Production of Cellulase and Xylanase by Aspergillus terreus KJ829487 Using Cassava Peels as Subtrates

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DOI: 10.4236/aim.2016.67050    1,669 Downloads   2,404 Views   Citations


Cassava (Manihot esculenta, Crantz) is one of the most important food plants in West Africa. Its peels are made up of cellulose, hemicellulose and lignin. This lignocellulolytic biomass can be converted using microbial enzymes to fermentable sugars which have wide range of biotechnological relevance in many fermentation processes. The aim of this study is to screen filamentous fungi from decaying cassava peels that are good producers of xylanases and cellulases. Decaying parts of cassava peels were obtained and brought to the laboratory for further work. Fungi were isolated, identified and screened for cellulase and xylanase production. Isolate with highest frequency of occurrence and enzyme production was identified using phenotypic and molecular method. Optimisation of growth conditions for enzymes production was monitored using the DNSA method, also saccharification of cassava peel were carried out using the enzymes obtained from the isolate. Aspergillus terreus KJ829487 was the predominant fungus. It produces cellulases and xylanases optimally at 40°C, pH 6 and 8, utilising carboxymethylcellulose (CMC) or xylose and yeast extracts as its carbon and nitrogen sources respectively. Saccharification of the peels yielded 584 mg/L glucose, 78 mg/L xylose and 66 mg/L rhamnose. Aspergillus terreus KJ829487 obtained from cassava peels have the ability to produce high concentration cellulases and xylanases which effectively hydrolysed the lignocelluloses’ biomass to fermentable sugars.

Cite this paper

Olanbiwoninu, A. and Odunfa, S. (2016) Production of Cellulase and Xylanase by Aspergillus terreus KJ829487 Using Cassava Peels as Subtrates. Advances in Microbiology, 6, 502-511. doi: 10.4236/aim.2016.67050.

Received 18 April 2016; accepted 19 June 2016; published 22 June 2016

1. Introduction

Cassava (Manihot esculenta, Crantz) peels are the main by-product from processing tuberous roots of cassava for human consumption. The peel is 1 - 4 mm thick and may account for 10% - 12% of the total dry matter of the root [1] . Cassava peels are lignocellulolytic biomass which is considered as an agricultural residue because it is discarded during processing. The degradation of this complex structure requires a complete enzymatic system.

Cellulose is a linear polysaccharide composed of β-1, 4-linked glucose molecules. Efficient hydrolysis of cellulose requires the action of a complex of cellulolytic enzymes that work synergistically: exo-1, 4-β-D-gluca- nases, endo-1-4-β-D-glucanases and 1,4-β-Dglucanases [2] . The production of cellulases by fungi and bacteria is widely disseminated in nature. Among fungi, the genera Trichoderma, Aspergillus, Penicillium, Humicola are described as cellulase producers, Aspergillus spp. is the major agents of decomposition and decay, therefore they produce a broad range of enzymes, including cellulases and xylanases and these reports have been well documented [3] - [8] . At present, there is an increasing demand for these enzymes, especially for bioconversion of agricultural resources and ethanol production because cellulase helps in hydrolyzing cellulose to produce glucose [9] .

Hemicellulose is a linear and branched heterogeneous polymer typically made up of five different sugars― L-arabinose, D-galactose, D-glucose, D-mannose, and D-xylose [10] . Xylanases are responsible for the hydrolysis of xylan and subsequently releasing xylo-oligosaccharides [11] . The hydrolysed products in the form of soluble sugars have extensive range of biotechnological relevance in many fermentation processes and functional food industry [12] . Literature review shows that, a large variety of microorganisms, including bacteria, yeast and filamentous fungi have been reported to produce xylanase [13] . From an industrial perspective, fungi are interesting due to higher extracellular release of xylanases, in addition to production of several auxiliary enzymes that are necessary for debranching of the substituted xylans [14] .

Lignin represents about 15% - 25% of lignocellulosic biomass and is a large cross-linked macromolecule composed of three monomers: p-coumaryl alcohol, coniferyl alcohol and sinapyl alcohol [15] . The enzymes responsible for lignin degradation are mainly lignin-peroxidase (LiP), manganese peroxidase (MnP), laccases and hydrogen peroxide-producing enzymes. A wide variety of microorganisms, including fungi, actinomycetes and bacteria, have been implicated in lignin biodegradation. Among them, white rot fungi have received extensive attention due to their powerful extracellular lignin-degrading enzymatic systems [16] . Other groups of fungi have also been reported as producers of lignolytic enzymes [17] .

