Human-β-defensins-1-3 and analogs do not require proton motive force for antibacterial activity against Escherichia coli
| Autor: | Viswanatha Krishnakumari, Kavin K. Packiyanathan, Ramakrishnan Nagaraj |
|---|---|
| Rok vydání: | 2013 |
| Předmět: |
chemistry.chemical_classification
beta-Defensins Chemiosmosis Chemistry Stereochemistry Cations Divalent Proton-Motive Force Microbial Sensitivity Tests Carbonyl cyanide m-chlorophenyl hydrazone medicine.disease_cause Microbiology Transport protein Divalent chemistry.chemical_compound Membrane Anti-Infective Agents Genetics medicine Escherichia coli Humans Magnesium Bacterial outer membrane Antibacterial activity Molecular Biology |
| Zdroj: | FEMS microbiology letters. 348(1) |
| ISSN: | 1574-6968 |
| Popis: | Human-β-defensins 1-3 (HBD-1-3) and their C-terminal analogs Phd-1-3 do not show antibacterial activity against Escherichia coli in the presence of mono- and divalent cations. Activity of peptides was examined against E. coli pretreated with carbonyl cyanide m-chlorophenylhydrazone (CCCP) and salt remedial Escherichia coli ftsEX, a deletion mutant of FtsEX complex [an ATP-binding cassette (ABC) transporter protein], in the presence of Na(+), Ca(2+), and Mg(2+). Activity was observed in the presence of Na(+) and Ca(2+), although not in the presence of Mg(2+) against E. coli, when proton motive force (PMF) was dissipated by CCCP. The peptides exhibited antibacterial activity against E. coli ftsEX even in the presence of Na(+) and Ca(2+). Our results indicate that HBD-1-3 and Phd-1-3 do not require PMF for their antibacterial activity. The absence of activity against E. coli in the presence of Na(+) and Ca(2+) ions is due to not only weakened electrostatic interactions with anionic membrane components, but also involvement of electrochemical gradients. However, Mg(2+) prevents electrostatic interaction of the peptides with the outer membrane resulting in loss of activity. |
| Databáze: | OpenAIRE |
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