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KMID : 1161520070110020175
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Animal Cells and Systems
2007 Volume.11 No. 2 p.175 ~ p.182
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Molecular cloning and characterization of lysozyme II from Artogeia rapae and its expression in Baculovirus?infected insect cells
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Bang In-Seok
Kang Chang-Soo
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Abstract
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The lysozyme II gene of cabbage butterfly Artogeia rapae was cloned from fat body of the larvae injected with E. coli and its nucleotide sequence was determined by the RACE?PCR. It has an open reading frame of 414 bp nucleotides corresponding to 138 amino acids including a signal sequence of 18 amino acids. The estimated molecular weight and the isoelectric point of the lysozyme II without the signal peptide were 13,649.38 Da and 9.11, respectively. The A. rapae lysozyme II (ARL II) showed the highest identity (81 %) in the amino acid sequence to Manduca sexta lysozyme among other lepidopteran species. The two catalytic residues (Glu32 and Asp50) and the eight Cys residue motifs, which are highly conserved among other c?type lysozymes in invertebrates and vertebrates, are also completely conserved. A phylogenetic analysis based on amino acid sequences indicated that the ARL II was more closely related to M. sexta, Hyphantria cunea, Heliothis virescens, and Trichoplusia ni lysozymes. The ARL II gene was expressed in Spodoptera frugiperda 21 insect cells and the recombinant ARL II (rARL II) was purified from cell?conditioned media by cation exchange column chromatography and reverse phase FPLC. The purified rARL II was able to form a clear zone in lysoplate assay against Micrococcus luteus. The lytic activity was estimated to be 511.41 U/mg, 1.53 times higher than that of the chicken lysozyme. The optimum temperature for the lytic activity of the rARL II was 50°C, the temperature dependency of the absolute lytic activity of rARL II was higher than that of the chicken lysozyme at low temperatures under 65°C.
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KEYWORD
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Artogeia rapae, Baculovirus expression, cDNA cloning, c-type lysozyme, Insect immunity
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