The present study was conducted to determine the effect of different concentrations of putrescine and spermidine at all stages of regeneration (callogenesis, somatic embryos multiplication, germination and rooting)) of date palm cultivar Barhee. Shoot tips were eradicated from 2-3 years old offshoots, surface sterilized and inoculated onto Murashiege and Skoog, 1962 (MS) medium supplemented with 20 mg/L 2,4-D and 3 mg/L N6-2-isopentyl adenine (2ip). Primary callus was obtained after 24 weeks on the nutrient medium. Calli were then transferred onto fresh MS medium containing 0.0, 50, 100 or 150 mg/L of putrescine or spermidine individually. Results were recorded after 12 weeks. A significant increase in embryonic callus fresh weights reached 4.093 g at the concentration 100mg/l of Spermidine and 3.817 g at 100 mg/L of putrescine. Embryogenic callus was developed on MS media using different concentration 0,50,100 or 150mg/L of putrescine or spermidine. Results indicated that the highest embryo number reached 28.67embryo at the concentration 100mg/L of spermidine. The highest significant root number 5.20 root/plant appeared with rooting medium supplemented 100mg/l of Spermidine. Addition of Putrescine as a supplement to the rooting medium at concentrations 100mg/l reached 2.60 root/plant. It is concluded that both putrescine and spermidine may play a positive role in increasing callus growth and regulation of somatic embryogenesis in Phoenix dactylifera var. Brahee tissue cultures.
