GEOMAR Helmholtz Centre for Ocean Research Kiel, RD3 Marine Microbiology, Düsternbrooker Weg 20, 24105 Kiel, Germany.
Department of Pharmacognosy, Faculty of Pharmacy, Minia University, Minia 61519, Egypt.
Bioorg Med Chem Lett. 2018 Feb 15;28(4):558-561. doi: 10.1016/j.bmcl.2018.01.062. Epub 2018 Feb 1.
A new cyclic hexapeptide, cyclo-(Gly-Leu-Val-IIe-Ala-Phe), named bacicyclin (1), was isolated from a marine Bacillus sp. strain associated with Mytilus edulis. The sequences of the amino acid building blocks of the cyclic peptide and its structure were determined by 1D- and 2D-NMR techniques. Marfey's analysis showed that the amino acid building blocks had L-configuration in all cases except for alanine and phenylalanine, which had D-configuration. Bacicyclin (1) exhibited antibacterial activity against the clinically relevant strains Enterococcus faecalis and Staphylococcus aureus with minimal inhibitory concentration values of 8 and 12 µM, respectively. These results demonstrate the potential of marine bacteria as a promising source for the discovery of new antibiotics.
一种新的环状六肽,环-(甘氨酸-亮氨酸-缬氨酸-异亮氨酸-丙氨酸-苯丙氨酸),命名为bacicyclin(1),从一种与贻贝相关的海洋芽孢杆菌菌株中分离得到。通过 1D 和 2D-NMR 技术确定了环状肽及其结构的氨基酸构建块的序列。Marfey 分析表明,除了丙氨酸和苯丙氨酸外,所有氨基酸构建块均具有 L-构型,而丙氨酸和苯丙氨酸则具有 D-构型。 Bacicyclin(1)对临床相关菌株粪肠球菌和金黄色葡萄球菌表现出抗菌活性,最小抑菌浓度值分别为 8 和 12 µM。这些结果表明海洋细菌作为发现新抗生素的有前途的来源具有潜力。