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碱性果胶酶在重组毕赤酵母中高效表达的关键因素研究
引用本文:王 芸,华兆哲,刘立明,堵国成,陈 坚. 碱性果胶酶在重组毕赤酵母中高效表达的关键因素研究[J]. 微生物学通报, 2008, 35(3): 0341-0345
作者姓名:王 芸  华兆哲  刘立明  堵国成  陈 坚
作者单位:1. 江南大学工业生物技术教育部重点实验室,无锡,214122
2. 江南大学工业生物技术教育部重点实验室,无锡,214122;江南大学食品科学技术国家重点实验室,无锡,214122
基金项目:国家重点基础研究发展计划(973计划);国家自然科学基金
摘    要:为提高重组毕赤酵母生产碱性果胶酶的产量和生产强度,在摇瓶条件下优化了重组毕赤酵母生产碱性果胶酶的关键因素。结果表明,以下条件:初始甘油浓度40g/L、初始甲醇浓度3.1g甲醇/gDCW、每24h添加0.51g甲醇/gDCW、诱导表达周期72h、250mL三角瓶诱导培养基装液量30mL、初始pH6,0,最适于菌体生长与产物表达。在此基础上,7L罐上通过恒速流加甘油进一步提高细胞密度,诱导阶段甲醇采取前期恒速流加和后期DO-stat,发酵结束菌体干重达80g/L,酶活为217U/mL,比摇瓶结果提高了66.2%。

关 键 词:碱性果胶酶  重组毕赤酵母  高效表达  甲醇诱导
修稿时间:2007-08-11

Key Factors of High-level Production of Polygalacturonate Lyase in Recombinant Pichia pastoris
WANG Yun,HUA Zhao-Zhe,LIU Li-Ming,DU Guo-Cheng and CHEN Jian. Key Factors of High-level Production of Polygalacturonate Lyase in Recombinant Pichia pastoris[J]. Microbiology China, 2008, 35(3): 0341-0345
Authors:WANG Yun  HUA Zhao-Zhe  LIU Li-Ming  DU Guo-Cheng  CHEN Jian
Affiliation:Key Laboratory of Industrial Biotechnology, Ministry of Education, Jiangnan University, Wuxi 214122;Key Laboratory of Industrial Biotechnology, Ministry of Education, Jiangnan University, Wuxi 214122;Key Laboratory of Industrial Biotechnology, Ministry of Education, Jiangnan University, Wuxi 214122;Key Laboratory of Industrial Biotechnology, Ministry of Education, Jiangnan University, Wuxi 214122;(1. Key Laboratory of Industrial Biotechnology, Ministry of Education, Jiangnan University, Wuxi 214122)(2. State Key Laboratory of Food Science and Technology, Jiangnan University, Wuxi 214122)
Abstract:The key factors on high-level polygalacturonate lyase (PGL) production in recombinant Pichia pastoris were investigated. In 250 mL shake flask, the optimal glycerol concentration, initial methanol concentration, methanol supplementation quantity, duration of induction, initial pH, medium volume were 40 g/L, 3.1 g Methanol/g DCW, 0.51 g Methanol/g DCW (in every 24 h), 72 h, pH6.0 and 30 mL, respectively. In 7 L fermentor, constant glycerol feeding, constant and DO-stat methanol feeding strategies were applied to enhance cell density and PGL production. Finally, the dry cell weight was 80 g/L, and the maximum yield of PGL was achieved to 217 U/mL, increased by 66.2% than that of flask level.
Keywords:Polygalacturonate lyase   Recombinant Pichia pastoris   High-level expression   Methanol induction
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