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dc.contributor.authorRodrigues, Rafael Torres de Souza
dc.contributor.authorChizzotti, Mario Luiz
dc.contributor.authorVital, Camilo Elber
dc.contributor.authorBaracat-Pereira, Maria Cristina
dc.contributor.authorBarros, Edvaldo
dc.contributor.authorBusato, Karina Costa
dc.contributor.authorGomes, Rafael Aparecido
dc.contributor.authorLadeira, Márcio Machado
dc.contributor.authorMartins, Taiane da Silva
dc.date.accessioned2017-11-01T10:47:11Z
dc.date.available2017-11-01T10:47:11Z
dc.date.issued2017-01-19
dc.identifier.issn19326203
dc.identifier.urihttps://doi.org/10.1371/journal.pone.0170294
dc.identifier.urihttp://www.locus.ufv.br/handle/123456789/12676
dc.description.abstractProteins are the major constituents of muscle and are key molecules regulating the metabolic changes during conversion of muscle to meat. Brazil is one of the largest exporters of beef and most Brazilian cattle are composed by zebu (Nellore) genotype. Bos indicus beef is generally leaner and tougher than Bos taurus such as Angus. The aim of this study was to compare the muscle proteomic and phosphoproteomic profile of Angus and Nellore. Seven animals of each breed previously subjected the same growth management were confined for 84 days. Proteins were extracted from Longissimus lumborum samples collected immediately after slaughter and separated by two-dimensional electrophoresis. Pro-Q Diamond stain was used in phosphoproteomics. Proteins identification was performed using matrix assisted laser desorption/ionization time-of-flight mass spectrometry. Tropomyosin alpha-1 chain, troponin-T, myosin light chain-1 fragment, cytoplasmic malate dehydrogenase, alpha-enolase and 78 kDa glucose-regulated protein were more abundant in Nellore, while myosin light chain 3, prohibitin, mitochondrial stress-70 protein and heat shock 70 kDa protein 6 were more abundant in Angus (P<0.05). Nellore had higher phosphorylation of myosin regulatory light chain-2, alpha actin-1, triosephosphate isomerase and 14-3-3 protein epsilon. However, Angus had greater phosphorylation of phosphoglucomutase-1 and troponin-T (P<0.05). Therefore, proteins involved in contraction and muscle organization, myofilaments expressed in fast or slow-twitch fibers and heat shock proteins localized in mitochondria or sarcoplasmic reticulum and involved in cell flux of calcium and apoptosis might be associated with differences in beef quality between Angus and Nellore. Furthermore, prohibitin appears to be a potential biomarker of intramuscular fat in cattle. Additionally, differences in phosphorylation of myofilaments and glycolytic enzymes could be involved with differences in muscle contraction force, susceptibility to calpain, apoptosis and postmortem glycolysis, which might also be related to differences in beef quality among Angus and Nellore.en
dc.formatpdfpt-BR
dc.language.isoengpt-BR
dc.publisherPublic Library of Science Onept-BR
dc.relation.ispartofseries12(1), e0170294, January 2017pt-BR
dc.rightsOpen Accesspt-BR
dc.subjectAnguspt-BR
dc.subjectNellorept-BR
dc.subjectBeef qualitypt-BR
dc.titleDifferences in beef quality between Angus (Bos taurus taurus) and Nellore (Bos taurus indicus) cattle through a proteomic and phosphoproteomic approachen
dc.typeArtigopt-BR
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