Blanco G, Fernández E, Fernández M J, Braña A F, Weissbach U, Künzel E, Rohr J, Méndez C, Salas J A
Departamento de Biología Funcional e Instituto Universitario de Oncología del Principado de Asturias, Universidad de Oviedo, Spain.
Mol Gen Genet. 2000 Jan;262(6):991-1000. doi: 10.1007/pl00008667.
A 2,580-bp region of the chromosome of Streptomyces argillaceus, the producer of the antitumor polyketide mithramycin, was sequenced. Analysis of the nucleotide sequence revealed the presence of two genes (mtmGIII and mtmGIV) encoding proteins that showed a high degree of similarity to glycosyltransferases involved in the biosynthesis of various antibiotics and antitumor drugs. Independent insertional inactivation of both genes produced mutants that did not synthesize mithramycin but accumulated several mithramycin intermediates. Both mutants accumulated premithramycinone, a non-glycosylated intermediate in mithramycin biosynthesis. The mutant affected in the mtmGIII gene also accumulated premithramycin A1, which contains premithramycinone as the aglycon unit and a D-olivose attached at C-12a-O. These experiments demonstrate that the glycosyltransferases MtmGIV and MtmGIII catalyze the first two glycosylation steps in mithramycin biosynthesis. A model is proposed for the glycosylation steps in mithramycin biosynthesis.
对产生抗肿瘤聚酮化合物光神霉素的泥质链霉菌染色体上一段2580 bp的区域进行了测序。核苷酸序列分析显示存在两个基因(mtmGIII和mtmGIV),它们编码的蛋白质与参与多种抗生素和抗肿瘤药物生物合成的糖基转移酶具有高度相似性。对这两个基因进行独立的插入失活产生了不合成光神霉素但积累了几种光神霉素中间体的突变体。两个突变体都积累了前光神霉素酮,它是光神霉素生物合成中的一种非糖基化中间体。受mtmGIII基因影响的突变体还积累了前光神霉素A1,它以前光神霉素酮为苷元单元,在C-12a-O处连接有一个D-橄榄糖。这些实验表明,糖基转移酶MtmGIV和MtmGIII催化光神霉素生物合成中的前两个糖基化步骤。提出了一个光神霉素生物合成中糖基化步骤的模型。