Performance of Chitosan/Glycerol Phosphate Hydrogel as a Support for Lipase Immobilization

Abstract

A biocompatible and biodegradable hybrid chitosan/glycerol phosphate hydrogel (CS-GP) was prepared and evaluated as support for enzyme immobilization. In this work a lipase sn-1,3 specific from Rhizopus oryzae was physically immobilized in CS-GP by adsorption (PA) and in CS-GP modified chemically with glutaraldehyde (CS-GP-GA) by covalent attachment (CA). The matrices (pure and chemically modified) and immobilized lipases were characterized by scanning electron microscopy (SEM), Fourier Transform Infrared Spectroscopy (FTIR) and thermogravimetric (TG) analysis. Moreover, a comparative study between free and immobilized lipase was provided in terms of pH, temperature, kinetic parameters and thermal stability. The catalytic properties of biocatalysts were assayed in olive oil hydrolysis. The maximum activities were found at 60◦C/pH 8.5 and 50◦C/pH 7.5 for lipase immobilized by PA and CA, respectively. Both immobilization process turned biocatalysts highly active, since they were stable for 120 days at low (-10◦C) temperatures and around 2-fold more stable than free lipase at 60◦C (high temperature). Thus, results revealed the potential application of chitosan/glycerol phosphate hydrogel (CS-GP) as matrix for lipase immobilization. Nevertheless, better performance was achieved when the lipase was immobilized by covalent attachment.

Keywords:
lipase; immobilization; chitosan; glycerol phosphate; hydrogel

1. Introduction

Hydrogels are three-dimensional polymeric structures able to absorb large quantities of water or biological fluids. Based on this, hydrogels are often classified into three categories depending on the nature of their network, namely entangled networks, covalently crosslinked networks and networks formed by secondary interactions. According to the literature, chitosan is one of the main compounds used in the synthesis of hydrogels¹. The development of chitosan hydrogel has been an area drawing intensive investigation and a large number of works have been reported on chitosan hydrogel and its potential use in various applications^2-6. The biochemical properties and the three-dimensional networks of chitosan hydrogel offer them wide applications in biomedical field including local drug delivery and tissue engineering⁷.

Several polymers have been used to prepare chitosan hybrid hydrogels, such as gelatin, collagen, carrageenan, alginate, polyvinyl alcohol (PVA), and carboxy-methyl-cellulose (CMC). The polyelectrolyte complexes of chitosan are formed with the purpose of obtaining more versatile hydrogels with different chemical and physical structures, which can improve your performance in specific industrial applications, such as medical and pharmaceutical^1,8. Among of the chitosan hybrid hydrogels, chitosan/glycerol phosphate hydrogel has received strong interest in medical and pharmaceuticals applications⁷. In recent years, chitosan/GP gels have already been used for repairing cartilage, bone and nerves; and also, functioned as injectable vehicles for delivering different drugs or bioactive molecules⁹. Glycerol phosphate is an organic compound naturally found in the body has been used as a catalyst to cause a sol-to-gel transition in chitosan solutions at physiological pH and temperature⁷.

The interest in modifying chitosan using different activation agents, and the use of polyelectrolyte complexes, have arisen recently mostly for applications in the field of enzyme immobilization. In recent time, various natural polymers, such as chitosan, have received great importance for immobilization which having excellent properties like biodegradability, eco-friendliness and biocompatibility for biomolecules¹⁰.

Immobilization of enzymes plays an import role within applied biotechnology. The main reason for immobilizing enzymes is the ability to isolate the biocatalyst from the reaction product and reuse it in order to increase productivity^11,12. Among the available enzymes, lipases (triacylglycerol alkyl hydrolases, EC 3.1.1.3) are versatile biocatalysts used in several industrial processes under aqueous or organic media. Thus, lipase immobilization has been widely studied, mainly due to its industrial importance¹³.

