4.7 Article

Efficacy of nisin derivatives with improved biochemical characteristics, alone and in combination with endolysin PlyP100 to control Listeria monocytogenes in laboratory-scale Queso Fresco

Journal

FOOD MICROBIOLOGY
Volume 94, Issue -, Pages -

Publisher

ACADEMIC PRESS LTD- ELSEVIER SCIENCE LTD
DOI: 10.1016/j.fm.2020.103668

Keywords

Listeria monocytogenes; Queso fresco; Nisin derivatives; Endolysin; PlyP100

Funding

  1. USDA Cooperative State Research, Education and Extension Service (Washington, DC) Hatch project [ILLU-698-339]
  2. Universidad Autonoma de Queretaro-University of Illinois Small Research Grants Program
  3. CONACyT (National Council of Science and Technology, Mexico) PhD scholarship
  4. Office of Naval Research [N000141612525]
  5. National Science Foundation [1553649]
  6. U.S. Department of Defense (DOD) [N000141612525] Funding Source: U.S. Department of Defense (DOD)

Ask authors/readers for more resources

This study utilized synthetic biology strategies to create a series of nisin A derivatives by substituting residues with positively charged amino acids, aiming to enhance control of L. monocytogenes in QF. The results showed that while nisin derivatives exhibited reduced antilisterial activity compared to nisin A, they were more stable under QF-like conditions, suggesting the potential for stabilized and enhanced control of L. monocytogenes in QF.
Nisin is an antimicrobial peptide that is commonly used as a food preservative and capable of inhibiting the pathogen Listeria monocytogenes. However, nisin is ineffective in controlling L. monocytogenes in Queso Fresco (QF). To address the challenge, in this work, we used synthetic biology strategies to create a series of nisin A derivatives by substituting residues 27, 30, 31 and 32 with positively charged amino acids (H, K and R). Our results showed that nisin derivatives exhibited reduced antilisterial activity in vitro compared to nisin A; however, they were all more stable under QF-like experimental conditions (pH 7 + 22% milk fat), notably H27/31K. Compared to nisin A, the derivatives H31K and V32K exhibited slight antilisterial improvement in QF and H27/ 31K was able to reduce the initial population of L. monocytogenes by up to 1.5 Log CFU/g. L. monocytogenes isolates exhibited similar susceptibility to nisin A or H27/31K after 7 or 14 days of nisin exposure in QF. Notably, when combined with endolysin PlyP100, the application of H27/31K resulted in non-enumerable levels of L. monocytogenes after 14 days of cold storage. Our results highlight the potential of bioengineered nisin derivatives for stabilized and enhanced control of L. monocytogenes in QF.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.7
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available