Spatial and temporal accumulation of mRNAs encoding two common lignin peroxidases in Phanerochaete chrysosporium.
Identifieur interne : 000D82 ( Main/Exploration ); précédent : 000D81; suivant : 000D83Spatial and temporal accumulation of mRNAs encoding two common lignin peroxidases in Phanerochaete chrysosporium.
Auteurs : S M Moukha [France] ; H A Wösten ; E J Mylius ; M. Asther ; J G WesselsSource :
- Journal of bacteriology [ 0021-9193 ] ; 1993.
Descripteurs français
- KwdFr :
- MESH :
- biosynthèse : ARN messager, Peroxidases.
- enzymologie : Champignons.
- génétique : Champignons, Peroxidases.
- Compartimentation cellulaire, Facteurs temps.
English descriptors
- KwdEn :
- MESH :
- chemical , biosynthesis : Peroxidases, RNA, Messenger.
- enzymology : Fungi.
- genetics : Fungi, Peroxidases.
- Cell Compartmentation, Time Factors.
Abstract
Accumulation of peroxidases and their mRNAs was localized in colonies of Phanerochaete chrysosporium sandwiched between perforated polycarbonate membranes. Northern (RNA) blot analyses of colonial rings and in situ hybridizations with specific probes for manganese(II)-dependent peroxidase (MnP-1) and lignin peroxidase (LiP H8) mRNAs indicated that the expression of MnP-1 and Lip H8 genes started simultaneously in the central area of 3-day-old colonies. With time the signals for both transcripts spread to more-peripheral areas while decreasing in intensity. Furthermore, the appearance of MnP protein, as detected with specific immune serum, immediately followed accumulation of the MnP-1 mRNA transcript. However, LiP protein could be detected only some time after accumulation of LiP H8 mRNA.
DOI: 10.1128/jb.175.11.3672-3678.1993
PubMed: 8501073
PubMed Central: PMC204772
Affiliations:
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Le document en format XML
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Northern (RNA) blot analyses of colonial rings and in situ hybridizations with specific probes for manganese(II)-dependent peroxidase (MnP-1) and lignin peroxidase (LiP H8) mRNAs indicated that the expression of MnP-1 and Lip H8 genes started simultaneously in the central area of 3-day-old colonies. With time the signals for both transcripts spread to more-peripheral areas while decreasing in intensity. Furthermore, the appearance of MnP protein, as detected with specific immune serum, immediately followed accumulation of the MnP-1 mRNA transcript. However, LiP protein could be detected only some time after accumulation of LiP H8 mRNA.</div></front></TEI><pubmed><MedlineCitation Status="MEDLINE" Owner="NLM"><PMID Version="1">8501073</PMID><DateCompleted><Year>1993</Year><Month>07</Month><Day>01</Day></DateCompleted><DateRevised><Year>2019</Year><Month>05</Month><Day>08</Day></DateRevised><Article PubModel="Print"><Journal><ISSN IssnType="Print">0021-9193</ISSN><JournalIssue CitedMedium="Print"><Volume>175</Volume><Issue>11</Issue><PubDate><Year>1993</Year><Month>Jun</Month></PubDate></JournalIssue><Title>Journal of bacteriology</Title><ISOAbbreviation>J Bacteriol</ISOAbbreviation></Journal><ArticleTitle>Spatial and temporal accumulation of mRNAs encoding two common lignin peroxidases in Phanerochaete chrysosporium.</ArticleTitle><Pagination><MedlinePgn>3672-8</MedlinePgn></Pagination><Abstract><AbstractText>Accumulation of peroxidases and their mRNAs was localized in colonies of Phanerochaete chrysosporium sandwiched between perforated polycarbonate membranes. Northern (RNA) blot analyses of colonial rings and in situ hybridizations with specific probes for manganese(II)-dependent peroxidase (MnP-1) and lignin peroxidase (LiP H8) mRNAs indicated that the expression of MnP-1 and Lip H8 genes started simultaneously in the central area of 3-day-old colonies. With time the signals for both transcripts spread to more-peripheral areas while decreasing in intensity. Furthermore, the appearance of MnP protein, as detected with specific immune serum, immediately followed accumulation of the MnP-1 mRNA transcript. However, LiP protein could be detected only some time after accumulation of LiP H8 mRNA.</AbstractText></Abstract><AuthorList CompleteYN="Y"><Author ValidYN="Y"><LastName>Moukha</LastName><ForeName>S M</ForeName><Initials>SM</Initials><AffiliationInfo><Affiliation>Laboratoire de Biotechnologie des Champignons Filamenteux, Faculté des Sciences de Luminy, Parc Scientifique et Technologique, Marseille, France.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Wösten</LastName><ForeName>H A</ForeName><Initials>HA</Initials></Author><Author ValidYN="Y"><LastName>Mylius</LastName><ForeName>E J</ForeName><Initials>EJ</Initials></Author><Author ValidYN="Y"><LastName>Asther</LastName><ForeName>M</ForeName><Initials>M</Initials></Author><Author ValidYN="Y"><LastName>Wessels</LastName><ForeName>J G</ForeName><Initials>JG</Initials></Author></AuthorList><Language>eng</Language><PublicationTypeList><PublicationType UI="D003160">Comparative Study</PublicationType><PublicationType 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sort="Asther, M" uniqKey="Asther M" first="M" last="Asther">M. Asther</name><name sortKey="Mylius, E J" sort="Mylius, E J" uniqKey="Mylius E" first="E J" last="Mylius">E J Mylius</name><name sortKey="Wessels, J G" sort="Wessels, J G" uniqKey="Wessels J" first="J G" last="Wessels">J G Wessels</name><name sortKey="Wosten, H A" sort="Wosten, H A" uniqKey="Wosten H" first="H A" last="Wösten">H A Wösten</name></noCountry><country name="France"><region name="Provence-Alpes-Côte d'Azur"><name sortKey="Moukha, S M" sort="Moukha, S M" uniqKey="Moukha S" first="S M" last="Moukha">S M Moukha</name></region></country></tree></affiliations></record>Pour manipuler ce document sous Unix (Dilib)
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