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基于遗传算法的光合细菌过氧化物酶电泳分析方法的建立
引用本文:牛红军,李飞莹,仇丽霞,杨官娥.基于遗传算法的光合细菌过氧化物酶电泳分析方法的建立[J].微生物学通报,2010,37(3):0465-0471.
作者姓名:牛红军  李飞莹  仇丽霞  杨官娥
作者单位:1. 山西医科大学药学院,山西,太原,030001
2. 山西医科大学卫生统计学教研室,山西,太原,030001
基金项目:国家自然科学基金项目(No. 30672621); 山西省自然科学基金项目(No. 2006011099); 山西省科技攻关项目(No. 051081); 山西医科大学博士启动基金项目(No. 03200811); 山西医科大学学生创新项目(No. 2009146)
摘    要:建立光合细菌中过氧化物酶的酸性聚丙烯酰胺凝胶电泳(A-PAGE)分析方法。以电泳图谱的谱带数和灰度为指标, 运用正交试验和遗传算法对该方法的电泳条件进行优化。实验结果表明, 当凝胶中Triton X-100含量为0.31%、菌体破碎时间为19 min、样品中Triton X-100含量为0.79%时, 可获得清晰的沼泽红假单胞菌过氧化物酶图谱; 当凝胶中Triton X-100含量为0.27%、菌体破碎时间为16 min、样品中Triton X-100含量为0.76%时, 可获得清晰的球形红细菌过氧化物酶图谱。本方法为光合细菌中过氧化物酶的分析提供了一种新的、简单、快速的手段。

关 键 词:光合细菌    过氧化物酶同工酶    聚丙烯酰胺凝胶电泳    遗传算法

Establishment of Gel Electrophoresis for the Analysis of Peroxidases in Photosynthetic Bacteria Based on Genetic Algorithm
NIU Hong-Jun,LI Fei-Ying,QIU Li-Xia and YANG Guan-E.Establishment of Gel Electrophoresis for the Analysis of Peroxidases in Photosynthetic Bacteria Based on Genetic Algorithm[J].Microbiology,2010,37(3):0465-0471.
Authors:NIU Hong-Jun  LI Fei-Ying  QIU Li-Xia and YANG Guan-E
Institution:1. School of Pharmaceutical Science, Shanxi Medical University, Taiyuan, Shanxi 030001, China;2. Department of Health Statistic, Shanxi Medical University, Taiyuan, Shanxi 030001, China;2. Department of Health Statistic, Shanxi Medical University, Taiyuan, Shanxi 030001, China;1. School of Pharmaceutical Science, Shanxi Medical University, Taiyuan, Shanxi 030001, China
Abstract:To establish the acid polyacrylamide gel electrophoresis (A-PAGE) analyzing method of peroxidase isoenzymes in photosynthetic bacteria. According to the number and the grey scale of bands, the conditions of the A-PAGE were optimized by the orthogonal design and the genetic algorithm. The results indicated that when the Triton X-100 concentration in the gels was 0.31%, the ultrasonic time was 19 min, the Triton X-100 concentration in the samples was 0.79%, the clear peroxidase isoenzyme zymograms of Rhodopseudomonas palustris were obtained, when the Triton X-100 concentration in the gels was 0.27%, the ultrasonic time was 16 min, the Triton X-100 concentration in the samples was 0.76%, the clear peroxidase isoenzyme zymograms of Rhodobacter sphaeroides were obtained. The paper set up a simple and rapid method for the analysis of peroxidase isoenzymes in photosynthetic bacteria.
Keywords:Photosynthetic bacteria  Peroxidase isoenzymes  Polyacrylamide gel electrophoresis  Genetic algorithm
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