TY - JOUR
T1 - Novel Antimicrobial Nano Bacteriocin
T2 - Lactic Acid Bacteria-Derived, Self-Assembled, and Enhanced for Superior Antimicrobial Activity
AU - Yi, Lanhua
AU - Li, Shengyang
AU - Xie, Miaomiao
AU - Chen, Bozhou
AU - Chen, Kaichao
AU - Wang, Zhouxia
AU - Zeng, Min
AU - Zhao, Qian
AU - Yang, Jiyu
AU - Tang, Yang
AU - Zhao, Wenxing
AU - Zeng, Ping
AU - Li, Xuecheng
AU - Wang, Jiaqi
AU - Zeng, Kaifang
AU - Zhong, Yuyue
AU - Chen, Sheng
PY - 2026/3/3
Y1 - 2026/3/3
N2 - As antimicrobial resistance emerges as a critical global health threat, food-grade bacteriocin, a kind of antimicrobial peptide (AMPs), offers promising new therapies but is hampered by poor stability and water solubility. To address this, we engineered a carrier-free self-assembly strategy: a novel bacteriocin from lactic acid bacteria in fermented food was modified to increase its hydrophobicity, enabling spontaneous formation of nano-antimicrobial bacteriocins (NAMBs) in TSB, LB, and MH media. These NAMBs exhibit a broader antimicrobial spectrum and enhanced potency against both Gram-positive and Gram-negative pathogens, including Listeria monocytogenes, Acinetobacter baumannii, and Vibrio parahaemolyticus, as evidenced by markedly reduced minimum inhibitory concentrations in vitro and superior therapeutic efficacy in infected mice in vivo. Mechanistic investigations reveal targeted disruption of cell envelope metabolism: in L. monocytogenes, NAMBs fortify the peptidoglycan layer while depleting wall teichoic acids and lipoteichoic acids, impairing carbohydrate metabolism and membrane transport; in A. baumannii, they downregulate fatty acid synthesis, disorder phospholipid composition, and weaken lipopolysaccharide integrity, culminating in membrane destabilization and cell death. These dual actions—disordering metabolic processes and remodeling bacterial cell walls or membranes—highlight the versatility of NAMBs. Our carrier-free self-assembly approach thus overcomes AMP stability and solubility limitations and paves the way for next-generation antimicrobial therapies. © 2026 Wiley-VCH GmbH.
AB - As antimicrobial resistance emerges as a critical global health threat, food-grade bacteriocin, a kind of antimicrobial peptide (AMPs), offers promising new therapies but is hampered by poor stability and water solubility. To address this, we engineered a carrier-free self-assembly strategy: a novel bacteriocin from lactic acid bacteria in fermented food was modified to increase its hydrophobicity, enabling spontaneous formation of nano-antimicrobial bacteriocins (NAMBs) in TSB, LB, and MH media. These NAMBs exhibit a broader antimicrobial spectrum and enhanced potency against both Gram-positive and Gram-negative pathogens, including Listeria monocytogenes, Acinetobacter baumannii, and Vibrio parahaemolyticus, as evidenced by markedly reduced minimum inhibitory concentrations in vitro and superior therapeutic efficacy in infected mice in vivo. Mechanistic investigations reveal targeted disruption of cell envelope metabolism: in L. monocytogenes, NAMBs fortify the peptidoglycan layer while depleting wall teichoic acids and lipoteichoic acids, impairing carbohydrate metabolism and membrane transport; in A. baumannii, they downregulate fatty acid synthesis, disorder phospholipid composition, and weaken lipopolysaccharide integrity, culminating in membrane destabilization and cell death. These dual actions—disordering metabolic processes and remodeling bacterial cell walls or membranes—highlight the versatility of NAMBs. Our carrier-free self-assembly approach thus overcomes AMP stability and solubility limitations and paves the way for next-generation antimicrobial therapies. © 2026 Wiley-VCH GmbH.
KW - antibacterial bacteriocin
KW - mechanisms of action
KW - nanoparticle
KW - peptide
KW - self-assembly
UR - http://www.scopus.com/inward/record.url?scp=105028284521&partnerID=8YFLogxK
UR - https://www.scopus.com/record/pubmetrics.uri?eid=2-s2.0-105028284521&origin=recordpage
U2 - 10.1002/adma.202511782
DO - 10.1002/adma.202511782
M3 - RGC 21 - Publication in refereed journal
SN - 0935-9648
VL - 38
JO - Advanced Materials
JF - Advanced Materials
IS - 13
M1 - e11782
ER -