Induction of Somatic Embryogenesis in Jatropha curcas

Author(s):  
Rosa M. Galaz-Ávalos ◽  
Heydi G. Martínez-Sánchez ◽  
Víctor M. Loyola-Vargas
2014 ◽  
Vol 35 (3se) ◽  
Author(s):  
Do Dang Giap ◽  
Nguyen Thi Kim Loan ◽  
Tran Trong Tuan ◽  
Le Thanh Tuan ◽  
Huynh Le Thien Tu ◽  
...  

2014 ◽  
Vol 47 ◽  
pp. 21-28 ◽  
Author(s):  
Anggi Nindita ◽  
Bambang Sapta Purwoko ◽  
Darda Efendi ◽  
Iswari S. Dewi

2018 ◽  
Vol 14 (4) ◽  
pp. 661-671
Author(s):  
Nguyen Thi Kim Loan ◽  
Do Dang Giap ◽  
Tran Trong Tuan ◽  
Nguyen Thi Thanh Hien ◽  
Nguyen Phuc Huy ◽  
...  

An efficient method for plant regeneration in Jatropha curcas L. via primary and secondary somatic embryogenesis culture from ex vitro leaves of 6-month-old plants was presented in this study. Leaves were cut into transverse thin cell layers (tTCLs) and cultured on MS medium supplemented with kinetin (KIN) at 0.5, 1.0, 1.5, and 2.0 mg/l in combination with indole-3-butyric acid (IBA) at 0.1, 0.5, and 1.0 mg/l or 2,4-dichlorophenoxyacetic acid (2,4-D) at 1.0, 1.5 and 2.0 mg/l . The highest embryogenic callus formation rate (89.3%) was obtained on medium supplemented with 1.0 mg/l KIN and 1.5 mg/l 2,4-D. The calli were selected for the study of primary somatic embryogenesis on MS medium containing 2,4-D (0.01, 0.03, 0.05, and 0.07 mg/l) or KIN (0.5, 1.0, 1.5, and 2.0 mg/l). The highest primary somatic embryos formation rate (76.67%) was achieved on MS medium supplemented with 1.0 mg/l KIN. The primary embryos were cultured on medium supplemented with KIN (0.1, 0.5, 1.0, 1.5, and 2.0 mg/l) combined with 0.2 mg/l indole-3-butyric acid (IBA) or 0.05 mg/l 2,4-D. The combination of 1.5 mg/l KIN and 0.05 mg/l 2,4-D was suitable for secondary embryos formation. Embryos proliferated rapidly, and the highest number of secondary embryos (77.5 embryos) wasobtained from a single primary embryos inoculated. Results also showed that the addition of proline (0.75 g/l) or spermidine (0.15 mM) to the culture medium increased the number of secondary embryos considerably. The fully developed plantlets exhibiting healthy roots and shoots were obtained when somatic embryos were sub-cultured onto B5 medium containing 1.5 mg/l IBA.


Author(s):  
Rupesh Kumar Singh ◽  
Eliel Ruiz-May ◽  
Luz María García-Pérez ◽  
Francisco R. Quiroz-Figueroa

GM Crops ◽  
2011 ◽  
Vol 2 (2) ◽  
pp. 110-117 ◽  
Author(s):  
Lin Cai ◽  
Lin Fu ◽  
Lianghui Ji

2007 ◽  
Vol 1 (3) ◽  
pp. 135-140 ◽  
Author(s):  
Timir baran Jha ◽  
Priyanka Mukherjee ◽  
Mukul Manjari Datta

2016 ◽  
Vol 4 (2) ◽  
pp. 76
Author(s):  
Tantri Dyah Ayu Anggraeni ◽  
Emy Sulistyowati ◽  
Rully Dyah Purwati

