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在伊丽莎白拟软柳珊瑚的共生双鞭毛虫共生藻Symbiodinium sp.中伪opterosin的生物合成。

Pseudopterosin biosynthesis in Symbiodinium sp., the dinoflagellate symbiont of Pseudopterogorgia elisabethae.

作者信息

Mydlarz Laura D, Jacobs Robert S, Boehnlein Jennifer, Kerr Russell G

机构信息

Interdepartmental Graduate Program in Marine Science, University of California, Santa Barbara, Santa Barbara, CA 93106, USA.

出版信息

Chem Biol. 2003 Nov;10(11):1051-6. doi: 10.1016/j.chembiol.2003.10.012.

Abstract

Investigations are reported that identify the biosynthetic source and origins of the pseudopterosins, pharmacologically important diterpene glycosides, in the gorgonian coral Pseudopterogorgia elisabethae. We report here the isolation of physiologically significant levels of endogenous pseudopterosins A, B, C, and D from purified symbionts identified as the dinoflagellate Symbiodinium sp. Biosynthetic studies in photosynthesizing symbiont isolates utilizing 14C-labeled inorganic carbon and the tritiated intermediate geranylgeranyl diphosphate yielded radiochemically pure pseudopterosins A through D and the first committed intermediate, elisabethatriene. The 14CO(2) uptake into the pseudopterosin pathway occurred at low levels compared to the 14CO(2) uptake into total lipids, suggesting a large reserve pool of the compounds. These results reveal for the first time that pseudopterosin biosynthesis is occurring within the algal symbiont and suggests the physiological implications of this biosynthesis.

摘要

据报道,已有研究确定了柳珊瑚Pseudopterogorgia elisabethae中具有重要药理活性的二萜糖苷类化合物——拟翼珊瑚素的生物合成来源和起源。我们在此报告,从被鉴定为共生甲藻Symbiodinium sp.的纯化共生体中分离出了具有生理意义水平的内源性拟翼珊瑚素A、B、C和D。利用14C标记的无机碳和氚化中间体香叶基香叶基二磷酸对光合共生体分离物进行的生物合成研究,产生了放射化学纯的拟翼珊瑚素A至D以及第一个关键中间体elisabethatriene。与14CO(2)进入总脂质的摄取量相比,14CO(2)进入拟翼珊瑚素途径的摄取量较低,这表明这些化合物存在大量储备库。这些结果首次揭示了拟翼珊瑚素的生物合成发生在藻类共生体内,并提示了这种生物合成的生理意义。

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