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Annular oxygenation and rearrangement products of cryptotanshinone by biotransformation with marine-derived fungi Cochliobolus lunatus and Aspergillus terreus.

Authors :
Wu, Jing-Shuai
Meng, Qin-Yu
Zhang, Ya-Hui
Shi, Xiao-Hui
Fu, Xiu-Mei
Zhang, Peng
Li, Xin
Shao, Chang-Lun
Wang, Chang-Yun
Source :
Bioorganic Chemistry. Oct2020, Vol. 103, pN.PAG-N.PAG. 1p.
Publication Year :
2020

Abstract

• Cryptotanshinone was transformed by two marine fungi to provide seven new products. • The products exhibited anti-neuroinflammatory and antibacterial activities. • These results revealed the potential of marine fungi to transform natural products. Structural modification of natural products by biotransformation with fungi is an attractive tool to obtain novel bioactive derivatives. In the present study, cryptotanshinone (1), a quinoid abietane diterpene from traditional Chinese medicine Salvia miltiorrhiza (Danshen), was transformed by two marine-derived fungi. By using Cochliobolus lunatus TA26-46, one new oxygenated and rearranged product (2), containing a 5,6-dihydropyrano[4,3- b chromene moiety, together with one known metabolite (10), were obtained from the converted broth of cryptotanshinone (1) with the isolated yields of 1.0% and 2.1%, respectively. While, under the action of Aspergillus terreus RA2905, seven new transformation products (3 – 9) as well as 10 with the fragments of 2-methylpropan-1-ol and oxygenated p -benzoquinone were produced and obtained with the isolated yields of 0.1%–1.3%. The structures of the new compounds were elucidated by comprehensive spectroscopic analysis including High Resolution Electrospray Ionization Mass Spectroscopy (HRESIMS), Nuclear Magnetic Resonance (NMR) and Electronic Circular Dichroism (ECD). The metabolic pathways of cryptotanshinone by these two fungi were presumed to be the opening and rearrangement of furan ring, and/or oxygenation of cyclohexane ring. Cryptotanshinone (1) and its metabolites displayed anti-inflammatory activities against NO production in LPS-stimulated BV-2 cells and antibacterial activities towards methicillin-resistant Staphylococcus aureus. These findings revealed the potential of marine fungi to transform the structures of natural products by biotransformation. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
00452068
Volume :
103
Database :
Academic Search Index
Journal :
Bioorganic Chemistry
Publication Type :
Academic Journal
Accession number :
145939932
Full Text :
https://doi.org/10.1016/j.bioorg.2020.104192