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Exploitation of Enzymes for the Production of Biofuels: Electrochemical Determination of Kinetic Parameters of LPMOs

Exploitation of Enzymes for the Production of Biofuels: Electrochemical Determination of Kinetic... applied sciences Article Exploitation of Enzymes for the Production of Biofuels: Electrochemical Determination of Kinetic Parameters of LPMOs 1 2 1 2 1, Dimitrios Zouraris , Anthi Karnaouri , Raphaela Xydou , Evangelos Topakas and Antonis Karantonis * Laboratory of Physical Chemistry and Applied Electrochemistry, School of Chemical Engineering, National Technical University of Athens, Zografou, 15780 Athens, Greece; dimzouraris@mail.ntua.gr (D.Z.); ch15611@mail.ntua.gr (R.X.) Biotechnology Laboratory, School of Chemical Engineering, National Technical University of Athens, Zografou, 15780 Athens, Greece; akarnaouri@chemeng.ntua.gr (A.K.); vtopakas@chemeng.ntua.gr (E.T.) * Correspondence: antkar@central.ntua.gr Abstract: Lytic polysaccharide monooxygenases (LPMOs) consist of a class of enzymes that boost the release of oxidised products from plant biomass, in an approach that is more eco-friendly than the traditional ones, employing harsh chemicals. Since LPMOs are redox enzymes, they could possibly be exploited by immobilisation on electrode surfaces. Such an approach requires knowledge of kinetic and thermodynamic information for the interaction of the enzyme with the electrode surface. In this work, a novel methodology is applied for the determination of such parameters for an LPMO from the filamentous fungus Thermothelomyces thermophila, MtLPMO9H. Keywords: LPMO; Fourier Transform ac Voltammetry (FTacV); cyclic voltammetry; Direct Electron Transfer (DET) Citation: Zouraris, D.; Karnaouri, A.; 1. Introduction Xydou, R.; Topakas, E.; Karantonis, A. Exploitation of Enzymes for the The exploitation of lignocellulosic biomass, such as wood and agricultural residues, Production of Biofuels: towards the production of fermentable sugars for the production of second-generation Electrochemical Determination of biofuels in an environmentally friendly way, requires of enzymatic degradation. This step Kinetic Parameters of LPMOs. Appl. has low energy requirements, selectivity, mild processing environment and no need of harsh Sci. 2021, 11, 4715. chemicals, in contrast to classical chemical methods, and it is catalyzed by a combination https://doi.org/10.3390/app11114715 of hydrolytic and oxidative enzymes [1,2]. Regarding the oxidation reactions, performing these steps in an electrochemical reactor, i.e., electroenzymatic synthesis of sugars, is a Received: 23 April 2021 promising approach for the production of such chemicals. In principle, when electrolysis is Accepted: 18 May 2021 combined with enzyme reactions, a redox enzyme is maintained in its active state through Published: 21 May 2021 an electrode process. This can be achieved by oxidation of or a reduction in a cofactor or a mediator on the electrode surface, or by direct electron transfer to the enzyme. Therefore, Publisher’s Note: MDPI stays neutral applying enzyme immobilization onto the electrode and combining bioelectrocatalysis with regard to jurisdictional claims in with traditional enzymatic hydrolysis offer perspectives for developing novel processes for published maps and institutional affil- the production of biofuels and other value-added materials from lignocellulose. iations. Lytic polysaccharide monooxygenases (LPMOs) are copper-dependent enzymes that have the capacity to cleave polysaccharides via an oxidative mechanism [3]. They are classified as Auxiliary Activities (AAs) in the Carbohydrate Active enZyme database (CAZy). More specifically, they are divided into seven families (AA9–11 and AA13–16) Copyright: © 2021 by the authors. based on their sequence similarities, with the majority of those that are studied thoroughly Licensee MDPI, Basel, Switzerland. belonging to the AA9 and AA10 families [4]. LPMOs act synergistically with other biomass- This article is an open access article degrading enzymes and significantly boost the hydrolytic performance of cellulase and distributed under the terms and hemicellulase cocktails, primarily by improving the accessibility of the enzymes to the conditions of the Creative Commons substrate [5,6]. Attribution (CC BY) license (https:// Until recently, the main theory regarding the mechanism of action of LPMOs involved creativecommons.org/licenses/by/ the introduction of a single oxygen atom from molecular oxygen into the substrate, while 4.0/). Appl. Sci. 2021, 11, 4715. https://doi.org/10.3390/app11114715 https://www.mdpi.com/journal/applsci Appl. Sci. 2021, 11, 4715 2 of 11 taking electrons from an external electron donor for their action [7]. More recently, Bis- saro et al., while examining an LPMO belonging to the AA10 family, supported the idea that the chemically relevant co-substrate of LPMO catalyzed oxidation is H O [8]. Regard- 2 2 less of the mechanism of the oxidative cleavage of the polysaccharidic substrate, in both cases, the reaction is initiated when the active center of the enzyme takes an electron from an external electron donor. The nature of the donors used in laboratory experimental setups include ascorbic acid, cysteine and reduced glutathione, but also a wide range of plant-derived phenols [9,10], lignin compounds [11] and photocatalytic and enzymatic systems [12]. The reported mechanisms for the initial reduction in LPMOs do not implicate any chemical steps other than a one-step, one-electron reaction. One interesting point regarding these enzymes, which could possibly be an advantage for their electrochemical exploitation, is that their copper-containing active center is not “buried” inside their structure but can be found on a solvent-exposed, flat surface [13]. This could facilitate their use as electrode coatings, by directly providing them with electrons from an electrode surface, while immobilized on the electrode surface. Other than their study, this characteristic could lead to the exploitation of the bioelectrocatalytic action of LPMOs towards the production of oxidised products (oligosaccharides and glucans) from biomass, in concert with hydrolytic enzymes, in the absence of any external reducing agent. This means that by providing electrons directly from an electrode surface to an immobilised LPMO, the enzyme could be utilised in bioconversions through bioelectrocatalysis focusing on product life cycles. The developed bioconversions will be carried out in predominantly aqueous media using enzymes, and therefore be characterised by a limited use of toxic reagents or solvents, requiring only an ambient temperature, in the absence of any reducing agent [14]. In order to test if the above task is feasible, a parameter that should be mentioned is the standard electron transfer rate constant (k ) between the immobilized electrode and the enzyme. This electron transfer rate should be rather fast, so that the electrocat- alytic current measured represents the rate of substrate turnover at the enzyme active site [15]. Among the electroanalytical methods, a technique that is very promising for the study of immobilised LPMOs is that of large amplitude fast Fourier