Abstract
Inflorescence induction and morphogenesis of regenerated flowers were investigated in vitro in Dioscorea zingiberensis C. H. Wright. Inflorescence induction was influenced by the type and concentration of phytohormones. When floral bud explants were incubated on a Murashige and Skoog medium containing a combination of 2.0 mg l−1 6-benzyladenine and 0.5 mg l−1 indole-3-butyric acid, the highest frequency of inflorescence induction was observed. However, in the presence of gibberellic acid, induction efficiency was reduced although node length of inflorescence was increased. Ontogenetic studies revealed that the inflorescence primordia originated directly from axillary epidermal cells of the perianth and bract of the explants after 7 days. In vitro, male flowers developed normally and blossomed after 90–100 days. In addition, some bisexual flowers were observed. These results demonstrated that there were differences in sexual differentiation of floral buds in vitro compared with that in vivo.
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Abbreviations
- BA:
-
6-Benzyladenine
- GA3 :
-
Gibberellic acid
- IAA:
-
Indole-3-acetic acid
- IBA:
-
Indole-3-butyric acid
- KT:
-
Kinetin
- MS:
-
Medium Murashige and Skoog medium
- NAA:
-
Naphthaleneacetic acid
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Acknowledgments
We greatly appreciate the help of Dr. Jihong Liu in revising this paper. This work was supported by grants from the Ph.D. Programs Foundation of Ministry of Education of China (No. 2005050416).
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Huang, XL., Yang, B., Hu, CG. et al. In vitro induction of inflorescence in Dioscorea zingiberensis . Plant Cell Tiss Organ Cult 99, 209–215 (2009). https://doi.org/10.1007/s11240-009-9595-x
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DOI: https://doi.org/10.1007/s11240-009-9595-x