Skip to main content
Log in

Cuticular permeance in relation to wax and cutin development along the growing barley (Hordeum vulgare) leaf

  • Original Article
  • Published:
Planta Aims and scope Submit manuscript

Abstract

The developing leaf three of barley provides an excellent model system for the direct determination of relationships between amounts of waxes and cutin and cuticular permeance. Permeance of the cuticle was assessed via the time-course of uptake of either toluidine blue or 14C-labelled benzoic acid ([14C] BA) along the length of the developing leaf. Toluidine blue uptake only occurred within the region 0–25 mm from the point of leaf insertion (POLI). Resistance—the inverse of permeance—to uptake of [14C] BA was determined for four leaf regions and was lowest in the region 10–20 mm above POLI. At 20–30 and 50–60 mm above POLI, it increased by factors of 6 and a further 32, respectively. Above the point of emergence of leaf three from the sheath of leaf two, which was 76–80 mm above POLI, resistance was as high as at 50–60 mm above POLI. GC-FID/MS analyses of wax and cutin showed that: (1) the initial seven fold increase in cuticular resistance coincided with increase in cutin coverage and appearance of waxes; (2) the second, larger and final increase in cuticle resistance was accompanied by an increase in wax coverage, whereas cutin coverage remained unchanged; (3) cutin deposition in barley leaf epidermis occurred in parallel with cell elongation, whereas deposition of significant amounts of wax commenced as cells ceased to elongate.

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

Abbreviations

BA:

Benzoic acid

FID:

Flame ionization detector

GC:

Gas chromatography

MS:

Mass spectrometry

PAR:

Photosynthetically active radiation

POE:

Point of emergence

POLI:

Point of leaf insertion

RH:

Relative humidity

SEM:

Scanning electron microscopy

References

  • Barnes J, Percy K, Paul N, Jones P, McLauchlin C, Mullineaux P, Creissen G, Wellburn A (1996) The influence of UV-B radiation on the physiochemical nature of tobacco (Nicotiana tabacum L.) leaf surface. J Exp Bot 47:99–109

    Article  CAS  Google Scholar 

  • Barthlott W, Neinhuis C (1997) Purity of the sacred lotus, or escape from the contamination in biological science. Planta 202:1–8

    Article  CAS  Google Scholar 

  • Eigenbrode SD (1996) Plant surface waxes and insect behaviour. In: Kerstiens G (ed) Plant cuticles—an integrated functional approach. BIOS Scientific Publishers Limited, Oxford, pp 201–222

    Google Scholar 

  • Espelie KE, Dean BB, Kolattukudy PE (1979) Composition of lipid-derived polymers from different anatomical regions of several plant species. Plant Physiol 64:1089–1093

    Article  PubMed  CAS  Google Scholar 

  • Franke R, Briesen I, Wojciechowski T, Faust A, Yephremov A, Nawrath C, Schreiber L (2005) Apoplastic polyesters in Arabidopsis surface tissues—a typical suberin and a particular cutin. Phytochemistry 66:2643–2658

    Article  PubMed  CAS  Google Scholar 

  • Fricke W (2002) Biophysical limitation of cell elongation in cereal leaves. Ann Bot 90:157–167

    Article  PubMed  Google Scholar 

  • Fricke W, Akhiyarova G, Veselov D, Kudoyarova G (2004) Rapid and tissue-specific changes in ABA and in growth rate in response to salinity in barley leaves. J Exp Bot 55:1115–1123

    Article  PubMed  CAS  Google Scholar 

  • Jeffree CE (1996) Structure and ontogeny of plant cuticles. In: Kerstiens G (ed) Plant cuticles—an integrated functional approach. BIOS Scientific Publishers Limited, Oxford, pp 33–82

    Google Scholar 

  • Jenks MA, Ashworth EN (1999) Plant epicuticular waxes: function production and genetics. Hortic Rev 23:1–68

    CAS  Google Scholar 

  • Jenks MA, Joly RJ, Peters PJ, Rich PJ, Axtell JD, Ashworth EN (1994) Chemically induced cuticle mutation affecting epidermal conductance to water vapor and disease susceptibility in Sorghum bicolor (L.) Moench. Plant Physiol 105:1239–1245

    PubMed  CAS  Google Scholar 

  • Jetter R, Schäffer S, Riederer (2000) Leaf cuticular waxes are arranged in chemically and mechanically distinct layers: evidence from Prunus laurocerasus L. Plant Cell Environ 23:619–628

    Article  CAS  Google Scholar 

  • Kerstiens G (1996a) Cuticular water permeability and its physiological significance. J Exp Bot 47:1813–1832

    Article  CAS  Google Scholar 

  • Kerstiens G (1996b) Signaling across the divide: a wider perspective of cuticular structure-function relationships. Trends Plant Sci 1:125–129

    Article  Google Scholar 

  • Kerstiens G (2006) Water transport in plant cuticles: an update. J Exp Bot 57:2493–2499

    Article  PubMed  CAS  Google Scholar 

  • Kirsch T, Kaffarnik F, Riederer M, Schreiber L (1997) Cuticular permeability of the three tree species Prunus laurocerasus L., Ginko biloba L. and Juglans regia L.: comparative investigation of the transport properties of intact leaves, isolated cuticles and reconstituted cuticular waxes. J Exp Bot 48:1035–1045

