Register      Login
Functional Plant Biology Functional Plant Biology Society
Plant function and evolutionary biology
RESEARCH ARTICLE

Hydration of Cuphea seeds containing crystallised triacylglycerols

Gayle M. Volk A , Jennifer Crane A , Ann M. Caspersen A , David Kovach B , Candice Gardner B and Christina Walters A C
+ Author Affiliations
- Author Affiliations

A USDA-ARS National Center for Genetic Resources Preservation, Fort Collins, CO 80521, USA.

B USDA-ARS North Central Regional Plant Introduction Station, Ames, IA 50011, USA.

C Corresponding author. Email: christina.walters@ars.usda.gov

D This paper originates from an International Symposium in Memory of Vincent R. Franceschi, Washington State University, Pullman, Washington, USA, June 2006.

Functional Plant Biology 34(4) 360-367 https://doi.org/10.1071/FP06291
Submitted: 8 November 2006  Accepted: 1 February 2007   Published: 19 April 2007

Abstract

Seeds that exhibit intermediate storage behaviour seem to die under conventional –18°C storage conditions. Cuphea wrightii A. Gray, C. laminuligera Koehne, C. carthagenensis (Jacq.) J.F. Macbr. and C. aequipetala Cav are considered sensitive to low temperature storage. The seeds of these species have triacylglycerols (TAG) that are crystalline at –18°C and melt when the seeds are warmed to >35°C. In contrast, seeds of tolerant species, C. lanceolata W.T. Aiton and C. hookeriana Walp., have TAG that crystallise at temperatures below –18°C and are fluid at 22°C. Cuphea seeds imbided while TAG are crystalline fail to germinate and exhibit visual damage. However, germination proceeded normally when dry seeds were warmed adequately to melt any crystalline TAG before imbibition. Reduced germination and cellular disruption including loss of lipid body compartmentation and fragmented protein bodies develop in seeds with crystalline TAG equilibrated to >0.1 g H2O g–1 DW. This damage cannot be reversed, even when seeds are dried before the damage can be visually detected. Results from this work reveal that the seeds of some species with intermediate type physiologies can be successfully placed into conventional –18 and –80°C storage facilities.

Additional keywords: intermediate storage behaviour, lipid, phase transition, seed, temperature, water.


Acknowledgements

This publication is dedicated in memory of Dr Vincent Franceschi whose enthusiasm and passion for cell biology was contagious. Mention of trade names or commercial products in this article is solely for the purpose of providing specific information and does not imply recommendation or endorsement by the US Department of Agriculture.


References


Bozzola JJ , Russell LD (1991) ‘Electron microscopy.’ (Jones and Bartlett Publishers: Boston)

Crane J, Miller AL, Van Rockel JW, Walters C (2003) Triacylglycerols determine the unusual storage physiology of Cuphea seed. Planta 217, 699–708.
Crossref | GoogleScholarGoogle Scholar | PubMed | open url image1

Crane J, Kovach D, Gardner C, Walters C (2006) Triacylglycerol phase and ‘intermediate’ seed storage physiology: a study of Cuphea carthagenensis. Planta 223, 1081–1089.
Crossref | GoogleScholarGoogle Scholar | PubMed | open url image1

del Cerro M, Cogen J, del Cerro C (1980) Stevenel’s blue, an excellent stain for optical microscopical study of plastic embedded tissues. Microscopica Acta 83, 117–121.
PubMed |
open url image1

Eira MTS, Silva EA Amaral da, De Castro RD, Dussert S, Walters C, Bewley JD, Hilhorst HWM (2006) Coffee seed physiology. Brazilian Journal of Plant Physiology 18, 149–163.
Crossref | GoogleScholarGoogle Scholar | open url image1

Ellis RH, Hong TD, Roberts EH (1990) An intermediate category of seed behavior? I. Coffee. Journal of Experimental Botany 41, 1167–1174.
Crossref | GoogleScholarGoogle Scholar | open url image1

Ellis RH, Hong TD, Roberts EH, Soetisna U (1991) Seed storage behaviour in Elaeis guineensis. Seed Science Research 1, 99–104. open url image1

Golovina EA, Hoekstra FA (2002) Membrane behavior as influenced by partitioning of amphiphiles during drying: a comparative study in anhydrobiotic plant systems. Comparative Biochemistry and Physiology 131, 545–558.
Crossref | GoogleScholarGoogle Scholar | PubMed | open url image1

Herman EM (1995) Cell and molecular biology of seed oil bodies. In ‘Seed development and germination’. (Eds J Kigel, G Galili) pp. 195–214. (Marcel Dekker: New York)

Hoekstra FA, Golovina EA, Buitink J (2001) Mechanisms of plant desiccation tolerance. Trends in Plant Science 6, 431–438.
Crossref | GoogleScholarGoogle Scholar | PubMed | open url image1

Hong TD , Linnington S , Ellis RH (1996) ‘Seed storage behaviour: a compendium. Handbook for genebanks No.4.’ (International Plant Genetic Resources Institute: Rome)

Hor YL, Kim YJ, Ugap A, Chabrillange N, Sinniah UR, Engelmann F, Dussert S (2005) Optimal hydration status for cryopreservation of intermediate oily seeds: Citrus as a case study. Annals of Botany 95, 1153–1161.
Crossref | GoogleScholarGoogle Scholar | PubMed | open url image1

McDonald MB (1999) Seed deterioration: physiology, repair and assessment. Seed Science and Technology 27, 177–237. open url image1

Sacandé M, Buitink J, Hoekstra FA (2000) A study of water relations in neem (Azadirachta indica) seed that is characterized by complex storage behaviour. Journal of Experimental Botany 51, 635–643.
Crossref | GoogleScholarGoogle Scholar | PubMed | open url image1

Small DM (1988) ‘The physical chemistry of lipids: from alkanes to phospholipids.’ (Plenum Press: New York)

Vertucci CW, Roos EE (1993) Theoretical basis of protocols for seed storage. II. The influence of temperature on optimal moisture levels. Seed Science Research 3, 201–213. open url image1

Volk GM, Crane J, Caspersen AM, Hill LM, Gardner C, Walters C (2006) Massive cellular disruption occurs during early imbibition of Cuphea seeds containing crystallized triacylglycerols. Planta 224, 1415–1426.
Crossref | GoogleScholarGoogle Scholar | PubMed | open url image1