Liu Xiuxia, Zhao Zihao, Zhang Wei, Sun Yang, Yang Yankun, Bai Zhonghu
National Engineering Laboratory for Cereal Fermentation Technology Jiangnan University Wuxi P. R. China.
The Key Laboratory of Industrial Biotechnology, Ministry of Education, School of Biotechnology Jiangnan University Wuxi P. R. China.
Eng Life Sci. 2017 Aug 14;17(10):1118-1125. doi: 10.1002/elsc.201700087. eCollection 2017 Oct.
Directly using the promoter associated with 5'-untranslated region of a high-protein-abundance gene from the genome may cause low expression activity of an expression system. A bicistronic expression part containing the short 5' coding sequence of the source gene and an embedded Shine-Dalgarno sequence can cause higher expression levels of the recombinant gene in a bicistronic cassette. Here, we evaluated two methods to construct expression parts and exploited genomic sequence sources to provide specific functional sequences to complete the expression system. The architecture of the bicistronic part increased the expression levels of target genes and performed more reliably than conventional expression parts with the same promoter and 5' untranslated region. For , the strongest bicistronic part, HP-BEP4, was obtained from a heterologous sequence source, leading to a 2.24-fold increase in the expression level of fluorescent protein over constitutively expressed pXMJ19 or the production of more than 100 mg/L single-chain variable fragment (scFv). It could meet the needs of overexpressing key genes in .
直接使用基因组中与高蛋白丰度基因5'非翻译区相关的启动子可能会导致表达系统的低表达活性。包含源基因短5'编码序列和嵌入的Shine-Dalgarno序列的双顺反子表达部分可在双顺反子盒中导致重组基因的更高表达水平。在这里,我们评估了两种构建表达部分的方法,并利用基因组序列来源提供特定功能序列以完善表达系统。双顺反子部分的结构提高了靶基因的表达水平,并且比具有相同启动子和5'非翻译区的传统表达部分表现得更可靠。例如,最强的双顺反子部分HP-BEP4是从异源序列来源获得的,导致荧光蛋白的表达水平比组成型表达的pXMJ19增加了2.24倍,或产生了超过100 mg/L的单链可变片段(scFv)。它可以满足在……中过表达关键基因的需求。