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甲基移位法呢基二磷酸衍生物是倍半萜环化酶的底物。

Methyl-Shifted Farnesyldiphosphate Derivatives Are Substrates for Sesquiterpene Cyclases.

机构信息

Institute of Organic Chemistry and Center of Biomolecular Drug Research (BMWZ), Leibniz Universität Hannover, Schneiderberg 1B, 30167 Hannover, Germany.

Symrise AG, Mühlenfeldstraße 1, 37603 Holzminden, Germany.

出版信息

Org Lett. 2020 Jun 5;22(11):4360-4365. doi: 10.1021/acs.orglett.0c01345. Epub 2020 May 20.

Abstract

New sesquiterpene backbones are accessible after biotransformation of presilphiperfolan-8β-ol synthase (BcBOT2), a fungal sesquiterpene synthase, with non-natural farnesyldiphosphates in which methyl groups are shifted by one position toward the diphosphate terminus. One of the macrocycles formed, a new germacrene A derivative, undergoes a Cope rearrangement to iso-β-elemene. Three of the new terpenoids show olfactoric properties that range from an intense peppery note to a citrus, ozone-like, and fruity scent.

摘要

经过真菌倍半萜合酶 BcBOT2(presilphiperfolan-8β-ol synthase)的生物转化,用非天然法呢基二磷酸(farnesyldiphosphates)作为前体,其中甲基向二磷酸末端移动一位,形成了新的倍半萜骨架。形成的大环之一,一种新的吉玛烷 A 衍生物,经历了 Cope 重排,生成异-β-榄香烯。三种新的萜类化合物具有从强烈的胡椒味到柑橘、臭氧和果香的气味特性。

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