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DNA uptake during electroporation of germinating pollen grains
Authors:Aref A Abdul-Baki  James A Saunders  Benjamin F Matthews  George W Pittarelli
Institution:

a Plant Molecular Biology Laboratory, Plant Sciences Institute, USDA-ARS, Beltsville, MD 20705, USA

b Germaplasm Quality & Enhancement Laboratory, Plant Sciences Institute, USDA-ARS, Beltsville, MD 20705, U.S.A.

Abstract:Electroporation of germinating pollen grains of Nicotiana gossei (L.) Domin under a variety of conditions showed that DNA was taken up by the pollen without detrimental effects on the viability of the pollen. By optimizing both the field strength of the electroporation pulse and the DNA concentration in the electroporation medium up to 6% of the donor DNA can be taken up by the germinating pollen while maintaining a pollen viability of 90%. Field strengths as high as 9 kV/cm could be applied to germinating pollen grains without detrimental effects on viability. Southern hybridizations demonstrated that DNA encoding the marker enzyme β-glucuronidase (GUS) was incorporated into electroporated pollen. Germinating pollen, treated in this manner, is capable of producing 300–400 seeds per capsule of viable seed when applied to the stigmas of compatible flowers of N. gossei which has been emasculated 4 days earlier.
Keywords:electroporation  pollen germination  DNA transfer  seed production  β-glucuronidase
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