Variation in culture,isoenzyme patterns and plastid DNA in the genusDaucus |
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Authors: | Benjamin F Matthews Kenneth G Wilson Lorin R DeBonte |
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Institution: | (1) Tissue Culture and Molecular Genetics Laboratory, U.S. Department of Agriculture, S&E, ARS, PPHI, 20705 Beltsville, Maryland;(2) Department of Botany, Miami University, 45056 Oxford, Ohio |
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Abstract: | Summary To identify markers for fusion and transformation studies, cell suspension cultures of four members of theDaucus genus were examined to determine differences in culture conditions, isoenzyme patterns, and plastid DNA. The four were:D. carota subsp.sativus cv. Danvers,D. carota subsp.gummifer, D. capillifolius, andD. pusillus. Under appropriate conditions, all four grew well as liquid cell suspension cultures and regenerated from protoplasts into
plants. Enzyme activities of homoserine dehydrogenase (HSDH) and alcohol dehydrogenase from cell culture extracts were analyzed
on electrophoretic gels. Although only one form of HSDH was present in eachDaucus line, the rate of migration of HSDH from cv. Danvers was different from that of the other cell lines. Multiple isoenzymic
forms of ADH were present in eachDaucus cultivar.
Camparison of endonuclease restriction fragment patterns from plastid DNAs digested by BamHI revealed only small differences
between plastid DNAs of cv. Danvers and subsp.Gummifer, whereas large differences were observed between cv. Danvers andD. pusillus plastid DNA patterns. No differences were found between cv. Danvers andD. capillifolius plastid DNA patterns when examined using eight different restriction enzymes. The data indicate that specific isoenzyme and
organelle DNA restriction fragment patterns will be useful markers for precise identification of genomes of differentDaucus species in somatic hybridization experiments.
This research was supported by the U.S. Department of Agriculture under Agreement 59-2246-1-1-737-0. |
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Keywords: | Daucus cell culture isoenzymes homoserine dehydrogenase chloroplast DNA |
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