In silico screening of 393 mutants facilitates enzyme engineering of amidase activity in CalB

Publikation: Bidrag til tidsskriftTidsskriftartikelForskningfagfællebedømt

  • Martin Robert Hediger
  • Luca De Vico
  • Julie Bille Rannes
  • Christian Jäckel
  • Werner Besenmatter
  • Allan Svendsen
  • Jensen, Jan Halborg
Our previously presented method for high throughput computational screening of mutant activity (Hediger et al., 2012) is benchmarked against experimentally measured amidase activity for 22 mutants of Candida antarctica lipase B (CalB). Using an appropriate cutoff criterion for the computed barriers, the qualitative activity of 15 out of 22 mutants is correctly predicted. The method identifies four of the six most active mutants with ≥3-fold wild type activity and seven out of the eight least active mutants with ≤0.5-fold wild type activity. The method is further used to screen all sterically possible (386) double-, triple- and quadruple-mutants constructed from the most active single mutants. Based on the benchmark test at least 20 new promising mutants are identified.
OriginalsprogEngelsk
Artikelnummere145
TidsskriftPeerJ
Vol/bind1
Antal sider15
DOI
StatusUdgivet - 2013

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