Molecular cloning and sequence analysis of chitinase cDNA from Mamestra brassicae
Author of the article:
Author's Workplace:
Key Words:Mamestra brassicae, chitinase, molecular cloning, sequence analysis
Abstract: Insect chitinase has great potential in biological control of insect pests. Total RNA was isolated from the whole body of Mamestra brassicae L. at prepupal stage. The cDNA sequence was cloned by RTPCR and rapid amplification of cDNA ends was conducted. The cDNA of 2 826 base pairs in length contained an open reading frame of 1 689 base pairs coding for a polypeptide of 562 amino acid residues with a predicted molecular weight of 62.6 kDa and pI 5.30. The deduced amino acid sequence of M. brassicae chitinase was predicted using the software Prosite, which indicated that it has two putative N-glycosylation sites and twenty two putative O-glycosylation sites. The predicted protein shared extensive similarites with those from other insects, expecially the lepidopteran insects. The cDNA sequence has been deposited in GenBank with accession No. FJ436415.