Biosynthesis, purification and characterization of endoglucanase from a xylanase producing strain Aspergillus niger B03

INDUSTRIAL MICROBIOLOGY

Biosynthesis, purification and characterization of endoglucanase from a xylanase producing strain Aspergillus niger B03

Georgi Todorov Dobrev; Boriana Yordanova Zhekova^*

Department of Biochemistry and Molecular Biology, University of Food Technologies, 26 Maritza Blvd., 4000 Plovdiv, Bulgaria

ABSTRACT

An extracellular endoglucanase was isolated from the culture liquid of xylanase producing strain Aspergillus niger B03. The enzyme was purified to a homogenous form, using consecutive ultrafiltration, anion exchange chromatography, and gel filtration. Endoglucanase was a monomer protein with a molecular weight of 26,900 Da determined by sodium dodecyl sulfate-polyacrylamide gel electrophoresis, and 28,800 Da determined by gel filtration. The optimal pH and temperature values for the enzyme action were 3.5 and 65ºC respectively. Endoglucanase was stable at 40ºC, pH 3.0 for 210 min. The substrate specificity of the enzyme was determined with carboxymethyl cellulose, filter paper, and different glycosides. Endoglucanase displayed maximum activity in the case of carboxymethyl cellulose, with a K_m value of 21.01 mg/mL. The substrate specificity and the pattern of substrate degradation suggested that the enzyme is an endoglucanase. Endoglucanase showed a synergism with endoxylanase in corn cobs hydrolysis.

Key words: endoglucanase; purification; characterization; Aspergillus niger; endoxylanase

INTRODUCTION

The hydrolysis of lignocellulosic biomass to fermenting sugars, which can be used for ethanol biosynthesis, is one of the possibilities for production of alternative energy sources. Annually about 7 million tons of lignocellulosic wastes from the grain-producing industry are deposited from the member-countries of the European Union (3). Lignocellulosic biomass includes various agricultural residues (straws, hulls, stems, and stalks), deciduous and coniferous woods, municipal biodegradable wastes, waste from the pulp and the paper industry and herbaceous energy crops. The composition of lignocellulosic biomass varies significantly. The main polysaccharide components are cellulose, representing 35-50 % of the biomass and xylan, which constitutes about 30 % (3).

The process of ethanol production from lignocellulosic biomass includes delignification of the plant biomass and hydrolysis of cellulose and hemycellulose to monosaccharides (2). The hydrolysis process can be performed by treatment with acids at high temperatures or by enzyme action. The acidic hydrolysis acquires a significant energy consumption and acid resisting equipment, which makes the process more expensive.

The enzymatic hydrolysis does not have these disadvantages. Because of the complex composition of lignocellulosic biomass, the synergistic action of several enzymes (endoglucanases, EC 3.2.1.4; β-glucosidases, EC 3.2.1.21; xylanases, EC 3.2.1.8 and β-xylosidases, EC 3.2.1.37) is needed for complete hydrolysis (22).

Lignocellulose degradation enzymes are produced by various groups of microorganisms, including moulds, bacteria, and yeasts. Filamentous fungi have been widely studied for their ability to produce cellulolytic and xylanolytic enzymes (1, 4). A characteristic feature of the mould strains is their ability to produce simultaneously cellulose and xylan degrading enzymes. Cellulases and xylanases produced by a certain strain may act synergistically during the hydrolysis of lignicellulosic biomass (10, 18, 19, 20).

The isolation, purification, and characterization of the separate enzymes, involved in lignocellulosic biomass hydrolysis give possibility for their effective application. The aim of the present research is to describe the biosynthesis, isolation and characterization of an endoglucanase from a xylanase producing strain Aspergillus niger B03.

MATERIALS AND METHODS

Strain Cultivation

The research was performed with an industrial xylanase producing strain Aspergillus niger B03 from Biovet JSC. For endoglucanase biosynthesis the strain was cultivated in 15 L laboratory bioreactor Aplikon as described previously (6, 7). The biomass was removed by filtration and the culture filtrate was used for the enzyme isolation.

Endoglucanase Purification

Endoglucanase purification was performed by ultrafiltration using 10 kDa membrane, anion-exchange chromatography and a subsequent gel filtration on a chromatographic system (Pharmacia biotech). Anion-exchange chromatography was carried out on a DEAE-Sephadex A50 column (2.6 x 40 cm) equilibrated with 10 mM sodium acetate buffer with pH 5.5. A sample, containing 51.25 mg of protein was loaded onto the column and the unbound protein was washed with the buffer solution. Elution was performed with gradient of NaCl at a flow rate of 9.6 mL/h. Fractions of 11 mL were collected, monitored at 280 nm, and assayed for CMCase activity and protein content. CMCase active fractions were subjected to gel filtration on Sephadex G 75 column (2.6 x 70.0 cm). Elution was performed with 0.05 M solution of NaCl at a flow rate of 19.8 mL/h, fractions of 7.0 mL were collected, and the standard assays were performed.