transform alternat- ing current voltammetry (FTacV), with which one can study both free and immobilised species, eliminating capacitance currents, a problem common in immobilised-on-electrode species [16–19]. In the past, this technique has been employed for the determination of the formal potential of immobilised LPMOs [20], as well as for the study of the direct electron transfer of multi-copper laccase like oxidases [6] and the interaction with epinephrine as a substrate [21]. Recently, a methodology for the extraction of the transfer coefficient a and the k for immobilised species has been proposed, but has yet to be applied experimen- tally [17]. In this work, this particular methology shall be employed for the extraction of the k an LPMO from the filamentous fungus Thermothelomyces thermophila, MtLPMO9H, and the calulated value of k shall be verified by numerical simulation. To our knowledge, k values for the interaction of an immobilized LPMO with an electrode surface is reported for the first time. 2. Materials and Methods Voltammetric experiments were performed in a single-compartment three-electrode cell consisting of a working electrode, a Pt wire as a counter electrode, and a AgjAgCl, KCl sat. reference electrode (+0.197 V vs. NHE). The aqueous solutions of about 5 mL consisted of 0.5 M acetate buffer (pH 6) as a supporting electrolyte. The working electrode consisted of a cobalt functionalised multi-walled carbon nan- otubes modified glassy carbon (GC) electrode, of 3 mm diameter. The immobilisation matrix was prepared as follows: A total of 1 g of commercial functionalised multi-wall carbon nanotubes (MWCNTs) (Hongwu Material, item No: C933-MC, Guangzhou, China) were added in a 150 mL solution with 20 % v/v. The suspension was stirred for 20 min at 120 C for further functionalization, until the liquid phase was evaporated. The solution Appl. Sci. 2021, 11, 4715 3 of 11 was left to dry overnight at 90 C until dry powder was collected. The powder was washed, then centrifuged 5 times with deionised water until the supernatant had a pH value of '7.0. This step ensured the removal of acetic acid excess. The obtained functionalised commercial MWCNTs (f-MWCNT) were left to dry at 90 C. Subsequently, the f-MWCNTs were mixed with 150 mL deionised water and 0.4227 g of (CH COO) Co4H O (MERCK) 3 2 2 leading to a loading 10 atom% Co on f-MWCNTs, which was then subjected to sonication at a low frequency (20 kHz) using a Hielscher (UIP500hd) sonicator (probe tip diameter of 22 mm) for 1 h. The solution was further left to dry and centrifuged (as described above) for the collection of the final product. The cobalt-functionalised MWCNTs (Co-f-MWCNTs) were stored in a desiccator at room temperature. For the immobilisation of the enzyme on the electrode, the following procedure was TM followed: A total of 0.005 g of Co-f-MWCNTs were suspended in 500 L of Nafion perfluorinated resin solution (concentration 5 wt% in lower aliphatic alcohols and water, Aldrich). Then, 8 L of the enzyme were mixed with 2 L of Co-f-MWCNTs suspension. Finally, 2 L of the resulting mix were left to dry on the GC electrode surface. MtLPMO9H was produced and purified to homogeneity as previously described [22]. After the purification the enzyme was divided in aliquots of 500 L, and stored at 15 C until use. Each aliquot was stored for a maximum time of 2 days at 4 C after its first use. The concentration of the purified enzyme was about 5.5 mg/mL, identified by the method introduced by Lowry et al. [23]. 3. Results 3.1. Cyclic Voltammetry As a first step in the examination of the interaction of the immobilised MtLPMO9H with the electrode surface via direct electron transfer, cyclic voltammetry was performed. MtLPMO9H was immobilised on a Co-f-MWCNTs modified GC electrode and the potential was scanned between 0.6 and 0.1 V at a scan rate of 0.1 V s . The voltammogram is presented in Figure 1 (black curve). Two rather faint peaks appear, one during the cathodic scan appearing at 0.252 V and one during the anodic scan at 0.281 V. Capacitance currents are evident in this voltammogram. The peak separation is estimated at 0.029 V, indicating a quasi-reversible reaction. The cyclic voltammetry of the Co-f-MWCNTs modified GC electrode in the absence of the enzyme is also present in Figure 1 (red curve). In this case, no redox peaks are detected, indicating that the redox peaks can indeed be attributed to the redox reaction of the enzyme and not any interference of the matrix. In order to extract the kinetic constant k and the transfer coefficient a from a cyclic voltammogram, assuming Butler–Volmer kinetics [24], one would take advantage of the correlation of the anodic and cathodic peak shift by varying the scan rate. However, these equations do not take the capacitance current and how it might affect the dependence of the peak shift into account. Moreover, at the higher scan rates which would be necessary in such a case, the capacitance would be more dominant, thus rendering the analysis even more difficult. One option would be to subtract the capacitance current from the total current in order to have only the Faradaic component and base the analysis on that alone. However, uncertainty rises for the precision of this approach in cases of non-ideal capacitance. The same uncertainty arises in case one would attempt to extract other magnitudes from the cyclic voltammogram, such as the surface coverage of the enzyme immobilised on the electrode surface. Appl. Sci. 2021, 11, 4715 4 of 11 0.281 V 0.5 −0.5 0.252 V −1 0 0.2 0.4 0.6 E / V vs Ag|AgCl, KCl sat. Figure 1. Experimental results: Cyclic voltammetry of MtLPMO9H immobilised on a Co-f-MWCNTs modified GC electrode (black) and Co-f-MWCNTs modified GC electrode without enzyme (red) at 25 C. Experimental conditions: acetate buffer 500 mM (pH 6) and v = 0.1 V s . Nonetheless, an interesting first approach to making an estimation of the value of the k would be to solve the equations for the immobilised species numerically in the case of cyclic voltammetry for different standard electron transfer kinetic constants. In order to do so, the problem has to be formulated, by considering an electrochemical reaction having formal electrode potential E , where both oxidised (E ) and reduced (E ) form of the Ox Red enzyme are immobilised on the electrode surface E + eGGGGGB E (1) FGGGGG Ox Red where k the cathodic kinetic constant and k the anodic one. The units for both kinetic c a constants are 1/s. Let us denote as G the initial surface concentration of E species and Ox assume a Butler–Volmer law for the rate constants aF 00 0 (EE ) RT k = k e (2) (1a)F 0 (EE ) RT k = k e (3) Thus, the current density expression of the Faradaic current during the redox reaction of the immobilised species can be given from Equation (4) as a funtion of the surface Ox coverage of the Ox species q = , with G the surface coverage of the E species 0 Ox Ox (1a)F 00 aF 00 0 0 (EE ) (EE ) RT RT i = G Fk [(1 q)e qe ] (4) where F is the Faraday constant and the coverage is found by solving the following differential equation, dq i = (5) dt F Assuming a cyclic voltammetry experiment where the potential starts from an initial value E and is scanned linearly towards more cathodic potentials