AUTHOR=Zeng Bo-Xuan , Yao Ming-Dong , Wang Ying , Xiao Wen-Hai , Yuan Ying-Jin 

TITLE=Metabolic Engineering of Saccharomyces cerevisiae for Enhanced Dihydroartemisinic Acid Production

JOURNAL=Frontiers in Bioengineering and Biotechnology

VOLUME=Volume 8 - 2020

YEAR=2020

URL=https://www.frontiersin.org/journals/bioengineering-and-biotechnology/articles/10.3389/fbioe.2020.00152

DOI=10.3389/fbioe.2020.00152

ISSN=2296-4185

ABSTRACT=Direct bioproduction of DHAA (dihydroartemisinic acid) rather than AA (artemisinic acid) as previous work would decrease the cost of artemisinin via the developed semi-biosynthesis way. The major challenge in microbial production of DHAA is how to efficiently manipulate consecutive key enzymes ADH1(artemisinic alcohol dehydrogenase), DBR2(artemisinic aldehyde Δ11(13) reductase) and ALDH1(aldehyde dehydrogenase) to redirect metabolic flux and elevate the ratio of DHAA to AA (artemisinic acid). Herein, DHAA biosynthesis was achieved in Saccharomyces cerevisiae by introducing series heterologous enzymes ADS (amorpha-4,11-diene synthase), CYP71AV1(amorphadiene oxidase), ADH1, DBR2 and ALDH1, obtaining initial DHAA/AA ratio at 2.53. The flux towards DHAA was enhanced by pairing fusion proteins DBR2-ADH1 and DBR2-ALDH1, leading to 1.75-fold increase in DHAA/AA ratio (to 6.97). Moreover, to promote the substrate preference of ALDH1 to dihydroartemisinic aldehyde (the intermediate for DHAA synthesis) than artemisinic aldehyde (the intermediate for AA synthesis), two rational engineering strategies, including downsizing the active pocket and enhancing the stability of enzyme/cofactor complex, were proposed to engineer ALDH1. It was found the mutant H194R, which showed better stability of the enzyme/NAD+ complex, obtained the highest DHAA to AA ratio at 3.73 among all the mutations. Then the mutant H194R was incorporated into above rebuilt fusion proteins, resulting in the highest ratio of DHAA to AA (10.05). Subsequently, the highest DHAA reported titer of 1.70 g/L (DHAA/AA ratio of 9.84) was achieved in 5L bioreactor fermentation. The study highlights the synergy of metabolic engineering and protein engineering in metabolic flux redirection, and would facilitate more efficient downstream chemical synthesis process.