In this context, this work investigates the biocompatible of chitosan/glycerol phosphate hydrogel (CS-GP) to immobilize a commercial food grade lipase sn-1,3 specific from Rhizopus oryzae. This lipase was chosen based on its potential previously identified to synthesize important products, such as structured lipids¹⁴. The lipase was immobilized on CS-GP by physical adsorption (PA) and covalent attachment (CA). The properties of both CS-GP support and immobilized derivatives were evaluated by Scanning electron microscopy (SEM), Fourier transform infrared spectroscopy (FTIR) and termogravimetry (TG). The influence of the temperature and pH on the biocatalyst activities was assessed by surface response methodology. Under the established conditions, the kinetic parameters and thermal stability of the immobilized derivatives were also determined and compared with those attained by the free lipase. To our knowledge, this is the first report of the use of chitosan/glycerol phosphate hydrogel as support for immobilizing microbial lipase.

2. Materials and Methods

A commercial food grade lipase from Rhizopus oryzae (L036P, Biocatalysts,Cardiff, England) in a crude form was used without further purification. High molecular weight chitosan (degree of deacetylation above 75%) and glycerol phosphate disodium salt were purchased from Sigma-Aldrich (St. Louis-USA). Glutaraldehyde 25% was used as cross-linker. Commercial olive oil with acidity of 0.5% (Carbonell^®) was purchased in a local market and used for hydrolytic activity experiments. Arabic gum was purchased from Synth/Brazil.

2.1. Preparation of CS-GP based supports

The CS-GP supports was prepared by dissolving chitosan (0.6 g) in 9 mL of hydrochloric acid (0.1 mol L^-1) followed by addition of 1.0 mL of disodium salt glycerol phosphate solution (0.560 g mL^-1) drop by drop under stirring. The product (CS-GP hydrogel) was then autoclaved at 121 ºC for 15 min, frozen in liquid nitrogen and lyophilized at -20ºC. Finally, the support was grounded to acquire powder form (CS-GP powder).

2.2. Lipase immobilization by physical adsorption (PA)

Initially, the CS-GP powder was soaked in anhydrous ethanol atproportion of 1: 1.5 (w v^-1) under stirring (50 rpm) for 6h at room temperature. After that period, ethanol excess was removed and lipase was addedin the ratio of 1:4 (w w^-1) (enzyme:support) together with buffer phosphate pH 7.0 (5 mmol L^-1) at a ratio of 1:60 (w w^-1) (support:solution). The system was maintained in contact for 18h at room temperature under stirring (50 rpm). Finally, the immobilized biocatalyst was filtered under vacuum and stored at 4 ºC.

2.3. Lipase immobilization by covalent attachment (CA)

The CS-GP powder was added to buffer phosphate pH 7.0 (0.2 mol L^-1) at a ratio of 1:1.2 (w v^-1). Then, glutaraldehyde solution (25%) was added at a ratio of 1:1.7 (w v^-1) (support:solution). The system was stirred at 50 rpm for 1 hour, filtered and washed with distilled water to remove the unbound glutaraldehyde (GA) and dried under vacuum to yield the CS-GP-GA (chitosan/glycerol phosphate hydrogel with glutaraldeyde) powder. After thar, buffer phosphate pH 7.0 (5 mmol L^-1) was added at a ratio of 1:60 (w w^-1) (support:solution). The system was maintained in contact for 18h at room temperature under stirring (50 rpm). Finally, the immobilized biocatalyst was filtered under vacuum and stored at 4 ºC.

2.4. Support and biocatalyst characterization

2.4.1. Scanning Electron Microscopy

Superficial morphologies of the CS-GP, CS-GP-GA and immobilized lipase were observed by Scanning Electron Microscopy (SEM) (Topcon/Singapore). The samples were coated with a gold film thickness of 16 nm (Bal-tec/USA).

2.4.2. Fourier transform infrared spectroscopy

Fourier transform infrared (FTIR) spectra were obtained in transmission mode on a FT-IR spectrometer Agilent Cary 630 (Agilent Technlogies/EUA) without further sample preparation.

