An Engineered Heat-Inducible Expression System for the Production of Casbene in .

Plants respond to heat stress by producing heat-shock proteins. These are regulated by heat-shock promoters containing regulatory elements, which can be harnessed to control protein expression both temporally and spatially. In this study, we designed heat-inducible promoters to produce the diterpene casbene in , through a multi-step metabolic pathway. To potentially increase gene transcription, we coupled heat-shock elements from Hsp101 or GmHsp17.3-B promoters, CAAT and TATA boxes from CaMV , and the 5'UTR from the tobacco mosaic virus. The resulting four chimeric promoters fused to a green fluorescent protein (GFP) reporter showed that the variant Ara2 had the strongest fluorescent signal after heat shock. We next created a 4-gene cassette driven by the promoter to allow for exogenous synthesis of casbene and transformed this multigene construct along with a selectable marker gene into . Metabolic analysis on the transgenic lines revealed that continuous heat outperforms heat shock, with up to 1 μg/mg DW of casbene detected after 32 h of uninterrupted 40 °C heat. These results demonstrate the potential of heat-inducible promoters as synthetic biology tools for metabolite production in plants.