Relative Effects of Uniconazole-p and other growth regulators on Micropropagation ratio of yam (Dioscorea spp.) plantlets at different growth phases

Authors

  • Morufat Oloruntoyin Balogun International Institute of Tropical Agriculture/University of Ibadan, Nigeria
  • Shou Yong Ng c/o N.Q. Ng, FAO Regional Office for Asia and the Pacific, 39 PhraAtit Road, Bangkok 10200, Thailand
  • Iyiola Fawole Professor of Genetics, Bells University of Science and Technology, Otta, Nigeria
  • Hironobu Shiwachi Department of International Agricultural Development, Tokyo University of Agriculture
  • Hidehiko Kikuno Department of International Agricultural Development, Tokyo University of Agriculture

Keywords:

Dioscorea, micropropagation, Uniconazole-p, Primary nodal complex, growth regulators,

Abstract

Scarcity of seed, pest and diseases are major constraints to yam production. Tissue culture techniques of meristem culture combined with heat therapy have been used to produce high-yielding virus-tested plantlets of root crops, which are later multiplied through micropropagation. However, the micropropagation rate is low in yam. We investigated in vitro, the rate of production of new nodes at some Plant growth regulator regimes applied at specific growth phases of yam. Three concentrations each of uniconazole-p (UP), gibberellic, jasmonic (JA) and naphthalene acetic (NAA) acids were applied at single node and primary nodal complex (PNC) formation phases in a split-plot design using two genotypes each of white and water yams. Number of nodes per plantlet was recorded after 16 weeks. The number of new nodes varied significantly with genotype by growth phase interaction and the main effect of PGRs. After 16 weeks, the control, 1.7 µM UP and 0.03 µM JA had highest means of 7, 9 and 8 nodes per plantlet compared to 2-3 nodes in the GA treatments. Thus, 4,900, 8,100 and 6,400 plantlets can be obtained in I year from a 100-node plant. In D. alata genotypes, addition of PGRs at PNC doubled the number of nodes per plantlet relative to addition at single node stage, while the effect of stage varied with genotype in D. rotundata. There is an important role for GA and its inhibitor-UP on the rate of yam micropropagation. Optimum multiplication rates can be achieved if the right PGR is applied at a standardized growth phase of a particular genotype. Earliness of genotypes seems to be a major factor that will determine the timing of application of PGRs.  

Author Biographies

Morufat Oloruntoyin Balogun, International Institute of Tropical Agriculture/University of Ibadan, Nigeria

Tissue Culture Specialist on the Yam Improvement for Income and Food Security in West Africa, IITA, Ibadan and Senior Lecturer (Geneticist), Department of Crop Protection and Environmental Biology, University of Ibadan, Nigeria

Shou Yong Ng, c/o N.Q. Ng, FAO Regional Office for Asia and the Pacific, 39 PhraAtit Road, Bangkok 10200, Thailand

Accomplished Tissue culture specialist, formerly at the International Institute of Tropical Agriculture, Ibadan, Nigeria

Iyiola Fawole, Professor of Genetics, Bells University of Science and Technology, Otta, Nigeria

Professor of Genetics

Hironobu Shiwachi, Department of International Agricultural Development, Tokyo University of Agriculture

Plant Physiologist

Hidehiko Kikuno, Department of International Agricultural Development, Tokyo University of Agriculture

Plant Physiologist

References

Agbaje, G.O. and Oyegbami, A. (2005).Survey on the adoption of yam minisett technology in South-Western Nigeria. Journal of Food Agriculture and Environment 3(2), 134-137.

Balogun M. O. 2005. Development of microtuber production and dormancy control protocols for yam (Dioscoreasp) germplasm conservation. PhD Thesis, University of Ibadan.

Bimbaun, E. H. , S. H. Lips and I. E. Nwana. 2002. An integrated approach to improve production of starch tubers. USDA Project Number: C13-153. Final report submitted to the U.S. Agency for International Development; Bureau for Global Problems. Online: http://pdf.usaid.gov/pdf_docs/PNACP601.pdf

Borges M, S. Meneses, N. Aguilera andJ. Vazquez.2004. Regeneration and multiplication of Dioscoreaalatagermplasm maintained in vitro. Plant Cell Tissue Organ Cult. 76: 87-89.