2.4.3. Thermogravimetry

Thermal stability and weight loss profiles were determined using a thermogravimetric analysis (TG) in the STA 449F3 Calorimeter (Netzsch/Germany) under Argon atmosphere in the temperature range from 30ºC to 500ºC, heating rate of 10 ºC min^-1 and mass 5.00 ± 0.50 mg.

2.5. Determination of optimal enzymatic activities and kinetic parameters

The effect of pH and temperature on the hydrolytic activities of free and immobilized lipases was assessed according to a 2² full factorial design with three replicates at the center points. Star points were added to the experimental design for free and lipase immobilized by CA in order to compose second order model. The activities were assayed by the hydrolysis of olive oil emulsion at a fixed proportion oil/water 1:1¹⁵.The experimental design results were analyzed using Statistica version 7 (StatSoft Inc., USA).

The influence of substrate concentration (Carbonell^® olive oil) on the hydrolytic activities was also analyzed in the hydrolysis assay varying the proportion of oil in the emulsion from 5 to 70% (v v^-1). Michaelis-Menten constant (K_m) and the maximum velocity (V_max) were calculated using OriginPro version 8 (Originlab Corporation).

2.6. Thermal and storage stability

Determination of the denaturation constant (k_d), half-life time (t_1/2) and the residual activity after differents time intervals (15, 30, 60, 90, 120 and 150 min) was made by incubated 1.0mL of the free lipase solution (0.5 mg mL^-1) or 0.1 g of immobilized lipase in the presence of 4 mL of buffer phosphate pH 7.0 (0.1 mol L^-1) at 60ºC and then cooled in an ice bath. The residual hydrolytic activity was calculated by the olive-oil emulsion method (as described above) and the parameters k_d and t_1/2 by Eq. 1 and Eq. 2, respectively, assuming a first order thermal denaturation.

(1) (1) $A=A_0{e}^{-k_{d}t}$

(2) $t_{1/2}=\frac{\ln 0.5}{-k_d}$

where A is the hydrolytic activity at time (t), A₀ is the hydrolytic activity at time t₀, k_d is the denaturation rate (min^-1), t is incubation time (min).

The samples of free and immobilized lipase was storage in low temperature (-10ºC) and storage stability was evaluate. Each 30 days the lipase activity was evaluate in a maximum period of 120 days.

3. Results and Discussion

3.1. Preparation of CS-GP support and immobilization efficiency

Chitosan hydrogels have been prepared with a variety of different geometries and formulations. In each preparation, the polymer binding is accomplished either by non covalent physical association, such as secondary forces (hydrogen, ionic, or hydrophobic bonding) and physical entanglements, or by covalent cross-linked chemical association⁷. Figures 1 and 2 show the hypothetical representation of the mechanism for the immobilization of lipase on CS-GP hydrogel by physical adsorption (PA) and covalent attachment (CA), respectively. Chitosan dissolves in acidic environments via protonation of its amine groups (NH₃⁺) that reacts with negative charge of oxygen from GP (PO6^5-) at pH < 6.5. The chitosan-glycerol phosphate electrostatic attraction via ammonia and phosphate groups is one of the effective interactions responsible for the sol-to-gel transition. It is proposed that for immobilization process by physical adsorption lipase is entrapped between the ionic bonds of chitosan and GP, resulting in the structure as shown in Figure 1. By covalent attachment, CS-GP was activated with glutaraldehyde to incorporate aldehyde groups on the support surface by reacting with the amino groups of CS-GP, aiming to render adequate functional groups to the covalent binding with the enzyme (Figure 2). The chemical activation resulted in bindings between the free aldehyde groups and amino groups (NH₂) of the lipase. In addition, lipase could still be trapped in the interstitial spaces formed between the polymer and glutaraldehyde.

Figure 1
Hypotetic representation of CS-GP matrix formation and lipase immobilization by physical adsorption.

Figure 2
Hypotetic representation of CS-GP matrix formation and and lipase immobilization by covallent atachment.

