Molecular Microbiology & Bioenergetics, Institute of Molecular Biosciences, Johann Wolfgang Goethe University Frankfurt/Main, Max-von-Laue- Str. 9, 60438, Frankfurt, Germany.
Microb Cell Fact. 2023 Sep 19;22(1):187. doi: 10.1186/s12934-023-02192-1.
Enzymes from thermophiles are of great interest for research and bioengineering due to their stability and efficiency. Thermophilic expression hosts such as Thermus thermophilus [T. thermophilus] can overcome specific challenges experienced with protein production in mesophilic expression hosts, such as leading to better folding, increased protein stability, solubility, and enzymatic activity. However, available inducible promoters for efficient protein production in T. thermophilus HB27 are limited.
In this study, we characterized the pilA4 promoter region and evaluated its potential as a tool for production of thermostable enzymes in T. thermophilus HB27. Reporter gene analysis using a promoterless β-glucosidase gene revealed that the pilA4 promoter is highly active under optimal growth conditions at 68 °C and downregulated during growth at 80 °C. Furthermore, growth in minimal medium led to significantly increased promoter activity in comparison to growth in complex medium. Finally, we proved the suitability of the pilA4 promoter for heterologous production of thermostable enzymes in T. thermophilus by producing a fully active soluble mannitol-1-phosphate dehydrogenase from Thermoanaerobacter kivui [T. kivui], which is used in degradation of brown algae that are rich in mannitol.
Our results show that the pilA4 promoter is an efficient tool for gene expression in T. thermophilus with a high potential for use in biotechnology and synthetic biology applications.
由于其稳定性和效率,来自嗜热生物的酶在研究和生物工程方面具有重要意义。嗜热表达宿主,如 Thermus thermophilus [T. thermophilus],可以克服在中温表达宿主中生产蛋白质时遇到的特定挑战,例如导致更好的折叠、增加蛋白质稳定性、溶解度和酶活性。然而,用于在 T. thermophilus HB27 中高效生产蛋白质的可诱导启动子有限。
在这项研究中,我们对 pilA4 启动子区域进行了表征,并评估了其作为在 T. thermophilus HB27 中生产耐热酶的工具的潜力。使用无启动子的β-葡萄糖苷酶基因进行报告基因分析表明,pilA4 启动子在 68°C 的最佳生长条件下具有高度活性,并在 80°C 生长时下调。此外,与在复杂培养基中生长相比,在基础培养基中生长导致启动子活性显著增加。最后,我们通过生产用于降解富含甘露醇的褐藻的 Thermoanaerobacter kivui [T. kivui] 的全活性可溶性甘露醇-1-磷酸脱氢酶,证明了 pilA4 启动子在 T. thermophilus 中异源生产耐热酶的适用性。
我们的结果表明,pilA4 启动子是 T. thermophilus 中基因表达的有效工具,具有在生物技术和合成生物学应用中高潜力。