Cargando…

Aflatoxin B(1) Degradation by a Pseudomonas Strain

Aflatoxin B(1) (AFB(1)), one of the most potent naturally occurring mutagens and carcinogens, causes significant threats to the food industry and animal production. In this study, 25 bacteria isolates were collected from grain kernels and soils displaying AFB(1) reduction activity. Based on its degr...

Descripción completa

Detalles Bibliográficos
Autores principales: Sangare, Lancine, Zhao, Yueju, Folly, Yawa Minnie Elodie, Chang, Jinghua, Li, Jinhan, Selvaraj, Jonathan Nimal, Xing, Fuguo, Zhou, Lu, Wang, Yan, Liu, Yang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4210884/
https://www.ncbi.nlm.nih.gov/pubmed/25341538
http://dx.doi.org/10.3390/toxins6103028
_version_ 1782341464868519936
author Sangare, Lancine
Zhao, Yueju
Folly, Yawa Minnie Elodie
Chang, Jinghua
Li, Jinhan
Selvaraj, Jonathan Nimal
Xing, Fuguo
Zhou, Lu
Wang, Yan
Liu, Yang
author_facet Sangare, Lancine
Zhao, Yueju
Folly, Yawa Minnie Elodie
Chang, Jinghua
Li, Jinhan
Selvaraj, Jonathan Nimal
Xing, Fuguo
Zhou, Lu
Wang, Yan
Liu, Yang
author_sort Sangare, Lancine
collection PubMed
description Aflatoxin B(1) (AFB(1)), one of the most potent naturally occurring mutagens and carcinogens, causes significant threats to the food industry and animal production. In this study, 25 bacteria isolates were collected from grain kernels and soils displaying AFB(1) reduction activity. Based on its degradation effectiveness, isolate N17-1 was selected for further characterization and identified as Pseudomonas aeruginosa. P. aeruginosa N17-1 could degrade AFB(1), AFB(2) and AFM(1) by 82.8%, 46.8% and 31.9% after incubation in Nutrient Broth (NB) medium at 37 °C for 72 h, respectively. The culture supernatant of isolate N17-1 degraded AFB(1) effectively, whereas the viable cells and intra cell extracts were far less effective. Factors influencing AFB(1) degradation by the culture supernatant were investigated. Maximum degradation was observed at 55 °C. Ions Mn(2+) and Cu(2+) were activators for AFB(1) degradation, however, ions Mg(2+), Li(+), Zn(2+), Se(2+), Fe(3+) were strong inhibitors. Treatments with proteinase K and proteinase K plus SDS significantly reduced the degradation activity of the culture supernatant. No degradation products were observed based on preliminary LC-QTOF/MS analysis, indicating AFB(1) was metabolized to degradation products with chemical properties different from that of AFB(1). The results indicated that the degradation of AFB(1) by P. aeruginosa N17-1 was enzymatic and could have a great potential in industrial applications. This is the first report indicating that the isolate of P. aeruginosa possesses the ability to degrade aflatoxin.
format Online
Article
Text
id pubmed-4210884
institution National Center for Biotechnology Information
language English
publishDate 2014
publisher MDPI
record_format MEDLINE/PubMed
spelling pubmed-42108842014-10-28 Aflatoxin B(1) Degradation by a Pseudomonas Strain Sangare, Lancine Zhao, Yueju Folly, Yawa Minnie Elodie Chang, Jinghua Li, Jinhan Selvaraj, Jonathan Nimal Xing, Fuguo Zhou, Lu Wang, Yan Liu, Yang Toxins (Basel) Article Aflatoxin B(1) (AFB(1)), one of the most potent naturally occurring mutagens and carcinogens, causes significant threats to the food industry and animal production. In this study, 25 bacteria isolates were collected from grain kernels and soils displaying AFB(1) reduction activity. Based on its degradation effectiveness, isolate N17-1 was selected for further characterization and identified as Pseudomonas aeruginosa. P. aeruginosa N17-1 could degrade AFB(1), AFB(2) and AFM(1) by 82.8%, 46.8% and 31.9% after incubation in Nutrient Broth (NB) medium at 37 °C for 72 h, respectively. The culture supernatant of isolate N17-1 degraded AFB(1) effectively, whereas the viable cells and intra cell extracts were far less effective. Factors influencing AFB(1) degradation by the culture supernatant were investigated. Maximum degradation was observed at 55 °C. Ions Mn(2+) and Cu(2+) were activators for AFB(1) degradation, however, ions Mg(2+), Li(+), Zn(2+), Se(2+), Fe(3+) were strong inhibitors. Treatments with proteinase K and proteinase K plus SDS significantly reduced the degradation activity of the culture supernatant. No degradation products were observed based on preliminary LC-QTOF/MS analysis, indicating AFB(1) was metabolized to degradation products with chemical properties different from that of AFB(1). The results indicated that the degradation of AFB(1) by P. aeruginosa N17-1 was enzymatic and could have a great potential in industrial applications. This is the first report indicating that the isolate of P. aeruginosa possesses the ability to degrade aflatoxin. MDPI 2014-10-23 /pmc/articles/PMC4210884/ /pubmed/25341538 http://dx.doi.org/10.3390/toxins6103028 Text en © 2014 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 license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Sangare, Lancine
Zhao, Yueju
Folly, Yawa Minnie Elodie
Chang, Jinghua
Li, Jinhan
Selvaraj, Jonathan Nimal
Xing, Fuguo
Zhou, Lu
Wang, Yan
Liu, Yang
Aflatoxin B(1) Degradation by a Pseudomonas Strain
title Aflatoxin B(1) Degradation by a Pseudomonas Strain
title_full Aflatoxin B(1) Degradation by a Pseudomonas Strain
title_fullStr Aflatoxin B(1) Degradation by a Pseudomonas Strain
title_full_unstemmed Aflatoxin B(1) Degradation by a Pseudomonas Strain
title_short Aflatoxin B(1) Degradation by a Pseudomonas Strain
title_sort aflatoxin b(1) degradation by a pseudomonas strain
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4210884/
https://www.ncbi.nlm.nih.gov/pubmed/25341538
http://dx.doi.org/10.3390/toxins6103028
work_keys_str_mv AT sangarelancine aflatoxinb1degradationbyapseudomonasstrain
AT zhaoyueju aflatoxinb1degradationbyapseudomonasstrain
AT follyyawaminnieelodie aflatoxinb1degradationbyapseudomonasstrain
AT changjinghua aflatoxinb1degradationbyapseudomonasstrain
AT lijinhan aflatoxinb1degradationbyapseudomonasstrain
AT selvarajjonathannimal aflatoxinb1degradationbyapseudomonasstrain
AT xingfuguo aflatoxinb1degradationbyapseudomonasstrain
AT zhoulu aflatoxinb1degradationbyapseudomonasstrain
AT wangyan aflatoxinb1degradationbyapseudomonasstrain
AT liuyang aflatoxinb1degradationbyapseudomonasstrain