Biología Funcional
Saila
María Gloria
Blanco Blanco
María Gloria Blanco Blanco-rekin lankidetzan egindako argitalpenak (30)
2017
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Branimycins B and C, Antibiotics Produced by the Abyssal Actinobacterium Pseudonocardia carboxydivorans M-227
Journal of Natural Products, Vol. 80, Núm. 2, pp. 569-573
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Pharmacological Potential of Phylogenetically Diverse Actinobacteria Isolated from Deep-Sea Coral Ecosystems of the Submarine Avilés Canyon in the Cantabrian Sea
Microbial Ecology, Vol. 73, Núm. 2, pp. 338-352
2016
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Atmospheric Dispersal of Bioactive Streptomyces albidoflavus Strains Among Terrestrial and Marine Environments
Microbial Ecology, Vol. 71, Núm. 2, pp. 375-386
2015
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Erratum to: Two Streptomyces Species Producing Antibiotic, Antitumor, and Anti-Inflammatory Compounds Are Widespread Among Intertidal Macroalgae and Deep-Sea Coral Reef Invertebrates from the Central Cantabrian Sea (Microb Ecol, (2014), DOI 10.1007/s00248-014-0508-0)
Microbial Ecology
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Myceligenerans cantabricum sp. nov., a barotolerant actinobacterium isolated from a deep cold-water coral
International Journal of Systematic and Evolutionary Microbiology, Vol. 65, pp. 1328-1334
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Two Streptomyces Species Producing Antibiotic, Antitumor, and Anti-Inflammatory Compounds Are Widespread Among Intertidal Macroalgae and Deep-Sea Coral Reef Invertebrates from the Central Cantabrian Sea
Microbial Ecology, Vol. 69, Núm. 3, pp. 512-524
2014
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Activation and silencing of secondary metabolites in Streptomyces albus and Streptomyces lividans after transformation with cosmids containing the thienamycin gene cluster from Streptomyces cattleya
Archives of Microbiology, Vol. 196, Núm. 5, pp. 345-355
2011
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Mutational analysis of the thienamycin biosynthetic gene cluster from Streptomyces cattleya
Antimicrobial Agents and Chemotherapy, Vol. 55, Núm. 4, pp. 1638-1649
2010
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Transcriptional organization of ThnI-regulated thienamycin biosynthetic genes in Streptomyces cattleya
Journal of Antibiotics, Vol. 63, Núm. 3, pp. 135-138
2008
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Identification of transcriptional activators for thienamycin and cephamycin C biosynthetic genes within the thienamycin gene cluster from Streptomyces cattleya
Molecular Microbiology, Vol. 69, Núm. 3, pp. 633-645
2003
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The biosynthetic gene cluster for the β-lactam carbapenem thienamycin in Streptomyces cattleya
Chemistry and Biology, Vol. 10, Núm. 4, pp. 301-311
2002
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Hybrid compounds generated by the introduction of a nogalamycin-producing plasmid into Streptomyces argillaceus
Journal of the Chemical Society. Perkin Transactions 1, pp. 1818-1825
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Rationally designed glycosylated premithramycins: Hybrid aromatic polyketides using genes from three different biosynthetic pathways
Journal of the American Chemical Society, Vol. 124, Núm. 21, pp. 6056-6062
2001
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Deoxysugar methylation during biosynthesis of the antitumor polyketide elloramycin by Streptomyces olivaceus: Characterization of three methyltransferase genes
Journal of Biological Chemistry, Vol. 276, Núm. 22, pp. 18765-18774
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Identification of a growth phase-dependent promoter in the rplJL operon of Streptomyces coelicolor A3(2)
Biochimica et Biophysica Acta - Gene Structure and Expression, Vol. 1517, Núm. 2, pp. 243-249
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Identification of a sugar flexible glycosyltransferase from streptomyces olivaceus, the producer of the antitumor polyketide elloramycin
Chemistry and Biology, Vol. 8, Núm. 3, pp. 253-263
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Towards the generation of novel antitumour agents from actinomycetes by combinatorial biosynthesis
NOVEL FRONTIERS IN THE PRODUCTION OF COMPOUNDS FOR BIOMEDICAL USE, VOL 1
2000
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Characterization of two glycosyltransferases involved in early glycosylation steps during biosynthesis of the antitumor polyketide mithramycin by Streptomyces argillaceus
Molecular and General Genetics, Vol. 262, Núm. 6, pp. 991-1000
1999
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Oxidative cleavage of premithramycin B is one of the last steps in the biosynthesis of the antitumor drug mithramycin
Chemistry and Biology, Vol. 6, Núm. 1, pp. 19-30
1998
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Novel hybrid tetracenomycins through combinatorial biosynthesis using a glycosyltransferase encoded by the elm genes in cosmid 16F4 and which shows a broad sugar substrate specificity
Journal of the American Chemical Society, Vol. 120, Núm. 41, pp. 10596-10601