| Literature DB >> 15123249 |
Bohdan Ostash1, Uwe Rix, Lily L Remsing Rix, Tao Liu, Felipe Lombo, Andriy Luzhetskyy, Oleksandr Gromyko, Chenchen Wang, Alfredo F Braña, Carmen Méndez, José A Salas, Victor Fedorenko, Jürgen Rohr.
Abstract
A 3 kb DNA fragment from the Streptomyces globisporus 1912 landomycin E (LaE) biosynthetic gene cluster (lnd) was completely sequenced. Three open reading frames were identified, lndGT4, lndZ4, and lndZ5, whose probable translation products resemble a glycosyltransferase, a reductase, and a hydroxylase, respectively. Studies of generated mutants from disruption and complementation experiments involving the lndGT4 gene allowed us to determine that LndGT4 controls the terminal L-rhodinose sugar attachment during LaE biosynthesis and that LndZ4/LndZ5 are responsible for the unique C11-hydroxylation of the landomycins. Generation of the novel landomycins F, G, and H in the course of these studies provided evidence for the flexibility of lnd glycosyltransferases toward their acceptor substrates and a basis for initial structure-activity relationships within the landomycin family of antibiotics.Entities:
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Year: 2004 PMID: 15123249 DOI: 10.1016/j.chembiol.2004.03.011
Source DB: PubMed Journal: Chem Biol ISSN: 1074-5521