Open access peer-reviewed chapter - ONLINE FIRST

SiO2-Based Materials for Immobilization of Enzymes

By Crina Anastasescu, Mihai Anastasescu, Ioan Balint and Maria Zaharescu

Submitted: March 27th 2019Reviewed: May 24th 2019Published: June 30th 2019

DOI: 10.5772/intechopen.87046

Downloaded: 96

Abstract

It is well known that SiO2-based nanomaterials were widely used as support material for many chemically active species but also for compounds with biological activity such as antibodies and enzymes, due to their lack of toxicity and high surface area. The hybrid materials resulted from associating enzymes with various morphologies of SiO2 inorganic matrix, especially obtained by sol-gel method, are meant to develop a higher enzymatic activity and increased lifetime but also the recovery and reutilization advantage. The present contribution emphasized the synthesis of SiO2 nanomaterials with different morphologies and their physicochemical characteristics including biocatalytic activity of immobilized enzymes on simple SiO2. The morphology-dependent behavior of SiO2 inorganic carriers obtained by sol-gel method was also emphasized. Accordingly, SEM investigations, nitrogen sorption, electrokinetic potential, and spectroscopic measurements are presented. p-Nitrophenyl acetate (p-NPA) was used for testing the enzymatic activity of as-prepared lipase-SiO2 hybrid materials.

Keywords

  • SiO2
  • sol-gel
  • enzymes
  • immobilization

1. Introduction

New multifunctional materials are required as practical solutions for competitive, affordable, and environmentally friendly technologies from industrial and healthcare areas. These should be also able to sustain and preserve various ecosystems and an appropriate quality of human life, gathering resources from border scientific fields: materials science, bioremediation, biocatalysis, and biomedicine [1].

Silica is largely studied material with high chemical and thermal stability, nontoxic and non-expensive, which can display a huge variety of morphologies, not only in natural state but also obtained by various synthetic routes. For these reasons, silica with high surface area (MCM 41, SBA 15) is intensively used as support for chemical active species [2] but also as inorganic host in hybrid complex for biological active compounds (enzymes) [3], especially those obtained in mild conditions, by sol-gel method [4]. These materials are recognized as appropriate carriers for biological compounds, preserving or increasing their intrinsic features [5]. In addition, tubular morphology of silica allows custom modification/functionalization of internal/external surfaces with chemical (metals, oxides) and biological (enzymes, antibodies) active compounds [6].

In this work we review various SiO2 morphologies obtained during our material development researches, pointing out their peculiar properties and advantages related to the immobilization of enzymes for potential practical applications.

2. Sol-gel synthesis of different SiO2 structures obtained by sol-gel method: sphere-, tube-, and veil-type morphologies

Our previous works reported sol-gel synthesis and characterization of SiO2 matrices with different morphologies (nanotubes, spheres, and veils) but also emphasized the multifunctional behavior of the as-obtained SiO2 materials, from the perspective of their chemical and biological activity. Firstly, spherical particles and hollow nanotubes with open ends, square shape, and high surface area (300 m2/g), [7, 8] were obtained at room temperature and atmospheric pressure, using DL tartaric acid as in situ generated template. The catalytic [9] and photocatalytic [10] activities of platinum-modified SiO2 nanotubes and spheres were further investigated and proven to be dependent on morphology of SiO2 matrix which bears (supports) the metallic active phase. SiO2 veils have been also obtained, and their composites have been used as support for platinum electrocatalyst [11].

Improvement of in situ generated template-assisted SiO2 synthesis and appropriate post-synthesis treatments allowed us to obtain nanotubes with intrinsic photo- and electrochemical activity due to high density of oxygen-related lattice defects [12, 13] but also to reveal the distinctive capacity of highly defected SiO2 and its composite SiO2-TiO2 to generate reactive oxygen species (ROS) with potential applications in biology and medicine [14].

SiO2 materials (nanotubes) have been proven to be biologically active for bioremediation processes, showing bactericidal and bacteriostatic effects on halotolerant microorganisms [15]. These type of materials have been successfully used as inorganic carriers in hybrid complex with enzymes [16], the enzymatic activity of the complex being dependent on morphological and textural properties of SiO2 matrices [17].

