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    <dc:title>Die antitumorwirksame Hybrid-Verbindung Premithramycinon H verweist indirekt auf ein tricyclisches Intermediat der Biosynthese des Aureolsäure-Antibiotikums Mithramycin</dc:title>
    <dc:creator cris:orcid="0000-0002-6680-6723">Felipe Lombó</dc:creator>
    <dc:creator>Eva Künzel</dc:creator>
    <dc:creator cris:orcid="0000-0001-7036-0608">Laura Prado</dc:creator>
    <dc:creator cris:orcid="0000-0002-3277-9085">Alfredo F. Braña</dc:creator>
    <dc:creator>Kai U. Bindseil</dc:creator>
    <dc:creator>Jürgen Frevert</dc:creator>
    <dc:creator cris:orcid="0000-0003-0330-8513">Daniel W. Bearden</dc:creator>
    <dc:creator cris:orcid="0000-0003-2729-841X">Cármen Méndez</dc:creator>
    <dc:creator cris:orcid="0000-0001-6495-3810">José A. Salas</dc:creator>
    <dc:creator cris:orcid="0000-0001-6447-5951">Jürgen Rohr</dc:creator>
    <dc:subject>mithramycin</dc:subject>
    <dc:subject>hybrid natural products</dc:subject>
    <dc:subject>biosynthetic intermediates</dc:subject>
    <dc:subject>tricyclic intermediate</dc:subject>
    <dc:subject>genetic recombination</dc:subject>
    <dc:subject>anticancer agents</dc:subject>
    <dc:subject>structure elucidation</dc:subject>
    <dc:description>Gen-Rekombinationsexperimente sind nicht nur nützlich für die Herstellung neuer Hybrid-Naturstoffe, sondern können auch hilfreich sein, um instabile Biosynthese-Zwischenprodukte abzufangen und Rückschlüsse auf deren Struktur zu ermöglichen. Premithramycinon H 1, ein biologisch aktives Hybridprodukt, das aus einer Mischung von Mithramycin- mit Tetracenomycin-Biosynthesegenen hervorgeht, ist hierfür ein gutes Beispiel.</dc:description>
    <dcterms:issued>2000</dcterms:issued>
    <dc:language>de</dc:language>
    <dc:type>info:eu-repo/semantics/article</dc:type>
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    <dc:identifier>https://doi.org/10.1002/(sici)1521-3757(20000218)112:4&lt;808::aid-ange808&gt;3.0.co;2-3</dc:identifier>
    <dcterms:isPartOf>Angewandte Chemie</dcterms:isPartOf>
    <dc:source>Angewandte Chemie</dc:source>
    <dc:identifier>urn:issn:0044-8249</dc:identifier>
    <dc:identifier>urn:issn:0932-2140</dc:identifier>
    <dcterms:bibliographicCitation>Angewandte Chemie, 2000, vol. 112, n. 4, p. 808-811</dcterms:bibliographicCitation>
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    <dc:title>The novel hybrid antitumor compound premithramycinone H provides indirect evidence for a tricyclic intermediate of the biosynthesis of the aureolic acid antibiotic mithramycin</dc:title>
    <dc:creator cris:orcid="0000-0002-6680-6723">Felipe Lombó</dc:creator>
    <dc:creator>Eva Künzel</dc:creator>
    <dc:creator cris:orcid="0000-0001-7036-0608">Laura Prado</dc:creator>
    <dc:creator cris:orcid="0000-0002-3277-9085">Alfredo F. Braña</dc:creator>
    <dc:creator>Kai U. Bindseil</dc:creator>
    <dc:creator>Jürgen Frevert</dc:creator>
    <dc:creator cris:orcid="0000-0003-0330-8513">Daniel W. Bearden</dc:creator>
    <dc:creator cris:orcid="0000-0003-2729-841X">Cármen Méndez</dc:creator>
    <dc:creator cris:orcid="0000-0001-6495-3810">José A. Salas</dc:creator>
    <dc:creator cris:orcid="0000-0001-6447-5951">Jürgen Rohr</dc:creator>
    <dc:subject>mithramycin</dc:subject>
    <dc:subject>hybrid natural products</dc:subject>
    <dc:subject>genetic recombination</dc:subject>
    <dc:subject>biosynthetic intermediates</dc:subject>
    <dc:subject>tricyclic intermediate</dc:subject>
    <dc:subject>structure elucidation</dc:subject>
    <dc:subject>anticancer agents</dc:subject>
