Activation of a Silent Gene Cluster from the Endophytic Fungus Talaromyces sp. Unearths Cryptic Azaphilone Metabolites.

IF 5.7 1区 农林科学 Q1 AGRICULTURE, MULTIDISCIPLINARY Journal of Agricultural and Food Chemistry Pub Date : 2024-07-04 DOI:10.1021/acs.jafc.4c03162
Xiaoling Huang, Dan Li, Bi Long, Haidi Li, Jing Li, Wenxuan Wang, Kangping Xu, Xia Yu
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Abstract

Fungal azaphilones have attracted widespread attention due to their significant potential as sources of food pigments and pharmaceuticals. Genome mining and gene cluster activation represent powerful tools and strategies for discovering novel natural products and bioactive molecules. Here, a putative azaphilone biosynthetic gene cluster lut from the endophytic fungus Talaromyces sp. was identified through genome mining. By overexpressing the pathway-specific transcription factor LutB, five new sclerotiorin-type azaphilones (1, 6, 8, and 10-11) together with seven known analogues (2-5, 7, 9, 12) were successfully produced. Compounds 8 and 9 exhibited antibacterial activity against Bacillus subtilis with MIC values of 64 and 16 μg/mL, respectively. Compound 11 showed cytotoxic activity against HCT116 and GES-1 with IC50 values of 10.9 and 4.9 μM, respectively, while 1, 4, 5, and 7-10 showed no obvious cytotoxic activity. Gene inactivation experiments confirmed the role of the lut cluster in the production of compounds 1-12. Subsequent feeding experiments unveiled the novel functional diversity of the dual megasynthase system. Furthermore, a LutC-LutD binary oxidoreductase system was discovered, and in combination with DFT calculations, the basic biosynthetic pathway of the sclerotiorin-type azaphilones was characterized. This study provided a good example for the discovery of new azaphilones and further uncovered the biosynthesis of these compounds.

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激活内生真菌 Talaromyces sp.的沉默基因簇,发现隐蔽的萘甲西隆代谢物。
真菌萘酮类化合物作为食品色素和药物来源的巨大潜力引起了广泛关注。基因组挖掘和基因簇激活是发现新型天然产品和生物活性分子的有力工具和策略。本文通过基因组挖掘,从内生真菌 Talaromyces sp.中发现了一个推测的萘甲酮生物合成基因簇 lut。通过过表达途径特异性转录因子 LutB,成功地生产出了五种新的硬化剂型萘酮(1、6、8 和 10-11)以及七种已知的类似物(2-5、7、9、12)。化合物 8 和 9 对枯草杆菌具有抗菌活性,其 MIC 值分别为 64 和 16 μg/mL。化合物 11 对 HCT116 和 GES-1 具有细胞毒性活性,IC50 值分别为 10.9 和 4.9 μM,而 1、4、5 和 7-10 没有明显的细胞毒性活性。基因失活实验证实了 lut 簇在产生 1-12 号化合物中的作用。随后的喂养实验揭示了双巨合成酶系统新的功能多样性。此外,还发现了 LutC-LutD 双氧化还原酶系统,并结合 DFT 计算,确定了硬化剂型唑类化合物的基本生物合成途径。该研究为发现新的唑萘酮提供了一个很好的范例,并进一步揭示了这些化合物的生物合成过程。
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来源期刊
Journal of Agricultural and Food Chemistry
Journal of Agricultural and Food Chemistry 农林科学-农业综合
CiteScore
9.90
自引率
8.20%
发文量
1375
审稿时长
2.3 months
期刊介绍: The Journal of Agricultural and Food Chemistry publishes high-quality, cutting edge original research representing complete studies and research advances dealing with the chemistry and biochemistry of agriculture and food. The Journal also encourages papers with chemistry and/or biochemistry as a major component combined with biological/sensory/nutritional/toxicological evaluation related to agriculture and/or food.
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