Okada Masahiro, Sugita Tomotoshi, Wong Chin Piow, Wakimoto Toshiyuki, Abe Ikuro
Graduate School of Pharmaceutical Sciences, The University of Tokyo , Bunkyo-ku, Tokyo 113-0033, Japan.
J Nat Prod. 2017 Apr 28;80(4):1205-1209. doi: 10.1021/acs.jnatprod.6b01152. Epub 2017 Mar 14.
A novel pyridinium with three indole moieties, tricepyridinium, was obtained from the culture of an Escherichia coli clone incorporating metagenomic libraries from the marine sponge Discodermia calyx. For the important structural elements of tricepyridinium to be investigated for antibacterial activity, tricepyridinium and its analogues were chemically synthesized. Tricepyridinium had antimicrobial activity, but not against E. coli, and cytotoxicity against P388 cells. Additional bioassays with its synthetic analogues revealed that the intriguing combination of the indole moieties, most likely derived from three tryptamines, as well as the pyridinium moiety were chiefly responsible for its potent biological activities.
一种带有三个吲哚基团的新型吡啶鎓盐——三吲哚吡啶鎓盐,是从一种大肠杆菌克隆的培养物中获得的,该克隆整合了来自海洋海绵萼海绵的宏基因组文库。为了研究三吲哚吡啶鎓盐的重要结构元素的抗菌活性,对三吲哚吡啶鎓盐及其类似物进行了化学合成。三吲哚吡啶鎓盐具有抗菌活性,但对大肠杆菌无活性,且对P388细胞具有细胞毒性。对其合成类似物进行的额外生物测定表明,吲哚基团(很可能源自三种色胺)与吡啶鎓基团的有趣组合是其强大生物活性的主要原因。