Publikation: The neomycin biosynthetic gene cluster of Streptomyces fradiae NCIMB 8233 : characterisation of an aminotransferase involved in the formation of 2-deoxystreptamine
Dateien
Datum
Autor:innen
Herausgeber:innen
ISSN der Zeitschrift
Electronic ISSN
ISBN
Bibliografische Daten
Verlag
Schriftenreihe
Auflagebezeichnung
URI (zitierfähiger Link)
DOI (zitierfähiger Link)
Internationale Patentnummer
Angaben zur Forschungsförderung
Projekt
Open Access-Veröffentlichung
Sammlungen
Core Facility der Universität Konstanz
Titel in einer weiteren Sprache
Publikationstyp
Publikationsstatus
Erschienen in
Zusammenfassung
The biosynthetic gene cluster of the 2-deoxystreptamine (DOS)-containing aminoglycoside antibiotic neomycin has been cloned for the first time by screening of a cosmid library of Streptomyces fradiae NCIMB 8233. Sequence analysis has identified 21 putative open reading frames (ORFs) in the neomycin gene cluster (neo) with significant protein sequence similarity to gene products involved in the biosynthesis of other DOS-containing aminoglycosides, namely butirosin (btr), gentamycin (gnt), tobramycin (tbm) and kanamycin (kan). Located at the 5′-end of the neo gene cluster is the previously-characterised neomycin phosphotransferase gene (apH). Three genes unique to the neo and btr clusters have been revealed by comparison of the neo cluster to btr, gnt, tbm and kan clusters. This suggests that these three genes may be involved in the transfer of a ribose moiety to the DOS ring during the antibiotic biosynthesis. The product of the neo-6 gene is characterised here as the L-glutamine : 2-deoxy-scyllo-inosose aminotransferase responsible for the first transamination in DOS biosynthesis, which supports the assignment of the gene cluster.
Zusammenfassung in einer weiteren Sprache
Fachgebiet (DDC)
Schlagwörter
Konferenz
Rezension
Zitieren
ISO 690
HUANG, Fanglu, Stephen F. HAYDOCK, Tatiana MIRONENKO, Dieter SPITELLER, Yanyan LI, Jonathan B. SPENCER, 2005. The neomycin biosynthetic gene cluster of Streptomyces fradiae NCIMB 8233 : characterisation of an aminotransferase involved in the formation of 2-deoxystreptamine. In: Organic & Biomolecular Chemistry. 2005, 3(8), pp. 1410-1418. ISSN 1477-0520. Available under: doi: 10.1039/B501199JBibTex
@article{Huang2005-04-21neomy-15515, year={2005}, doi={10.1039/B501199J}, title={The neomycin biosynthetic gene cluster of Streptomyces fradiae NCIMB 8233 : characterisation of an aminotransferase involved in the formation of 2-deoxystreptamine}, number={8}, volume={3}, issn={1477-0520}, journal={Organic & Biomolecular Chemistry}, pages={1410--1418}, author={Huang, Fanglu and Haydock, Stephen F. and Mironenko, Tatiana and Spiteller, Dieter and Li, Yanyan and Spencer, Jonathan B.} }
RDF
<rdf:RDF xmlns:dcterms="http://purl.org/dc/terms/" xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:rdf="http://www.w3.org/1999/02/22-rdf-syntax-ns#" xmlns:bibo="http://purl.org/ontology/bibo/" xmlns:dspace="http://digital-repositories.org/ontologies/dspace/0.1.0#" xmlns:foaf="http://xmlns.com/foaf/0.1/" xmlns:void="http://rdfs.org/ns/void#" xmlns:xsd="http://www.w3.org/2001/XMLSchema#" > <rdf:Description rdf:about="https://kops.uni-konstanz.de/server/rdf/resource/123456789/15515"> <dc:creator>Huang, Fanglu</dc:creator> <dc:creator>Spiteller, Dieter</dc:creator> <dc:creator>Li, Yanyan</dc:creator> <dc:contributor>Huang, Fanglu</dc:contributor> <dcterms:rights rdf:resource="https://rightsstatements.org/page/InC/1.0/"/> <dcterms:isPartOf rdf:resource="https://kops.uni-konstanz.de/server/rdf/resource/123456789/28"/> <dc:language>eng</dc:language> <dspace:isPartOfCollection rdf:resource="https://kops.uni-konstanz.de/server/rdf/resource/123456789/28"/> <dcterms:title>The neomycin biosynthetic gene cluster of Streptomyces fradiae NCIMB 8233 : characterisation of an aminotransferase involved in the formation of 2-deoxystreptamine</dcterms:title> <dcterms:bibliographicCitation>Publ. in: Organic & biomolecular chemistry ; 3 (2005), 8. - pp. 1410-1418</dcterms:bibliographicCitation> <dc:date rdf:datatype="http://www.w3.org/2001/XMLSchema#dateTime">2011-09-01T12:18:19Z</dc:date> <dc:creator>Haydock, Stephen F.</dc:creator> <dc:creator>Mironenko, Tatiana</dc:creator> <dc:contributor>Haydock, Stephen F.</dc:contributor> <foaf:homepage rdf:resource="http://localhost:8080/"/> <dc:rights>terms-of-use</dc:rights> <dcterms:abstract xml:lang="eng">The biosynthetic gene cluster of the 2-deoxystreptamine (DOS)-containing aminoglycoside antibiotic neomycin has been cloned for the first time by screening of a cosmid library of Streptomyces fradiae NCIMB 8233. Sequence analysis has identified 21 putative open reading frames (ORFs) in the neomycin gene cluster (neo) with significant protein sequence similarity to gene products involved in the biosynthesis of other DOS-containing aminoglycosides, namely butirosin (btr), gentamycin (gnt), tobramycin (tbm) and kanamycin (kan). Located at the 5′-end of the neo gene cluster is the previously-characterised neomycin phosphotransferase gene (apH). Three genes unique to the neo and btr clusters have been revealed by comparison of the neo cluster to btr, gnt, tbm and kan clusters. This suggests that these three genes may be involved in the transfer of a ribose moiety to the DOS ring during the antibiotic biosynthesis. The product of the neo-6 gene is characterised here as the L-glutamine : 2-deoxy-scyllo-inosose aminotransferase responsible for the first transamination in DOS biosynthesis, which supports the assignment of the gene cluster.</dcterms:abstract> <dc:contributor>Spiteller, Dieter</dc:contributor> <dc:contributor>Mironenko, Tatiana</dc:contributor> <void:sparqlEndpoint rdf:resource="http://localhost/fuseki/dspace/sparql"/> <dc:creator>Spencer, Jonathan B.</dc:creator> <bibo:uri rdf:resource="http://kops.uni-konstanz.de/handle/123456789/15515"/> <dc:contributor>Spencer, Jonathan B.</dc:contributor> <dcterms:available rdf:datatype="http://www.w3.org/2001/XMLSchema#dateTime">2011-09-01T12:18:19Z</dcterms:available> <dc:contributor>Li, Yanyan</dc:contributor> <dcterms:issued>2005-04-21</dcterms:issued> </rdf:Description> </rdf:RDF>