Filamentous fungi are good examples of microorganisms that produce cellulase and xylanase on industrial scale and they can easily be obtained from lignocellulolytic biomass. The aim of this study is to screen filamentous fungi from decaying lignocellulolytic agricultural waste products that are good producers of xylanases and cellulases.

2. Materials and Methods

2.1. Collection of Samples

Decaying parts of cassava peels were collected from the dumping site of a cassava processing site in Old-Ife Road, Ibadan, Oyo State, Nigeria.

2.2. Strain Isolation and Identification

The filamentous fungi were isolated from the decaying parts of cassava peels and the technique of [17] James and Natalie, 2001 was used for identification using Lactophenol blue stain. The identification was done by placing a drop of the stain on clean slide, using a mounting needle; small portion of the mycelium from the fungal cultures was removed and placed in a drop of lactophenol. The mycelium was spread on the slide and gently covered with a cover slip applying small pressure so as to eliminate air bubbles. The slide was mounted in an optical microscope (Olympus CH) and observed using 10 and 40× lenses respectively. The species obtained were identified in accordance to [18] .

2.3. Selection of Isolate

Aspergillus terreus was the most predominant fungus present. Therefore, it was selected for further studies.

2.4. Enzymes Assay Substrate

Xylan powder and carboxymethylcellulose (CMC) powder was used for assay of xylanase and carboxymethylcellulase enzyme. The purpose of the assay is to check the purity of these enzymes. The powders were obtained from Sigma-Aldrich Incorporation, Germany.

2.5. Screening of Isolates for Enzyme Production

Each fungal isolates obtained were screened for cellulase and xylanase production. Chemically defined media composed of KH2PO4 (1 g/L), MgSO4・7H2O (0.5 g/L), yeast extract (1 g/L), CaCl2・2H2O (0.14 g/L), CMC or Xylan (10 g/L) and thiamine (0.0025 g/L) were prepared [19] . The media were dispensed into screw capped bottles and sterilized at 121˚C for fifteen minutes in an autoclave. After cooling, the medium was inoculated with one disk of agar of the fungal mycelium obtained by using a sterile cork borer (9 mm). Uninoculated medium served as control. After growth had been allowed to proceed for the required length of time at the required temperature, the cultures were centrifuged using refrigerated centrifuge (IEC, Centra, MP4R Model) at 3000 rpm for 15 minutes. Culture supernatant (1 ml) was added to 9ml of the substrate containing 0.55% w/v of CMC (carboxymethyl cellulose) in 0.55 M acetate buffer pH 5.5 for cellulase and 1.0% w/v of xylan in 0.2 M acetate buffer pH 4.5 for xylanase (hemicellulase) assay. Subsequently, they were incubated at 45˚C for 1 hour. Each reaction was halted by adding a drop of 5 M NaOH. To estimate the amount of reducing sugars released, dinitrosalicyclic acid (DNSA) reagent (1 ml) was added to 1ml of the filtrate―CMC/xylan reaction mixture and boiled at 100˚C for 10 minutes in a water bath [20] . After cooling, the absorbance was determined at 540 nm using a Jenway 6405/VIS spectrophotometer. The absorbance of standard aqueous solutions of D-glucose and xylose of various concentrations (0 - 10 mgml) at 540 nm was determined and used to construct a graph of percentage absorbance as related to mg of glucose or xylose per ml. The amount of reducing sugar produced by 1 ml of fungi filtrate from the CMC assay medium and xylan assay medium was calculated from this graph. Cellulolytic and hemicellulolytic activities of the filtrates were then expressed in terms of the amount of total reducing sugars (RS) per ml.

2.6. Molecular Identification of Fungus

The internal transcribed spacer (ITS) sequence of the fungus was amplified by polymerase chain reaction (PCR) with the primers ITS1 (5-CTTGGTCATTTAGAGGAAGTAA-31) and ITS2 (5-TCCTCCGCTTATTGATATGC- 31). The amplification was performed using a PCR cycler under the following cycling parameters: 94˚C for 4 minutes, followed by 37 cycles of 30s at 92˚C, 30s at 55˚C and 1min at 68˚C with final extension of 68˚C for 1 minute. Sequencing of the purified PCR amplicon was done using ABI Bigdye 3.1 cycle sequencing kit (Applied Biosystems, California, USA) on ABI 3730XL and the nucleotide sequence determined by automated sequencer by Laragen Inc., Culver City California. The nucleotide sequences of ITS1/ITS2 of the isolate was aligned and analyzed by using Basic Local Alignment Search Tool (BLAST) program available at [21] .

