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An extra copy of the β-glucosidase gene improved the cellobiose fermentation capability of an engineered strain

3 Biotech. 2019-09-01; 
Hyo Jin Kim, Won-Heong Lee, Timothy Lee Turner, Suryang Kwak, Yong-Su Jin
Products/Services Used Details Operation
PCR Cloning and Subcloning … The CloneEZ ® PCR Cloning Kit (GenScript, Piscataway, NJ, USA) was used to assemble the gh1-1 and pRS424 PCR products. All vectors were introduced into E. coli Top10 and the transformants were selected on Luria–Bertani agar medium containing 100 µg/mL ampicillin … Get A Quote

摘要

In a previously engineered recombinant, the cellobiose fermentation rate was significantly lower than the glucose fermentation rate. Thus, we implemented a genome-wide perturbation library to find gene targets for improving the cellobiose fermentation capability of the yeast strain. Unexpectedly, we discovered a transformant that contained an additional β-glucosidase gene (-), possibly through homologous recombination between the plasmids. The additional β-glucosidase led to the fastest cellobiose fermentation activity among all the transformants evaluated, and the strain demonstrated significantly higher β-glucosidase activity than the control strain, especially during the initial exponential growth phase.... More

关键词

Cellobiose fermentation, Genome-wide overexpression library, Gh1-1, Homologous recombination, Saccharomyces cerevisiae