New anthracycline metabolites produced by the aklavinone 11-hydroxylase gene in Streptomyces galilaeus ATCC 31133

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dc.contributor.authorHang Sub Kim-
dc.contributor.authorYoung Soo Hong-
dc.contributor.authorYoung Ho Kim-
dc.contributor.authorO J Yoo-
dc.contributor.authorJung Joon Lee-
dc.date.accessioned2017-04-19T08:45:27Z-
dc.date.available2017-04-19T08:45:27Z-
dc.date.issued1996-
dc.identifier.issn0021-8820-
dc.identifier.urihttps://oak.kribb.re.kr/handle/201005/3750-
dc.description.abstractTransformation of Streptomyces galilaeus ATCC 31133 with the aklavinone 11-hydroxylase gene (dnrF) resulted in the production of many red pigments. The new metabolites were purified and their structures were determined as 11-hydroxylated aclacinomycin A, B and T by spectral analysis. This result indicated that the dnrF was stably expressed in the strain S. galilaeus ATCC 31133 to give rise to hybrid aclacinomycins. In addition, a new aclacinomycin analog named 11-hydroxyaclacinomycin X was isolated from the same culture. Its structure was elucidated as 2'''-amino-11-hydroxyaclacinomycin Y. It showed strong cytotoxicity against several human tumor cell lines, especially leukemia and melanoma cell lines.-
dc.publisherSpringer-Nature Pub Group-
dc.titleNew anthracycline metabolites produced by the aklavinone 11-hydroxylase gene in Streptomyces galilaeus ATCC 31133-
dc.title.alternativeNew anthracycline metabolites produced by the aklavinone 11-hydroxylase gene in Streptomyces galilaeus ATCC 31133-
dc.typeArticle-
dc.citation.titleJournal of Antibiotics-
dc.citation.number4-
dc.citation.endPage360-
dc.citation.startPage355-
dc.citation.volume49-
dc.contributor.affiliatedAuthorHang Sub Kim-
dc.contributor.affiliatedAuthorYoung Soo Hong-
dc.contributor.affiliatedAuthorYoung Ho Kim-
dc.contributor.affiliatedAuthorJung Joon Lee-
dc.contributor.alternativeName김항섭-
dc.contributor.alternativeName홍영수-
dc.contributor.alternativeName김영호-
dc.contributor.alternativeName유욱준-
dc.contributor.alternativeName이정준-
dc.identifier.bibliographicCitationJournal of Antibiotics, vol. 49, no. 4, pp. 355-360-
dc.identifier.doi10.7164/antibiotics.49.355-
dc.description.journalClassY-
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Ochang Branch Institute > Chemical Biology Research Center > 1. Journal Articles
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