2.7. Enzyme Production and Extracts

Isolate was grown in a 250 ml glass bottle containing 10 g of substrate (cassava peel) and yeast extract as a nitrogen source. Moisture content was adjusted to 20% - 40% (w/w) by adding distilled water and sterilized at 121˚C for 15 minutes. The bottle was inoculated with 5 mls of the fungi grown for 7 days (1 × 106 spores/ml) and incubated at 30˚C for 5 - 7 days. Experiment was carried out in triplicates.

At the end of the incubation period, 0.1 M citrate buffer with pH 4.8 was added to give a total of 50 ml/flask. The flasks were shaken using an orbital shaker at 150 rpm for 1 hr then filtered to obtain clear filtrate for determining enzyme activity.

2.8. Optimization of Cultural Conditions for Enzyme Production

The isolate was grown in chemically defined media composed of KH2PO4 (1 g/L), MgSO4∙7H2O (0.5 g/L), yeast extract (1 g/L), CaCl2∙2H2O (0.14 g/L), CMC/xylan (10 g/L) and thiamine (0.0025 g/L) according to [22] .

2.9. Effect of Temperature on Cellulase and Xylanase Activity

The isolate was grown in chemically defined medium in a concentration of 1 × 106 spores ml−1 and incubated at temperatures of 27˚C, 40˚C, 50˚C, 60˚C and 70˚C for 5 days. All were done in triplicates. After incubation, the content of the flask was centrifuged and the cell free supernatant was assayed for cellulose and xylanase synthesis using the DNSA method to estimate the amount of reducing sugars released.

2.10. Effect of pH on Cellulase and Xylanase Activity

The isolate was grown in chemically defined medium with a concentration of 1 × 106 spores ml−1, adjusting the pH from 6 to 10 and incubated for 5 days. After incubation, the content of the flask was centrifuged and the cell free supernatant was assayed for cellulase and xylanase synthesis using the DNSA method to estimate the amount of reducing sugars released.

2.11. Effect of Carbon Source on Cellulase and Xylanase Activity

The isolate was grown in chemically defined medium with a concentration of 1 × 106 spores’ ml−1. The carbon source was substituted using glucose, xylose, raffinose, carboxymethylcellulose, mannitol and lactose. Incubation was done at the optimum pH and temperature for 5 days. After incubation, the content of the flask were centrifuged and the cell free supernatant was analyzed for cellulose and xylanase as analyzed for cellulose and xylanase synthesis using the DNSA method to estimate the amount of reducing sugars released.

2.12. Effect on Nitrogen Source on Cellulase and Xylanase Activity

The isolate was grown in chemically defined medium with a concentration of 1.0 × 106 spores ml−1. The nitrogen source was substituted using peptone, urea, (NH4)2SO4, NaNO3 and yeast extract. Incubation was done at the optimum temperature, pH and carbon source and incubated accordingly for 5 days. After incubation, the content of the flask was centrifuged and the cell free supernatant was assayed for cellulase and xylanase synthesis using the DNSA method to estimate the amount of reducing sugars released.

2.13. Enzyme Assay

The cellulase and xylanase was assayed by incubating 1 ml of crude enzyme with 9 ml of 0.55 M sodium acetate buffer pH 5.5 containing 0.55% w/w CMC and 0.2 M acetate buffer pH 4.5 containing 1.0% w/v xylan at 45˚C for 1 hour. The amount of reducing sugars released was determined by the 3, 5-dinitrosalicyclic acid (DNS) method [20] .

2.14. Enzyme Activity

This is determined based on one unit (u) of the enzyme activity i.e. the amount of enzyme required to release 1 unit of products (glucose or xylose) from cassava peels per minute under the assay conditions. In this study, the enzyme activities are expressed as units per gram of cassava peels (U/g).

2.15. Alkali Pretreatment by NaOH

Twenty grammes of cassava peel was suspended in 80 mls of 0.01 M to 3 M sodium hydroxide (NaOH), incubated at room temperature for 1 h in a 500 ml beaker for cold treatment while for heat treatment the beakers were placed in an autoclave at temperature between 100˚C and 135˚C with exposure time varying from 15min to 60 mins. The solid residues were collected and washed thoroughly with tap water until neutral pH was reached prior to enzymatic hydrolysis [23] .

