Invited Talk: Lactic acid production using C1 or C6 carbon source
International Conference Biomolecular Engineering ICBE
2018
ICBE Asia 2018: International Conference on Biomolecular Engineering
General Submissions
Session 2: Translational Biomolecular Engineering
Monday, January 8, 2018 - 2:00pm to 2:35pm
Biorefinery is defined as producing useful chemicals and fuels mainly via microbial fermentation. Currently, glucose and other biomass-derived sugars are used as major carbon sources for microbial fermentation, but other abundant and inexpensive carbon sources such as CO2, CO and methane are considered as promising alternatives to sugars in biorefinery. We engineer Saccharomyces cerevisiae and Methylomonas sp. DH-1 to produced D-lactic acid using glucose and methane, respectively. Both organisms cannot naturally produce lactic acid. Therefore L or D form-specific lactic acid can be produced by introducing stereo-specific heterologous lactate dehydrogenase. By eliminating ethanol and glycerol production pathways, and adaptive laboratory evolution to increase lactate tolerance, we generate S. cerevisiae strain, which can produced D-lactic acid under acidic conditions with high titer, yield, and productivity. Methylomonas sp. DH-1 is a methanotroph which can use methane as a sole carbon and energy source. By adaptive laboratory evolution, lactic acid-tolerant strain is generated. Expression of D form-specific lactate dehydrogenase gene in the evolved strain leads to about 8-fold increase in D-lactic acid production from methane compared to that in wild type strain.