A Staphylococcus capitis strain with unusual bacteriocin production.
Christiane SzekatMichaele JostenJasmin RickmeyerMax CrüsemannGabriele BierbaumPublished in: Microbial biotechnology (2023)
Staphylococcus capitis is a member of the human and mammal skin microbiomes and is considered less harmful than Staphylococcus aureus. S. capitis subsp. urealyticus BN2 was isolated from a cat and expressed strong antibacterial activity against a range of Gram-positive species, most notably including S. aureus strains with resistance to methicillin (MRSA) and strains with intermediate resistance to vancomycin (VISA). These latter strains are normally relatively resistant to bacteriocins, due to cell wall and cell membrane modifications. Genomic sequencing showed that the strain harboured at least two complete gene clusters for biosynthesis of antagonistic substances. The complete biosynthetic gene cluster of the well-known lantibiotic gallidermin was encoded on a large plasmid and the mature peptide was present in isopropanol cell extracts. In addition, a chromosomal island contained a novel non-ribosomal peptide synthetase (NRPS) gene cluster. Accidental deletion of two NRPS modules and partial purification of the anti-VISA activity showed that this novel bacteriocin represents a complex of differently decorated, non-ribosomal peptides. Additionally, a number of phenol-soluble modulins (PSMs) was detected by mass spectrometry of whole cells. Producing these compounds, the strain was able to outcompete several S. aureus strains, including MRSA and VISA, in tube cultures.
Keyphrases
- staphylococcus aureus
- methicillin resistant staphylococcus aureus
- escherichia coli
- copy number
- cell wall
- biofilm formation
- genome wide
- mass spectrometry
- single cell
- endothelial cells
- genome wide identification
- induced apoptosis
- crispr cas
- gene expression
- stem cells
- high resolution
- induced pluripotent stem cells
- gram negative
- cell cycle arrest
- oxidative stress
- cystic fibrosis
- reduced graphene oxide
- quantum dots
- ms ms
- silver nanoparticles
- high performance liquid chromatography
- recombinant human