Simulated gastrointestinal digestion of nisin and interaction between nisin and bile

Loading...
Thumbnail Image
Files
3698.pdf(1.42 MB)
Accepted Version
Date
2017-08-14
Authors
Gough, Ronan
O'Connor, Paula M.
Rea, Mary C.
Gómez-Sala, Beatriz
Miao, Song
Hill, Colin
Brodkorb, André
Journal Title
Journal ISSN
Volume Title
Publisher
Elsevier Ltd.
Research Projects
Organizational Units
Journal Issue
Abstract
Nisin, an antimicrobial peptide showing activity against many Gram positive bacteria, is widely used as a food preservative. The simulated gastrointestinal digestion of nisin (variant A) was studied using the in vitro INFOGEST digestion method. Following oral, gastric and small intestinal digestion, there was no intact nisin in the system and the nisin was primarily digested by pancreatin. After digestion, six nisin fragments (1–11, 1–12, 1–20, 1–21, 1–29 and 1–32) were identified by reversed phase high performance liquid chromatography and mass spectroscopy and four of these nisin fragments (1–20, 1–21, 1–29 and 1–32) demonstrated low antibacterial activity against Lactococcus lactis HP in agar diffusion activity assays. Additionally, it was observed that bile salts form a complex with nisin. This was examined by atomic force microscopy, turbidity and dynamic light scattering, which showed that this interaction resulted in significantly larger bile salt micelles. The presence of bile salts at physiological levels significantly altered the relative amounts of the nisin fragments 1–12, 1–20 and 1–29 produced during an in vitro digestion. This study highlights the importance of including bile in simulated digestions of antimicrobial peptides in order to obtain a more accurate simulation of the in vivo digestion products and their activity.
Description
Keywords
Nisin , Digestion , Bile , Antimicrobial peptide , Surfactant
Citation
Gough, R., O'Connor, P. M., Rea, M. C., Gómez-Sala , B., Miao, S., Hill, C. and Brodkorb, A (2017) 'Simulated gastrointestinal digestion of nisin and interaction between nisin and bile', LWT - Food Science and Technology, 86, pp. 530-537. doi:10.1016/j.lwt.2017.08.031
Link to publisher’s version