Abstract
The glyceraldehyde-3-phosphate dehydrogenase (GAP) gene from the thermotolerant yeast strain Pichia thermomethanolica BCC16875 was characterized. To investigate the efficiency of the GAP promoter for heterologous expression, especially at high temperature in various carbon sources, the promoter was employed for constitutive expression of a phytase reporter gene. The results showed that this promoter was able to drive efficient expression of phytase at 30 °C; the native promoter was highly robust compared with the heterologous GAP promoter from Pichia pastoris. More importantly, the GAP promoter was shown to be able to function at higher temperatures up to 42 °C, which could be useful for large-scale protein production to help reduce cooling costs in the fermenter. Expression in different carbon sources revealed that the GAP promoter was functional in glucose-, glycerol-, and methanol-containing media, with the highest level of expression in YPD medium. This strong promoter will help promote high expression of heterologous protein expression in P. thermomethanolica, especially in large-scale fermentation. In addition, a new tool for heterologous expression in yeast has been gained.
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Acknowledgments
We thank Mr. Wuttichai Mhuantong for technical assistance and Dr. Philip J. Shaw for critically editing the manuscript. Financial support (P-09-00108) from National Center for Genetic Engineering and Biotechnology, Thailand is greatly appreciated.
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Harnpicharnchai, P., Promdonkoy, P., Sae-Tang, K. et al. Use of the glyceraldehyde-3-phosphate dehydrogenase promoter from a thermotolerant yeast, Pichia thermomethanolica, for heterologous gene expression, especially at elevated temperature. Ann Microbiol 64, 1457–1462 (2014). https://doi.org/10.1007/s13213-013-0765-z
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DOI: https://doi.org/10.1007/s13213-013-0765-z