Direct organogenesis from shoot tip of Egyptian New Valley date palm cultivars

Mona Bakr, Amal F. M. Zein El Din, I. Shams El Din, I. Ibrahim, R. Taha
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Abstract

Shoot tip explants of superior date palm cultivars Sewi, Tamr El wady, Hegazi and one individual unknown female from El-Kharga city (called Faleg or Meghel) were grown in the New Valley region and cultured on three different starting culture media MS+10mg/l 2,4-D+3.0mg/l 2iP ( M1), MS+ 10mg/l NAA+ 3.0mg/l 2iP (M2) and MS+30 mg/l NAA+20mg/l 2iP(M3) for eight months (two months interval). All culture media were supplemented with 40g/l sucrose, 2.0 g/l PVP, and 3.0 g/l activated charcoal and solidified with gelrite at 2.0 g/l. After eight months, some morphological responses were noticed as direct shoot buds, direct embryogenesis and callus. Depending on these responses, different culture media with different combinations of auxin and cytokinin were used to differentiate and multiply these cultures. Results indicated that the highest direct shoot bud percentage was formed on M1 medium while the highest direct embryo percentage was formed on M2.Induced direct shoot buds that transferred to the half strength of 2,4D then transferred to auxin free medium showed the highest multiplied rate as clusters. Maximum shoot number was obtained when transferring these clusters to a modified medium supplemented with 3/4 MS salt + 2.0 mg/l BA+ 0.5 mg/l Kinetin+ 0.25 mg/l 2iP+ 1.0 mg/l IAA. Meanwhile, induced direct embryos transferred to a modified medium supplemented with 1/2 MS+ 0.25 mg/l ABA + 0.5 mg/l Kinetin+ 0.25 mg/l 2iP showed the highest secondary embryo number. All induced shoots were rooted successfully and transferred to the greenhouse.
埃及新谷枣树品种茎尖的直接器官发生
选用优质枣椰树品种Sewi、Tamr El wady、Hegazi和来自El- kharga市的一株未知雌枣椰树(Faleg或Meghel)的茎尖外植体,在新谷地区以MS+10mg/l 2,4- d +3.0mg/l 2iP(M1)、MS+10mg/l NAA+ 3.0mg/l 2iP(M2)和MS+ 30mg /l NAA+20mg/l 2iP(M3)三种不同的起始培养基培养8个月(间隔2个月)。所有培养基分别添加40g/l蔗糖、2.0 g/l PVP和3.0 g/l活性炭,并用2.0 g/l的明胶固化。8个月后,出现了直接芽、直接胚和愈伤组织等形态反应。根据这些反应,使用不同的培养基和不同的生长素和细胞分裂素组合来分化和繁殖这些培养物。结果表明,在M1培养基上直接芽率最高,而在M2培养基上直接胚率最高。将诱导的直芽转移到2、4D的一半强度,再转移到无生长素的培养基上,成簇繁殖率最高。将这些簇转移到添加3/4 MS盐+ 2.0 mg/l BA+ 0.5 mg/l Kinetin+ 0.25 mg/l 2iP+ 1.0 mg/l IAA的改良培养基中,获得最大芽数。在1/2 MS+ 0.25 mg/l ABA + 0.5 mg/l Kinetin+ 0.25 mg/l 2iP的培养基中,直接诱导胚的次生胚数最高。诱导苗均生根成功,移栽温室。
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