Generally, sol-gel synthesis of tubular SiO2 materials was conducted in line with Nakamura and Matsui’s work [18], modifications of synthetic procedure being done in respect to particular applications.

Thin and larger SiO2 nanotubes in addition to spherical SiO2 are meant to function as inorganic host for immobilized enzymes, and, accordingly, their previously synthesis has been reported [7, 17]. Better control of synthesis conditions allowed an optimization of their morphology and structure, in order to be appropriate for an inorganic carrier. Generally, these materials are resulting from a template-assisted sol-gel process, consisting in hydrolysis and condensation reactions conducted in the presence of DL tartaric acid, in respect to well-defined and well-controlled synthetic parameters which will be exposed in what comes. By selecting proper temperature, concentration of started solution, and in situ organic template development, not only morphological changes (observed in SEM captured images) can be induced but also structural ones, resulting in highly defected surfaces with increased chemical reactivity [12].

In this sense, we used a mixture of tetraethyl orthosilicate (TEOS) (Alfa Aesar, 99%), absolute ethanol (Riedel-de Haen), ammonia (25% w/w aq. Alfa Aesar), and DL tartaric acid (TA) as internal templating agent. The involved molar ratio was 1 (TEOS):0.07 (tartaric acid):43 (ethanol):36 (H2O), at 20°C. A subsequent addition of ammonia (25%), drop by drop, triggers the formation of the final synthesis product, a white and dense suspension being observed. The whole synthetic procedure is performed in mild conditions, at room temperature (25°). One hour aging time is allowed followed by filtering, washing with ultrapure water (Milli-Q system, 18 MΩcm), and drying at 100°C for 3 hours. Typically, the post-synthesis thermal treatment involves calcination for 3 h at 500°C with a heating rate of 0.5°C/minute (Scheme 1).

Scheme 1.

Schematic representation of the SiO2-NT preparation route.

This synthesis route leads to hollow and large nanotubes, together with a minor percent of spherical particles. The sample will be denoted in what comes as SiO2TL sample (TL meaning large tubes) (Figure 1).

Figure 1.

(a–d) SEM images at different magnifications of large tubes (SiO2TL)—unpublished results; (e, f) TEM images of large tubes (SiO2TL). (e, f) Reprinted from [7] with permission from Elsevier).

A faster addition of aqueous ammonia to similar reaction mixture favors the formation of solid spheres instead of nanotubes. Their diameters are about hundreds of nanometers, the samples being denoted as SiO2S (S—spheres) (Figure 2).

Figure 2.

SEM images of SiO2 spheres (SiO2S). (Reprinted from [17]).

For obtaining thinner (20–50 nm diameter) and longer nanotubes, denoted as SiO2Tt (Tt meaning thin tubes) (Figure 3), the working temperature decreased at 0°C, and the molar ratio of reactants changed according to the following values: 1 (TEOS):0.03 (tartaric acid):18 (ethanol):10 (H2O).

Figure 3.

SEM images of thin tubes (SiO2Tt). (Reprinted from [17]).

These synthetic conditions allow to obtain not only a better morphological homogeneity than in previous case but also an increased chemical reactivity of the SiO2 tubular surfaces; their functionalization with NH2 groups proved to be favored, which is an appropriate functional feature for an efficient inorganic carrier.

The control of the above-described synthesis parameters allows to achieve various and reproducible morphologies. Briefly, the diversity regarding the morphology (spheres and veils) but also the different textural properties of the nanotubes is closely related to the experimental conditions governing both the SiO2 sol and in situ template generation.

Accordingly, adjustments concerning the SiO2 sol formation are resulting in appearance of the veil-type morphology (Figure 4).

Figure 4.

SEM images of sol-gel SiO2 veils (SiO2v). (Unpublished results).

In addition, by using meso-tartaric acid instead of DL tartaric acid, small spherical particles (around 40 nm) have been obtained (Figure 5).

Figure 5.

TEM images of spherical SiO2 nanoparticles (SiO2s). (Reprinted from [7] with permission from Elsevier).

If DL tartaric acid is replaced by oxalic acid, tubular morphology is maintained. Figure 6 shows the resulted tubes sized (characterized) at micrometric scale both in diameter and length. These experimental achievements are in line with the literature data [19].

