Skip to main content
Log in

Morphological and AFLP diversity in Thaumatococcus daniellii, the source of the protein sweetener thaumatin

  • Notes on Neglected and Underutilized Crops
  • Published:
Genetic Resources and Crop Evolution Aims and scope Submit manuscript

Abstract

Thaumatococcus daniellii is a perennial African wild edible plant. Fruit arils from natural populations are the source of the protein sweetener, thaumatin. There are relatively few documented examples of its cultivation, however it has great potential as an intercrop for cultivation under rubber or cocoa. Across the species range there is notable diversity in leaf and fruit morphology. In this study, T. daniellii populations from four provenances in Ghana and Cameroon (separated by the Dahomey Gap) were compared for leaf and fruit morphology in situ and in an experiment using plants grown from sampled rhizomes planted under rubber in a single location in Cameroon. When collected rhizomes from four provenances were planted at one location, the samples from the local provenance produced the largest plants and fruits, and there was less morphological variation between samples from different provenances than was recorded in situ. In situ morphological differences were notable between north–south separated provenances in each country. Fruit collected in situ was analysed for aril thaumatin content and significant variation was found between provenances (1.08–2.00%). Amplified fragment length polymorphism (AFLP) was used to assess genetic diversity among the four provenances and 54% of loci were polymorphic. Cluster analysis of AFLP data separated samples of T. daniellii according to geographical origin. Maximum genetic diversity was found between provenances separated across the Dahomey Gap.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Fig. 1
Fig. 2
Fig. 3
Fig. 4
Fig. 5

Similar content being viewed by others

References

  • Abbiw DK (1990) The useful plants of Ghana: West African uses of wild and cultivated plants. Intermediate Technology Publications/Royal Botanic Gardens, Kew

    Google Scholar 

  • Andersson L (1998) Marantaceae. In: Kubitzki K, Huber PJ, Rudall PS, Stevens PS, Stützel T (eds) The families and genera of vascular plants: flowering plants—monocotyledons. Springer, Berlin, pp 278–293

    Google Scholar 

  • Belaj A, Satovic Z, Cipriani G, Baldoni L, Testolin R, Rallo L, Trujillo I (2003) Comparative study of the discriminating capacity of RAPD, AFLP and SSR markers and of their effectiveness in establishing genetic relationships in olive. Theor Appl Genet 107:736–744

    Article  PubMed  CAS  Google Scholar 

  • Booth AH (1958) The Niger, the Volta and the Dahomey Gap as geographic barriers. Evolution 12:48–62

    Article  Google Scholar 

  • Boy C, Waliszewski WS (2009) Extraction of thaumatin from Thaumatococcus daniellii arils. Protocol, Natex UK Ltd, Sandy

    Google Scholar 

  • Cardoso SRS, Provan J, Lira CDF, Pereira LDOR, Ferreira PCG, Cardoso MA (2005) High levels of genetic structuring as a result of provenance fragmentation in the tropical tree species Caesalpinia echinata Lam. Biodivers Conserv 14:1047–1057

    Article  Google Scholar 

  • Chalmers K, Waugh R, Sprent J, Simons A, Powell W (1992) Detection of genetic variation between and within provenances of Gliricidia sepium and G. maculata using RAPD markers. Heredity 69:465–472

    Article  PubMed  Google Scholar 

  • Chao CCT, Devanand PS, Chen JJ (2005) AFLP analysis of genetic relationships among Calathea species and cultivars. Plant Sci 168:1459–1469

    Article  CAS  Google Scholar 

  • Dhetchuvi MJB (1996) Taxonomie et phytogéographie des Marantaceae et des Zingiberaceae de l’Afrique Centrale (Gabon, Congo, Zaire, Rwanda et Brundi). Ph.D. Université Libre de Bruxelles, Bruxelles, Belgium

  • Dhetchuvi MM, Diafouka A (1993) Thaumatococcus daniellii (Benn.) Benth. var. puberulifolius Dhetchuvi and Diafouka (Marantaceae), une nouvelle variété d’Afrique Centrale. Belg J Bot 126:206–208

    Google Scholar 

  • Drummond RSM, Keeling DJ, Richardson TE, Gardner RC, Wright SD (2000) Genetic analysis and conservation of 31 surviving individuals of a rare New Zealand tree, Metrosideros bartlettii (Myrtaceae). Mol Ecol 9:1149–1157

    Article  PubMed  CAS  Google Scholar 

  • Dupont LM, Jahns S, Marret F, Ning S (2000) Vegetation change in equatorial West Africa: time-slices for the last 150 ka. Palaeogeogr Palaeoclimatol Palaeoecol 155:95–122