Cabrera M, R. Gómez, M. Basail, A. Santos, V. Medero, J. Lopez, A. Rayas, M. García and J. Ventura.2005. Production of yam microtubers using a temporary immersion system.Plant Cell Tissue Organ Cult. 83: 103-107

Cabrera M, R. Gómez, E. Espinosa, J. López, V. Medero, M. Basail and A. Santos. 2011. Yam (Dioscorea alata L.) microtuber formation in Temporary Immersion System as planting material. Biotecnologia Applicada vol.28 no.4.

Chu P. E. and R. Ribeiro. 2002. Growth and carbohydrate changes in shoot cultures of Dioscorea species as influenced by photoperiod, exogenous sucrose and cytokinin concentractions. Plant Cell Tissue Organ Cult. 70: 241-249

FAO, 2013. Food and Agricultural Organization of the United Nations. www.fao.org/statistics/en/ FAO, Rome

Graebe J.E. 1987. Gibberellin biosynthesis and control. Ann. Rev. Plant Physiol. 38:419-465.Izumi K., I. Yamaguchi, A. Wada, H. Oshio and N. Takanashi. 1984. Effects of a new growth retardant {(E)-1-(4-chlorophenyl)-4, 4-dimethyl-2-(1,2,4-triazol-1-yl)-1-penten-3-ol (S-330) }on the growth and gibberellin content of rice plant. Plant Cell Physiology 25:611-617.

Ironkwe, A.G. 2005. Adoption of yam minisett technology by women farmers in Abia State, Nigeria. An unpublished M.Sc. Thesis in the Department of Rural Sociology and Extension, Michael Okpara University of Agriculture, Umudike, Abia State. Pp 75-81. Nigeria.

Malaurie B, O. Pungu and M. Trouslot.1995a. Effect of growth regulators concentrations on morphological development of meristem tips in Dioscorea cayenensis-rotundata complex and D. praehensilis. Plant Cell, Tissue and Organ Cult. 41: 229-235

Malaurie B, O. Pungu and M. F. Trouslot.1995b. Influence of meristem-tip size and location on morphological development in Dioscorea cayenensis-rotundata complex and D. praehensilis. Plant Cell Tissue Organ.Cult. 42: 215-218.

Mantell. S.H., S.Q. Haque. and A.P. Whitehall. 1980. Apical meristem tip culture for virus eradication of flexuous viruses in yams (Dioscoreaalata). Tropical Pest Management. 26(2): 170-179.

Mayong V.M., Smith J., Weber G.K., Jagtap S.S., Oyewole B. 1996. Macro-characterization of Agricultural Systems in West Africa: An Overview. Resource and Crop Management Monograph No. 21, IITA, Ibadan, Nigeria.

Matsumoto, R. H; Shiwachi, H. Kikuno, K. Irie and H. Toyohara. (2010) Effect of collecting time of scions and, treatment of gibberellins and uniconazol-P on the growth of vine cuttings in water yam (Dioscorea alata L.). Japanese Society for Tropical Agriculture, Research for Tropical Agriculture Vol. 3, Extra issue 2, pp51-52. October 09-10, Okinawa, Japan.

Medero V, L. Del Sol and M. García. 1999. Metodología para la propagación del clon de ñame Blanco o Pelú. Resúmenes del BioCat 99, Granma Cuba 5-7 de Octubre pp. 12

Mitchell. S.A., H.N Asemota. and M.H. Ahmad. 1995a. Factors affecting the in vitro

establishment of Jamaican Yams (Dioscoreaspp) from nodal pieces. J. Sci. Food Agric.

-550.

Mitchell, S.A.. H.N Asernota. and M.H. Ahmad. 1995b. Effects of Explant source. Culture medium strenght and Growth regulators on the in vitro propagation of three Jamaican yams (Dioscoea cayenensis, D. trifida and D. rotundata). J. Sci. Food Agric. 67.173-180.

Murashige T. and Skoog F. 1962. A revised medium for rapid growth and bioassays with Tobacco tissue cultures. Physiologia Plantarium 15: 473 - 497

Ng, S.Y.C, 1984. Meristem culture and multiplication. In: International Institute of Tropical Agriculture Annual Report, 1983, Ibadan, Nigeria, pp 133-134.

