The aureolic acid family of antitumor compounds: structure, mode of action, biosynthesis, and novel derivatives-Reference-Cited by-同舟云学术

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The aureolic acid family of antitumor compounds: structure, mode of action, biosynthesis, and novel derivatives

Published:2006-09-30 Issue:1 Volume:73 Page:1-14
ISSN:0175-7598
Container-title:Applied Microbiology and Biotechnology
language:en
Short-container-title:Appl Microbiol Biotechnol

Author:

Lombó Felipe,Menéndez Nuria,Salas José A.,Méndez Carmen

Publisher

Springer Science and Business Media LLC

Subject

Applied Microbiology and Biotechnology,General Medicine,Biotechnology

Link

http://link.springer.com/content/pdf/10.1007/s00253-006-0511-6.pdf

Reference70 articles.

1. Bianchi N, Rutigliano C, Passadore M, Tomassetti M, Pippo L, Mischiati C, Feriotto G, Gambari R (1997) Targeting of the HIV-1 long terminal repeat with chromomycin potentiates the inhibitory effects of a triplex-forming oligonucleotide on Sp1-DNA interactions and in vitro transcription. Biochem J 326:919–927

2. Blanco G, Fu H, Méndez C, Khosla C, Salas JA (1996) Deciphering the biosynthetic origin of the aglycone of the aureolic acid group of anti-tumor agents. Chem Biol 3:193–196

3. Blanco G, Fernández E, Fernández MJ, Braña AF, Weissbach U, Künzel E, Rohr J, Méndez C, Salas JA (2000) Characterization of two glycosyltransferases involved in early glycosylation steps during biosynthesis of the antitumor polyketide mithramycin by Streptomyces argillaceus. Mol Gen Genet 262:991–1000

4. Blanco G, Patallo EP, Braña AF, Trefzer A, Bechthold A, Rohr J, Méndez C, Salas JA (2001) Identification of a sugar flexible glycosyltransferase from Streptomyces olivaceus, the producer of the antitumor polyketide elloramycin. Chem Biol 8:253–263

5. Blumauerova M, Lipavska H, Stajner K, Vanek Z (1976) The study of variability and strain selection in Streptomyces atroolivaceus. III. Isolation and preliminary characteristics of mutants impaired in the biosynthesis of mithramycin. Folia Microbiol (Praha) 21:285–293

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