IN VITRO DIRECT AND INDIRECT PROPAGATION OF BLACKBERRY (RUBUS SP.)
Badr-Elden, A., Nower, A., Abdallah, A., Albeah, H. (2016). IN VITRO DIRECT AND INDIRECT PROPAGATION OF BLACKBERRY (RUBUS SP.). EKB Journal Management System, 2(Special issue (2) for the first International Conference of Genetic Engineering and Biotechnology), 89-100. doi: 10.21608/rjab.2016.59891
Awatef M. Badr-Elden; Ahmed A. Nower; Adel A. Abdallah; Hind A. Albeah. "IN VITRO DIRECT AND INDIRECT PROPAGATION OF BLACKBERRY (RUBUS SP.)". EKB Journal Management System, 2, Special issue (2) for the first International Conference of Genetic Engineering and Biotechnology, 2016, 89-100. doi: 10.21608/rjab.2016.59891
Badr-Elden, A., Nower, A., Abdallah, A., Albeah, H. (2016). 'IN VITRO DIRECT AND INDIRECT PROPAGATION OF BLACKBERRY (RUBUS SP.)', EKB Journal Management System, 2(Special issue (2) for the first International Conference of Genetic Engineering and Biotechnology), pp. 89-100. doi: 10.21608/rjab.2016.59891
Badr-Elden, A., Nower, A., Abdallah, A., Albeah, H. IN VITRO DIRECT AND INDIRECT PROPAGATION OF BLACKBERRY (RUBUS SP.). EKB Journal Management System, 2016; 2(Special issue (2) for the first International Conference of Genetic Engineering and Biotechnology): 89-100. doi: 10.21608/rjab.2016.59891

IN VITRO DIRECT AND INDIRECT PROPAGATION OF BLACKBERRY (RUBUS SP.)

Research Journal of Applied Biotechnology
Article 8, Volume 2, Special issue (2) for the first International Conference of Genetic Engineering and Biotechnology, June 2016, Page 89-100  XML PDF (1.02 MB)
Document Type: Original Article
DOI: 10.21608/rjab.2016.59891
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Authors
Awatef M. Badr-Elden1; Ahmed A. Nower email 1; Adel A. Abdallah2; Hind A. Albeah1
1Plant Biotechnology Department, Genetic Engineering and Biotechnology Research Institute, University of Sadat City, Egypt
2Environmental studies & Research Institute, University of Sadat City, Egypt
Abstract
In vitro direct and indirect propagation of blackberry (Rubus sp.) were studied. Blackberry explants are easily oxidized, so the uses of the running tap water for washing about one hour before sterilization allowed avoiding the oxidation. The disinfection process was represented using different concentrations of Clorox (10, 15, 20%) with exposure times (5 and 10 min.), the best treatment being achieved by the concentration of (10% for 5 min.) for shoot tips and (5% for 5min) for leaves disinfectant. A normal growth and development occurred only in the BA of the multiplication, but at Kin or TDZ decreased in the shoots growth was induced. Maximum volume of callus induction and callus % were produced at TDZ or 2mg/l NAA or 2,4-D each alone from leaf explants. Addition of 2.0mg/l TDZ into media increased the callus induction from in vitro leaves than ex vitro leaves and having the best response. The highest responses of organogenesis obtained from In-vitro leaves than ex vitro leaves. The increased rooting of shoots appeared when MS reduced to ½ salts strength and produced highest leaves number, plant length (cm) and roots number. While, MS reduced to ¼ salts strength resulted in tallest of roots (2.72 cm). The rooting of plants derived from ½ MS salt strength medium give highest leaves number, plant length, roots number and roots length than other strengths of MS after two months from acclimatization in greenhouses.
Keywords
Acclimatization; Callus; in Vitro; multiplication; Organogenesis
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