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作 者:吴益民[1] 王洪军[1] 孙艳[2] 吴琼[3] 冯立[1] 张志强[1] 杨青[1] 杨国平[1]
机构地区:[1]沈阳军区疾病预防控制中心,沈阳110034 [2]沈阳药科大学,沈阳110016 [3]吉林大学药学院,长春130012
出 处:《中国抗生素杂志》2007年第10期599-601,614,共4页Chinese Journal of Antibiotics
基 金:辽宁省教育厅青年人才基金资助课题(No.05L433)
摘 要:目的利用已含有血红蛋白基因(vgb)的红色糖多孢基因工程重组菌,探讨vgb表达产物对重组糖多孢红霉菌提高红霉素产率的影响。方法用SDS-PAGE、Western blot方法鉴定血红蛋白,用葡萄糖浓度与总蛋白质含量比较原始菌株与重组菌株的差别。结果红色糖多孢基因工程重组菌与原始菌株比较,重组菌株发酵过程葡萄糖浓度的变化出现在第二时段(约38h),原始菌株达到了0.4g/L,而重组菌株只有0.25g/L;第三时段原始菌株出现了游离葡萄糖浓度高峰而重组菌株未出现。在两个菌株中生物物质浓度[以总蛋白质(g/L)表示]存在不同,重组菌株比原始菌株约低27%。红霉素效价,原始菌株和重组菌株分别为3.98和5.15g/L,相当于重组菌株提高红霉素体积产率约29%。结论重组红色糖多孢菌表达了透明颤菌血红蛋白,提高了红霉素产率,对解决抗生素工业和基因工程菌高密度发酵有良好的应用前景。Objective To study the exprssion of Vitreoscilla hemoglobin gene (vgb) in the Saccharopoblyspoura erythraea and its effect on erythromycin production. Method A vgb gene was integrated into the chromosomal DNA of Sac. erythraea by electrotransformation and the recombinant Sac. erythraea was obtained. The VHb was identified with SDS-PAGE and Western blotting method. Glucose concentrations and total protein content in original Sac. erythraea and recombinant strain fermentation processes were determined and compared with auto-biochemical assay. The erythromycin titers were tested with cylinder plate method. Results At the second stage of fermentation, glucose concentration of original strain reached 0.4g/L at about 38h and that of recombinant strain was 0.25g/L ; at the third stage, a glucose concentration peak appeared in original strain while none did in recombinant. The total protein content of recombinant was lower than that of original strain by 27%. The titres of erythromycin in original strain and recombinant were 3.98 and 5.15g/L, respectively, i.e. the the erythromycin production of recombinant was increased by 29% compared with that of original strain. Conclusion vgb gene was expressed in recombinant Sac. erythraea, which increased erythromycin production and showed a bright application prospect of antibiotic-gene engineering strain.
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