Big Chemical Encyclopedia

Chemical substances, components, reactions, process design ...

Articles Figures Tables About

Polysaccharides mechanisms

RP Scherer, Zydis tablets or (polysaccharide mechanical forces ... [Pg.672]

I. Dea, E. Morris, D. Rees, J. Welsh, H. Barnes and J. Price, Associations of like and unlike polysaccharides mechanism and specificity in galactoraannans, interacting bacterial polysaccharides, and related systems. Carbohydr. Res., 57 (1977) 249. [Pg.926]

This enzyme catalyzes the hydrolysis of 1,4-a-D-glucosidic bonds in polysaccharides (mechanism, 2.4.2.5), effecting successive removals of maltose units from the nonreducing end. Hydrolysis is linked to a Walden inversion at C-1, giving rise to 3-maltose. This inversion, which can be detected polarimetrically, represents a definite characteristic of an exoglycanase. [Pg.333]

Associations of Like and Unlike Polysaccharides Mechanism and Specificity in Galactomannans, Interacting Bacterial Polysaccharides, and Related Systems. Carbo-hyd. Res. 57, 249 (1977). [Pg.246]

Cation (Section 1 2) Positively charged ion Cellobiose (Section 25 14) A disacchande in which two glu cose units are joined by a 3(1 4) linkage Cellobiose is oh tamed by the hydrolysis of cellulose Cellulose (Section 25 15) A polysaccharide in which thou sands of glucose units are joined by 3(1 4) linkages Center of symmetry (Section 7 3) A point in the center of a structure located so that a line drawn from it to any element of the structure when extended an equal distance in the op posite direction encounters an identical element Benzene for example has a center of symmetry Cham reaction (Section 4 17) Reaction mechanism m which a sequence of individual steps repeats itself many times usu ally because a reactive intermediate consumed m one step is regenerated m a subsequent step The halogenation of alkanes is a chain reaction proceeding via free radical intermediates... [Pg.1278]

Dextran gels have been utilized since the late 1950s (1) for the separation of biopolymers. First attempts on Sephadex (2-5) and Sephadex/Sepharose (6-8) systems are documented for hydrolyzed and native starch glucans. Up until now, particularly for the preparative and semipreparative separation of polysaccharides, a range of efficient and mechanically stable Sephacryl gels (9-14) have been developped. [Pg.465]

Agarose gels have been used for more than two decades to separate polysaccharides (17-22). In particular, Sepharose CL 2B is widely used (6-8) to separate native starch, but continuously improved mechanical and chemical stability made all of the Sepharose CL gels perfect systems for the analysis of high molecular and broad distributed polysaccharides (23-28). [Pg.479]

Cell wall Peptidoglycan a rigid framework of polysaccharide cross-linked by short peptide chains. Some bacteria possess a lipopolysaccharide- and protein-rich outer membrane. Mechanical support, shape, and protection against swelling in hypotonic media. The cell wall is a porous nonselective barrier that allows most small molecules to pass. [Pg.25]

Polysaccharide-based CSPs incorporate derivatives of cellulose and amylose adsorbed on silica gel. The selectivity of these CSPs depends upon the nature of the substituents introduced during the derivatization process. The secondary structure of the modified polysaccharide is believed to play a role in selectivity, but the chiral recognition mechanisms have not been fully elucidated [55]. [Pg.309]

To gain an insight into the likely hydrolytic behavior of sulfated simple sugars and polysaccharides, Brimacombe, Foster, Hancock, Overend, and Stacey carried out a rigorous set of experiments with the cyclic sulfates of cyclohexane cis-and trims-1,2-diol as model compounds. The results were interpreted on the reasonable assumption that, in all cases, the cyclic sulfates initially afford a diol monosulfate. Examples of both S-0 and C-0 bond cleavage were encountered. A qualitative reaction mechanism was proposed for use as a working hypothesis for the hydrolysis of sugar sulfates. [Pg.16]

Another major drawback of polysaccharides is their hydrophilic nature leading to low degrees of adhesion between fiber and matrix [11]. Moisture absorption takes place by three types of mechanisms namely diffusion, capillarity, and transport via micro cracks [2]. Among the three, diffusion is considered to be the major mechanism. Water absorption largely depends on the water-soluble or hygroscopic components embedded in the matrix, which acts as a semipermeable membrane. While, fiber/matrix adhesion and fiber architecture also affect the moisture absorption. The results of the water sorption experiment showed an interesting trend. The extent of water uptake was not very significant and also did not increase linearly with amount of filler (Table-2). [Pg.122]

The results of the mechanical properties can be explained on the basis of morphology. The scanning electron micrographs (SEM) of fractured samples of biocomposites at 40 phr loading are shown in figure. 3. It can be seen that all the bionanofillers are well dispersed into polymer matrix without much agglomeration. This is due to the better compatibility between the modified polysaccharides nanoparticles and the NR matrix (Fig. 4A and B). While in case of unmodified polysaccharides nanoparticles the reduction in size compensates for the hydrophilic nature (Fig. 3C and D). In case of CB composites (Fig. 3E) relatively coarse, two-phase morphology is seen. [Pg.128]

The process by which cells take up large molecules is called endocytosis. Some of these molecules (eg, polysaccharides, proteins, and polynucleotides), when hydrolyzed inside the cell, yield nutrients. Endocytosis provides a mechanism for regulating the content of certain membrane components, hormone receptors being a case in point. Endocytosis can be used to learn more about how cells function. DNA from one cell type can be used to transfect a different cell and alter the latter s function or phenotype. A specific gene is often employed in these experiments, and this provides a unique way to smdy and analyze the regulation of that gene. DNA transfection depends upon endocytosis endocy-... [Pg.428]


See other pages where Polysaccharides mechanisms is mentioned: [Pg.14]    [Pg.91]    [Pg.14]    [Pg.91]    [Pg.34]    [Pg.42]    [Pg.295]    [Pg.296]    [Pg.300]    [Pg.413]    [Pg.480]    [Pg.272]    [Pg.100]    [Pg.155]    [Pg.488]    [Pg.106]    [Pg.14]    [Pg.218]    [Pg.684]    [Pg.858]    [Pg.47]    [Pg.444]    [Pg.81]    [Pg.83]    [Pg.196]    [Pg.243]    [Pg.46]    [Pg.126]    [Pg.201]    [Pg.203]    [Pg.212]    [Pg.242]    [Pg.232]    [Pg.140]    [Pg.423]    [Pg.43]    [Pg.117]    [Pg.5]   
See also in sourсe #XX -- [ Pg.139 , Pg.140 , Pg.141 , Pg.142 , Pg.143 , Pg.144 , Pg.145 , Pg.146 , Pg.147 , Pg.148 , Pg.149 , Pg.150 ]




SEARCH



Mechanism in the formation of polysaccharide gels

Polysaccharide biosynthesis insertion mechanism

Polysaccharide gels mechanism

Polysaccharides block mechanism

Polysaccharides monomeric mechanism

Sulphated polysaccharide mechanisms of action

© 2024 chempedia.info