Microbial Production of γ-Curcumene in Metabolically Engineered Escherichia coli Using a Novel γ-Curcumene Synthase from Parthenium argentatum
Discuss this preprint
Start a discussion What are Sciety discussions?Listed in
This article is not in any list yet, why not save it to one of your lists.Abstract
Background Terpenoids are attractive targets for sustainable biomanufacturing because of their structural diversity and potential applications in fuels and high-value chemicals. Among sesquiterpenes, γ-curcumene is a promising yet underexplored molecule, and its efficient microbial production has not been established. In this study, we identified a previously uncharacterized γ-curcumene synthase from Parthenium argentatum (PaCS) and evaluated its use for microbial γ-curcumene production in metabolically engineered Escherichia coli . Results Sequence analysis revealed that PaCS is phylogenetically distinct from the previously reported γ-curcumene synthase from Pogostemon cablin . When expressed in an E. coli strain carrying a heterologous mevalonate pathway, PaCS predominantly produced γ-curcumene, with only minor formation of (−)-α-bisabolol. Product identity was confirmed by GC–MS and NMR analyses. Biochemical characterization of recombinant PaCS showed maximal activity at 35°C and pH 8.5, with Mg²⁺ as the preferred divalent metal ion. For microbial production, culture conditions and host background were evaluated, and the evolved strain SBA01 showed the best performance. In fed-batch fermentation, the engineered strain produced up to 1.1 g/L γ-curcumene in terrific broth and 1.03 g/L in modified R medium. In addition, purified γ-curcumene was chemically hydrogenated to bisabolane and dihydro-ar-curcumene, demonstrating its utility as a precursor for fuel-related sesquiterpene hydrocarbons. Conclusions This study establishes a microbial production platform for γ-curcumene using a novel γ-curcumene synthase from P. argentatum and metabolically engineered E. coli . The results expand the available terpene synthase toolbox and provide a foundation for the biosynthesis and downstream upgrading of γ-curcumene-derived molecules. These findings support the broader use of synthetic biology and metabolic engineering for the production of non-native sesquiterpenes from renewable carbon sources.