The variables influencing laccase production by white-rot fungus Ganoderma sp. rckk-02 were optimized employing response surface methodology. Malt extract (6.0% w/v), lignin (0.5% w/v) and pH (5.5) were found to be the most significant factors for enhanced laccase production by 7 fold (226.0 U/ml) as compared to unoptimized growth conditions (32.0 U/ml). The N-terminal sequence of laccase revealed its distinct amino acid profile (S- I- R- N- S- G), which suggested it as a novel enzyme. The Far-UV CD spectrum of the laccase showed single broad negative trough at around 213 nm, a typical signature of all β proteins. The laccase was found to fall in the range of middle redox potential laccases. Purified laccase at dosage of 2.5 Ug−1 body weight when supplemented with pelleted diet of rats, a significant improvement (p < 0.05) in nutrients digestibility without causing any elevation of blood stress enzymes was observed.
White rot fungi are known to be the potential producer of ligninolytic enzymes i.e. mangnese peroxidase, lignin peroxidase and laccases. Among these, laccases are one of the widely studied oxidoreductases and majority of them contain four copper ions per molecule. They catalyze single-electron oxidation of a wide variety of organic and inorganic substrates including mono-, di-, polyphenols, methoxyphenols, aromatic amines and ascorbate with concomitant four-electron reduction of oxygen to water1. This makes laccases useful for their varied applications in several biotechnological processes such as phenolics elimination for stabilization and browning of fruit juices, beer/wine, in bleaching of paper pulp, decolourization of dyes and textile effluents, oxidation-reduction reaction in biosensors development, PAHs and other xenobiotics degradation for soil bioremediation, production of complex polymers in organic synthesis and mild oxidizing agent in cosmetics development2. In addition, its being an efficient lignin degrading biocatalyst, has been applied in biopulping but scarcely been tried for its possible application in improving the bioavailability of nutrients and digestibility of animal feed, especially for monogastric diets.
Laccase can either act on feed components prior to or after consumption i.e. within the gastrointestinal tract3. However, to make use of laccase commercially viable in feed improvement, its production level should be high as well as it should be nontoxic to animals. The critical safety evaluation of the enzymes used for improving animal feed is must and tests involving rat models have been found essential to provide some preliminary indication of possible cellular mutagenicity, potential carcinogenicity and teratogenecity during the developmental stages3,4,5. Furthermore, random addition of enzymes to diets without consideration for specific situations, toxicity and substrate targets will only discourage or delay on- farm adoption of enzyme technology6. Therefore, we have also selected the rat model for evaluation of efficiency of laccase in improvement of pelleted diets specifically for monogastric animals. Thus for producing higher amount of such enzymes researchers have gained interest in minimizing the cost of enzyme preparation to be used as ruminants diet supplement7. Thereby, designing and optimization of fermentation media for the most economical production is one of the most important task.
The objectives of this work were to optimize production of laccase with middle redox potential from an indigenous white rot fungus, Ganoderma sp. rckk-02 using response surface methodology under liquid static cultivation conditions, its characterization and its evaluation for possible application as animal feed supplement.
Laccase production from Ganoderma sp. rckk-02, when grown under static cultivation conditions, started after 48 h of incubation (3.8 U/ml) and reached maximum (32 U/ml) after 240 h and declined thereafter (Graph not shown).
Response surface methodology (RSM)
For the selection of the key factors like carbon source, nitrogen source and trace metal one factor at a time strategy was adopted followed by Plackett-Burman Design (PBD). Thereafter, RSM employing CCRD was used to optimize individual concentrations of selected variables viz. malt extract, lignin and pH, identified to possess maximum influence on laccase production from Ganoderma sp. rckk-02. Table 2 depicts the CCRD analysis along with experimental and predicted responses obtained in each individual experiment. The regression equations obtained after the analysis of variance (ANOVA) gave the level of laccase produced as a function of the initial values of malt extract, pH and lignin (Table 3). The final response equation that represented a suitable model for laccase production is given below: Y = 224.97 + 10.12A − 2.33B − 2.08C − 34.35A2 − 17.79B2 − 7.41C2 − 5.25AB + 1AC + 1.13A3 + 0.083B3 + 0.083C3, where Y is laccase production; A is malt extract; B is lignin; and C is pH.
