Efficient L-Alanine Production by a Thermo-Regulated Switch in Escherichia coli.

Abstract

L-Alanine has important applications in food, pharmaceutical and veterinary and is used as a substrate for production of engineered thermoplastics. Microbial fermentation could reduce the production cost and promote the application of L-alanine. However, the presence of L-alanine significantly inhibit cell growth rate and cause a decrease in the ultimate L-alanine productivity. For efficient L-alanine production, a thermo-regulated genetic switch was designed to dynamically control the expression of L-alanine dehydrogenase (alaD) from Geobacillus stearothermophilus on the Escherichia coli B0016-060BC chromosome. The optimal cultivation conditions for the genetically switched alanine production using B0016-060BC were the following: an aerobic growth phase at 33°C with a 1-h thermo-induction at 42°C followed by an oxygen-limited phase at 42°C. In a bioreactor experiment using the scaled-up conditions optimized in a shake flask, B0016-060BC accumulated 50.3g biomass/100g glucose during the aerobic growth phase and 96g alanine/100g glucose during the oxygen-limited phase, respectively. The L-alanine titer reached 120.8g/l with higher overall and oxygen-limited volumetric productivities of 3.09 and 4.18g/lh, respectively, using glucose as the sole carbon source. Efficient cell growth and L-alanine production were reached separately, by switching cultivation temperature. The results revealed the application of a thermo-regulated strategy for heterologous metabolic production and pointed to strategies for improving L-alanine production.