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Introduction ,[object Object],[object Object],[object Object]
Advantage ,[object Object],[object Object],[object Object],Disadvantage ,[object Object],[object Object],[object Object],[object Object],Plastid Transformation  Agrobacterium Transformation  Advantage Disadvantage ,[object Object],[object Object]
Seed sterilization Preinduction callus Preculture of callus Callus induction inoculation Culture  A. Tumefaciens harboring pCAMBIA1301 in AB medium Preparation of inoculum Co-cultivation selection Shoot regeneration X-Gluc solution Examination of expression of GUS rooting potting Material and Methods – Agro bacterium transformation at 28 o C +16 h light +8 h dark cycle 3 weeks at 28 o C  In dark 3 days Co-cultivation 2 mins 3 days 3 days
Continue… Material and Methods – Biolistic transformation
 
[object Object],[object Object],[object Object],[object Object],[object Object]
Chloroplast from leaves & DNA Isolated Two homologous fragments are amplified and purified Cloned into pBluescript SK (MB) - pSKE & pSKF sequencing vectors are constructed Double digested with Sac II & Bam H I & fragment inserted in pSKF Vector Rice homologous fragment -  pREF Pu16S was digested by Sac I Cut was blunted with klenow fragments and again cut with Hind III Modified 16s promoter (150BP) Digested product was cloned into PT393 between xbal site & hind III site Expression vector p16ST PAZ – Digested by Xba I Cut was blunted and again cut with Hind III Product contain Bar sequence & it was purified Inserted into  p16ST B/W Sac I – Hind III site Intermediate vector p16STB was formed Cut with Bam H I – DNA fragments Cloned into  pREF  – b/w Bam H I site Rice chloroplast pRB
Construction of chloroplast transformation vector Source : LIYi-nü  etal
Results and discussion ,[object Object],[object Object],Figure 1: (A) Calli co-cultured on a sterilized filter paper placed on 30 mL  solid N6D  (B) Co-cultured calli on solid medium were subjected to hygromycin selection for 7 days.  (C) Co-cultured calli on solid medium were subjected to hygromycine selection for 7 days and stained with X-Gluc solution. (D)Calli co-cultured on three pieces of filter paper moistened with 5.5 mL of N6D medium (E) Co-cultured calli on liquid medium were subjected to hygromycin selection for 7 days.  (F) Co-cultured calli on liquid medium were subjected to hygromycine selection for 7 days and stained with X-Gluc solution Three pieces of filter paper moistened with 5.5 mL of N6D medium+ 100mg/L of L-cysteine give calli without browning
[object Object],[object Object],[object Object],In this experiment, 0-15mg/L of acetosyringone at 25 o C is suitable
[object Object],[object Object]
transplastomic rice lines - Biolistic transformation Molecular identification of the bar gene in transplastomic rice plants - Chloroplast transformation bar  gene was identified in transplatomic rice plants by using Southern blotting - Chloroplast transformation
Recommendation ,[object Object],[object Object],[object Object]
References Ozawa Kenjirou (2009) Establisment of a high efficiency  Agrobacterium- mediated transformation system of rice ( Oryza sativa  L.).  Plant Science , 176 : 522-527 Ozawa Kenjirou and Takaiwa Fumio (2010) Highly efficient  Agrobacterium- mediated transformation of suspension-cultured cell clusters of rice ( Oryza sativa  L.).  Plant Science , 179 : 333-337. Olhoft PM,  Somers DA (2001) L-Cysteine increases Agrobacterium-mediated T-DNA delivery into soybean cotyledonary-node cells,  Plant Cell Rep .  20 :706–711. Enrı´quez-Obrego´ n GA, Prieto-Samso´ nov DL, de la Riva GA, M. Pe´ rez, G. Selman-Housein, R.I. Va´zquez-Pado´ n (1999) Agrobacterium-mediated Japonica rice transformation:a procedure assisted by an antinecrotic treatment,  Plan. Cell Tissue Org. Cult . 59 : 159–168. Potrykus I (1991) Gene transfer to plants: assessment of published approaches and results , Annu. Rev. Plant Physiol. Plant Mol. Biol.   42 : 205–225. LI Yi-nu (2009) Establishment of a Gene Expression System in Rice Chloroplast and Obtainment of PPT-Resistant Rice Plants,  Agricultural Sciences in China.  8(6) 643-651. Hiratsuka J, Shimada  (1989) The complete sequence of the rice (Oryza sativa) chloroplast genome: intermolecular recombination between distinct tRNA genes accounts for a major plastid DNA inversion during the evolution of the cereals.  Molecular and General Genetics ,  217,  185-194 Boynton J E (1988), Chloroplast transformation in  Chlamydomonas  with high velocity micro projectiles, Science,  240 , 1534-1538

