| Literature DB >> 31576747 |
Christopher B Eiben1, Tristan de Rond2, Clayton Bloszies3, Jennifer Gin4,5,6, Jennifer Chiniquy4,5,6, Edward E K Baidoo4,5,6, Christopher J Petzold4,5,6, Nathan J Hillson4,5,6, Oliver Fiehn3, Jay D Keasling4,5,7,8.
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 E. coli 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 13C 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.Entities:
Keywords: HDMAPP; HIPP; homodimethylallyl pyrophosphate; homoisopentenyl pyrophosphate; juvenile hormones; mevalonate pathway; terpenes
Mesh:
Substances:
Year: 2019 PMID: 31576747 DOI: 10.1021/acssynbio.9b00230
Source DB: PubMed Journal: ACS Synth Biol ISSN: 2161-5063 Impact factor: 5.110