Expression and purification of cyto-insectotoxin (Cit1a) using silkworm larvae targeting for an antimicrobial therapeutic agent
Author(s) -
M. P. Ali,
Katsuhiko Yoshimatsu,
Tomohiro Suzuki,
Tatsuya Kato,
Enoch Y. Park
Publication year - 2014
Publication title -
applied microbiology and biotechnology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.074
H-Index - 221
eISSN - 1432-0614
pISSN - 0175-7598
DOI - 10.1007/s00253-014-5728-1
Subject(s) - antimicrobial , antimicrobial peptides , bombyx mori , biology , peptide , green fluorescent protein , bombycidae , bacteria , fusion protein , microbiology and biotechnology , biochemistry , cecropin , protease , gene , recombinant dna , enzyme , genetics
Antimicrobial peptides (AMPs), both synthetic and from natural sources, have raised interest recently as potential alternatives to antibiotics. Cyto-insectotoxin (Cit1a) is a 69-amino-acid antimicrobial peptide isolated from the venom of the central Asian spider Lachesana tarabaevi. The synthetic gene Cit1a fused with the enhanced green fluorescent protein (EGFP) gene was expressed as the EGFP-Cit1a fusion protein using a cysteine protease-deleted Bombyx mori nucleopolyhedrovirus (BmNPV-CP(-)) bacmid in silkworm larva and pupa. The antimicrobial effect of the purified protein was assayed using disk diffusion and broth microdilution methods. The minimum inhibitory concentration of EGFP-Cit1a was also measured against several bacterial strains and showed similar antimicrobial activity to that of the synthetic Cit1a reported earlier. The EGFP-Cit1a fusion protein showed antibiotic activity toward gram-positive and gram-negative bacteria at the micromolar concentration level. These results show that active Cit1a can be produced and purified in silkworm, although this peptide is insecticidal. This study demonstrates the potential of active Cit1a purified from silkworms to use as an antimicrobial agent.
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