Ng, S.Y.C. 1988.In vitro tuberization in white yam (Dioscorearotudatan.Poir).Plant Cell, Tissue and Organ Culture 14: 121-128.

Ng, S.Y.C. 1992.Micropropagation of white yam (D. rotundata. poir), In: Biotechnology in Agriculture Forestry, High-tech and micropropagation III (ed. Y.P.S. Bajaj), Berlin Heidelberg, Springer -Ver lag, Vol 19 pp. 135-159.

Okagami, N. 1978. Dormancy in Dioscorea: Sprouting promotion by inhibitors of protein synthesis on bulbils and rhizomes. Plant Cell Physiology 19(2):221-227.

Onjo, M., B. J. Park and M. Hayashi. 2001. Effects of plant growth regulators on plantlet growth and enlargement of microtubers of water yam (Dioscorea alata) in vitro. Japanese journal of tropical agriculture 45(2): 145-147.

Ovono, P.O., C. Kevers and J. Dommes. 2007. Axillary proliferation and tuberisation of Dioscoreacayenensis.D. rotundata complex. Plant Cell, Tissue and Organ Culture. Volume 91, Issue 2, pp 107-114

Oyelami Olayemi, 2011. Identification of appropriate media combination with plant growth regulators to generate shoots from meristem culture on in vitro plantlets of yam. M. Sc. Dissertation, University of Ibadan, Nigeria.

Park, B. J., M. Onjo, S. Tominaga, H.Shiwachi and M. Hayashi. 2003. Relationship between the dormancy and its release and external factors in tubers of water yam (Dioscorea alata L) Japanesee Journal of Tropical agriculture 47(1) 42-50.

Poornima GN and Ravishankar RV. 2007. Invitro propagation of white yams, Dioscoreaoppositifolian (Linn) and Dioscoreapentphylla (Linn.). African Journal of Biotechnology.Vol. 6 (20). Pp. 2348-2352.

Rademacher. W. 1991. Biochemical effects of plant growth retardants. In Plant Biochemical

regulators (Ed H.W. Gausman). Pp. 169-200.

Salazar, R. y R. Hoyos. 2007. Multiplicación y tuberización de ñame (Dioscoreaalata L.) en sistema de inmersión. Revista Facultad Nacional de Agronomía, Medellín 60(2): 3907-3921.

Sengupta. J.. S.C. Mitra. and A.K. Sharma; 1984. Organogenesis and tuberization in Cultures

of Dioscorea floribunda. Plant Cell Tiss. Org. Cult. 3.325-33 1.

Snedecor, G.W. and W.G. Cochran. 1967. Statistical Methods. The Iowa State University Press, Iowa, U.S.A. 593pp.

Statistical Analysis Systems (SAS). Copyright 1999-2000.SAS (r) Proprietary Software Release 8.2 (TS2M0), SAS Institute Inc., Cary, NC, USA.

Wickham LD, H.C. Passam and L.A.Wilson. 1981. Tuber germination and early growth in four edible Dioscorea species. Ibid. 47: 87-95.

Wickham LD, H.C. Passam and L.A.Wilson. 1982. The origin, development and germination of bulbils in two Dioscorea species. Annals of Botany 50: 621-627.

Watt M. P. (2012). The status of temporary immersion system (TIS) technology for plant micropropagation.African Journal of Biotechnology Vol. 11(76), pp. 14025-14035.

Yan H, Yang L, Li Y (2011). Improved growth and quality of Dioscorea fordii Prain et Burk and Dioscorea alata plantlets using a temporary immersion system. African Journal of Biotechnology. 10: 19444-19448.

Ziv M. 1990. The effect of growth retardants on shoot proliferation and morphogenesis in liquid cultured Gladiolus plants. Acta Horti 280207-214.

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Published

2015-03-26

How to Cite

Balogun, M. O., Ng, S. Y., Fawole, I., Shiwachi, H., & Kikuno, H. (2015). Relative Effects of Uniconazole-p and other growth regulators on Micropropagation ratio of yam (Dioscorea spp.) plantlets at different growth phases. JOURNAL OF ROOT CROPS, 40(2), 5–11. Retrieved from https://journal.isrc.in/index.php/jrc/article/view/194

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