| Peer-Reviewed

In Vitro Germination and Direct Shoot Induction of Yeheb (Cordeauxia Edulis Hemsl.)

Received: 21 November 2014    Accepted: 4 December 2014    Published: 18 December 2014
Views:       Downloads:
Abstract

‘Yeheb’ (Cordeauxia edulis Hemsl) is a multipurpose and evergreen shrub and endemic to southeastern corner of Ethiopia and Somalia. It is adapted to low and irregular rainfall and survives a very long dry season. It has enormous economic and food security role to the pastoralist of Somali in Ethiopia. However, the plant is threatened with extinction due to overexploitation and its’ poor natural regeneration capacity. In addition, ‘yeheb’ is usually reported having limited reproductive capacities and often have very specific and limited conditions for seed germination, flowering and seed shelf life. Therefore, to overcome these propagation challenges, an experiment was conducted with the aim of developing a protocol for the in vitro regeneration of ‘yeheb’ from cotyledonary node. The result of these studies revealed that seed was washed by 5% sodium hypochlorite for ten min in aseptic condition found to be more effective in surface sterilization. The sterilized seed cultured on half strength of Gamborg (B5) medium was found to be the most suitable medium for germination (26.67%).The highest shoot initiation percentage (89 % of explants produces shoots), number of shoots per explant and number of leaf per shoot were obtained from cotyledonary node explants cultured on Murashige and Skoog (MS) media supplemented with 2.00 mg. l-1 N6-benzylaminopurine (BAP) within nine weeks. While, the highest shoot length and shoot fresh weight were recorded from control (free BAP) and 6.00 mg. l-1 BAP, respectively. The highest shoot multiplication (4.56 number of shoot induced) and elongation (2.97cm) were obtained from the induced shoot were cut and placed on MS media supplemented with 2.00 mg. l 1BAP+6.00 mg. l-1of gibberellic acid (GA3) and free BAP+6.00 mg. l-1 of GA3, respectively. The elongated shoots were transferred to different media supplemented with various types and levels of hormones but none of them induced root. As a conclusion, this is the first attempt for direct in vitro regeneration of C. edulis and permissible result for cryopreservation.

Published in Agriculture, Forestry and Fisheries (Volume 3, Issue 6)
DOI 10.11648/j.aff.20140306.13
Page(s) 452-458
Creative Commons

This is an Open Access article, distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution and reproduction in any medium or format, provided the original work is properly cited.

Copyright

Copyright © The Author(s), 2024. Published by Science Publishing Group

Keywords

BAP, Cotyledonary Node, Germination, In Vitro, GA3 Shoot Induction, Shoot Elongation

