Wang Xue, Gao Yang-Le, Zhang Ming-Liang, Zhang Huai-Dong, Huang Jian-Zhong, Li Li
Engineering Research Center of Industrial Microbiology, College of Life Sciences, Fujian Normal University, Fuzhou 350117, China.
Engineering Research Center of Industrial Microbiology, College of Life Sciences, Fujian Normal University, Fuzhou 350117, China; State Key Laboratory of Bioactive Substance and Function of Natural Medicines, Institute of Materia Medica, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing 100050, China.
J Biotechnol. 2020 Feb 10;309:85-91. doi: 10.1016/j.jbiotec.2020.01.002. Epub 2020 Jan 8.
Ascomycete fungi Cordyceps are widely used in traditional Chinese medicine, and numerous investigations have been carried out to uncover their biological activities. However, primary researches on the physiological effects of Cordyceps were committed using crude extracts. At present, there are only a few compounds which were comprehensively characterized from Cordyceps, partial owing to the low production. In order to scientifically take advantage of Cordyceps, we used the strategy of genome mining to discover bioactive compounds from Cordyceps militaris. We found the putative biosynthetic gene cluster of the acyl-CoA:cholesterol acyltransferase inhibitor beauveriolides in the genome of C. militaris, and produced the compounds by heterologous expression in Aspergillus nidulans. Production of beauveriolide I and III also was detected in both ferment mycelia and fruiting bodies of C. militaris. The possible biosynthetic pathway was proposed. Our studies unveil the active compounds of C. militaris against atherosclerosis and Alzheimer's disease and provide the enzyme resources for the biosynthesis of new cyclodepsipeptide molecules.
子囊菌纲真菌虫草在传统中药中广泛应用,人们已开展大量研究以揭示其生物活性。然而,对虫草生理效应的初步研究使用的是粗提物。目前,从虫草中全面鉴定出的化合物仅有少数几种,部分原因是产量较低。为科学利用虫草,我们采用基因组挖掘策略从蛹虫草中发现生物活性化合物。我们在蛹虫草基因组中发现了酰基辅酶A:胆固醇酰基转移酶抑制剂白僵菌素的推定生物合成基因簇,并通过在构巢曲霉中的异源表达产生了这些化合物。在蛹虫草的发酵菌丝体和子实体中也检测到了白僵菌素I和III的产生。提出了可能的生物合成途径。我们的研究揭示了蛹虫草中对抗动脉粥样硬化和阿尔茨海默病的活性化合物,并为新环缩肽分子的生物合成提供了酶资源。