中性内切型纤维素酶在毕赤酵母中高水平表达的研究  

High-level Production of Neutral Endoglucanase 1 in Pichia pastoris

作　　者：丁少军[1] 宋美静[1] 杨红军[1] 邢增涛[2] 周蕊[1] 曹杰[1] 

机构地区：[1]南京林业大学生物工程系,南京210037 [2]上海农业科学院食用菌研究所,上海201106

出　　处：《生物工程学报》2006年第1期71-76,共6页Chinese Journal of Biotechnology

基　　金：国家自然科学基金资助项目(No.30271058);校高层次留学回国人才引进基金项目~~

摘　　要：中性内切型纤维素酶在纺织及造纸工业具有重要的应用,为了进一步提高从我国草菇中克隆的一种新的中性内切型纤维素酶(EG1)在Pichiapastoris中的表达水平,我们进行了提高基因拷贝数及高密度发酵等多种手段实现其高水平表达的研究。在前期研究的基础上,利用对已整合eg1的重组子再转化的方法,从含有2000μgLZeocin的YPDSZ平板上筛选到高抗Zeocin转化子,在摇瓶培养条件下,该转化子表达量比原来提高了3.8倍,在pH4～8条件下均有稳定表达,接种量(OD600=5.0)表达水平最好,提高甲醇的诱导浓度对表达有显著的促进作用。用3.2L发酵罐进行了高密度发酵,甲醇诱导95.5h后达到最高值,比摇瓶培养再提高了6.4倍,因此利用高抗Zeocin转化子及高密度发酵的手段,使EG1的表达水平提高了34倍,蛋白表达量达8.80mgmL,EG1酶活达到543.36IUmL,实现了中性内切纤维素酶的高水平表达,本研究将大大促进建立我国纺织用纤维素酶大规模高效生产技术。The gene（eg1） encoding for novel endoglueanase 1 was cloned previously from Chinese straw mushroom Volvariella volvacea. EG1 has high thermal stability and optimal pH at neutral and shows great potential in textile and paper industry applications. To improve the expression level of EG1 in Pichia pastoris, the increasing copy number of clone, and its high cell density fermentation in 3.2L fermenter for its high-level expression were investigated in this work. By electro-transformation of pPICZaB-egl into GS115EG11 integrated with single copy of egl gene, A resistant transformant with 3.8 times higher level expression than GS115EG11 was screened from YPDSZ plate containing 2000p.g/mL of Zeocin. The effect of initial cell density, pH and methanol on its expression and biomass accumulation was evaluated in shaking culture. Optimal EG1 production was observed when initial cell density 0D6oo was 5.0. EG1 production and biomass accumulation did not seem to vary when cells were induced at different pH values. Both of EG1 and cell density were found to increase with higher methanol concentrations, reaching 62.48 IU/mL and 31.7 （ OD600 ） respectively after 120 h induction with 2.0% （ V/V） methanol compared to 30.24 IU/mL and 17.79 （ OD600 ） with 0.25% methanol induction. EG1 expression was further increased by 6.4 times higher than shaking culture after 95.5 hours induction with methanol in fed-batch fermentation, so totally 34 times higher than that for GS115EG11 was achieved by screening of high Zeocin resistant clone and high cell density fermentation. The production of EG1 with 543.36IU/mL CMC activity and 8.80mg/mL protein expression was obtained in Pichia pastoris.

关 键 词：中性内切型纤维素酶 毕赤酵母 高水平表达 

分 类 号：Q786[生物学—分子生物学]