The coefficient of determination (R2) was calculated to be 0.9998 for laccase production and thus the model could explain 99.98% variability in the response. The R2 value provided a measure of variability in the observed response values, which could be explained by the experimental factors and their interactions. The closer the R2 value is to 1.00, stronger the model is and the better it predicts8. Predicted R2 (0.9931) was found to be very close to the adjusted R2 (0.9993) for laccase yield, which shows number of terms in the model relative to the number of squares of points in the design. The adjusted R2 corrects the R2 value for the sample size and number of terms in the model. If there are many terms in the model and the sample size is not very large, the adjusted R2 may be noticeably smaller than predicted R2. The purpose of statistical analysis is to determine the experimental factors, which generate signals that are large in comparison to noise. The adequate precision measuring the signal to noise ratio was found to be 131.839 for laccase production. A signal to noise ratio greater than 4 is desirable. The model is thus fit and can be used to navigate the design space. The model F-value of 1981.84 and values of Prob > F (<0.05) indicated that model terms are significant (Table 3).
Three-dimensional response surface curves were plotted to study the interaction among different physiochemical parameters to find out optimum laccase production from Ganoderma sp. rckk-02. The plots were generated by plotting the response (Laccase production) using the Z-axis against two independent variables while keeping the other independent variables at their O-level.
An interaction between the two parameters (pH and lignin) gave a higher enzyme yield at lignin concentration of 0.5% (w/v) and pH 5.5 (Fig. 1a, d). The response between pH and malt extract at O-level of lignin indicated that a moderately acidic pH (5.5) was desirable, since laccase production from Ganoderma sp. rckk-02 is sensitive to pH (optimum range pH 5.0–5.8) (Fig. 1b). Response surface plot of the interaction between malt extract and lignin, while keeping pH at O-level is depicted in Figure 1c where, a linear increase in laccase production was observed when malt extract concentration increased up to 6.0% (w/v) and thereafter it declined steadily. Moreover, a linear increase in the laccase production with increase in lignin level from 0.4 to 0.5% (w/v) was recorded.
To validate and confirm these predictions, experiments were designed with random levels of factors within and outside the design space. Validation was carried out under conditions predicted by the model (varying levels of pH, lignin and malt extract). The experimental values were found to be very close to the predicted values and hence, the model was successfully validated.
Purification of laccase
Extracellular laccase from Ganoderma sp. rckk-02 was purified to homogeneity. Crude enzyme was precipitated and concentrated using ammonium sulphate and ultrafiltration column (10 kDa), respectively, resulting into 2.42 fold purification. The final fold purification of laccase was estimated as 9.3, with a yield of 8.7%. Conventional multi-step procedures have generally been followed for complete purification of laccase that follow almost similar protocol involving concentration step (ammonium sulphate or acetone precipitation) followed by dialysis, ion-exchange chromatography and gel-filtration9.
The purity of the enzyme was checked by native PAGE, SDS-PAGE and zymogram analysis (Fig. 2). On the native PAGE, the purified enzyme showed a single band of 68 kDa. The zymogram analysis of laccase using guaiacol revealed colored band within 30 min of incubation, coinciding with Coomassie stained protein band on Native PAGE. The purified enzyme showed a single band of approximately 62 kDa molecular weight on 10% SDS-PAGE following Coomassie staining. In order to accurately determine the molecular mass of laccase protein, the enzyme was analysed on MALDI-ToF mass spectra.
