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Computational exploration of New Delhi Metallo-β-lactamase 1 (NDM-1) inhibitory peptides derived from Lacticaseibacillus paracasei HM-1 fermented camel milk

Year: 2026
Type: article
Abstract: • Camel milk fermented with L. paracasei HM-1 yielded potent antimicrobial peptides. • Fermentates showed strong activity against MDR B. cereus, S. Typhimurium, E. coli , and S. aureus . • LC–MS/MS identified >2000 peptides; 46 showed high predicted bioactivity scores. • Multiple peptides (e.g., AAQNLLACGVALGALR) strongly interacted with NDM-1 active sites. • Docking and MD simulations revealed stable peptide–NDM-1 binding and inhibitory potential. • Lead peptide AAQNLLACGVALGALR displayed highest affinity and stable multi-residue interactions. Silent pandemic of antimicrobial resistance (AMR) necessitates exploring natural antibiotic alternatives like antimicrobial peptides (AMPs). In a similar quest, present study investigated the antimicrobial potential of AMPs derived from Lacticaseibacillus paracasei HM1 fermented camel milk (FCM) proteins against multi drug resistant Bacillus cereus (BC), Staphylococcus aureus (SA), Escherichia coli (EC), and Salmonella Typhimurium (ST). Antibacterial assays suggested potent antibacterial activity of FCM-AMPs against BC (20.0±1.0mm), SA (12.0±0.7mm), EC (14.0±0.5mm), and ST (20.0±0.6mm). Further, identification, and in silico analysis of these AMPs revealed that peptides CCFSSCAMR, KCCFSSCAMR, AAQNLLACGVALGALR, FLPPLQPAVMVPFLQPK, and LLPAPPLLR showed potent interaction and binding with β-lactamase giving insights into their antimicrobial mechanisms. The research findings indicate FCM derived AMPs as potent antibacterial agents targeting both cell membrane and antibiotic degrading enzymes. Going ahead, further validation, safety assessment, and clinical trials will be essential to develop these peptides into effective antimicrobial therapies against AMR pathogens.
Source: Future Foods
Language: English
Subfield: Microbiology
Open Access status: gold
Estimated APC paid: $1,990
OpenAlex ID: W7160410683
FWCI:
Cites: 54
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