Home About us Contact
|
Home About us Contact | ||
|
|
||
Wall Polysaccharides (wall + polysaccharide)
Kinds of Wall Polysaccharides Selected AbstractsCombined cell wall polysaccharide, mycotoxin and bacterial lipopolysaccharide exposure and inflammatory cytokine responsesAPMIS, Issue 7 2009LENE JOHANNESSEN Human exposure to environmental microbes occurs regularly. Microbial compounds may interact with each other to affect cellular responses. We hypothesized that interactions between microbial compounds could modulate inflammatory cytokine responses in vitro. We investigated monocyte production of the pro-inflammatory cytokine tumour necrosis factor-, (TNF-,) and the regulatory cytokine interleukin-10 (IL-10) after combined exposure to the fungal cell wall polysaccharide mannan and to the ,-glucan laminarin, the mycotoxin citrinin and bacterial lipopolysaccharide (LPS). Interactions between the cell wall microbial compounds were estimated statistically in a general linear mixed model. We found that LPS (100 ng/ml) and the used ,-glucan (up to 1000 ,g/ml) significantly interacted with each other to reduce TNF-, production. Mannan (up to 100 ,g/ml) did not interact with the ,-glucan, but interacted with LPS. IL-10 production was induced by LPS only. The mycotoxin citrinin did not induce cytokine production, but was toxic to the cells in a dose- and time-dependent manner. However, non-toxic doses of citrinin reduced LPS-induced IL-10 production while LPS-induced TNF-, production was not similarly reduced by citrinin. In conclusion, interactions between microbial compounds can modulate cellular inflammatory cytokine production and experimental investigations of one compound at a time could give misleading conclusions about these combined effects. [source] Molecular determinants of ligand specificity in family 11 carbohydrate binding modules , an NMR, X-ray crystallography and computational chemistry approachFEBS JOURNAL, Issue 10 2008Aldino Viegas The direct conversion of plant cell wall polysaccharides into soluble sugars is one of the most important reactions on earth, and is performed by certain microorganisms such as Clostridium thermocellum (Ct). These organisms produce extracellular multi-subunit complexes (i.e. cellulosomes) comprising a consortium of enzymes, which contain noncatalytic carbohydrate-binding modules (CBM) that increase the activity of the catalytic module. In the present study, we describe a combined approach by X-ray crystallography, NMR and computational chemistry that aimed to gain further insight into the binding mode of different carbohydrates (cellobiose, cellotetraose and cellohexaose) to the binding pocket of the family 11 CBM. The crystal structure of C. thermocellum CBM11 has been resolved to 1.98 Å in the apo form. Since the structure with a bound substrate could not be obtained, computational studies with cellobiose, cellotetraose and cellohexaose were carried out to determine the molecular recognition of glucose polymers by CtCBM11. These studies revealed a specificity area at the CtCBM11 binding cleft, which is lined with several aspartate residues. In addition, a cluster of aromatic residues was found to be important for guiding and packing of the polysaccharide. The binding cleft of CtCBM11 interacts more strongly with the central glucose units of cellotetraose and cellohexaose, mainly through interactions with the sugar units at positions 2 and 6. This model of binding is supported by saturation transfer difference NMR experiments and linebroadening NMR studies. [source] Cell wall hemicelluloses as mobile carbon stores in non-reproductive plant tissuesFUNCTIONAL ECOLOGY, Issue 5 2007G. HOCH Summary 1As essential compounds of plant cell walls, hemicelluloses account for about a quarter of all plant biomass worldwide. 2In seed cotyledons and endosperm of species from several plant families, hemicelluloses are used as mobile carbon reserves. Whether cell wall hemicelluloses of non-reproductive plant tissue are multifunctional molecules, which can also serve as carbon sources during periods of enhanced carbon demand, is still equivocal. 3This review summarizes the current understanding of a possible reserve function of hemicelluloses. Although several descriptive and experimental studies suggested at least partial mobility of cell wall polysaccharides in mature, non-reproductive plant tissues, there is still a need for a broad-scale, ecophysiological exploration of the actual nature of hemicelluloses beyond their structural function. 4The chemical heterogeneity of hemicelluloses may be the major problem for precise quantitative analyses on a large, comparative scale. 5Because of the abundant distribution of hemicelluloses in plants, the existence of a significant mobile carbohydrate pool in cell walls of non-reproductive organs would shed rather new light on plant carbon relations in a source-sink context. 