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 

TITLE=Transcriptional Analysis of Acinetobacter sp. neg1 Capable of Degrading Ochratoxin A

JOURNAL=Frontiers in Microbiology

VOLUME=7

YEAR=2017

URL=https://www.frontiersin.org/journals/microbiology/articles/10.3389/fmicb.2016.02162

DOI=10.3389/fmicb.2016.02162

ISSN=1664-302X

ABSTRACT=<p>Ochratoxin A (OTA) is a nephrotoxic and potentially carcinogenic mycotoxin produced by several species of <italic>Aspergillus</italic> and <italic>Penicillium</italic>, contaminating grapes, wine and a variety of food products. We recently isolated from OTA contaminated soil vineyard a novel free-living strain of <italic>Acinetobacter</italic> sp. <italic>neg1</italic>, 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 <italic>in vitro</italic> 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 <italic>Acinetobacter</italic> sp. <italic>neg1</italic> strain and that OTA degrading reaction triggers the modulation of further catabolic activities.</p>