A method for long-term micropropagation of Phaseolus coccineus L. |
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Authors: | F Vaquero C Robles M L Ruiz |
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Institution: | (1) Departamento de Genética, Facultad de Biología, Universidad de León, 24071 León, Spain |
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Abstract: | A method for long-term plant regeneration of Phaseolus coccineus L, is described. Shoot-tips and cotyledonary nodes cultured on a Murashige and Skoog medium supplemented with N6-benzylaminopurine, 10 M, and -naphthaleneacetic acid, 1 M, formed multiple bud-shoots. These shoots were transferred to medium containing BAP 1 M, NAA 0.1 M, and gibberellic acid 3 M to promote shoot growth and further shoot multiplication. Rooting was achieved in medium with 11 M indole-3-acetic acid. Rooted plants grew to maturity and were fertile. Cultures have maintained their ability to regenerate plants for more than two years. A sample of 30 regenerated plants (R0) was tested for chromosome number, all of them being diploid; seven isozymatic systems were electrophpretically analyzed in 82 R0 regenerated plants. No differences were observed in their electrophoretic patterns in comparison with those shown by seedlings. Histological studies revealed the origin of buds from calluses via organogenesis.Abbreviations BAP
N6-benzylaminopurine
- 2,4-D
2,4-dichlorophenoxyacetic acid
- GA3
gibberellic acid
- IAA
indole-3-acetic acid
- MS
Murashige and Skoog (1962) medium
- NAA
-naphthaleneacetic acid
- ADH
alcohol dehydrogenase
- GOT
glutamic-oxaloacetic transaminase
- MDH
malate dehydrogenase
- 6PGD
6-phosphogluconate dehydrogenase
- PGI
Phosphoglucose isomerase
- PGM
phosphoglucose mutase
- SK
shikimate dehydrogenase |
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Keywords: | Phaseolus cocdneus Plant regeneration Chromosome number Isozymes |
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