4.7 Article

Lipase bound cellulose nanofibrous membrane via Cibacron Blue F3GA affinity ligand

Journal

JOURNAL OF MEMBRANE SCIENCE
Volume 330, Issue 1-2, Pages 288-296

Publisher

ELSEVIER SCIENCE BV
DOI: 10.1016/j.memsci.2008.12.064

Keywords

Cellulose; Nanofibrous; Lipase enzyme; Affinity membranes; Cibacron Blue F3GA

Funding

  1. National Textile Center [M02-CD05]
  2. Jastro-Shields Graduate Research at the University of California, Davis

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Cellulose (Cell) nanofibrous membranes were prepared by nucleophilic reaction of the cellulose hydroxyl with the triazinyl chloride of Cibacron Blue F3GA (CB) ligand and studied as affinity membranes for lipase enzyme. Cell nanofibrous membranes containing fibers with 200 nm average diameters were prepared by electrospinning of cellulose acetate (CA). followed by alkaline hydrolysis. The CB capacity of the Cell nanofibrous membranes was optimized by lengthening the nucleophilic reaction time and increasing CB concentration and ionic strength. The equilibrium adsorption isotherms of CB on the Cell nanofibrous membranes followed a typical Langmuir monolayer adsorption behavior. At 242 mg CB/g of Cell, the maximum lipase adsorption capacity (q(m)) and the dissociation constant (K-d) values were 41.02 mg/g and 0.25 mg/mL, respectively. Optimal lipase adsorption capacity was obtained at pH 4.0, its isoelectric point, with added NaCl on Cell membranes 86 mg CB capacity per g of Cell. A facile lipase loading capacity of 16.21 mg/g of CB-Cell was achieved under moderated conditions and could be optimized to reach at least 150 mg/g. The CB-Cell bound lipase had similar catalytic rate and retained 86.2% activity as in its free form. These findings clearly show that the CB bound Cell nanofibrous membrane is a highly efficient ultra-high specific porous support for lipase enzyme and is potentially versatile for immobilizing other enzymes and as affinity membrane for proteins. (C) 2009 Elsevier B.V. All rights reserved.

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