Abstract
A pair of proper primers were designed and synthesized for Polymerase Chain Reaction (PCR) of anti-bacterial gene aiiA which encodes protein aiiA from marine bacterial genome, according to the gene sequences of aiiA. The plasmid pMD18-ZD02aiiA was constructed after PCR testing of aiiA gene. The gene sequence of aiiA was amplified with proper primers (with active locations by enzymes BamHIand EcoRI) from molding board of pMD18-ZD02aiiA and linked into expression vector pET-17b after it was hydrolyzed by enzymes of BamHI and EcoRI. And then plasmids pET-ZD02aiiA was constructed. The results of hydrolyzation of enzymes, PCR amplification and sequencing demonstrated that the target gene fragments were inserted into vector pET-17b correctly, the sequences of gene aiiA and frame of reading codes were right. Thus, it may provide base for the recombinant express and induced express of anti-bacterial gene from marine bacterium.
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Acknowledgments
This work was supported by grants from Science and Technology Plan Project of Guangdong Province (2009B020311003), Science and Technology Plan Project of Jiangsu Province (BN2010038), Special Scientific Research Funds for Central Non-profit Institutes, Chinese Academy of Fishery Sciences (2010TS01), Production, Learning and Research Project of Guangdong Province (2011B090400151).
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Ding, X., Yin, B., Zhang, S., Tang, W., Sun, W., Zhou, S. (2013). Construction of Recombinant Expression Vector of Anti-Bacterial Gene aiiA from Marine Bacterium. In: Du, W. (eds) Informatics and Management Science V. Lecture Notes in Electrical Engineering, vol 208. Springer, London. https://doi.org/10.1007/978-1-4471-4796-1_28
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DOI: https://doi.org/10.1007/978-1-4471-4796-1_28
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