Hordein patterns characterization in Mexican malting barley cultivars

A group of storage proteins highly abundant in cereal seeds are the prolamins, characterized by the frequent presence of proline in their sequence. The barley prolamins are known as hordeins. The aim of this study was to obtain the hordein banding patterns for five different Mexican barley cultivars...

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Detalles Bibliográficos
Autores: Salgado-Albarrán, Marisol, Herrera-Díaz, Jorge, Dinkova, Tzvetanka D.
Tipo de recurso: artículo
Estado:Versión publicada
Fecha de publicación:2015
País:México
Institución:UNIVERSIDAD NACIONAL AUTÓNOMA DE MÉXICO
Repositorio:TIP Revista especializada en ciencias químico-biológicas
Idioma:español
OAI Identifier:oai:ojs.ojs.escire.net:article/93
Acceso en línea:http://tip.zaragoza.unam.mx/index.php/tip/article/view/93
Access Level:acceso abierto
Palabra clave:Barley (Hordeum vulgare); mass spectrometry; hordeins; malt; banding patterns
Cebada (Hordeum vulgare); espectrometría de masas; hordeínas; malta; patrones de bandeo
Descripción
Sumario:A group of storage proteins highly abundant in cereal seeds are the prolamins, characterized by the frequent presence of proline in their sequence. The barley prolamins are known as hordeins. The aim of this study was to obtain the hordein banding patterns for five different Mexican barley cultivars in mature seeds. In addition, the hordein patterns in processed malt of four mexican and a canadian (Metcalfe) barley cultivars were obtained. Mass Spectrometry (MS), using distinct digestion protocols, identified differential bands in the patterns. Major differences in the seed patterns between cultivars consisted in discrete bands at 100 kDa, 65 kDa and in the range of 37 to 45 kDa. In malt, the patterns were highly contrasting among Mexican cultivars as well as in Metcalfe, suggesting that hordein processing during germination and malt processing is particular to each cultivar. Finally, the MS identification demonstrated that trypsin digestion is appropriate to distinguish B and γ hordeins in malt, whereas sequential digestion with chymotrypsin and trypsin allows the identification of C hordeins in seed.