Plant Productions

Micropropagation of Polianthes tuberosa L. Through Direct Organogenesis

Mohammad Hosein Daneshvar; Mehri Havil; Amin Lotfi Jalal Abadi

Volume 45, Issue 2 , September 2022, , Pages 277-286

https://doi.org/10.22055/ppd.2022.36928.1973

Abstract

IntroductionPolianthes tuberosa L. is one of the most important ornamental bulbous plants in tropical and subtropical regions that is cultivating in some regions of Iran. Due to the ... Read More IntroductionPolianthes tuberosa L. is one of the most important ornamental bulbous plants in tropical and subtropical regions that is cultivating in some regions of Iran. Due to the transmission of fungal and bacterial diseases, propagation by bulbs is not affordable. Tissue culture is a good way to produce uniform and disease-free seedling. Therefore, in vitro cultivation of tuberose is a suitable solution to commercial reproduction. Materials and MethodsTo investigate the best method of micropropagation of Polianthes tuberosa, this study was conducted in three experiments (proliferation, root formation and adaptation). The explants used in this study were lateral buds. Ethyl alcohol (70%) and dilute laundry bleach (5.25% active chlorine), benomyl fungicide and dishwashing liquid were used to eliminate surface contamination of the explants. In the first experiment, the effect of different plant growth regulators and MS medium (MS, ½ MS, ¼ MS) on shoot formation of lateral bud was investigated. Lateral bud explants were cultured in MS medium with various plant growth regulators including KIN (0.25, 0.5, 0.1, 0.2 and 0.4 mg / L), BAP (0.25 (0.5, 0.1 and 2.0 mg / l) and then the length and number of shoots were evaluated. After forming shoots in the propagation medium, they were transferred to a new environment to form roots.The root formation experiment included tree levels of NAA concentrations, (0.5, 0.75 and 1 mg/L) in combination with 0.2 mg/L IBA and control (without growth regulator). Adaptation experiment with 5 Substrate of bed including Peat Moss, Cocopeat, Sand, Peat Moss with Cocopeat (1: 1) and Sand with Cocopeat and Peat Moss (1: 1: 1) was conducted. Results and DiscussionThe results showed that there was a significant difference between various types of plant growth regulators (PGR) and MS culture media at different concentrations and no branch was produced without the use of PGR. In shoot prolifferation experiment, the maximum number of shoots (4.8) was obtained from lateral bud explants in MS medium with 0.25 mg / l BAP in combination with 0.25 mg / l KIN. The highest length of lateral shoot shoots (3.75 cm) was observed in MS medium with 0.25 mg / l KIN in combination with 0.25 mg / l BAP.The results of root formation experiment showed that the highest number of roots was observed in MS medium containing 0.5 mg / l NAA and 0.2 mg / l IBA and the lowest number of roots in control (without plant growth regulator). Treatment of 0.5 mg / l NAA with 0.2 mg / l IBA had the highest root length (1.22 cm). The lowest root length was also observed in the control (without plant growth regulator). In the adaptation test, no significant difference was observed between treatments in survival rate. ConclusionThe results of this study showed that the shoot organogenesis is controlled by the cytokinin with MS medium in different concentrations. It should be mentioned that cytokinin had an important role in the synthesis of RNA, stimulation of the production of protein and the activity of some enzymes. Also, the results showed that the use of cytokinin alone has a beneficial effect on shoot organogenesis.

Microtuberization Efficiency of Three Potato (Solanum tuberosum L.) Cultivars under Osmotic Stress in vitro