Determination of Endoglucanase Molecular Weight

The molecular weight of endoglucanase was determined by sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-PAGE) and gel filtration. SDS-PAGE was performed by the method of Laemli (11) with 10.0 % polyacrylamide gel at a constant current of 10 mA. The following protein calibration kit (Merck) was used: ovotransferrin (78,000 Da), albumin (66,250 Da), ovalbumin (45,000 Da), carbonic anhydrase (30,000 Da), myoglobin (17,200 Da), cytochrome c (12,300 Da). The staining procedure was done with Coomassie Blue R-350. Gel filtration was performed as described above using the following protein calibration kit: cytochrome c (12,300 Da), carbonic anhydrase (30,000 Da), ovalbumin (45,000 Da), and bovine albumin (67,000 Da).

Effect of pH and Temperature on Endoglucanase Activity and Stability

The effect of pH and temperature was evaluated in the range of pH 2.5-8.0 (pH interval 0.5) and temperature of 30-90ºC (temperature interval 5ºC) by performing the CMCase activity assay. Citrate-phosphate buffer solutions were used for pH profile determination. Thermal and pH stabilities were determined by pre-incubating the enzyme at various temperatures, notably, 40ºC and 60ºC, at pH 3.0, 5.0 and 7.0 for up to 210 min. At every 15 min a sample was withdrawn and the residual activity of the enzyme was determined.

Estimation of Endoglucanase Substrate Specificity and Kinetic Parameters

The substrate specificity of endoglucanase was tested with 10 mg/mL carboxymethyl cellulose (CMC), cellobiose, and methyl glycoside (Sigma) by determination of the reducing sugars released. When 1.0 mM ρ-nitrophenyl-β-D-glucopyranoside (Sigma) was used as a substrate, the activity was determined as described by Ponpium (17). The enzyme activity against filter paper was determined with 50 mg Whatman No 1 filter paper soaked in 1.8 mL of 100 mM sodium acetate buffer with pH 5. The enzyme reaction was performed at 50ºC for 60 min and the increase in reducing sugars was assayed.

Kinetic parameters were determined using CMC as a substrate in the range of 4.0-9.0 mg/mL initial concentration by applying Lineweaver-Burk transformation.

Hydrolysis of CMC by Endoglucanase

CMC hydrolysis was studied in the case of 10.0 mg/mL CMC with 0.08 U of endoglucanase at pH 5.0 and 40ºC. The relative viscosity of CMC solution was measured with an Oswald viscometer (5) and the reducing sugars content in the reaction mixture was determined.

Synergism of Endoglucanase and Endoxylanase Action

The synergistic effect of endoglucanase and endoxylanase was evaluated by the hydrolysis degree of corn cobs. Endoxylanase was isolated from the culture liquid of Aspergillus niger B03 as described previously (8). Three samples, containing respectively endoglucanase, endoxylanase and both enzyme preparations were prepared. 10 mg/mL of corn cobs (milled to <1 mm) were suspended in 100 mM sodium acetate buffer with pH 5.0 and 3.2 U of endoglucanase and 70 U of endoxylanase were added per one gram of substrate. The hydrolysis was performed at 40ºC for up to 10 h. At certain time intervals the reducing sugars released were determined. The synergistic effect is evaluated in comparison to the theoretical values of the reducing sugars, formed by both enzyme preparations.

Determination of CMCase Activity

CMCase activity was determined by mixing 0.2 mL enzyme solution with 1.8 mL of 10.0 mg/mL CMC solution in 100 mM sodium acetate buffer with pH 5.0, at 50ºC for 15 min and the reducing sugars released were determined. One unit of CMCase activity was defined as the amount of enzyme, forming 1 μmol of reducing sugars per one minute under the assay conditions.

Assays

The concentration of reducing sugars was determined by the dinitrosalicylic acid method (13). Protein content was assayed by the Lowry method (12) with bovine serum albumin (Sigma) as a standard. Biomass concentration was determined by the dry weight after drying at 105ºC.

RESULTS AND DISCUSSION

Biosynthesis of Endoglucanase

The dynamics of biosynthesis and Aspergillus niger growth in submerged cultivation in 15 L stirred and aerated laboratory bioreactor is shown on Fig. 1. The period within 15-35 h was the log phase of the strain growth and it was characterized with a sharp increase of biomass production and outlet CO_2. Endoglucanase biosynthesis began after 45 h of fermentation. According to biomass and CO₂ production more significant increase in endoglucanase biosynthesis was observed at the end of log phase and continued during the stationary phase of strain growth.

After 20 h of fermentation a tendency of decrease in pH of the culture medium was observed (data not shown). Significant increase in CMCase activity was observed at pH within 3.0-4.0. Maximum enzyme activity (3.7 U/mL) was achieved after 95 h of fermentation at pH 4.0.

Reducing sugars concentration gradually decreased during the process. Increase in CMCase activity and medium pH began after the complete run out of reducing sugars, which is probably due to the use of the obtained organic acids as carbon source.

Purification and Molecular Weight of Endoglucanase

The extracellular endoglucanase produced by Aspergillus niger B03 was purified using three consecutive steps (ultrafiltration and column chromatography). A summary of the purification procedure is presented in Table 1. The ultrafiltration step yielded 91.35 % of CMCase activity in the retentate. For further purification, the retentate was subjected to anion-exchange chromatography on DEAE-Sephadex A50 (Fig. 2). Only one peak showing CMCase activity was detected.

