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Transient expression of ELN gene in tobacco plant / Mona Ahmed Mohamed Abdelghani ; Supervised Naglaa Abdelmoneam Abdallah , Abdel Hadi Abdallah , Ghada Aboelheba

By: Contributor(s): Material type: TextLanguage: English Publication details: Cairo : Mona Ahmed Mohamed Abdelghani , 2015Description: 67 P. : charts , photographs ; 25cmOther title:
  • فى نبات الدخان ELNالتعبير المؤقت لجين ال [Added title page title]
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Dissertation note: Thesis (M.Sc.) - Cairo University - Faculty of Agriculture - Department of Genetics Summary: Plant molecular farming (PMF) is an important growing prospective approach in plant biotechnology. It includes production of recombinant pharmaceutical and industrial proteins in large quantities from engineered plants. Elastin is a major protein component of elastic fibers. They provide tissues with the required resilience and elasticity. In this work, Nicotiana tabacum leaves were used as a bioreactor for the expression and production of the full human tropoelastin protein; the precursor protein of elastin. The agrobacterium- mediated transient expression system into Nicotiana tabacum was used via syringe agroinfiltration to provide a fast and convenient way to produce recombinant proteins with a greater expression overall the plant leaf. This study aimed to establish an efficient and rapid system for transiently expression and production of human recombinant tropoelastin protein in transgenic N. tabacum plants. Modified sequence of the elastin (ELN) gene was biosynthesized and cloned into pCambia1390 vector to be transferred into N. tabacum. Optimization of codon usage for the human tropoelastin gene, without changing the primary structure of the protein was carried out to ensure high expression in tobacco plants. The obtained data proved that the 5th day post-infiltration is the optimum interval to obtain the maximum production of the recombinant protein. Southern blot analysis was able to detect the 2175 bps fragment representing the ELN orf. On the other hand, ELN -expression within plant{u2019}s tissue was visualized by RT-PCR within 3 to 10 days post agroinfiltration. At the protein level, western and ELISA confirmed the expression of recombinant tropoelastin protein
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Thesis قاعة الرسائل الجامعية - الدور الاول المكتبة المركزبة الجديدة - جامعة القاهرة Cai01.07.10.M.Sc.2015.Mo.T (Browse shelf(Opens below)) Not for loan 01010110067366000
CD - Rom مخـــزن الرســائل الجـــامعية - البدروم المكتبة المركزبة الجديدة - جامعة القاهرة Cai01.07.10.M.Sc.2015.Mo.T (Browse shelf(Opens below)) 67366.CD Not for loan 01020110067366000

Thesis (M.Sc.) - Cairo University - Faculty of Agriculture - Department of Genetics

Plant molecular farming (PMF) is an important growing prospective approach in plant biotechnology. It includes production of recombinant pharmaceutical and industrial proteins in large quantities from engineered plants. Elastin is a major protein component of elastic fibers. They provide tissues with the required resilience and elasticity. In this work, Nicotiana tabacum leaves were used as a bioreactor for the expression and production of the full human tropoelastin protein; the precursor protein of elastin. The agrobacterium- mediated transient expression system into Nicotiana tabacum was used via syringe agroinfiltration to provide a fast and convenient way to produce recombinant proteins with a greater expression overall the plant leaf. This study aimed to establish an efficient and rapid system for transiently expression and production of human recombinant tropoelastin protein in transgenic N. tabacum plants. Modified sequence of the elastin (ELN) gene was biosynthesized and cloned into pCambia1390 vector to be transferred into N. tabacum. Optimization of codon usage for the human tropoelastin gene, without changing the primary structure of the protein was carried out to ensure high expression in tobacco plants. The obtained data proved that the 5th day post-infiltration is the optimum interval to obtain the maximum production of the recombinant protein. Southern blot analysis was able to detect the 2175 bps fragment representing the ELN orf. On the other hand, ELN -expression within plant{u2019}s tissue was visualized by RT-PCR within 3 to 10 days post agroinfiltration. At the protein level, western and ELISA confirmed the expression of recombinant tropoelastin protein

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