Abstract

BackgroundGeraniol is an acyclic monoterpene alcohol, which exhibits good prospect as a gasoline alternative. Geraniol is naturally encountered in plants at low concentrations and an attractive target for microbial engineering. Geraniol has been heterologously produced in Escherichia coli, but the low titer hinders its industrial applications. Moreover, bioconversion of geraniol by E. coli remains largely unknown.ResultsRecombinant overexpression of Ocimum basilicum geraniol synthase, Abies grandis geranyl diphosphate synthase, and a heterotic mevalonate pathway in E. coli BL21 (DE3) enabled the production of up to 68.6 ± 3 mg/L geraniol in shake flasks. Initial fed-batch fermentation only increased geraniol production to 78.8 mg/L. To further improve the production yield, the fermentation conditions were optimized. Firstly, 81.4 % of volatile geraniol was lost during the first 5 h of fermentation in a solvent-free system. Hence, isopropyl myristate was added to the culture medium to form an aqueous-organic two-phase culture system, which effectively prevented volatilization of geraniol. Secondly, most of geraniol was eventually biotransformed into geranyl acetate by E. coli, thus decreasing geraniol production. For the first time, we revealed the role of acetylesterase (Aes, EC 3.1.1.6) from E. coli in hydrolyzing geranyl acetate to geraniol, and production of geraniol was successfully increased to 2.0 g/L under controlled fermentation conditions.ConclusionsAn efficient geraniol production platform was established by overexpressing several key pathway proteins in engineered E. coli strain combined with a controlled fermentation system. About 2.0 g/L geraniol was obtained using our controllable aqueous-organic two-phase fermentation system, which is the highest yield to date. In addition, the interconversion between geraniol and geranyl acetate by E. coli was first elucidated. This study provided a new and promising strategy for geraniol biosynthesis, which laid a basis for large-scale industrial application.

Highlights

  • Geraniol is an acyclic monoterpene alcohol, which exhibits good prospect as a gasoline alternative

  • Geraniol has been successfully heterologously produced in Escherichia coli and S. cerevisiae

  • A recent study demonstrated that geranyl diphosphate (GPP) accumulation in yeast bearing mutated farnesyl diphosphate synthase (FPPS) enabled geraniol formation in the absence of a heterologous geraniol synthase probably through endogenous dephosphorylation [11, 14]

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Summary

Introduction

Geraniol is an acyclic monoterpene alcohol, which exhibits good prospect as a gasoline alternative. Geraniol has been heterologously produced in Escherichia coli, but the low titer hinders its industrial applications. Geraniol has been successfully heterologously produced in Escherichia coli and S. cerevisiae. Geraniol can be generated even in the absence of specific GPPS or mutated FPPS in E. coli by overexpressing an Ocimum basilicum geraniol synthase (GES), the GPP release mechanism remains unclear [16]. By co-overexpression of a FPPS mutant and GES in S. cerevisiae, 5 mg/L geraniol was obtained after 7 days of culture [11]. Production of geraniol was further increased to 36.04 mg/L in S. cerevisiae harboring both regulator gene MAF1 and GES after 48 h of culture by overexpressing key rate-limiting enzymes of the MVA pathway [17]. The titer is still too low for industrial applications

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