A novel cecropin‐like peptide from black soldier fly, Hermetia illucens: Isolation, structural and functional characterization. Issue 2 (March 2017)
- Record Type:
- Journal Article
- Title:
- A novel cecropin‐like peptide from black soldier fly, Hermetia illucens: Isolation, structural and functional characterization. Issue 2 (March 2017)
- Main Title:
- A novel cecropin‐like peptide from black soldier fly, Hermetia illucens: Isolation, structural and functional characterization
- Authors:
- Park, Soon‐Ik
Yoe, Sung Moon - Abstract:
- Abstract: Cecropins are basic antibacterial peptides that have potent antimicrobial activities. We induced and purified a novel antimicrobial peptide exhibiting activity against Gram‐negative bacteria from the immunized hemolymph of Hermetia illucens larvae . The immunized hemolymph was extracted, and the novel cecropin‐like peptide 1 (CLP1) was purified using solid‐phase extraction and reverse‐phase chromatography. The purified CLP1 demonstrated a molecular weight of 4, 840 Da, as determined by matrix‐assisted laser desorption/ionization‐time‐of‐flight (MALDI‐TOF). From analysis of CLP1 by N‐terminal amino acid sequencing using Edman degradation, combined with MALDI‐TOF and rapid amplification of cDNA ends‐polymerase chain reaction (RACE‐PCR), the amino acid sequence of the mature peptide was determined to be GWRKRVFKPVEKFGQRVRDAGVQGIAIAQQGANVLATARGGP PQQG. In NCBI BLAST, the amino acid sequence of CLP1 was found to be 60 % identical to the Drosophila melanogaster cecropin C. In silico analysis revealed that CLP1 was suggested to be part of the cecropin superfamily of AMPs characterized as cationic, linear, α‐helical, and amphipathic polypeptides. Analysis of the minimal inhibitory concentration (MIC) and the minimal bactericidal concentration (MBC) showed that CLP1 exerted antibacterial effects against Gram‐negative bacteria. The expression of CLP1 transcripts in several tissues after bacterial challenge was measured by quantitative real‐time PCR. CLP1 expression wasAbstract: Cecropins are basic antibacterial peptides that have potent antimicrobial activities. We induced and purified a novel antimicrobial peptide exhibiting activity against Gram‐negative bacteria from the immunized hemolymph of Hermetia illucens larvae . The immunized hemolymph was extracted, and the novel cecropin‐like peptide 1 (CLP1) was purified using solid‐phase extraction and reverse‐phase chromatography. The purified CLP1 demonstrated a molecular weight of 4, 840 Da, as determined by matrix‐assisted laser desorption/ionization‐time‐of‐flight (MALDI‐TOF). From analysis of CLP1 by N‐terminal amino acid sequencing using Edman degradation, combined with MALDI‐TOF and rapid amplification of cDNA ends‐polymerase chain reaction (RACE‐PCR), the amino acid sequence of the mature peptide was determined to be GWRKRVFKPVEKFGQRVRDAGVQGIAIAQQGANVLATARGGP PQQG. In NCBI BLAST, the amino acid sequence of CLP1 was found to be 60 % identical to the Drosophila melanogaster cecropin C. In silico analysis revealed that CLP1 was suggested to be part of the cecropin superfamily of AMPs characterized as cationic, linear, α‐helical, and amphipathic polypeptides. Analysis of the minimal inhibitory concentration (MIC) and the minimal bactericidal concentration (MBC) showed that CLP1 exerted antibacterial effects against Gram‐negative bacteria. The expression of CLP1 transcripts in several tissues after bacterial challenge was measured by quantitative real‐time PCR. CLP1 expression was negligible throughout the body before immunization, and was mostly evident in the fat body after immunization. … (more)
- Is Part Of:
- Entomological research. Volume 47:Issue 2(2017:Mar.)
- Journal:
- Entomological research
- Issue:
- Volume 47:Issue 2(2017:Mar.)
- Issue Display:
- Volume 47, Issue 2 (2017)
- Year:
- 2017
- Volume:
- 47
- Issue:
- 2
- Issue Sort Value:
- 2017-0047-0002-0000
- Page Start:
- 115
- Page End:
- 124
- Publication Date:
- 2017-03
- Subjects:
- cecropin -- Hermetia illucens -- antimicrobial peptide
Insects -- Korea -- Periodicals
Entomology -- Periodicals
595.709519 - Journal URLs:
- http://firstsearch.oclc.org ↗
http://onlinelibrary.wiley.com/journal/10.1111/(ISSN)1748-5967 ↗
http://www.blackwell-synergy.com/loi/enr ↗
http://www.blackwellpublishing.com/journal.asp?ref=1738-2297&site=1 ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1111/1748-5967.12226 ↗
- Languages:
- English
- ISSNs:
- 1738-2297
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 3778.605000
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 315.xml