Analysis of the cell wall binding domain in bacteriocin-like lysin LysL from Lactococcus lactis LAC460.
Samira MokhtariYanru LiPer Erik Joakim SarisTimo M TakalaPublished in: Archives of microbiology (2024)
Wild-type Lactococcus lactis strain LAC460 secretes prophage-encoded bacteriocin-like lysin LysL, which kills some Lactococcus strains, but has no lytic effect on the producer. LysL carries two N-terminal enzymatic active domains (EAD), and an unknown C-terminus without homology to known domains. This study aimed to determine whether the C-terminus of LysL carries a cell wall binding domain (CBD) for target specificity of LysL. The C-terminal putative CBD region of LysL was fused with His-tagged green fluorescent protein (HGFPuv). The HGFPuv_CBDlysL gene fusion was ligated into the pASG-IBA4 vector, and introduced into Escherichia coli. The fusion protein was produced and purified with affinity chromatography. To analyse the binding of HGFPuv_CBDLysL to Lactococcus cells, the protein was mixed with LysL-sensitive and LysL-resistant strains, including the LysL-producer LAC460, and the fluorescence of the cells was analysed. As seen in fluorescence microscope, HGFPuv_CBDLysL decorated the cell surface of LysL-sensitive L. cremoris MG1614 with green fluorescence, whereas the resistant L. lactis strains LM0230 and LAC460 remained unfluorescent. The fluorescence plate reader confirmed the microscopy results detecting fluorescence only from four tested LysL-sensitive strains but not from 11 tested LysL-resistant strains. Specific binding of HGFPuv_CBDLysL onto the LysL-sensitive cells but not onto the LysL-resistant strains indicates that the C-terminus of LysL contains specific CBD. In conclusion, this report presents experimental evidence of the presence of a CBD in a lactococcal phage lysin. Moreover, the inability of HGFPuv_CBDLysL to bind to the LysL producer LAC460 may partly explain the host's resistance to its own prophage lysin.
Keyphrases
- escherichia coli
- single molecule
- induced apoptosis
- cell wall
- cell cycle arrest
- energy transfer
- binding protein
- endoplasmic reticulum stress
- dna binding
- wild type
- cell surface
- signaling pathway
- genome wide
- nitric oxide
- cystic fibrosis
- hydrogen peroxide
- small molecule
- gene expression
- dna methylation
- label free
- gold nanoparticles
- liquid chromatography
- ms ms
- reduced graphene oxide
- candida albicans
- pi k akt
- multidrug resistant
- capillary electrophoresis