Department of Microbial Drugs, Helmholtz Centre for Infection Research and German Centre for Infection Research (DZIF), partner site Hannover/Braunschweig, Inhoffenstrasse 7, 38124 Braunschweig, Germany.
Department of Chemistry, Faculty of Science, University of Dschang, P.O. Box 67, Dschang, Cameroon.
Molecules. 2017 Oct 9;22(10):1674. doi: 10.3390/molecules22101674.
Extracts from an endophytic fungus isolated from the roots of the Algerian plant showed prominent antimicrobial activity in a screening for novel antibiotics. The producer organism was identified as by means of morphological studies and molecular phylogenetic methods. Studies on the secondary metabolite production of this strain in various culture media revealed that the major components from shake flasks were massarilactones D () and H () as well as two new furanone derivatives for which we propose the trivial names (5)--gregatin B () and graminin D (). Scale-up of the fermentation in a 10 L bioreactor yielded massarilactone D and several further metabolites. Among those were three new anthranilic acid derivatives (-), two known anthranilic acid analogues ( and ) and three cyclopeptides (-). Their structures were elucidated on the basis of extensive spectroscopic analysis (1D- and 2D-NMR), high-resolution mass spectrometry (HRESIMS), and the application of the modified Mosher's method. The isolated metabolites were tested for antimicrobial and cytotoxic activities against various bacteria, fungi, and two mammalian cell lines. The new Metabolite and Compound exhibited antimicrobial activity while Compound showed cytotoxicity activity against KB3.1 cells.
从阿尔及利亚植物根部分离出的内生真菌提取物在新型抗生素筛选中表现出显著的抗菌活性。通过形态学研究和分子系统发育方法,确定产生菌为。对该菌株在不同培养基中的次生代谢产物生产研究表明,摇瓶中的主要成分是 massarilactones D () 和 H () 以及两种新的呋喃酮衍生物,我们将其命名为(5)-gregatin B () 和 graminin D ()。在 10 L 生物反应器中放大发酵,得到了 massarilactone D 和其他几种代谢产物。其中包括三个新的邻氨基苯甲酸衍生物(-)、两个已知的邻氨基苯甲酸类似物(和)和三个环肽(-)。根据广泛的光谱分析(1D 和 2D-NMR)、高分辨率质谱(HRESIMS)以及改进的 Mosher 方法的应用,确定了它们的结构。分离得到的代谢产物对各种细菌、真菌和两种哺乳动物细胞系进行了抗菌和细胞毒性测试。新代谢物和化合物表现出抗菌活性,而化合物对 KB3.1 细胞表现出细胞毒性活性。