Effect of Plant Growth Regulators on Somatic Embryogenesis and Plantlet Development of Turkey Berry (Solanum torvum SW)

In the present study it was reported on direct somatic embryogenesis and plant regeneration from cotyledon and leaf explants of Turkey berry/pea egg plant (Solanum torvum SW), a medicinally important plant. Somatic embryogenesis has several advantages over other routes of in vitro plant regeneration. Somatic embryogenesis was induced directly from cotyledon and leaf explants on MS medium fortified with BAP (0.5 mg/L)+NAA (0.5-6.0 mg/L). High percentage of somatic embryogenesis (90%), maximum number of somatic embryos formation (62±0.18) along with high percentage (76%) conversion of somatic embryos into bipolar embryos was observed on cotyledon explants in 0.5 mg/L BAP+2.5 mg/L NAA. At the same concentration of BAP (0.5 mg/L)+NAA (2.5 mg/L) also resulted on the maximum percentage of somatic embryogenesis (92%), the highest number of somatic embryos formation (88±0.15) and the highest percentage (76%) of somatic embryos conversion into bipolar embryos in leaf explants. A mixture of globular, heart and torpedo-shaped embryos were germinated on MS medium supplemented with 0.5 mg/L IAA+1.0-4.0 mg/L BAP. Maximum germination frequency (75±0.14) of somatic embryos and plantlet formation was found in 0.5 mg/L IAA+2.0 mg/L BAP, but they didn’t germinate on ½ MSO and MSO media. The survival rate of regenerated plants after field transfer was recorded to be 75%. These regenerated plants were found morphologically similar to donor plants. The present protocol can be used for conservation of the species and also for genetic transformation experiments in S. torvum.

Banana Cultivars Microshoot Induction and Plantlet Formation Using Cytokinin and Auxin

<p>Banana is a horticultural plant with very high potentials, which contains carbohydrates and vitamins that are useful in fulfilling people's food and nutritional needs. Hence, this study aims to produce superior banana seedlings and develop a protocol for their mass production using a plant <em>in vitro</em> culture technique. This was a two stage-experiment i.e. microshoot production and plantlet formation. The result showed that Gebyar cultivar produced more shoots than the Kepok Kuning<em> </em>cultivar, with an average of 4.25 microshoots explant^-1. However, Kepok Kuning produced more leaves than Gebyar,<em> </em>with an average of 4.64 leaves plantlet^-1. Banana shoots cultured on the media containing Indole-3-acetic acid (IAA) at a concentration of 2.5 µM produced the highest leaves number. Meanwhile, those cultured on the media containing 1-Naphthalenesacetic acid (NAA) at a concentration of 7.5 µM produced the highest roots number. A Murashige and Skoog (MS) medium supplemented with 6-Benzylaminopurine (BAP) up to 30 µM and the one supplemented with 7.5 μM of NAA are suitable for Kepok Kuning and Gebyar<em> </em>cultivars micropropagation with regard to microshoot induction and plantlet formation, respectively.</p>

Increasing the somatic embryogenesis frequency of Panax vietnamensis Ha et Grushv. by disinfection of leaf explant using nano silver and the addition of nano silver in culture medium

Somatic embryo is a developmental method for mass multiplication of valuable medicinal plants. In this study, leaf explants of Ngoc Linh ginseng were disinfected with nano silver at different concentrations and exposure times to eliminate infectious agents and induce embryogenic callus for the production of somatic embryos. The results show that the lowest contamination rate (20.00%) was observed when leaf explants were treated with 0.5 g/L nano silver for 15 minutes while the highest embryogenic callus induction rate (72.22%) and fresh weight (0.77 g) was determined at 0.2 g/L nano silver for 20 minutes. High frequency of somatic embryogenesis formation and germination were occurred on MS medium supplemented 1.0 mg/L 2,4-D; 0.5 mg/L NAA; 0.2 mg/L Kin and 1.6 mg/L nanosilver. After 8 weeks of culture, the number somatic embryos derived from nano silver treated-leaves was increased 2 times than non-treated explants. Addition of 1.0 mg/L NAA and 1.2 mg/L nano silver was showed the highest shoot and root length, root number, fresh and dry weight of plantlets. This research showed that pre-treatment and supplement of nano silver in culture medium is potentially useful for improving embryogenesis frequency, and plantlet formation of Ngoc Linh ginseng cultured in vitro.