against time at a certain scan rate v , and the scan is reversed at a time t , the applied potential can be expressed as in Equation (6) E = E vt + vjt t j (6) I R R In order to also include capacitance in the problem, we shall assume a contribution to the current, which can be expressed as follows dE i = C (7) C dl dt I / μA Appl. Sci. 2021, 11, 4715 5 of 11 where C is the specific capacitance of the double layer. The total current density, i, shall dl be expressed as a sum of the Faradaic and the capacitance contributions, t t i(t) = i (t) + C v (8) F dl j t t j By solving the problem numerically, the cyclic voltammograms are presented in Figure 2, for different k values. The other parameteres used for this example are 0 6 2 2 00 1 G = 5.1 10 mol m , C = 1 F m , E = 0 V, v = 0.1 V s . For the different dl k values, the peak separation values are presented in Table 1. From these values, one would expect that based on the peak separation of the experimental results at 0.1 V s at 0 1 0.029 V, a rough estimation of the k value should be around 5 s . −1 −2 −0.2 0.2 E / V Figure 2. Computational results: Cyclic voltammetry for different k values. Parameter values: 0 6 2 2 00 1 0 G = 5.1 10 mol m , C = 1 F m , E = 0 V, v = 0.1 V s and k = 100 (black), 20 (red), dl 10 (blue), 5 (green), 2 (orange) and 1 s (orange). Table 1. Peak separation values for an immobilised species assuming v = 0.1 V s and ideal capacitance. 0 1 k /s DE/V 100 0.000 20 0.008 10 0.014 5 0.026 2 0.059 1 0.098 3.2. FT Alternating Current Voltammetry Before attempting to extract the k , FTacV was performed on a Co-f-MWCNTs mod- ified GC electrode with and without MtLPMO9H. The cathodic 5th harmonic in acetate buffer 500 mM, pH 6 for A = 0.2 V and f = 5 is presented in Figure 3. In the case of the immobilised enzyme (black curve) a set of intense peaks around the principle peak at 0.25 V. On the other hand, in the absence of the MtLPMO9H, a faint peak of small amplitude appears at 0.2 V (red curve), leading to the conclusion that the high amplitude harmonic is indeed due to the enzyme and not the immobilization matrix. Then, FTacV was performed so as to apply the methodology introduced [17] for the extraction of the k . At this point, the methodology is summarized: 1. A harmonic h is chosen, being free of capacitance currents. This harmonic is recorded at a fixed amplitude and decreasing frequencies; (rev) 2. The limiting value of the normalized peak height, I / f , of the principal peak is p,h determined. For this frequency, f , the reaction is at the reversible region; -2 i / A m Appl. Sci. 2021, 11, 4715 6 of 11 3. If the transfer coefficient is to be determined, the shift in the potential of the principal peak is plotted as a function of the logarithm of the inverse frequency, 1/ f . Linear regression is performed in the region of high frequencies and the transfer coefficient is determined; 4. The principal peak height I of a quasi-reversible harmonic is determined and the p,h (rev) value I /I is calculated; p,h p,h 5. The kinetic constant is determined from the graph representing the dependance of (rev) I /I on log(k / f ). p,h p,h 1.5 0.5 0.6 0.5 0.4 0.3 0.2 0.1 0 E / V vs Ag|AgCl, KCl sat. Figure 3. Experimental results: 5th harmonics of MtLPMO9Himmobilised on a Co-f-MWCNTs modified GC electrode (black) and Co-f-MWCNTs modified GC electrode without the enzyme (red) at 25 C. Experimental conditions: acetate buffer 500 mM, pH 6, A = 0.20 V and f = 5. Therefore, as a first step, FTacV was performed for two amplitudes, 0.2 and 0.25 V, at frequencies of 5, 3, 1, 0.5, 0.2 and 0.1 Hz. The scan rate was adjusted at each case accordingly in order to fullfill the slow scan rate approximation and render the experiment independent of this factor [16,19]. The cathodic scan of the 4th and the 5th harmonics are presented in Figures 4 and 5, respectively, for A = 0.2 and 0.25 V. Looking at both the amplitudes employed, there is no intense deformation in the harmonics that would suggest a transfer coefficient that would deviate beyond the range of 0.4–0.6; thus, regard- ing the dominant peak [17], no significant errors would be inserted in the preliminary analysis in case an a = 0.5 is assumed. Moreover, both 4th and 5th harmonic seem free of capacitance contribution. As a second step, the trend of the main observable, i.e., the peak height of the prin- ciple peaks, is to be observed. In both cases, typical 4th and 5th harmonics for quasi- reversible reactions of immobilised species are presented for the higher applied frequencies (Figures 4a,c and 5a,c). Apparently, as the frequency is decreased, the amplitude of the harmonics decreases, as predicted theoretically. The trend of the normalized peak height of the principle peaks, I / f , on frequency is presented in Figures 4b,d and 5b,d. By ob- p,h serving these figures, it is evident that a saturation in the peak height of the dominant peak is observed for a frequency of 0.1 Hz. This indicates that reversibility is reached (rev) by that point, and the height of the dominant peak of the reversible harmonic, I has p,h been determined. (rev) As a next step, a quasi-reversible harmonic is chosen and the ratio I /I is calcu- p,h p,h (rev) lated, where I is the normalised peak current for a quasi-reversible harmonic and I p,h p,h the normalised peak current for the reversible harmonic at a certain A and a. For all the combinations of amplitudes and harmonics, the chosen frequency for the quasi-reversible harmonic is that of 5 Hz, while for the peak of the reversible harmonic, it is 0.1 Hz. Let (rev) (rev) us now use the example of I /I and I /I for 0.25 V. The respective estimated p,4 p,5 p,4 p,5 values are 0.57 and 0.6, respectively. I / μA 5 Appl. Sci. 2021, 11, 4715 7 of 11 As a final step, these values shall be used for the estimation of the k from the nomo- (rev) 0 1 grams of I /I against the log(k f ). These nomograms are calculated for a = 0.5 p,h p,h (Figure 6a for the 4th harmonic and Figure 6b for the 5th). The same procedure is done for the amplitude of A = 0.2 V. By taking an average of the extracted values, the k is estimated at 4.6  2.6 s . 3 (b) 0.8 (a) 2 0.6 1 0.4 0 0.2 0.6 0.5 0.4 0.3 0.2 0.1 0 −1 −0.5 0 0.5 E / V vs Ag|AgCl, KCl sat. log f / Hz 2 (d) 0.6 (c) 1.5 1 0.4 0.5 0 0.2 0.6 0.5 0.4 0.3 0.2 0.1 0 −1 −0.5 0 0.5 E / V vs Ag|AgCl, KCl sat. log f / Hz Figure 4. Experimental results: (a) 4th harmonics, (b) normalised peak height of the 4th harmonic, (c) 5th harmonics and (d) normalised peak height of the 5th harmonic, of MtLPMO9H immobilised on a Co-f-MWCNTs modified GC electrode at 25 C. Experimental conditions: acetate buffer 500 mM, pH 6, A = 0.2 V, and f = 5 (black), 3 (red), 1 (blue), 0.5 (green), 0.2 (orange) and 0.1 (magenta) Hz. 10 4 (b) (a) 3.5 2.5 1.5 0 1 0.5 0.4 0.3 0.2 0.1 0 −1 −0.5 0 0.5 E / V vs Ag|AgCl KCl sat log f / Hz 8 (d) 3 (c) 2.5 4 2 2 1.5 0 1 −1 0 0.5 0.4 0.3 0.2 0.1 0 −0.5 0.5 E / V vs Ag|AgCl KCl sat log f / Hz Figure 5. Experimental results: (a) 4th harmonics, (b) normalised peak height of the 4th harmonic, (c) 5th harmonics and (d) normalised peak height of the 5th harmonic, of MtLPMO9H immobilised on a Co-f-MWCNTs modified GC electrode at 25 C. Experimental conditions: acetate buffer 500 mM, pH 6, A = 0.25 V, and f = 5 (black), 3 (red), 1 (blue), 0.5 (green), 0.2 (orange) and 0.1 (magenta) Hz. I / μA I / μA I / μA I / μA 5 4 5 4 -1 -1 -1 I f / μA s -1 I f / μA s p,5 I f / μA s p,4 I f / μA s p,4 p,5 Appl. Sci. 2021, 11, 4715 8 of 11 (a) 0.8 0.6 0.4 0.2 (b) 0.8 0.6 0.4 0.2 −4 −3 −1 0 1 −2 2 0 -1 log(k f ) Figure 6. Computational results: Dependence of the normalised principal peak height for the (a) 4th and (b) 5th harmonic of an immobilised species. Parameters: a = 0.5 and A = 0.2 (black) and 0.25 V (red). In order to validate the value of k , found experimentally, FTacV experiments were 0 1 simulated numerically for k equal to 4.6 s and a equal to 0.57. In order to do so, Equation (5) was solved numerically where the potential ramp is perturbed by a sinusoidal of amplitude A and frequency f , E = E vt + vjt t j + A sin 2p f t (9) I R R 0 and the harmonics where calculated from the current obtained by multiplying the current density, Equation (4) with the electrode surface S. Apparently, both the surface area S and the surface concentration of the oxidized form of the enzyme G are unknown and are expected to vary between different immobilisation experiments. Therefore, the factor G S was chosen by trial-and-error. The simulation results (red curves) together with the 0 13 corresponding experimental plots (black curves) for A = 0.2, G S = 3 10 mol and 0 12 A = 0.25 V, G S = 1.2 10 mol and f = 1 Hz, are presented in Figure 7a,b, respectively. A rather good agreement is observed, implying a satisfactory estimation of k . I / I I / I p,5 p,5,rev p,4 p,4,rev Appl. Sci. 2021, 11, 4715 9 of 11 0.5 (a) 0.4 0.3 0.2 0.1 0.6 0.5 0.4 0.3 0.2 0.1 0 E / V vs Ag|AgCl, KCl sat. (b) 2.5 1.5 0.5 0.5 0.4 0.3 0.2 0.1 0 E / V vs Ag|AgCl KCl sat Figure 7. Experimental (black) versus computational (red dashed line) of the 5th harmonic of MtLPMO9H immobilised on a Co-f-MWCNTs modified GC electrode at 25 C. Experimental condi- tions: acetate buffer 500 mM, pH 6, f = 1 Hz and (a) A = 0.2 and (b) 0.25 V. Computational 0 13 parameters: a=0.57, f = 1 Hz, (a) A = 0.2 V, G S = 3  10 mol and (b) A = 0.25 V, 0 0 0 12 G S = 1.2 10 mol. 4. Discussion MtLPMO9H was immobilised on an electrode surface, ensuring that direct electron transfer is indeed possible for this enzyme with the immobilisation method used with an indication that, for the conventional scan, rated when using cyclic voltammetry, the kinetics were quasi-reversible. The signal was governed by capacitance, a common feature for immobilised enzymes on electrode surfaces. Despite this, still, an initial estimation of the standard electron transfer rate constant was intented through the computational reproduction of cyclic voltammograms. From the peak separation, it was predicted that 0 1 the k would be around 5 s , assuming an a equal to 0.5. Then FTacV was performed for two different amplitudes as various frequencies in order to assure that both quasi-reversibility and reversibility are achieved in order to apply the methodology to extract the k of immobilised species using FTacV. The extracted value was at 4.6 2.6 s being in good accordance with what was expected from cyclic voltammetry. In order to validate the k value obtained experimentally, FTacV experiments were simulated numerically and a rather good agreement was found for transfer coefficient a equal to 0.57. In order to approximate the peak heights of the voltammograms, different values of G S were used for the two different amplitudes. At this point, the validity of 0 1 the G S used shall be ascertained. Since the enzyme concentration is 5.5 mg mL and 8 L were utilised, and they were dilluted in 10 L to a final concentration of 4.4 mg mL . From this, 2 L were used, and, taking into consideration that the molecular weight of the enzyme is 65 kDa [22], the maximum moles that can be 1.35  10 . Considering that not all of the enzymes would be bound to the matrix and from what was bound, not all would be oriented in such a way so as to interact with the enzyme, the values used for I / μA i / μA 5 Appl. Sci. 2021, 11, 4715 10 of 11 the simulation seem to be valid. Nevertheless, it has to be pointed out that the proposed experimental methodology for obtaining kinetic parameters does not require knowledge of the surface concentration of the immobilised species or the the value of the surface area. In general, it is common practice to compare computational with experimental results in order to ascertain the validity of the parameters used for the computational ones. The computational fits tend to reproduce most of the features of the voltammogram, just as in this case, where the basic features of the harmonics presented are fitted rather well [25,26]. Regarding the precision of the comparison of the computational harmonics with the experimental ones, it should also be taken into account that the above analysis is valid only if the assumptions of the model are closely met, where the immobilised species must behave as a Langmuirian monolayer and a dispersion of the electrochemical transfer rates should be absent. Otherwise, where kinetic or thermodynamic dispersion is present, more elaborate models have to be considered [27–29]. The influence of kinetic and thermodynamic dispersion might affect the waveform of the voltammograms [30], and other theories such as that of Marcus–Hush can applied, instead of the Butler–Volmer law [31]. Yet, in this case, the Butler–Volmer law seems to be rather sufficient for this case. To conclude, with the k value that was estimated, it seems that, under the right conditions, it is feasible to render the system reversible and take advantage of it for bioelectrocatalytic purposes. Thus, it could be proven to be rather resourceful in such applications. Author Contributions: Conceptualization, D.Z. and A.K. (Antonis Karantonis); methodology, D.Z.; software, A.K. (Antonis Karantonis); validation, D.Z. and A.K. (Antonis Karantonis); formal analysis, R.X., D.Z.; investigation, D.Z.; resources, A.K. (Antonis Karantonis), E.T.; data curation, D.Z.; writing— original draft preparation, D.Z., A.K. (Antonis Karantonis); writing—review and editing, A.K. (Antonis Karantonis), A.K. (Anthi Karnaouri), E.T.; supervision, A.K. (Antonis Karantonis), E.T.; project administration, A.K. (Antonis Karantonis); funding acquisition, A.K. (Antonis Karantonis). All authors have read and agreed to the published version of the manuscript. Funding: The research work was supported by the Hellenic Foundation for Research and Inno- vation (H.F.R.I.) under the “First Call for H.F.R.I. Research Projects to support Faculty members and Researchers and the procurement of high-cost research equipment grant” (Project Number: HFRI-FM17-3090). Institutional Review Board Statement: Not applicable. Informed Consent Statement: Not applicable. Data Availability Statement: Data sharing not applicable. Acknowledgments: Chr. Argirusis and P. Pandis are aknowledged for providing the Co-f-MWCNTs. Conflicts of Interest: The authors declare no conflict of interest. References 1. Eibinger, M.; Ganner, T.; Bubner, P.; Rošker, S.; Kracher, D.; Haltrich, D.; Ludwig, R.; Plank, H.; Nidetzky, B. 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Exploitation of Enzymes for the Production of Biofuels: Electrochemical Determination of Kinetic Parameters of LPMOs

