Next Article in Journal
Dynamics of the Toxin Cylindrospermopsin and the Cyanobacterium Chrysosporum (Aphanizomenon) ovalisporum in a Mediterranean Eutrophic Reservoir
Next Article in Special Issue
Screening a Strain of Aspergillus niger and Optimization of Fermentation Conditions for Degradation of Aflatoxin B1
Previous Article in Journal
Bt Toxin Modification for Enhanced Efficacy
Previous Article in Special Issue
Efficacy of Active Carbon towards the Absorption of Deoxynivalenol in Pigs
Article Menu

Export Article

Correction published on 2 September 2015, see Toxins 2015, 7(9), 3538-3539.

Open AccessArticle
Toxins 2014, 6(10), 3028-3040; doi:10.3390/toxins6103028

Aflatoxin B1 Degradation by a Pseudomonas Strain

1
Institute of Agro-products Processing Science and Technology, Chinese Academy of Agricultural Sciences, Beijing 100193, China
2
Key Laboratory of Agro-products Processing, Ministry of Agriculture, Beijing 100193, China
These authors contributed equally to this work.
*
Author to whom correspondence should be addressed.
Received: 23 September 2014 / Revised: 28 September 2014 / Accepted: 8 October 2014 / Published: 23 October 2014
(This article belongs to the Special Issue Detoxification of Mycotoxins)
View Full-Text   |   Download PDF [758 KB, uploaded 23 October 2014]   |  

Abstract

Aflatoxin B1 (AFB1), 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 AFB1 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 AFB1, AFB2 and AFM1 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 AFB1 effectively, whereas the viable cells and intra cell extracts were far less effective. Factors influencing AFB1 degradation by the culture supernatant were investigated. Maximum degradation was observed at 55 °C. Ions Mn2+ and Cu2+ were activators for AFB1 degradation, however, ions Mg2+, Li+, Zn2+, Se2+, Fe3+ 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 AFB1 was metabolized to degradation products with chemical properties different from that of AFB1. The results indicated that the degradation of AFB1 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. View Full-Text
Keywords: aflatoxin; degradation; culture supernatant; Pseudomonas aeruginosa N17-1 aflatoxin; degradation; culture supernatant; Pseudomonas aeruginosa N17-1
This is an open access article distributed under the Creative Commons Attribution License which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. (CC BY 4.0).

Supplementary material

Scifeed alert for new publications

Never miss any articles matching your research from any publisher
  • Get alerts for new papers matching your research
  • Find out the new papers from selected authors
  • Updated daily for 49'000+ journals and 6000+ publishers
  • Define your Scifeed now

SciFeed Share & Cite This Article

MDPI and ACS Style

Sangare, L.; Zhao, Y.; Folly, Y.M.E.; Chang, J.; Li, J.; Selvaraj, J.N.; Xing, F.; Zhou, L.; Wang, Y.; Liu, Y. Aflatoxin B1 Degradation by a Pseudomonas Strain. Toxins 2014, 6, 3028-3040.

Show more citation formats Show less citations formats

Related Articles

Article Metrics

Article Access Statistics

1

Comments

[Return to top]
Toxins EISSN 2072-6651 Published by MDPI AG, Basel, Switzerland RSS E-Mail Table of Contents Alert
Back to Top