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The self-assembly of a cyclic lipopeptides mixture secreted by a B. megaterium strain and its implications on activity against a sensitive Bacillus species.
- Source :
-
PloS one [PLoS One] 2014 May 09; Vol. 9 (5), pp. e97261. Date of Electronic Publication: 2014 May 09 (Print Publication: 2014). - Publication Year :
- 2014
-
Abstract
- Cyclic lipopeptides are produced by a soil Bacillus megaterium strain and several other Bacillus species. In this work, they are detected both in the Bacillus intact cells and the cells culture medium by MALDI-TOF mass spectrometry. The cyclic lipopeptides self-assemble in water media producing negatively charged and large aggregates (300-800 nm of mean hydrodynamic radius) as evaluated by dynamic light scattering and zeta-potential analysis. The aggregate size depends on pH and ionic strength. However, it is not affected by changes in the osmolarity of the outer medium suggesting the absence of an internal aqueous compartment despite the occurrence of low molecular weight phospholipids in their composition as determined from inorganic phosphorus analysis. The activity against a sensitive Bacillus cereus strain was evaluated from inhibition halos and B. cereus lysis. Essential features determining the antibiotic activity on susceptible Bacillus cereus cells are the preserved cyclic moiety conferring cyclic lipopeptides resistance to proteases and the medium pH. The aggregates are inactive per se at the pH of the culture medium which is around 6 or below. The knock out of the sensitive cells only takes place when the aggregates are disassembled due to a high negative charge at pH above 6.
- Subjects :
- Bacillus cereus drug effects
Hydrogen-Ion Concentration
Lipopeptides pharmacology
Peptides, Cyclic pharmacology
Phosphorus analysis
Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization
Surface-Active Agents chemistry
Bacillus megaterium metabolism
Lipopeptides biosynthesis
Microbial Interactions physiology
Peptides, Cyclic biosynthesis
Protein Aggregates
Soil Microbiology
Subjects
Details
- Language :
- English
- ISSN :
- 1932-6203
- Volume :
- 9
- Issue :
- 5
- Database :
- MEDLINE
- Journal :
- PloS one
- Publication Type :
- Academic Journal
- Accession number :
- 24816927
- Full Text :
- https://doi.org/10.1371/journal.pone.0097261