纤维二糖
木糖
生物化学
化学
发酵
乳酸
木质纤维素生物量
代谢工程
乳酸发酵
食品科学
纤维素
生物
纤维素酶
细菌
酶
遗传学
作者
Timothy L. Turner,Guochang Zhang,Eun Joong Oh,Vijay Subramaniam,Andrew Adiputra,Vimal Subramaniam,Christopher D. Skory,Ji Yeon Jang,Byung Jo Yu,In Park,Yong‐Su Jin
摘要
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. Biotechnol. Bioeng. 2016;113: 1075–1083. © 2015 Wiley Periodicals, Inc.
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