Figure 6.

SEM images of extra large SiO2 tubes (SiO2TXL) obtained with oxalic acid as template. (Unpublished results).

3. Modification of SiO2 tubular matrices with gold nanoparticles

According to literature data, most of the enzymatic immobilization tests on silica are based on electrostatic interactions, resulting in direct adsorption [20, 21]. Gold nanoparticles deposed on silica surface proved to increase the capacity of SiO2 materials to load the target enzymes [22].

In this sense, gold modification of SiO2 matrices was performed both by direct impregnation of SiO2 powder with a solution of HAuCl4 3H2O and by deposition of metallic nanoparticles after functionalization of silica surface with 3-(triethoxysilyl)-propylamine.

Direct modification of SiO2 materials with gold was done using 0.2 g of previously thermally treated SiO2 (500°C, 3 hours) and an aqueous solution of 0.01 M HAuCl4 3H2O (49%, Sigma-Aldrich), in order to achieve 2% Au (weight percent). The resulted mixture has been stirred (500 rpm) at room temperature for 5 hours and then calcined 1 h at 300°C with a heating rate of 0.5 deg/min.

The same procedure has been respected for gold modification of SiO2 surface after functionalization with organic groups (Scheme 2), which consists in refluxing for 12 hours of a mixture containing 0.2 g SiO2, 5 ml absolute ethanol, and 50 microliters (μl) of 3-(triethoxysilyl)-propylamine (C9H23NO3Si, 99%, Sigma-Aldrich).

Scheme 2.

Schematic representation of the Au-modified SiO2-NT preparation route.

After washing with ethanol, filtering, and drying, the recovered powder is added to a gold aqueous solution (HAuCl4 3H2O, 0.01 M) and stirred (500 rpm) at room temperature for 5 hours. An aqueous solution of NaBH4 (Sigma-Aldrich) is used for reduction of ionic (Au3+) to metallic gold, followed by washing, filtering, and calcinations of the recovered product at 500°C for 1 hour, maintaining the same heating rate as for direct impregnation (0.5 deg/min).

The average size of deposited metal nanoparticles evaluated from TEM and X-ray diffraction (XRD) measurements ranged in 5–15 nm domain.

Figure 7.

FTIR spectra of SiO2 spheres (SiO2S), SiO2 thin tubes (SiO2Tt), and SiO2 large tubes (SiO2TL).

Figure 8.

SEM images of gold-modified silica thin tubes, by direct impregnation (AuSiO2Tt). (Unpublished results).

4. Morphological and structural characterization of simple and gold-modified SiO2

In order to evaluate the various morphologies displayed by SiO2 sol-gel materials as a result of ranging the synthetic parameters and to emphasize the fully desired characteristics of SiO2 matrices for development of hybrid structures with enzymatic activity, scanning and transmission electron microscopies (SEM, TEM), Fourier transform infrared and FTIR-ATR, diffuse reflectance UV-Vis spectroscopy, and XRD measurements were performed.

4.1. Characterization of bare SiO2 materials

4.1.1. Scanning and transmission electron microscopy (SEM and TEM)

SEM investigations (Figure 1, for the SiO2TL sample) clearly show the tubular morphology as major phase of the SiO2 powders resulted from the sol-gel process.

SEM images from Figure 1a–d reveal a small percent of rounded particles, most of them being attached on the external surface of the tubes. This observation is in line with reported literature data about SiO2 tubular matrices obtained in mild conditions, by sol-gel process [18]. Their average external diameter is around 200 nm, the length overcoming 1 μm. An accurate perspective on the wall structure of these large nanotubes (SiO2TL) is achieved by TEM images from Figure 1e,f. So, thick walls with porous structure, empty core, and open ends of the nanotubes could be observed.

Figure 2 shows the presence of solid, big spheres with an average diameter of 200 nm, no other morphologies being present.

