| Literature DB >> 26524688 |
Timothy L Turner1,2, Guo-Chang Zhang1,2, Eun Joong Oh1,2, Vijay Subramaniam2, Andrew Adiputra3, Vimal Subramaniam3, Christopher D Skory4, Ji Yeon Jang5, Byung Jo Yu5, In Park5, Yong-Su Jin6,7.
Abstract
Efficient and rapid production of value-added chemicals from lignocellulosic biomass is an important step toward a sustainable society. Lactic acid, used for synthesizing the bioplastic polylactide, has been produced by microbial fermentation using primarily glucose. Lignocellulosic hydrolysates contain high concentrations of cellobiose and xylose. Here, we constructed a recombinant Saccharomyces cerevisiae strain capable of fermenting cellobiose and xylose into lactic acid. Specifically, genes (cdt-1, gh1-1, XYL1, XYL2, XYL3, and ldhA) coding for cellobiose transporter, β-glucosidase, xylose reductase, xylitol dehydrogenase, xylulokinase, and lactate dehydrogenase were integrated into the S. cerevisiae chromosomes. The resulting strain produced lactic acid from cellobiose or xylose with high yields. When fermenting a cellulosic sugar mixture containing 10 g/L glucose, 40 g/L xylose, and 80 g/L cellobiose, the engineered strain produced 83 g/L of lactic acid with a yield of 0.66 g lactic acid/g sugar (66% theoretical maximum). This study demonstrates initial steps toward the feasibility of sustainable production of lactic acid from lignocellulosic sugars by engineered yeast.Entities:
Keywords: Saccharomyces cerevisiae; cellobiose; lactate dehydrogenase; lactic acid; metabolic engineering
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Year: 2015 PMID: 26524688 DOI: 10.1002/bit.25875
Source DB: PubMed Journal: Biotechnol Bioeng ISSN: 0006-3592 Impact factor: 4.530