Characterization of laccase
Effect of pH and temperature on laccase activity
Purified laccase was active over acidic pH range (3.0–5.5) with maximum activity at pH 4.5. Laccase was highly stable at pH ranging from 3.0 to 5.0. The enzymes retained almost 50% activity even after 6 h incubation at pH 6, whereas, at pH 5 it showed almost 95% residual activity.
Laccase showed maximum temperature stability at 30°C and was observed to retain 100% residual activity even after 150 min. However, the laccase stability started to decline at temperatures 60°C and above with 30–77% residual activity (Fig. 3a). Purified laccase had temperature optima at 50°C hence the subsequent experiments during enzyme characterization were performed at 50°C (Fig. 3b).
Effect of substrate concentration
Laccase activity increased with increasing substrate concentration and maximum value was observed with 4.5 mM guaiacol and 4 mM ABTS, thereafter enzyme activity gradually declined. Laccase had a Km of 217 μM and 77 μM and Vmax of 92.59 μmoles/ml/min and 250 μmoles/ml/min for guaiacol and ABTS, respectively.
Effect of metal ions
Metal ions are known to bind to the enzyme and alter its activity by stabilization or destabilization of the protein conformation. The laccase from Ganoderma sp. rckk-02 was observed to be affected differently with majority of metal ions in a concentration dependent manner. Maximum inhibition of laccase was observed with CoCl2 and HgCl2 inhibited laccase maximally. The enzyme was comparatively stable in presence of CaCl2, MnSO4, FeCl3, ZnSO4 and BaCl2 (0.5–3 mM) with a significant inhibition only at very high concentrations i.e. 10 mM of the metal ions. Exceptionally, CuSO4 and CuCl2 showed 100% stability at 0.5 to 10 mM.
Effect of surfactants and detergents
Laccase from Ganoderma sp. rckk-02 was found to be moderately stable in both ionic as well as non-ionic surfactants. The enzyme retained almost 52% relative laccase activity at 0.5 mM concentration of Triton X-100 and all tweens except Tween 20, where it had 39% residual activity. Detergents such as SDS and CTAB did not show any noticeable effect on enzyme activity at 5 and 10 mM concentration.
The N-terminal sequence of laccase from Ganoderma sp. rckk-02 was determined (S I R N S G) and compared with various fungi reported elsewhere10 (Table 4). N-terminal sequencing of Ganoderma sp. rckk-02, through MALDI-ToF had resulted into very distinct amino acid profile. From the results, it is suggested that the laccase from Ganoderma sp. rckk-02 may be a novel laccase and encoded by different laccase genes.
Far-UV CD spectrum of laccase
The Far-UV CD spectrum of the purified laccase showed single, broad negative trough at around 213 nm, which is a typical signature of all β-proteins (Fig. 4). The spectrum depicted different intensities of secondary structural element. The content of the secondary structure was estimated using K2D software, which fit to β-structure with 8% α-helix and has higher proportion of β-sheet i.e. 44%. The information generated was similar to the known structure of several laccases. These enzymes (with the full complement of copper atoms) consist mainly of antiparallel β-barrels as observed in the Trametes versicolor11.
Redox potential of laccase
Laccases can be divided in to three groups as a function of potential: low, middle and high potential laccases, having redox potential of 430, 430–710 and 780 mV, respectively12. Laccase from Ganoderma sp. rckk-02 was observed to have redox potential of 630 mV, hence belongs to middle redox potential laccases.
In vivo rat trial of laccase supplemented diets
Dry matter and Nutrient digestibility
Except for the digestibility of crude protein which was comparable among rats of all the groups, the rats supplemented with laccase at a dose level of 2.5 units g−1 body weight (T2) digested significantly (p < 0.01) more dry matter (DM), organic matter (OM), ether extract (EE), crude fibre (CF), nitrogen free extract (NFE) and total carbohydrate (T-CHO) than those without laccase supplementation (T1) or those supplemented with 5 units of laccase g−1 body weight (T3) (Table 5). However, at 5% level of significance (p < 0.05), the digestibility of DM, OM and T-CHO was higher in the rats on 5.0 units laccase supplementation per g body weight (T3) in comparison to those devoid of laccase supplementation.