Figure 3 presents thin nanotubes (SiO2Tt) (average diameter ~50 nm) like predominant morphology, spherical entities being present on their surface but as smaller percent than for the previous tubular sample (SiO2TL). From this point of view, it is obvious that the sample has a high degree of homogeneity. Also, the tubes are thinner and much longer than previous ones, the ratio between the external and internal diameters being also decreased. Despite their impressive length, similar to that of the fibers, the SEM images captured at 1 μm scale bar show a good contrast between their walls and empty cores. This means high surface (both internal and external) areas are available for interaction (contact) with enzymes. In addition to BET results, these images indicate a facile access but also a potential confinement [23] of the enzymes inside the tubes which could favor an increased degree of enzymatic immobilization.

Figure 4 presents images of a single and distinct morphology obtained by sol-gel method, namely, SiO2 veils. In addition to the previously reported application, as support and part in composite structures [11], many potential applications could exploit the lack of toxicity but especially the great structural and morphological homogeneity of this SiO2 matrix, especially in biomaterial range.

Figures 5 and 6 are also relevant for the influence of the synthesis parameters on the morphological features of the synthesized material. The change of the organic template leads to rounded, quite undefined nanoparticles characterized by the SEM images from Figure 5 and the modified tubular morphology being exposed in Figure 6. These images are recorded for a sample whose characteristics have been tailored by the oxalic acid used as template. Huge tubes can be observed and enlarged especially as diameters (up to 5 μm).

4.1.2. Fourier transform infrared spectroscopy (FTIR)

Taking into account the target application for these SiO2-based materials, namely, the immobilization of enzymes, the information obtained by FTIR regarding the structural characteristics of SiO2 inorganic matrix and its interaction with functional organic groups are useful.

The relevant vibration bands observed from FTIR spectra of the spherical and tubular SiO2 samples (Figure 7) are similar; small variations could be perceived especially regarding their intensity and the presence of silanol groups (Si-OH), which is an important issue from the perspective of further functionalization of silica surface with 3-(triethoxysilyl)-propylamine (APTES) and, subsequently, the deposition of gold on the surface.

According to our previous collected results and literature data, the large peak from 1124 cm−1 is due to Si-O stretching from SiO2 [7], and its shoulder (1200 cm−1) is assigned to asymmetric vibration of Si-O-Si [24]. One more tiny shoulder located around ~ 960 cm−1 could indicate the presence of silanol groups [25], especially for spherical SiO2 (SiO2S) but unperceivable for the sample containing large tubes (SiO2TL). Its spectrum indicates also less structural, free OH groups and adsorbed water, generally evaluated from the development of a broadband ranging in 3350–3600 cm−1 domain [26, 27]. The presence of OH groups on silica surface could promote the hydrogen bonding formation with functional groups of enzymes [28]. According to the reported data [8], the peak located at 847 cm−1 is due to νs(Si-O-Si), and the peak appearing to 484 cm−1 is determined by δ(Si-O-Si).

In order to identify and characterize gold nanoparticles deposited on the surface of thin tubes by direct impregnation of powder with gold precursor solution, SEM analysis (Figure 8a) was performed. A very large size distribution associated with a weak dispersion of gold nanoparticles could be observed.

In the case of gold deposition after surface functionalization with APTES, smaller gold nanoparticles were expected to result. Figure 9a presents a SEM image of the metal-modified nanotubes, but gold nanoparticles are unperceivable because of their reduced dimensions as a result of previous surface functionalization. Accordingly, TEM analysis was performed, and the images from Figure 9b show smaller gold nanoparticles with average diameter around 7 nm, deposited on external surface of nanotubes which bear as well spherical particles of SiO2. Also, a loss of transparency could be observed in the case of functionalized samples. Images from Figures 8 and 9 emphasize more efficient gold deposition after functionalization of SiO2 tubular surface, exhibiting small, well-dispersed gold nanoparticles which should successfully bind the enzymes.

Figure 9.

(a) SEM images of SiO2 thin tubes modified with gold after functionalization with APTES (AuSiO2TtF). (b) TEM images of SiO2 thin tubes modified with gold after functionalization with APTES (AuSiO2TtF). (Unpublished results).

