Structural insight on assembly-line catalysis in terpene biosynthesis

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作者
Jacque L. Faylo
Trevor van Eeuwen
Hee Jong Kim
Jose J. Gorbea Colón
Benjamin A. Garcia
Kenji Murakami
David W. Christianson
机构
[1] Roy and Diana Vagelos Laboratories,Department of Biochemistry and Biophysics, Perelman School of Medicine
[2] Department of Chemistry,Biochemistry and Molecular Biophysics Graduate Group, Perelman School of Medicine
[3] University of Pennsylvania,undefined
[4] University of Pennsylvania,undefined
[5] University of Pennsylvania,undefined
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Nature Communications | / 12卷
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摘要
Fusicoccadiene synthase from Phomopsis amygdali (PaFS) is a unique bifunctional terpenoid synthase that catalyzes the first two steps in the biosynthesis of the diterpene glycoside Fusicoccin A, a mediator of 14-3-3 protein interactions. The prenyltransferase domain of PaFS generates geranylgeranyl diphosphate, which the cyclase domain then utilizes to generate fusicoccadiene, the tricyclic hydrocarbon skeleton of Fusicoccin A. Here, we use cryo-electron microscopy to show that the structure of full-length PaFS consists of a central octameric core of prenyltransferase domains, with the eight cyclase domains radiating outward via flexible linker segments in variable splayed-out positions. Cryo-electron microscopy and chemical crosslinking experiments additionally show that compact conformations can be achieved in which cyclase domains are more closely associated with the prenyltransferase core. This structural analysis provides a framework for understanding substrate channeling, since most of the geranylgeranyl diphosphate generated by the prenyltransferase domains remains on the enzyme for cyclization to form fusicoccadiene.
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