September
2009
Volume
86
Number
5
Pages
487
—
491
Authors
Hind Mokrane,1,2,3
Bert Lagrain,3
Kurt Gebruers,3
Christophe M. Courtin,3
Kristof Brijs,3
Paul Proost,4 and
Jan A. Delcour3,5
Affiliations
Laboratoire des produits bioactifs et de la valorisation de la biomasse, Ecole Normale Supérieure, BP 92, Kouba, Alger, Algérie.
Département Génie de l'environnement, Ecole Nationale Polytechnique, BP 182, El Harrach, Alger, Algérie.
Laboratory of Food Chemistry and Biochemistry and Leuven Food Science and Nutrition Research Centre (LFoRCe), K.U. Leuven, Kasteelpark Arenberg 20, bus 2463, B-3001 Leuven, Belgium.
Laboratory of Molecular Immunology, K.U. Leuven, Minderbroedersstraat 10, B-3000 Leuven, Belgium.
Corresponding author. Phone: +32(0)16321634. Fax: +32(0)16321997. E-mail: jan.delcour@biw.kuleuven.be
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RelatedArticle
Accepted June 5, 2009.
Abstract
ABSTRACT
The prolamins in seven Algerian Sahara sorghum cultivars of varying seed shape and color were investigated. Protein contents ranged from 12 to 16%. Prolamins were the major protein fraction. They could be separated according to degree of disulfide cross-linking. Kafirin monomers and low molecular weight polymers could be extracted with 70% ethanol, whereas highly cross-linked kafirins additionally needed a reducing agent to become extractable. Kafirin monomers of α-, β- and γ-type were purified and N-terminally sequenced. For the first time, δ-kafirin was identified at the protein level. The study clearly revealed intercultivar differences between protein levels. The joint use of SDS-PAGE, SE-HPLC, and RP-HPLC allowed discriminating among cultivars based on the differences in prolamin levels and composition.
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© 2009 AACC International, Inc.