African Journal of Biotechnology

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Afr. J. Biotechnol.


Vol. 2 No. 7


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Aly  IN 

Verreet JA


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African Journal of Biotechnology Vol. 2 (7), pp. 206210, July 2003

ISSN 1684-5315  © 2003 Academic Journals

 

Full Length Research Paper

Comparison of multi-locus enzyme and protein gel electrophoresis in the discrimination of five Fusarium species isolated from Egyptian cottons

Ibrahim N. Aly1,  Mohmed A. Abdel-Sattar1, Kamel A. Abd-Elsalam2,3*  Mohmed S. Khalil2 and Joseph A. Verreet3

1 Suez Canal University, Faculty of Agriculture, Ismailia, Egypt.

2 Agricultural Research Center, Plant Pathology Research Institute, Giza, Egypt.

3 Christian Albrechts Universität zu Kiel, Institut für Phytopathologie, Kiel, Germany.

 

*Corresponding author; phone: (49 431) 880 2993; fax: (49 431) 880 1583; e-mail: kaabdelsalam@msn.com

Accepted 21 May 2003  

 
    Abstract

 

 

 

Electrophoretic studies of multilocus-enzymes (MLEE) and whole-cell protein (SDS-PAGE) were carried out in order to evaluate the parity between different methods for the characterization of five Fusarium species recovered from cotton-growing areas in Egypt by numerical taxonomy methods. The obtained data revealed that SDS-PAGE and esterase isozymes are more efficient in grouping isolates in their respective species while peroxidase and malate dehydrogenase isozyme has much limited resolution in organizing all isolates in their respective species-specific clusters. A low correlations was detected between geographical origin of isolates and genetic diversity. Results indicate that the estimated inter-specific variation may be more pronounced with protein markers than with isoyzmes when the two approaches are applied to the same populations. The level of genetic variability detected within and between Fusarium spp. accessions with protein and esterase isoyzmes analysis suggests that it is a reliable, efficient, and effective marker technology for determining genetic relationships in Fusarium genus.

 

Key words: Cotton, Fusarium, Isozymes, polyacrylamide gel electrophoresis.  

  

 

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