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基于基因组的藤黄属植物中呫吨酮类化合物II型聚酮合酶生物合成途径及其抗真菌活性分析。

Genome-based analysis of the type II PKS biosynthesis pathway of xanthones in and their antifungal activity.

作者信息

Liu Ling-Li, Liu Hong-Fei, Gao Hua-Hua, Yang Zheng-Zhong, Feng Xiao-Lan, Gao Jin-Ming, Zhao Jian-Bang

机构信息

Shaanxi Key Laboratory of Natural Products & Chemical Biology, College of Chemistry & Pharmacy, Northwest A&F University Yangling 712100 Shaanxi People's Republic of China

College of Information Engineering, Northwest A&F University Yangling 712100 Shaanxi People's Republic of China

出版信息

RSC Adv. 2019 Nov 15;9(64):37376-37383. doi: 10.1039/c9ra07345k. eCollection 2019 Nov 13.

Abstract

The ethyl acetate extract from the liquid fermentation of Aw99c exhibited high and broad antifungal activities against plant pathogenic fungi. Bioassay guide fractionation led to the discovery of two xanthones, citreamicin ε and θ. The draft genome sequence of Aw99c was analyzed by a similarity-based approach to elucidate the pathway for the citreamicins. A 48 kb citreamicin () gene cluster with 51 open reading frames encoding type II polyketide synthases and unique polyketide tailoring enzymes was proposed based on the genome analysis and the chemical structure derivation. antifungal assay showed that citreamicin ε exhibited significant growth inhibition against the plant pathogenic fungi with MIC values ranging from 1.56 to 12.5 μM. The cellular structural change of treated with citreamicin ε was detected by SEM and the result showed that citreamicin ε caused disruptive surface of the mycelia.

摘要

Aw99c液体发酵的乙酸乙酯提取物对植物病原真菌表现出高效且广泛的抗真菌活性。生物测定导向的分级分离导致发现了两种呫吨酮,即柠檬霉素ε和θ。通过基于相似性的方法分析了Aw99c的基因组草图序列,以阐明柠檬霉素的合成途径。基于基因组分析和化学结构推导,提出了一个48 kb的柠檬霉素()基因簇,其具有51个编码II型聚酮合酶和独特聚酮修饰酶的开放阅读框。抗真菌试验表明,柠檬霉素ε对植物病原真菌表现出显著的生长抑制作用,MIC值范围为1.56至12.5 μM。通过扫描电子显微镜检测了用柠檬霉素ε处理后的细胞结构变化,结果表明柠檬霉素ε导致菌丝体表面破坏。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4a7b/9075769/43f7d1c979e4/c9ra07345k-f1.jpg

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