References
[1] Ali, H.M., 1988. Cordeauxia edulis: Production and Forage Quality in Central Somalia. Thesis for the degree of Master of Science in Rangeland Resources, National University of Somalia, Somalia.
[2] Teketay, D. and Eshete, A., 2004. Status of indigenous fruits in Ethiopia. In: Chikamai B, Eyog-Matig O, Mbogga M (eds.) Review and Appraisal on the Status of Indigenous Fruits in Eastern Africa: A Report Prepared for IPGRI-SAFORGEN in the Framework of AFRENA/FORENESSA, Kenya Forestry Research Institute, Nairobi, Kenya, pp 3-35.
[3] Miège, J. and Miège, M.N., 1978. Cordeauxia edulis a Caesalpinaceae of Arid Zones of East Africa, Caryologic, blastogenic and biochemical features. Potential aspects for nutrition. Economic Botany, 32: 336-345.
[4] Drechsel, P. and Zech, W., 1988. Site conditions and nutrient status of Cordeauxia edulis (Caesalpiniaceae) in its natural habitat in central Somalia. Economic Botany, 42: 242–249.
[5] Hemming, C.F., 1972. The vegetation of the northern region of Somalia Republic. Proceeding of Linnaeus Social London, 177:173-250.
[6] Watson, R.M., Tippett, C.J., Becket, J.J. and Scholes, V., 1982. Somali Democratic Republic, Central Rangelands Survey, London. Resource Management and Research, 1:3–10
[7] N.A.S (National Academy of Science), 1979. Tropical legumes: Resource for the Future, Nat Acad. Sci. Washington DC, pp261.
[8] Brink, M., 2006.Cordeauxia edulis Hemsl Record from Protobase. PROTA (Plant resources of tropical Africa / Ressourcesvégétales de l’Afriquetropicale), Wageningen, Netherlands http://database.prota.org/search.htm (Accessed on September 14, 2011)
[9] Booth, F.E.M. and Wickens, G.E., 1988. Non-timber uses of selected arid zone trees and shrubs in Africa. FAO Conservation Guide 19, 52-58.
[10] FAO, 1988. Traditional food plants, Food and nutrition paper 42:224-27.
[11] Assefa, F., Bollini, R. and Kleiner, D., 1997. Agricultural potential of little used tropical legumes with special emphasis on Cordeauxia edulis (Ye-eb nut) and Sphenostylisstenocarpa (African yam bean). Giessener Beiträge zur Entwicklungsforschung, 24:237–242.
[12] Bally, P.R.O., 1966. Miscellaneous notes on the flora of Tropical East Africa, 29. Enquiry into the occurrence of the Yeheb nut (Cordeauxia edulis Hemsl.) in the Horn of Africa.Candollea 21 (1), 3-11.
[13] Liew, J., 2003. Desiccation tolerance of yeheb (Cordeauxia edulis Hemsl.) seeds.Thesis for the degree of Master of Science in Agriculture, SLU, Ultuna, Sweden.
[14] Mussa, M., 2010.Cordeauxia edulis (yeheb): resource status, utilization and management in Ethiopia. Thesis for the degree of Philosophiae Doctor, University of Wales.
[15] Murashige, T. and Skoog, F., 1962.A revised medium for rapid growth and bioassays with tobacco tissue cultures. Physiologia Plantarum, 15: 473-497.
[16] Gamborg, O.L., Murashige, T., Thorpe, T.A. and Vasil, I.K., 1976.Plant tissue culture media. In Vitro, 12:473-478.
[17] SAS Institute Inc., 2002. Statistical Analysis Software, Version 9.0. Cary, North Carolina, USA.
[18] Pierik, R.L.M., 1997. In vitro culture of higher plants. Kluwer Acadamic publishers. Wageningen Agricultural University, The Netherland, pp 1-72.
[19] Alvarez, V.M., Ferreira, A.G., and Nunes, V.F., 2006. Seed disinfestation methods for in vitro cultivation of epiphyte orchids from Southern Brazil. HorticulturaBrasileira 24: 217-220.
