Improved heterologous protein expression in the chloroplast of Chlamydomonas reinhardtii through promoter and 5′ untranslated region optimization

Summary Microalgae have the potential to be a valuable biotechnological platform for the production of recombinant proteins. However, because of the complex regulatory network that tightly controls chloroplast gene expression, heterologous protein accumulation in a wild‐type, photosynthetic‐competent algal chloroplast remains low. High levels of heterologous protein accumulation have been achieved using the psbA promoter/5′ untranslated region (UTR), but only in a psbA ‐deficient genetic background, because of psbA/D1‐dependent auto‐attenuation. Here, we examine the effect of fusing the strong 16S rRNA promoter to the 5′ UTR of the psbA and atpA genes on transgene expression in the chloroplast of Chlamydomonas reinhardtii . We show that fusion of the 16S promoter had little impact on protein accumulation from the psbA 5′ UTR in a psbA ‐deficient genetic background. Furthermore, the 16S/psbA promoter/UTR fusion was silenced in the presence of wild‐type levels of D1 protein, confirming that the psbA 5′ UTR is the primary target for D1‐dependent auto‐repression. However, fusion of the 16S promoter to the atpA 5′ UTR significantly boosts mRNA levels and supports high levels of heterologous protein accumulation in photosynthetic‐competent cells. The 16S/atpA promoter/UTR drove LUXCT protein accumulation to levels close to that of psbA in a psbA− background, and drove expression of a human therapeutic protein to levels only twofold lower than the psbA 5′ UTR. The 16S/atpA promoter/UTR combination should have utility for heterologous protein production when expression from a photosynthetic‐competent microalgal strain is required.