TY - JOUR
T1 - Engineering Yarrowia lipolytica for Efficient Synthesis of Geranylgeraniol
AU - Wang, Kaifeng
AU - Yin, Mingxue
AU - Sun, Mei Li
AU - Zhao, Quanyu
AU - Ledesma-Amaro, Rodrigo
AU - Ji, Xiao Jun
AU - Lin, Lu
N1 - Publisher Copyright:
© 2024 American Chemical Society.
PY - 2024/9/18
Y1 - 2024/9/18
N2 - Geranylgeraniol (GGOH) is a crucial component in fragrances and essential oils, and a valuable precursor of vitamin E. It is primarily extracted from the oleoresin of Bixa orellana, but is challenged by long plant growth cycles, severe environmental pollution, and low extraction efficiency. Chemically synthesized GGOH typically comprises a mix of isomers, making the separation process both challenging and costly. Advancements in synthetic biology have enabled the construction of microbial cell factories for GGOH production. In this study, Yarrowia lipolytica was engineered to efficiently synthesize GGOH by expressing heterologous phosphatase genes, enhancing precursor supplies of farnesyl diphosphate, geranylgeranyl pyrophosphate, and acetyl-CoA, and downregulating the squalene synthesis pathway by promoter engineering. Additionally, optimizing fermentation conditions and reducing reactive oxygen species significantly increased the GGOH titer to 3346.47 mg/L in a shake flask. To the best of our knowledge, this is the highest reported GGOH titer in shaking flasks to date, setting a new benchmark for terpenoid production.
AB - Geranylgeraniol (GGOH) is a crucial component in fragrances and essential oils, and a valuable precursor of vitamin E. It is primarily extracted from the oleoresin of Bixa orellana, but is challenged by long plant growth cycles, severe environmental pollution, and low extraction efficiency. Chemically synthesized GGOH typically comprises a mix of isomers, making the separation process both challenging and costly. Advancements in synthetic biology have enabled the construction of microbial cell factories for GGOH production. In this study, Yarrowia lipolytica was engineered to efficiently synthesize GGOH by expressing heterologous phosphatase genes, enhancing precursor supplies of farnesyl diphosphate, geranylgeranyl pyrophosphate, and acetyl-CoA, and downregulating the squalene synthesis pathway by promoter engineering. Additionally, optimizing fermentation conditions and reducing reactive oxygen species significantly increased the GGOH titer to 3346.47 mg/L in a shake flask. To the best of our knowledge, this is the highest reported GGOH titer in shaking flasks to date, setting a new benchmark for terpenoid production.
KW - Yarrowia lipolytica
KW - geranylgeraniol
KW - geranylgeranyl pyrophosphate synthase
KW - metabolic engineering
KW - reactive oxygen species
UR - http://www.scopus.com/inward/record.url?scp=85203290889&partnerID=8YFLogxK
U2 - 10.1021/acs.jafc.4c06749
DO - 10.1021/acs.jafc.4c06749
M3 - 文章
C2 - 39241196
AN - SCOPUS:85203290889
SN - 0021-8561
VL - 72
SP - 20568
EP - 20581
JO - Journal of Agricultural and Food Chemistry
JF - Journal of Agricultural and Food Chemistry
IS - 37
ER -