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Improving the ability of astragalus trigonus L. to produce apigenin using modern genetic techniques / Ahmede Gamal Eldin Mohei Eldin Seif Eldin ; Supervised Ahmed Nagib Elsayed Sharaf , Naglaa Abdelmonem Abdallah , Nagwa Ibrahim Abdflfattah Elarabi

By: Contributor(s): Material type: TextTextLanguage: English Publication details: Cairo : Ahmed Gamal Eldin Mohei Eldin Seif Eldin , 2018Description: 105 P. : charts , facsimiles ; 25cmOther title:
  • تحسين قدرة نبات القتاد على انتاج الأبيجنين باستخدام التقنيات الوراثية الحديثة [Added title page title]
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Dissertation note: Thesis (Ph.D.) - Cairo University - Faculty of Agriculture - Department of Genetics Summary: Astragalus trigonus considered an important medical plant had been used as traditional medicine, which improve the resistance to viral infections, hepatoprotective, heart tonic, nephritis and diabetes. For the purpose of genetic conservation of the Astragalus trigonus, an efficient and repeatable in vitro propagation system from the hypocotyl explants was developed. Murashige and Skoog medium (MS) included various concentration and /or of a-naphthaleneacetic acid (NAA), benzylamino-purine (BAP), thidiazuron (TDZ) and kinetin (KIN) was used for shoot initiation.The number of shoot/explants was high (14 shoots) in the presence of 0.5 mg/l NAA and 0.5 mg/l BAP. Elongated shoots were successfully rooted in MS medium supplemented with 1.0 mg/l NAA. High similarity percentage was detected among the in vitro regenerated plant with the mother plants as reveled by the molecular marker analysis; random amplified polymorphic DNA (RAPD) and inter simple sequence repeats (ISSR). The data obtained from both of RAPD and ISSR analyses showed 35.2 % polymorphism among the regenerated and their mother plants. The protocol in this study can be applied to conserve the endangered Astragalus trigonus. in order to enhancement the apigenin callus induction was achieved on MS supplemented with 0.5 mg/l 2,4-D and the elicitation with jasmonic acid, salicylic acid, chitosan and yeast extract was tested
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Thesis Thesis قاعة الرسائل الجامعية - الدور الاول المكتبة المركزبة الجديدة - جامعة القاهرة Cai01.07.10.Ph.D.2018.Ah.I (Browse shelf(Opens below)) Not for loan 01010110076998000
CD - Rom CD - Rom مخـــزن الرســائل الجـــامعية - البدروم المكتبة المركزبة الجديدة - جامعة القاهرة Cai01.07.10.Ph.D.2018.Ah.I (Browse shelf(Opens below)) 76998.CD Not for loan 01020110076998000

Thesis (Ph.D.) - Cairo University - Faculty of Agriculture - Department of Genetics

Astragalus trigonus considered an important medical plant had been used as traditional medicine, which improve the resistance to viral infections, hepatoprotective, heart tonic, nephritis and diabetes. For the purpose of genetic conservation of the Astragalus trigonus, an efficient and repeatable in vitro propagation system from the hypocotyl explants was developed. Murashige and Skoog medium (MS) included various concentration and /or of a-naphthaleneacetic acid (NAA), benzylamino-purine (BAP), thidiazuron (TDZ) and kinetin (KIN) was used for shoot initiation.The number of shoot/explants was high (14 shoots) in the presence of 0.5 mg/l NAA and 0.5 mg/l BAP. Elongated shoots were successfully rooted in MS medium supplemented with 1.0 mg/l NAA. High similarity percentage was detected among the in vitro regenerated plant with the mother plants as reveled by the molecular marker analysis; random amplified polymorphic DNA (RAPD) and inter simple sequence repeats (ISSR). The data obtained from both of RAPD and ISSR analyses showed 35.2 % polymorphism among the regenerated and their mother plants. The protocol in this study can be applied to conserve the endangered Astragalus trigonus. in order to enhancement the apigenin callus induction was achieved on MS supplemented with 0.5 mg/l 2,4-D and the elicitation with jasmonic acid, salicylic acid, chitosan and yeast extract was tested

Issued also as CD

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