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Somatic Embryogenesis (somatic + embryogenesi)
Selected AbstractsSomatic embryogenesis and multiple-shoot formation from seed-derived shoot apical meristems of rhodesgrass (Chloris gayana Kunth)GRASSLAND SCIENCE, Issue 3 2007Takahiro Gondo Abstract High-frequencies of somatic embryogenesis and multiple-shoot formation were achieved with seed-derived shoot apical meristems of rhodesgrass (Chloris gayana Kunth). Shoot apices as initial explants were isolated from aseptically germinated seedlings, and cultured in vitro. Embryogenic calli and the multiple shoots were induced and maintained on MS basal medium with various combinations of 2,4-dichlorophnoxyacetic acid (2,4-D) and 6-benzylaminopurine (BAP), the two most effective treatments being 2.0 mg L,1 2,4-D and 0.1 mg L,1 2,4-D + 2.0 mg L,1 BAP. These embryogenic calli and multiple-shoot formations could be used as alternative regenerable target tissues for genetic transformation using particle bombardment of rhodesgrass. [source] Predicting the regenerative capacity of conifer somatic embryogenic cultures by metabolomicsPLANT BIOTECHNOLOGY JOURNAL, Issue 9 2009Andrew R. Robinson Summary Somatic embryogenesis in gymnosperms is an effective approach to clonally propagating germplasm. However, embryogenic cultures frequently lose regenerative capacity. The interactions between metabolic composition, physiological state, genotype and embryogenic capacity in Pinus taeda (loblolly pine) somatic embryogenic cultures were explored using metabolomics. A stepwise modelling procedure, using the Bayesian information criterion, generated a 47 metabolite predictive model that could explain culture productivity. The model performed extremely well in cross-validation, achieving a correlation coefficient of 0.98 between actual and predicted mature embryo production. The metabolic composition and structure of the model implied that variation in culture regenerative capacity was closely linked to the physiological transition of cultures from the proliferation phase to the maturation phase of development. The propensity of cultures to advance into this transition appears to relate to nutrient uptake and allocation in vivo, and to be associated with the tolerance and response of cultures to stress, during the proliferation phase. [source] Stress-induced somatic embryogenesis in vegetative tissues of Arabidopsis thalianaTHE PLANT JOURNAL, Issue 1 2003Miho Ikeda-Iwai Summary Somatic embryogenesis is an obvious experimental evidence of totipotency, and is used as a model system for studying the mechanisms of de-differentiation and re-differentiation of plant cells. Although Arabidopsis is widely used as a model plant for genetic and molecular biological studies, there is no available tissue culture system for inducing somatic embryogenesis from somatic cells in this plant. We established a new tissue culture system using stress treatment to induce somatic embryogenesis in Arabidopsis. In this system, stress treatment induced formation of somatic embryos from shoot-apical-tip and floral-bud explants. The somatic embryos grew into young plantlets with normal morphology, including cotyledons, hypocotyls, and roots, and some embryo-specific genes (ABI3 and FUS3) were expressed in these embryos. Several stresses (osmotic, heavy metal ion, and dehydration stress) induced somatic embryogenesis, but the optimum stress treatment differed between different stressors. When we used mannitol to cause osmotic stress, the optimal conditions for somatic embryogenesis were 6,9 h of culture on solid B5 medium containing 0.7 m mannitol, after which the explants were transferred to B5 medium containing 2,4-dichlorophenoxyacetic acid (2,4-D, 4.5 µm), but no mannitol. Using this tissue culture system, we induced somatic embryogenesis in three major ecotypes of Arabidopsis thaliana, Ws, Col, and Ler. [source] The effect of genotype and culture medium on somatic embryogenesis and plant regeneration from mature embryos of fourteen apomictic cultivars of buffel grass (Cenchrus ciliaris L.)GRASS & FORAGE SCIENCE, Issue 1 2006E. L. Colomba Abstract Buffel grass (Cenchrus ciliaris L.) is an important apomictic grass used as forage for ruminant livestock. Biotechnological methods provide opportunities for producing new germplasm. Mature embryos of fourteen buffel grass apomictic cultivars (2n = 4x = 36) were used to induce embryogenic callus formation using a basal medium supplemented with 3% sucrose and with the testing of five concentrations of 2,4-dichlorophenoxyacetic acid (2,4-D) and four concentrations of 6-benzylaminopurine (BAP). The effects of cultivar and culture medium on callus induction