By Peter Ulvskov

Plant Polysaccharides, a very good new quantity in Wiley-Blackwell’s profitable Annual Plant stories sequence, covers the polysaccharides and proteins that shape the elemental structure of the plant mobilephone wall, and the genes that encode the mobile equipment that synthesizes them.The quantity makes a speciality of the evolution of the various households of genes whose items are required to make a selected form of polysaccharide, bringing cognizance to the categorical biochemical houses of the proteins to the extent of sorts of sugar linkages they make.Beautifully illustrated in complete color all through, this unheard of new quantity offers innovative updated details on such vital themes as cellphone wall biology, composition and biosynthesis, glycosyltransferases, hydroxyproline-rich glycoproteins, enzymatic amendment of plant mobilephone wall polysaccharides, glycan engineering in transgenic crops, and polysaccharide nanobiotechnology.Drawing jointly a few of the world’s top specialists in those parts, the editor, Peter Ulvskov, has supplied a landmark quantity that's crucial examining for plant and crop scientists, biochemists, molecular biologists and geneticists. All libraries in universities and study establishmentswhere plant sciences, agriculture, organic, biochemical and molecular sciences are studied and taught must have copies of this crucial quantity.

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Additional info for Annual Plant Reviews, Plant Polysaccharides: Biosynthesis and Bioengineering (Volume 41)

Sample text

Xylanases Some 2AcXyl or 3AcXyl. In Poales, some Fer-Ara and 2AcAra Man, Gal, oligosaccharides. Mannanase Heavily galactosylated mannans in some seeds. Little studied in primary cell walls Man-Glc, ManMan, Man, Glc Mannanase Well known in secondary walls of xylem. Some Man residues 2- or 3-O-acetylated Glc Lichenase, cellulase Only in Poales and Equisetum. Glc Laminarinase Mainly in wounded tissues, wallregenerating protoplasts, and phloem sieve-tubes ? 3 Rhamnogalacturonan-II domains RG-II is a small but exceedingly complex pectic domain.

E. g.

G. g. Selaginella). MeGal is abundant in all lycopodiophytes tested but not in bryophytes or euphyllophytes. MeRha is abundant in homosporous (but not heterosporous) lycopodiophytes. It is a component of their RG-II, in place of Rha (Matsunaga et al. 2004); however, the total MeRha content (Popper & Fry 2004) seriously exceeds what would be required for the modest RG-II content, suggesting that the MeRha of homosporous lycopodiophyte walls is not confined to RG-II. Many lycopodiophyte walls are rich in Man, although the polysaccharides involved have not been characterized.

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