Zhu Taicheng, Guo Meijin, Sun Chen, Qian Jiangchao, Zhuang Yingping, Chu Ju, Zhang Siliang
State Key Laboratory of Bioreactor Engineering, East China University of Science and Technology, 130 Meilong Rd, P.O. Box 329#, Shanghai, 200237, People's Republic of China.
Biotechnol Lett. 2009 May;31(5):679-84. doi: 10.1007/s10529-009-9917-4. Epub 2009 Jan 19.
A battery of Pichia pastoris transformants, G1, G6, A2, A3, C3, carrying 1, 6, 12, 18 and 29 copies of porcine insulin precursor (PIP) gene, were employed to investigate the genetic stability of these multi-copy P. pastoris strains. Both G6 and C3 maintained their original copy numbers in serial culture without methanol induction for 35 generations. With methanol as an inducer and carbon source, G1 and G6 remained stable but the average copy numbers (ACNs) of PIP gene in A2, A3, C3 were decreased to 10, 10 and 15 copies, respectively, after 96 h of induction in shake-flask culture. A PIP copy number distribution analysis of fermentation samples of C3 indicated that the majority of yeast cells have partially or completely lost their PIP genes. In 5-l fermentor culture, the ACNs of PIP gene in A2, A3, C3 were also decreased to 10, 15, 21 copies, respectively, after 72 h of methanol induction.
一组毕赤酵母转化子,G1、G6、A2、A3、C3,分别携带1、6、12、18和29个拷贝的猪胰岛素前体(PIP)基因,用于研究这些多拷贝毕赤酵母菌株的遗传稳定性。G6和C3在无甲醇诱导的连续培养35代中均保持其原始拷贝数。以甲醇作为诱导剂和碳源,在摇瓶培养中诱导96小时后,G1和G6保持稳定,但A2、A3、C3中PIP基因的平均拷贝数(ACN)分别降至10、10和15个拷贝。对C3发酵样品的PIP拷贝数分布分析表明,大多数酵母细胞已部分或完全丢失其PIP基因。在5升发酵罐培养中,甲醇诱导72小时后,A2、A3、C3中PIP基因的ACN也分别降至10、15、21个拷贝。