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applied sciences Article Exploitation of Enzymes for the Production of Biofuels: Electrochemical Determination of Kinetic Parameters of LPMOs 1 2 1 2 1, Dimitrios Zouraris , Anthi Karnaouri , Raphaela Xydou , Evangelos Topakas and Antonis Karantonis * Laboratory of Physical Chemistry and Applied Electrochemistry, School of Chemical Engineering, National Technical University of Athens, Zografou, 15780 Athens, Greece; dimzouraris@mail.ntua.gr (D.Z.); ch15611@mail.ntua.gr (R.X.) Biotechnology Laboratory, School of Chemical Engineering, National Technical University of Athens, Zografou, 15780 Athens, Greece; akarnaouri@chemeng.ntua.gr (A.K.); vtopakas@chemeng.ntua.gr (E.T.) * Correspondence: antkar@central.ntua.gr Abstract: Lytic polysaccharide monooxygenases (LPMOs) consist of a class of enzymes that boost the release of oxidised products from plant biomass, in an approach that is more eco-friendly than the traditional ones, employing harsh chemicals. Since LPMOs are redox enzymes, they could possibly be exploited by immobilisation on electrode surfaces. Such an approach requires knowledge of kinetic and thermodynamic information for the interaction of the enzyme with the electrode surface. In this work, a novel methodology is applied for the determination of such parameters for an LPMO from the filamentous fungus Thermothelomyces thermophila, MtLPMO9H. Keywords: LPMO; Fourier Transform ac Voltammetry (FTacV); cyclic voltammetry; Direct Electron Transfer (DET) Citation: Zouraris, D.; Karnaouri, A.; 1. Introduction Xydou, R.; Topakas, E.; Karantonis, A. Exploitation of Enzymes for the The exploitation of lignocellulosic biomass, such as wood and agricultural residues, Production of Biofuels: towards the production of fermentable sugars for the production of second-generation Electrochemical Determination of biofuels in an environmentally friendly way, requires of enzymatic degradation. This step Kinetic Parameters of LPMOs. Appl. has low energy requirements, selectivity, mild processing environment and no need of harsh Sci. 2021, 11, 4715. chemicals, in contrast to classical chemical methods, and it is catalyzed by a combination https://doi.org/10.3390/app11114715 of hydrolytic and oxidative enzymes [1,2]. Regarding the oxidation reactions, performing these steps in an electrochemical reactor, i.e., electroenzymatic synthesis of sugars, is a Received: 23 April 2021 promising approach for the production of such chemicals. In principle, when electrolysis is Accepted: 18 May 2021 combined with enzyme reactions, a redox enzyme is maintained in its active state through Published: 21 May 2021 an electrode process. This can be achieved by oxidation of or a reduction in a cofactor or a mediator on the electrode surface, or by direct electron transfer to the enzyme. Therefore, Publisher’s Note: MDPI stays neutral applying enzyme immobilization onto the electrode and combining bioelectrocatalysis with regard to jurisdictional claims in with traditional enzymatic hydrolysis offer perspectives for developing novel processes for published maps and institutional affil- the production of biofuels and other value-added materials from lignocellulose. iations. Lytic polysaccharide monooxygenases (LPMOs) are copper-dependent enzymes that have the capacity to cleave polysaccharides via an oxidative mechanism [3]. They are classified as Auxiliary Activities (AAs) in the Carbohydrate Active enZyme database (CAZy). More specifically, they are divided into seven families (AA9–11 and AA13–16) Copyright: © 2021 by the authors. based on their sequence similarities, with the majority of those that are studied thoroughly Licensee MDPI, Basel, Switzerland. belonging to the AA9 and AA10 families [4]. LPMOs act synergistically with other biomass- This article is an open access article degrading enzymes and significantly boost the hydrolytic performance of cellulase and distributed under the terms and hemicellulase cocktails, primarily by improving the accessibility of the enzymes to the conditions of the Creative Commons substrate [5,6]. Attribution (CC BY) license (https:// Until recently, the main theory regarding the mechanism of action of LPMOs involved creativecommons.org/licenses/by/ the introduction of a single oxygen atom from molecular oxygen into the substrate, while 4.0/). Appl. Sci. 2021, 11, 4715. https://doi.org/10.3390/app11114715 https://www.mdpi.com/journal/applsci Appl. Sci. 2021, 11, 4715 2 of 11 taking electrons from an external electron donor for their action [7]. More recently, Bis- saro et al., while examining an LPMO belonging to the AA10 family, supported the idea that the chemically relevant co-substrate of LPMO catalyzed oxidation is H O [8]. Regard- 2 2 less of the mechanism of the oxidative cleavage of the polysaccharidic substrate, in both cases, the reaction is initiated when the active center of the enzyme takes an electron from an external electron donor. The nature of the donors used in laboratory experimental setups include ascorbic acid, cysteine and reduced glutathione, but also a wide range of plant-derived phenols [9,10], lignin compounds [11] and photocatalytic and enzymatic systems [12]. The reported mechanisms for the initial reduction in LPMOs do not implicate any chemical steps other than a one-step, one-electron reaction. One interesting point regarding these enzymes, which could possibly be an advantage for their electrochemical exploitation, is that their copper-containing active center is not “buried” inside their structure but can be found on a solvent-exposed, flat surface [13]. This could facilitate their use as electrode coatings, by directly providing them with electrons from an electrode surface, while immobilized on the electrode surface. Other than their study, this characteristic could lead to the exploitation of the bioelectrocatalytic action of LPMOs towards the production of oxidised products (oligosaccharides and glucans) from biomass, in concert with hydrolytic enzymes, in the absence of any external reducing agent. This means that by providing electrons directly from an electrode surface to an immobilised LPMO, the enzyme could be utilised in bioconversions through bioelectrocatalysis focusing on product life cycles. The developed bioconversions will be carried out in predominantly aqueous media using enzymes, and therefore be characterised by a limited use of toxic reagents or solvents, requiring only an ambient temperature, in the absence of any reducing agent [14]. In order to test if the above task is feasible, a parameter that should be mentioned is the standard electron transfer rate constant (k ) between the immobilized electrode and the enzyme. This electron transfer rate should be rather fast, so that the electrocat- alytic current measured represents the rate of substrate turnover at the enzyme active site [15]. Among the electroanalytical methods, a technique that is very promising for the study of immobilised LPMOs is that of large amplitude fast Fourier transform alternat- ing current voltammetry (FTacV), with which one can study both free and immobilised species, eliminating capacitance currents, a problem common in immobilised-on-electrode