جستجوی مقالات مرتبط با کلیدواژه « shoot regeneration » در نشریات گروه « زراعت »

Crocus flower, which belongs to Iridaceae family, is one of the most important ornamental bulbous plants. The propagation of Crocus vernus L. by corm is not commercially affordable due to transmission of fungal and bacterial diseases as well as the long dormancy period which takes 4 to 5 months. Thus, in vitro culture of Crocus vernus is a suitable solution for commercial reproduction. Plant tissue culture technique would be a better alternative for improving quality and production.

In order to micropropagate ornamental saffron, the effect of different culture media on direct organogenesis experiment was conducted in factorial arrangement in a completely randomized design with 3 replications in the tissue culture lab of the Department of Horticulture at Agricultural Sciences and Natural Resources University of Khuzestan from 2015 to 2016. The explants used in this experiment were latheral and terminal buds which were evaluated in 10 hormons treatments and control in the Murashige and Skoog medium (MS). To eliminate surface contamination, the explants were first immersed under water for 30 minutes after placing the corms. Next, they were placed in high temperature Benlate fungicide solution (55° C) for 30 minutes. Then, they were put in 70% ethanol (ethyl alcohol) for 30 seconds and 15% Sodium hypochlorite solution for 6 minutes. The explants were finally washed three times with sterile distilled water under the air flow bench. The effects of plant growth regulators including BAP (0.5, 1.0, 2.0 mg/l), TDZ (0.5, 0.75, 1.0 mg/l), Kin (0.5, 1.0, 2.0 mg/l) and 0.1mg/l IBA in direct regeneration were investigated.

The results showed that the kind of plant growth regulators (PGR) and the explant type are very important in regeneration of Crocus vernus so that we can not secure any shoots without PGR. In direct organogenesis experiment, the maximum number of multiple shoots (15.84) was obtained from apical bud explant in MS medium supplemented with 5/0 mg/l TDZ along with 5/0 mg/l BAP, 5/0 mg/l KIN and 1/0 mg/l IBA, after 10 weeks, that had a significant difference with other treatments at 1% Duncan test. We observed 2.o mg/l BAP along with 1/0 mg/l IBA had the greatest effect on the number of corms.

The results showed the shoot regeneration is controlled by the ratio of cytokinin with auxin. It should be mentioned that cytokinin plays a role in the synthesis of RNA, stimulation of the production of protein, and the activity of some enzymes. The results also indicated that the use of cytokinin along with auxin has a beneficial effect on shoot regeneration.

Daenensis thyme (Thymus daenensis Celak) is one of the important medicinal plant that belongs to the family Labiatae. The leaves and flowering branches of this plant has a number of important compounds such as Thymol, Carvacrol, Btaptyn and Parasymyn. The present study was performed in order to determine the optimum of plant growth regulators (auxin and cytokinin) for production of in vitro plantlet using apical bud and hypocotyl explants. The seeds after sterilization were germinated on MS medium. The explants were cultured on the medium containing various concentrations of BAP and Kin for study of in vitro micropropagation. Hypocotyl explants were cultured on the medium containing various combinations of BAP and NAA for callus induction and shoot regeneration. In study of micropropagation, the mean comparison showed the highest number of shoot, leaf and bud obtained in MS medium containing 2.5 mg l-1 Kin in the apical explants. In study of regeneration, the mean comparison showed the highest percentage of shoot regeneration and mean of shoot number were obtained on MS medium supplemented with 1.5 mg l-1 BAP + 0.6 mg l-1 NAA in hypocotyl explants. Overall, Kin was most effective plant growth regulator on micropropagation and comination of BAP and NAA had most effect on regeneration of Daenensis thyme.

Anthemis hyalina DC. is one of the most important herbal medicine plants and is used for anti-allergy and curing skin rashes or acne. To date there is no report for in vitro culture of this species and the present study was performed for the first time with the aim of obtaining the optimized treatment for shoot regeneration. In this research the effect of different plant growth regulators NAA (0, 0.1, 0.5, 1.5 mg L-1) and BA (0, 1, 3 mg L-1) on callus induction and shoot regeneration in leaf and immature embryo explants was investigated. This experiment has been carried out as factorial in a completely randomized design with four replications. The results showed the significant effects of all main factors and interactions on measured traits in 0.01 probability level. The highest frequency of shoot regeneration for leaf explant was observed on the medium containing 1 mg L-1 BA. In embryo explant the best treatment for shoot regeneration was 3 mg L-1 BA.

One of the major advantages of in vitro culture of African violet (Saintpaulha ionantha) is production of new cultivars and propagation of their chimera which might not be propagated by the other methods. In this study, we tested the effects of silver nanoparticles on the sterilization rate (antifungal and antibacterial activity), regeneration and shoot formation of African violet "Pink Amiss" explants. These nanoparticles were synthesized from pomegranate peels and Damask rose petals extracts. We used a completely randomized design test with factorial arrangement to investigate various volumetric ratios of plant extracts to silver nitrate (1:20, 1:10, 1:5 and 1:1) on the culture contaminations. Using silver nanoparticles synthesized by the plant extracts, especially Damask rose petals extract resulted in no fungal and bacterial contamination in the African violet explants after 1 and 3 weeks as compared to the control, and silver nitrate (1mM). All tested concentrations of the silver nanoparticles significantly (P ≤ 0.05) controlled both bacterial and fungal contaminations. The 1:20 ratio of plant extracts to silver nitrate showed the best control. In addition, the highest regeneration (%52) and shoot regeneration (%38) was observed in this treatment. In conclusion, we suggest using silver nanoparticles synthesized by plant extracts for sterilization of in Vitro Culture for African Violet rather than using other chemicals such as silver nitrate.

Ocimum basilicum L. (sweet basil), from Lamiaceae family, is rich in aromatic essential oils and valuable in industry for its pharmaceutical, aromatic properties. The present study has focused on tissue culture of O. basilicum using leaf explants from in vitro germinated plants. The current study has been fulfilled based on completely randomized design with 5 replications using MS (Murashige and Skoog) medium with different concentrations of BAP (0, 1 mgl-1) and 2,4-D (0,0.5,1mgl-1). After callus formation the calluses were transferred on new MS media with (1, 3 & 5 mgl-1) BAP in combination with 0.2 mgl-1 NAA, for regeneration. The highest average number of shoots occurred in the medium containing 1 mgl-1 BAP and 0.2 mg-1 NAA. The presence of NAA inhibited root formation, when combined with different concentrations of BAP.