Isolation and characterization of three pairs of verrucosidin epimers from the marine sediment-derived fungus Penicillium cyclopium and configuration revision of penicyrone A and related analogues
Li, Yan-He1,2,3; Mandi, Attila4; Li, Hong-Lei2,3,5; Li, Xiao-Ming2,3,5; Li, Xin2,3,5; Meng, Ling-Hong2,3,5; Yang, Sui-Qun2,3,5; Shi, Xiao-Shan2,3,5; Kurtan, Tibor4; Wang, Bin-Gui1,2,3,5
刊名MARINE LIFE SCIENCE & TECHNOLOGY
2023-05-28
页码9
关键词Marine-derived fungus Penicillium cyclopium Verrucosidin derivatives TDDFT-ECD calculations Mosher's method Antimicrobial activity
ISSN号2096-6490
DOI10.1007/s42995-023-00173-2
通讯作者Kurtan, Tibor(kurtan.tibor@science.unideb.hu) ; Wang, Bin-Gui(wangbg@ms.qdio.ac.cn)
英文摘要Verrucosidins, a methylated alpha-pyrone class of polyketides rarely reported upon, have been implicated in one or more neurological diseases. Despite the significance of verrucosidins as neurotoxins, the absolute configurations of most of the derivatives have not been accurately characterized yet. In this study, three pairs of C-9 epimeric verrucosidin derivatives, including the known compounds penicyrones A and B (1a/1b) and 9-O-methylpenicyrones A and B (2a/2b), the new compounds 9-O-ethylpenicyrones A and B (3a/3b), together with the related known derivative verrucosidin (4), were isolated and identified from the culture extract of Penicillium cyclopium SD-413, which was obtained from the marine sediment collected from the East China sea. Their structures were established based on an in-depth analysis of nuclear magnetic resonances (NMR) and mass spectroscopic data. Determination of the absolute configurations of these compounds was accomplished by Mosher's method and time-dependent density functional theory (TDDFT) calculations of electronic circular dichroism (ECD) and optical rotation (OR). The configurational assignment of penicyrone A demonstrated that the previously reported C-6 absolute configuration of verrucosidin derivatives needs to be revised from (6S) to (6R). The 9R/9S epimers of compounds 1-3 were found to exhibit growth inhibition against some pathogenic bacteria, indicating that they have potential as lead compounds for the creation of antimicrobial agents.
资助项目National Natural Science Foundation of China[U2006203] ; National Major Science and Technology Infrastructure from the Chinese Academy of Sciences ; National Research, Development, and Innovation Office[FK134653] ; National Research, Development, and Innovation Office[KEXUE2020GZ02] ; Governmental Information-Technology Development Agency (KIFUE) ; Senior User Project of RV KEXUE ; [K138672]
WOS关键词DERIVATIVES ; ECD
WOS研究方向Marine & Freshwater Biology
语种英语
出版者SPRINGERNATURE
WOS记录号WOS:000995924400001
内容类型期刊论文
源URL[http://ir.qdio.ac.cn/handle/337002/183168]  
专题海洋研究所_实验海洋生物学重点实验室
通讯作者Kurtan, Tibor; Wang, Bin-Gui
作者单位1.Univ Chinese Acad Sci, Sch Marine Sci, Beijing 100049, Peoples R China
2.Qingdao Natl Lab Marine Sci & Technol, Lab Marine Biol & Biotechnol, Qingdao 266071, Peoples R China
3.Chinese Acad Sci, Inst Oceanol, CAS & Shandong Prov Key Lab Expt Marine Biol, Qingdao 266071, Peoples R China
4.Univ Debrecen, Dept Organ Chem, Egyet Ter 1, H-4032 Debrecen, Hungary
5.Chinese Acad Sci, Ctr Ocean Mega Sci, Qingdao 266071, Peoples R China
推荐引用方式
GB/T 7714
Li, Yan-He,Mandi, Attila,Li, Hong-Lei,et al. Isolation and characterization of three pairs of verrucosidin epimers from the marine sediment-derived fungus Penicillium cyclopium and configuration revision of penicyrone A and related analogues[J]. MARINE LIFE SCIENCE & TECHNOLOGY,2023:9.
APA Li, Yan-He.,Mandi, Attila.,Li, Hong-Lei.,Li, Xiao-Ming.,Li, Xin.,...&Wang, Bin-Gui.(2023).Isolation and characterization of three pairs of verrucosidin epimers from the marine sediment-derived fungus Penicillium cyclopium and configuration revision of penicyrone A and related analogues.MARINE LIFE SCIENCE & TECHNOLOGY,9.
MLA Li, Yan-He,et al."Isolation and characterization of three pairs of verrucosidin epimers from the marine sediment-derived fungus Penicillium cyclopium and configuration revision of penicyrone A and related analogues".MARINE LIFE SCIENCE & TECHNOLOGY (2023):9.
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