The invention discloses a direct polygerm-generation regeneration
plant culture method by the isolated culture of beet
epicotyl. The invention also discloses a decapitated
epicotyl exophyte. The invenThe invention discloses a direct polygerm-generation regeneration
plant culture method by the isolated culture of beet
epicotyl. The invention also discloses a decapitated epicotyl exophyte. The invention utilizes an epicotyl exophyte and the decapitated epicotyl exophyte to establish a
gene-independent, simple and rapid beet isolated culture regeneration
plant culture technology which directly intion utilizes an epicotyl exophyte and the decapitated epicotyl exophyte to establish a
gene-independent, simple and rapid beet isolated culture regeneration plant culture technology which directly induces polygerm generation, elongation and rootage; by the formulation of a culture medium and the optimizing screen of carbon sources, the
browning degree of the exophyte is lowered to the lightest deduces polygerm generation, elongation and rootage; by the formulation of a culture medium and the optimizing screen of carbon sources, the
browning degree of the exophyte is lowered to the lightest degree, an exophyte can have the maximum generation
bud number more than or equal to 3 and the regeneration
bud rootage rate higher than 90 percent, and a regeneration plant with a full root, a full stagree, an exophyte can have the maximum generation
bud number more than or equal to 3 and the regeneration bud rootage rate higher than 90 percent, and a regeneration plant with a full root, a full stalk and full leaves can be obtained by only 3 to 4 months. The invention has low malformed
seedling rate and lays a foundation for the hereditary improvement of beet breeds applied in production duringlk and full leaves can be obtained by only 3 to 4 months. The invention has low malformed
seedling rate and lays a foundation for the hereditary improvement of beet breeds applied in production during
gene engineering.
gene engineering.