آمار
| تعداد نشریات | 45 |
| تعداد شمارهها | 1,493 |
| تعداد مقالات | 18,210 |
| تعداد مشاهده مقاله | 58,933,329 |
| تعداد دریافت فایل اصل مقاله | 20,392,601 |
In Vitro Propagation of Damask Rose Using the Temporary Immersion System | ||
| Journal of Plant Physiology and Breeding | ||
| مقاله 2، دوره 6، شماره 2، اسفند 2016، صفحه 9-18 اصل مقاله (521.88 K) | ||
| نوع مقاله: Research Paper | ||
| نویسندگان | ||
| Ali Bosh1؛ Ahmad Moieni* 2؛ Hamid Dehghani2؛ Zahra Movahedi3 | ||
| 1MSc, Department of Agricultural Biotechnology, Tarbiat Modares University, Tehran, Iran | ||
| 2Associate Prof., Department of Plant Breeding and Biotechnology, Faculty of Agriculture, Tarbiat Modares University, Tehran, Iran | ||
| 3Assistant Prof., Department of Agronomy and Plant Breeding, Faculty of Agriculture, Malayer University, Malayer, Iran | ||
| چکیده | ||
| For centuries, Damask rose has been one of the most popular species of the rose family. Damask rose can be propagated using vegetative methods such as micropropagation. In this research, the use of temporary immersion system was reported for the first time for Damask rose micropropagation. For this reason, a traditional temporary immersion system was designed to facilitate its micropropagation. To optimize this system, the effects of the BAP concentration, immersion time, explant size, number of explants per temporary immersion unit were investigated in the independent experiments using completely randomized design. Temporary immersion system was also compared with the solid and liquid media. The highest shoot number per explant was obtained from a temporary immersion system using an immersion time of 3 min every 150 min (11.8 shoots), a modified MS medium with 6 mg l-1 BAP (12.33 shoots) and explants with shoot length of 4 cm (12.45 shoots). Results indicated that the temporary immersion system was significantly better than solid and liquid media for the shoot number per explant (10.66, 2.56 and 5.66, respectively). | ||
| کلیدواژهها | ||
| BAP؛ Explant؛ Immersion time؛ Micropropagation؛ Rosa damascena Mill | ||
| مراجع | ||
|
Achuthan CR, Babu BH and Padikkala, 2003. Antioxidant and hepatoprotective effects of Rosa damascena. Pharmaceutical Biology 41: 357-361
Adelberg JW and Simpson EP, 2002. Intermittent immersion vessel apparatus and process for plant propagation. Internl. S/N: PCT/US01/06586
Aitken-Christie J, Kozai T and Takayama S, 1995.Automation in plant tissue culture. General introduction and overview. In: Aitken-Christie et al. (Eds). Automation and Environment Control in Plant Tissue Culture. Pp. 1-18. Kluwer Acad. Publ., Dordrecht, the Netherlands.
Akdemir H, Su¨zerer V, Onay A, Tilkat E, Ersali Y and Ciftci YO, 2014. Micropropagation of the pistachio and its rootstocks by temporary immersion system. Plant Cell Tissue and Organ Culture 117: 65–76.
Basim E and Basim H, 2003. Antibacterial activity of Rosa damascena essential oil. Fitoterapia 74: 394–396
Escalona M, Lorenzo JC, González B, Daquinta M, González JL, Desjardins Y and Borroto CG, 1999. Pineapple (Ananas comosus L. Merr) micropropagation in temporary immersion systems. Plant Cell Reports 18: 743-748.
Escalona M, Samson G, Borroto C and Desjardins Y, 2003. Physiology of effects of temporary immersion bioreactors on micropropagated pineapple plantlets. In Vitro Cellular and Developmental Biology-Plant 39: 651-656.
Etienne H, Bertrand B, Anthony F, Côte F and Berthouly M, 1997a. L’embryogenèse somatique: un outil pour l’amélioration génétique du caféier. In: 17th International Scientific Colloquium on Coffee. 21-25 June, Nairobi, Kenya. Pp. 457–465. ASIC Publishers, Paris, France.
Etienne H, Dechamp E, Etienne BD and Bertrand B, 2006. Bioreactors in coffee micropropagation. Brazilian Journal of Plant Physiology 18 (1): 45-54.
Etienne H, Lartaud M, Michaux–Ferrière N, Carron MP, Berthouly M and Teisson C, 1997b. Improvement of somatic embryogenesis in Hevea brasiliensis (Müll. Arg.) using the temporary immersion technique. In Vitro Cellular and Developmental Biology-Plant 33: 81–87.