Free lipase showed average activity of 11276.9 ± 236.4 U g^-1. According to the immobilization procedures, the covalent attachment provided better performance (average activity of 439.8 ± 11.2 U g^-1) in comparison with the lipase immobilized by physical adsorption, which revealed average activity of 406.3 ± 15.8 U g^-1. Such results indicated that the use of glutaraldehyde slight increased the linkage between the enzyme and the support.

3.2. Characterization of CS-GP supports and the immobilized lipase preparations

3.2.1. FTIR

The efficiency of both immobilization procedures in relation to the lipase incorporation on the support was assessed by Fourier transformed infrared spectroscopy (FTIR). FTIR technique was used to identify and characterize the chemical bonds and functional groups based on the principle that each type of bond has a characteristic absorption wavelength represent as an upward peak on a charted spectrum¹⁶. Figure 3a and Figure 3b show that the spectra of CS-GP and CS-GP-GA supports. Both materials exhibited bands at 3000-3500 cm^-1 corresponding to stretching vibration of the OH group suggesting the presence of intramolecular water^17,18. Other common bands occurred between 1900-1200 cm^-1 due to the presence of the amine group in the material^19,20. The band at 1100-900cm^-1 is probably due to the binding of polysaccharides characteristic of CO²¹. Such profiles were expected since both materials have amino or amide linkage in their composition. Nevertheless, according to Beppu et al. (2007), the CS-GA crosslinking shows an increase in the absorption at 1655 cm^-1 due to imine bonds (N=C)²². In addition, ethylenic and free-aldehydic shoulders at 1562 and 1720 cm^-1 were observed relatively to the intensity of other peaks²². An increase in the C-H stretch bond at 2936 cm^-1 and a decrease in the peak at 1100 cm^-1 were also observed by these authors, indicating the presence of aliphatic amino groups²².

Figure 3
(a) Fourier Transformed Infrared Specta of (black) chitosan-glycerol phosphate support, and (grey) chitosan-glycerol phosphate crosslinked with glutaraldehyde. (b) Fourier Transformed Infrared Specta of (black) free lipase, (light grey) system lipase immobilized by physical absorption, and (dark grey) system lipase immobilized by covalent attachement.

The immobilization of lipase by PA and CA can be confirmed by the presence of characteristics peaks of lipase on these spectra (Fig. 3b). Free enzyme displayed a typical spectrum of proteins with bands associated to their characteristic amide group (CONH). The band of 1700-1600 cm^-1 is related to the amide I vibration and C = O carboxylic acid^17,18 (Fig 3b). The band in the range of 1600-1510 cm^-1 present in the lipase immobilized by physical absorption spectrum, but not found in the free lipase and CS-GP spectra, refers to the N-H bond with contribution of C=N vibrational^23-25, suggesting an interaction between the enzyme and support (NH bending)^19,21.

3.2.2. SEM

Morphological evidences also suggested interactions among CS, GP, GA and lipase. Figure 4 (a-d) shows the SEM micrographs of the CS-GP and CS-GP-GA supports and lipase immobilized by PA and CA. Figure 4a shows CS-GP micrograph. Sheet-shaped particles can be observed, while CS-GP-GA micrograph (Fig. 4b) show a dense and compact structure with some particles attached. It may be inferred that cross-linking with glutaraldehyde reduced the superficial porosity of the CS-GP-GA and increased the materials' interactions.

Figure 4
Scanning Electron Microscopy images of (a) CS-GP, (b) CS-GP-GA, (c) lipase immobilized by physical absorption (PA) and (d) lipase immobilized by covalent attachement (CA).

Comparing both immobilized derivatives (Fig. 4c and 4d), it can be observed that the system lipase immobilized by PA (on CS-GP support) shows more superficial pores than the system lipase immobilized on CS-GP-GA (by CA). Such difference was expected, since the structure of CS-GP-GA support is crosslinked by the activation with GA and showed smaller and fewer pores.

