In this study,the seeds of wild Petunia Juss.were used as explants to investigate the optimal condition for tissue culture.Several different kinds and concentrations of growth regulators were adopted to produce more m...In this study,the seeds of wild Petunia Juss.were used as explants to investigate the optimal condition for tissue culture.Several different kinds and concentrations of growth regulators were adopted to produce more multiple bud clumps,callus or roots in this study.The experiments may provide experimental foundation for the rapid propagation technology and establishment of tissue culture system for wild Petunia Juss.展开更多
The effects of sterilization pretreatment, sampling time and growth regulators on callus formation, explant contamination and adventitious bud induction from stems of balsam pear （Momordica charantia L.） were invest...The effects of sterilization pretreatment, sampling time and growth regulators on callus formation, explant contamination and adventitious bud induction from stems of balsam pear （Momordica charantia L.） were investigated. Sterilized for 6 rain with 0.1% （w/v） mercuric chloride solution is an essential sterilization method for stems. June and July proved to be better for material taking, followed by May. The callus formation rate of balsam pears reached the highest when medium added with IBA 1.0mg/L and BA 2.0 mg/L, while the optimum medium for adventitious bud induction was MS added with IBA 0.5mg/L and BA 4.0 mg/L. And it will provide theoretical and technical basis for rapid propagation and breeding.展开更多
In an attempt to propagate and conserve the rare, showy bulbous plants of Iris bismarckiana, newly recorded to the flora of Jordan and to contribute to the conservation the wild lris species in Jordan, a simple rapid,...In an attempt to propagate and conserve the rare, showy bulbous plants of Iris bismarckiana, newly recorded to the flora of Jordan and to contribute to the conservation the wild lris species in Jordan, a simple rapid, time consuming protocol has been developed using plant regeneration via somatic embryogenesis. Somatic embryogenesis was induced in zygotic embryo culture on Murashige and Skoog （MS） medium supplemented with 2,4-dichlorophenoxy acetic acid （8 mg/L） as the sole plant growth regulator, where both embryogenesis calli and somatic embryos were induced. Separation of embryos from embryo clusters was necessary to enhance the frequency of germination. Germination was stimulated by separation of embryos successfully from embryo clusters and transferred onto fresh MS medium. Data obtained were analyzed as a complete random design with three replications. Calli fragments that were transferred to embryogenesis induction medium （EIM） produced white embryo-like globular structures within two weeks. Within three more weeks, clusters of structures at various stages of development could be found on the same callus. The applied technique is rewarding and encouraging for further research on the endangered wild species of Iris in Jordan.展开更多
The balsum pear （Momordica charantia L. ） anthers in the monokaryotic stage of microspore development were cultured in this experiment. Different Plant growth regulators＇ combinations, base media and carbon sources...The balsum pear （Momordica charantia L. ） anthers in the monokaryotic stage of microspore development were cultured in this experiment. Different Plant growth regulators＇ combinations, base media and carbon sources were studied for callus formation and organ differentiation from balsum pear anthers. The result showed that the best media for callus inducement was： MS＋BA 0.5 mg/L＋NAA 0.2 mg/L＋ 2, 4-D 0.5 mg/L＋KT 2.0 mg/L, with 3% sugar and 0.8% agar. The best media to induce roots from balsum pear anther callus was： MS＋NAA 0.05 rag/L＋ KT 0.5 rag/L, with 3% sugar and 0.8% agar. Most of adventitious roots from callus were triploid（2N=3X=33）展开更多
The study was carried out to induce variations and stimulate callus induction, plant regeneration from different explants of two tomato （Lycopersicon esculentum Mill.） cultivars Trescantos and super Regina by using ...The study was carried out to induce variations and stimulate callus induction, plant regeneration from different explants of two tomato （Lycopersicon esculentum Mill.） cultivars Trescantos and super Regina by using tissue culture technique and Sodium azide as a chemical mutagens at concentrations （0.0, 2.0 and 4.0） mM under salinity stress condition at the levels（3.0, 6.0 and 9.0） dS/m. Different plant growth regulators were tested for their potentials in callus induction. The results revealed that treated seeds with SA （sodium azide） at concentration （2.0） mM increased seed germination percentage, seedling height and root length as compare to control treatment. While （4.0） mM concentration cause a reduction in all parameters mentioned above. Concerning to callus induction both cultivars showed a different response against different tested media with varying concentrations of plant growth regulators and despite their variable response to all tested media a combination of （2.0） mg from Kinetin （KIN） and lndol acetic acid （IAA） was found to be the most effective as compare to other treatments. Moreover, when callus transferred to a stressed media the variation was observed in explants fresh weight, and high reduction with the increment of salt level were recorded. Similarly the regeneration efficiency from stressed callus were observed at the level 3.0 and 6.0 dS/m while 9.0 dS/m the callus failed to regenerate plants for all three explants of both tomato cultivars.展开更多
基金Supported by Talent Introduction Project of Anhui Science and Technology University(ZRC2007147)General Project of Natural Scientific Research from Education Department of Anhui Province(KJ2010B052,KJ2010B294)
文摘In this study,the seeds of wild Petunia Juss.were used as explants to investigate the optimal condition for tissue culture.Several different kinds and concentrations of growth regulators were adopted to produce more multiple bud clumps,callus or roots in this study.The experiments may provide experimental foundation for the rapid propagation technology and establishment of tissue culture system for wild Petunia Juss.
