Characterisation and stabilisation of recombinant Humicola insolens endoglucanase produced in Pichia pastoris
Cellulases are industrially important hydrolytic enzymes that are applicable in the bioconversion of cellulosic biomass to simple sugars. In this work, Pichia pastoris carrying an endoglucanase cDNA (CMC3) from a thermophilic fungus, Humicola insolens, was grown in a 30 L bioreactor to produce rec...
| Main Authors: | , , , , , , |
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| Format: | Article |
| Language: | English |
| Published: |
Penerbit Universiti Kebangsaan Malaysia
2015
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| Online Access: | http://journalarticle.ukm.my/8723/ http://journalarticle.ukm.my/8723/ http://journalarticle.ukm.my/8723/1/44_1_25.pdf |
| Summary: | Cellulases are industrially important hydrolytic enzymes that are applicable in the bioconversion of cellulosic biomass to
simple sugars. In this work, Pichia pastoris carrying an endoglucanase cDNA (CMC3) from a thermophilic fungus, Humicola
insolens, was grown in a 30 L bioreactor to produce recombinant CMC3 in a fed-batch cultivation mode. After optimisation
of the cultivation conditions, a total of 5.3 gL-1 proteins were obtained in a 20 L working volume after a 40 h induction with
methanol. CMC3 expresses a β-1,4-endoglucanase with a specific activity of 62.83 U mg-1, demonstrating its specificity for
hydrolysing carboxymethyl cellulose as a substrate. No detectable hydrolysis on Sigmacell® cellulose, Avicel or beechwood
xylan was observed. The recombinant CMC3 displayed moderate thermostability, being stable at up to 50°C for more than
72 h. Metal ions such as Mn²+ and Co²+ enhanced the CMC3 activity, while Ni+, Zn²+ and Cu²+ inhibited the enzyme
activity. The CMC3 produced in P. pastoris was stable under long-term storage, retaining 84% and 75% of its initial activity
after 4 months of storage at 4°C and 25°C, respectively. The addition of stabilisers further improved the enzyme stability by
7% and 5% at 4°C and 25°C, respectively. |
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