
doi: 10.1038/12884
pmid: 10471932
DNA family shuffling of 26 protease genes was used to create a library of chimeric proteases that was screened for four distinct enzymatic properties. Multiple clones were identified that were significantly improved over any of the parental enzymes for each individual property. Family shuffling, also known as molecular breeding, efficiently created all of the combinations of parental properties, producing a great diversity of property combinations in the progeny enzymes. Thus, molecular breeding, like classical breeding, is a powerful tool for recombining existing diversity to tailor biological systems for multiple functional parameters.
Recombination, Genetic, Proteasome Endopeptidase Complex, Hot Temperature, Recombinant Fusion Proteins, Serine Endopeptidases, Hydrogen-Ion Concentration, Protein Engineering, Peptide Fragments, Enzyme Stability, Subtilisins, Selection, Genetic, Gene Library, Peptide Hydrolases
Recombination, Genetic, Proteasome Endopeptidase Complex, Hot Temperature, Recombinant Fusion Proteins, Serine Endopeptidases, Hydrogen-Ion Concentration, Protein Engineering, Peptide Fragments, Enzyme Stability, Subtilisins, Selection, Genetic, Gene Library, Peptide Hydrolases
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