species [16–19]. In the past, this technique has been employed for the determination of the formal potential of immobilised LPMOs [20], as well as for the study of the direct electron transfer of multi-copper laccase like oxidases [6] and the interaction with epinephrine as a substrate [21]. Recently, a methodology for the extraction of the transfer coefficient a and the k for immobilised species has been proposed, but has yet to be applied experimen- tally [17]. In this work, this particular methology shall be employed for the extraction of the k an LPMO from the filamentous fungus Thermothelomyces thermophila, MtLPMO9H, and the calulated value of k shall be verified by numerical simulation. To our knowledge, k values for the interaction of an immobilized LPMO with an electrode surface is reported for the first time. 2. Materials and Methods Voltammetric experiments were performed in a single-compartment three-electrode cell consisting of a working electrode, a Pt wire as a counter electrode, and a AgjAgCl, KCl sat. reference electrode (+0.197 V vs. NHE). The aqueous solutions of about 5 mL consisted of 0.5 M acetate buffer (pH 6) as a supporting electrolyte. The working electrode consisted of a cobalt functionalised multi-walled carbon nan- otubes modified glassy carbon (GC) electrode, of 3 mm diameter. The immobilisation matrix was prepared as follows: A total of 1 g of commercial functionalised multi-wall carbon nanotubes (MWCNTs) (Hongwu Material, item No: C933-MC, Guangzhou, China) were added in a 150 mL solution with 20 % v/v. The suspension was stirred for 20 min at 120 C for further functionalization, until the liquid phase was evaporated. The solution Appl. Sci. 2021, 11, 4715 3 of 11 was left to dry overnight at 90 C until dry powder was collected. The powder was washed, then centrifuged 5 times with deionised water until the supernatant had a pH value of '7.0. This step ensured the removal of acetic acid excess. The obtained functionalised commercial MWCNTs (f-MWCNT) were left to dry at 90 C. Subsequently, the f-MWCNTs were mixed with 150 mL deionised water and 0.4227 g of (CH COO) Co4H O (MERCK) 3 2 2 leading to a loading 10 atom% Co on f-MWCNTs, which was then subjected to sonication at a low frequency (20 kHz) using a Hielscher (UIP500hd) sonicator (probe tip diameter of 22 mm) for 1 h. The solution was further left to dry and centrifuged (as described above) for the collection of the final product. The cobalt-functionalised MWCNTs (Co-f-MWCNTs) were stored in a desiccator at room temperature. For the immobilisation of the enzyme on the electrode, the following procedure was TM followed: A total of 0.005 g of Co-f-MWCNTs were suspended in 500 L of Nafion perfluorinated resin solution (concentration 5 wt% in lower aliphatic alcohols and water, Aldrich). Then, 8 L of the enzyme were mixed with 2 L of Co-f-MWCNTs suspension. Finally, 2 L of the resulting mix were left to dry on the GC electrode surface. MtLPMO9H was produced and purified to homogeneity as previously described [22]. After the purification the enzyme was divided in aliquots of 500 L, and stored at 15 C until use. Each aliquot was stored for a maximum time of 2 days at 4 C after its first use. The concentration of the purified enzyme was about 5.5 mg/mL, identified by the method introduced by Lowry et al. [23]. 3. Results 3.1. Cyclic Voltammetry As a first step in the examination of the interaction of the immobilised MtLPMO9H with the electrode surface via direct electron transfer, cyclic voltammetry was performed. MtLPMO9H was immobilised on a Co-f-MWCNTs modified GC electrode and the potential was scanned between 0.6 and 0.1 V at a scan rate of 0.1 V s . The voltammogram is presented in Figure 1 (black curve). Two rather faint peaks appear, one during the cathodic scan appearing at 0.252 V and one during the anodic scan at 0.281 V. Capacitance currents are evident in this voltammogram. The peak separation is estimated at 0.029 V, indicating a quasi-reversible reaction. The cyclic voltammetry of the Co-f-MWCNTs modified GC electrode in the absence of the enzyme is also present in Figure 1 (red curve). In this case, no redox peaks are detected, indicating that the redox peaks can indeed be attributed to the redox reaction of the enzyme and not any interference of the matrix. In order to extract the kinetic constant k and the transfer coefficient a from a cyclic voltammogram, assuming Butler–Volmer kinetics [24], one would take advantage of the correlation of the anodic and cathodic peak shift by varying the scan rate. However, these equations do not take the capacitance current and how it might affect the dependence of the peak shift into account. Moreover, at the higher scan rates which would be necessary in such a case, the capacitance would be more dominant, thus rendering the analysis even more difficult. One option would be to subtract the capacitance current from the total current in order to have only the Faradaic component and base the analysis on that alone. However, uncertainty rises for the precision of this approach in cases of non-ideal capacitance. The same uncertainty arises in case one would attempt to extract other magnitudes from the cyclic voltammogram, such as the surface coverage of the enzyme immobilised on the electrode surface. Appl. Sci. 2021, 11, 4715 4 of 11 0.281 V 0.5 −0.5 0.252 V −1 0 0.2 0.4 0.6 E / V vs Ag|AgCl, KCl sat. Figure 1. Experimental results: Cyclic voltammetry of MtLPMO9H immobilised on a Co-f-MWCNTs modified GC electrode (black) and Co-f-MWCNTs modified GC electrode without enzyme (red) at 25 C. Experimental conditions: acetate buffer 500 mM (pH 6) and v = 0.1 V s . Nonetheless, an interesting first approach to making an estimation of the value of the k would be to solve the equations for the immobilised species numerically in the case of cyclic voltammetry for different standard electron transfer kinetic constants. In order to do so, the problem has to be formulated, by considering an electrochemical reaction having formal electrode potential E , where both oxidised (E ) and reduced (E ) form of the Ox Red enzyme are immobilised on the electrode surface E + eGGGGGB E (1) FGGGGG Ox Red where k the cathodic kinetic constant and k the anodic one. The units for both kinetic c a constants are 1/s. Let us denote as G the initial surface concentration of E species and Ox assume a Butler–Volmer law for the rate constants aF 00 0 (EE ) RT k = k e (2) (1a)F 0 (EE ) RT k = k e (3) Thus, the current density expression of the Faradaic current during the redox reaction of the immobilised species can be given from Equation (4) as a funtion of the surface Ox coverage of the Ox species q = , with G the surface coverage of the E species 0 Ox Ox (1a)F 00 aF 00 0 0 (EE ) (EE ) RT RT i = G Fk [(1 q)e qe ] (4) where F is the Faraday constant and the coverage is found by solving the following differential equation, dq i = (5) dt F Assuming a cyclic voltammetry experiment where the potential starts from an initial value E and is scanned linearly towards more cathodic potentials against time at a certain scan rate v , and the scan is reversed at a time t , the applied potential can be expressed as in Equation (6) E = E vt + vjt t j (6) I R R In order to also