http://www.cnr.it/ontology/cnr/individuo/prodotto/ID274523
A multiplex, bead-based array for profiling plant-derived components in complex food matrixes (Articolo in rivista)
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- Label
- A multiplex, bead-based array for profiling plant-derived components in complex food matrixes (Articolo in rivista) (literal)
- Anno
- 2013-01-01T00:00:00+01:00 (literal)
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#doi
- 10.1007/s00216-013-7434-8 (literal)
- Alternative label
Elena Ponzoni, Diego Breviario, *Alessandro Mautino, Silvia Gianì, Laura Morello (2013)
A multiplex, bead-based array for profiling plant-derived components in complex food matrixes
in Analytical & bioanalytical chemistry (Print); Springer, Heidelberg (Germania)
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- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#autori
- Elena Ponzoni, Diego Breviario, *Alessandro Mautino, Silvia Gianì, Laura Morello (literal)
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- Istituto Biologia e Biotecnologia Agraria-Consiglio Nazionale delle Ricerche, Via Bassini 15, 20133 Milano, Italy
*Bioclarma, Via Nizza 52, 10126 Torino, Italy (literal)
- Titolo
- A multiplex, bead-based array for profiling plant-derived components in complex food matrixes (literal)
- Abstract
- Authentication of processed food ingredients is
becoming an important issue for customers, and some DNAbased
analytical methods have been developed, especially for
animal products. As food products typically contain several
different ingredients, a current challenge is to increase the
multiplexing capacity of DNA-based methods, to develop
\"all-in-one\" assays. Oligonucleotide-coupled, bead-based
suspension arrays are sensitive and reproducible multiplex
analytical tools. We applied the Multi-Analyte Profile
(xMAP(TM)) technology to develop an assay able to
concurrently detect five different plant components in mixed
flours and in processed feed and food. Capture probes were
targeted to species-specific DNA polymorphisms present
within the first intron of plant ?-tubulin genes, which can be
amplified by the tubulin-based polymorphism-amplification
method (TBP-PCR). The workflow is very simple and
straightforward, consisting of a PCR amplification step with
universal primers, followed by the direct hybridization assay.
Results are highly reproducible. For each single plant species,
the absolute detection limit was as low as one target DNA
copy. In complex mixtures of flours derived from seeds or
from commercial dry \"pasta,\" relative limits of detection
ranged, in weight, from 2 % for soybean to less than 0.5 %
for wheat. The specificity of the capture probes and the high
sensitivity of the method allowed the successful determination
of the analytical composition of three feeds as well as eleven
food samples, such as snacks, biscuits, and pasta. The
multiplexing ability of the assay (up to 100 different analytes)
provides scalability and flexibility, in response to specific
needs. (literal)
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