Graduate School of Pharmaceutical Sciences, Kitasato University, Tokyo, Japan.
J Antibiot (Tokyo). 2013 Jan;66(1):37-41. doi: 10.1038/ja.2012.83. Epub 2012 Nov 21.
An enzyme assay for bacterial undecaprenyl pyrophosphate (UPP) synthase was performed to screen microbial culture broths for inhibitors of UPP synthase. During the course of this screening program, an EtOH extract of a rice culture of Penicillium brasilianum FKI-3368 was found to inhibit UPP synthase activity. From activity-guided purification, a new compound-designated spirohexaline was isolated together with the structurally related and known viridicatumtoxin by ethyl acetate extraction silica gel and octadecylsilane column chromatographies and high-performance liquid chromatography. The structure of spirohexaline was elucidated by spectroscopic analysis, including NMR. Spirohexaline and viridicatumtoxin have a common hexacycline structure produced by fusion of a tetracycline-type ring with a spiro-type ring. They inhibited UPP synthase activity with IC₅₀ values of 9.0 and 4.0 μM, respectively.
一种用于细菌十一碳烯焦磷酸(UPP)合酶的酶测定法被用于筛选微生物培养物中的 UPP 合酶抑制剂。在该筛选计划的过程中,从 Penicillium brasilianum FKI-3368 的水稻培养物的 EtOH 提取物中发现了抑制 UPP 合酶活性的物质。通过活性导向的纯化,从乙酸乙酯提取物硅胶和十八烷基硅烷柱色谱和高效液相色谱中分离出一种新的化合物,命名为螺六氢萘,并与结构相关的已知的绿僵菌素一起分离出来。通过包括 NMR 在内的光谱分析阐明了螺六氢萘的结构。螺六氢萘和绿僵菌素具有由四环型环与螺型环融合产生的共同的六环结构。它们抑制 UPP 合酶的活性,IC₅₀ 值分别为 9.0 和 4.0 μM。