Functional expression of theSpodoptera exiguachitinase to examine the virtually screened inhibitor candidates

Abstract Chitinase is responsible for insect chitin hydrolyzation, which is a key process in insect molting and pupation. However, little is known about the chitinase of Spodoptera exigua ( Se Chi). In this study, based on the Se Chi gene (ADI24346) identified in our laboratory, we constructed the recombinant baculovirus P-Chi for the expression of recombinant Se Chi (r Se Chi) in Hi5 cells. The r Se Chi was purified by chelate affinity chromatography, and the purified protein showed activity comparable with that of a commercial Sg Chi, suggesting that we harvested active Se Chi for the first time. The purified protein was subsequently tested for enzymatic properties and revealed to exhibit its highest activity at pH 8 and 40 C. Using homology modeling and molecular docking techniques, the three-dimensional model of Se Chi was constructed and screened for inhibitors. In two rounds of screening, twenty compounds were selected. With the purified r Se Chi, we tested each of the twenty compounds for inhibitor activity against r Se Chi, and seven compounds showed obvious activity. This study provided new information for the chitinase of beet armyworm and for chitinase inhibitor development.