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Fig. 2 | Biotechnology for Biofuels

Fig. 2

From: Investigation of a thermostable multi-domain xylanase-glucuronoyl esterase enzyme from Caldicellulosiruptor kristjanssonii incorporating multiple carbohydrate-binding modules

Fig. 2

Relative activity of the GH10 domain (red square) and the GH10 domain with both N-terminal CBM22 domains (blue circle) over a range of different pHs. Sodium acetate buffer was used up to pH 5.5, sodium phosphate from pH 6 to 8, and Tris for pH 8.5 and 9. The results are presented as the average of triplicate experiments with standard errors

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