    <dc:description>Gene recombination experiments are not only useful for the generation of novel hybrid natural products, but can also be helpful in intercepting unstable biosynthetic intermediates to allow conclusions to be made about their structures. Premithramycinone H (1), a biologically active hybrid which results from a mixture of mithramycin and tetracenomycin biosynthetic genes, is a good example of this strategy.</dc:description>
    <dcterms:issued>2000</dcterms:issued>
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    <dc:identifier>https://doi.org/10.1002/(sici)1521-3773(20000218)39:4&lt;796::aid-anie796&gt;3.0.co;2-n</dc:identifier>
    <dcterms:isPartOf>Angewandte Chemie International Edition</dcterms:isPartOf>
    <dc:source>Angewandte Chemie International Edition</dc:source>
    <dc:identifier>urn:issn:1433-7851</dc:identifier>
    <dc:identifier>urn:issn:1521-3773</dc:identifier>
    <dcterms:bibliographicCitation>Angewandte Chemie International Edition, 2000, vol. 39, n. 4, p. 796-799</dcterms:bibliographicCitation>
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    <dc:title>ChemInform Abstract: Enantiospecific Synthesis of Dihydropyridines from Chiral Enamines.</dc:title>
    <dc:creator cris:orcid="0000-0002-1600-7878">Esther Caballero</dc:creator>
    <dc:creator cris:orcid="0000-0003-2623-1256">Pilar Puebla</dc:creator>
    <dc:creator>M. SANCHEZ</dc:creator>
    <dc:creator cris:orcid="0000-0002-3311-5846">Manuel Medarde</dc:creator>
    <dc:creator cris:orcid="0000-0001-7036-0608">Laura Prado</dc:creator>
    <dc:creator cris:orcid="0000-0002-0578-0611">Arturo San Feliciano</dc:creator>
    <dc:subject>enantiospecific synthesis</dc:subject>
    <dc:subject>dihydropyridines</dc:subject>
    <dc:subject>chiral enamines</dc:subject>
    <dc:subject>asymmetric synthesis</dc:subject>
    <dc:subject>pyridine synthesis</dc:subject>
    <dc:description>Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable via the “References” option.</dc:description>
    <dcterms:issued>1996</dcterms:issued>
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    <dc:identifier>https://doi.org/10.1002/chin.199647137</dc:identifier>
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    <dc:identifier>urn:issn:0009-2975</dc:identifier>
    <dc:identifier>urn:issn:0931-7597</dc:identifier>
    <dcterms:bibliographicCitation>ChemInform, 1996, vol. 27, n. 47</dcterms:bibliographicCitation>
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    <dc:title>Towards the Generation of Novel Antitumour Agents from Actinomycetes by Combinational Biosynthesis</dc:title>
    <dc:creator>J. A. Salas</dc:creator>
    <dc:creator>Gloria Blanco</dc:creator>
    <dc:creator cris:orcid="0000-0002-3277-9085">Alfredo F. Braña</dc:creator>
    <dc:creator>Ernestina Fernández</dc:creator>
    <dc:creator>Ma José Palomo Fernández</dc:creator>
    <dc:creator>Jose Garcia Bernrdo</dc:creator>
    <dc:creator>Ana Gonzalez</dc:creator>
    <dc:creator cris:orcid="0000-0002-6680-6723">Felipe Lombó</dc:creator>
    <dc:creator cris:orcid="0000-0001-7036-0608">Laura Prado</dc:creator>
    <dc:creator cris:orcid="0000-0003-3505-3762">Luís M. Quirós</dc:creator>
    <dc:creator cris:orcid="0000-0001-9891-0843">César Sánchez</dc:creator>
    <dc:creator cris:orcid="0000-0003-2729-841X">Cármen Méndez</dc:creator>
    <dc:subject>anticancer agents</dc:subject>
    <dc:subject>actinomycetes</dc:subject>
    <dc:subject>combinatorial biosynthesis</dc:subject>
    <dc:subject>natural product discovery</dc:subject>
    <dc:subject>secondary metabolites</dc:subject>
    <dc:subject>anticancer drug discovery</dc:subject>
    <dcterms:issued>2001</dcterms:issued>
