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Isoenzyme and cotyledon protein variation for identification of black beans (Phaseolus vulgaris L.) with similar seed morphology
Authors:D. R. Driedger  B. M. Watts  A. Hussain  L. G. Elias
Affiliation:(1) Department of Foods and Nutrition, University of Manitoba, R3T 2N2 Winnipeg, Manitoba, Canada;(2) Present address: National Agri-Food Technology Centre, 810 Phillips Street, R1N 3J9 Portage la Prairie, Manitoba, Canada;(3) Agriculture Canada/Research Station, 195 Dafoe Road, R3T 2M9 Winnipeg, Manitoba, Canada;(4) Division of Agricultural and Food Sciences, Institute of Nutrition of Central America and Panama, Carretera Roosevelt, Zona 11, Guatemala City, Guatemala C.A.
Abstract:Summary Methods developed to identify genetically diverse varieties of beans (Phaseolus vulgaris L.) were applied to closely related lines that were difficult to distinguish on the basis of seed morphology. Seedling tissues and seeds of black beans, were examined electrophoretically for isoenzyme and cotyledon proteinn protein patterns. Seven enzymes, extracted from seeds or from seedling stem, root or leaf tissues, were compared for polymorphism. Peptidase, polyphenol oxidase, phosphoglucoisomerase and glutamate oxaloacetate transaminase patterns were the same for all lines. Some differences were observed for acid phosphatase, peroxidase and esterase patterns, but complete discrimination of the six selected lines was not possible on the basis of isoenzyme patterns alone. Using polyacrylamide gel electrophoresis (PAGE) of dissociated 0.1 M acetic acid soluble proteins at pH 3.1 (acid-PAGE), or sodium dodecyl sulphate PAGE (SDS-PAGE) of residual protein extracts, all but one pair of samples in each case could be distinguished from the other samples. Using both techniques all of the lines could be identified unequivocally.
Keywords:acid-PAGE  black bean  common bean  cotyledon proteins  isoenzyme  Phaseolus vulgaris  protein variation  SDS-PAGE
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