include capacitance in the problem, we shall assume a contribution to the current, which can be expressed as follows dE i = C (7) C dl dt I / μA Appl. Sci. 2021, 11, 4715 5 of 11 where C is the specific capacitance of the double layer. The total current density, i, shall dl be expressed as a sum of the Faradaic and the capacitance contributions, t t i(t) = i (t) + C v (8) F dl j t t j By solving the problem numerically, the cyclic voltammograms are presented in Figure 2, for different k values. The other parameteres used for this example are 0 6 2 2 00 1 G = 5.1 10 mol m , C = 1 F m , E = 0 V, v = 0.1 V s . For the different dl k values, the peak separation values are presented in Table 1. From these values, one would expect that based on the peak separation of the experimental results at 0.1 V s at 0 1 0.029 V, a rough estimation of the k value should be around 5 s . −1 −2 −0.2 0.2 E / V Figure 2. Computational results: Cyclic voltammetry for different k values. Parameter values: 0 6 2 2 00 1 0 G = 5.1 10 mol m , C = 1 F m , E = 0 V, v = 0.1 V s and k = 100 (black), 20 (red), dl 10 (blue), 5 (green), 2 (orange) and 1 s (orange). Table 1. Peak separation values for an immobilised species assuming v = 0.1 V s and ideal capacitance. 0 1 k /s DE/V 100 0.000 20 0.008 10 0.014 5 0.026 2 0.059 1 0.098 3.2. FT Alternating Current Voltammetry Before attempting to extract the k , FTacV was performed on a Co-f-MWCNTs mod- ified GC electrode with and without MtLPMO9H. The cathodic 5th harmonic in acetate buffer 500 mM, pH 6 for A = 0.2 V and f = 5 is presented in Figure 3. In the case of the immobilised enzyme (black curve) a set of intense peaks around the principle peak at 0.25 V. On the other hand, in the absence of the MtLPMO9H, a faint peak of small amplitude appears at 0.2 V (red curve), leading to the conclusion that the high amplitude harmonic is indeed due to the enzyme and not the immobilization matrix. Then, FTacV was performed so as to apply the methodology introduced [17] for the extraction of the k . At this point, the methodology is summarized: 1. A harmonic h is chosen, being free of capacitance currents. This harmonic is recorded at a fixed amplitude and decreasing frequencies; (rev) 2. The limiting value of the normalized peak height, I / f , of the principal peak is p,h determined. For this frequency, f , the reaction is at the reversible region; -2 i / A m Appl. Sci. 2021, 11, 4715 6 of 11 3. If the transfer coefficient is to be determined, the shift in the potential of the principal peak is plotted as a function of the logarithm of the inverse frequency, 1/ f . Linear regression is performed in the region of high frequencies and the transfer coefficient is determined; 4. The principal peak height I of a quasi-reversible harmonic is determined and the p,h (rev) value I /I is calculated; p,h p,h 5. The kinetic constant is determined from the graph representing the dependance of (rev) I /I on log(k / f ). p,h p,h 1.5 0.5 0.6 0.5 0.4 0.3 0.2 0.1 0 E / V vs Ag|AgCl, KCl sat. Figure 3. Experimental results: 5th harmonics of MtLPMO9Himmobilised on a Co-f-MWCNTs modified GC electrode (black) and Co-f-MWCNTs modified GC electrode without the enzyme (red) at 25 C. Experimental conditions: acetate buffer 500 mM, pH 6, A = 0.20 V and f = 5. Therefore, as a first step, FTacV was performed for two amplitudes, 0.2 and 0.25 V, at frequencies of 5, 3, 1, 0.5, 0.2 and 0.1 Hz. The scan rate was adjusted at each case accordingly in order to fullfill the slow scan rate approximation and render the experiment independent of this factor [16,19]. The cathodic scan of the 4th and the 5th harmonics are presented in Figures 4 and 5, respectively, for A = 0.2 and 0.25 V. Looking at both the amplitudes employed, there is no intense deformation in the harmonics that would suggest a transfer coefficient that would deviate beyond the range of 0.4–0.6; thus, regard- ing the dominant peak [17], no significant errors would be inserted in the preliminary analysis in case an a = 0.5 is assumed. Moreover, both 4th and 5th harmonic seem free of capacitance contribution. As a second step, the trend of the main observable, i.e., the peak height of the prin- ciple peaks, is to be observed. In both cases, typical 4th and 5th harmonics for quasi- reversible reactions of immobilised species are presented for the higher applied frequencies (Figures 4a,c and 5a,c). Apparently, as the frequency is decreased, the amplitude of the harmonics decreases, as predicted theoretically. The trend of the normalized peak height of the principle peaks, I / f , on frequency is presented in Figures 4b,d and 5b,d. By ob- p,h serving these figures, it is evident that a saturation in the peak height of the dominant peak is observed for a frequency of 0.1 Hz. This indicates that reversibility is reached (rev) by that point, and the height of the dominant peak of the reversible harmonic, I has p,h been determined. (rev) As a next step, a quasi-reversible harmonic is chosen and the ratio I /I is calcu- p,h p,h (rev) lated, where I is the normalised peak current for a quasi-reversible harmonic and I p,h p,h the normalised peak current for the reversible harmonic at a certain A and a. For all the combinations of amplitudes and harmonics, the chosen frequency for the quasi-reversible harmonic is that of 5 Hz, while for the peak of the reversible harmonic, it is 0.1 Hz. Let (rev) (rev) us now use the example of I /I and I /I for 0.25 V. The respective estimated p,4 p,5 p,4 p,5 values are 0.57 and 0.6, respectively. I / μA 5 Appl. Sci. 2021, 11, 4715 7 of 11 As a final step, these values shall be used for the estimation of the k from the nomo- (rev) 0 1 grams of I /I against the log(k f ). These nomograms are calculated for a = 0.5 p,h p,h (Figure 6a for the 4th harmonic and Figure 6b for the 5th). The same procedure is done for the amplitude of A = 0.2 V. By taking an average of the extracted values, the k is estimated at 4.6  2.6 s . 3 (b) 0.8 (a) 2 0.6 1 0.4 0 0.2 0.6 0.5 0.4 0.3 0.2 0.1 0 −1 −0.5 0 0.5 E / V vs Ag|AgCl, KCl sat. log f / Hz 2 (d) 0.6 (c) 1.5 1 0.4 0.5 0 0.2 0.6 0.5 0.4 0.3 0.2 0.1 0 −1 −0.5 0 0.5 E / V vs Ag|AgCl, KCl sat. log f / Hz Figure 4. Experimental results: (a) 4th harmonics, (b) normalised peak height of the 4th harmonic, (c) 5th harmonics and (d) normalised peak height of the 5th harmonic, of MtLPMO9H immobilised on a Co-f-MWCNTs modified GC electrode at 25 C. Experimental conditions: acetate buffer 500 mM, pH 6, A = 0.2 V, and f = 5 (black), 3 (red), 1 (blue), 0.5 (green), 0.2 (orange) and 0.1 (magenta) Hz. 10 4 (b) (a) 3.5 2.5 1.5 0 1 0.5 0.4 0.3 0.2 0.1 0 −1 −0.5 0 0.5 E / V vs Ag|AgCl KCl sat log f / Hz 8 (d) 3 (c) 2.5 4 2 2 1.5 0 1 −1 0 0.5 0.4 0.3 0.2 0.1 0 −0.5 0.5 E / V vs Ag|AgCl KCl sat log f / Hz Figure 5. Experimental results: (a) 4th harmonics, (b) normalised peak height of the 4th harmonic, (c) 5th harmonics and (d) normalised peak height of the 5th harmonic, of MtLPMO9H immobilised on a Co-f-MWCNTs modified GC electrode at 25 C. Experimental conditions: acetate buffer 500 mM, pH 6, A = 0.25 V, and f = 5 (black), 3 (red), 1 (blue), 0.5 (green), 0.2 (orange) and 0.1 (magenta) Hz. I / μA I / μA I / μA I / μA 5 4 5 4 -1 -1 -1 I f / μA s -1 I f / μA s p,5 I f / μA s p,4 I f / μA s p,4 p,5 