Plant cells walls

Ice formation is both beneficial and detrimental. Benefits, which include the strengthening of food stmctures and the removal of free moisture, are often outweighed by deleterious effects that ice crystal formation may have on plant cell walls in fmits and vegetable products preserved by freezing. Ice crystal formation can result in partial dehydration of the tissue surrounding the ice crystal and the freeze concentration of potential reactants. Ice crystals mechanically dismpt cell stmctures and increase the concentration of cell electrolytes which can result in the chemical denaturation of proteins. Other quaHty losses can also occur (12). 

Hemicellulose [9034-32-6] is the least utilized component of the biomass triad comprising cellulose (qv), lignin (qv), and hemiceUulose. The term was origiaated by Schulze (1) and is used here to distinguish the nonceUulosic polysaccharides of plant cell walls from those that are not part of the wall stmcture. Confusion arises because other hemicellulose definitions based on solvent extraction are often used in the Hterature (2—4). The term polyose is used in Europe to describe these nonceUulosic polysaccharides from wood, whereas hemicellulose is used to describe the alkaline extracts from commercial pulps (4). The quantity of hemicellulose in different sources varies considerably as shown in Table 1. 

R. D. Preston, The Physical Biology of Plant Cell Walls, Chapman and Had, London, 1974. 

G. O. AspiuaU, iu F. Loewus ed.. Biogenesis of Plant Cell Wall Polysaccharides, Academic Press, Inc., New York, 1973. 

Historically, dietary fiber referred to iasoluble plant cell wall material, primarily polysaccharides, not digested by the endogenous enzymes of the human digestive tract. This definition has been extended to iaclude other nondigestible polysaccharides, from plants and other sources, that are iacorporated iato processed foods. Cellulose [9004-34-6] (qv) is fibrous however, lignin [9005-53-2] (qv) and many other polysaccharides ia food do not have fiberlike stmctures (see also Carbohydrates). 

Detergent Methods. The neutral detergent fiber (NDF) and acid detergent fiber (ADF) methods (2), later modified for human foods (13), measure total insoluble plant cell wall material (NDF) and the cellulose—lignin complex (ADF). The easily solubilized pectins and some associated polysaccharides, galactomaimans of legume seeds, various plant gums, and seaweed polysaccharides are extracted away from the NDF. They caimot be recovered easily from the extract, and therefore the soluble fiber fraction is lost. 

Glucomannans (GM) and galactoglucomannans (GGM), common constituents of plant cell walls, are the major hemicellulosic components of the secondary cell walls of softwoods, whereas in the secondary cell walls of hardwoods they occur in minor amounts. They are suggested to be present together with xylan and fucogalactoxyloglucan in the primary cell walls of higher plants [192]. These polysaccharides were extensively studied in the 1960s [6,193]. 

Figures 3 and 5 from Biochimie, vol 85, Perez S, Rodrigues-Carvajal MA, Doco T (2003) A complex plant cell wall polysaccharide rhamnogalactmonan 11. A structure in quest of a function. p 109-pl21...

Role of Microtubules in Cytokinesis and in Plant Cell Wall Formation... 

Kacurakova, M., Capek, P., Sasinkova, V., WeUner, N. Ebringerova, A. (2000). FT-IR study of plant cell wall model compounds pectic polysaccharides and hemicelluloses. Carbohydrate Polymers, Vol. 43,2, (October 2000), pp. (195-203), ISSN 0144-8617... 

The ability of PO to interact with the acetyl residues of chitin allows us to compare them with monovalent lectins (i.e. extensins) which when binding with hemicellulose are only affected in a medium with a high ionic strength (Brownleader et al., 2006). As a rule, POs are bound with the plant cell wall and act as its modifiers. Some POs can form complexes with an extensin of cell walls (Brownleader et al., 2006). Consequently, chitin-specific sites that are capable of interacting with polysaccharides exist in the molecules of PO, and these sites can resemble the membrane receptor binding sites or else be similar to the domains of heparinbinding proteins (Kim et al., 2001). 

Carpita N. Tierney M. Campbell M. (2001) Molecular biology of the plant cell wall Searching for genes that define structure, architecture and dynamics // Plant Mol. Biol. V. 47. P. 1- 5. 

Gorshkova T. A. (2007) Plant Cell Wall as a Dynamic System (in Russian), Nauka, Moscow. 

Ryan, C.A., Bishop, P.D., Walker-Simmons, M., Brown, W. Graham, J. (1985). The role of pectic fragments of the plant cell wall in response to biological stresses. In Cellular and Molecular Biology of Plant Stress, ed. J.L. Key T. Kosuge, pp. 319-34. New York Alan R. Liss. 

Plant cell walls are made of bundles of cellulose chains laid down in a cross-hatched pattern that gives cellulose strength in all directions. Hydrogen bonding between the chains gives cellulose a sheetlike structure. 

Dietary fibre, which comprises all the non-digestible structural carbohydrates of plant cell walls and any associate lignin, provides a further example of a complex food-borne factor which cannot be classified as a nutrient, and which continues to generate debate over such issues as definition and analytical techniques. However, whatever the unresolved complexities, dietary fibre has a lengthy history and had proved itself eminently suitable as a component of functional food products long before the term was even coined. 

Other galacturonic acid-containing plant cell wall polysaccharides... 

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