Suberin

Short description: Hydrophobic lipid polyester in plant cell walls

Suberin, cutin and lignins are complex, higher plant epidermis and periderm cell-wall macromolecules, forming a protective barrier. Suberin, a complex polyester biopolymer, is lipophilic, and composed of long chain fatty acids called suberin acids, and glycerol. Suberins and lignins are considered covalently linked to lipids and carbohydrates, respectively, and lignin is covalently linked to suberin, and to a lesser extent, to cutin.[1][2][3] Suberin is a major constituent of cork, and is named after the cork oak, Quercus suber. Its main function is as a barrier to movement of water and solutes.

## Anatomy and physiology

Suberin is highly hydrophobic and a somewhat 'rubbery' material. In roots, suberin is deposited in the radial and transverse/tangential cell walls of the endodermal cells. This structure, known as the Casparian strip or Casparian band, functions to prevent water and nutrients taken up by the root from entering the stele through the apoplast. Instead, water must bypass the endodermis via the symplast. This allows the plant to select the solutes that pass further into the plant. It thus forms an important barrier to harmful solutes.[4] For example, mangroves use suberin to minimize salt intake from their littoral habitat.

Suberin is found in the phellem layer of the periderm (or cork). This is outermost layer of the bark. The cells in this layer are dead and abundant in suberin, preventing water loss from the tissues below. Suberin can also be found in various other plant structures. For example, they are present in the lenticels on the stems of many plants and the net structure in the rind of a netted melon is composed of suberised cells.

## Structure and biosynthesis

Suberin consists of two domains, a polyaromatic and a polyaliphatic domain.[5] The polyaromatics are predominantly located within the primary cell wall, and the polyaliphatics are located between the primary cell wall and the cell membrane. The two domains are supposed to be cross-linked. The exact qualitative and quantitative composition of suberin monomers varies in different species. Some common aliphatic monomers include α-hydroxyacids (mainly 18-hydroxyoctadec-9-enoic acid) and α,ω-diacids (mainly octadec-9-ene-1,18-dioic acid). The monomers of the polyaromatics are hydroxycinnamic acids and derivatives, such as feruloyltyramine.

In addition to the aromatics and aliphatics components, glycerol has been reported a major suberin component in some species. The role of glycerol is proposed to interlink aliphatic monomers, and possibly also to link polyaliphatics to polyaromatics, during suberin polymer assembly. The polymerization step of aromatic monomers has been shown to involve a peroxidase reaction.

The biosynthesis of the aliphatic monomers shares the same upstream reactions with cutin biosynthesis, and the biosynthesis of aromatics shares the same upstream reactions with lignin biosynthesis.

Phlobaphen also occurs in the polyaromatic part of the suberin mixture.

## References

1. ↑ Lewis, N. G.; Yamamoto, E.; Wooten, J. B.; Just, G.; Ohashi, H.; Towers, G. H. (1987). "Monitoring biosynthesis of wheat cell-wall phenylpropanoids in situ". Science 237 (4820): 1344–6. doi:10.1126/science.237.4820.1344. PMID 17801473. Bibcode: 1987Sci...237.1344L.
2. ↑ Graça, J. (2015). "Suberin: The biopolyester at the frontier of plants". Frontiers in Chemistry 3: 62. doi:10.3389/fchem.2015.00062. PMID 26579510. Bibcode: 2015FrCh....3...62G.
3. ↑ Bernards, M.A. (March 2002). "Demystifying suberin". Canadian Journal of Botany 80 (3): 227–240(14). doi:10.1139/b02-017.
4. ↑ Kolattukudy, P. E. (1984). "Biochemistry and function of cutin and suberin". Canadian Journal of Botany 62 (12): 2918–2933. doi:10.1139/b84-391. ISSN 0008-4026.
5. ↑ Kolattukudy, P. E. (1980). "Biopolyester Membranes of Plants: Cutin and Suberin". Science 208 (4447): 990–1000. doi:10.1126/science.208.4447.990. ISSN 0036-8075. PMID 17779010. Bibcode: 1980Sci...208..990K.

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Types of phenylpropanoids

Classes of phenylpropanoids|

* Hydroxycinnamic acids
* Chromones (Furanochromones)
* Cinnamaldehydes
* Monolignols
* Coumarins
* Chalcones
* Flavonoids
* Phenylpropenes
* Stilbenoids
* Lignans
* Lignins
* Suberins

Examples|

* Rhododendrin

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