6Consequently, a reserve function of hemicelluloses questions the conventional division of cell compounds into structural (i.e. immobile) and non-structural (i.e. mobile) compounds. [source] Characterisation of Chilean hazelnut (Gevuina avellana) tissues: light microscopy and cell wall polysaccharidesJOURNAL OF THE SCIENCE OF FOOD AND AGRICULTURE, Issue 3 2003Fernando Dourado Abstract By applying several differential staining techniques and light microscopy, the structure and composition of Chilean hazelnut (Gevuina avellana) seeds were analysed. The structure of the G avellana seed is very simple, with a thin, heavily lignified seed coat and two voluminous cotyledons. The embryo food reserves are uniformly distributed over the cotyledon cells. The cell wall polysaccharides were recovered from the alcohol-insoluble residue by mild treatment with warm chlorite solution and sequential extraction with alkali solutions of increasing concentration. FT-IR spectra in the 1200,850,cm,1 region were used together with chemometric techniques to distinguish the hemicellulosic and pectic polysaccharides in the extracts. The most abundant extracts were fractionated by graded precipitation in ethanol. A xyloglucan was identified by 1H and 13C NMR as the major hemicellulosic polysaccharide, with a sugar composition of 4Glc:3.5Xyl:1Gal:0.5Fuc. The hazelnut cell walls are composed of equivalent amounts of pectic polysaccharides, xyloglucans and cellulose. © 2003 Society of Chemical Industry [source] Cell wall polysaccharides of bush butter (Dacryodes edulis (G Don) HJ Lam) fruit pulp and their evolution during ripeningJOURNAL OF THE SCIENCE OF FOOD AND AGRICULTURE, Issue 8 2001Crépin Ella Missang Abstract Cell wall material was isolated as alcohol-insoluble solids (AIS) from bush butter endocarp tissue at different stages of ripeness. AIS were then extracted with 0.05,M CDTA followed by increasing concentrations of KOH (0.05, 1 and 4,M respectively). The chemical extractions solubilised a total of 51.6,60.6% of AIS, the yields of CDTA extracts accounting for approximately 9.6,12.2% of AIS. The extracts as well as the residues were analysed for their sugar composition and protein and starch contents. CDTA extracted the bulk of uronic acid in AIS, but the uronic acid content (after dialysis) of these extracts showed a significant decrease as the fruits ripened (from 439 to 252,mg,g,1 between the first and the last degree of ripeness). Analysis of the CDTA extracts by anion exchange and size exclusion chromatography showed a gradual appearance of new pectic populations at low degrees of methylation and low molecular weights, indicating that CDTA-soluble pectins are demethylated and depolymerised during ripening. The dilute alkali (0.05,M KOH) extracts were essentially composed of proteins in addition to a minor quantity of pectin. The 1,M KOH and principally 4,M KOH treatments led to the extraction of hemicelluloses, mainly xyloglucan-like and mannan-like polymers. These extracts also contained substantial amounts of protein and starch. No variation related to the degree of ripeness was visible in the sugar composition of the alkali extracts. The molecular weight distribution of the hemicelluloses did not change with the degree of ripeness. The final residues accounted for 21.4,27.3% of AIS and were mostly composed of glucose (827,908,mg,g,1). All these results suggested that only CDTA-soluble pectins were involved in bush butter fruit softening. © 2001 Society of Chemical Industry [source] Extensive solubilization and depolymerization of cell wall polysaccharides during avocado (Perseaamericana) ripening involves concerted action of polygalacturonase and pectinmethylesterasePHYSIOLOGIA PLANTARUM, Issue 4 2000Kazuyuki Wakabayashi During the ripening of avocado (Persea americana Mill.) fruit, water-soluble polyuronides increased dramatically, concomitant with marked downshifts in molecular mass. Treatment of cell walls from pre-ripe fruit with purified avocado polygalacturonase (PG, EC 3.2.1.15) promoted the release and molecular mass downshift of polyuronides. The polyuronides released by PG were similar in size distribution to water-soluble polyuronides from fruit at intermediate stages of ripening. Polyuronides released from pre-ripe fruit by PG, although of relatively high molecular mass, were not further degraded upon additional incubation with fresh enzyme. Similarly, water-soluble polyuronides prepared from fruit at intermediate stages of ripening were largely resistant to the action of purified PG in vitro. When polyuronides derived from fruit at intermediate stages of ripening were treated with weak alkali or pectinmethylesterase (PME, EC 3.1.1.11), extensive molecular mass downshifts occurred in response to incubation with PG. These results suggest that PG plays the central role in polyuronide degradation in