Appl. Sci. 2021, 11, 4715 8 of 11 (a) 0.8 0.6 0.4 0.2 (b) 0.8 0.6 0.4 0.2 −4 −3 −1 0 1 −2 2 0 -1 log(k f ) Figure 6. Computational results: Dependence of the normalised principal peak height for the (a) 4th and (b) 5th harmonic of an immobilised species. Parameters: a = 0.5 and A = 0.2 (black) and 0.25 V (red). In order to validate the value of k , found experimentally, FTacV experiments were 0 1 simulated numerically for k equal to 4.6 s and a equal to 0.57. In order to do so, Equation (5) was solved numerically where the potential ramp is perturbed by a sinusoidal of amplitude A and frequency f , E = E vt + vjt t j + A sin 2p f t (9) I R R 0 and the harmonics where calculated from the current obtained by multiplying the current density, Equation (4) with the electrode surface S. Apparently, both the surface area S and the surface concentration of the oxidized form of the enzyme G are unknown and are expected to vary between different immobilisation experiments. Therefore, the factor G S was chosen by trial-and-error. The simulation results (red curves) together with the 0 13 corresponding experimental plots (black curves) for A = 0.2, G S = 3 10 mol and 0 12 A = 0.25 V, G S = 1.2 10 mol and f = 1 Hz, are presented in Figure 7a,b, respectively. A rather good agreement is observed, implying a satisfactory estimation of k . I / I I / I p,5 p,5,rev p,4 p,4,rev Appl. Sci. 2021, 11, 4715 9 of 11 0.5 (a) 0.4 0.3 0.2 0.1 0.6 0.5 0.4 0.3 0.2 0.1 0 E / V vs Ag|AgCl, KCl sat. (b) 2.5 1.5 0.5 0.5 0.4 0.3 0.2 0.1 0 E / V vs Ag|AgCl KCl sat Figure 7. Experimental (black) versus computational (red dashed line) of the 5th harmonic of MtLPMO9H immobilised on a Co-f-MWCNTs modified GC electrode at 25 C. Experimental condi- tions: acetate buffer 500 mM, pH 6, f = 1 Hz and (a) A = 0.2 and (b) 0.25 V. Computational 0 13 parameters: a=0.57, f = 1 Hz, (a) A = 0.2 V, G S = 3  10 mol and (b) A = 0.25 V, 0 0 0 12 G S = 1.2 10 mol. 4. Discussion MtLPMO9H was immobilised on an electrode surface, ensuring that direct electron transfer is indeed possible for this enzyme with the immobilisation method used with an indication that, for the conventional scan, rated when using cyclic voltammetry, the kinetics were quasi-reversible. The signal was governed by capacitance, a common feature for immobilised enzymes on electrode surfaces. Despite this, still, an initial estimation of the standard electron transfer rate constant was intented through the computational reproduction of cyclic voltammograms. From the peak separation, it was predicted that 0 1 the k would be around 5 s , assuming an a equal to 0.5. Then FTacV was performed for two different amplitudes as various frequencies in order to assure that both quasi-reversibility and reversibility are achieved in order to apply the methodology to extract the k of immobilised species using FTacV. The extracted value was at 4.6 2.6 s being in good accordance with what was expected from cyclic voltammetry. In order to validate the k value obtained experimentally, FTacV experiments were simulated numerically and a rather good agreement was found for transfer coefficient a equal to 0.57. In order to approximate the peak heights of the voltammograms, different values of G S were used for the two different amplitudes. At this point, the validity of 0 1 the G S used shall be ascertained. Since the enzyme concentration is 5.5 mg mL and 8 L were utilised, and they were dilluted in 10 L to a final concentration of 4.4 mg mL . From this, 2 L were used, and, taking into consideration that the molecular weight of the enzyme is 65 kDa [22], the maximum moles that can be 1.35  10 . Considering that not all of the enzymes would be bound to the matrix and from what was bound, not all would be oriented in such a way so as to interact with the enzyme, the values used for I / μA i / μA 5 Appl. Sci. 2021, 11, 4715 10 of 11 the simulation seem to be valid. Nevertheless, it has to be pointed out that the proposed experimental methodology for obtaining kinetic parameters does not require knowledge of the surface concentration of the immobilised species or the the value of the surface area. In general, it is common practice to compare computational with experimental results in order to ascertain the validity of the parameters used for the computational ones. The computational fits tend to reproduce most of the features of the voltammogram, just as in this case, where the basic features of the harmonics presented are fitted rather well [25,26]. Regarding the precision of the comparison of the computational harmonics with the experimental ones, it should also be taken into account that the above analysis is valid only if the assumptions of the model are closely met, where the immobilised species must behave as a Langmuirian monolayer and a dispersion of the electrochemical transfer rates should be absent. Otherwise, where kinetic or thermodynamic dispersion is present, more elaborate models have to be considered [27–29]. The influence of kinetic and thermodynamic dispersion might affect the waveform of the voltammograms [30], and other theories such as that of Marcus–Hush can applied, instead of the Butler–Volmer law [31]. Yet, in this case, the Butler–Volmer law seems to be rather sufficient for this case. To conclude, with the k value that was estimated, it seems that, under the right conditions, it is feasible to render the system reversible and take advantage of it for bioelectrocatalytic purposes. Thus, it could be proven to be rather resourceful in such applications. Author Contributions: Conceptualization, D.Z. and A.K. (Antonis Karantonis); methodology, D.Z.; software, A.K. (Antonis Karantonis); validation, D.Z. and A.K. (Antonis Karantonis); formal analysis, R.X., D.Z.; investigation, D.Z.; resources, A.K. (Antonis Karantonis), E.T.; data curation, D.Z.; writing— original draft preparation, D.Z., A.K. (Antonis Karantonis); writing—review and editing, A.K. (Antonis Karantonis), A.K. (Anthi Karnaouri), E.T.; supervision, A.K. (Antonis Karantonis), E.T.; project administration, A.K. (Antonis Karantonis); funding acquisition, A.K. (Antonis Karantonis). All authors have read and agreed to the published version of the manuscript. Funding: The research work was supported by the Hellenic Foundation for Research and Inno- vation (H.F.R.I.) under the “First Call for H.F.R.I. Research Projects to support Faculty members and Researchers and the procurement of high-cost research equipment grant” (Project Number: HFRI-FM17-3090). Institutional Review Board Statement: Not applicable. Informed Consent Statement: Not applicable. Data Availability Statement: Data sharing not applicable. Acknowledgments: Chr. Argirusis and P. Pandis are aknowledged for providing the Co-f-MWCNTs. Conflicts of Interest: The authors declare no conflict of interest. References 1. Eibinger, M.; Ganner, T.; Bubner, P.; Rošker, S.; Kracher, D.; Haltrich, D.; Ludwig, R.; Plank, H.; Nidetzky, B. 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Journal

Applied Sciences – Multidisciplinary Digital Publishing Institute

Published: May 21, 2021

Keywords: LPMO; Fourier Transform ac Voltammetry (FTacV); cyclic voltammetry; Direct Electron Transfer (DET)

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