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Four Classes of Structurally Unusual Peptides from Two Marine-Derived Fungi: Structures and Bioactivities

机译:来自两种海洋衍生真菌的四类结构异常肽:结构和生物活性

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The structures and biological properties of peptides produced by two genera of marine-derived fungi, an atypical Acremonium sp., and a Metarrhizium sp. were explored. The Acremonium strain was isolated from a marine sponge and has previously been shown by our group to produce peptides from the efrapeptin and RHM families. The isolation and structure elucidation of the new linear pentadecapeptides efrapeptins Eα (>1), H (>2) and N-methylated octapeptides RHM3 (>3) and RHM4 (>4) were carried out through a combination of 1D and 2D NMR techniques and tandem MS. Additional known efrapeptins E, F, G and the known syctalidamides A and B were also isolated. The absolute configurations of >1 – >4 are proposed to be the same as the original compound families. The marine-sponge derived Metarrhizium sp. was shown to produce destruxin cyclic depsipeptides including A, B, B2, desmethyl B, E chlorohydrin and E2 chlorohydrin. Efrapeptins Eα (>1), F and G each displayed IC50s of 1.3 nM against H125 cells, and destruxin E2 chlorohydrin displayed an IC50 of 160 nM against HCT-116 cells. An initial therapeutic assessment suggested a continuous (168 h) exposure of at least 2 ng/ml, or a daily (24 h) exposure of at least 300 ng/ml for H125 cells treated with efrapeptin G, and a continuous (168 h) exposure of at least 190 ng/ml for HCT-116 cells treated with destruxin E2 chlorohydrin, will cause 90% tumor cell death in vitro.
机译:由两个海洋衍生真菌,一个非典型的顶孢菌属和一个Metarrhizium菌产生的肽的结构和生物学特性。被探索了。 Acremonium菌株是从海洋海绵中分离出来的,我们的研究小组先前已证明该菌株可从efrapeptin和RHM家族生产肽。新型线性五肽七肽efrapeptinsEα(> 1 ),H(> 2 )和N-甲基化八肽RHM3(> 3 )的分离和结构解析和RHM4(> 4 )是通过1D和2D NMR技术以及串联MS进行的。还分离了另外的已知的rapepteptin E,F,G以及已知的syctalidamides A和B。建议> 1 – > 4 的绝对配置与原始化合物家族相同。海洋海绵衍生的Metarrhizium sp。显示出可产生destruxin环状二肽肽,包括A,B,B2,去甲基B,E氯醇和E2氯醇。 EfrapeptinsEα(> 1 ),F和G分别对H125细胞显示1.3 nM的IC50,destruxin E2氯代醇对HCT-116细胞显示IC50的160 nM。最初的治疗评估表明,连续(168 h)暴露于至少2 ng / ml,或每天(24 h)暴露于至少300 ng / ml,用efrapeptin G处理过的H125细胞,以及连续(168 h)暴露于至少190 ng / ml的经destruxin E2氯醇处理的HCT-116细胞将在体外导致90%的肿瘤细胞死亡。

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