The digestibility of neutral detergent fibre (NDF), acid detergent fibre (ADF), cellulose and hemicellulose was significantly (p < 0.01) higher in rats supplemented with 2.5 units laccase enzyme g−1 body weight (T2) (Table 5) as compared to the digestibility of these fibre fractions in rats on diets without (T1) or with 5 units g−1 body weight laccase supplementation. Though it was comparable at 1% level of significance, the digestibility of all the fibre fractions was superior (p < 0.05) in rats of T3 group, which received 5 units laccase g−1 body weight when compared to those on control diet (T1) having no laccase supplementation. Moderate level of enzyme supplementation was found superior in improving animal performance in the present study and similar observation was reported by Beauchemin et al. (2003) where, high level of enzyme addition can be less effective than low levels and the optimum level may depend on the diet6. Nsereko et al. (2002) has also observed similar results and speculated that application of a moderate level of enzyme to the ruminant feeds caused some beneficial disruption of the surface structure of the feed either before or after ingestion24. Application of ligninolytic enzymes as feed supplements promises to be the simplest method for digestibility improvement. However, mechanistic model for ruminal or gut activity of exogenous enzyme supplementation is not very well studied (Graminha et al. 2008)25. Beauchemin et al. (2003) extensively discussed the application of exogenous enzymes on animal feed and the mechanisms by which nutrient utilization is improved6. Moreover, ruminant animals (e.g., cattle and sheep) have the advantage of alloenzymatic digestion provided by rumen microflora, which enables ruminants to obtain nutrients from complex feed matrices that are not made available through autoenzymatic digestion. Accordingly, ruminants are able to subsist on diets comprised, for example, entirely of forages. Pigs, chickens and other monogastric animals lack the alloenzymes from rumen microflora, so for these species to derive optimal nutrient benefit from complex feed matrices it is necessary to provide added enzyme supplementation not available from resident intestinal microflora (Pariza and Cook, 2010)3.
Blood enzyme activity
The activity (U/L) of SGPT (ALT) and SGOT (AST) did not vary significantly (p > 0.05) due to dietary variations (Table 6). The activity of SGPT (ALT) was found to be within the normal physiological range (35.1 ± 13.3 U/L) but that of SGOT (AST) was marginally higher than the normal range (42.9 ± 10.1 U/L) on all the diets as reported for rats earlier13. The LDH activity was significantly (p < 0.05) higher in rats supplemented with 5 units of laccase g−1 body weight (T3) but comparable between rats fed control diet (T1) and diet supplemented with 2.5 units of laccase g−1 body weight (T2) and was almost within the normal range (46.6 ± 22.0) as has been observed by Kaneko et al13.
The increase in laccase yield from Ganoderma sp. rckk-02 with increase in lignin concentration might be due to (a) synthesis of inducible laccase isozymes14 and (b) combinatorial effect of laccase and HOBT (a heterocyclic compound with N-OH moiety which can be oxidized by laccase to its nitroxide radical). These redicals act as proximal oxidant of lignin which depolymerizes lignin and give rise to phenolics (ferulic acid, vanillic acid, 3–4 dihydroxy benzoic acid) as well as non phenolic structural polymers15,16. The phenolics produced would have served the dual purpose of acting as both substrate and inducer for laccase biosynthesis. This observation is well supported by existing reports in literature regarding laccase induction. Mansur et al.14 have reported addition of veratryl alcohol enhanced laccase production by 10-fold from a lignin-degrading basidiomycete. 2,5-xylidine was reported to be the most effective inducer for production of laccase from Cyathus bulleri and Pycnoporus cinnabarinus10,17. Fungal laccases typically exhibit pH optima in the acidic range. While the pH optima for the oxidation of ABTS are generally lower than 4.0, phenolic compounds like DMP, guaiacol and syringaldazine exhibit higher values i.e. 4.0–7.018. The enzyme activity at higher pH is decreased by the binding of a hydroxide anion to the T2/T3 coppers of laccase, which blocks the internal electron transfer from T1 to T2/T3 centres19. Not only the rate of oxidation but also the reaction products can differ according to pH. This may be due to abiotic follow-up reactions of primary radicals formed by laccase. The stability of fungal laccases is generally higher at acidic pH18.