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Genetically modified rice using three transformation methods

  • 1.  
  • 2.
  • 3.
  • 4. Seed sterilization Preinduction callus Preculture of callus Callus induction inoculation Culture A. Tumefaciens harboring pCAMBIA1301 in AB medium Preparation of inoculum Co-cultivation selection Shoot regeneration X-Gluc solution Examination of expression of GUS rooting potting Material and Methods – Agro bacterium transformation at 28 o C +16 h light +8 h dark cycle 3 weeks at 28 o C In dark 3 days Co-cultivation 2 mins 3 days 3 days
  • 5. Continue… Material and Methods – Biolistic transformation
  • 6.  
  • 7.
  • 8. Chloroplast from leaves & DNA Isolated Two homologous fragments are amplified and purified Cloned into pBluescript SK (MB) - pSKE & pSKF sequencing vectors are constructed Double digested with Sac II & Bam H I & fragment inserted in pSKF Vector Rice homologous fragment - pREF Pu16S was digested by Sac I Cut was blunted with klenow fragments and again cut with Hind III Modified 16s promoter (150BP) Digested product was cloned into PT393 between xbal site & hind III site Expression vector p16ST PAZ – Digested by Xba I Cut was blunted and again cut with Hind III Product contain Bar sequence & it was purified Inserted into p16ST B/W Sac I – Hind III site Intermediate vector p16STB was formed Cut with Bam H I – DNA fragments Cloned into pREF – b/w Bam H I site Rice chloroplast pRB
  • 9. Construction of chloroplast transformation vector Source : LIYi-nü etal
  • 10.
  • 11.
  • 12.
  • 13. transplastomic rice lines - Biolistic transformation Molecular identification of the bar gene in transplastomic rice plants - Chloroplast transformation bar gene was identified in transplatomic rice plants by using Southern blotting - Chloroplast transformation
  • 14.
  • 15. References Ozawa Kenjirou (2009) Establisment of a high efficiency Agrobacterium- mediated transformation system of rice ( Oryza sativa L.). Plant Science , 176 : 522-527 Ozawa Kenjirou and Takaiwa Fumio (2010) Highly efficient Agrobacterium- mediated transformation of suspension-cultured cell clusters of rice ( Oryza sativa L.). Plant Science , 179 : 333-337. Olhoft PM, Somers DA (2001) L-Cysteine increases Agrobacterium-mediated T-DNA delivery into soybean cotyledonary-node cells, Plant Cell Rep . 20 :706–711. Enrı´quez-Obrego´ n GA, Prieto-Samso´ nov DL, de la Riva GA, M. Pe´ rez, G. Selman-Housein, R.I. Va´zquez-Pado´ n (1999) Agrobacterium-mediated Japonica rice transformation:a procedure assisted by an antinecrotic treatment, Plan. Cell Tissue Org. Cult . 59 : 159–168. Potrykus I (1991) Gene transfer to plants: assessment of published approaches and results , Annu. Rev. Plant Physiol. Plant Mol. Biol. 42 : 205–225. LI Yi-nu (2009) Establishment of a Gene Expression System in Rice Chloroplast and Obtainment of PPT-Resistant Rice Plants, Agricultural Sciences in China. 8(6) 643-651. Hiratsuka J, Shimada (1989) The complete sequence of the rice (Oryza sativa) chloroplast genome: intermolecular recombination between distinct tRNA genes accounts for a major plastid DNA inversion during the evolution of the cereals. Molecular and General Genetics , 217, 185-194 Boynton J E (1988), Chloroplast transformation in Chlamydomonas with high velocity micro projectiles, Science, 240 , 1534-1538

Editor's Notes

  1. three pieces of filter paper moistened with 5.5 mL of N6D medium+ 100mg/L of L-cysteine give calli without browning
  2. 0-15mg/L of acetosyringone at 25 o C