Hoshino Shotaro, Ozeki Masahiro, Wong Chin Piow, Zhang Huiping, Hayashi Fumiaki, Awakawa Takayoshi, Morita Hiroyuki, Onaka Hiroyasu, Abe Ikuro
Graduate School of Pharmaceutical Sciences, The University of Tokyo.
Institute of Natural Medicine, University of Toyama.
Chem Pharm Bull (Tokyo). 2018;66(6):660-667. doi: 10.1248/cpb.c18-00143.
Mycolic acid-containing bacteria (MACB) are known to activate cryptic natural product biosynthesis in co-cultures with actinobacteria. We cultured Actinosynnema mirum NBRC 14064, a producer of the mono-cyclic polyene macrolactam mirilactam A (6), with the MACB Tsukamurella pulmonis TP-B0596. As a result, three novel compounds (mirilactams C-E, 1-3) were produced in the co-culture conditions. Compounds 1-3 were likely derived from 6 by epoxidation and subsequent spontaneous cyclization. The chemical structures and stereochemistries of 1-3 were determined by spectroscopic analyses (NMR and MS), conformational searches in the optimized potentials for liquid simulations-3 (OPLS3) force field, and calculations of electronic circular dichroism (ECD).
含分枝菌酸的细菌(MACB)已知在与放线菌共培养时会激活隐秘天然产物的生物合成。我们将单环多烯大环内酰胺米利内酰胺A(6)的产生菌——放线链霉菌NBRC 14064与MACB——肺塔库菌TP-B0596进行了共培养。结果,在共培养条件下产生了三种新化合物(米利内酰胺C - E,1 - 3)。化合物1 - 3可能是由6通过环氧化和随后的自发环化衍生而来。通过光谱分析(核磁共振和质谱)、在液体模拟优化势 - 3(OPLS3)力场中的构象搜索以及电子圆二色性(ECD)计算确定了1 - 3的化学结构和立体化学。