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Nisin is a bacteriocin that is globally employed as a biopreservative in food systems to control gram-positive, and some gram-negative, bacteria. Here we tested the bioactivity of nisin A-producing Lactococcus lactis NZ9700 and producers of bioengineered variants thereof against representatives of the gram-negative genus Thermus, which has been associated with the pink discoloration defect in cheese. Starting with a total of 73 nisin variant-producing Lactococcus lactis, bioactivity against Thermus was assessed via agar diffusion assays, and 22 variants were found to have bioactivity greater than or equal to that of the nisin A-producing control. To determine to what extent this enhanced bioactivity was attributable to an increase in specific activity, minimum inhibitory concentrations were determined using the corresponding purified form of these 22 nisin A derivatives. From these experiments, nisin M17Q and M21F were identified as peptides with enhanced antimicrobial activity against the majority of Thermus target strains tested. In addition, several other peptide variants were found to exhibit enhanced specific activity against a subset of strains.
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http://dx.doi.org/10.3168/jds.2020-19350 | DOI Listing |
Front Microbiol
August 2025
School of Bioengineering, Qilu University of Technology, Shandong Academy of Science, Jinan, China.
The nisin-controlled gene expression (NICE) system is an efficient and promising gene expression system for . To enhance the expression efficiency of the NICE system in ATCC19258, an inducible expression vector, pNZ8148-PnisA-gfp-PnisR-nisR-nisK, containing the regulatory element NisR/K and the promoter PnisR, was first constructed using the basic plasmid pNZ8148. Green fluorescent protein (GFP), as the reporter protein, was cloned downstream of PnisA in the vector pNZ8148 to detect protein expression.
View Article and Find Full Text PDFOrg Lett
September 2025
State Key Laboratory of Natural Product Chemistry, College of Chemistry and Chemical Engineering, Lanzhou University, Lanzhou 730000, P. R. China.
A photoredox approach is described for converting dehydroalanine (Dha) residues in peptides to aspartic acid (Asp). Using ammonium formate as a CO radical source under mild conditions, Dha is functionalized in a traceless manner.The protocol is compatible with peptide substrates, including fully unprotected, the complex antimicrobial peptide nisin.
View Article and Find Full Text PDFInt J Mol Sci
July 2025
NICM Health Research Institute, Western Sydney University, Penrith, NSW 2751, Australia.
Lymphoma continues to pose a serious challenge to global health, underscoring the urgent need for new therapeutic strategies. Recently, the gut microbiome has been shown to play a potential role in regulating immune responses and influencing cancer progression. However, its molecular mechanisms of action in lymphoma remain poorly understood.
View Article and Find Full Text PDFFront Bioeng Biotechnol
July 2025
Bioprocessing Technology Institute (BTI), Agency for Science, Technology and Research (A*STAR), Singapore, Singapore.
Introduction: Cultivated meat, produced by in vitro cell culture in bioreactors, offers a sustainable alternative to traditional meat sources. A significant challenge in its production is the high cost of mitogenic growth factors, which are essential supplements in serum-free media for cultivating meat cells. One strategy to reduce cost involves minimizing purification cost by using a food-grade host to secrete growth factors.
View Article and Find Full Text PDFInt J Mol Sci
July 2025
NICM Health Research Institute, Western Sydney University, Penrith, NSW 2751, Australia.
Lymphoma continues to pose a significant global health burden, highlighting the urgent need for novel therapeutic strategies. Recent advances in microbiome research have identified gut-microbiota-derived metabolites, or postbiotics, as promising candidates in cancer therapy. This study investigates the antiproliferative and mechanistic effects of two postbiotics, Nisin (N) and Urolithin B (UB), individually and in combination, against the human lymphoma cell line HKB-11.
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