USE OF ISOZYME ELECTROPHORESIS TO DIFFERENTIATE AMONG ISOLATES OF Macrophomina phaseolina
Aly, A., Abdel-Sattar, M., Omar, M. (2008). USE OF ISOZYME ELECTROPHORESIS TO DIFFERENTIATE AMONG ISOLATES OF Macrophomina phaseolina. EKB Journal Management System, 33(3), 1909-1925. doi: 10.21608/jpp.2008.131661
A. A. Aly; M. A. Abdel-Sattar; M. R. Omar. "USE OF ISOZYME ELECTROPHORESIS TO DIFFERENTIATE AMONG ISOLATES OF Macrophomina phaseolina". EKB Journal Management System, 33, 3, 2008, 1909-1925. doi: 10.21608/jpp.2008.131661
Aly, A., Abdel-Sattar, M., Omar, M. (2008). 'USE OF ISOZYME ELECTROPHORESIS TO DIFFERENTIATE AMONG ISOLATES OF Macrophomina phaseolina', EKB Journal Management System, 33(3), pp. 1909-1925. doi: 10.21608/jpp.2008.131661
Aly, A., Abdel-Sattar, M., Omar, M. USE OF ISOZYME ELECTROPHORESIS TO DIFFERENTIATE AMONG ISOLATES OF Macrophomina phaseolina. EKB Journal Management System, 2008; 33(3): 1909-1925. doi: 10.21608/jpp.2008.131661

USE OF ISOZYME ELECTROPHORESIS TO DIFFERENTIATE AMONG ISOLATES OF Macrophomina phaseolina

Journal of Plant Production
Article 11, Volume 33, Issue 3, March 2008, Pages 1909-1925    PDF (1.48 M)
Document Type: Original Article
DOI: 10.21608/jpp.2008.131661
Authors
A. A. Aly1; M. A. Abdel-Sattar2; M. R. Omar1
1Plant Pathology Research Institute, Agric. Res. Center, Giza, Egypt.
2Dept. of Agric. Bot., Faculty of Agric., Suez Canal Univ., Ismailia, Egypt.
Abstract
The banding patterns of malate dehydrogenase (EC1.1.1.37), glycerol dehydrogenase (EC1.1.1.72), peroxidase (EC1.11.1.7), esterase (EC3.1.1.1), and acid phosphatase (EC3.1.3.2) were determined by polyacrylamide gel electrophoresis for 28 isolates of Macrophomina phaseolina. A total of 96 phenotypes was detected for all the enzymes. Esterase gave the greatest number of polymorphic banding patterns. Cluster analysis of the isozyme banding patterns by the unweighted pair-group method based on arithmetic means placed the isolates in several groups; however, geographic origin of the isolates or source (host) did not exhibit clear correlation with the isozyme electrophoretic grouping results.
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