4.1.3. Diffuse reflectance UV-Vis spectroscopy performed on silica and gold-modified silica thin tubes

The main objective of this investigation was to observe the surface plasmon resonance (SPR) phenomenon which is related to gold nanoparticles contained by the analyzed samples. As it could be seen from Figure 10, a large peak appears around 500 nm for the gold-modified SiO2 samples, this being more impressive when gold is deposited after functionalization of SiO2 thin tubes (AuSiO2TtF).

Figure 10.

UV-Vis spectra of silica and gold-modified silica tubes by direct impregnation (AuSiO2Tt) and after functionalization (AuSiO2TtF). (Unpublished results).

4.1.4. X-ray diffraction (XRD)

The XRD results are presented in Figure 11, where the broad diffraction band located at 2ϴ = 21.5° is characteristic to the amorphous structure of SiO2 and the maxima from 2ϴ = 38.17, 44.3, 64.5, 77.5° are typical for metallic gold. The average crystallite size of the gold deposited after functionalization of silica surface, calculated with Williamson-Hall method, is 7.5 nm, much smaller than for the other sample (~ 15 nm).

Figure 11.

XRD spectra of gold-modified silica thin tubes by direct impregnation (AuSiO2Tt) and after functionalization (AuSiO2TtF). (Unpublished results).

4.1.5. Fourier transform infrared spectroscopy (FTIR)

Analysis of spectra from Figures 13 and 14 (details of general spectrum from Figure 12) shows that after silica thin tube functionalization, its spectra do not present the specific vibrations of Si-OH (~ 960 cm−1), free or bounded OH groups, and adsorbed water (3350–3600 cm−1). This supports the idea that 3-(triethoxysilyl)-propylamine is anchored by the OH groups of the tubular silica surface.

Figure 12.

General FTIR spectra of simple, functionalized, and gold-modified SiO2 thin tubes: SiO2 (SiO2Tt), SiO2-APTES (SiO2TtF), and AuSiO2-APTES (AuSiO2TtF). (Unpublished results).

Figure 13.

FTIR spectra of simple, functionalized, and gold-modified SiO2 thin tubes: SiO2 (SiO2Tt), SiO2-APTES (SiO2TtF), and AuSiO2-APTES (AuSiO2TtF) in 900–1000 cm−1region. (Unpublished results).

Figure 14.

FTIR spectra of simple, functionalized, and gold-modified SiO2 thin tubes: SiO2 (SiO2Tt), SiO2-APTES (SiO2TtF), and AuSiO2-APTES (AuSiO2TtF) in 3000–4000 cm−1region. (Unpublished results).

Figure 15.

FTIR-ATR spectrum of thin tubes (SiO2TtF) functionalized with 3-(triethoxysilyl)-propylamine. (Unpublished results).

Figure 16.

FTIR-ATR spectrum of gold-modified thin tubes (AuSiO2TtF) after functionalization with 3-(triethoxysilyl)-propylamine. (Unpublished results).

Figure 17.

N2 adsorption-desorption isotherms (a) and the pore size distribution obtained from the desorption branch (b) for the SiO2Tt samples before lipase immobilization; (c and d) the same curves recorded after lipase immobilization. (Reprinted from [17]).

Figure 18.

(a) FTIR-ATR spectra recorded from supernatant solution after immobilization of lipase on different SiO2 samples in phosphate buffer solution, revealing the 3271 cm−1 peak. (Reprinted from [17]); (b) FTIR-ATR spectra recorded from supernatant solution after immobilization of lipase on SiO2Tt and AuSiO2Tt supports. (Unpublished results).

Figure 19.

(a) The electrokinetic potential of lipase-bare SiO2 hybrid systems. (Adapted from [17]); (b) Gold-modified SiO2Tt together with developed lipase hybrid complex. (Unpublished results).

4.1.6. FTIR-ATR spectroscopy performed on functionalized (APTES) SiO2 thin tubes

FTIR-ATR measurements were done in order to check the functionalization of SiO2Tt surface with functional groups of 3-(triethoxysilyl)-propylamine.

Figure 15 identifies the peak located at 1635 cm−1 which, according to the literature data, is attributed to the twisting vibration of N-H in addition to the band from 3000 to 2900 cm−1 due to the stretching vibration of the CH2 which proves the successful functionalization of silica with APTES [29, 30].