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    <dc:identifier>https://doi.org/10.1007/0-306-46885-9_23</dc:identifier>
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    <dc:source>Focus on biotechnology</dc:source>
    <dc:identifier>urn:issn:1569-268X</dc:identifier>
    <dcterms:bibliographicCitation>Focus on biotechnology, 2001, p. 383-399</dcterms:bibliographicCitation>
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    <dc:title>The mtmVUC genes of the mithramycin gene cluster in Streptomyces argillaceus are involved in the biosynthesis of the sugar moieties</dc:title>
    <dc:creator cris:orcid="0000-0002-3487-2806">Aída González</dc:creator>
    <dc:creator>Lily L. Remsing</dc:creator>
    <dc:creator cris:orcid="0000-0002-6680-6723">Felipe Lombó</dc:creator>
    <dc:creator>M. J. Fernández</dc:creator>
    <dc:creator cris:orcid="0000-0001-7036-0608">Laura Prado</dc:creator>
    <dc:creator cris:orcid="0000-0002-3277-9085">Alfredo F. Braña</dc:creator>
    <dc:creator>Eva Künzel</dc:creator>
    <dc:creator cris:orcid="0000-0001-6447-5951">Jürgen Rohr</dc:creator>
    <dc:creator cris:orcid="0000-0003-2729-841X">Cármen Méndez</dc:creator>
    <dc:creator cris:orcid="0000-0001-6495-3810">José A. Salas</dc:creator>
    <dc:subject>mithramycin</dc:subject>
    <dc:subject>Streptomyces argillaceus</dc:subject>
    <dc:subject>sugar synthesis</dc:subject>
    <dc:subject>glycosylation</dc:subject>
    <dc:subject>C-methyltransferase</dc:subject>
    <dc:subject>polyketide biosynthesis</dc:subject>
    <dc:subject>glycosyltransferases</dc:subject>
    <dc:subject>insertional inactivation</dc:subject>
    <dcterms:issued>2001</dcterms:issued>
    <dc:language>en</dc:language>
    <dc:type>info:eu-repo/semantics/article</dc:type>
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    <dc:identifier>https://doi.org/10.1007/s004380000372</dc:identifier>
    <dcterms:isPartOf>Molecular &amp; General Genetics: MGG</dcterms:isPartOf>
    <dc:source>Molecular &amp; General Genetics: MGG</dc:source>
    <dc:identifier>urn:issn:1617-4615</dc:identifier>
    <dc:identifier>urn:issn:1617-4623</dc:identifier>
    <dcterms:bibliographicCitation>Molecular &amp; General Genetics: MGG, 2001, vol. 264, n. 6, p. 827-835</dcterms:bibliographicCitation>
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    <dc:title>Analysis of two chromosomal regions adjacent to genes for a type II polyketide synthase involved in the biosynthesis of the antitumor polyketide mithramycin in Streptomyces argillaceus</dc:title>
    <dc:creator cris:orcid="0000-0001-7036-0608">Laura Prado</dc:creator>
    <dc:creator cris:orcid="0000-0002-6680-6723">Felipe Lombó</dc:creator>
    <dc:creator cris:orcid="0000-0002-3277-9085">Alfredo F. Braña</dc:creator>
    <dc:creator cris:orcid="0000-0003-2729-841X">Cármen Méndez</dc:creator>
    <dc:creator cris:orcid="0000-0001-6447-5951">Jürgen Rohr</dc:creator>
    <dc:creator cris:orcid="0000-0001-6495-3810">José A. Salas</dc:creator>
    <dc:subject>mithramycin</dc:subject>
    <dc:subject>type II polyketide synthase</dc:subject>
    <dc:subject>Streptomyces argillaceus</dc:subject>
    <dc:subject>polyketide biosynthesis</dc:subject>
    <dc:subject>oxygenase</dc:subject>
    <dc:subject>reductase</dc:subject>
    <dc:subject>gene replacement</dc:subject>
    <dc:subject>biosynthetic gene clusters</dc:subject>
    <dc:subject>anticancer natural products</dc:subject>
    <dc:subject>biosynthetic pathway</dc:subject>
    <dcterms:issued>1999</dcterms:issued>
    <dc:language>en</dc:language>