Banafsheh Jamshidi; Marzieh Ghanbari Jahromi; Amir Mousavi

Volume 45, Issue 1 , May 2022, , Pages 109-122

https://doi.org/10.22055/ppd.2020.30032.1782

Abstract

IntroductionPotato (Solanum tuberosum L.) is one of the most important crops worldwide. It is vegetatively propagated using pieces or whole potato tubers, but a virus infection causes ... Read More IntroductionPotato (Solanum tuberosum L.) is one of the most important crops worldwide. It is vegetatively propagated using pieces or whole potato tubers, but a virus infection causes crop reduction to almost a half or even one third, which varies from place to place and from season to another. Micropropagation is the practice of rapidly multiplying stock plant material to produce many progeny plants, using modern plant tissue culture methods. Microtuberization in potato needs the right interaction between several factors such as cyto, sucrose and osmotic stress. The purpose of present study was to investigate microtuberization efficiency of three potato cultivars under osmotic stress and in vitro conditions. Materials and MethodsThis experiment was carried out based on completely randomized design (CRD) in three replications. Potato seeds of three cultivars (Agria, Savalan and HPS-II/67) were cultured on Murashige and Skoog (MS) medium. After proliferation, plantlets were transferred to the media containing nine treatments with polyethylene glycol hydrogel (PEG) at four levels (0.003, 0.006, 0.009, 0.012 M), sorbitol at four levels (0.1, 0.2, 0.3, and 0.4 M). For this purpose, potato quality, microtuberization percentage, proline concentration, chlorophyll content, and Catalase (CAT) and superoxide dismutase (SOD) activities were measured. Results and DiscussionThe results showed that plantlets grown under non-stressed conditions (control) possessed higher rates of leaf number, new shoot length and proliferation index compared to the under stressed conditions. Agria cultivar presented better growth characteristics under stressed conditions compared to other experimental cultivars. The highest potato destruction was observed at 0.012 M PEG in Savalan cultivar followed by 0.4 M sorbitol in all cultivars. Microtuberization percentage increased in all three cultivars by stress conditions, in which it increased with progressing in stress levels. The greatest percentage of microtuberization was obtained from Agria cultivar at 0.003 M PEG. Compared to the control, proline concentration, and also CAT and SOD activities increased under stress conditions. Moreover, total chlorophyll content decreased under the stress conditions in comparison to the control. Generally, based on the results, maximum rates of microtuberization and viability were observed in Agria followed by HPS-II/67, and the highest microtuber weight was obtained in HPS-II/67 cultivar. When plants are faced to stress conditions like osmotic stress, free radicals such as reactive oxygen species (ROS) increases. On the other hand, plants use different strategies to scavenge the generated ROS. The reduction of chlorophyll content and increases of antioxidant enzyme activities are due to increase of ROS under osmotic stress conditions. ConclusionAt slight stress conditions, potato plants utilize the strategy to generate more tuber. Therefore, the lower concentrations of PEG can be introduced as a stimulator of microtuber.

Effect of hormonal compositions on micropropagation of fifteen cultivars of Gerbera (Gerbera jamesonii Bolus ex Hooker f.)

M. Kharrazi; A. Sharifi; F. Keykha Akhar; A. Bagheri; Y. M. Moradian

Volume 40, Issue 4 , March 2018, , Pages 91-102

https://doi.org/10.22055/ppd.2018.13443

Abstract

Background and objectives Gerbera is one of the most important ornamental plants that used as cut flower and potted plant. The common methods of propagation does not have performance ... Read More Background and objectives Gerbera is one of the most important ornamental plants that used as cut flower and potted plant. The common methods of propagation does not have performance for supplying the global demand of this ornamental plant. So the most common method for commercial propagation of gerbera is micropropagation. Material and methods In this study, effect of different hormonal treatments and cultivars on micropropagation and rooting of gerbera shoot tip explant was evaluated. Shoot tip explants were first washed with running tap water for 30 min then they were surface sterilized by dipping in 1.5% sodium hypochlorite solution for 5 min and rinsed with sterile distilled water, followed by immersing in 0.1 % mercuric chloride solution for 5 min. After Sterilization with mercuric chloride solution, capitulum was washed with sterile distilled water. Subsequent washing was done with sterile distilled water three times. Sterilization with sodium hypochlorite solution and mercuric chloride and final rinse with sterile distilled water were done under laminar air flow hood. In the proliferation phase, MS medium containing 1 mg/l BA or KIN in combination with 0.1 mg/l IAA or hormone-free medium, 3% sucrose, 8 g/l agar was used. For rooting of propagated plantlets, ½ MS medium containing 1 mg/l IBA, IAA, 2IP or ½ MS hormone-free medium, 3% sucrose, 8 g/l agar was used. After 4 weeks different parameters such as number of plantlet, height of plantlet, number of main root, root length, number of secondary root were measured. Cultivars that was used in this experiment are as follows: 1: ‘Aventura’, 2: ‘Barones’, 3: ‘Mayfair’, 4: ‘Cacharelle’, 5: ‘Real’, 6: ‘Sorbet’, 7: ‘Dalma’, 8: ‘Goldy’, 9: ‘Panama’, 10: ‘Lancaster’, 11: ‘Dune’, 12: ‘Bellavue’, 13: ‘Blinddate’, 14: ‘Applause’, 15: ‘Sunway’. Results and discussion The results showed that in all studied cultivars, the medium containing BA lead to producing the highest number of plantlet. So using the medium containing BA in propagation phase is recommended for obtaining the highest number of plantlet. Also the results showed that the rooting of gerbera plantlets was affected by cultivar and suitable hormonal composition for rooting of each cultivar was different. However, the appropriate acclimation of produced plantlets is so important. Although the length and number of roots in ½ MS medium was at the average of other treatments, but propagated plantlets from this medium, had a suitable acclimation capacity. Moreover, additional cost for utilization of rooting hormones was reduced and therefore commercial production cost decreased. So application of this medium for rooting of different gerbera cultivars is recommended. Finally acclimation of rooted plantlet was done in cocopeat and perlite medium, with 95% success.