and plant regeneration were evaluated. Significant differences were observed among the fourteen cultivars and the five concentrations of 2,4-D (P < 0·01). Values for embryogenic callus production varied from 0 to 86·7. Most cultivars showed the highest level of embryogenic callus production on the medium with the concentration of 3 mg L,1 2,4-D. The addition of different BAP concentrations in combination with 2,4-D in the medium inhibited embryogenic callus growth and did not permit plant regeneration. The data clearly demonstrated that the genotype and concentrations of 2,4-D had significant effects both on the frequency of embryonic callus formation from mature embryos and on the subsequent efficiency of plant regeneration of apomictic cultivars of buffel grass. Cultivars Biloela and Nunbank showed the greatest efficiency in in vitro culture response. [source] Optimization of culture conditions for plant regeneration of Panicum spp. through somatic embryogenesisGRASSLAND SCIENCE, Issue 1 2010Mi-Suk Seo Abstract We developed a rapid and efficient shoot regeneration system for Panicum spp. by adjusting the regeneration medium and studying the responses of different genotypes and the influence of explant types (mature seed, immature embryo and shoot apex). We used Panicum meyerianum (Nees) and Panicum longijubatum (Stapf) which were shown to perform well, to select the optimal medium for shoot regeneration. The highest frequency of shoot regeneration was obtained on Murashige and Skoog medium supplemented with 30 g L,1 maltose and 1 mg L,1 N-phenyl-N,-[(1,2,3-thidiazol-5-yl) urea]. The callus formed green spots after 1 week of culture and showed primary green shoots after 2 weeks. In this system, the calli derived from mature seed of nine Panicum genotypes showed large variation in shoot regeneration ability: from 0 to 69.9% in the frequency of shoot formation and from 0 to 8.4 in the number of shoots per callus. Guineagrass (Panicum maximum Jacq.) showed no ability and switchgrass (Panicum virgatum L.) showed low ability to regenerate from mature seed-derived calli; however, both were able to be regenerated from immature embryos and calli derived from shoot apices. We developed an efficient protocol for high shoot regeneration of various Panicum genotypes which provides a foundation for efficient tissue culture and genetic improvement of Panicum. [source] Somatic embryogenesis and multiple-shoot formation from seed-derived shoot apical meristems of rhodesgrass (Chloris gayana Kunth)GRASSLAND SCIENCE, Issue 3 2007Takahiro Gondo Abstract High-frequencies of somatic embryogenesis and multiple-shoot formation were achieved with seed-derived shoot apical meristems of rhodesgrass (Chloris gayana Kunth). Shoot apices as initial explants were isolated from aseptically germinated seedlings, and cultured in vitro. Embryogenic calli and the multiple shoots were induced and maintained on MS basal medium with various combinations of 2,4-dichlorophnoxyacetic acid (2,4-D) and 6-benzylaminopurine (BAP), the two most effective treatments being 2.0 mg L,1 2,4-D and 0.1 mg L,1 2,4-D + 2.0 mg L,1 BAP. These embryogenic calli and multiple-shoot formations could be used as alternative regenerable target tissues for genetic transformation using particle bombardment of rhodesgrass. [source] IN VITRO SOMATIC EMBRYOGENESIS AND REGENERATION OF SOMATIC EMBRYOS FROM PIGMENTED CALLUS OF KAPPAPHYCUS ALVAREZII (DOTY) DOTY (RHODOPHYTA, GIGARTINALES),JOURNAL OF PHYCOLOGY, Issue 3 2003C. R. K. Reddy In vitro somatic embryogenesis and regeneration of somatic embryos to whole plants through micropropagules was successfully demonstrated from pigmented uniseriate filamentous callus of Kappaphycus alvarezii (Doty) Doty in axenic cultures. More than 80% of the explants cultured on 1.5% (w/v) agar-solidified Provasoli enriched seawater (PES) medium showed callus development. The callus induction rate was consistently higher for laboratory-adapted plants. The excised callus grew well in subcultures and maintained its growth for prolonged periods if transferred to fresh medium in regular intervals. Some subcultured calli (<10%) did undergo transformation and produced densely pigmented spherical or oval-shaped micropropagules (1,5 mm in diameter) that subsequently developed into young plantlets in liquid PES medium. The micropropagule production was further improved through somatic embryogenesis by a novel method of culturing thin slices of pigmented callus with naphthaleneacetic acid (NAA) or a mixture of NAA and 6-benzylaminopurine. Transfer of embryogenic callus along with tiny somatic embryos to liquid medium and swirling on orbital shaker facilitated rapid growth and morphogenesis of somatic