    Google Scholar 

  • Dutech C, Seiter J, Petronelli P, Joly HI, Jarne P (2002) Evidence of low gene flow in a neotropical clustered tree species in two rainforest stands of French Guiana. Mol Ecol 11:725–738

    Article  PubMed  CAS  Google Scholar 

  • Ellis AG, Weis AE, Gaut BS (2006) Evolutionary radiation of “stone plants” in the genus Argyroderma (Aizoaceae): unraveling the effects of landscape, habitat, and flowering time. Evolution 60:39–55

    PubMed  Google Scholar 

  • Fry CH, Keith S, Urban K (1982–2004) The birds of Africa, vols 1–7. Academic Press, London

  • Gaudeul M, Till-Bottraud I, Barjon F, Manel S (2004) Genetic diversity and differentiation in Eryngium alpinum L. (Apiaceae): comparison of AFLP and microsatellite markers. Heredity 92:508–518

    Article  PubMed  CAS  Google Scholar 

  • Hamrick JL, Godt MJW, Murawski DA, Loveless MD (1991) Correlations between species traits and allozyme diversity: implications for conservation biology. In: Falk DA, Holsinger KE (eds) Genetics and conservation of rare plants. Oxford University Press, Oxford, pp 75–86

    Google Scholar 

  • Hawthorn WD (1996) Holes and sums of parts in Ghanaian forest: regeneration, scale and sustainable use. Proc R Soc Edinb 104B:75–176

    Google Scholar 

  • Keller J (2001) Marantaceae. In Hanelt P, Institute of Crop Plant Research (eds) Mansfeld’s encyclopedia of agricultural and horticultural crops. Springer-Verlag, Berlin, vol 5, pp 2405–2411

  • Kerényi Z, Zeller K, Hornok L, Leslie JF (1999) Molecular standardization of mating type terminology in the Gibberella fujikuroi species complex. Appl Environ Microbiol 65:4071–4076

    PubMed  Google Scholar 

  • Leistner OA (2000) Seed plants of southern tropical Africa: families and genera. National Botanical Institute, Pretoria, p 409

    Google Scholar 

  • Ley AC, Claßen-Bockhoff R (2005) Floral diversity of African Marantaceae. Poster presented at: XVII international botanical congress, 17–23 July, Austria Centre, Vienna, Austria

  • Ley AC, Claßen-Bockhoff R (2009) Pollination syndromes in African Marantaceae. Ann Bot 104:41–56

    Article  PubMed  Google Scholar 

  • Liu J-J, Sturrock R, Ekramoddoullah AKM (2010) The superfamily of thaumatin-like proteins: its origin, evolution, and expression towards biological function. Plant Cell Rep 29:419–436

    Article  PubMed  CAS  Google Scholar 

  • Lynch M, Milligan BG (1994) Analysis of provenance genetic structure with RAPD markers. Mol Ecol 3:91–99

    Article  PubMed  CAS  Google Scholar 

  • Meléndez-Ackerman EJ, Speranza P, Kress WJ, Rohena L, Toledo E, Cortés C, Treece D, Gitzendanner M, Soltis P, Soltis D (2005) Microevolutionary processes inferred from AFLP and morphological variation in Heliconia bihai (Heliconiaceae). Int J Plant Sci 166:781–794

    Article  Google Scholar 

  • Murray MG, Thompson WF (1980) Rapid isolation of high molecular weight plant DNA. Nucleic Acids Res 8:4321–4326

    Article  PubMed  CAS  Google Scholar 

  • Mwase WF, Bjørnstad Å, Stedje B, Bokosi JM, Kwapata MB (2006) Genetic diversity of Uapaca kirkiana Muel. Årg. provenances as revealed by amplified fragment length polymorphisms (AFLPs). Afr J Biotechnol 5:1205–1213

    CAS  Google Scholar 

  • Myburg AA, Remington DL, O’Malley DM, Sederoff RR, Whetten RW (2001) High-throughput AFLP analysis using infrared dye-labelled primers and an automated DNA sequencer. BioTechniques 30:348–357

    PubMed  CAS  Google Scholar 

  • Onwueme IC, Onochie BE, Sofowora EA (1979) Cultivation of T. [Thaumatococcus] daniellii—the sweetener. World Crops 31:106–109, 111

  • Peakall R, Smouse PE (2006) Genalex 6: genetic analysis in excel. Provenance genetic software for teaching and research. Mol Ecol Notes 6:288–295

    Article  Google Scholar 

  • Peakall R, Smouse PE, Huff DR (1995) Evolutionary implications of allozyme and RAPD variation in diploid provenances of dioecious buffalograss Buchloë dactyloides. Mol Ecol 4:135–147

