Chemical synthesis and cloning of human Β-endorphin gene inEscherichia coli
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Abstract
Total synthesis of human Β-endorphin gene has been designed for the expression in bacterial system. Eight individual oligonucleotides corresponding to the Β-endorphin gene were chemically synthesized and joined through the enzyme-catalyzed reaction. The final yield of the 111-nucleotide-long synthetic Β-endorphin gene construct was about 10% of the total oligonucleotide used. The synthetic human Β-endorphin gene was cloned into the bacteriumEscherichia coli, using pUC8 vector and shown to have the correct nucleotide sequences as designed.
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Β-endorphin human gene oligonucleotide synthesis recombinant DNA Escherichia coliPreview
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© Humana Press Inc. 1995