The SPT15 gene encodes a Saccharomyces cerevisiae TATA-binding protein, which is able to globally control the transcription levels of various metabolic and regulatory genes. In this study, a SPT15 gene mutant (S42N, S78R, S163P, and I212N) was expressed in S. cerevisiae BY4741 (BSPT15-M3), of which effects on fermentative yeast properties were evaluated in a series of culture types. By applying different nitrogen sources and air supply conditions in batch culture, organic nitrogen sources and microaerobic condition were decided to be more favorable for both cell growth and ethanol production of the BSPT15-M3 strain than the control S. cerevisiae BY4741 strain expressing the SPT15 gene (BSPT15wt). Microaerobic fed-batch cultures of BSPT15-M3 with glucose shock in the presence of high ethanol content resulted in a 9.5–13.4% higher glucose consumption rate and ethanol productivity than those for the BSPT15wt strain. In addition, BSPT15-M3 showed 4.5 and 3.9% increases in ethanol productivity from cassava hydrolysates and corn starch in simultaneous saccharification and fermentation processes, respectively. It was concluded that overexpression of the mutated SPT15 gene would be a potent strategy to develop robust S. cerevisiae strains with enhanced cell growth and ethanol production abilities.
Bibliographical noteFunding Information:
This work was financially supported by the National Research Foundation of Korea (NRF) Grant (2016R1A2B4010842) and the Advanced Biomass R&D Center (ABC) of Korea Grant (2011-0031359) funded by the Korean Ministry of Science, ICT and Future Planning and also by the R&D Program of MOTIE/KEIT (10049675).
© 2017, Springer-Verlag Berlin Heidelberg.
- Microaerobic fermentation
- Osmotic tolerance
- Saccharomyces cerevisiae
- Simultaneous saccharification and fermentation
ASJC Scopus subject areas
- Applied Microbiology and Biotechnology