TY - JOUR
T1 - Engineered Biosynthesis of Phenol Using Acetate as the Carbon Source in Escherichia coli
AU - Feng, Jiao
AU - Zhao, Yan
AU - Liu, Zhendi
AU - Wang, Xin
AU - Xu, Sheng
AU - Chen, Kequan
N1 - Publisher Copyright:
© 2025 American Chemical Society.
PY - 2025/2/3
Y1 - 2025/2/3
N2 - Acetate is a prospective nonfood carbon source generated from one-carbon feedstocks and lignocellulose in biomanufacturing. This study aimed to efficiently biosynthesize phenol from acetate using engineered Escherichia coli. To achieve this sustainable route, we first constructed ten engineered E. coli strains by introducing the heterogeneous phenol synthesis pathway and enhancing the acetate assimilation pathway, with the strain BL9 exhibiting optimal phenol production. Subsequently, five metabolic engineering strategies were implemented for boosting phenol production, including activating the glyoxylate cycle by deleting iclR, relieving the repression of TyrR, replacing the bottleneck enzyme with AroGfbr, identifying and reinforcing rate-limiting steps in the shikimate pathway, and constructing a precursor phosphoenolpyruvate recycling module. These strategies resulted in a boost in the phenol titer of the engineered strain TPL6 to 0.454 g/L. Finally, a systematic optimization of the fermentation conditions was achieved. Through fed-batch fermentation combined with in situ extraction, the phenol titer was raised to 2.01 g/L, 38 times over the initial flask production. This is the first study to biosynthesize phenol from acetate, and it highlights the great potential of metabolically engineered E. coli.
AB - Acetate is a prospective nonfood carbon source generated from one-carbon feedstocks and lignocellulose in biomanufacturing. This study aimed to efficiently biosynthesize phenol from acetate using engineered Escherichia coli. To achieve this sustainable route, we first constructed ten engineered E. coli strains by introducing the heterogeneous phenol synthesis pathway and enhancing the acetate assimilation pathway, with the strain BL9 exhibiting optimal phenol production. Subsequently, five metabolic engineering strategies were implemented for boosting phenol production, including activating the glyoxylate cycle by deleting iclR, relieving the repression of TyrR, replacing the bottleneck enzyme with AroGfbr, identifying and reinforcing rate-limiting steps in the shikimate pathway, and constructing a precursor phosphoenolpyruvate recycling module. These strategies resulted in a boost in the phenol titer of the engineered strain TPL6 to 0.454 g/L. Finally, a systematic optimization of the fermentation conditions was achieved. Through fed-batch fermentation combined with in situ extraction, the phenol titer was raised to 2.01 g/L, 38 times over the initial flask production. This is the first study to biosynthesize phenol from acetate, and it highlights the great potential of metabolically engineered E. coli.
KW - Escherichia coli
KW - acetate
KW - biosynthesis
KW - metabolic engineering
KW - phenol
UR - http://www.scopus.com/inward/record.url?scp=85216092507&partnerID=8YFLogxK
U2 - 10.1021/acssuschemeng.4c08437
DO - 10.1021/acssuschemeng.4c08437
M3 - 文章
AN - SCOPUS:85216092507
SN - 2168-0485
VL - 13
SP - 1657
EP - 1666
JO - ACS Sustainable Chemistry and Engineering
JF - ACS Sustainable Chemistry and Engineering
IS - 4
ER -