Temperature profiles of laccase activity are almost similar with other extracellular ligninolytic enzymes with optima between 50°C and 70°C18. On the other hand laccase from Ganoderma lucidum has been reported with highest activity at 25°C 20. Laccase from Ganoderma sp. rckk-02 exhibited higher temperature optima compared to other fungi studied earlier but especially when compared to Ganoderma lucidum20,21. Thus the higher temperature optima make the enzyme of wider utility in various biotechnological applications. The kinetic parameters obtained for ABTS and guaiacol fall well within the ranges reported for other laccases9. Earlier fungal laccase from G. lucidum has been reported to be more stable on different concentration (0.5–5.0 mM) of heavy metals i.e. Mn2+, Ca2+, Zn2+, Cu2+ and Mg2+21. Contrary to that Baldrian18 has discussed the sensitivity of laccases toward heavy metal ions. The stability of this enzyme in presence of various heavy metals makes it an efficient agent in the treatment of wastewater containing heavy metals. While, the detergent could not change enzyme considerable which could be due to the reduction of the unproductive enzyme adsorption to the substrate22. Stability of laccase from Ganoderma sp. rckk-02 in both ionic and nonionic surfactants makes it robust enzyme for diverse applications.
To the best of our knowledge, the N-terminal sequencing of laccase from Ganoderma sp. rckk-02 is not identical to many known laccases but is closer to various wood degrading fungi. As reported previously, the N-terminal amino acid sequence of most fungal laccases (A/G-I-G-P-V/T) appears to be conserved and quite homologus in terms of primary sequences/conserved sequences10. Whereas, earlier reports of the CD spectrum of the laccase protein from C. bulleri indicated 37% α-helix and 26% β-sheet, which differed significantly from our findings23.
Moderate level of enzyme supplementation was found superior in improving animal performance in the present study and similar observation was reported by Beauchemin et al.6 where, high level of enzyme addition can be less effective than low levels and the optimum level may depend on the diet. Nsereko et al.24 has also observed similar results and speculated that application of a moderate level of enzyme to the ruminant feeds caused some beneficial disruption of the surface structure of the feed either before or after ingestion. Application of ligninolytic enzymes as feed supplements promises to be the simplest method for digestibility improvement. However, mechanistic model for ruminal or gut activity of exogenous enzyme supplementation is not very well studied25. Beauchemin et al.6 extensively discussed the application of exogenous enzymes on animal feed and the mechanisms by which nutrient utilization is improved. Moreover, ruminant animals (e.g., cattle and sheep) have the advantage of alloenzymatic digestion provided by rumen microflora, which enables ruminants to obtain nutrients from complex feed matrices that are not made available through autoenzymatic digestion. Accordingly, ruminants are able to subsist on diets comprised, for example, entirely of forages. Pigs, chickens and other monogastric animals lack the alloenzymes from rumen microflora, so for these species to derive optimal nutrient benefit from complex feed matrices it is necessary to provide added enzyme supplementation not available from resident intestinal microflora3.
The enzyme ALT and AST are widely reported in the case of hepatitis, cirrhosis, metastatic carcinoma and myocardial infarction26,27. LDH, an oxidoreductase, catalyzes the inter-conversion of lactate and pyruvate. LDH is most often measured to evaluate the presence of tissue or cell damage28. The laccase from Ganoderma sp. rckk-02 appears to have different properties compared to other laccases and it holds potential to be a suitable candidate for animal feed supplement.
