http://www.cnr.it/ontology/cnr/individuo/prodotto/ID283639
Mass Spectrometry-based proteomic approach in Oenococcus oeni (O. oeni) enological starter (Articolo in rivista)
- Type
- Label
- Mass Spectrometry-based proteomic approach in Oenococcus oeni (O. oeni) enological starter (Articolo in rivista) (literal)
- Anno
- 2014-01-01T00:00:00+01:00 (literal)
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#doi
- 10.1021/pr4012798 (literal)
- Alternative label
Napoli A, Aiello, D., Aiello, G., Cappello, M.S., Di Donna, L., Mazzotti, F., Materazzi, S., Fiorillo, M., Sindona G. (2014)
Mass Spectrometry-based proteomic approach in Oenococcus oeni (O. oeni) enological starter
in Journal of proteome research (Print)
(literal)
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#autori
- Napoli A, Aiello, D., Aiello, G., Cappello, M.S., Di Donna, L., Mazzotti, F., Materazzi, S., Fiorillo, M., Sindona G. (literal)
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- Note
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- Department of Chemistry and Chemical Technologies, University of Calabria, Via P. Bucci, Cubo 12/D, 87036 Arcavacata di Rende (CS), Italy
CNR, Institute of Science of Food Production (ISPA), Lecce, Italy
Department of Chemistry, \"Sapienza\" University of Rome, Rome, Italy (literal)
- Titolo
- Mass Spectrometry-based proteomic approach in Oenococcus oeni (O. oeni) enological starter (literal)
- Abstract
- A simple procedure is proposed for selective protein
solubilization and trypsin digestion, followed by off-line liquid chromatography-
matrix assisted laser desorption ionization mass spectrometry (LC-
MALDI MS) analysis of Oenococcus oeni (O. oeni) bacterium. Peptides were
identified from tryptic digests using sequencing by tandem mass
spectrometry and database searches. Cytoplasmic and membrane related
proteins (MRP) were identified in the O. oeni bacterium. MS/MS data
analysis points out 13 peptides having one point mutation from 9 proteins.
The major microheterogeneity was found for Zn-dependent alcohol
dehydrogenase (Zn-ADH, Q04GE6) and 60 kDa chaperonin (GroEL,
Q04E64) that are involved in methionine catabolism and post-translational
protein folding, respectively. MS/MS data processing also leads to the
identification of 34 unique phosphorylation sites from 19 phosphoproteins. (literal)
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