Zhang Juan, Cai Yanqiu, Du Guocheng, Chen Jian, Wang Miao, Kang Zhen
The Key Laboratory of Industrial Biotechnology, Ministry of Education, School of Biotechnology, Jiangnan University, Wuxi, 214122, P. R. China.
School of Biotechnology, Jiangnan University, Wuxi, 214122, P. R. China.
J Microbiol. 2017 Jul;55(7):538-544. doi: 10.1007/s12275-017-6514-4. Epub 2017 Jun 30.
Cutinase as a promising biocatalyst has been intensively studied and applied in processes targeted for industrial scale. In this work, the cutinase gene tfu from Thermobifida fusca was artificially synthesized according to codon usage bias of Saccharomyces cerevisiae and investigated in Saccharomyces cerevisiae. Using the α-factor signal peptide, the T. fusca cutinase was successfully overexpressed and secreted with the GAL1 expression system. To increase the cutinase level and overcome some of the drawbacks of induction, four different strong promoters (ADH1, HXT1, TEF1, and TDH3) were comparatively evaluated for cutinase production. By comparison, promoter TEF1 exhibited an outstanding property and significantly increased the expression level. By fed-batch fermentation with a constant feeding approach, the activity of cutinase was increased to 29.7 U/ml. The result will contribute to apply constitutive promoter TEF1 as a tool for targeted cutinase production in S. cerevisiae cell factory.
角质酶作为一种有前景的生物催化剂,已得到深入研究并应用于工业规模的生产过程。在本研究中,根据酿酒酵母的密码子使用偏好,人工合成了来自嗜热栖热放线菌的角质酶基因tfu,并在酿酒酵母中进行了研究。利用α-因子信号肽,通过GAL1表达系统成功实现了嗜热栖热放线菌角质酶的过表达和分泌。为了提高角质酶水平并克服诱导的一些缺点,对四个不同的强启动子(ADH1、HXT1、TEF1和TDH3)在角质酶生产方面进行了比较评估。相比之下,启动子TEF1表现出优异的性能,显著提高了表达水平。通过恒速补料分批发酵,角质酶活性提高到了29.7 U/ml。该结果将有助于将组成型启动子TEF1用作酿酒酵母细胞工厂中靶向生产角质酶的工具。