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Updated: Nov 18, 2025

A Method to Assess Bacteriocin Effects on the Gut Microbiota of Mice
Published on: July 25, 2017
Anticancer and antimicrobial potential of enterocin 12a from Enterococcus faecium
Preeti Sharma1, Sumanpreet Kaur1, Bhupinder Singh Chadha1
1Department of Microbiology, Guru Nanak Dev University, Amritsar, Punjab, 143005, India.
A novel bacteriocin, enterocin 12a, effectively combats multidrug-resistant Gram-negative bacteria and selectively inhibits human cancer cell proliferation, showing promise as a dual-action therapeutic agent.
Area of Science:
- Microbiology and Biotechnology
- Cancer Research
- Drug Discovery
Background:
- Rising infections from Gram-negative bacteria in neutropenic cancer patients necessitate novel therapeutics.
- Bacteriocins, prokaryotic cationic proteins, show potential as antimicrobial and anticancer agents.
Purpose of the Study:
- To purify and characterize a novel bacteriocin with potential dual anticancer and antimicrobial properties.
- To evaluate the antimicrobial spectrum and anticancer activity of the purified bacteriocin.
Main Methods:
- Purification and characterization of enterocin 12a from *Enterococcus faecium*.
- Antimicrobial susceptibility testing against multidrug-resistant Gram-negative and Gram-positive pathogens.
- Assessment of anticancer activity against human cancer cell lines and normal cells using cell proliferation assays and morphological analysis.
Main Results:
- A 65 kDa broad-spectrum enterocin 12a was purified, exhibiting potent activity against multidrug-resistant Gram-negative bacteria (*Salmonella*, *Shigella*, *Vibrio*, *E. coli*) and *Listeria monocytogenes*.
- Enterocin 12a demonstrated selective dose-dependent inhibition of human cancer cell line proliferation without affecting normal peripheral blood mononuclear cells.
- Mass spectrometry revealed partial homology of enterocin 12a with a redox protein from *E. faecalis*.
Conclusions:
- Enterocin 12a is a novel bacteriocin with significant anticancer properties against human cell lines and minimal toxicity to non-malignant cells.
- Further investigation of enterocin 12a's anticancer potential in preclinical animal models is warranted.
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