All animal experiments were performed at Department of Zoology, University of Delhi, in accordance with current guidelines of the Organization for Economic Cooperation and Development (OECD)29 and Igmoris Draft, March 2008. All animal experiments were performed in strict compliance with Indian laws in an ethical way dually approved by Institutional Ethical committee.
Chemicals and Feed materials
Guaiacol and protein markers were purchased from Sigma - Aldrich Corporation, USA. All other media components and chemicals used were of highest purity grade available commercially. All the kits for biochemical assays were purchased from Teco Diagnostics, Anaheim, CA 92807. Wheat straw and other feed ingredients were purchased locally.
Microorganism and culture conditions
Laccase producing basidiomycetous fungus Ganoderma sp. rckk-02 was isolated from stump of Euclyptica lanceolata, Delhi ridge forest, New Delhi, India (Accession No. GenBank: AJ749970.1). The culture was grown and maintained on malt extract agar (MEA) containing (g/l): Malt extract 20.0, KH2PO4 0.5, MgSO4·7H2O 0.5, Ca(NO3)2·4H2O 0.5, pH 5.4 at 30°C 17. Laccase production under RSM was carried out in 50 ml malt extract broth (MEB) in 250 ml Erlenmeyer flasks. Each flask was inoculated with 8 fungal discs (7 mm each) from the periphery of 5-day-old cultures of Ganoderma sp. rckk-02 and incubated for 11 days at 30°C under static cultivation conditions. HOBT (1- Hydroxybenzotriazole) was filter sterilized through 0.22 μm membrane (Millipore, Germany) and added to each flask on day 5 at a final concentration of 1.0 mM for induction of laccase production. The fungal mass was separated from fermentation broth by centrifugation at 4000× g for 20 min at 4°C and the supernatant was used for estimating laccase activity.
Statistical analysis and modeling
Response surface methodology (RSM)
For the selection of the key factors like carbon source, nitrogen source and trace metal one factor at a time was adopted followed by Plackett-Burman Design (PBD) (data not shown). Thereafter, RSM employing CCRD was carried out to optimize the levels of variables identified to possess maximum influence on laccase production from Ganoderma sp. rckk-02. The level of three independent variables viz. malt extract (A), lignin (B) and pH (C), chosen for this study were optimized by the statistical software package ‘DESIGN-EXPERT 6.0, (Stat-Ease, Inc., USA). Each factor in the design was studied at five different levels (Table 1). A set of 20 experiments was carried out and all variables were taken at a central coded value considered as zero. The minimum and maximum ranges of variables used and the full experimental plan with respect to their values in actual and coded form is also given in Table 2. Upon completion of experiments, the average maximum laccase production was taken as response (Y). A second order polynomial equation was fitted to the data by a multiple regression method. The quadratic model for predicting the optimal point was expressed according to the following quadratic equation:
Where Y is predicted response; β0 is intercept; β1, β2, β3 are linear coefficients and β12, β23, β13 are interaction coefficients. Eq. (1) was analyzed using DESIGN EXPERT software to estimate the responses of the dependent variables and regression analysis of experimental data. The quality of the fit of the quadratic model equation was expressed by the coefficient of determination (R2) and its statistical significance was checked by Fishers test value (F-value).
Laccase activity was determined using Guaiacol as substrate following the method described elsewhere17. Guaiacol (10 mM) prepared in 100 mM citrate phosphate buffer (pH 5.0) was used as substrate. One unit (U) of laccase was defined as the change in absorbance of 0.01/ml/min at 470 nm. The protein content was estimated by standard Lowry's method using bovine serum albumin as the standard.
Purification of laccase
The culture broth (950 ml) was filtered through Whatman filter no. 1 and centrifuged at 13,000× g for15 min at 10°C. The protein extract was concentrated using an Amicon Ultra-15 membrane filter (Millipore, Germany). Partial purification of laccase from the culture filtrate was carried out by addition of finely ground ammonium sulfate at three different saturation levels, i.e., 0–20%, 20–40% and 40–80%. After overnight incubation at 4°C, the culture filtrate was centrifuged at 9,000× g for 20 min. Precipitates were dissolved in 20 mM citrate-phosphate buffer (pH 5.4) and dialysed overnight against same buffer at 4°C.
