초록 ▼

A process is provided for inducing direct somatic embryogenesis in Pooideae and rapidly regenerating fertile plants by first culturing isolated immature scutella cells in culture medium comprising auxin, cytokinin and polyamine in amounts effective to cause direct formation of primary embryos withou

A process is provided for inducing direct somatic embryogenesis in Pooideae and rapidly regenerating fertile plants by first culturing isolated immature scutella cells in culture medium comprising auxin, cytokinin and polyamine in amounts effective to cause direct formation of primary embryos without an intervening callus stage, at least until at least one primary embryo reaches the globular developmental stage, the auxin being present in greater proportion than cytokinin. A second step includes either a) culturing the primary embryos under conditions to regenerate plantlets, and culturing the primary embryos in regeneration medium; or b) culturing the primary embryos at the globular developmental stage and no longer than the coleoptilar stage in culture medium comprising auxin, cytokinin, and polyamine in amounts effective to cause induction of secondary embryo formation, at least until secondary embryogenesis is detected, the cytokinin being present in greater proportion than auxin, and culturing the secondary embryos under conditions to regenerate plantlets.

대표청구항 ▼

What is claimed is: 1. A process for inducing direct somatic embryogenesis in Pooideae and rapidly regenerating fertile plants, comprising the steps of: a) culturing isolated immature scutella cells of Pooideae in or on a culture medium comprising auxin, cytokinin and polyamine in amounts effective

