2010
DOI: 10.1016/j.biortech.2010.06.115
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Magnetic mesoporous silica nanoparticles: Fabrication and their laccase immobilization performance

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Cited by 183 publications
(86 citation statements)
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“…This may have been caused by restricted mobility of the bound enzyme and reduced accessibility of the substrate to the active site. Similar higher K m for immobilized enzyme has been reported for silica immobilized laccase [34]. The K m for b-glucosidase immobilized on Eupergit C was ten times higher than that of the free enzyme [35].…”
Section: Kinetic Characterization Of the Immobilized Proteasesupporting
confidence: 79%
“…This may have been caused by restricted mobility of the bound enzyme and reduced accessibility of the substrate to the active site. Similar higher K m for immobilized enzyme has been reported for silica immobilized laccase [34]. The K m for b-glucosidase immobilized on Eupergit C was ten times higher than that of the free enzyme [35].…”
Section: Kinetic Characterization Of the Immobilized Proteasesupporting
confidence: 79%
“…Silica nanoparticles are attractive candidates as inorganic, nanoscale (less than or equal to 100 nm in diameter) materials that have received considerable attention in recent years, particularly in medicine, due to their inert, biocompatible, biodegradable, thermally and chemically stable properties [1][2][3][4] as well as their inexpensive synthesis [5]. In particular, mesoporous silica nanoparticles (MSNPs) have received interest as carriers for many applications, including pharmaceutical drug delivery, gene therapy, enzyme immobilization, catalytic chemistry, ion exchange, biosensing and bioimaging [6][7][8][9][10][11][12]. Furthermore, the ordered pore network, high pore volume and surface area, and silanol-containing surface [13] as well as the biodegradation of silica in the natural environment into relatively harmless silicic acid by-products make this an attractive proposition.…”
Section: Introductionmentioning
confidence: 99%
“…The solution to this problem is to use immobilized enzymes that are more stable and therefore reusable. Enzyme immobilization, especially for decolorization of azo dyes, has been introduced using some polymeric carriers including polyamide 6,6 fibers , alginate/ gelatin blend with PEG (Ping et al 2008), porous poly (GMA/EGDMA) (Arica et al 2009), and silica (Wang et al 2010). However, some of these polymers have low mechanical strength, durability, and/or high cost.…”
Section: Introductionmentioning
confidence: 99%