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甲羟戊酸途径的多效性促成非经典萜类化合物的产生。

Mevalonate Pathway Promiscuity Enables Noncanonical Terpene Production.

作者信息

Eiben Christopher B, de Rond Tristan, Bloszies Clayton, Gin Jennifer, Chiniquy Jennifer, Baidoo Edward E K, Petzold Christopher J, Hillson Nathan J, Fiehn Oliver, Keasling Jay D

机构信息

Department of Bioengineering , University of California , San Francisco , California 94143 , United States.

Center for Marine Biotechnology and Biomedicine, Scripps Institution of Oceanography , University of California San Diego , La Jolla , California 92093 , United States.

出版信息

ACS Synth Biol. 2019 Oct 18;8(10):2238-2247. doi: 10.1021/acssynbio.9b00230. Epub 2019 Oct 2.

Abstract

Lepidoptera (butterflies and moths) make the six-carbon compounds homoisopentenyl pyrophosphate (HIPP) and homodimethylallyl pyrophosphate (HDMAPP) that are incorporated into 16, 17, and 18 carbon farnesyl pyrophosphate (FPP) analogues. In this work we heterologously expressed the lepidopteran modified mevalonate pathway, a propionyl-CoA ligase, and terpene cyclases in to produce several novel terpenes containing 16 carbons. Changing the terpene cyclase generated different novel terpene product profiles. To further validate the new compounds we confirmed C propionate was incorporated, and that the masses and fragmentation patterns were consistent with novel 16 carbon terpenes by GC-QTOF. On the basis of the available farnesyl pyrophosphate analogues lepidoptera produce, this approach should greatly expand the reachable biochemical space with applications in areas where terpenes have traditionally found uses.

摘要

鳞翅目昆虫(蝴蝶和飞蛾)能合成六碳化合物高异戊烯基焦磷酸(HIPP)和高二甲烯丙基焦磷酸(HDMAPP),这些化合物会被整合到含有16、17和18个碳原子的法呢基焦磷酸(FPP)类似物中。在这项研究中,我们在[具体内容缺失]中异源表达了鳞翅目昆虫修饰的甲羟戊酸途径、一种丙酰辅酶A连接酶和萜烯环化酶,以生产几种含16个碳原子的新型萜类化合物。改变萜烯环化酶会产生不同的新型萜类产物谱。为了进一步验证这些新化合物,我们证实了丙酸盐被整合进去,并且通过气相色谱-四极杆飞行时间质谱(GC-QTOF)确定其质量和碎片模式与新型16碳萜类化合物一致。基于鳞翅目昆虫产生的现有法呢基焦磷酸类似物,这种方法应能极大地扩展可触及的生化空间,并应用于萜类化合物传统上有应用的领域。

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