination><MedlinePgn>108-12</MedlinePgn></Pagination><Abstract><AbstractText>Dot blot analyses showed that more ligninase H8 mRNA was present in ammonium sufficient cultures of Phanerochaete chrysosporium than in ammonium limited cultures. Reverse transcription followed by polymerase chain reaction and DNA sequencing verified that H8 mRNA was present under both conditions. Fast protein liquid chromatography profiles indicated that H8 was present but lacked heme in ammonium sufficient cultures. These data indicated that H8 was transcribed and translated by day 5 under ammonium sufficient conditions, but was inactive due to lack of heme.</AbstractText></Abstract><AuthorList CompleteYN="Y"><Author ValidYN="Y"><LastName>Johnston</LastName><ForeName>C G</ForeName><Initials>CG</Initials><AffiliationInfo><Affiliation>Biotechnology Center, Utah State University, Logan 84322-4705.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Aust</LastName><ForeName>S D</ForeName><Initials>SD</Initials></Author></AuthorList><Language>eng</Language><GrantList CompleteYN="Y"><Grant><GrantID>ES04922</GrantID><Acronym>ES</Acronym><Agency>NIEHS NIH HHS</Agency><Country>United States</Country></Grant></GrantList><PublicationTypeList><PublicationType UI="D016428">Journal Article</PublicationType><PublicationType UI="D013487">Research Support, U.S. Gov't, P.H.S.</PublicationType></PublicationTypeList></Article><MedlineJournalInfo><Country>United States</Country><MedlineTA>Biochem Biophys Res Commun</MedlineTA><NlmUniqueID>0372516</NlmUniqueID><ISSNLinking>0006-291X</ISSNLinking></MedlineJournalInfo><ChemicalList><Chemical><RegistryNumber>0</RegistryNumber><NameOfSubstance UI="D003470">Culture Media</NameOfSubstance></Chemical><Chemical><RegistryNumber>0</RegistryNumber><NameOfSubstance UI="D012333">RNA, Messenger</NameOfSubstance></Chemical><Chemical><RegistryNumber>EC 1.11.1-</RegistryNumber><NameOfSubstance UI="C086881">ligninase H8</NameOfSubstance></Chemical><Chemical><RegistryNumber>EC 1.11.1.-</RegistryNumber><NameOfSubstance UI="D010544">Peroxidases</NameOfSubstance></Chemical><Chemical><RegistryNumber>EC 1.13.-</RegistryNumber><NameOfSubstance UI="D010105">Oxygenases</NameOfSubstance></Chemical><Chemical><RegistryNumber>EC 1.14.99.-</RegistryNumber><NameOfSubstance UI="C044391">ligninase</NameOfSubstance></Chemical></ChemicalList><CitationSubset>IM</CitationSubset><MeshHeadingList><MeshHeading><DescriptorName UI="D000363" MajorTopicYN="N">Agaricales</DescriptorName><QualifierName UI="Q000201" MajorTopicYN="Y">enzymology</QualifierName><QualifierName UI="Q000235" MajorTopicYN="N">genetics</QualifierName><QualifierName UI="Q000254" MajorTopicYN="N">growth & development</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D003470" MajorTopicYN="N">Culture Media</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D007438" MajorTopicYN="N">Introns</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D010105" MajorTopicYN="N">Oxygenases</DescriptorName><QualifierName UI="Q000096" MajorTopicYN="Y">biosynthesis</QualifierName><QualifierName UI="Q000235" MajorTopicYN="N">genetics</QualifierName><QualifierName UI="Q000302" MajorTopicYN="N">isolation & purification</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D010544" MajorTopicYN="N">Peroxidases</DescriptorName><QualifierName UI="Q000096" MajorTopicYN="Y">biosynthesis</QualifierName><QualifierName UI="Q000235" MajorTopicYN="N">genetics</QualifierName><QualifierName UI="Q000302" MajorTopicYN="N">isolation & purification</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D016133" MajorTopicYN="N">Polymerase Chain Reaction</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D012333" MajorTopicYN="N">RNA, Messenger</DescriptorName><QualifierName UI="Q000032" MajorTopicYN="N">analysis</QualifierName><QualifierName UI="Q000096" MajorTopicYN="N">biosynthesis</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D014158" MajorTopicYN="Y">Transcription, Genetic</DescriptorName></MeshHeading></MeshHeadingList></MedlineCitation><PubmedData><History><PubMedPubDate PubStatus="pubmed"><Year>1994</Year><Month>4</Month><Day>15</Day></PubMedPubDate><PubMedPubDate PubStatus="medline"><Year>1994</Year><Month>4</Month><Day>15</Day><Hour>0</Hour><Minute>1</Minute></PubMedPubDate><PubMedPubDate PubStatus="entrez"><Year>1994</Year><Month>4</Month><Day>15</Day><Hour>0</Hour><Minute>0</Minute></PubMedPubDate></History><PublicationStatus>ppublish</PublicationStatus><ArticleIdList><ArticleId IdType="pubmed">8166678</ArticleId><ArticleId IdType="pii">S0006291X84714215</ArticleId><ArticleId IdType="doi">10.1006/bbrc.1994.1421</ArticleId></ArticleIdList></PubmedData></pubmed><affiliations><list></list><tree><noCountry><name sortKey="Aust, S D" sort="Aust, S D" uniqKey="Aust S" first="S D" last="Aust">S D Aust</name><name sortKey="Johnston, C G" sort="Johnston, C G" uniqKey="Johnston C" first="C G" last="Johnston">C G Johnston</name></noCountry></tree></affiliations></record>Pour manipuler ce document sous Unix (Dilib)
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