Expression and Characterization of Calcium- and Zinc-Tolerant Xylose Isomerase from G10.

The enzyme xylose isomerase (E.C. 5.3.1.5, XI) is responsible for the conversion of an aldose to ketose, especially xylose to xylulose. Owing to the ability of XI to isomerize glucose to fructose, this enzyme is used in the food industry to prepare high-fructose corn syrup. Therefore, we studied the characteristics of XI from G10, a thermophilic bacterium. First, the gene coding for XI () was inserted into the pET-21a(+) expression vector and the construct was transformed into the competent cell BL21 (DE3). The expression of recombinant XI was induced in the absence of isopropyl-thio-β-galactopyranoside and purified using Ni-NTA affinity chromatography. The optimum temperature of recombinant XI was 80°C and measurement of the heat stability indicated that 55% of residual activity was maintained after 2 h incubation at 60°C. The optimum pH was found to be 7.5 in sodium phosphate buffer. Magnesium, manganese, and cobalt ions were found to increase the enzyme activity; manganese was the most effective. Additionally, recombinant XI was resistant to the presence of Ca²⁺ and Zn²⁺ ions. The kinetic properties, and , were calculated as 81.44 mM and 2.237 μmol/min/mg, respectively. Through redundancy analysis, XI of G10 was classified into a family containing type II XIs produced by the genera , , and . These results suggested that the thermostable nature of XI of G10 may be advantageous in industrial applications and food processing.