Plant Regeneration via Somatic Embryogenesis in Solanum nigrum L. (Black nightshade) (Solanaceae)

Aim: To study the effect of various plant growth regulators (PGRs) for induction of somatic embryogenesis and plantlet formation from cotyledon and leaflet explants in S. nigrum (night shade) an important medicinal plant used in treatment of digestive problems and skin infections. Place and Duration of Study: Department of Biotechnology, Kakatiya university, Warangal. Telangana, India, 3 years. Methodology: Cotyledon (0.8 cm2) and leaflet explants (0.8-1.0 cm2) from 3 week and 4 week old were cultured on MS medium supplemented with 30 g/L sucrose along with different concentrations of 0.5 mg/L BAP+NAA (0.5 – 6.0 mg/L) . Results: Maximum percentage of somatic embryogenesis was observed in cotyledon(89%) and leaf (98%) explants on MS medium augmented with 0.5mg/L BAP in combination with 2.0 mg/L NAA whereas the highest number of somatic embryos per explant (86 ± 0.19) was formed in leaflet explant. Conclusion: Somatic embryogenesis was induced from both cotyledon and leaf explants. Since it is threatened and medicinally important species S. nigrum, the present protocol can be used for its conservation and genetic transformation experiments.

Effects of Leaf Age and Exogenous Hormones on Callus Initiation, Rooting Formation, Bud Germination, and Plantlet Formation in Chinese Fir Leaf Cuttings

To guide the cultivation of superior Chinese fir plantlets, we designed an L16(4)4 orthogonal experiment to determine how leaf age and exogenous hormones influence key growth processes in leaf cuttings. Hormone concentration and treatment duration significantly affected leaf cuttings in all three age categories; 6-benzylaminopurine (6-BA), 1-naphthaleneacetic acid (NAA), and treatment time exerted the strongest effects on callus initiation rates. Additionally, NAA had the largest effect on the rooting rate across all cuttings, and all three hormones significantly influenced the bud germination rate. Based on our experimental results, expected optimal treatments for callus initiation were 10 mg∙L−1 indole-3-butyric acid (IBA) for 10 min, 30 mg∙L−1 NAA for 15 min, and 10 mg∙L−1 NAA plus 30 mg∙L−1 IBA for 10 min. For the rooting rate, the expected optimal treatment was 50 mg∙L−1 NAA and 40 mg∙L−1 IBA for 5–20 min. Finally, for bud germination, optimal treatments were 20 min of immersion in water, 30 mg∙L−1 6-BA plus 50 mg∙L−1 NAA for 15 min, and 30 mg∙L−1 6-BA for 5 min. Plantlet formation only occurred in the <one-year-old leaves, and at very low rates (maximum 5.8%); this outcome is likely attributable to the mother plant’s relatively old age (five years). Plantlet formation from cuttings is dependent on ensuring the rooting rate after callus initiation. Therefore, to promote rooting rates and bud germination, we recommend leaving more xylem at the base of leaf cuttings.

Optimized in vitro plant regeneration of the biodiesel plant Jatropha curcas L.: the effects of using seeds at different stages of maturity as starting materials

<em>Jatropha curcas</em> L. is an important biofuel plant that can be regenerated <em>in</em> <em>vitro</em> using seeds. The fruits of <em>J. curcas</em> do not reach maturity at the same time although they are on the same bunch. This study was undertaken to evaluate the effect of seeds, from fruits at different stages of maturity, on <em>in</em> <em>vitro</em> plantlet formation. Callus was induced on Murashige and Skoog medium using different concentrations of 2,4 dichlorophenoxyacetic acid (2,4-D) and 6 benzylaminopurine (BAP). 2,4D at a concentration of 3.0 mg/L and BAP at 1.0 mg/L were found to be optimum for callus formation. <em>In vitro</em> plantlets obtained on BAP were smaller with thicker hypocotyl and thicker roots. On the other hand, seeds from mature fruits gave better results for <em>in</em> <em>vitro</em> plantlet regeneration on 1.0 mg/L BAP without any rooting medium. A combination of sand and soil were used for acclimatization. Best results were obtained when sand and soil were used in equal amounts. Results also showed that seed maturity is an important factor for <em>in vitro</em> plant regeneration of<em> J. curcas</em> and that root formation <em>in vitro</em> does not require additional plant growth regulator substance.