TY - JOUR
T1 - Production of acetol from glycerol using engineered Escherichia coli
AU - Zhu, Hongliang
AU - Yi, Xianyang
AU - Liu, Yi
AU - Hu, Hongbo
AU - Wood, Thomas K.
AU - Zhang, Xuehong
N1 - Funding Information:
This work was supported by 973 Programs of China ( 2012CB721005 ).
PY - 2013/12
Y1 - 2013/12
N2 - Escherichia coli Lin43 is a strain which has some mutations in glycerol kinase (GlpK) and the repressor for the glycerol 3-phosphate regulon (GlpR). When exposed to glycerol, it quickly accumulates lethal levels of methylglyoxal, which is a precursor of acetol; acetol is important for the manufacture of polyols, acrolein, dyes, and skin tanning agents. This work reports the engineering of E. coli Lin 43 for the conversion of glycerol into acetol. First, the glyoxalase system was interrupted by deleting the gloA gene, which increased the acetol yield by 32%. In addition, the aldehyde reductase YqhD was overexpressed which led to an increase of acetol production by 11.4-fold. Acetol production was optimized by varying the cell density, glycerol concentration, supplemental carbon source, pH and temperature. Under the optimal conditions (OD600=20, 20g/L glycerol, 2g/L succinate, pH 7.0, and 28°C), we obtained 5.4g/L acetol in 21h.
AB - Escherichia coli Lin43 is a strain which has some mutations in glycerol kinase (GlpK) and the repressor for the glycerol 3-phosphate regulon (GlpR). When exposed to glycerol, it quickly accumulates lethal levels of methylglyoxal, which is a precursor of acetol; acetol is important for the manufacture of polyols, acrolein, dyes, and skin tanning agents. This work reports the engineering of E. coli Lin 43 for the conversion of glycerol into acetol. First, the glyoxalase system was interrupted by deleting the gloA gene, which increased the acetol yield by 32%. In addition, the aldehyde reductase YqhD was overexpressed which led to an increase of acetol production by 11.4-fold. Acetol production was optimized by varying the cell density, glycerol concentration, supplemental carbon source, pH and temperature. Under the optimal conditions (OD600=20, 20g/L glycerol, 2g/L succinate, pH 7.0, and 28°C), we obtained 5.4g/L acetol in 21h.
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U2 - 10.1016/j.biortech.2013.09.062
DO - 10.1016/j.biortech.2013.09.062
M3 - Article
C2 - 24113547
AN - SCOPUS:84885162016
SN - 0960-8524
VL - 149
SP - 238
EP - 243
JO - Bioresource technology
JF - Bioresource technology
ER -