It is obvious from Figure 16 that the chemical “fingerprint” of the SiO2 inorganic matrix is preserved, but the organic groups identified in previous spectrum are strongly flattened, due to the thermal treatment applied after functionalization and gold modification, respectively. As expected, the broadband (3400–3600 cm−1) related to OH groups and adsorbed water is clearly diminished, as well as the band from 2900 to 3000 cm−1 (the stretching vibration due to CH2 from APTES).

5. Synthesis, characterization, and catalytic activity of hybrid complex lipase-inorganic matrices (SiO2, AuSiO2Tt)

5.1. Synthesis of lipase-SiO2 complex

Generally, the design of hybrid structures like enzyme-inorganic carrier is looking to preserve or increase the catalytic activity of free enzymes but especially to extend its lifetime and endurance in relation to parameters governing its proximity (pH, temperature) [31]. In addition to this, enzymatic immobilizations have the advantage of reusability which is an important issue especially for those biocatalysts meant to sustain valuable biotechnologies. For instance, free and immobilized lipase is used in esterification, transesterification, reactions [32, 33], and different biotechnological applications [34].

According to literature data, gold nanoparticles could increase the enzyme loading on inorganic carriers, acting as efficient support for enzymes [35]. Few but important potential medical applications are centered on the use of lipase immobilized on gold nanoparticles as electrochemical sensor for triglycerides from human serum [36].

The literature results indicate the isoelectric point of lipase from Rhizopus oryzae and silica at pH 7.6 and 3, respectively [21]. In order to achieve an electrostatic attraction between SiO2 supports and lipase, our immobilization experiments were conducted at pH 6.3 where lipase is slightly positively charged.

Briefly, hybrid complex material consisting in lipase-inorganic support (SiO2Tt, AuSiO2Tt) was obtained according to the previous reported work [17] concerning the generation of biocatalyst lipase-SiO2 matrices. Lipase (Rhizopus oryzae, Sigma-Aldrich) in phosphate buffer (pH 6.3) was mixed with SiO2 and Au/SiO2 powder (0.02 g) also dispersed in phosphate buffer and magnetically stirred 24 h (100°C). The solid product containing lipase immobilized on SiO2 and Au/SiO2 powder was separated from supernatant by centrifugation and washed several times with phosphate buffer and water in order to be further evaluated from the perspective of total organic carbon content, FTIR-ATR and PZC measurements, and enzymatic tests as well.

5.2. Characterization of lipase-SiO2 complex

5.2.1. BET measurements

The textural properties of tubular and spherical silica, correlated with total organic carbon measurement on their lipase derivative hybrid complex, were previously evaluated and reported [17].

Accordingly, a surface area (SBET) about 18 and 14m2/g, respectively, was found for large tubes (SiO2TL) and spherical (SiO2S) samples. In the case of large tubes, mesopores of 3 nm were identified, which are probably located in the walls of the nanotubes but improper for the lipase immobilization (the diameter of Rhizopus oryzae being ~ 5 nm). SEM and TEM images (Figure 1) show an internal diameter of ~200 nm, and total organic carbon measurements [17] indicate the best lipase loading on SiO2Tt sample (30 mg/g). It is obvious that the internal surfaces are accessible for lipase immobilization.

Spherical SiO2 matrices (SiO2S) show a large size distribution of pores, ranging from 3 to 5 nm and from 10 to 30 nm. Probably, the last value is due to voids of packed spheres and could hardly allow the enzymatic immobilization, but leaching could be favored too.

Figure 17 presents the data related to SiO2 tubular thin tube sample (SiO2Tt).

From BET analysis, the value of the specific surface area (SBET) was found to be 107.83 m2/g. The shape of adsorption and desorption branches is typical for cylindrical pores with open ends. The pore size distribution is very large, spanning from 10 to 100 nm. By correlating these results with SEM images (Figure 3), it can be assumed that the internal diameters of these thin tubes are ranging between 10 and 50 nm. The well-defined peak from 3 nm can be attributed to the mesoporosity of wall nanotubes, similar to larger ones (SiO2TL). These properties are drastically changed by the lipase adsorption; the broad peak ranging between 10 and 100 nm is not present anymore. This proves that the immobilization of lipase on SiO2Tt sample is in fact a confinement inside the core of the nanotubes which can assure an increased stability against post-immobilization leaching. Total organic carbon analysis sets the capacity of loading the lipase around 15 mg/g, lower than for larger tubes but better than for spherical ones.