What is claimed is: 1. A process for inducing direct somatic embryogenesis in Pooideae and rapidly regenerating fertile plants, comprising the steps of: a) culturing isolated immature scutella cells of Pooideae in or on a culture medium comprising auxin, cytokinin and polyamine in amounts effective to cause direct formation of primary embryos without an intervening callus stage, at least until at least one primary embryo reaches the globular developmental stage, the auxin being present in greater proportion than the cytokinin; and one of the following steps selected from: b) culturing one or more of the primary embryos from step (a) under conditions conducive to regeneration of plantlets from the primary embryos, and culturing the primary embryo in or on a regeneration medium; or c) culturing one or more of the primary embryos at the globular developmental stage and no longer than the coleoptilar stage from step (a) in or on a culture medium comprising auxin, cytokinin, and polyamine in amounts effective to cause induction of secondary embryo formation, at least until secondary embryogenesis is detected, the cytokinin beina present in greater proportion than the auxin, and culturing one or more of the secondary embryos under conditions conducive to regeneration of plantlets from the secondary embryos. 2. The process of claim 1, wherein, in step (a), the ratio of auxin to cytokinin in the culture medium is from about 5 μM auxin per 1 μM cytokinin to about 20 μM auxin per 1 μM cytokinin. 3. The process of claim 2, wherein, in step (a) the culture medium includes the plant growth regulators: i) from about 15 μM auxin to about 45 μM auxin; ii) from about 15 μM polyamine to about 45 μM polyamine; and iii) from about 1 μM cytokinin to about 5 μM cytokinin. 4. The process of claim 1, wherein, in step (a), the ratio of auxin to cytokinin in the culture medium is about 14 μM auxin per 1 μM cytokinin. 5. The process of claim 4, wherein, in step (a), the culture medium includes the plant growth regulators of: i) about 30 μM auxin; ii) about 30 μM polyamine; and iii) about 2 μM cytokinin. 6. The process of claim 1, wherein, in step (a), the culture medium is DSEM medium. 7. The process of claim 3, wherein steps (a) and (b) are conducted, and the regeneration medium is MS medium. 8. The process of claim 7, further comprising, before step (b) , the step of culturing the primary embryo under conditions conducive to germination of the primary embryos until germination of at least one of the primary embryos commences. 9. The process of claim 8, wherein the germination step comprises culturing the primary embryo in or on a culture medium which comprises polyamine in an amount effective to cause germination of the primary embryos, and which is essentially free of either auxin or cytokinin. 10. The process of claim 9, wherein the culture medium comprises from about 15 μM polyamine to about 45 μM polyamine. 11. The process of claim 9, wherein the culture medium comprises about 30 μM polyamine. 12. The process of claim 9, wherein the germination step comprises culturing the primary embryo in or on GEM medium. 13. The process of claim 7, further comprising the step of culturing the plantlets under conditions conducive to induction of root formation until the plantlets form roots. 14. The process of claim 13, further comprising the step of transplanting the plantlets to soil and growing them to maturity. 15. The process of claim 14, wherein the scutella cells are selected from the genera consisting of Triticum, Hordeum, Secale, Avena, Dactylis, and Bromus. 16. The process of claim 15, wherein the scutella cells are selected from the group consisting of Triticum durum amphiploids, Hordeum vulgare, Triticum aestivum, Triticum durum, Triticum monococum, Triticum urartu, Secale cereale, and Avena sativa scutella cells. 17. The process of claim 15, wherein the scutella cells of step (a) are free of a germ. 18. The process of claim 17, which further includes, after step (a), cutting the scutellum carrying the primary embryo into a plurality of pieces prior to culturing in step (b). 19. The process of claim 18, wherein the scutellum carrying the primary embryo is cut into two to four pieces. 20. The process of claim 15, wherein step (a) further comprises the step of introducing foreign DNA into the scutella cells or primary embryo so that the foreign DNA becomes stably integrated into the genome of the cells. 21. The process of claim 20, wherein the foreign DNA is introduced into the scutella cells or primary embryo by particle bombardment or by Agrobacterium-mediated transformation. 22. The process of claim 21, wherein the foreign DNA is introduced into the scutella cells or primary embryo in step (a) during the development of the primary embryo. 23. The process of claim 22, wherein the foreign DNA is introduced into the scutella cells between zero to five days after commencement of tissue culture. 24. The process of claim 22, wherein the foreign DNA is introduced into the scutella cells or the primary embryo after two days following commencement of tissue culture. 25. The process of claim 22, wherein after the foreign DNA has been introduced, the scutella cells or primary embryo are transferred to a media for steps (a) and (b) which includes a selective agent to identify a transformed plant cell that has incorporated the foreign DNA. 26. The process of claim 25, wherein the transformed plant cell is cultured in media to support regeneration of transformants. 27. The process of claim 26, which further comprises confirming expression of the foreign DNA in the transformants by one or both of polymerase chain reaction and Southern blot analyses. 28. The process of claim 3, wherein, in step (c), the ratio of auxin to cytokinin in the culture medium is from about 0.05 μM auxin per 1 μM cytokinin to about 0.2 μM auxin per 1 μM cytokinin. 29. The process of claim 28, wherein, in step (c), the culture medium includes the plant growth regulators: i) from about 5 μM auxin to about 15 μM auxin; ii) from about 15 μM polyamine to about 45 μM polyamine; and iii) from about 50 μM cytokinin to about 200 μM cytokinin. 30. The process of claim 3, wherein, in step (c) the ratio of auxin to cytokinin is about 0.1 μM auxin per 1.0 μM cytokinin. 31. The process of claim 30, wherein, in step (c), the culture medium includes the plant growth regulators of: i) about 11 μM auxin; ii) about 30 μM polyamine; and iii) about 110 μM cytokinin. 32. The process of claim 3, wherein, in step (c), the culture medium is SEM medium. 33. The process of claim 32, wherein step (c) comprises culturing the secondary embryo in or on a regeneration medium. 34. The process of claim 33, wherein the regeneration medium is MS medium. 35. The process of claim 33, further comprising, before step (c), the step of culturing the secondary embryo under conditions conducive to germination of the secondary embryos until germination of at least one of the secondary embryos commences. 36. The process of claim 35, wherein the germination step comprises culturing the secondary embryo in or on a culture medium which comprises polyamine in an amount effective to cause germination of the secondary embryos, and which is essentially free of either auxin or cytokinin. 37. The process of claim 36, wherein the culture medium comprises from about 15 μM polyamine to about 45 μM polyamine. 38. The process of claim 36, wherein the culture medium comprises about 30 μM polyamine. 39. The process of claim 36, wherein the germination step comprises culturing the secondary embryo in or on GEM medium. 40. The process of claim 33, further comprising the step of culturing the plantlets under conditions conducive to induction of root formation until the plantlets form roots. 41. The process of claim 40, further comprising the step of transplanting the plantlets to soil and growing them to maturity. 42. The process of claim 41, wherein the scutella cells are selected from the genera consisting of Triticum, Hordeum, Secale, Avena, Dactylis, and Bromus. 43. The process of claim 42, wherein the scutella cells are selected from the group consisting of Triticum durum amphiploids, Hordeum vulgare, Triticum aestivum, Triticum durum, Triticum monococum, Triticum urartu, Secale cereale, and Avena sativa scutella cells. 44. The process of claim 42, wherein the scutella cells of step (a) are free of a germ. 45. The process of claim 44, which further includes, after step (a), cutting the primary embryo into a plurality of pieces before culturing in step (c). 46. The process of claim 45, wherein the primary embryo is cut into two to four pieces. 47. The process of claim 45, which further comprises, before step (c), the step of cutting the primary embryo carrying the secondary embryo into a plurality of pieces, or cutting a germinating leaf if developed, to obtain a high frequency of germination of secondary embryo. 48. The process of claim 47, wherein the primary embryos carrying the secondary embryo is cut into two pieces. 49. The process of claim 42, wherein step (a) further comprises the step of introducing foreign DNA into the scutella cells or the primary embryo so that the foreign DNA becomes stably integrated into the genome of the cells. 50. The process of claim 49, wherein the foreign DNA is introduced into the scutella cells or primary embryo by particle bombardment or by Agrobacterium-mediated transformation. 51. The process of claim 50, wherein the foreign DNA is introduced into the scutella cells or the primary embryo in step (a) during the development of the primary embryo. 52. The process of claim 51, wherein the foreign DNA is introduced into the scutella cells or the primary embryo between zero to five days after commencement of tissue culture. 53. The process of claim 51, wherein the foreign DNA is introduced into the scutella cells or the primary embryo after two days following commencement of tissue culture. 54. The process of claim 51, wherein after the foreign DNA has been introduced, the scutella cells or primary embryo are transferred to a media for step (c), and optionally for step (a), which includes a selective agent to identify a transformed plant cell that has incorporated the foreign DNA. 55. The process of claim 54, wherein the transformed plant cell is cultured in media to support regeneration of transformants. 56. The process of claim 55, which further comprises confirming expression of the foreign DNA in the transformants by one or both of polymerase chain reaction and Southern blot analyses.