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Fig. 3 | Biotechnology for Biofuels

Fig. 3

From: A thermostable bacterial lytic polysaccharide monooxygenase with high operational stability in a wide temperature range

Fig. 3

Thermal unfolding of mgLPMO10. The apparent melting temperatures (Tm(app)) were determined by differential scanning calorimetry (DSC) by heating the full-length mgLPMO10-holo (approximately 0.4 g/L) at 1 °C/min from 25 °C to 100 °C in 50 mM sodium phosphate buffer (pH 6.0). The experiment was repeated for the apo version of the protein (mgLPMO10apo) and the holo catalytic domain (mgLPMO10CD)

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