Production of Multiple Talaroenamines from Penicillium malacosphaerulum via One-Pot/Two-Stage Precursor-Directed Biosynthesis

• Published in: Journal of natural products (Washington, D.C.) Vol. 85; no. 9; pp. 2168 - 2176
• Main Authors: Zhang, Zhenzhen, He, Xueqian, Zhang, Xiaomin, Li, Dehai, Wu, Guangwei, Liu, Zhenzhen, Niu, Chao, Yang, Lanping, Song, Wenting, Li, Zhanlin, Wang, Zhenhui
• Format: Journal Article
• Language: English
• Published: WASHINGTON American Chemical Society and American Society of Pharmacognosy 23.09.2022; Amer Chemical Soc
• Subjects: Chemistry, Medicinal; Life Sciences & Biomedicine; Pharmacology & Pharmacy; Plant Sciences; Science & Technology; GENERATION; ASSAY; ANALOGS; DERIVATIVES
• ISSN: 0163-3864; 1520-6025
• DOI: 10.1021/acs.jnatprod.2c00394

Nineteen new talaroenamine derivatives, talaroenamines F1–F19 (1–19), were isolated from the Yellow River wetland derived Penicillium malacosphaerulum HPU-J01 by use of a one-pot/two-stage precursor-directed biosynthesis approach. During this approach, the initial precursor p-methylaniline was first used as a carrier to capture the biologically synthesized cyclohexanedione to produce talaroenamine F, and then the other aniline derivatives were employed to replace the p-methylaniline fragment of talaroenamine F to generate the final products. LC–MS analysis showed that only four compounds (2, 8, 10, and 12) could be produced by the traditional precursor-directed biosynthesis in which the aniline precursors were added simultaneously. Compound 14 was cytotoxic against the K562 cell line with an IC50 value of 2.2 μM. This work demonstrated the one-pot/two-stage precursor-directed biosynthesis could improve substrate acceptance leading to the production of diverse talaroenamines.