rhKPI/AβPP大规模发酵及纯化工艺  

Large scale fermentation process and purification for rhKPI/AβPP in Pichia pastoris

作　　者：贺巾超[1] 杨莉莉[1] 马杰[1] 颜波群[2] 韩树海[1] 侯立中[1] 颜炜群[1] 

机构地区：[1]吉林大学再生医学科学研究所生物化学研究室,吉林长春130021 [2]吉林大学第四医院消化内科,吉林长春130011

出　　处：《吉林大学学报（医学版）》2006年第2期278-281,共4页Journal of Jilin University：Medicine Edition

基　　金：国家高技术研究发展计划(863计划)资助课题(2004AA205020)

摘　　要：目的：在毕赤酵母（Pichia pastoris）中高效表达AβPP中的Kunitz型蛋白酶抑制剂的结构域（KPI／AβPP），利用80L的发酵罐优化发酵条件，制备rhKPI／AβSPP。方法：克隆kpi基因插入到pPICZα，构建真核表达载体pPICZμ-kpi，经核酸测序确证后，电转化毕赤酵母菌株X-33，筛选高表达rhKPI／AβPP工程菌。结果：筛选出的高表达工程菌采用80L发酵罐甲醇诱导补料批式发酵，在pH3．3、纯氧浓度22％～30％、罐内压力为12psi、甲醇诱导60h时产量1．0g·L^-1。纯化的rhKPI／AβPP经SDS-PAGE分析显示单一区带，相对分子质量6750。质谱测定其相对分子质量为6750，抑制胰蛋白酶的比活性为8．4EPU·mg^-1。结论：克隆、构建、筛选出高效表达rhKPI／AβPP的毕赤酵母工程菌，并建立了稳定的发酵和纯化工艺。Objective To study the efficient expression of a Kunitz-type protease inhibitor （KPI） domain of the Alzheimer＇s disease related to amyloid β-protein precursor, and produce rhKPI/AβPP by optimizing fermentation papameters on large scale using Pichia pastoris as host system. Methods KPI/AβPP gene was inserted into expression vector pPICZa and the resulted recombinant vector was transformed into the Pichia pastoris. Then KPI/AβPP was expressed in 80L fermentor with optimizing parameters and the broth was harvested and purified with SP Sepharose. Results KPI/AβPP gene could be induced by methanol and expressed with the maximal yield of 1.0 g · L^-1. The expressed product was purified from the fermentating culture. Analytic results revealed that resulted product with relative molecular mass of about 6 750 inhibited the serine protease activities. Conclusion rhKPI/AβPP can be expressed in Pichia pastoris on large scale. A stable fermentation and purification technology is successfully set up.

关 键 词：rhKPI/AβPP 毕赤酵母 发酵 

分 类 号：Q78[生物学—分子生物学]