食品科学 ›› 2012, Vol. 33 ›› Issue (10): 57-60.doi: 10.7506/spkx1002-6630-201210012

• 工艺技术 • 上一篇    下一篇

从毕赤酵母中提取外源重组蛋白的超声破碎条件及优化

戴佳锟1,2,3,李 燕4,马 齐1,2,关正君3,张 超3,张艳婷3,赵荣荣3,尉亚辉3,*   

  1. 1.陕西省科学院酶工程研究所 2.陕西省酶工程技术中心 3.西北大学生命科学学院,西部资源生物与现代生物技术省部共建重点实验室 4.陕西省微生物研究所
  • 出版日期:2012-05-25 发布日期:2012-05-07
  • 基金资助:
    陕西省科学院科技计划项目(2011K-17);西北大学自主创新类项目(10YZZ36)

Optimization of Ultrasonic Treatment for Recovery of Recombinant Protein from Pichia pastoris

DAI Jia-kun1,2,3,LI Yan4,MA Qi1,2,GUAN Zheng-jun3,ZHANG Chao3,ZHANG Yan-ting3, ZHAO Rong-rong3,WEI Ya-hui3,*   

  1. (1. Institute of Enzyme Engineering, Shaanxi Academy of Sciences, Xi,an 710600, China ;2. Enzyme Engineering Technology Center of Shaanxi, Xi,an 710600, China ;3. Key Laboratory of Resource Biology and Biotechnology in Western China, College of Life Science, Northwest University, Xi,an 710069, China;4. Shaanxi Provincial Institute of Microbiology, Xi,an 710043, China)
  • Online:2012-05-25 Published:2012-05-07

摘要: 建立适用于从毕赤酵母菌中提取外源重组蛋白的超声破碎方法。采用Western Blotting免疫印记技术检测从毕赤酵母菌中提取的外源人脂联素蛋白活性,并以外源人脂联素蛋白活性作为考察指标,采用单因素和L9(33)正交试验设计,对超声破碎条件进行优化。结果表明:在外源人脂联素蛋白活性最高的情况下,超声破碎条件为超声破碎功率450W、时间25min、时间间隔(工作时间:间歇时间)10:10(s/s),此时细胞破碎率为(67.8±2.1)%。若在超声破碎时添加1mmol/L PMSF,虽对细胞破碎率并无显著影响,但外源人脂联素蛋白活性将会明显增高。

关键词: 毕赤酵母, 超声破碎法, 人脂联素蛋白, Western Blotting免疫印记技术

Abstract: In order to establish an appropriate ultrasonic treatment method for the recovery of recombinant protein from Pichia pastoris, the activity of human-adiponectin recombinant protein was evaluated by Western Blotting analysis. A L9(33) orthogonal array design based on single-factor tests was employed to optimize the conditions for ultrasonic treatment. The results showed that the optimal ultrasonic treatment conditions were ultrasonic power of 450 W, ultrasonic treatment time of 25 min and ultrasonic treatment interval of 10 s. Under the optimal ultrasonic treatment conditions, the breaking rate of cell walls was (67.8 ± 2.1)%. The activity of human-adiponectin recombinant protein could be significantly improved by adding 1 mmol/L of PMSF although the addition of PMSF had no effect on breaking rate of cell walls.

Key words: Pichia pastoris, ultrasonication, human-adiponectin protein, Western Blotting analysis

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