A cDNA coding mutated cecropin CMIV from Bombyx mori was synthesized a
ccording to its amino acid sequence using E. coil biased codons. The g
ene was cloned into the fusion expression vector pEZZ318 and was expre
ssed in E. coli HB101. The fusion protein produced was purified by aff
inity chromatography to yield 26 mg/L fusion product. The anti-bacteri
al activities of recombinant cecropin CMIV were recovered after cleava
ge by chemical method.