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    <dc:identifier>https://doi.org/10.1007/s004380050960</dc:identifier>
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    <dc:identifier>urn:issn:0026-8925</dc:identifier>
    <dc:identifier>urn:issn:1432-1874</dc:identifier>
    <dcterms:bibliographicCitation>Molecular &amp; General Genetics: MGG, 1999, vol. 261, n. 2, p. 216-225</dcterms:bibliographicCitation>
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    <dc:title>Oxidative cleavage of premithramycin B is one of the last steps in the biosynthesis of the antitumor drug mithramycin</dc:title>
    <dc:creator cris:orcid="0000-0001-7036-0608">Laura Prado</dc:creator>
    <dc:creator>Ernestina Fernández</dc:creator>
    <dc:creator>Ulrike Weiβbach</dc:creator>
    <dc:creator>Gloria Blanco</dc:creator>
    <dc:creator cris:orcid="0000-0003-3505-3762">Luís M. Quirós</dc:creator>
    <dc:creator cris:orcid="0000-0002-3277-9085">Alfredo F. Braña</dc:creator>
    <dc:creator cris:orcid="0000-0003-2729-841X">Cármen Méndez</dc:creator>
    <dc:creator cris:orcid="0000-0001-6447-5951">Jürgen Rohr</dc:creator>
    <dc:creator>José A. Salas</dc:creator>
    <dc:subject>oxidative cleavage</dc:subject>
    <dc:subject>Streptomyces argillaceus</dc:subject>
    <dc:subject>Baeyer-Villiger oxidation</dc:subject>
    <dc:subject>lactone ring opening</dc:subject>
    <dc:subject>type II polyketide synthase</dc:subject>
    <dc:subject>anticancer natural products</dc:subject>
    <dcterms:issued>1999</dcterms:issued>
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    <dc:identifier>https://doi.org/10.1016/s1074-5521(99)80017-9</dc:identifier>
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    <dc:identifier>urn:issn:1879-1301</dc:identifier>
    <dcterms:bibliographicCitation>CHEMISTRY &amp; BIOLOGY, 1999, vol. 6, n. 1, p. 19-30</dcterms:bibliographicCitation>
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    <dc:title>The structures of premithramycinone and demethylpremithramycinone, plausible early intermediates of the aureolic acid group antibiotic mithramycin</dc:title>
    <dc:creator cris:orcid="0000-0001-6447-5951">Jürgen Rohr</dc:creator>
    <dc:creator>Ulrike Weißbach</dc:creator>
    <dc:creator>Claus Beninga</dc:creator>
    <dc:creator>Eva Künzel</dc:creator>
    <dc:creator cris:orcid="0000-0002-0644-8696">Karsten Siems</dc:creator>
    <dc:creator>Kai U. Bindseil</dc:creator>
    <dc:creator cris:orcid="0000-0002-6680-6723">Felipe Lombó</dc:creator>
    <dc:creator cris:orcid="0000-0001-7036-0608">Laura Prado</dc:creator>
    <dc:creator cris:orcid="0000-0002-3277-9085">Alfredo F. Braña</dc:creator>
    <dc:creator cris:orcid="0000-0003-2729-841X">Cármen Méndez</dc:creator>
    <dc:creator cris:orcid="0000-0001-6495-3810">José A. Salas</dc:creator>
    <dc:subject>mithramycin</dc:subject>
    <dc:subject>antibiotic biosynthesis</dc:subject>
    <dc:subject>structure elucidation</dc:subject>
    <dc:description>The structures of premithramycinone and its demethyl analogue suggest that the aureolic acid antibiotics are biosynthetically formed via a tetracycline-type, and not a tetracenomycin-type, folded decaketide.</dc:description>
    <dcterms:issued>1998</dcterms:issued>
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    <dc:identifier>urn:issn:1364-548X</dc:identifier>
    <dcterms:bibliographicCitation>Chemical Communications, 1998, n. 3, p. 437-438</dcterms:bibliographicCitation>
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    <dc:title>Towards the generation of novel antitumour agents from actinomycetes by combinatorial biosynthesis</dc:title>
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