ripening avocado fruit cell walls and that partial de-esterification is necessary for the increase in the susceptibility of polyuronides to PG. Differences in the patterns of polyuronide depolymerization in avocado fruit compared with the more thoroughly characterized tomato fruit are discussed. [source] Autohydrolysis of plant xylans by apoplastic expression of thermophilic bacterial endo-xylanasesPLANT BIOTECHNOLOGY JOURNAL, Issue 3 2010Bernhard Borkhardt Summary The genes encoding the two endo-xylanases XynA and XynB from the thermophilic bacterium Dictyoglomus thermophilum were codon optimized for expression in plants. Both xylanases were designed to be constitutively expressed under the control of the CaMV 35S promoter and targeted to the apoplast. Transient expression in tobacco and stable expression in transgenic Arabidopsis showed that both enzymes were expressed in an active form with temperature optima at 85 °C. Transgenic Arabidopsis accumulating heterologous endo-xylanases appeared phenotypically normal and were fully fertile. The highest xylanase activity in Arabidopsis was found in dry stems indicating that the enzymes were not degraded during stem senescence. High levels of enzyme activity were maintained in cell-free extracts from dry transgenic stems during incubation at 85 °C for 24 h. Analysis of cell wall polysaccharides after heat treatment of wildtype and transgenic extracts from dry stems showed a decrease in the molecular weight of xylans from transgenic stems. [source] Plant cell wall biosynthesis: genetic, biochemical and functional genomics approaches to the identification of key genesPLANT BIOTECHNOLOGY JOURNAL, Issue 2 2006Naser Farrokhi Summary Cell walls are dynamic structures that represent key determinants of overall plant form, plant growth and development, and the responses of plants to environmental and pathogen-induced stresses. Walls play centrally important roles in the quality and processing of plant-based foods for both human and animal consumption, and in the production of fibres during pulp and paper manufacture. In the future, wall material that constitutes the major proportion of cereal straws and other crop residues will find increasing application as a source of renewable fuel and composite manufacture. Although the chemical structures of most wall constituents have been defined in detail, the enzymes involved in their synthesis and remodelling remain largely undefined, particularly those involved in polysaccharide biosynthesis. There have been real recent advances in our understanding of cellulose biosynthesis in plants, but, with few exceptions, the identities and modes of action of polysaccharide synthases and other glycosyltransferases that mediate the biosynthesis of the major non-cellulosic wall polysaccharides are not known. Nevertheless, emerging functional genomics and molecular genetics technologies are now allowing us to re-examine the central questions related to wall biosynthesis. The availability of the rice, Populus trichocarpa and Arabidopsis genome sequences, a variety of mutant populations, high-density genetic maps for cereals and other industrially important plants, high-throughput genome and transcript analysis systems, extensive publicly available genomics resources and an increasing armoury of analysis systems for the definition of candidate gene function will together allow us to take a systems approach to the description of wall biosynthesis in plants. [source] Arabidopsis XXT5 gene encodes a putative ,-1,6-xylosyltransferase that is involved in xyloglucan biosynthesisTHE PLANT JOURNAL, Issue 1 2008Olga A. Zabotina Summary The function of a putative xyloglucan xylosyltransferase from Arabidopsis thaliana (At1g74380; XXT5) was studied. The XXT5 gene is expressed in all plant tissues, with higher levels of expression in roots, stems and cauline leaves. A T-DNA insertion in the XXT5 gene generates a readily visible root hair phenotype (root hairs are shorter and form bubble-like extrusions at the tip), and also causes the alteration of the main root cellular morphology. Biochemical characterization of cell wall polysaccharides isolated from xxt5 mutant seedlings demonstrated decreased xyloglucan quantity and reduced glucan backbone substitution with xylosyl residues. Immunohistochemical analyses of xxt5 plants revealed a selective decrease in some xyloglucan epitopes, whereas the distribution patterns of epitopes characteristic for other cell wall polysaccharides remained undisturbed. Transformation of xxt5 plants with a 35S::HA-XXT5 construct resulted in complementation of the morphological, biochemical and immunological phenotypes, restoring xyloglucan content and composition to wild-type levels. These data provide evidence that XXT5 is a xyloglucan ,-1,6-xylosyltransferase, and functions in the biosynthesis of xyloglucan. [source] | |||||||||||||