The gel filtration column HiPrep 16/60 Sephacryl S 100 HR (GE Healthcare, USA) was equilibrated and washed with 20 mM citrate-phosphate buffer (pH 5.5). The column was loaded with concentrated protein sample containing laccase activity and were eluted with the same buffer at the flow rate of 0.5 ml/min using a Pump P-920 (ÄKTA basic 100, GE Healthcare, USA). Fractions containing laccase activity were pooled and loaded on to a DEAE cellulose anion exchange column (10 cm × 2.8 cm), which was equilibrated and washed with 50 mM sodium phosphate buffer, pH 6.0. The enzyme was eluted with a linear gradient of NaCl (0–1.0 M) at the flow rate of 0.5 mL/min and was monitored for absorbance at 280 nm.
Molecular mass determination
Fractions containing laccase activity were pooled and applied on a Resource-Q (GE Healthcare, USA) column and eluted with a linear gradient from 0 to 0.5 M NaCl. Peak fractions were pooled and concentrated by ultrafiltration using an Amicon Ultra-15 membrane. The enzyme purity and molecular weight of laccase from Ganoderma sp. rckk-02 were determined by SDS-PAGE as per the standard procedure. The molecular weight of the purified native laccase was confirmed by gel filtration on Sephadex G-100.
Effect of pH and temperature on laccase activity
The enzyme activity was assayed in the pH range of 3.0–7.5 using buffers of varying pH (citrate-phosphate, pH 3.0–6.5; phosphate buffer, pH 6.0–7.5). Activity was expressed as percentage relative activity with respect to maximum activity, which was considered as 100%. The optimum pH was determined by incubating the enzyme in buffers of varying pH (5.0 and 7.0) for 4 h at room temperature (25 ± 1°C). Effect of temperature on laccase activity was determined by incubating the reaction mixture at different temperatures varying from 30 to 90°C under standard assay conditions.
Thermostability of laccase
The temperature stability of laccase was determined by incubating the enzyme sample at various temperatures ranging from 30 to 80°C for 210 h and the residual activity was determined.
Effect of various inhibitors and metal ions
The effect of various inhibitors viz. Ethylenediamine tetraacetate (EDTA), β-mercaptoethanol, Dithiothreitol (DTT) and urea on laccase activity was determined by incubating the enzyme at a final concentration ranging from 0.5–10.0 mM for 30 min at room temperature and then measuring the residual activity following the standard assay conditions. The effect of various metal ions on laccase activity was studied by incubating the enzyme with various metal ions at concentrations ranging from 0.5–10 mM at room temperature for 30 min.
Effect of surfactants
The effect of surfactants (SDS, tweens, CTAB, triton-x-100) on purified laccase activity was determined by incubating the enzyme with surfactant of concentrations ranging from 0.5 –10 mM for 30 min at room temperature.
Effect of substrate concentration on enzyme activity and determination of Km and Vmax for different substrates
Michaelis-Menten constant (Km- substrate concentration at which rate of reaction is half the maximum rate of reaction) and maximum rate of reaction (Vmax) were determined by using guaiacol and ABTS as substrates at concentration ranging from 0.5–5 mM in 20 mM citrate-phosphate buffer (pH 5.0). The values of Km and Vmax were calculated from Lineweaver-Burk plot.
N-terminal amino acid sequence analysis
Purified laccase from Ganoderma sp. rckk-02 was separated by native PAGE, blotted to polyvinylidene difluoride (PVDF) membranes and stained with Coomassie Brillient Blue. The PVDF membranes containing the purified protein blot were processed for N-terminal amino acid sequence analysis by Trypsin degradation on a MALDI-ToF (Bruker Daltonik, GmbH, Germany).