embryos into micropropagules that grew into whole plants in subsequent cultivation in the sea. The daily growth rate of one tissue cultured plant was monitored for seven generations in field and found to be as high as 1.5,1.8 times over farmed plants. The prolific somatic embryogenesis together with high germination potential of somatic embryos observed in this study offers a promising tool for rapid and mass clonal production of seed stock of Kappaphycus for commercial farming. [source] Changes in phosphatidylinositol and phosphatidylinositol monophosphate kinase activities during the induction of somatic embryogenesis in Coffea arabicaPHYSIOLOGIA PLANTARUM, Issue 2 2003María Julissa Ek-Ramos Evidence was obtained for the presence of phosphatidylinositol (PIK) and phosphatidylinositol monophosphate kinase (PIPK) at different developmental stages during somatic embryogenesis in Coffea arabica L. by in vitro phosphorylation of endogenous lipids in the presence of [,- 32P]ATP followed by thin-layer chromatography. The results indicate the existence of a relationship between the development stages that were analysed and the kinases found. In cells without differentiated structures (EC, embryogenic calli) phosphatidylinositol kinase and phosphatidylinositol monophosphate 5-kinase (EC 2.7.1.68) activities were present. These activities increased significantly in the first differentiated stage (PREG, preglobular structures) and decreased as the development stages advanced. Phosphatidylinositol monophosphate (PIP) formation decreased from the globular (GLO) to the cotyledonary (COT) stage. The PIP fraction contained both isomers, PI 3-P and PI 4-P. This demonstrates PI3K (EC 2.7.1.137) and PI4K (EC 2.7.1.67) activity during somatic embryogenesis in Coffea arabica L. When wortmannin, an inhibitor of PI3K and PI4K activities, was included in an in vitro assay, a dose-dependent inhibition of the formation of both isomers was observed. The addition of wortmannin to the induction medium during the PREG stage reduced the number of normal embryos. Our results suggest that PI and PIP kinases and the formation of certain phosphoinositides may play roles in the regulation of somatic embryo development in Coffea arabica L. [source] Biotechnology of the Banana: A Review of Recent ProgressPLANT BIOLOGY, Issue 5 2000G. R. Rout Abstract: A number of biotechnological tools have been developed which could help breeders to evolve new plant types to meet the demand of the food industry in the next century. Available techniques for the transfer of genes could significantly shorten the breeding procedures and overcome some of the agronomic and environmental problems which would otherwise not be possible through conventional methods. In vitro protocols have been standardized to allow commercially viable propagation of desired clones of Musa. An overview of the regeneration of banana by direct and indirect organogenesis, and somatic embryogenesis is presented in this article. In addition, the use of several other biotechnological techniques to enrich the genome of banana, such as selection of somaclonal variants, screening for various useful characteristics, cryopreservation, genetic transformation and molecular genetics are reviewed. In conclusion, the improvement of banana through modern biotechnology should help ensure food security by stabilizing production levels in sustainable cropping systems geared towards meeting domestic and export market demands. [source] Somatic Embryogenesis in Leguminous PlantsPLANT BIOLOGY, Issue 2 2000P. Lakshmanan Abstract: This review examines recent advances in the induction and development of somatic embryos in leguminous plants. Emphasis has been given to identify the current trends and successful strategies for the establishment of somatic embryogenic systems, particularly in the economically important species. It appears that, in legumes, somatic embryogenesis can be realized relatively easily especially in young meristematic tissues such as immature embryos and developing leaves. In the majority of the species examined, chlorophenoxyacetic acids remained the most active inductive compounds; however, the new generation growth regulators such as thidiazuron are emerging as successful alternatives for high-frequency direct regeneration of somatic embryos, even from well differentiated explant tissues. Low-frequency embryo production, poor germination and conversion of somatic embryos into plantlets and somaclonal variation are the major impediments limiting the utility of somatic embryogenesis for biotechnological applications in legumes. These limitations, however, may be considerably reduced in the near future, as more newly developed