Gao Min-Jie, Zhan Xiao-Bei, Gao Peng, Zhang Xu, Dong Shi-Juan, Li Zhen, Shi Zhong-Ping, Lin Chi-Chung
Key Laboratory of Industrial Biotechnology, Ministry of Education, School of Biotechnology, Jiangnan University, Wuxi, 214122, China.
Appl Biochem Biotechnol. 2015 May;176(2):493-504. doi: 10.1007/s12010-015-1590-6. Epub 2015 Apr 15.
Various induction strategies were investigated for effective porcine interferon-α (pIFN-α) production by Pichia pastoris in a 10 L fermenter. We found that pIFN-α concentration could be significantly improved with the strategies of low-temperature induction or methanol/sorbitol co-feeding. On this basis, a combinational strategy of induction at lower temperature (20 °C) with methanol/sorbitol co-feeding has been proposed for improvement of pIFN-α production. The results reveal that maximal pIFN-α concentration and antiviral activity reach the highest level of 2.7 g/L and 1.8 × 10(7) IU/mg with the proposed induction strategy, about 1.3-2.1 folds higher than those obtained with other sub-optimal induction strategies. Metabolic analysis and online multi-variable measurement results indicate that energy metabolic enrichment is responsible for the performance enhancement of pIFN-α production, as a large amount of ATP could be simultaneously produced from both formaldehyde oxidation pathway in methanol metabolism and tricarboxylic acid (TCA) cycle in sorbitol metabolism. In addition, the proposed combinational induction strategy enables P. pastoris to be resistant to high methanol concentration (42 g/L), which conceivably occur associating with the error-prone methanol over-feeding. As a result, the proposed combinational induction strategy simultaneously increased the targeted protein concentration and operational stability leading to significant improvement of pIFN-α production.
研究了多种诱导策略,以在10 L发酵罐中通过毕赤酵母有效生产猪干扰素-α(pIFN-α)。我们发现,采用低温诱导或甲醇/山梨醇共进料策略可显著提高pIFN-α浓度。在此基础上,提出了低温(20°C)诱导与甲醇/山梨醇共进料的组合策略,以提高pIFN-α的产量。结果表明,采用所提出的诱导策略,pIFN-α的最大浓度和抗病毒活性达到最高水平,分别为2.7 g/L和1.8×10(7) IU/mg,比其他次优诱导策略获得的水平高约1.3至2.1倍。代谢分析和在线多变量测量结果表明,能量代谢富集是pIFN-α生产性能提高的原因,因为在甲醇代谢中的甲醛氧化途径和山梨醇代谢中的三羧酸(TCA)循环都可以同时产生大量ATP。此外,所提出的组合诱导策略使毕赤酵母能够耐受高甲醇浓度(42 g/L),这可能与容易出错的甲醇过量进料有关。因此,所提出的组合诱导策略同时提高了目标蛋白浓度和操作稳定性,从而显著提高了pIFN-α的产量。