Suberin is a lipophilic macromolecule found in specialized plant cell walls, wherever insulation or protection towards the surroundings is needed. Suberized cells form the periderm, the tissue that envelops secondary stems as part of the bark, and develop as the sealing tissue after wounding or leaf abscission. Suberin is a complex polyester built from poly-functional long-chain fatty acids (suberin acids) and glycerol. The suberin acids composition of a number of plant tissues and species is now established, but how the polyester macromolecule is assembled within the suberized cell walls is not known. In the last years contributions from several areas have however significantly enriched our understanding of suberin. The primary structure of the polyester, i.e. how the suberin acids and glycerol are sequentially linked was revealed, together with the stereochemistry of the mid-chain functional groups some suberin acids have; solid-state NMR studies showed the presence of methylene chains spatially separated and with different molecular mobility; biophysical studies showed the membrane behaviour of suberin acids derivatives, allowing new insights on structure-properties relationships; and a number of candidate genes were conclusively related to suberin biosynthesis. The comprehension of suberin as a macromolecule will be essential to understand its vital protective roles in plants and how they will deal with eventual environmental changes. Suberin is also expected to be a source for high-performing bio-based chemicals, taking advantage of the structural uniqueness of their constituent suberin acids.

The surface of most aerial plant organs is covered with a cuticle that provides protection against multiple stress factors including dehydration. Interest on the nature of this external layer dates back to the beginning of the 19th century and since then, several studies facilitated a better understanding of cuticular chemical composition and structure. The prevailing undertanding of the cuticle as a lipidic, hydrophobic layer which is independent from the epidermal cell wall underneath stems from the concept developed by Brongniart and von Mohl during the first half of the 19th century. Such early investigations on plant cuticles attempted to link chemical composition and structure with the existing technologies, and have not been directly challenged for decades. Beginning with a historical overview about the development of cuticular studies, this review is aimed at critically assessing the information available on cuticle chemical composition and structure, considering studies performed with cuticles and isolated cuticular chemical components. The concept of the cuticle as a lipid layer independent from the cell wall is subsequently challenged, based on the existing literature, and on new findings pointing towards the cell wall nature of this layer, also providing examples of different leaf cuticle structures. Finally, the need for a re-assessment of the chemical and structural nature of the plant cuticle is highlighted, considering its cell wall nature and variability among organs, species, developmental stages, and biotic and abiotic factors during plant growth.

Eucalypt wood (Eucalyptus globulus) was heated in an oven for 2–24 h at 170–200°C and in an autoclave with superheated and saturated steam for 2–12 h at 190–210°C. The chemical composition of untreated wood and thermally treated wood with different mass losses in the range of 1.1–11.9% was studied by summative analysis, and the composition of dichloromethane, ethanol and water extracts was determined by gas chromatography mass spectometry (GC-MS). The hemicelluloses degraded first, mainly regarding the arabinose and xylose moieties. Lignin degraded at a slower rate and cellulose was only slightly affected under severe treatment conditions. The extractive content increased first with heat treatment and decreased later on. Almost all of the original extractives disappeared and new compounds were formed, such as anhydrosugars, mannosan, galactosan, levoglucosan and two C₅ anhydrosugars. The most prominent lignin derived compounds were syringaldehyde, syringic acid and sinapaldehyde. The main difference between autoclave and oven treated samples was the appearance of more oxidized extractives for the oven treatment.