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组织工程新材料蜘蛛拖丝蛋白的重组培养
引用本文:章文贤,李敏,涂桂云,黄智华.组织工程新材料蜘蛛拖丝蛋白的重组培养[J].中国组织工程研究与临床康复,2003,7(20):2782-2784.
作者姓名:章文贤  李敏  涂桂云  黄智华
作者单位:福建师范大学生物工程学院生化与分子生物学系,福建省福州市,350007
基金项目:国家教委资助项目(JA02158),福建省自然科学基金重大项目(2001F006)~~
摘    要:目的通过对重组蜘蛛拖丝蛋白基因工程菌pNS2生长的培养基进行优化,为获取大量蜘蛛拖丝蛋白提供条件。方法采用单因子试验和正交试验对培养基进行优化。结果获得优化的培养基组成:葡萄糖5.0g/L、蛋白胨5.0g/L、磷酸二氢钾(KH2PO4)15.0g/L、微量元素母液15.0g/L、硫酸镁(MgSO4)0.8g/L、柠檬酸1.7g/L。培养基优化后,工程菌的生长量提高了60.6%。结论优化的培养基为基因工程菌pNS2大规模生产蜘蛛拖丝蛋白奠定了基础。

关 键 词:生物医学工程  生物相容性材料  培养基  正交试验
文章编号:1671-5926(2003)20-2782-03
修稿时间:2003年3月4日

Recombinant culture of spider dragline silk protein as a new tissue engineering material
Wen-Xian Zhang,Min Li,Gui-Yun Tu,Zhi-Hua Huang,Coll ege of Bioengi-neering,Fujian Normal University,Fuzhou ,Fujian P rovince,Chi na.Recombinant culture of spider dragline silk protein as a new tissue engineering material[J].Journal of Clinical Rehabilitative Tissue Engineering Research,2003,7(20):2782-2784.
Authors:Wen-Xian Zhang  Min Li  Gui-Yun Tu  Zhi-Hua Huang  Coll ege of Bioengi-neering  Fujian Normal University  Fuzhou  Fujian P rovince  Chi na
Institution:Wen-Xian Zhang,Min Li,Gui-Yun Tu,Zhi-Hua Huang,Coll ege of Bioengi-neering,Fujian Normal University,Fuzhou 350007,Fujian P rovince,Chi na
Abstract:Aim To optimize the medium for the growth of genetic e n -gineering Escherichia coli pNS2,pr oviding a nice condition for the mass cul ture of spider dragline silk proteins.Methods The single-factor experi-ments and the orthogonal experiment s were adopted to opitimize the medi-ums.Result s The optimized culture medium consis ted of 5.0g /L Glucose,5.0g /L Pe ptone,15.0g /L KH 2 PO 4 ,15.0g /L Trance elements storeso-lution,0.8g /L MgSO 4 ,1.7g /L Citric acid.The growth of en gineering bacteria increased 6 0.6%in the optimized culture.Conclusion The opti-mized culture medium is u sed for genetic engineering Escherichia coli pN S2to produce the recombinant sp ider dr agline silk protein in a large scale.
Keywords:biomedical engin eering  biocompatible materials  cul-ture media  orthogonal test  
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