Harris RE and Mason EB, 1983. Two machines for in vitro propagation of plants in liquid media. Canadian Journal of Plant Science 63: 311–316.
Horn WAH, 1992. Micropropagation of rose. In: Bajaj YPS (Ed). Biotechnology in Agriculture and Forestry. Vol. 20. High-tech and Micropropagation IV. Pp. 320-342. Springer, Germany.
Hvoslef-Eide AK and Preil W, 2005. Liquid Culture Systems for In Vitro Plant Propagation. Springer, Dordrecht.
Jabbarzadeh Z and Khosh-Khui M, 2005. Factors affecting tissue culture of Damask rose (Rosa damascene Mill.). Scientia Horticulturae 105: 475-482.
Krueger S, Robacker C and Simonton W, 1991. Culture of Amelanchier × grandiflorain a programmable micropropagation apparatus. Plant Cell Tissue and Organ Culture 27: 219–226.
Kumar A, Sood A, Palni UT, Gupta AK and Palni LMS, 2001. Micropropagation of Rosa damascene Mill. from mature bushes using thidiazuron. The Journal of Horticultural Science and Biotechnology 76: 30-34.
Levin R, Stav R, Alper Y and Watad AA, 1998. A technique for repeated non-axenic subculture of plant tissues in a bioreactor on liquid medium containing sucrose. Plant Tissue Culture Biotechnology 3: 41–45.
Mahmood N, Piacente S, Pizza C, Burke A, Khan A and Hay A, 1996. The anti-HIV activity and mechanisms of action of pure compounds isolated from Rosa damascene. Biochemical and Biophysical Research Communications 229: 73–79.
Mahmoudi Noodezeh H, Moieni A and Baghizadeh F, 2012. In vitro propagation of the Damask rose (Rosa damascena Mill.). In vitro Cellular and Development Biology-Plant 48: 530-538.
Martre P, Lacan D, Just D and Teisson C, 2001. Physiological effects of temporary immersion on Hevea brasiliensis (Müll. Arg.) callus. Plant Cell Tissue and Organ Culture 67: 25–35.
Nikbakht A, Kafi M, Mirmasomi M and Babalar M, 2005. Micropropagation of Damask Rose (Rosa damascene Mill.) cvs. Azaran and Ghamsar. International Journal of Agriculture and Biology 7: 535-538.
Ozkan G, Sagdic O, Baydar NG and Baydar H, 2004. Antioxidant and antibacterial activities of Rosa damascene flower extracts. Food Science and Technology International10: 277-281.
Quiala E, Can˜al MJ, Meijo´n M, Rodriguez R, Chave´z M, Valledon L, Feria M and Barbo´n R, 2012. Morphological and physiological responses of proliferating shoots of teak to temporary immersion and BA treatments. Plant Cell Tissue and Organ Culture 109: 223–234.
Salekjalali M, 2012. Phloroglucinol, BAP and NAA enhance axillary shoot proliferation and other growth indicators in in vitro culture of Damask Rose (Rosa damascene Mill.). American-Eurasian Journal of Agricultural and Environmental Sciences 12 (7): 960 -966.
Skirvin RM, Chu MC and Young HJ, 1990. Rose. In: Ammirato PV, Evans D, Sharp WR and Bajaj YPS (Eds). Handbook of Plant Cell Culture. Vol. 5. Ornamental species. Pp. 716-743. McGraw Hill, New York, USA.
Steinmacher DA, Guerra MP, Saare-Surminski K and Lieberei R, 2011. A temporary immersion system improves in vitro regeneration of peach palm through secondary somatic embryogenesis. Annals of Botany 108: 1463–1475.
Teisson C and Alvard D, 1995. A new concept of plant in vitro cultivation in liquid medium: temporary immersion. In: Terzi M, Cella R and Falavigna A (Eds). Current Issues in Plant Molecular and Cellular Biology. Pp. 105-109. Kluwer Academic Publisher.
Traoré A, Maximova SN and Guiltinan MJ, 2003. Micropropagation of Theobroma cacao L. using somatic embryo-derived plants. In vitro Cellular and Development Biology-Plant 409: 1-7.
Vidal N, Correa B, Rial E, Regueira M, Sa´nchez C and Cuenca B, 2015. Comparison of temporary and continuous immersion systems for micropropagation of axillary shoots of chestnut and willow. Acta Horticulturae 1083: 227–233.
| ||
|
آمار تعداد مشاهده مقاله: 868 تعداد دریافت فایل اصل مقاله: 1,502 |
||