Characterization of Endolysin LysG77YL from Bacillus licheniformis-Infecting Bacteriophage G77YL and Application as an Antimicrobial Agent
Nanjoo Park, Yerin Cho, Yerin Kang, Minsuk Kong

TL;DR
This paper describes a new endolysin from a bacteriophage that effectively targets and reduces Bacillus licheniformis in dairy products.
Contribution
The study introduces LysG77YL_EAD, a stable and potent endolysin with broad activity against Bacillus strains.
Findings
LysG77YL_EAD showed broader and more potent antibacterial activity than the full-length enzyme.
The endolysin retained high activity under various pH, salt, and temperature conditions.
Treatment with LysG77YL_EAD reduced B. licheniformis in milk by 4 log CFU/ml within 30 min.
Abstract
Bacillus licheniformis is a spore-forming, Gram-positive bacterium widely found in nature and frequently associated with spoilage in dairy products due to its extracellular enzyme production. To develop a targeted biocontrol strategy, a novel lytic phage, G77YL, was isolated from the Gyeongchun Line Forest Trail in South Korea. Host range analysis revealed that G77YL specifically infects several strains of B. licheniformis. Genome analysis indicated that it is a virulent phage devoid of lysogeny-related genes and encodes a glycosyl hydrolase family 25 endolysin, designated as LysG77YL. The endolysin (LysG77YL) and its enzymatically active domain (LysG77YL_EAD) were cloned, expressed, and purified. Lytic assays demonstrated that LysG77YL_EAD exhibited broader and more potent antibacterial activity than the full-length enzyme, targeting all Bacillus strains tested, including eight B.…
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Taxonomy
TopicsBacteriophages and microbial interactions · Monoclonal and Polyclonal Antibodies Research · Biopolymer Synthesis and Applications
