利用大肠杆菌工程菌生产2,3-二磷酸甘油酸的研究  

Study on production of 2,3-BPG with recombinant E.coli strain

作　　者：黄晚[1] 郑茂发[1] 黄伟达[1] 

机构地区：[1]复旦大学生物化学与分子生物学系,上海200433

出　　处：《东北师大学报（自然科学版）》2010年第3期150-155,共6页Journal of Northeast Normal University(Natural Science Edition)

基　　金：国家自然科学基金资助项目(30873153)

摘　　要：通过基因工程的方法,将表达人源BPGM(bisphosphoglycerate mutase二磷酸甘油酸变位酶,E.C.2.7.5.4.)的质粒转化入大肠杆菌内,并进行培养条件的优化摸索,通过向培养基内加入葡萄糖使大肠杆菌大量发酵生产2,3-BPG(2,3-bisphosphoglycerate,2,3-二磷酸甘油酸).结果表明,当培养基中葡萄糖质量浓度为10 g/L,诱导时间为4 h,大肠杆菌工程菌表达的2,3-BPG含量最高.如果诱导后加入终质量分数为0.5%的Tween 80可以有效促进2,3-BPG分泌到培养基中.诱导后4 h添加新培养基,补加葡萄糖可以使2,3-BPG的产量提高1倍,达到7.5 mmol/L.2,3-BPG（2,3-bisphosphoglycerate）is one of the intermediate products in glycolytic pathway,which catalyzes by an enzyme named BPGM（bisphosphoglycerate mutase E.C.2.7.5.4）.The BPGM only exists in erythrocyte.In this paper,used recombinant E.coli strain to express BPGM in the cell,with input of glucose into the LB to induce the production of 2,3-BPG.Used malachite green method for determination of inorganic phosphate to detect 2,3-BPG.The results showed that,when the concentration of glucose is 10 g/L,and the induce time is 4 hours,it reached the highest productivity of 2,3-BPG,approximately at a level of 3.75 mmol/L.In the mean while,with the input Tween 80 to the final concentration at 0.5% can promote the 2,3-BPG to come out of the E.coli into the LB.

关 键 词：2 3-二磷酸甘油酸 二磷酸甘油酸变位酶 糖酵解 

分 类 号：Q789[生物学—分子生物学]