Natural Products Research Institute, College of Pharmacy, Seoul National University, 1 Gwanak-ro, Gwanak-gu, Seoul 08826, Republic of Korea.
Department of Pharmacy, Yonsei Institute of Pharmaceutical Sciences, and Department of Integrative Biotechnology and Translational Medicine, Yonsei University, 85 Songdogwahak-ro, Yeonsu-gu, Incheon 21983, Republic of Korea.
J Org Chem. 2021 Aug 20;86(16):11149-11159. doi: 10.1021/acs.joc.1c00360. Epub 2021 May 12.
Two new nonribosomal peptides, bonnevillamides D and E ( and ), have been discovered in sp. UTZ13 isolated from the carrion beetle, . Combinational analysis of the UV, MS, and NMR spectroscopic data revealed that their planar structures were comprised of dichlorinated linear peptides containing nonproteinogenic amino acid residues, such as 4-methylazetidinecarboxylic acid and 4--acetyl-5-methylproline. The configurations of bonnevillamides D and E ( and ) were determined based on ROESY correlations, the advanced Marfey's method, phenylglycine methyl ester derivatization, molecular modeling, and circular dichroism spectroscopy. The nonribosomal peptide synthetase biosynthetic pathway of bonnevillamides D and E has been proposed using bioinformatic analysis of the whole-genome sequence data of sp. UTZ13. Their biological activity toward the aggregation of amyloid-β, which is one of the key pathogenic proteins in Alzheimer's disease, was evaluated using a thioflavin T assay and gel electrophoresis. Bonnevillamides D and E reversed the fibril formation by inducing the monomerization of amyloid-β aggregates.
从腐肉甲虫中分离到的 sp. UTZ13 产生了两种新的非核糖体肽,bonnevillamides D 和 E(1 和 2)。综合分析紫外、质谱和核磁共振谱数据表明,它们的平面结构由含有非蛋白氨基酸残基的二氯线性肽组成,如 4-甲基氮杂环丁烷羧酸和 4--乙酰基-5-甲基脯氨酸。bonnevillamides D 和 E(1 和 2)的构型是基于 ROESY 相关、高级 Marfey 法、苯甘氨酸甲酯衍生化、分子建模和圆二色性光谱确定的。通过对 sp. UTZ13 全基因组序列数据的生物信息学分析,提出了 bonnevillamides D 和 E 的非核糖体肽合成途径。使用硫代黄素 T 测定法和凝胶电泳评估了它们对淀粉样蛋白-β聚集的生物活性,淀粉样蛋白-β是阿尔茨海默病的关键致病蛋白之一。bonnevillamides D 和 E 通过诱导淀粉样蛋白-β 聚集物的单体化来逆转纤维形成。