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Identification and Antimicrobial Activity of Medium-Sized and Short Peptides from Yellowfin Tuna (Thunnus albacares) Simulated Gastrointestinal Digestion

Due to the rapidly increasing resistance to conventional antibiotics, antimicrobial peptides are emerging as promising novel drug candidates. In this study, peptide fragments were obtained from yellowfin tuna muscle by simulated gastrointestinal digestion, and their antimicrobial activity towards Gr...

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Autores principales: Cerrato, Andrea, Capriotti, Anna Laura, Capuano, Federico, Cavaliere, Chiara, Montone, Angela Michela Immacolata, Montone, Carmela Maria, Piovesana, Susy, Zenezini Chiozzi, Riccardo, Laganà, Aldo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7555217/
https://www.ncbi.nlm.nih.gov/pubmed/32867059
http://dx.doi.org/10.3390/foods9091185
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author Cerrato, Andrea
Capriotti, Anna Laura
Capuano, Federico
Cavaliere, Chiara
Montone, Angela Michela Immacolata
Montone, Carmela Maria
Piovesana, Susy
Zenezini Chiozzi, Riccardo
Laganà, Aldo
author_facet Cerrato, Andrea
Capriotti, Anna Laura
Capuano, Federico
Cavaliere, Chiara
Montone, Angela Michela Immacolata
Montone, Carmela Maria
Piovesana, Susy
Zenezini Chiozzi, Riccardo
Laganà, Aldo
author_sort Cerrato, Andrea
collection PubMed
description Due to the rapidly increasing resistance to conventional antibiotics, antimicrobial peptides are emerging as promising novel drug candidates. In this study, peptide fragments were obtained from yellowfin tuna muscle by simulated gastrointestinal digestion, and their antimicrobial activity towards Gram-positive and Gram-negative bacteria was investigated. In particular, the antimicrobial activity of both medium- and short-sized peptides was investigated by using two dedicated approaches. Medium-sized peptides were purified by solid phase extraction on C18, while short peptides were purified thanks to a graphitized carbon black sorbent. For medium-sized peptide characterization, a peptidomic strategy based on shotgun proteomics analysis was employed, and identification was achieved by matching protein sequence database by homology, as yellowfin tuna is a non-model organism, leading to the identification of 403 peptides. As for short peptide sequences, an untargeted suspect screening approach was carried out by means of an inclusion list presenting the exact mass to charge ratios (m/z) values for all di-, tri- and tetrapeptides. In total, 572 short sequences were identified thanks to a customized workflow dedicated to short peptide analysis implemented on Compound Discoverer software.
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spelling pubmed-75552172020-10-19 Identification and Antimicrobial Activity of Medium-Sized and Short Peptides from Yellowfin Tuna (Thunnus albacares) Simulated Gastrointestinal Digestion Cerrato, Andrea Capriotti, Anna Laura Capuano, Federico Cavaliere, Chiara Montone, Angela Michela Immacolata Montone, Carmela Maria Piovesana, Susy Zenezini Chiozzi, Riccardo Laganà, Aldo Foods Article Due to the rapidly increasing resistance to conventional antibiotics, antimicrobial peptides are emerging as promising novel drug candidates. In this study, peptide fragments were obtained from yellowfin tuna muscle by simulated gastrointestinal digestion, and their antimicrobial activity towards Gram-positive and Gram-negative bacteria was investigated. In particular, the antimicrobial activity of both medium- and short-sized peptides was investigated by using two dedicated approaches. Medium-sized peptides were purified by solid phase extraction on C18, while short peptides were purified thanks to a graphitized carbon black sorbent. For medium-sized peptide characterization, a peptidomic strategy based on shotgun proteomics analysis was employed, and identification was achieved by matching protein sequence database by homology, as yellowfin tuna is a non-model organism, leading to the identification of 403 peptides. As for short peptide sequences, an untargeted suspect screening approach was carried out by means of an inclusion list presenting the exact mass to charge ratios (m/z) values for all di-, tri- and tetrapeptides. In total, 572 short sequences were identified thanks to a customized workflow dedicated to short peptide analysis implemented on Compound Discoverer software. MDPI 2020-08-27 /pmc/articles/PMC7555217/ /pubmed/32867059 http://dx.doi.org/10.3390/foods9091185 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Cerrato, Andrea
Capriotti, Anna Laura
Capuano, Federico
Cavaliere, Chiara
Montone, Angela Michela Immacolata
Montone, Carmela Maria
Piovesana, Susy
Zenezini Chiozzi, Riccardo
Laganà, Aldo
Identification and Antimicrobial Activity of Medium-Sized and Short Peptides from Yellowfin Tuna (Thunnus albacares) Simulated Gastrointestinal Digestion
title Identification and Antimicrobial Activity of Medium-Sized and Short Peptides from Yellowfin Tuna (Thunnus albacares) Simulated Gastrointestinal Digestion
title_full Identification and Antimicrobial Activity of Medium-Sized and Short Peptides from Yellowfin Tuna (Thunnus albacares) Simulated Gastrointestinal Digestion
title_fullStr Identification and Antimicrobial Activity of Medium-Sized and Short Peptides from Yellowfin Tuna (Thunnus albacares) Simulated Gastrointestinal Digestion
title_full_unstemmed Identification and Antimicrobial Activity of Medium-Sized and Short Peptides from Yellowfin Tuna (Thunnus albacares) Simulated Gastrointestinal Digestion
title_short Identification and Antimicrobial Activity of Medium-Sized and Short Peptides from Yellowfin Tuna (Thunnus albacares) Simulated Gastrointestinal Digestion
title_sort identification and antimicrobial activity of medium-sized and short peptides from yellowfin tuna (thunnus albacares) simulated gastrointestinal digestion
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7555217/
https://www.ncbi.nlm.nih.gov/pubmed/32867059
http://dx.doi.org/10.3390/foods9091185
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