Chemical Biology Research Center, KRIBB, 30 Yeongudanji-ro, Ochang-eup, Chungbuk 363-883, Korea.
J Microbiol Biotechnol. 2012 Nov;22(11):1478-81. doi: 10.4014/jmb.1206.06026.
Geldanamycin (GM) and its analogs are important anticancer agents that inhibit heat shock protein (Hsp) 90, which is a major chaperone protein in cancer cells. Accordingly, based on interest in obtaining novel natural GM derivatives, the potential of Streptomyces hygroscopicus JCM4427, a GM producer, was explored for novel natural GM derivative(s), resulting in the discovery of new GM analogs as a biosynthetic shunt product and intermediates from its fermentation broth. In this study, the fermentation, isolation, structure determination, and biological activity of the compounds, two new tetracyclic thiazinogeldanamycin (1) and 19-hydroxy-4,5-dihydrogeldanamycin (3), together with the three known 4,5-dihydrothiazinogeldanamycin (2), reblastatin (4), and 17-demethoxy-reblastatin (5), are described.
金霉素(GM)及其类似物是重要的抗癌药物,可抑制热休克蛋白(Hsp)90,它是癌细胞中的主要伴侣蛋白。因此,基于获得新型天然 GM 衍生物的兴趣,对产生 GM 的吸水链霉菌 JCM4427 的潜力进行了探索,以期发现新的 GM 类似物作为生物合成支路产物及其发酵液中的中间体。在这项研究中,描述了化合物的发酵、分离、结构确定和生物活性,包括两个新的四环噻嗪金霉素(1)和 19-羟基-4,5-二氢金霉素(3),以及三种已知的 4,5-二氢噻嗪金霉素(2)、雷帕霉素(4)和 17-去甲氧基-雷帕霉素(5)。