Utilization of Indirect Regeneration to Induce Micropropagation of Fritillaria imperialis L. on in vitro Culture

Mojtaba Rahimi; Mohammad Hosein Daneshvar

Volume 39, Issue 4 , March 2017, , Pages 31-42

https://doi.org/10.22055/ppd.2017.12066

Abstract

Background and Objectives Iran is home of one of the most delightful and graceful flower of Fritillaria in the world. Its habitation is commonly expanded on the vast areas: growing ... Read More Background and Objectives Iran is home of one of the most delightful and graceful flower of Fritillaria in the world. Its habitation is commonly expanded on the vast areas: growing in beds, borders, backgrounds and rock gardens. Besides, it is also suitable for naturalizing and excellent for cut flowers. Fritillaria imperialis as a medicinal plant has pharmaceutical purpose in which possesses a health beneficial essence that used in production of mucus and cough medicine. In addition, extractions of plant tissues contain certain of properties which affect to reduce blood pressure and blood sugar. Unfortunately, the habitation of this ornamental plant is under threat and majority of its habitation already being to ruin due to human activities and urbanization. The propagation of Fritillaria through offsets (bulblets) is prolonging approach which takes approximately 3-4 years. Whereas, using tissue culture technique for flower production is required less time probably within a few months and economically has a huge advantage due to low cost and a numerous plant production in a short time. Materials and methods This research was carried out in four experiments: callus formation, bulblet production, root formation and acclimatization. In the present study, a factorial experiment was assigned as completed randomized design (CRD) with three replications. In the first experiment, leaf primordia and scale explants were cultured on MS medium supplemented with different concentrations of NAA and IBA in order to produce callus formation. In the second experiment, the calli were cultured on organogenesis medium which were contained MS medium supplement, with kin. and TDZ, after 6 and 12 weeks. In the third experiment, the bulblets were transferred into rooting media, which were contained MS medium supplemented with different concentrations of NAA (0, 0.5, 1.0 and 2.0 mg/l). In the fourth experiment, after washing the bulblet whit warm distilled water (40ᵒC) that contain 2.0 mg/l benlate fungicide, they then were planted into the pots containing sterilized perlite, cocopeat and perlite along with cocopeat. Results In the first experiment, the results demonstrated that the highest weight of callus (3.29g) was sustained in scale explants on basal MS medium which was supplemented with 0.5mg/l NAA along with 0.5mg/l IBA. In second experiment, the result indicated that the numerous of bulblets were developed on MS medium supplemented with 0.5mg/l TDZ along with 0.5mg/l kin. Which of these, the callus scale were produced on MS medium supplemented with 0.5mg/l NAA. In the third experiment, in order to retain rooting the bulblets, they were cultured on MS medium supplemented with different concentration of NAA. The result elucidated that the large quantity of roots (7.7) were obtained from leaf primordia on MS medium supplemented with 1.0mg/l NAA. In the fourth experiment, rooted bulblets were washed with warm distilled water for 5-10min, and then they were transferred into pots with perlite, cocopeat and perlite + cocopeat. Discussion The results revealed information that the rooted bulblets from scale growing on cocopeat substrate had retained the most diameter (21.64mm) as compared to other treatments. The finding results under this investigation strongly suggested that using micropropagation it is definitely a possible trend to abolish the barriers which caused to deteriorate of Fritillaria imperiallis.

Investigation into micropropagation of Narcissus tazetta L. from leaf explant

N I; S K; S K

Volume 36, Issue 4 , March 2014, , Pages 15-28

Abstract

Narcissus tazetta is one of the most important ornamental bulbous species endemic to Iran. Micropropagation of Narcissus tazetta is an important method for rapid propagation and disease ... Read More

An Investigation in to Micropropagation and the Effect of Colchicine on In Vitro Ploidy Induction in Narcissus (Narcissus tazetta)

M. Ahmadi Majd; H. Sarikhani; M. Chaichi; A. Kashi

Volume 35, Issue 4 , March 2013, , Pages 93-103

Abstract

In this research, micropropagation of Narcissus tazetta was investigated by using bulb twin-scale explants using four different concentrations of BA (0, 0.5, 1 and 2 mg/l) and, therefore, ... Read More

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Keywords = micropropagation

Micropropagation of Polianthes tuberosa L. Through Direct Organogenesis

Abstract

Microtuberization Efficiency of Three Potato (Solanum tuberosum L.) Cultivars under Osmotic Stress in vitro

Abstract

Effect of hormonal compositions on micropropagation of fifteen cultivars of Gerbera (Gerbera jamesonii Bolus ex Hooker f.)

Abstract

Utilization of Indirect Regeneration to Induce Micropropagation of Fritillaria imperialis L. on in vitro Culture

Abstract

Investigation into micropropagation of Narcissus tazetta L. from leaf explant

Abstract

An Investigation in to Micropropagation and the Effect of Colchicine on In Vitro Ploidy Induction in Narcissus (Narcissus tazetta)

Abstract