Arabinogalactans structure

Within the scope of this review, the contributions of the last decade concerning cell-wall polysaccharides isolated from woody and other plant tissues will be reviewed according to the above-proposed classification of hemicelluloses including larch arabinogalactans. The present review article updates and extends previous reviews [3-5] and will focus in particular on new investigated plant sources, isolation methods, structural features, physicochemical and various functional properties of hemicelluloses. Attention will also be paid to the modification of isolated hemicelluloses or hemicellulosic materials and the appHcation possibiUties of hemicelluloses and their derivatives, including their use for the production of composite materials and other biomaterials. 

Arabinogalactans (AGs) are widely spread throughout the plant kingdom. Many edible and inedible plants are rich sources of these polysaccharides. AGs occur in two structurally different forms described as type I and type II, associated with the pectin cell-wall component by physical bonds and some of them are covalently linked to the complex pectin molecule as neutral side chains. Commercial pectins always contain AG 10-15%). AG of type I has a linear (1 4)-y0-o-Galp backbone, bearing 20-40% of of-L-Ara/ residues (1 5)-linked in short chains, in general at position 3. It is commonly found in pectins from citrus, apple and potato [6]. Recently, this AG type has been isolated from the skin of Opuntia ficus indica pear fruits [372]. 

Keywords Arabinogalactans Bioactivity Medicinal plants Rhamnogalacturonans Pectins Structure-activity relations... 

Fig. 2 Average structure of the hairy or ramified region of an apectic substance, with a rhamnogalacturonan I backbone substituted at position 4 of the rhamnose units with arabinan and arabinogalactan type II side chains...

Fig. 7 Structure of the Arabinogalactan type II polymer from Larch...

Black pepper contains several polysaccharides of which one shows a strong effect as an immune enhancer based on the fact that the polymer is an anti-complementary polysaccharide. The polysaccharide has an Mw of approx. 40 kD. It is composed basically of rhamnose, arabinose, galactose and galac-turonic acid, and shows a high binding capacity for the Yariv reagent. This indicates that the side chain of the polymer is of the arabinogalactan type II, which is a common structure for several polysaccharides with an effect on the complement system [70]. 

Fincher, G. B. Stone, B. A., Clarke, A. E. (1983). Arabinogalactan-protein Structure, synthesis and function. Annual Review of Plant Physiology, Vol.34, (June 1983), pp. 47-70, ISSN 0066-4294. 

The cell walls of mycobacteria contain three structures peptidoglycan, an arabinogalactan polysaccharide and long chain hydroxy fatty acids (mycolic acids) which are all covalently linked. Additional non-covalently attached lipid components found in the wall include glycolipids, various phospholipids and waxes. The lipid-rich nature of the mycobacterial wall is responsible for the characteristic acid-fastness on staining and serves as a penetration barrier to many antibiotics. Isoniazid and ethambutol have long been known as specific antimycobacterial agents but their mechanisms of action have only recently become more clearly understood. 

J.W. Van de Vis, Characterization and mode of action of enzymes degrading galactan structures of arabinogalactans. Thesis Wageningen Agricultural University (1994). 

Hydrolysis of mannan-type polysaccharides by P-mannanase is dependent on substitution on and within the main-chain as well as the source of the P-mannanase employed. Characterisation of reaction products can be used to define the sub-site binding requirements of the enzymes as well as the fine-structures of the polysaccharides. Action of c/xt/o-arabinanase and em/o-galactanase on arabinans and arabinogalactans is described. Specific assays for ndo-arabinanase and arabinan (in fruit-juice concentrates) are reported. 

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