详细信息
Transcriptional investigation of the effect of mixed feeding to identify the main cellular stresses on recombinant Pichia pastoris ( EI收录)
文献类型:期刊文献
英文题名:Transcriptional investigation of the effect of mixed feeding to identify the main cellular stresses on recombinant Pichia pastoris
作者:Zhu, Taicheng[1,2]; Hang, Haifeng[2]; Chu, Ju[2]; Zhuang, Yingping[2]; Zhang, Siliang[2]; Guo, Meijin[2]
机构:[1] Institute of Microbiology, Chinese Academy of Sciences, Beijing 100101, China; [2] State Key Laboratory of Bioreactor Engineering, East China University of Science and Technology, 130 Meilong Rd., Shanghai 200237, China
年份:2013
卷号:40
期号:2
起止页码:183
外文期刊名:Journal of Industrial Microbiology and Biotechnology
收录:EI(收录号:20242616517336)
语种:英文
外文关键词:Genes - Insulin - Metabolism - Methanol - Physiology - Recombinant proteins - Yeast
摘要:Heterologous protein expression using Pichia pastoris causes metabolic stress on the physiology of host cells, which may compromise the yields of secreted foreign proteins. Thus, understanding these metabolic stresses during secretory expression allows us to circumvent these undesirable effects. We investigated the effect of co-feeding two alternative carbon resources, sorbitol and yeast extract (YE), on the physiology of A3, a P. pastoris strain carrying 18 copies of the porcine insulin precursor (PIP) gene. Comparative transcriptional analysis was performed on 13 selected genes involved in important cellular processes. Results showed that co-feeding of either sorbitol or YE along with methanol improved the performance of A3. The co-feeding of YE enhanced the specific growth rate of A3 and the specific PIP productivity. However, the oxidative stress in the yeast cells increased. The co-feeding of methanol and sorbitol increased the specific growth rate of A3 but did not affect the specific PIP productivity. The transcriptional results suggested that sorbitol may have repressed the expression of foreign proteins. These observations will not only guide the application of mixed feeding strategies but also give a deeper understanding of the metabolic burden in the secretory expression of foreign proteins. ? 2013 Society for Industrial Microbiology and Biotechnology.
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