Center for Marine Science, Department of Chemistry and Biochemistry, University of North Carolina Wilmington , 5600 Marvin K. Moss Lane, Wilmington, North Carolina 28409, United States.
J Nat Prod. 2018 Feb 23;81(2):349-355. doi: 10.1021/acs.jnatprod.7b00829. Epub 2018 Feb 6.
We report a mass-spectrometry-based metabolomics study of a laboratory-cultured strain of Microcystis aeruginosa (UTEX LB2385), which has led to the discovery of five peptides (1-5) belonging to the microginin class of linear cyanopeptides. The structures and configurations of these peptides were determined by spectroscopic analyses and chemical derivitization. The microginin peptides described herein are the first reported derivatives containing N-methyl methionine (1, 5) and N-methyl methionine sulfoxide (2-4). The two tripeptide microginin analogues (4, 5) identified represent the smallest members of this peptide family. Their angiotensin-converting enzyme (ACE) inhibitory activity was also investigated. Microginin 527 (4) was the most potent of the group, with an IC of 31 μM.
我们报告了一项基于质谱的蓝藻(UTEX LB2385)培养菌株的代谢组学研究,该研究发现了五个属于微囊藻素线性蓝藻肽类的肽(1-5)。这些肽的结构和构型通过光谱分析和化学衍生化确定。本文报道的微囊藻素肽是第一个报道的含有 N-甲基蛋氨酸(1、5)和 N-甲基蛋氨酸亚砜(2-4)的衍生物。鉴定出的两种三肽微囊藻素类似物(4、5)代表了该肽家族中最小的成员。还研究了它们的血管紧张素转化酶(ACE)抑制活性。微囊藻素 527(4)是该组中最有效的,IC 为 31 μM。