[20] Vujanovic, V., Arnaud, S.T.M. and Barabé, D., 2000.Viability testing of orchid seed and the promotion of coloration and germination.Annals of Botany, 86:79-86.
[21] George, E. F., Hall, M.A. and Klerk, G.D., 2008. Plant Propagation by Tissue Culture 3rd Edition, Publication by Springer, Netherlands.
[22] Altaf, N., 2006. In vitro bud culture of Kinnow tree, Pak. J. Bot. 38(3): 597-601.
[23] Kant, T., Prajapati S. and Parmar, A.K., 2010. Efficient micropropagation from cotyledonary node cultures of Commiphora wightii (Arn.)
[24] Roshetko, J.M., 1995. Albiziasaman: pasture improvement, shade, timber and more (NFTA 95-02). Winrock International, Morrilton, Arkansas. http://www.winrock.org/ forestry/factpub/factsh/a_saman.htm. (Accessed on September 14, 2011).
[25] Mittal, A., Agarwal, R., Gupta, S.C., 1989.In vitro development of plantlets from axillary buds of Acacia auriculiformis. Plant Cell, Tissue and Organ Culture, 19: 65–70.
[26] Dewan, A., Nanda, K., Gupta, S.C., 1992. In vitro micropropagation of Acacia nilotica sub sp. Indica Brenan via cotyledonary nodes. Plant Cell Reports, 12: 18–21.
[27] Singh, H. P., Singh, S., Saxena, R.P., Singh, R.K., 1993. In vitro bud break in axillary nodal segments of mature trees of Acacia nilotica. Indian Journal Plant Physiol. 36:21–24.
[28] Aha, Y.J., and Chen, G.Q., 2008. High frequency regeneration through adventitious shoot formation in caster bean (Riceinus communis L.). In Vitro Cellular and Developmental Biology -Planta, 43:9-15.
[29] Vengadesan, G. and Pijut, M.P., 2009. In vitro propagation of northern red oak (Quercusrubra L.)In Vitro Cellular and Developmental Biology – Planta, 45:474–482.
[30] Alam, I., Sharmin, S.A., Mondal, S.C., Alam, M., Khalekuzzaman, M. and Anisuzzaman, M., 2010. In vitro micropropagation through cotyledonary node culture of caster bean (Riceinus communis L.). Australian Journal of crop science, 4(2):81-84.
[31] Naghmouchi, S., Khouja, M.L., Rejib, M.N. and Boussaid, M., 2008. Effect of growth regulators and explant origin on in vitro propagation of Ceratonia siliqua L. via cuttings. Biotechnol. Agron. Soc. Environ.:12 (3):251-258.
[32] Thomas, T. and Blakesley, D. 1987 .Practical and potential uses of Cytokinin in agriculture and horticulture. In: Bonga, J. M., and Durzan, D.J.,(eds) Cell and tissue culture in trees, vol. 1 Amsterdam: Martinus Nijhoff Publishers.37p.
[33] Eyob, S., 2009.Promotion of seed germination, subsequent seedling growth and in vitro propagation of korarima Aframomum corrorima Braun. Journal of Medicinal Plants Research, 3(9):652-659.
[34] Payghamzadeh, K. and Kazemitabar, S.K, 2011. In vitro propagation of walnut. African Journal of Biotechnology, 10(3):290-311.
[35] Chitra D.S.V. and G., Padmaja, 1999. Clonal propagation of mulberry through invitroculture of nodal explants. Scientia Hort. 80: 289-298.
[36] Deore, A.J. and Johnson, A.T., 2008. High frequency plant regeneration from leaf-disc culture of Jatropha curcas L.: an important biodiesel crop. Plant Biotechnology Rep., 2:7-11.
[37] Najafabadi, A.J. and Hamidoghli, Y., 2009. Micropropagation of thornless trailing blackberry (Robus sp.) by axillary bud explant. Australian Journal of crop science, 3:191-194.
Cite This Article
  • APA Style

