Cargando…
Transcriptional Analysis of Acinetobacter sp. neg1 Capable of Degrading Ochratoxin A
Ochratoxin A (OTA) is a nephrotoxic and potentially carcinogenic mycotoxin produced by several species of Aspergillus and Penicillium, contaminating grapes, wine and a variety of food products. We recently isolated from OTA contaminated soil vineyard a novel free-living strain of Acinetobacter sp. n...
Autores principales: | , , , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2017
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5220012/ https://www.ncbi.nlm.nih.gov/pubmed/28119679 http://dx.doi.org/10.3389/fmicb.2016.02162 |
_version_ | 1782492551357399040 |
---|---|
author | Liuzzi, Vania C. Fanelli, Francesca Tristezza, Mariana Haidukowski, Miriam Picardi, Ernesto Manzari, Caterina Lionetti, Claudia Grieco, Francesco Logrieco, Antonio F. Thon, Michael R. Pesole, Graziano Mulè, Giuseppina |
author_facet | Liuzzi, Vania C. Fanelli, Francesca Tristezza, Mariana Haidukowski, Miriam Picardi, Ernesto Manzari, Caterina Lionetti, Claudia Grieco, Francesco Logrieco, Antonio F. Thon, Michael R. Pesole, Graziano Mulè, Giuseppina |
author_sort | Liuzzi, Vania C. |
collection | PubMed |
description | Ochratoxin A (OTA) is a nephrotoxic and potentially carcinogenic mycotoxin produced by several species of Aspergillus and Penicillium, contaminating grapes, wine and a variety of food products. We recently isolated from OTA contaminated soil vineyard a novel free-living strain of Acinetobacter sp. neg1, ITEM 17016, able to degrade OTA into the non-toxic catabolic product ochratoxin α. Biochemical studies suggested that the degradation reaction proceeds via peptide bond hydrolysis with phenylalanine (Phe) release. In order to identify genes responsible for OTA degradation we performed a differential gene expression analysis of ITEM 17016 grown in the presence or absence of the toxin. Among the differentially expressed genes, six peptidases up-regulated at 6 h were identified. The degrading activity of the carboxypeptidase PJ_1540 was confirmed in vitro in a heterologous system. The enrichment analysis for Gene Ontology terms confirmed that OTA degradation proceeds through peptidase activities and revealed the over-representation of pathways related to Phe catabolism. These results indicate that Phe may represent an energy source for this Acinetobacter sp. neg1 strain and that OTA degrading reaction triggers the modulation of further catabolic activities. |
format | Online Article Text |
id | pubmed-5220012 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-52200122017-01-24 Transcriptional Analysis of Acinetobacter sp. neg1 Capable of Degrading Ochratoxin A Liuzzi, Vania C. Fanelli, Francesca Tristezza, Mariana Haidukowski, Miriam Picardi, Ernesto Manzari, Caterina Lionetti, Claudia Grieco, Francesco Logrieco, Antonio F. Thon, Michael R. Pesole, Graziano Mulè, Giuseppina Front Microbiol Microbiology Ochratoxin A (OTA) is a nephrotoxic and potentially carcinogenic mycotoxin produced by several species of Aspergillus and Penicillium, contaminating grapes, wine and a variety of food products. We recently isolated from OTA contaminated soil vineyard a novel free-living strain of Acinetobacter sp. neg1, ITEM 17016, able to degrade OTA into the non-toxic catabolic product ochratoxin α. Biochemical studies suggested that the degradation reaction proceeds via peptide bond hydrolysis with phenylalanine (Phe) release. In order to identify genes responsible for OTA degradation we performed a differential gene expression analysis of ITEM 17016 grown in the presence or absence of the toxin. Among the differentially expressed genes, six peptidases up-regulated at 6 h were identified. The degrading activity of the carboxypeptidase PJ_1540 was confirmed in vitro in a heterologous system. The enrichment analysis for Gene Ontology terms confirmed that OTA degradation proceeds through peptidase activities and revealed the over-representation of pathways related to Phe catabolism. These results indicate that Phe may represent an energy source for this Acinetobacter sp. neg1 strain and that OTA degrading reaction triggers the modulation of further catabolic activities. Frontiers Media S.A. 2017-01-09 /pmc/articles/PMC5220012/ /pubmed/28119679 http://dx.doi.org/10.3389/fmicb.2016.02162 Text en Copyright © 2017 Liuzzi, Fanelli, Tristezza, Haidukowski, Picardi, Manzari, Lionetti, Grieco, Logrieco, Thon, Pesole and Mulè. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Microbiology Liuzzi, Vania C. Fanelli, Francesca Tristezza, Mariana Haidukowski, Miriam Picardi, Ernesto Manzari, Caterina Lionetti, Claudia Grieco, Francesco Logrieco, Antonio F. Thon, Michael R. Pesole, Graziano Mulè, Giuseppina Transcriptional Analysis of Acinetobacter sp. neg1 Capable of Degrading Ochratoxin A |
title | Transcriptional Analysis of Acinetobacter sp. neg1 Capable of Degrading Ochratoxin A |
title_full | Transcriptional Analysis of Acinetobacter sp. neg1 Capable of Degrading Ochratoxin A |
title_fullStr | Transcriptional Analysis of Acinetobacter sp. neg1 Capable of Degrading Ochratoxin A |
title_full_unstemmed | Transcriptional Analysis of Acinetobacter sp. neg1 Capable of Degrading Ochratoxin A |
title_short | Transcriptional Analysis of Acinetobacter sp. neg1 Capable of Degrading Ochratoxin A |
title_sort | transcriptional analysis of acinetobacter sp. neg1 capable of degrading ochratoxin a |
topic | Microbiology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5220012/ https://www.ncbi.nlm.nih.gov/pubmed/28119679 http://dx.doi.org/10.3389/fmicb.2016.02162 |
work_keys_str_mv | AT liuzzivaniac transcriptionalanalysisofacinetobacterspneg1capableofdegradingochratoxina AT fanellifrancesca transcriptionalanalysisofacinetobacterspneg1capableofdegradingochratoxina AT tristezzamariana transcriptionalanalysisofacinetobacterspneg1capableofdegradingochratoxina AT haidukowskimiriam transcriptionalanalysisofacinetobacterspneg1capableofdegradingochratoxina AT picardiernesto transcriptionalanalysisofacinetobacterspneg1capableofdegradingochratoxina AT manzaricaterina transcriptionalanalysisofacinetobacterspneg1capableofdegradingochratoxina AT lionetticlaudia transcriptionalanalysisofacinetobacterspneg1capableofdegradingochratoxina AT griecofrancesco transcriptionalanalysisofacinetobacterspneg1capableofdegradingochratoxina AT logriecoantoniof transcriptionalanalysisofacinetobacterspneg1capableofdegradingochratoxina AT thonmichaelr transcriptionalanalysisofacinetobacterspneg1capableofdegradingochratoxina AT pesolegraziano transcriptionalanalysisofacinetobacterspneg1capableofdegradingochratoxina AT mulegiuseppina transcriptionalanalysisofacinetobacterspneg1capableofdegradingochratoxina |