International Journal of Biological Macromolecules 51 (2012) 18–24
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International Journal of Biological Macromolecules
jo u rn al hom epa ge: www.elsevier.com/locate/ijbiomac
Modification and characterization of cellulosic cotton fibers for efficient
immobilization of urease
M. Monier
∗
, A.M.A. El-Sokkary
Chemistry Department, Faculty of Science, Mansoura University, Mansoura, Egypt
a r t i c l e i n f o
Article history:
Received 10 April 2012
Accepted 19 April 2012
Available online 26 April 2012
Keywords:
Cotton
Grafting
Urease
Acrylonitrile
a b s t r a c t
Cotton fibers were first grafted by polyacrylonitril in the presence of KMnO
4
and oxalic acid as a combined
redox initiator. Moreover, modification of the grafted cotton fibers was done by changing the nitrile
group ( CN) into hydrazidine group through the reaction with hydrazine hydrate, then the fibers were
activated by glutaraldehyde to introduce free aldehyde groups which were able to react with amino
groups of urease to form Schiff’s base, and result in cotton fibers immobilized urease. The efficiency of
the immobilization was evaluated by examining the relative enzymatic activity of enzyme before and
after the immobilization of urease. The results showed that the optimum temperature of immobilized
urease was 35
◦
C, which was higher than that of the free enzyme (30
◦
C), and the immobilized urease
exhibited a higher relative activity than that of free urease over 35
◦
C. The optimal pH for immobilized
urease was 6.5, which was lower than that of the free urease (pH 7.0), and the immobilization resulted
in stabilization of enzyme over a wider pH range. The kinetic constant value (K
m
) of immobilized urease
was higher than that of the free urease. However, the thermal and operational stabilities of immobilized
urease have been improved greatly.
© 2012 Elsevier B.V. All rights reserved.
1. Introduction
Cellulose is the most abundant natural, polysaccharide in the
world. It has been used as a material for centuries in all types of
practical uses. Social concerns for sustainable green products are
encouraging the efficient exploitation of cellulose [1].
Cellulosic cotton fibers are generally strong, with high mechani-
cal properties. In addition, they are also hydrophilic, but insoluble in
water, stable to chemicals, non-toxic to living bodies, reproducible,
recyclable and biocompatible. With these specific and promising
characteristics of cotton, modification techniques to promote these
original properties or to add new functionalities to cellulose have
been studied. Chemical modifications have been positioned at the
center of the field of cellulose modification [2,3].
Chemical treatment of cellulose materials using oxidizing
agents is quite a frequent technique in cellulose chemistry aim-
ing to functionalize cellulose with some active functional groups.
During the oxidation of cellulose, aldehyde, ketone and carboxyl
groups may be formed in the cellulose, depending on the nature
of the oxidizing agent and the conditions of oxidation. Most
oxidations proceed with low selectivity. Oxidations reactions of
∗
Corresponding author. Tel.: +20 10 03975988.
E-mail address: monierchem@yahoo.com (M. Monier).
cellulose with periodate were carried out with a high selectiv-
ity [4–10]. This reaction takes place between C
2
–C
3
bond of the
glucopyranoside ring and leads to the formation of two aldehyde
groups at C
2
and C
3
positions; the resulting compound is the dialde-
hyde cellulose (DAC).
Another type of important chemical modification has been
extensively studied many years ago which is grafting of different
vinyl monomers onto polysaccharides with the aim of obtaining
different functional products. Composite is a term given to the
products of graft copolymerization reaction of polysaccharide and
vinyl monomer in the presence of initiator [11–15].
These graft copolymerization reactions have been carried out by
different initiation techniques such as gamma irradiation [16–19]
and chemical initiation [20].
Modifications of cellulose and its derivatives through graft
copolymerization of different vinyl monomers gives new materials
for composite membranes [20,11] metal ion sorption and enzyme
immobilization [12].
Urease which catalyzes the degradation of urea to ammonia and
carbon dioxide, has been used in an immobilized form in kidney
machines for blood detoxification. According to one report approx-
imately half a million patients worldwide are being supported by
hemodialysis [21]. Urease occupies a unique place in enzymology in
that it has been the first enzyme to be crystallized. Its immobilized
form has found broad applications, such as blood detoxification in
0141-8130/$ – see front matter © 2012 Elsevier B.V. All rights reserved.
http://dx.doi.org/10.1016/j.ijbiomac.2012.04.019