<p>Jarak pagar (Jatropha curcas L.) merupakan tanaman penghasil minyak nabati sebagai bahan baku bio-diesel. Selama ini, kebutuhan bahan tanam diperoleh dari benih dan setek. Teknik mikropropagasi khususnya melalui embriogenesis somatik merupakan alternatif untuk penyediaan bahan tanam dalam jumlah besar dengan waktu relatif lebih singkat. Jenis eksplan, genotipe, dan kondisi fisiologis tanaman donor serta jenis dan kondisi fisik mediummerupakan faktor utama yang mempengaruhi keberhasilan embriogenesis somatik. Penelitian ini dilakukan untuk mengetahui eksplan dan komposisi media yang tepat untuk induksi kalus embriogenesis somatik, perkecambahan embrio somatik dan pertumbuhan tunas hasil embriogenesis somatik. Penelitian dilaksanakan di laboratorium Kultur Jaringan, Balai Penelitian Tanaman Pemanis dan Serat mulai bulan April sampai dengan November 2011, meliputi tiga tahap, yaitu 1) menguji komposisi media untuk induksi kalus embriogenesis somatik antara lain M1=MS+0,5 mg/l BAP+0,5 mg 2,4 D; M2= MS+1 mg/l BAP +0,5 mg/l 2,4 D; M3= MS+0,5 mg/l BAP+0,2 mg/l TDZ, dan M4= MS+1 mg/l BAP+0,2 mg/l TDZ; 2) menguji komposisi media untuk induksi perkecambahan embrio somatik antara lain MK1= MS+0,5 mg/l BAP+0,1 mg/l NAA dan MK2= MS+0,5 mg/l BAP+0,4 mg/l IBA; dan 3) menguji komposisi media untuk pertumbuhan tunas embrio somatik antara lain MP1= MS+0,5 mg/l BAP+0,1 mg/l IBA dan MP2= MS+0,5 mg/l BAP+0,1 mg/l IAA. Bahan tanam yang digunakan adalah genotipe IP-3A dan IP-3M dengan sumber eksplan kotiledon dan daun. Hasil penelitian menunjukkan kombinasi MS+0,5 mg/l BAP+0,2 mg/l TDZ dengan sumber eksplan kotiledon paling sesuai untuk induksi kalus embriogenesis somatik. Genotipe IP-3M memiliki respon yang lebih baik disbanding IP-3A dan stabil dari tahap induksi kalus embriogenis somatik, induksi perkecambahan embrio somatik, dan pertumbuhan tunas embrio somatik.</p><p> </p><p>Jatropha (Jatropha curcas L.) is an oil producing plants as source of bio-diesel. Planting materials usually are obtained from seeds and stem-cuttings. Micro-propagation techniques especially through somatic embryo-genesis is an alternative to provide a large number of planting material in a relatively short time. Explant sources, genotype and physicological conditions of donor plants, also composition and physical condition of medium are the main factors affecting the successful of somatic embryogenesis. The study was conducted to determine the most suitable combination of explant and media composition for embryogenic calli induc-tion, somatic embryo germination, and shoots growth derived from somatic embryogenesis. The experiment was conducted in the Tissue Culture Laboratory, of Indonesian Sweetener and Fiber Crops Research Insti-tute from April to November 2011 covering three phases: 1) testing media composition to induce somatic embryogenic calli i.e. M1=MS+0.5 mg/l BAP+0.5 mg 2.4 D; M2 = MS+1 mg/l BAP+0.5 mg/l 2.4 D; M3 = MS+0.5 mg/l BAP+0.2 mg/l TDZ and M4 = MS+1 mg/l BAP+ 0.2 mg/l TDZ; 2) testing media composition to induce somatic embryo germination i.e. MK1 = MS+0.5 mg/l BAP+0.1 mg/l NAA and MK2 = MS+0.5 mg/l BAP+0.4 mg/l IBA; and 3) testing media composition to induce somatic embryo shoot growth i.e. MP1 = MS+0.5 mg/l BAP+0.1 mg/l IBA and MP2= MS+0.5 mg/l BAP+0.1 mg/l IAA. Plant material used are genotype IP-3A and IP-3M with cotyledone and leaf as explant sources. The results showed that combination of MS+0.5 mg/l BAP+0.2 mg/l TDZ and cotyledons as explants source is the most suitable for somatic embryogenic calli. IP-3M genotype showed a better response to IP-3A and stable from induction of somatic embryogenic calli, somatic embryo germination, and somatic embryo shoots growth.</p>


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