On this stage of the purification procedure the enzyme did not appear as a single band on SDS-PAGE, which imposed the need of further purification by gel filtration with Sephadex G75. After this step endoglucanase was detected as a single band on the electropherogram, indicating a homogeneous enzyme (Fig. 3).

The molecular weight of the purified endoglucanase was determined to be 26,900 Da by SDS-PAGE and 28,800 Da by gel filtration. The close values, achieved by both methods suggested it to be a monomer protein.

Effect of pH and Temperature on Enzyme Activity and Stability

The effect of pH and temperature was studied with the homogenous and the crude endoglucanase (data not shown). Both enzyme preparations showed maximal CMCase activity at pH 3.5, and 80 % relative activity was detected in the range of pH 2.5-4.5.

The homogenous and the crude enzyme preparations showed a high activity at high temperature values. The optimal temperature value was 65ºC and both enzymes displayed over 90 % of their maximal activity at 75ºC. The crude endoglucanase showed catalytic activity (25 % of maximal one) even at 95ºC. This property of endoglucanase is important for its application.

An important feature of the industrially applied enzymes is their stability. The enzyme showed a good stability at low values of pH (data not shown). When endoglucanase was incubated at 40ºC and pH 3.0, the enzyme retained 92 % of its activity for 210 min. For comparison in the case of pH 7.0, endoglucanase was totally inactivated for 90 min. At higher temperature values (60ºC and pH 3.0) the enzyme showed 60 % residual activity for 45 min.

Substrate Specificity and Kinetic Parameters of Endoglucanase

The substrate specificity of the homogenous enzyme preparation was studied with CMC, filter paper, cellobiose, methyl glycoside and ρ-nitrophenyl-β-D-glucopyranoside. The enzyme showed highest activity against CMC. The activity was lower, when filter paper was used as a substrate. The enzyme did not degrade low molecular substrates such as cellobiose, methyl glycoside, and ρ-nitrophenyl-β-D-glucopyranoside. These results indicated that the enzyme is an endoglucanase – it displayed high activity against CMC, low activity against filter paper, and did not act on glycosides. Similar results were reported for the endoglucanase produced by Aspergillus kawachii (9).

The kinetic parameters of endoglucanase were determined in the case of CMC as a substrate. K_m value was estimated to be 21.01 mg/mL, and V_max was 0.31 mg/mL.min. The established value of K_m was significantly higher than the values reported for other endoglucanases from Aspergillus - K_m = 14 mg/mL (16), K_m = 5 mg/mL (21), which showed lower affinity of the isolated endoglucanase against substrate CMC.

CMC Hydrolysis by Endoglucanase

CMC hydrolysis was studied by assaying the change in the relative viscosity and the reducing sugars content (Fig. 4). A sharp decrease of CMC viscosity and a corresponding increase in reducing sugars content was detected during the first 15 min of the reaction. The rates of viscosity decrease and reducing sugars increase were reduced after 15 min of reaction. These results confirmed the hypothesis that the enzyme is an endoglucanase.

Synergism of Endoglucanase and Endoxylanase Action

The synergistic effect of endoglucanase and endoxylanase was studied by performing hydrolysis of corn cobs by the single and combined action of both enzymes (Fig. 5). The corn cobs used were a complex substrate, containing 9.57 % β-glucans and 35.56 % arabonoxylans (6). The results showed that the substrate is more effectively hydrolyzed by the combined action of endoglucanase and endoxylanase in comparison to the separate enzymes. Furthermore, a synergistic effect was observed. The concentration of reducing sugars formed by both enzymes was higher than the theoretically calculated value. At the end of the process the increase was about 50 %. These results may be explained by the degradation of xylan networks between cellulose microfibrils, which allows endoglucanase to degrade cellulose microfibrils in the deeper structure (14). Similar synergistic effect was reported for other xylan and cellulose degrading enzymes (14, 15).

CONCLUSION

An endoglucanase was isolated from the culture liquid from a xylanase producing strain Aspergillus niger B03. The enzyme was highly active against CMC, it showed lower activity against filter paper, did not act on β-glycosides, and caused a decrease in CMC viscosity. These results indicated that the enzyme is an endoglucanase. The isolated endoglucanase degraded complex substrates as corn cobs in synergism with an endoxylanase, which allows the enzyme to be applied in hydrolysis of lignocellulosic biomass.

ACKNOWLEDGEMENTS

The authors acknowledge Biovet Ltd. for giving the xylanase producing strain Aspergillus niger B03. The work was supported by the Grant-in-Aid VU-AN-6/2005 for Scientific Research of Priority area (Agricultural science) from the Ministry of Education of Bulgaria.

Submitted: January 29, 2010; Returned to authors for corrections: April 15, 2011; Approved: January 16, 2012.

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Publication Dates

• Publication in this collection
  02 May 2012
• Date of issue
  Mar 2012

History

• Received
  29 Jan 2010
• Accepted
  16 Jan 2012
• Reviewed
  15 Apr 2011