2.16. Acid Pretreatment by H2SO4

The 2% cassava peels was hydrolyzed with acid (sulphuric acid) of different concentrations ranging from 0.01 to 3 M. The hydrolysis conditions were performed at 121˚C for 30 min. The hydrolysates were separated by a centrifuge at 6500 rpm for 10 min. Each sample was neutralized by 1 M NaOH solution for analysis of reducing sugar with DNSA method. The acid concentration that gave a maximum reduce sugars was chosen. The selected acid concentration was applied to determine the optimum temperature for cassava peel hydrolysis. A temperature range used in this study was between 100˚C and 135˚C and hydrolysis time was from 15 to 60 min for heat treatment. Cold treatment was done by incubating suspended cassava peel in 0.01 M to 3 M sulphuric acid for 1h. The solid residues were collected and neutralized with 2 M NaOH and then washed thoroughly with tap water until neutral pH was reached prior to enzymatic hydrolysis [19] .

2.17. Saccharification of Pretreated Cassava Peel

Following enzyme extraction, fungal cells were eliminated from the crude enzyme and one gram of pretreated cassava peel was saccharified with 5 ml of crude enzymes (3 U/mL) of cellulase and xylanase respectively. The mixtures were incubated at 45˚C for 3 days in an orbital shaker. The glucose and xylose yields were analyzed using gas chromatography (HP-6890 powered with HP ChemStation Rev, A 09.01 [1206] Software) with a BPX70 column and a flame ionization detector, detector temperature is 325˚C the protocol of [24] was used.

3. Results

3.1. Isolation of Fungi

Thirteen fungal isolates were obtained from rotten cassava peels. Seven species of the genus Aspergillus were isolated; three species of Penicillium, two species of Rhizopus and Streptomyces and one Candida were also obtained. They were identified as Rhizopusoryzae, Aspergillus terreus, Penicillium expansum, Penicillium atrovenetum, Fusarium poae, Streptomyces nitrosporeus and Candida valida. A. terreus have the highest percentage occurrence and morphologically it was observed to have a black to dark brown colour; it has a velvety appearance, and it also has short aerial hyphae with black spots, the conidial head is columnar while the conidial globose is slightly ellipsoidal.

3.2. Screening for Fungi Producing Cellulase and Xylanase

The cellulase and xylanase production by fungal isolates are represented in Figure 1 Aspergillus terreus produced the highest concentration of cellulase and xylanase respectively (2.7 U/mL and 3.4 U/mL) while Candida valida produced the lowest concentration of 0.55 U/ml and 1.0 U/mL for both cellulase and xylanase.

3.3. Molecular Identification of Isolates

The nucleotide sequences were subjected to the basic alignment search tool (BLAST) (http// where similarities and analysis was made from existing sequences in the database. The best cellulase or xylanase producers showed a 99% identity with Aspergillus terreus and given ascension number KJ829487.

3.4. Optimization of Conditions for Cellulase and Xylanase Production

3.4.1. Effect of pH

Five pH values ranging from 6 to 10 were picked for this study. The optimal pH for cellulase and xylanase production using cassava peels as the sole source of carbon was 6 and 8 producing 2.8 U/mL and 3.4 U/mL respectively (Figure 2).

3.4.2. Effect of Temperature

In this study, the production of cellulase and xylanase by Aspergillus terreus KJ829487 was determined after varying the temperature of incubation from 27˚C to 70˚C. The greatest enzymatic production occurred at 40˚C (Figure 3) for both cellulase and xylanase production (2.8 U/mL and 3.4 U/mL), for the culture at 50˚C to 70˚C, the enzymatic activities decline.

3.4.3. Effect of Nitrogen Sources

In this study, the supplementation of organic and inorganic nitrogen sources stimulated the cellulase and xylanase yield and activity, with the organic sources yielding higher concentration more than the inorganic ones. The organic nitrogen used for this study are peptone, urea and yeast extract and the inorganic nitrogen used are

Figure 1. Cellulase and xylanase concentration of fungi isolated from rotten cassava peels in Ibadan.

Figure 2. Effect of pH on cellulase and xylanase production by Aspergillus terreus KJ829487.

Figure 3. Effect of temperature on cellulase and xylanase production by Aspergillus terreus KJ829487.

