Bio-based production of chemicals is important for sustainable chemical industry. Here,
Escherichia coli is metabolically engineered to produce 1,3-diaminopropane (1,3-DAP), a monomer for polyamide. Comparison of heterologous C
4 and C
5 pathways for 1,3-DAP production by
in silico flux analysis revealed that the C
4 pathway employing
Acinetobacter baumannii dat and
ddc genes, encoding 2-ketoglutarate 4-aminotransferase and L-2,4-diaminobutanolate decarboxylase, respectively, was more efficient. In a strain having feedback resistant aspartokinases, the
ppc and
aspC genes were overexpressed to increase flux towards 1,3-DAP synthesis. Also, knocking out
pfkA was found to increase 1,3-DAP production by applying 128 synthetic small RNAs. Overexpression of the
ppc and
aspC genes in the
pfkA deleted strain resulted in even higher production of 1,3-DAP. Fed-batch fermentation of the final engineered
E. coli strain allowed production of 13 g/L of 1,3-DAP in a glucose minimal medium. [This work was supported by the Technology Development Program to Solve Climate Changes on Systems Metabolic Engineering for Biorefineries from the Ministry of Science, ICT and Future Planning (MSIP) through the National Research Foundation (NRF) of Korea (NRF-2012M1A2A2026556 and NRF-2012M1A2A2026557).]