5.2.2. FTIR-ATR measurements

Our reported data containing the FTIR-ATR results registered on lipase-SiO2 hybrid complex [17] indicated the presence of lipase and its specific vibration bands both in supernatant and onto solid tubular and spherical SiO2 supports (Figure 18).

The previous reported capacity of unmodified SiO2 matrices to load lipase was found to fit to the following sequence: SiO2TL > SiO2Tt > SiO2S (Figure 18a).

The comparison of Figure 18a,b highlights especially the peak from 3271 cm−1 (marking the stretching vibration of the NH group). In this sense, it appears that lipase from supernatant solution (of the derivative hybrid complex of gold-modified SiO2Tt) is less emphasized. This observation means a higher capacity of gold-modified sample to uptake lipase than the bare SiO2Tt carrier. Thus, the gold modification of silica looks to be successful and worth to be further investigated.

5.2.3. The electrokinetic potential

The electrokinetic potential (ξ) measurements (Figure 19) bring information related to the electrostatic interactions established between the surfaces of inorganic carrier and enzyme, which is actually a decisive parameter for an efficient enzymatic immobilization by direct adsorption.

The lipase immobilization on SiO2 and gold-modified SiO2 matrices was performed at pH 6.3 in phosphate buffer solution. In these conditions, the silica should be negatively charged and lipase slightly positive. Our previous results [17] indicate highly negative values of electrokinetic potential (ξ), especially for spherical samples. After immobilization (Figure 19a), these values slightly change, probably due to the lipase adsorption on the external surface of SiO2 matrices. From the above-presented data, the immobilization of lipase on SiO2Tt sample takes place especially inside the nanotubes.

Figure 19b displays the values of electrokinetic potential (ξ) for gold-modified thin nanotubes, both by direct impregnation (AuSiO2Tt) and after functionalization with APTES (AuSiO2TtF), before and after lipase immobilization. It is obvious that the deposition of gold after surface functionalization is more efficient in terms of the inorganic host ability to immobilize the lipase, this fact being illustrated in Figure 19b as a shift of the electrokinetic potential (ξ) to more positive values.

5.3. Catalytic activity of lipase-SiO2 complex

Our previously reported data [17] are concerning the catalytic activity of lipase from Rhizopus oryzae immobilized on bare tubular and spherical SiO2 matrices for hydrolysis reaction of p-nitrophenyl acetate (p-NPA).

Briefly, the hybrid complex newly formed is suspended in dimethyl sulfoxide (DMSO) and phosphate buffer at pH 7.8. One hour of incubation at 37°C is allowed, and the liquid phase was separated by centrifugation for measuring the reaction products by UV-Vis.

The best biocatalyst in terms of highest product amount (p-nitrophenyl) proved to result from lipase immobilization on SiO2 thin tubes. For this reason, gold nanoparticle modification of this inorganic matrix should result in optimization of structural and functional properties of its derivative hybrid complex with lipase. This aspect was addressed by the above-presented structural characterization of gold-modified SiO2Tt support, and its derivative complex and further investigations regarding their enzymatic activity will be performed.

6. Conclusions

Sol-gel method proves to be an efficient tool for obtaining well-defined SiO2-based multifunctional materials (bio-/photocatalysis, bioremediation processes, electrochemistry).

SiO2 inorganic carriers obtained by in situ generated template-assisted sol-gel method revealed morphology-dependent behavior regarding lipase (Rhizopus oryzae) immobilization and enzymatic activity of the derivative hybrid complex.

Gold modification of functionalized (APTES) SiO2 tubular surfaces improves the degree of enzymatic immobilization.

Conflict of interest

The authors declare no conflict of interest.

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Crina Anastasescu, Mihai Anastasescu, Ioan Balint and Maria Zaharescu (June 30th 2019). SiO<sub>2</sub>-Based Materials for Immobilization of Enzymes [Online First], IntechOpen, DOI: 10.5772/intechopen.87046. Available from:

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