(NH4)2SO4 and NaNO3. Yeast extract showed the highest cellulase and xylanase production (2.8 U/mL, 3.8 U/mL) and this is represented in the Figure 4.

3.4.4. Effect of Carbon Sources

The ability of A. terreus KJ829487 to utilize different carbon sources was monitored using various types of carbon (Figure 5) because the production of enzymes is related to the type and concentration of carbon source in the medium [25] . Addition of carboxymethyl cellulose (CMC) to the medium was most effective for cellulase production with 2.7 U/mL (Figure 5) concentration of cellulase produced, while xylose induces highest production of xylanase (3.2 U/mL).

3.4.5. Saccharification of Pretreated Cassava Peels

Enzymatic hydrolysis of pretreated cassava peels with A. terreus KJ829487 enzymes produced highest concentration of glucose (584 mg/L), xylose (78 mg/L) and rhamnose (66 mg/L) from dilute acid pretreated peels.

4. Discussion

The predominance of A. terreus in this study is in conformity with the work of [26] who stated that A. terreus

Figure 4. Effect of nitrogen sources on cellulase and xylanase production by Aspergillus terreus KJ829487.

Figure 5. Effect of carbon sources on cellulase and xylanase production by Aspergillus terreus KJ829487.

group are typically soil organisms, abundant in soil and decaying litter and a great variety of materials useful to man which includes grains, straw and forage products, cotton and other fibrous materials. [27] reported in their work on the optimization of cellulase production by A. terreus the ability of the organism to produce high concentration of cellulase enzymes. Also, [28] confirmed that Aspergillus sp. have the capability to produce large amounts of cellulolytic enzymes. Utilization of pH is considered as an important factor during enzyme production. According to [29] , they have been able to establish that cellulase and xylanase experience of most filamentous fungi are pH dependent. [30] reported an optimum of pH 5 and 8 for cellulase and xylanase during enzyme production of Trichoderma viride. The optimum temperature for growth of fungus may not necessarily be the optimum temperature for production of enzymes, although incubation temperature is a critical factor in enzyme production according to [31] . The result for the cellulase production at 40˚C is in accordance with the work of [32] , who also obtained a maximum temperature of 40˚C for A. terreus AV49 using pretreated groundnut shell as substrate, this observation is similar to previous studies carried out by [33] and [27] . Optimal temperature for xylanase in this work is obtained at 40˚C and this is not in agreement with the work of [31] who obtained an optimal temperature for xylanase activity at 28˚C for A. niger, while [34] reported 35˚C for A. terreus UL4206 and [35] reported optimum temperature for xylanase production by A. sulphurous cultivated from agro industrial wastes to be between 30˚C and 45˚C. [36] also reported that organic nitrogen sources are more suitable for the optimal production of cellulase and xylanase. [37] establish the fact that addition of yeast extract always lead to an increase in cellulase and xylanase production by A. terreus which explains the high production of enzymes using yeast extract in this study. [38] and [39] , reported that using CMC is the most favourable carbon source for screening cellulolytic fungi. Also, [40] supports the use of xylose as carbon source to improve xylanase production in filamentous fungi. Basic principle underlying acid pretreatment method is that the acid removes the hemicellulosic components of the peels thereby exposing the cellulose to enzymatic digestion [41] . At this point the cellulose is extremely susceptible to hydrolysis [42] . This shows that acid hydrolysis significantly (P < 0.05) enhanced saccharification of cassava peels with the isolate enzyme. Pretreatment or hydrolysis with sulphuric acid has removed and hydrolysed hemicellulose to their monomeric constituent and lignin-hemicellulose cellulose interactions partially disrupted [43] . This pretreatment therefore solubilised the cellulose making it amenable to attack by the cellulase produced by the isolates. The acid disrupts the hydrogen bonding between cellulose chains, converting it to a completely amorphous state, thereby forming a homogenous gelatin with the acid. At this point the cellulose is extremely susceptible to hydrolysis [44] . [45] reported that dilute sulphuric acid hydrolysis is the best processing options for desirable characteristics like low cost of chemicals for pretreatment, minimal waste production, limited size reduction, fast reaction and production of high concentration of sugars.

5. Conclusion

Aspergillus terreus KJ829487 obtained from cassava peels have the ability to produce high concentrations of cellulases and xylanases which can be applied for effective bioconversion of cassava peels to fermentable sugars that can be further processed for manufacturing of value added products.


*Corresponding author.

Conflicts of Interest

The authors declare no conflicts of interest.


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