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

Genetic Resources and Crop Evolution, Nov 2011

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.

Article PDF cannot be displayed. You can download it here:

https://link.springer.com/content/pdf/10.1007%2Fs10722-011-9771-9.pdf

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

Genetic Resources and Crop Evolution January 2012, Volume 59, Issue 1, pp 151–161 | Cite as Morphological and AFLP diversity in Thaumatococcus daniellii, the source of the protein sweetener thaumatin AuthorsAuthors and affiliations Wojciech S. WaliszewskiFergus L. SinclairKatherine A. Steele Notes on Neglected and Underutilized Crops First Online: 05 November 2011 219 Downloads 3 Citations 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. KeywordsDNA fingerprinting Genetic diversity Intercropping Marantaceae Thaumatin Thaumatococcus daniellii West Africa Wild edible plant  This is a preview of subscription content, log in to check access. Notes 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. References Abbiw DK (1990) The useful plants of Ghana: West African uses of wild and cultivated plants. Intermediate Technology Publications/Royal Botanic Gardens, KewGoogle 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 278–293Google 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 107:736–744PubMedCrossRefGoogle Scholar Booth AH (1958) The Niger, the Volta and the Dahomey Gap as geographic barriers. Evolution 12:48–62CrossRefGoogle Scholar Boy C, Waliszewski WS (2009) Extraction of thaumatin from Thaumatococcus daniellii arils. Protocol, Natex UK Ltd, SandyGoogle 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 14:1047–1057CrossRefGoogle 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 69:465–472PubMedCrossRefGoogle Scholar Chao CCT, Devanand PS, Chen JJ (2005) AFLP analysis of genetic relationships among Calathea species and cultivars. Plant Sci 168:1459–1469CrossRefGoogle 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, BelgiumGoogle Scholar Dhetchuvi MM, Diafouka A (1993) Thaumatococcus daniellii (Benn.) Benth. var. puberulifolius Dhetchuvi and Diafouka (Marantaceae), une nouvelle variété d’Afrique Centrale. Belg J Bot 126:206–208Google 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 9:1149–1157PubMedCrossRefGoogle 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 155:95–122Google 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 11:725–738PubMedCrossRefGoogle 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 60:39–55PubMedGoogle Scholar Fry CH, Keith S, Urban K (1982–2004) The birds of Africa, vols 1–7. Academic Press, LondonGoogle Scholar 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 92:508–518PubMedCrossRefGoogle 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 75–86Google Scholar Hawthorn WD (1996) Holes and sums of parts in Ghanaian forest: regeneration, scale and sustainable use. Proc R Soc Edinb 104B:75–176Google 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 2405–2411Google Scholar Kerényi Z, Zeller K, Hornok L, Leslie JF (1999) Molecular standardization of mating type terminology in the Gibberella fujikuroi species complex. Appl Environ Microbiol 65:4071–4076Pu (...truncated)


This is a preview of a remote PDF: https://link.springer.com/content/pdf/10.1007%2Fs10722-011-9771-9.pdf
Article home page: http://link.springer.com/article/10.1007/s10722-011-9771-9

Wojciech S. Waliszewski, Fergus L. Sinclair, Katherine A. Steele. Morphological and AFLP diversity in Thaumatococcus daniellii, the source of the protein sweetener thaumatin, Genetic Resources and Crop Evolution, 2011, pp. 151-161, Volume 59, Issue 1, DOI: 10.1007/s10722-011-9771-9