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. 2011 Sep 23;286(45):39179–39187. doi: 10.1074/jbc.M111.283929

FIGURE 3.

FIGURE 3.

Characterization of HspB. A, pH dependence of HspB stability. The enzyme was incubated overnight in buffers of various pH at 25 °C. B, thermostability of HspB. The enzyme was incubated in Tris-HCl buffer (50 mm, pH 8.0) at varying temperatures for 30 min. C, effects of metal salts on HspB stability. CK, without metal salt; Na, Na+; Ni, Ni2+; Co, Co2+; Ca, Ca2+; Cu, Cu2+; Mn, Mn2+; Zn, Zn2+; Mg, Mg2+; K, K+; Mo, MoO42−; W, WO42−. D, oxygen consumption of the HspB reaction. ▲, ●, and ■ indicate the oxygen declines from different initial concentrations. For the above four experiments, enzyme activity was determined according to the standard assay at 25 °C and pH 8.0.