Far-UV CD spectrum of laccase
Far-UV CD spectrum of purified laccase was determined in 10 mM Sodium Cacodylate buffer (pH 5.2) in a Jacob J-810 Spectropolarimeter (Jasco Corporation, Japan). Laccase was properly dialyzed in the sodium cacodylate buffer at a protein concentration of 0.5 mg/ml. The parameters used for the measurement were: sensitivity, 100 mdeg; wavelength, 200–250 nm; data pitch, 0.2 nm; in continuous scanning mode. The scan speed was set at 50 nm/min with a response of 1 s and b and width at 1 nm23.
The redox potential of laccase was determined using cyclic voltammetry (CV) following the method described by Dutton (1978)30.
In vivo animal trial
Animals housing and laccase feeding
Thirty six weaned male rats (Holtzman strain, n = 36) of uniform body weight and 30–32 day old were procured from Department of Zoology,University of Delhi, Delhi and divided into three (T1, T2 and T3) experimental groups as described earlier5. Each group consisted of three replicates of four rats each in a completely randomized design. The animals were acclimatized for 5 days on normal pelleted diet (concentrate and wheat straw; 50:50) before the start of feeding trial. They were housed in cages fitted with feeders, waterers and with facilities for the collection of feaces. Tap water was used for drinking and supplied ad libitum and the temperature and relative humidity of the room was maintained at 26°C ± 5°C and 50–55%, respectively.
The rats of group T2 and T3 were daily offered partially purified laccase enzyme (2.5 and 5.0 units g−1 body weight) from Ganoderma sp. rckk-02 in drinking water through out the experimental period. T1 group was offered pure tap water devoid of laccase.
Determinations of Body weights, feed efficiency, dry matter (DM) utilization and nutrient digestibility studies
Measured quantity of the pelleted composite diets was offered daily morning in a way to meet ad libitum and had access to it at all times. Individual body weights were recorded at weekly intervals before offering feed and water. The efficiency of feed and DM utilization was calculated as unit (g) intake per unit (g) gain. A digestibility trial of 4 d duration was conducted on all the experimental rats, involving total collection method to assess. Feed and faecal samples were analyzed for various proximate principles and fibre fractions as per the standard methods of Association of Official Agricultural Chemist (AOAC)31,32,33. Nitrogen in wet faeces was estimated with the help of CHNS analyzer (Model Elementar – Vario EL III).
Determination of blood enzyme activity
Blood was collected from rats of all the groups through ocular puncture with the help of heparinised capillary tubes into sterile stoppard glass tubes for the estimation of the activity of target enzymes. Thereafter, plasma was obtained and collected by centrifuging the blood at 4000 rpm for 5 min. Blood was analysed for the activity of alanine aminotransferase (ALT), aspartate aminotransferase (AST) as per the methods described by Henry (1974)26 and Young et al. (1975)27 and lactate dehydrogenase (LDH)) was analyzed as per the method of Babson and Babson (1973)34. The data were statistically analyzed using one way analysis of variance (ANOVA) as per the method of Snedecor and Cochran (1989)35.
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This work was supported by research grant received from Department of Biotechnology, Government of India, New Delhi. The authors are also thankful to Ms. Arti Jain, JRF, Department of Chemistry, University of Delhi, Delhi for her assistance during estimation of redox potential of laccase. The assistance of Dr. Bijender Singh, Dept. of Microbiology, M. D. University, Rohtak in executing the statistical model for optimization of enzyme production is highly acknowledged. Author BS also wishes to acknowledge Council of Scientific and Industrial Research for Senior Research Fellowship award.
The authors declare no competing financial interests.
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Sharma, K., Shrivastava, B., Sastry, V. et al. Middle-redox potential laccase from Ganoderma sp.: its application in improvement of feed for monogastric animals. Sci Rep 3, 1299 (2013). https://doi.org/10.1038/srep01299
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