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Directed enzyme evolution: climbing fitness peaks one amino acid at a time

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CURRENT OPINION IN CHEMICAL BIOLOGY
卷 13, 期 1, 页码 3-9

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ELSEVIER SCI LTD
DOI: 10.1016/j.cbpa.2009.01.017

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资金

  1. Ruth M Kirschstein National Research Service [F32 GM076964]
  2. NIH [R01 GM074712-01A1]
  3. Institute for Collaborative Biotechnologies
  4. Jacobs Institute for Molecular Medicine
  5. Department of Energy

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Directed evolution can generate a remarkable range of new enzyme properties. Alternate substrate specificities and reaction selectivities are readily accessible in enzymes from families that are naturally functionally diverse. Activities on new substrates can be obtained by improving variants with broadened specificities or by step-wise evolution through a sequence of more and more challenging substrates. Evolution of highly specific enzymes has been demonstrated, even with positive selection alone. It is apparent that many solutions exist for any given problem, and there are often many paths that lead uphill, one step at a time.

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