Institute of Marine Drugs, School of Pharmaceutical Sciences, Guangxi Key Laboratory of Efficacy Study on Chinese Materia Medica, Guangxi University of Chinese Medicine, NO. 13 Wuhe Rood, Nanning 530200, China.
J Agric Food Chem. 2021 Apr 21;69(15):4392-4401. doi: 10.1021/acs.jafc.0c07415. Epub 2021 Apr 9.
Sugarcane smut, caused by , is one of the most devastating fungal diseases affecting sugarcane worldwide. To develop a potent sugarcane smut fungicide, secondary metabolites of marine-derived were isolated and screened for inhibitory activities, which led to the discovery of five new 24-membered macrolactins, bamemacrolactins A-E (-), with being the most potent inhibitor. The antifungal mechanism of was studied by assessing its effects on mycelial morphology and the cell wall. Differential proteomics were used to analyze proteins in upon treatment with bamemacrolactin C and to elucidate its antifungal mechanism. A total of 533 differentially expressed proteins were found. After the Gene Ontology and Kyoto Encyclopedia of Genes and Genomes pathway analyses, eight target proteins were selected, and their functions were discussed. Six of the eight proteins were reported as antifungal targets. The target proteins are involved in the oxidative phosphorylation pathway. Therefore, the potent inhibition of by compound is most likely through oxidative phosphorylation and targeting a series of enzymes.
甘蔗黑粉病由 引起,是全球范围内影响甘蔗的最具破坏性的真菌病害之一。为了开发有效的甘蔗黑粉病杀菌剂,从海洋来源的 中分离并筛选了次生代谢产物,以评估其抑制活性,从而发现了五个新的 24 元大环内酯,bamemacrolactins A-E (-),其中 是最有效的抑制剂。通过评估对菌丝形态和细胞壁的影响来研究 对 的抗真菌机制。通过差异蛋白质组学分析 处理 bamemacrolactin C 后的蛋白质,以阐明其抗真菌机制。共发现 533 个差异表达蛋白。经过基因本体论和京都基因与基因组百科全书途径分析,选择了 8 个目标蛋白,并讨论了它们的功能。这 8 个目标蛋白中有 6 个被报道为抗真菌靶标。靶蛋白参与氧化磷酸化途径。因此,化合物 对 的强烈抑制作用很可能是通过氧化磷酸化和针对一系列酶起作用的。