화학공학소재연구정보센터
Journal of Bioscience and Bioengineering, Vol.97, No.5, 305-309, 2004
Biophysical analysis of heat-induced structural maturation of glutamate dehydrogenase from a hyperthermophilic archaeon
Tertiary structure of the recombinant glutamate dehydrogenase from Thermococcus kodakaraensis KOD1 (Tk-rGDH) converts into an intact form induced by the heat treatment. This phenomenon, heat-induced structural maturation, means that high temperature plays an important role in the proper folding and oligomerization of Tk-rGDH. In this work, we analyzed the heat-induced structural maturation of Tk-rGDH by differential scanning microcalorimetry (DSC), circular dichroism (CD), and activity measurements. In DSC measurements, the peak of adsorption of non-heated Tk-rGDH (nh-Tk-rGDH) was two times smaller than that of Tk-rGDH heated at 70degreesC for 30 min (h-Tk-rGDH). The transition temperature (T-m) of h-Tk-rGDH was 115degreesC, which was about 3degreesC higher than that of nh-Tk-rGDH. In the presence of 0.5 M NaCl, the nh-Tk-rGDH showed two peaks at 107degreesC and 114degreesC, while the h-Tk-rGDH showed a single peak at 115.7degreesC. The heat-induced conformational change process was monitored by changes in CD intensity at 222 nm, and the result showed that heat-induced structural maturation is irreversible. The heat treatment at 70degreesC showed the highest enhancement in activity, which was 15% larger than that of heat-treated Tk-rGDH at 40degreesC. The results indicate that heat-induced structural maturation involves an irreversible process, transforming the non-heated form to the stable and active form.