Palmira De Bellis

Dr. Palmira De Bellis

Institute of Sciences of Food Production (ISPA), National Research Council (CNR), Via G. Amendola, 122/O 70126 Bari, Italy
orcid

Research Focus & Metrics

Academic Career Length

26Years (2001-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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1 May 2010 in International Journal of Food Microbiology
Verified
Journal Article
Closed access
PBPalmira De Bellis
Palmira De Bellis
Francesca ValerioFrancesca Valerio
Francesca Valerio
ASAngelo Sisto
Angelo Sisto
SLStella Lisa Lonigro
Stella Lisa Lonigro
PLPaola Lavermicocca
Paola Lavermicocca

1 September 2009 in Systematic and Applied Microbiology
Verified
Journal Article
Closed access
Francesca ValerioFrancesca Valerio
Francesca Valerio
MFMara Favilla
Mara Favilla
PBPalmira De Bellis
Palmira De Bellis
ASAngelo Sisto
Angelo Sisto
SCSilvia de Candia
Silvia de Candia
PLPaola Lavermicocca
Paola Lavermicocca

1 June 2012 in International Journal of Food Microbiology
Verified
Journal Article
Closed access
Francesca ValerioFrancesca Valerio
Francesca Valerio
PBPalmira De Bellis
Palmira De Bellis
MBM. Di Biase
M. Di Biase
SLS.L. Lonigro
S.L. Lonigro
Barbara GiussaniBarbara Giussani
Barbara Giussani
ASAngelo Sisto
Angelo Sisto

1 April 2006 in Applied and Environmental Microbiology
Verified
Journal Article
Closed access
Francesca ValerioFrancesca Valerio
Francesca Valerio
PBPalmira De Bellis
Palmira De Bellis
SLStella Lisa Lonigro
Stella Lisa Lonigro
Lorenzo MorelliLorenzo Morelli
Lorenzo Morelli
AVAngelo Visconti
Angelo Visconti
PLPaola Lavermicocca
Paola Lavermicocca
The ability of potentially probiotic strains of Lactobacillus plantarum and Lactobacillus paracasei to survive on artichokes for at least 90 days was shown. The anchorage of bacterial strains to artichokes improved their survival in simulated gastrointestinal digestion. L. paracasei IMPC2.1 was further used in an artichoke human feeding study involving four volunteers, and it was shown that the organism could be recovered from stools.

1 March 2008 in International Journal of Food Microbiology
Verified
Journal Article
Closed access
Francesca ValerioFrancesca Valerio
Francesca Valerio
PBPalmira De Bellis
Palmira De Bellis
SLStella L. Lonigro
Stella L. Lonigro
AVAngelo Visconti
Angelo Visconti
PLPaola Lavermicocca
Paola Lavermicocca

27 November 2015 in Toxins
Verified
Journal Article
Open access
PDF file
PBPalmira De Bellis
Palmira De Bellis
MTMariana Tristezza
Mariana Tristezza
EHEdith Miriam Haidukowski
Edith Miriam Haidukowski
Francesca FanelliFrancesca Fanelli
Francesca Fanelli
ASAngelo Sisto
Angelo Sisto
Francesco GriecoFrancesco Grieco
Francesco Grieco
Ochratoxin A (OTA) is a mycotoxin with a main nephrotoxic activity contaminating several foodstuffs. In the present report, five soil samples collected from OTA-contaminated vineyards were screened to isolate microorganisms able to biodegrade OTA. When cultivated in OTA-supplemented medium, OTA was converted in OTα by 225 bacterial isolates. To reveal clonal relationships between isolates, molecular typing by using an automated rep-PCR system was carried out, thus showing the presence of 27 different strains (rep-PCR profiles). The 16S-rRNA gene sequence analysis of an isolate representative of each rep-PCR profiles indicated that they belonged to five bacterial genera, namely Pseudomonas, Leclercia, Pantoea, Enterobacter, and Acinetobacter. However, further evaluation of OTA-degrading activity by the 27 strains revealed that only Acinetobacter calcoaceticus strain 396.1 and Acinetobacter sp. strain neg1, consistently conserved the above property; their further characterization showed that they were able to convert 82% and 91% OTA into OTα in six days at 24 °C, respectively. The presence of OTα, as the unique OTA-degradation product was confirmed by LC-HRMS. This is the first report on OTA biodegradation by bacterial strains isolated from agricultural soils and carried out under aerobic conditions and moderate temperatures. These microorganisms might be used to detoxify OTA-contaminated feed and could be a new source of gene(s) for the development of a novel enzymatic detoxification system.