growth regulators with specific morphogenic targets become available for experimentation. From the published data, it is apparent that more effort should be given to develop repetitive embryogenic systems with high frequency of germination and regeneration, since such systems will find immediate application in mass propagation and other crop improvement programmes. As our understanding of various morphogenic processes, including growth and differentiation of zygotic embryos, is fast expanding, it is conceivable that development of highly efficient somatic embryogenic systems with practical application can be anticipated, at least for the important leguminous crops, in the foreseeable future. [source] Micropropagation of self-rooting juvenile clones by secondary somatic embryogenesis in Hevea brasiliensisPLANT BREEDING, Issue 2 2010Y. W. Hua With 2 figures and 5 tables Abstract Micropropagation of self-rooting juvenile clones in Hevea brasiliensis was established for two clones CATAS 7-33-97 and CATAS 88-13 through the following three steps: induction of primary embryos, embryo multiplication by secondary somatic embryogenesis in three successive cycles from a single culture of primary embryo and plant regeneration. The embryo multiplication coefficients of the two clones increased in the first cycle and reached the maximum in the second and the third cycle at the same rate. Significant effects of origins of embryo fragments and calcium on secondary embryogenesis were detected, the highest ratios of the regenerated embryos to primary embryos appeared, when embryo fragments close to the base of embryos were used and incubated in Murashige and Skoog (MS)-based callogenesis medium with 6.0 mm CaCl2 for CATAS 88-13 and 9.0 mm CaCl2 for CATAS 7-33-97. The highest rates of plant conversion were produced on MS-based plant regeneration medium with 4.5 and 9.0 ,m 2,4-D for CATAS 7-33-97 (85.0%) and 13.5 ,m for CATAS 88-13 (75.0%), being higher than other reports (60%). Finally, the application of this system was discussed. [source] Stress-induced somatic embryogenesis in vegetative tissues of Arabidopsis thalianaTHE PLANT JOURNAL, Issue 1 2003Miho Ikeda-Iwai Summary Somatic embryogenesis is an obvious experimental evidence of totipotency, and is used as a model system for studying the mechanisms of de-differentiation and re-differentiation of plant cells. Although Arabidopsis is widely used as a model plant for genetic and molecular biological studies, there is no available tissue culture system for inducing somatic embryogenesis from somatic cells in this plant. We established a new tissue culture system using stress treatment to induce somatic embryogenesis in Arabidopsis. In this system, stress treatment induced formation of somatic embryos from shoot-apical-tip and floral-bud explants. The somatic embryos grew into young plantlets with normal morphology, including cotyledons, hypocotyls, and roots, and some embryo-specific genes (ABI3 and FUS3) were expressed in these embryos. Several stresses (osmotic, heavy metal ion, and dehydration stress) induced somatic embryogenesis, but the optimum stress treatment differed between different stressors. When we used mannitol to cause osmotic stress, the optimal conditions for somatic embryogenesis were 6,9 h of culture on solid B5 medium containing 0.7 m mannitol, after which the explants were transferred to B5 medium containing 2,4-dichlorophenoxyacetic acid (2,4-D, 4.5 µm), but no mannitol. Using this tissue culture system, we induced somatic embryogenesis in three major ecotypes of Arabidopsis thaliana, Ws, Col, and Ler. [source] Influence of antibiotic cefotaxime on somatic embryogenesis and plant regeneration in indica riceBIOTECHNOLOGY JOURNAL, Issue 10 2006Deepinder Grewal Dr. Abstract An antibiotic, cefotaxime (OmnataxÔ) has been found to promote somatic embryogenesis and subsequent plant regeneration in vitro in indica-type basmati rice cultures. Response was highly genotype specific. The number, mass and morphology of the calli formed on the scutellar tissues were dependent on the growth medium (with or without cefotaxime). The embryogenic nature of nodular calli was confirmed through histological analysis and their plant regeneration ability. The calli of variety Pusa basmati 1 grown on medium supplemented with cefotaxime (100 mg/L) exhibited up to 70.5% plant regeneration as compared to control (51.51%). Plants regenerated from emryogenic calli were phenotypically normal and identical to seed-derived plants and exhibited normal fertility. A limited humidity and an optimal aeration of the culture tubes further enhanced the frequency of somatic embryogenesis and plant regeneration. [source] | |||||||||||||