3.2.3. TG

Thermal stability of supports and the immobilized samples was evaluated by thermogravimetric analysis. The TG curves and their derivatives (DTG) of all samples are displayed in Figure 5a-d. The first mass loss occurred around 100-150ºC and is attributed to the evaporation of superficial water and degradation of low molecular weight species, such as amino acids, peptides and oligomers²⁶.

Figure 5
Termogravimetric analysis (TG) and Derivative TG curves of (a) CS-GP,(b) CS-GP-GA, (c) free lipase(d) lipase immobilized by physical adsorption (PA), and (e) lipase immobilized by covalent attachment (CA).

By analyzing thermal stability of the supports without enzyme (Fig. 5a and 5b), it can be observe that the presence of glutaraldehyde has altered the mechanism of degradation of the CS-GP-GA compared to the CS-GP. Only 3% of mass was lose by CS-GP-GA around 300-350 ºC, while CS-GP lost 21% at this same temperature range. The mass loss at around 300ºC is due to the polymer degradation and removal of intramolecular water. It can also be attributed to the dehydration of the saccharide rings and depolymerization²⁷.

On the other hand, a mass loss of 22% was observed for the crosslinked support (CS-GP-GA) at 475ºC, which can be attributed to the polymer degradation. Nevertheless, the residual mass at 500ºC for CS-GP and CS-GP-GA were 65 and 75%, respectively. These results suggest that the presence of glutaraldehyde increased the stability of the support.

Similar behavior was observed comparing the lipases immobilized by PA and CA (Fig. 5d an 5e). The mass loss of the system lipase immobilized by PA at 300ºC was 39%, while the system lipase immobilized by PA lost only 3% at this temperature. The reduced mass loss of the system lipase immobilized by PA can be due to the three-dimensional structure of CS-GP-GA, which made difficult its decomposition and protected the lipase from degradation. In contrast, free lipase lost more than half of its mass at this temperature (52%, Fig. 5c). Therefore, both systems increased thermal stability of the immobilized lipase at 300ºC.

The residual mass at 500ºC for free lipase, lipase immobilized by PA and lipase immobilized by CA were 25, 45 and 55%, indicating that the immobilization procedures increased thermal stability of lipase and the presence of glutaraldehyde made the system more thermally stable.

3.3. Kinetics properties of the lipases immobilized by PA and CA

The enzyme kinetics parameters K_m and V_max were measured from nonlinear regression technique aiming to determine the catalytic effectiveness of the immobilized lipases in relation to the free lipase. The apparent V_max value indicated the maximum reaction rate and the K_m value indicated the substrate affinity and enzyme conformational changes, while the catalytic efficiency (V_max/K_m) indicated the overall cumulative effect of V_max and K_m on enzyme activity²⁸. The activities of free and immobilized lipases at different substrate concentrations were determined and the kinetic constants were calculated (Table 1).

Table 1
Activities of free and immobilized lipases at different substrate concentrations. Kinetic parameters (k_m and V_max) of free and immobilized lipase. Catalytic efficiency and variation (R²).

Lipase	km	Vmax	Catalytic efficiency	R2
	(mM)	(U/g)	(Vmax/Km)
Free lipase	1153.1	21113.2	18.31	0.98
Immobilized by PA	2806.4	638.2	0.23	0.97
Immobilized by CA	771	369.4	0.48	0.94

Free lipase showed a value of Km 1153.1 ± 239.8 mM and lipase immobilized by PA and CA showed values of 2806.4 ± 953.5 mM and 771.0 ± 245.7 mM, respectively. These results reveal that the affinity of the lipase immobilized by PA towards the substrate decreased 2.4 times while the lipase immobilized by CA enhanced the affinity 1.5 times. In case of immobilization by CA, probably, the covalent attachment aids the scattering of lipases into the support matrix, so that higher substrate concentration was experienced around the immobilized lipase²⁹. Otherwise, a possible explanation for higher K_m value determined on the lipase immobilized by PA may be the modifications in the zeta potential, since CS-GP particles without crosslink with GA can change the zeta potential of substrate, thus leading to change of electric attraction between enzyme and substrate³⁰.