    Yohannes Seyoum, Firew Mekbib. (2014). In Vitro Germination and Direct Shoot Induction of Yeheb (Cordeauxia Edulis Hemsl.). Agriculture, Forestry and Fisheries, 3(6), 452-458. https://doi.org/10.11648/j.aff.20140306.13

    Copy | Download

    ACS Style

    Yohannes Seyoum; Firew Mekbib. In Vitro Germination and Direct Shoot Induction of Yeheb (Cordeauxia Edulis Hemsl.). Agric. For. Fish. 2014, 3(6), 452-458. doi: 10.11648/j.aff.20140306.13

    Copy | Download

    AMA Style

    Yohannes Seyoum, Firew Mekbib. In Vitro Germination and Direct Shoot Induction of Yeheb (Cordeauxia Edulis Hemsl.). Agric For Fish. 2014;3(6):452-458. doi: 10.11648/j.aff.20140306.13

    Copy | Download

  • @article{10.11648/j.aff.20140306.13,
      author = {Yohannes Seyoum and Firew Mekbib},
      title = {In Vitro Germination and Direct Shoot Induction of Yeheb (Cordeauxia Edulis Hemsl.)},
      journal = {Agriculture, Forestry and Fisheries},
      volume = {3},
      number = {6},
      pages = {452-458},
      doi = {10.11648/j.aff.20140306.13},
      url = {https://doi.org/10.11648/j.aff.20140306.13},
      eprint = {https://article.sciencepublishinggroup.com/pdf/10.11648.j.aff.20140306.13},
      abstract = {‘Yeheb’ (Cordeauxia edulis Hemsl) is a multipurpose and evergreen shrub and endemic to southeastern corner of Ethiopia and Somalia. It is adapted to low and irregular rainfall and survives a very long dry season. It has enormous economic and food security role to the pastoralist of Somali in Ethiopia. However, the plant is threatened with extinction due to overexploitation and its’ poor natural regeneration capacity. In addition, ‘yeheb’ is usually reported having limited reproductive capacities and often have very specific and limited conditions for seed germination, flowering and seed shelf life. Therefore, to overcome these propagation challenges, an experiment was conducted with the aim of developing a protocol for the in vitro regeneration of ‘yeheb’ from cotyledonary node. The result of these studies revealed that seed was washed by 5% sodium hypochlorite for ten min in aseptic condition found to be more effective in surface sterilization. The sterilized seed cultured on half strength of Gamborg (B5) medium was found to be the most suitable medium for germination (26.67%).The highest shoot initiation percentage (89 % of explants produces shoots), number of shoots per explant and number of leaf per shoot were obtained from cotyledonary node explants cultured on Murashige and Skoog (MS) media supplemented with 2.00 mg. l-1 N6-benzylaminopurine (BAP) within nine weeks. While, the highest shoot length and shoot fresh weight were recorded from control (free BAP) and 6.00 mg. l-1 BAP, respectively. The highest shoot multiplication (4.56 number of shoot induced) and elongation (2.97cm) were obtained from the induced shoot were cut and placed on MS media supplemented with 2.00 mg. l 1BAP+6.00 mg. l-1of gibberellic acid (GA3) and free BAP+6.00 mg. l-1 of GA3, respectively. The elongated shoots were transferred to different media supplemented with various types and levels of hormones but none of them induced root. As a conclusion, this is the first attempt for direct in vitro regeneration of C. edulis and permissible result for cryopreservation.},
     year = {2014}
    }
    

    Copy | Download

  • TY  - JOUR
    T1  - In Vitro Germination and Direct Shoot Induction of Yeheb (Cordeauxia Edulis Hemsl.)
    AU  - Yohannes Seyoum
    AU  - Firew Mekbib
    Y1  - 2014/12/18
    PY  - 2014
    N1  - https://doi.org/10.11648/j.aff.20140306.13
    DO  - 10.11648/j.aff.20140306.13
    T2  - Agriculture, Forestry and Fisheries
    JF  - Agriculture, Forestry and Fisheries
    JO  - Agriculture, Forestry and Fisheries
    SP  - 452
    EP  - 458
    PB  - Science Publishing Group
    SN  - 2328-5648
    UR  - https://doi.org/10.11648/j.aff.20140306.13
    AB  - ‘Yeheb’ (Cordeauxia edulis Hemsl) is a multipurpose and evergreen shrub and endemic to southeastern corner of Ethiopia and Somalia. It is adapted to low and irregular rainfall and survives a very long dry season. It has enormous economic and food security role to the pastoralist of Somali in Ethiopia. However, the plant is threatened with extinction due to overexploitation and its’ poor natural regeneration capacity. In addition, ‘yeheb’ is usually reported having limited reproductive capacities and often have very specific and limited conditions for seed germination, flowering and seed shelf life. Therefore, to overcome these propagation challenges, an experiment was conducted with the aim of developing a protocol for the in vitro regeneration of ‘yeheb’ from cotyledonary node. The result of these studies revealed that seed was washed by 5% sodium hypochlorite for ten min in aseptic condition found to be more effective in surface sterilization. The sterilized seed cultured on half strength of Gamborg (B5) medium was found to be the most suitable medium for germination (26.67%).The highest shoot initiation percentage (89 % of explants produces shoots), number of shoots per explant and number of leaf per shoot were obtained from cotyledonary node explants cultured on Murashige and Skoog (MS) media supplemented with 2.00 mg. l-1 N6-benzylaminopurine (BAP) within nine weeks. While, the highest shoot length and shoot fresh weight were recorded from control (free BAP) and 6.00 mg. l-1 BAP, respectively. The highest shoot multiplication (4.56 number of shoot induced) and elongation (2.97cm) were obtained from the induced shoot were cut and placed on MS media supplemented with 2.00 mg. l 1BAP+6.00 mg. l-1of gibberellic acid (GA3) and free BAP+6.00 mg. l-1 of GA3, respectively. The elongated shoots were transferred to different media supplemented with various types and levels of hormones but none of them induced root. As a conclusion, this is the first attempt for direct in vitro regeneration of C. edulis and permissible result for cryopreservation.
    VL  - 3
    IS  - 6
    ER  - 

    Copy | Download

Author Information
  • Dry land Crop Research Department, Somali Region Pastoral and Agro-pastoral Research, Jijiga, Ethiopia

  • School of Plant sciences, Haramaya University (HU), Dire Dewa, Ethiopia

  • Sections