TY - JOUR
T1 - Metabolic engineering of
T2 - Escherichia coli for production of non-natural acetins from glycerol
AU - Zada, Bakht
AU - Joo, Seongjoon
AU - Wang, Chonglong
AU - Tseten, Tenzin
AU - Jeong, Seong Hee
AU - Seo, Hogyun
AU - Sohn, Jung Hoon
AU - Kim, Kyung Jin
AU - Kim, Seon Won
AU - Zada, Bakht
N1 - Publisher Copyright:
© The Royal Society of Chemistry.
PY - 2020/11/21
Y1 - 2020/11/21
N2 - Mono-, di- and triacetin are three glycerol esters which are usually synthesized via costly and environmentally unfriendly chemical synthesis methods. Here, Escherichia coli is metabolically engineered for the production of mono-, di- and triacetin using glycerol as a substrate. First, a novel biosynthetic route of mono- and diacetin is established by overexpression of a native enzyme, maltose O-acetyltransferase (MAA). Next, the biosynthetic pathway is extended to produce a mixture of mono-, di- and triacetin by overexpression of chloramphenicol-O-acetyltransferase (CAT). By successive strategies, including heterologous gene expression, metabolic engineering, and culture optimization, a recombinant E. coli is enabled to produce more than 27 g L-1 of a mixture of mono-, di- and triacetin in shake flask cultures, which is a >650-fold increase over the initial production of 0.04 g L-1. In vitro studies confirm the acetylation of glycerol to mono- and diacetin by MAA, and the additional acetylation to triacetin by CAT. When crude glycerol is used as a substrate, the engineered strain produced a total of 25.9 g L-1 of the acetin mixture, about the same as that achieved from pure glycerol. To our knowledge, this is the first successful report of microbial production of the artificial chemicals, acetins.
AB - Mono-, di- and triacetin are three glycerol esters which are usually synthesized via costly and environmentally unfriendly chemical synthesis methods. Here, Escherichia coli is metabolically engineered for the production of mono-, di- and triacetin using glycerol as a substrate. First, a novel biosynthetic route of mono- and diacetin is established by overexpression of a native enzyme, maltose O-acetyltransferase (MAA). Next, the biosynthetic pathway is extended to produce a mixture of mono-, di- and triacetin by overexpression of chloramphenicol-O-acetyltransferase (CAT). By successive strategies, including heterologous gene expression, metabolic engineering, and culture optimization, a recombinant E. coli is enabled to produce more than 27 g L-1 of a mixture of mono-, di- and triacetin in shake flask cultures, which is a >650-fold increase over the initial production of 0.04 g L-1. In vitro studies confirm the acetylation of glycerol to mono- and diacetin by MAA, and the additional acetylation to triacetin by CAT. When crude glycerol is used as a substrate, the engineered strain produced a total of 25.9 g L-1 of the acetin mixture, about the same as that achieved from pure glycerol. To our knowledge, this is the first successful report of microbial production of the artificial chemicals, acetins.
UR - http://www.scopus.com/inward/record.url?scp=85096740287&partnerID=8YFLogxK
U2 - 10.1039/d0gc02395g
DO - 10.1039/d0gc02395g
M3 - Article
AN - SCOPUS:85096740287
SN - 1463-9262
VL - 22
SP - 7788
EP - 7802
JO - Green Chemistry
JF - Green Chemistry
IS - 22
ER -