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Endolysin gp11 of the Curtobacterium phage Ayka could potentially be an active component of the new antibacterial agent to prevent wilt caused by Curtobacterium flaccumfaciens pv.
The isolation and characterisation of five novel lytic bacteriophages that specifically target K. grimontii are described and provides a basis for further evaluation of their potential in phage therapy.
Detailed analysis of the genome and structural proteome of phage Miki is presented, including in silico predictions and modeling of receptor-binding proteins, including central and proximal fibers resembling the adsorption apparatus of Escherichia phage T5.
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