Cork

Cork is the name given to the plant tissue that derives from the phellogen (a type of cambium) and has suberized cell walls. Typically these are found in the ‘bark’ of roots and stems that undergo secondary growth. Suberization also occurs in the Casparian band and in cells immediately below wounds.

Keywords: cork; periderm; phellogen; suberin; cell wall

Figure 1. Examples of suberized cork tissues. The outer cork cells of the gymnosperm bark pictured at left represent the most abundant form of suberized cork in above-ground plants. The potato tuber, on the right, has a highly suberized periderm that is only five to six cell layers thick, but helps this storage organ maintain a high water content, even with prolonged storage. In the centre, a champagne cork illustrates one of the major industrial uses for suberized cork tissues.
Figure 2. Schematic diagram of a typical wood stem periderm. The phellogen is evident as a single continuous layer of rectangular, radially flattened cells. Note the position of the phellogen relative to the vascular cambium. Cells to the outside of the phellogen become suberized and form the phellem, or cork. Cells to the inside of the phellogen form the phelloderm, a segment of living parenchyma cells. The common term ‘bark’ refers to all the tissues outside of the vascular cambium, including both the phloem and periderm.
Figure 3. Electron micrograph of a suberized potato tuber cell wall. The picture is of a potato tuber cell that has been induced to suberize by wounding. Notice the multilamellar bands (arrow) between the cell wall and the plasma membrane. Bar, 0.5 m.
Figure 4. The chemical components of ‘suberin’. The major aliphatic components are the long-chain (i.e. C16–C32) fatty acids, alcohols, -hydroxyalkanoic acids and ,-dioic acids and glycerol. The dioic acids are considered diagnostic for suberized tissues. Minor components include 9,10-epoxy-18-hydroxy- and 9,10,18-trihydroxy-octadecanoic acids as well as 9,10-epoxy- and 9,10-dihydroxy-1,18-octadecandioic acids. For the aliphatics, only the C18 octadecanes are shown. The aromatic components include the hydroxycinnamic acids, hydroxycinnamoyl amides and monolignols. Hydroxycinnamic acids can either be esterified to the aliphatic components, either directly or through glycerol, or covalently crosslinked to each other via C–C and C–O–C bonds as well as to other aromatic components and cell wall polysaccharides.
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 References
    Bernards MA and Lewis NG (1998) The macromolecular aromatic domain in suberized tissue: a changing paradigm. Phytochemistry 47: 915–933.
    Cordiero N, Belgacem MN, Silvestre AJD, Neto CP and Gandini A (1998) Cork suberin as a new source of chemicals. I. Isolation and chemical characterization of its composition. Biological Macromolecules 22: 71–80.
    book Esau K (1977) Anatomy of Seed Plants, 2nd edn. New York: John Wiley & Sons.
    Gil AM, Lopes MH, Neto CP and Callaghan PT (2000) An NMR microscopy study of water absorption in cork. Journal of Materials Sciences 35: 1891–1900.
    Graça J and Pereira H (2000) Suberin structure in potato periderm: glycerol, long-chain monomers and glyceryl and feruloyl dimers. Journal of Agriculture and Food Chemistry 48: 5476–5483.
    Holloway PJ (1983) Some variations in the composition of suberin from the cork layers of higher plants. Phytochemistry 22: 495–502.
    Lulai EC and Corsini DL (1998) Differential deposition of suberin phenolic and aliphatic domains and their roles in resistance to infection during potato tuber (Solanum tuberosum L.) wound-healing. Physiological and Molecular Plant Pathology 53: 209–222.
    Matzke K and Reiderer M (1991) A comparative study into the chemical constitution of cutins and suberins from Picea abies (L.) Karst., Quercus robur L., and Fagus sylvatica L. Planta 185: 233–245.
 Further Reading
    book Bernards MA and Razem FA (2001) "The poly(phenolic) domain of potato suberin: a non-lignin cell wall bio-polymer". Phytochemistry (in press).
    book Bracegirdle B and Miles PH (1971) An Atlas of Plant Structure. London: Heinemann Educational Books.
    Davin LB and Lewis NG (1992) Phenylpropanoid metabolism: biosynthesis of monolignols, lignans and neolignans, lignins and suberins. Recent Advances in Phytochemistry 26: 325–375.
    Graça J and Pereira H (1997) Cork suberin: a glyceryl based polymer. Holzforschung 51: 225–234.
    Kolattukudy PE (1980) Biopolyester membranes of plants: cutin and suberin. Science 208: 990–1000.
    Kolattukudy PE (1984) Biochemistry and function of cutin and suberin. Canadian Journal of Botany 62: 2918–2933.
    Lapierre C, Pollet B and Negrel J (1996) The phenolic domain of potato suberin: structural comparison with lignins. Phytochemistry 42: 949–953.
    Oven P, Torelli N, Shortle WC and Zupani (1999) The formation of a ligno-suberised layer and necrophylactic periserm in beech bark (Fagus sylvatica L.). Flora 194: 137–144.
    Vogt E, Schönherr J and Schmidt HW (1983) Water permeability of periderm membranes isolated enzymatically from potato tubers (Solanum tuberosum L.). Planta 158: 294–301.
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How to Cite close
Bernards, Mark A(Feb 2002) Cork. In: eLS. John Wiley & Sons Ltd, Chichester. http://www.els.net [doi: 10.1038/npg.els.0002080]