As expected, V_max values for the immobilized lipases were reduced from V_max 21113.2 ± 1907.5 U/g for the free lipase to 638.2 ± 131.6 U/g and 369.4 ± 41.7 U/g for the lipases immobilized by PA and CA, respectively. This behavior can be attributed to the agglomeration formed by small hydrogel particles imposing diffusion limitations between biocatalyst and substrate. Changes on the enzyme microenvironment due to action of the GA crosslink agent could be also interfere the reaction rate of the lipase immobilized by CA.

The catalytic efficiency is a cumulative factor expressed by the ratio of V_max to K_m. Both immobilized lipases showed lower values of catalytic efficiency compared with the free lipase (Table 1). Between the immobilized biocatalysts, the lipase immobilized by CA was 2 times more efficient than the lipase immobilized by PA.

3.4. Effect of pH and temperature on the activity of free lipase and lipase immobilized by PA and CA

A experimental designwas performed to attain the optimal conditions of pH (X₁) and temperature (X₂) for hydrolytic activities of both free and immobilized lipases. For the lipase immobilized by PA, a full factorial design was used while for free and lipase immobilized by CA, star points were inserted to compose a second order model.

The experimental design is shown in Table 2, along with the experimental results. Free lipase and lipase immobilized by CA showed the highest lipolytic activities, 17682.97 ± 1482.41 U g^-1 and 547.04 ± 16.65 U g^-1, respectively at the central point (pH 7.5 and 50ºC), while lipase immobilized by CA attained 575.45±10.79 Ug^-1at highest level point (pH 8.5 and 60ºC). These results suggest that an increase of 56.8% occured in the lipase activity after the combination of variations in the pH and temperature. For the free lipase an increase of 24.3 % and 41.6 % for immobilized lipase by CA and PA, respectively.

Table 2
Experimental design and hidrolytic activity obtained for different combination of pH and temperature.

Tests	Real variable (coded variable)	Hidrolytic Activity (U/g)
	pH	Temperature (ºC)	Free Lipase	Immobilized PA	Immobilized CA
1	6.5 (-1)	60 (+1)	15565.25 ± 2011.84	149.32 ± 4.84	329.78 ± 33.89
2	6.5 (-1)	40 (-1)	7359.08 ± 105.89	100.02 ± 2.83	76.13 ± 21.44
3	8.5 (+1)	60 (+1)	8788.54 ± 317.66	575.45 ± 10.79	70.33 ± 8.97
4	8.5 (+1)	40 (-1)	12388.67 ± 741.20	542.40 ± 4.28	328.89 ± 24.74
5	7.5 (0)	50 (0)	15988.80 ± 423.54	486.11 ± 7.68	423.28 ± 10.08
6	7.5 (0)	50 (0)	17682.97 ± 1482.41	529.13 ± 6.84	547.04 ± 16.65
7	7.5 (0)	50 (0)	16253.51 ± 1005.92	434.69 ± 7.73	482.41 ± 7.70
8	6.1 (-α)	50 (0)	11012.15 ± 635.32	-	253.38 ± 45.13
9	8.9 (+α)	50 (0)	12759.27 ± 1279.63	-	186.71 ± 13.40
10	7.5 (0)	36 (-α)	12176.90±1270.63	-	248.83 ± 20.19
11	7.5 (0)	64 (+α)	5664.91±158.83	-	146.03 ± 40.78

The individual effects and variable interactions (pH and temperature) in the hydrolitic activities for free and immobilized lipases were estimated with aid of Statistica 7.0, considering a confidence level of 95%, significance p ≤ 0.05 and Fisher's statistical test for analyzis of variance. The models were checked by the R², which indicates the value of sample variation for hidrolytic activities attributed to the studied variables. The results obtained from the statistical studies were shown in Table 3.

