Showing 4 results for C. Ghobadi
M. Mohamadi Bazargani, B. E. S. Tabatabaei, A. Rezaei, C. Ghobadi,
Volume 8, Issue 2 (summer 2004)
Abstract
Optimizing regeneration of cotton plant in two variety (Sahel and Varamin) via shoot apex was done in order to Agrobacterium-mediated transformation. In this reaserch shoot apexes of two varieties were isolated from four or five day seedling and were placed on a special medium of shooting (modified MS without hormon).In order to select the best rooting media, The Statistical Analysis explants that produce shoot and leaves in a CRBD with 4 replicates and 4 rooting treatments: 1) modified MS without hormon, 2) ½ MS with 0.1 mg/lit IBA, 3) ½ MS with 0.1 mg/lit NAA, 4) ½ MS with 0.1 mg/lit IAA. The statistical analysis indicated that the best for both varieties, was medium with 0.1 mg/lit IBA and rooting percentage of Varamin is better than sahel in all of media.
T. Mahmoodi-Ghehsareh, B. E. Sayed-Tabatabaei, C. Ghobadi, A. Mirlohi,
Volume 8, Issue 3 (fall 2004)
Abstract
The significance of haploid plants as genetic and plant breeding tools has been recognized for a long time. Haploid production techniques including anther culture, isolated microspore culture and intergeneric hybridization between wheat × Hordeum bulbosum and wheat × maize have been used to produce homozygous lines which accelerate breeding programs. In this study, wheat × maize hybridization and anther culture techniques were used for haploid production in six wheat genotypes. The results showed that 70.7% of regenerated plants through anther culture were albino plants and only 29.2 % were green, while the plants produced through wheat × maize method were all green. Ploidy variation was not observed in plants regenerated through wheat × maize hybridization. It was concluded that wheat × maize crosses would be an appropriate and practical method for haploid production in different wheat genotypes, which in comparison with the anther culture method has a higher efficiency.
A. Yamchi, F. Rastgar Jazii, C. Ghobadi, A. Mousavi, A. A. Karkhanehee,
Volume 8, Issue 4 (winter 2005)
Abstract
Proline as a key osmoregulating solute in plants plays an overriding role in osmotic pressure adjustment of the cell under water stress conditions. In plant, a bifunctional enzyme delta-1-pyrroline-5-carboxylate synthetase (p5cs) promotes and directs proline synthesis during drought stress conditions. The activity of this enzyme is strongly induced to increase proline concentration within the cell to prevent the impact of water deficit. In this study, the sequence coded for p5cs enzyme under the control of the cauliflower mosaic virus 35S promoter was cloned into a plasmid containing gus and nptII genes. The construct pBI121-p5cs was then transferred into Agrobacterium tumefaciens C58 (pGV3101) and used for producing transgenic tobacco(Nicotiana tabacum cv. Xanthi) plants. The amplification of a 765 bp band within p5cs gene from transferred plants and forming deep blue color in leaf tissues of the explants indicated the successful introduction of p5cs construct into nuclear genome of tobacco plants through Agrobacterium-mediated transformation. The two-month old plants growing under normal condition besides the five-day seedlings under drought stress were subjected to determination of proline concentration. Comparison of P5cs product levels between control and water tolerated plants indicated an increase of proline of about 96.91 to 1330.891 mg/g and of 204.454 to 2039.77 mg/g in plants under normal irrigation and under drought stress, conditions respectively. The significant difference between the levels of proline product in control and transgenic plants under different growing conditions demonstrated the expression of targeted gene (p5cs) in engineered tobacco plants that may pave the way to overcome the water stress problem in agronomically useful crops.
M. Bahar, M. R. Mohammadi, C. Ghobadi,
Volume 10, Issue 4 (winter 2007)
Abstract
The identification of potato cultivars is a recurrent objective of potato research. The research is prompted by the increasing number of potato cultivars and the importance of seed purity. In developing a reliable method for identification of the imported potato cultivars and determining their genetic relationship, the capacity of 10 polymorphic simple sequence repeat markers (SSRs) was evaluated for the analysis of 28 commercial cultivars of potato. The number of alleles detected at different loci ranged from 3 to 10 alleles with a total of 57 for all loci and a mean of 5.7 alleles per locus. In the 28 potato cultivars analyzed, the number of heterozygous genotypes per locus varied between 6 to 28 with an average number of heterozygous genotypes per locus of 18, considering the 10 loci studied. Based on the resulting dendrogram of jacquard's similarity coefficient and UPGMA analysis, the potato cultivars were placed in two major groups. However, the results from similarity coefficient confirmed the close phylogenetic relationships among members in each cluster. The dendrogram derived from SSRs data clustered together Kenebek, Florida and Atlantic which are known as American potato cultivars, but Stanbuli, an old cultivar in Iran, was placed in concert with European cultivars. This finding might be an indication that this cultivar along with other unidentified cultivars, growing in local fields, has been introduced from European countries to Iran. The results obtained illustrate the appropriate utility of SSRs to assess genetic relationships of potato cultivars and develop a PCR- based tool for evaluation of potato seed purity.
