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Directed Evolution of Human Cu,Zn-SOD Under Artificial Oxidant Pressures
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作者 gou xiao jun LI Chun lei +5 位作者 KONG Xiang duo ZHU Shi zhen ZHANG Hong ying WANG xiao ping ZHANG Jin LIU Tian yun 《Chemical Research in Chinese Universities》 SCIE CAS CSCD 2002年第3期294-298,共5页
Cu,Zn SOD is a highly conserved enzyme and the controversy about its evolutionary possibility in the near future has been lively. In order to further our understanding of the future fate of human Cu,Zn SOD, we adopt... Cu,Zn SOD is a highly conserved enzyme and the controversy about its evolutionary possibility in the near future has been lively. In order to further our understanding of the future fate of human Cu,Zn SOD, we adopted a strategy relating to the directed evolution to study how the mutants of human Cu,Zn SOD respond to different oxidative stress. After five rounds of screening, we found a mutant that can survive under harsh pressures and DNA sequencing proves that it shows a mutation responsible for the phenomenon. However, under natural pressure, our screening comes to nothing. Then we may draw the following conclusions: the evolution of biological macromolecules in some respect depends on their surroundings and if they are too familiar with a certain environment, they may embody evolutionary inertia. 展开更多
关键词 Human Cu Zn SOD Directed evolution SCREENING
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Cloning of Promoter of Chinese Bean GRP 1.8 Gene and Characterization of Its Function in Transgenic Tobacco Plants
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作者 LU Hai JIANG Xiang ning +3 位作者 LI Feng lan ZENG Qing yin LIU Wei gou xiao jun 《Chemical Research in Chinese Universities》 SCIE CAS CSCD 2002年第3期290-293,共4页
In order to learn the expression pattern of GRP1 8(glycine rich protein) gene promoter in transgenic plants and to explore its potential application in plant genetic engineering for vascular specific expression of... In order to learn the expression pattern of GRP1 8(glycine rich protein) gene promoter in transgenic plants and to explore its potential application in plant genetic engineering for vascular specific expression of interested genes, GRP 1 8 promoter was amplified by PCR from Chinese bean genomic DNA. The intermediate vector was constructed by inserting vascular specific expression promoter of GRP 1 8 gene in vector pBI 101. The regenerated tobacco plants obtained were analyzed by PCR to select the putative transgenic plants. The histochemical localization of GUS( β D glucosidase) activity indicates that as for that of GRP 1 8 promoter we can confer the vascular specific expression of GUS gene. 展开更多
关键词 Chinese Bean Promoter of GRP 1 8 gene Transgenic tobacco plants
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