Luzhetskyy Andriy, Taguchi Takaaki, Fedoryshyn Marta, Dürr Clemens, Wohlert Sven-Eric, Novikov Volodymyr, Bechthold Andreas
Albert-Ludwigs-Universität, Institut für Pharmazeutische Wissenschaften, Stefan-Meier-Strasse 19, 79104 Freiburg, Germany.
Chembiochem. 2005 Aug;6(8):1406-10. doi: 10.1002/cbic.200500018.
The glycosyltransferase LanGT2 is involved in the biosynthesis of the hexasaccharide side chain of the angucyclic antibiotic landomycin A. Its function was elucidated by targeted gene inactivation of lanGT2. The main metabolite of the obtained mutant was identified as tetrangulol (4), the progenitor of the landomycin aglycon (7). The lack of the sugar side chain indicates that LanGT2 catalyzes the priming glycosyl transfer in the hexasaccharide biosynthesis: the attachment of a D-olivose to O-8 of the polyketide backbone. Heterologous expression of urdGT2 from S. fradiae Tü2717 in this mutant resulted in the production of a novel C-glycosylated angucycline (6).
糖基转移酶LanGT2参与蒽环类抗生素地霉素A六糖侧链的生物合成。通过对lanGT2进行靶向基因失活阐明了其功能。所得突变体的主要代谢产物被鉴定为四方醇(4),即地霉素苷元(7)的前体。糖侧链的缺失表明LanGT2催化六糖生物合成中的起始糖基转移:将D-橄榄糖连接到聚酮骨架的O-8上。来自弗氏链霉菌Tü2717的urdGT2在该突变体中的异源表达导致产生了一种新型的C-糖基化蒽环类化合物(6)。