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Research Detail

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M. Ashraful Habib
Agriculture  Research  &  Development,  International Rice Research Institute, Bangladesh

M. Abdul Muktadir
Grain Legume Breeding, Faculty of Agriculture  and  Environment,  The  University  of  Sydney,  Centre  for  Carbon  Water  and  Food  (CCWF),  380  Werombi Road, Camden, Brownlow Hill, NSW 2570, Australia. 

M. Rezwan Kabir
Biotechnology  Division,  Bangladesh  Agricultural  Research  Institute,  Gazipur-1701,  Bangladesh

M.  A. Khaleque Mian
Department of Genetics and Plant  Breeding, Bangabandhu Sheikh Mujibur Rahman Agricultural University, Gazipur-1706. Bangladesh

M. A. Yousuf Akhond 
Biotechnology  Division,  Bangladesh  Agricultural  Research  Institute,  Gazipur-1701,  Bangladesh

Five eggplant cultivars were cultured on MS supplemented with 0.5 mg/l 2,4-D,  resulting  in  the  development  of  embryogenic  calli.  When  the  calli  were  sub-cultured onto growth regulator free MS, BARI Begun-4 produced the highest  number of embryos (64) per explant followed by BARI Begun-1 (57). Later both  the  superior  varieties  in  terms  of  embryo  production  were  cultured  on  MS  having  0.5,  1.0,  1.5  and  2.0  mg/l  2,4-D  along  with  a  control.  BARI  Begun-4  produced the highest number of embryos (67) on MS supplemented with 1.0  mg/l  2,4-D  which  was  closely  followed  by  BARI  Begun?1  (62).  Regenerated  plantlets were successfully established in soil following acclimation.   

   Optimization, Somatic embryogenesis, Solanum melongena
  Horticulture Research Center, Bangladesh Agricultural Research Institute, Gazipur-1701, Bangladesh
  
  
  Crop-Soil-Water Management
  Brinjal

To determine the Optimization of Somatic Embryogenesis Protocol for Locally Adapted Eggplant (Solanum melongena L.) Varieties in Bangladesh.

Seeds of four eggplant varieties BARI Begun-1, BARI Begun-4, BARI Begun-5,  BARI  Begun-6  and  an  elite  local  cultivar  Islampuri  were  collected  from  the  Horticulture  Research  Center,  Bangladesh  Agricultural  Research  Institute,  Gazipur-1701. Seeds were first dipped into 100% ethanol for 20-30 seconds  followed by 4 washings with sterile distilled water. After that Tween 20 (3-5  drops) were added in 100 ml 2% sodium hypochlorite solution (40% Clorox).   Seeds were dipped in a 50 ml conical flask containing the prepared solution for  20 minutes with frequent shaking followed by 4 washings with sterile distilled  water. Finally, 25 - 30 seeds were inoculated in each small jar containing 30 ml  agar solidified half strength of MS with 3% sucrose for supporting seedling  development and kept in dark for 8 - 10 days at 25°C and 60 - 70% relative  humidity.    Hypocotyl  segments  of  8  - 10  day old  in vitro  grown  seedlings  of  aforementioned eggplant cultivars were used as explants. About 5 mm long  segments taken from the apical portion of the hypocotyl were inoculated on  culture media (Muktadir 2008) prepared as per treatment combinations. Culture  conditions were maintained by keeping the cultures in dark for five weeks then  transferred to light. Temperature was set at 25ºC with a light illumination of 2000-3000 lux from fluorescent lamps maintained  under the photoperiod of (16L/8D) and at 60- 70% relative humidity.   Initially the cultivars were evaluated for embryogenic response on medium  supplemented with 0.5 mg/l 2,4-D. Three replicates and 12 explants per replicate  had been used. Fifty embryos per replicate were used for embryo germination  and  plantlet  development.  Later,  two  best  performing  varieties  were  tested  against four different concentrations (0.5, 1.0, 1.5 and 2.0 mg/l) of 2,4-D along  with a control following the same methodology mentioned previously. The experiment was laid out in single factor CRD with three replications and  results  were  analyzed  by  using  MSTAT-C  program.  Differences  among  the  means were compared following DMRT test at 5% level of significance. 

  Plant Tissue Cult. & Biotech. 26(1): 77-83, 2016 (June).
  
Funding Source:
1.   Budget:  
  

Percentage of in vitro embryo germination derived from different treatments  also showed significant differences. Germination was maximum from 1.0 mg/l  2,4-D  derived  embryos  for  both  the  varieties  which  indicated  statistical  superiority to rest of the treatments. In vitro germinated embryos were successfully  transferred  to  soil  in  pots  following  acclimated.  Ex  vitro  establishment was the best in plantlets derived from 0.5 mg/l 2,4-D treatment and  had no statistical difference with 1.0 mg/l 2,4-D derived plantlets. The interaction  of  genotype  and  growth  regulators  in  regeneration  either  organogenesis  or  somatic embryogenesis is a common phenomenon  and in the present work this influence was clearly manifested in different  phases of regeneration.

  Journal
  


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