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...
Autores principales: | , , , , , , , , , |
---|---|
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 |