Table 3
Estimation of the effects of variables, standard error and the p value for the hydrolytic activity of free lipase and immobilized by PA and CA.

Variable	Free Enzyme			Immobilized by PA			Immobilized by CA
	Effect	Standard Error	p	Effect	Standard Error	p	Effect	Standard Error	p
Média	16631.77	± 526.11	0.0100*	341.79	± 23.64	0.0048*	484.27	± 35.73	0.0054*
X1 (Linear)	176.48	± 647.69	0.8108	434.26	± 47.28	0.0116*	-25.26	± 43.99	0.6238
X1 (Quadratic)	-4460.76	± 777.49	0.0291*				-270.56	± 52.81	0.0360*
X2 (Linear)	-1139.08	± 647.69	0.2207	41.18	± 47.28	0.4757	-37.58	± 43.99	0.4829
X2 (Quadratic)	-7486.07	± 777.49	0.0106*				-293.63	± 52.80	0.0308*
X1 X2	-5903.15	± 911.38	0.0230*	- 8.13	± 47.28	0.8794	-256.14	± 61.90	0.0537

According to the Student's T test, both variablesshowed negative and significant quadratic effects for the free and lipase immobilized by CA and interaction was significant only for free enzyme within the experimental range studied at a 95 % ofconfidence level (Table 3). At the same confidence level, the lipase immobilized by PA showed only significant linear effect for the variable pH.

From these results, statistical models could be composed with the coefficients correspondent to the significant effects. For the lipase immobilized by CA a linear model was fitted as no significant value was given by checking the curvature (p = 0.059). The coefficients related to non significant effects were excluded from the model, except when it was necessary to maintain hierarchy³¹. The models are given in Table 4.

Table 4
Analysis of variance of the model that represents the hydrolytic activity of free lipase as function of pH (X₁) and temperature (X₂).

Source	Free lipase				Immobilized lipase by CA				Immobilized lipase by PA
	SS	DF	F	p	SS	DF	F	p	SS	DF	F	p
X1 (L)	61665	1	0.0742	0.8108	188577.4	1	84.3517	0.0117*	1263.3	1	0.3297	0.6238
X1 (Q)	27341476	1	32.9175	0.0291*		-	-	-	100576.8	1	26.249	0.0365*
X2 (L)	2569044	1	3.0930	0.2207	1695.4	1	0.7583	0.4757	2796.8	1	0.7299	0.4829
X2 (Q)	77003800	1	92.7080	0.0106*		-	-	-	118465.9	1	30.9177	0.0308*
X1 X2	34847180	1	41.9539	0.0230*	66.0	1	0.0295	0.8794	65589.8	1	17.1179	0.0537
Lack of fit	27265712	3	10.9421	0.0849	34329.9	1	15.3560	0.0594	3470.1	3	0.3019	0.8260
Pure error	1661213	2			4471.2	2			7663.3	2
Total SS	151525162	10			229139.9	6			251518.4	10

The statistical significance of these models was evaluated by the F test (Table 4), which revealed that they were significant at 95% confidence level, without lack of fit. Also, the determination coefficient (R²) indicates that the modelscan explain more 80% of the variability. Thus, the fitted equations were considered adequate for describing the activity as a function of the studied variables and were used to plot the response surfaces as shown in Figure 6 (a-c).

Figure 6
Response surface for: (a) free lipase, (b) lipase immobilized lipase by physical absorption (PA), and (c) lipase immobilized by covalent attachment (CA).

By considering the adjusted models, optimized conditions determined for each evaluated system were: free enzyme (48.8 ºC and pH 7.6); immobilized lipase by PA (60ºC and pH 8.5) and immobilized lipase by CA (49.5 ºC and pH 7.5).

Upon immobilization process, optimum temperature values were incresead due to the interaction between the enzyme and the surface support that can result in a more rigid structure for the protein molecule, resulting in a more stable active globular form of the biocatalystat higher temperatures.