    Article  CAS  Google Scholar 

  • Kunst L, Samuels AL (2003) Biosynthesis and secretion of plant cuticular wax. Prog Lipid Res 42:51–80

    Article  PubMed  CAS  Google Scholar 

  • Lendzian KJ, Schönherr (1983) In vivo study of cutin synthesis in leaves of Clivia minitia Reg. Planta 158:70–75

    Article  CAS  Google Scholar 

  • Lequeu J, Fauconnier M-L, Chammaï A, Bronner R, Blée E (2003) Formation of plant cuticle: evidence for the occurrence of the peroxygenase pathway. Plant J 36:155–164

    Article  PubMed  CAS  Google Scholar 

  • Marinari C, Wolters-Arts M (2000) Complex waxes. Plant Cell 12:1795–1798

    Article  Google Scholar 

  • Merida T, Schönherr J, Schmidt HW (1981) Fine structure of plant cuticles in relation to water permeability: the fine structure of the cuticle of Clivia miniata Reg. Leaves. Planta 152:259–267

    Article  Google Scholar 

  • Niederl S, Kirsch T, Riederer M, Schreiber L (1998) Co-permeability of 3H-labeled water and 14C-labeled organic acids across isolated plant cuticles: investigating cuticular paths of diffusion and predicting cuticular transpiration. Plant Physiol 116:117–123

    Article  CAS  Google Scholar 

  • Rhee Y, Hlousek-Radojcic A, Ponsamuel J, Liu D, Post-Beitenmiller D (1998) Epicuticular wax accumulation and fatty acid elongation activities are induced during leaf development in leeks. Plant Physiol 116:901–911

    Article  PubMed  CAS  Google Scholar 

  • Richardson A, Franke R, Kerstiens G, Jarvis M, Schreiber L, Fricke W (2005) Cuticular wax deposition in growing barley (Hordeum vulgare) leaves commences in relation to the point of emergence of epidermal cells from the sheaths of older leaves. Planta 222:472–483

    Article  PubMed  CAS  Google Scholar 

  • Riederer M, Schönherr J (1988) Development of plant cuticles–fine structure and cutin composition of Clivia miniata Reg. Leaves. Planta 174:127–138

    Article  CAS  Google Scholar 

  • Riederer M, Schreiber L (2001) Protecting against water loss: analysis of the barrier properties of plant cuticles. J Exp Bot 52:2023–2032

    Article  PubMed  CAS  Google Scholar 

  • Ristic Z, Jenks MA (2002) Leaf cuticle and water loss in maize lines differing in dehydration avoidance. J Plant Physiol 159:654–651

    Article  Google Scholar 

  • Šantrůček J, Šimáňová E, Karbulková Šimková M, Schreiber L (2004) A new technique for measurement of water permeability of stomatous cuticular membranes isolated from Hedera helix leaves. J Exp Bot 55:1411–1422

    Article  PubMed  CAS  Google Scholar 

  • Schmidt HW, Schönherr (1982) Development of plant cuticles–occurrence and role of non-ester bonds in cutin of Clivia miniata Reg. Leaves. Planta 156:380–384

    Article  CAS  Google Scholar 

  • Schreiber L, Schönherr J (1992) Analysis of foliar uptake of pesticides in barley leaves: role of epicuticular waxes and compartmentation. Pestic Sci 36:213–221

    Article  CAS  Google Scholar 

  • Schreiber L, Schönherr J (1993) Mobilities of organic compounds in reconstituted cuticular wax of barley leaves: determination of diffusion coefficients. Pestic Sci 38:353–361

    Article  CAS  Google Scholar 

  • Suh MC, Samuels AL, Jetter R, Kunst L, Pollard M, Ohlrogge J, Beisson F (2005) Cuticular lipid composition, surface structure, and gene expression in Arabidopsis stem epidermis. Plant Physiol 139:1649–1665

    Article  PubMed  CAS  Google Scholar 

  • Tanaka T, Tanaka H, Machida C, Watanabe M, Machida Y (2004) A new method for rapid visualization of defects in leaf cuticle reveals five intrinsic patterns of surface defects in Arabidopsis. Plant J 37:139–146

    Article  PubMed  CAS  Google Scholar 

  • Vogg G, Fischer S, Leide J, Emmanuel E, Jetter R, Levy AA, Riederer M (2004) Tomato fruit cuticular waxes and the effects on transpiration barrier properties: functional characterisation of a mutant deficient in a very-long-chain fatty acid β-ketoacyl-CoA synthase. J Exp Bot 55:1401–1410

    Article  PubMed  CAS  Google Scholar 

Download references

Acknowledgments

This research was supported by the UK Biotechnology and Biological Sciences Research Council (BBSRC), Grant 61/P18283 (to W.F.) and a studentship of the University of Paisley.

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Wieland Fricke.

Rights and permissions

Reprints and permissions

About this article

Cite this article

Richardson, A., Wojciechowski, T., Franke, R. et al. Cuticular permeance in relation to wax and cutin development along the growing barley (Hordeum vulgare) leaf. Planta 225, 1471–1481 (2007). https://doi.org/10.1007/s00425-006-0456-0

Download citation

  • Received:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s00425-006-0456-0

Keywords

Navigation