文摘The effects of sterilization pretreatment, sampling time and growth regulators on callus formation, explant contamination and adventitious bud induction from stems of balsam pear （Momordica charantia L.） were investigated. Sterilized for 6 rain with 0.1% （w/v） mercuric chloride solution is an essential sterilization method for stems. June and July proved to be better for material taking, followed by May. The callus formation rate of balsam pears reached the highest when medium added with IBA 1.0mg/L and BA 2.0 mg/L, while the optimum medium for adventitious bud induction was MS added with IBA 0.5mg/L and BA 4.0 mg/L. And it will provide theoretical and technical basis for rapid propagation and breeding.
文摘In an attempt to propagate and conserve the rare, showy bulbous plants of Iris bismarckiana, newly recorded to the flora of Jordan and to contribute to the conservation the wild lris species in Jordan, a simple rapid, time consuming protocol has been developed using plant regeneration via somatic embryogenesis. Somatic embryogenesis was induced in zygotic embryo culture on Murashige and Skoog （MS） medium supplemented with 2,4-dichlorophenoxy acetic acid （8 mg/L） as the sole plant growth regulator, where both embryogenesis calli and somatic embryos were induced. Separation of embryos from embryo clusters was necessary to enhance the frequency of germination. Germination was stimulated by separation of embryos successfully from embryo clusters and transferred onto fresh MS medium. Data obtained were analyzed as a complete random design with three replications. Calli fragments that were transferred to embryogenesis induction medium （EIM） produced white embryo-like globular structures within two weeks. Within three more weeks, clusters of structures at various stages of development could be found on the same callus. The applied technique is rewarding and encouraging for further research on the endangered wild species of Iris in Jordan.
基金The authors would like to thank Dr. WANG Xiao-rong and DENG Qun-xian for their help in the tests. This study was supported by the Education Bureau Science Foundation of Sichuan Province （No. 2005A003） and the Sichuan Agricultural University Science Foundation （No. 3305）.
文摘The balsum pear （Momordica charantia L. ） anthers in the monokaryotic stage of microspore development were cultured in this experiment. Different Plant growth regulators＇ combinations, base media and carbon sources were studied for callus formation and organ differentiation from balsum pear anthers. The result showed that the best media for callus inducement was： MS＋BA 0.5 mg/L＋NAA 0.2 mg/L＋ 2, 4-D 0.5 mg/L＋KT 2.0 mg/L, with 3% sugar and 0.8% agar. The best media to induce roots from balsum pear anther callus was： MS＋NAA 0.05 rag/L＋ KT 0.5 rag/L, with 3% sugar and 0.8% agar. Most of adventitious roots from callus were triploid（2N=3X=33）
文摘The study was carried out to induce variations and stimulate callus induction, plant regeneration from different explants of two tomato （Lycopersicon esculentum Mill.） cultivars Trescantos and super Regina by using tissue culture technique and Sodium azide as a chemical mutagens at concentrations （0.0, 2.0 and 4.0） mM under salinity stress condition at the levels（3.0, 6.0 and 9.0） dS/m. Different plant growth regulators were tested for their potentials in callus induction. The results revealed that treated seeds with SA （sodium azide） at concentration （2.0） mM increased seed germination percentage, seedling height and root length as compare to control treatment. While （4.0） mM concentration cause a reduction in all parameters mentioned above. Concerning to callus induction both cultivars showed a different response against different tested media with varying concentrations of plant growth regulators and despite their variable response to all tested media a combination of （2.0） mg from Kinetin （KIN） and lndol acetic acid （IAA） was found to be the most effective as compare to other treatments. Moreover, when callus transferred to a stressed media the variation was observed in explants fresh weight, and high reduction with the increment of salt level were recorded. Similarly the regeneration efficiency from stressed callus were observed at the level 3.0 and 6.0 dS/m while 9.0 dS/m the callus failed to regenerate plants for all three explants of both tomato cultivars.