To confirm these models, assays were carried out under the established conditions and the differences between the experimentaland theoretical values were lower than 5%.

3.5. Thermal and storage stability of the lipases immobilized by PA and CA

Aiming to evaluate the irreversible loss of enzymatic activity on exposure to high temperature, in this case 60ºC, the thermal stability of free and immobilized lipases was determined. The profile of thermal deactivation is illustrated in Figure 7. As expected, the immobilization process stabilized the enzyme, since free lipase maintain only 20% of its original activity after an incubation period of 150 min, while the immobilized enzyme by PA and CA remained 40% and 45%, respectively, of their original activities. This behavior is in accordance with the results obtained by TG curves that indicated an enhancement in the thermal stability of lipase after immobilization.

Figure 7
Thermal deactivation for: (square) free lipase, (star) lipase immobilized by physical absorption (PA), and (sphere) lipase immobilized by covalent attachment (CA).

Based on these results, the thermal deactivation constant (k_d) and half-life time of free and immobilized lipases was determined by fitting a model of first order deactivation. The half-life time (t_1/2) is the time which takes for the activity to reduce to a half of the original activity and inversely proportional to the rate of denaturation (k_d). The results present in Table 5 reveal that the model adjusted to the results (R² > 0.97) and showed that both immobilized lipases were about 2 times more stable than the free lipase.

Table 5
Thermal inactivation constant (k_d) and half-life of free and immobilized lipases.

	t½ (h)	kd (h-1)	R2
Free lipase	0.98	0.70	0.97
Immobilized by PA	1.9	0.37	0.98
Immobilized by CA	2.0	0.35	0.99

This improvement in thermal stability was also reported by Fernandes et al., (2014)²⁷ and Silva et al. (2012)³². They obtained an increase of 25 and 80% using lipase from Candida antarctica immobilized on hydrogel and PHBV, respectively. Da Ros et al., (2010)³³ immobilized the lipase from Bulkoderia cepacia on SiO₂-PVA and Nb₂O₅ and found an increase half-life of 17 and 7 times respectively, while Silva et al., (2011)²⁶ immobilized the same lipase on epoxySiO₂chitosanand found a 30 times increase.

At low temperature, both the immobilized derivatives showed good storage stability, since after 120 days they retained 80% (immobilized by CA) and 70% (immobilized by PA) of its original activity, as can be observed in Figure 8.

Figure 8
Storage stability for: (black) free lipase, (striped) lipase immobilized by physical absorption (PA), and (plaid) lipase immobilized by covalent attachment (CA).

4. Conclusions

The incorporation of the enzyme on the support took place differently depending on the method used. The immobilization by PA happened by the entrapment of lipase between the ionic bonds of chitosan and GP while CA occurred by bindings between the free aldehyde groups and amino groups (NH₂) of the lipase. The addition of glutaraldehyde caused a modification both on the surface of the support making it more compact, dense and less porous as in the structure that assumed a three-dimensional conformation. As a result, there was a greater affinity of the enzyme for this support CS-GP-GA and the thermal decomposition of the CS-GP-GA support and the lipase immobilized by CA occurred in three stages and not in two as occurred in all other cases. The value of V_max was negatively affected by the particle agglomeration of the support that made diffusion difficult in both immobilizations. In addition, an interdependence between pH and temperature was noted, since activity values were higher when compared to the activity of these variables alone. Finally, immobilization improved the enzyme stability as it exhibited a greater hydrolytic activity compared to the free enzyme after 150 min. Therefore, CS-GP supports can potentially be used for lipase immobilization, and the CA method presented the best performance.

5. Acknowledgements

The authors thank the financial support from CAPES (Coordenação de Aperfeiçoamento de Pessoal de Nível Superior) and FAPEMIG (Fundação de Amparo à Pesquisa de Minas Gerais).

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Publication Dates

• Publication in this collection
  29 June 2017
• Date of issue
  2017

History

• Received
  17 Jan 2017
• Reviewed
  09 May 2017
• Accepted
  21 May 2017