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Heterologous expression and characterization of a high redox potential laccase from Coriolopsis polyzona MUCL 38443
Pinar, Orkun Tamerler, Candan Yazgan Karataş, Ayten
Pinar, Orkun
Tamerler, Candan
Yazgan Karataş, Ayten
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Abstract
In this study, a novel laccase gene, named as Cplcc1, and its corresponding cDNA were isolated and characterized from the
Coriolopsis polyzona MUCL 38443 strain. The Cplcc1 gene consists of a 1563-bp open reading frame encoding a protein of 520 amino acids with a 20-residue putative signal peptide. The size of the Cplcc1 gene is 2106 bp and it contains ten introns and five potential N-glycosylation sites. Additionally, the isolated full-length Cplcc1 cDNA was successfully expressed in Pichia pastoris. The heterologous expression conditions were also optimized and the highest activity value increased to 800 U L–1 with 1.5% methanol, 0.8 mM CuSO4, and 0.6% L-alanine supplementation. The recombinant laccase was partially purified and the molecular weight was found as approximately 54 kDa. The maximum oxidation activity was observed for 2,2-azinobis-(3-ethylbenzothiazoline-6-sulfonic acid) (ABTS) at pH 3.0. The optimal temperature was found as 70 °C. On the other hand, at 30 °C, the enzyme was stable for more than a week and its half-life was longer than 8 h. The Km, Vmax, kcat, and kcat Km
–1 values of the recombinant laccase were identified as 0.137 mM, 288.6 µmol min–1 L–1, 5.73 × 105 min–1, and 4.18 × 106 min–1 mM–1,respectively. Sodium azide, L-cysteine, and SDS were found as usual inhibitors.
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2017
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TÜBİTAK
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Pinar_2017.pdf
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Keywords
Coriolopsis polyzona, Enzyme activity, Heterologous expression, Laccase, Pichia pastoris, Purification
Citation
Pinar, O., BEHAR, C. T., & KARATAŞ, A. (2017). Heterologous expression and characterization of a high redox potential laccase from Coriolopsis polyzona MUCL 38443. Turkish Journal of Biology, 41(2), 278-291.