Preparation and Characterization of Immobilized Lipase from Pseudomonas Cepacia onto Magnetic Cellulose Nanocrystals

Sci Rep. 2016 Feb 4:6:20420. doi: 10.1038/srep20420.

Abstract

Magnetic cellulose nanocrystals (MCNCs) were prepared and used as an enzyme support for immobilization of Pseudomonas cepacialipase (PCL). PCL was successfully immobilized onto MCNCs (PCL@MCNC) by a precipitation-cross-linking method. The resulting PCL@MCNC with a nanoscale size had high enzyme loading (82.2 mg enzyme/g) and activity recovery (95.9%). Compared with free PCL, PCL@MCNC exhibited significantly enhanced stability and solvent tolerance, due to the increase of enzyme structure rigidity. The observable optimum pH and temperature for PCL@MCNC were higher than those of free PCL. PCL@MCNC manifested relatively higher enzyme-substrate affinity and catalytic efficiency. Moreover, PCL@MCNC was capable of effectively catalyzing asymmetric hydrolysis of ketoprofenethyl ester with high yield of 43.4% and product e.e. of 83.5%. Besides, immobilization allowed PCL@MCNC reuse for at least 6 consecutive cycles retaining over 66% of its initial activity. PCL@MCNC was readily recycled by magnetic forces. Remarkably, the as-prepared nanobiocatalyst PCL@MCNC is promising for biocatalysis.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Bacterial Proteins / chemistry
  • Bacterial Proteins / isolation & purification
  • Bacterial Proteins / metabolism
  • Biocatalysis
  • Cellulose / chemistry
  • Enzyme Stability
  • Enzymes, Immobilized
  • Hydrogen-Ion Concentration
  • Hydrolysis
  • Ketoprofen / metabolism
  • Lipase / chemistry*
  • Lipase / isolation & purification
  • Lipase / metabolism*
  • Magnetite Nanoparticles / chemistry*
  • Pseudomonas / enzymology*
  • Temperature

Substances

  • Bacterial Proteins
  • Enzymes, Immobilized
  • Magnetite Nanoparticles
  • Cellulose
  • Ketoprofen
  • Lipase