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Expression and characterization of LacMP, a novel fungal laccase of Moniliophthora perniciosa FA553.

Biotechnology letters (2015-06-22)
Huiping Liu, Chaofan Tong, Bing Du, Shuli Liang, Ying Lin
RÉSUMÉ

To characterize a putative laccase gene, LacMP, of Moniliophthora perniciosa FA553 that had been screened using a genome mining approach, then cloned and expressed in Pichia pastoris. The purified recombinant LacMP was ~57 kDa with a maximum laccase activity of 232 U/l. The optimal pH for oxidation reactions with 2,2'-azino-bis(3-ethylbenzothiazoline-6-sulfonic acid), syringaldazine, guaiacol and 2,6-dimethoxyphenol, were 6, 7.5, 6.5, and 6.5, respectively. The laccase activity was optimal at 60, 45, 45, and 55 °C for the four respective substrates. LacMP was stable at pH 6-8 and <30 °C. Li(+), K(+), Co(2+), Ni(2+), Mn(2+), and Mg(2+) at 1 mM had no obvious effect on its activity. Given that LacMP has optimal activity under neutral and alkaline oxidation reaction conditions, it could be a potential candidate for industrial biocatalytic applications.

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Sigma-Aldrich
Gaïacol, oxidation indicator
Sigma-Aldrich
Gaïacol, natural, ≥99%, FG
Sigma-Aldrich
2,6-Diméthoxyphénol, 99%
Sigma-Aldrich
2,6-Diméthoxyphénol, ≥98%, FG
Sigma-Aldrich
Syringaldazine, indicator for laccase and peroxidase activity
Sigma-Aldrich
2,6-Diméthoxyphénol, natural, ≥96%
Sigma-Aldrich
Syringaldazine, 98%