    Article  CAS  Google Scholar 

  • Pfennig DW, Wund MA, Snell-Rood EC, Cruickshank T, Schlichting CD, Moczek AP (2010) Phenotypic plasticity’s impacts on diversification and speciation. Trends Ecol Evol 25:459–467

    Article  PubMed  Google Scholar 

  • Prince LM, Kress WJ (2006) Phylogenetic relationships and classification in Marantaceae: insights from plastid DNA sequence data. Taxon 55:281–296

    Article  Google Scholar 

  • Rohlf FJ (2000) NTSYSpc: numerical taxonomy and multivariate analysis system. Exeter Software, New York

    Google Scholar 

  • Russell JR, Weber JC, Booth A, Powell W, Sotelo-Montes C, Dawson IK (1999) Genetic variation of Calycophyllum spruceanum in the Peruvian Amazon Basin, revealed by amplified fragment length polymorphism (AFLP) analysis. Mol Ecol 8:199–204

    Article  Google Scholar 

  • Saitou N, Nei M (1987) The neighbor-joining method: a new method for reconstructing phylogenetic trees. Mol Biol Evol 4:406–425

    PubMed  CAS  Google Scholar 

  • Techaprasan J, Klinbunga S, Jenjittikul T (2008) Genetic relationships and species authentication of Boesenbergia (Zingiberaceae) in Thailand based on AFLP and SSCP analyses. Biochem Syst Ecol 36:408–416

    CAS  Google Scholar 

  • Termote C, Van Damme P, Djailo BD (2011) Eating from the wild: Turmub, Mbole and Bali traditional knowledge on non-cultivated edible plants, District Tshopo, DRCongo. Genet Resour Crop Evol 58:585–618

    Article  Google Scholar 

  • Venkatachalam L, Sreedhar RV, Bhagyalakshmi N (2008) The use of genetic markers for detecting DNA polymorphism, genotype identification and phylogenetic relationships among banana cultivars. Mol Phylogenet Evol 47:974–985

    Article  PubMed  CAS  Google Scholar 

  • Vos P, Hogers R, Bleeker M, Reijans M, Lee TVD, Hornes M, Frijters A, Pot J, Peleman J, Kuiper M, Zabeau M (1995) AFLP: a new technique for DNA fingerprinting. Nucleic Acids Res 23:4407–4414

    Article  PubMed  CAS  Google Scholar 

  • Waliszewski WS, Oppong S, Hall JB, Sinclair FL (2005) Implications of local knowledge of the ecology of a wild super sweetener for its domestication and commercialization in west and central Africa. Econ Bot 59:231–243

    Article  Google Scholar 

  • White F (1979) The Guineo-Congolian region and its relationships to other Phytochoria. Bulletin du Jardin botanique national de Belgique/Bulletin van de National Plantentuin van België 49:11–55

    Article  Google Scholar 

  • White F (1983) The vegetation of Africa. UNESCO natural resources 20. UNESCO, Paris

    Google Scholar 

  • Woodhead M, Russell J, Squirrell J, Hollingsworth PM, Mackenzie K, Gibby M, Powell W (2005) Comparative analysis of provenance genetic structure in Athyrium distentifolium (Pteridophyta) using AFLPs and SSRs from anonymous and transcribed gene regions. Mol Ecol 14:1681–1695

    Article  PubMed  CAS  Google Scholar 

Download references

Acknowledgments

We thank the communities of Nsuta and Gbledi-Gbogame villages in Ghana and Etome and Mebanga in Cameroon for assistance with field work and the Wildlife Conservation Society (Cameroon), the Forest Services Division (FSD) (Tarkwa) and Forest Im-Pex (Ghana) for logistical support. The Cameroon Development Corporation kindly provided land for experimental field trials and access to their laboratories. We thank M. Lyonga for field assistance and maintenance of experimental trials and C. Boy for advice on thaumatin extraction. This work was funded by grants from The Natural Resources International Foundation (NRIF), The Gen Foundation, The Society for Experimental Biology, The Sir Richard Stapley Educational Trust, The Sir William Roberts Scholarship and Natex UK Ltd.

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Katherine A. Steele.

Rights and permissions

Reprints and permissions

About this article

Cite this article

Waliszewski, W.S., Sinclair, F.L. & Steele, K.A. Morphological and AFLP diversity in Thaumatococcus daniellii, the source of the protein sweetener thaumatin. Genet Resour Crop Evol 59, 151–161 (2012). https://doi.org/10.1007/s10722-011-9771-9

Download citation

  • Received:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s10722-011-9771-9

Keywords

Navigation