1.Filamentous fungal sesterterpenoids and their synthases.
Chinese Journal of Biotechnology 2016;32(12):1631-1641
Although the number of sesterterpenoids is fewer than other terpenoids reported, they have presented a wide range of biological activities and medicinal value. Reported filamentous fungal sesterterpene synthases are special on bifunctional two catalytically independent domains: prenyltransferase and terpene cyclase, but less specific on substrates selection and diverse ways of cyclization. This article reviews the research advances in filamentous fungal sesterterpenoids and their synthases, especially describes filamentous fungal sesterterpenoids and the structure and function characteristics of sesterterpene synthase.
Cyclization
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Fungi
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chemistry
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enzymology
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Sesterterpenes
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chemistry
2.Two new sesquiterpenoids from basidiomycete Tyromyces chioneus.
Hua GUO ; Tao FENG ; Zheng-Hui LI ; Ji-Kai LIU
Acta Pharmaceutica Sinica 2014;49(11):1578-1581
Two new sesquiterpenoids, named as tyromols A and B (1 and 2), were isolated from cultures of basidiomycete Tyromyces chioneus, along with two previously reported 15-hydroxy-6 α, 12-epoxy-7β, 10αH, 11βH-spiroax-4-ene (3) and agripilol C (4). Compounds 1-4 were separated and purified by silica gel, RP-18, Sephadex LH-20 column chromatography. Their structures were elucidated on the basis of extensive spectroscopic analysis including IR, MS, 1D and 2D NMR experiments.
Basidiomycota
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chemistry
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Magnetic Resonance Spectroscopy
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Sesquiterpenes
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chemistry
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isolation & purification
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Sesterterpenes
3.3-Anhydro-6-hydroxy-ophiobolin A displays high in vitro and in vivo efficacy against influenza A virus infection.
Song WANG ; Xiaoqin LUO ; Ruoxiang YAN ; Quanxin WANG ; Qiuyue QI ; Xiaojuan CHI ; Lanlan ZHANG ; Ziding YU ; Binxiang CAI ; Ji-Long CHEN ; Hongwei LIU
Protein & Cell 2016;7(11):839-843