Improved activity and thermostability of Bacillus pumilus lipase by directed evolution

  • Akbulut N
  • Tuzlakoĝlu Öztürk M
  • Pijning T
 et al. 
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Abstract

To improve enzymatic activity of Bacillus pumilus lipases, DNA shuffling was applied to two lipase genes from local B. pumilus isolates. Using a high-throughput activity assay, the mutant with highest activity was selected. This chimeric mutant (L3-3), carrying two crossover positions and three point mutations, has a specific activity 6.4 and 8.2 times higher than the two parent enzymes. The mutant also is more tolerant to various detergents and organic solvents, and has a 9 times longer half-life at 50. °C. Homology modeling of mutant L3-3, based on the highly homologous B. subtilis lipase A, shows that the increased thermostability is likely due to structural rigidification and reduced surface hydrophobicity. Increased specific activity may result from the location of mutations close to the active site. Together, our results show that it is possible to evolve, by DNA shuffling, B. pumilus lipase variants with improved applicability as biocatalysts, even if the two parent enzymes are highly similar. © 2013 Elsevier B.V.

Author-supplied keywords

  • 3D homology model
  • Bacillus pumilus lipase
  • Biocatalyst
  • DNA shuffling
  • Directed evolution
  • Thermostability

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Authors

  • Tjaard PijningGroningen University Faculty of Science and Engineering

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  • Nagihan Akbulut

  • Merve Tuzlakoĝlu Öztürk

  • Saliha Işsever Öztürk

  • Füsun Gümüşel

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