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Wall complex

Fig. 2a-c. Morphology of an empty capsule. Capsules were produced fromo.6% HV alginate/o.6% cellulose sulfate/1.2% polymethylene-co-guanidine/r% calcium chloride. The reaction time was 30 s. The capsule size is approximately r.6o mm while the membrane thickness is 0.033 mm a the wall complex is clearly evident b progression in the membrane thickness 0.073 mm with reaction time r8o s c progression in the membrane thickness o.ro6 mm with reaction time 300 s... [Pg.66]

The Lipoarabinomannan Components of the Cell Wall Complex of Mycobacterium tuberculosis NPOEs in Chemoselective, Regioselective and Three-Component Double Differential Clycosidations... [Pg.345]

About one-fourth or more of the lignin is in the middle lamella-primary wall complex. The remainder is within the holoceliulose system of the cell walls. [Pg.1751]

Grabber, J. H., Ralph, J., Hatfield, R. D., Quideau, S., Kuster T., Pell, A. N., 1996, Dehydrogenation polymcr-ccl 1 wall complexes as a model for lignified grass walls, J. Agric. Food Chem. 44 1453-1459. [Pg.138]

Binding of the metals to the cell wall complex the wall of root cells is directly exposed to the metals available in the soil water phase. From a few to about 80% of the total root metal content was found to be associated with the root cell walls in various dicotyledonous plants (Ernst, 1972, 1974 Farago et al., 1980). Metals can be electrostatically bound to carboxylic functions of pectins and to charged groups of wall proteins even more complex chemical bounds can occur. Moreover, amorphous metal precipitates as phosphate, carbonate and silicate have been reported (Ernst et al., 1990). [Pg.166]

Recent interest in oligoarabinans, have been triggered by their presence in the lipoarabinoman-nan polysaccharide component of the cell wall complex of mycobacteria [85]. Several research groups have employed -pentenyl arabinofuranosides in their approaches to oligoarabinans. [Pg.591]

K. N. Jayaprakash, J. Lu, and B. Fraser-Reid, Synthesis of a lipomannan component of the cell-wall complex of Mycobacterium tuberculosis is based on Paulsen s concept of donor/acceptor match, Angew. Chem. Int. Ed., 44 (2005) 5894-5898. [Pg.156]

Solid-State NMR of Glycopeptide Antibiotics with Bacterial Cell Wall Complexes Conclusions... [Pg.198]

For the ESR experiments, intact tissues lxlx4mm were equilibrated at pH 5 in water for 15 min. and decanted this procedure was repeated thrice. About 10-40 mg dry weight of cell wall complex was used for each treatment combination. Samples were equilibrated 22 2° in 10 ml of various concentrations of Mn (1, 1 ), Mn with Ca (18) or Cu ... [Pg.176]

Other information may help to solve treatment problems in the future. One important chemical constituent has been overlooked the protein, ex-tensin, associated with the primary wall (8). Extensin is a structural protein similar to collagen. It may have a quinone tannage, which gives the strongest known cross-links to protein and makes it insoluble. Extensin is located (1-5%) in the most persistent part of the cell wall, the middle lamellaprimary wall complex. Its presence there must have something to do with the persistence of this complex. [Pg.11]

Pectin analysis also needs more refining and emphasis. Pectic substances are a group of related substances (protopectin, pectin, and pectic acids), each with specific chemical characteristics (9). Both the protopectin and the pectic acid, pectinic acid, form insoluble complexes with metals, especially calcium. These too, like the protein, are concentrated in the persistent middle lamella-primary wall complex. [Pg.11]

Lignin makes up to 15-35% of fresh wood, with 60-80% of the lignin located in the secondary wall. The middle lamella-primary wall complex has the higher concentration (0.6-0.9 g/g), as compared to the secondary wall (0.2-0.3 g/g). In the cell wall, lignin, hemicellulose, and pectin fill the interstices between the cellulose microfibrils. Lignin may be bound to hemi-celluloses, the most unstable of the biopolymers in wood, and thus hemicellulose loss would expose the lignin to chemical changes. [Pg.11]

Scanning electron microscopy (SEM) before and after histochemical extraction of lignin with peracetic acid has shown the location of cellulose and lignin and the persistence of the middle lamella-primary wall complex in archaeological wood buried for 2500 years (ii). [Pg.12]

Figure 13. Scanning electron micrograph of transverse section of air-dried Picea sp. from a 1200 A.D. Thule site Herschel Island. The fractured surface shows oil-swollen secondary cell walls of latewood tracheids separated from the primary wall complex. This is shown in detail in Figure 14. The earlywood tracheids appear normal. Figure 13. Scanning electron micrograph of transverse section of air-dried Picea sp. from a 1200 A.D. Thule site Herschel Island. The fractured surface shows oil-swollen secondary cell walls of latewood tracheids separated from the primary wall complex. This is shown in detail in Figure 14. The earlywood tracheids appear normal.
With respect to the TMI the zeolite framework behaves like an anion, a solvent or a ligand. The ions are usually introduced from aqueous solution as hexaquo floating complexes [M(OH2)6]". Upon partial dehydration they become stabilized as wall complexes bound in part to the framework and in part to remain-... [Pg.377]

A major development has been to provide easy release of parts from the mold. Special mold treatments and careful physical removal of parts were required, increasing the cost. PURs now incorporate an internal mold release (IMR) agent that improves part performance and process economics. However, thin-walled, complex parts may require the use of release agents on the mold. Material developments are under way to rectify this situation. [Pg.284]

Other encapsulations utilize more or less similar methods for the formation of the capsule wall. Complex coacervation utilizes the reaction of an anionic water-soluble polymer with a cationic material to form the shell wall that separates from the solution. As the coacervate separates from the solution, it will tend to coat suspended particles with a protective shell. The shell wall is then hardened with a cross-linking agent. In situ polymerization is used to form urea formaldehyde or melamine formaldehyde shells by using heat to cross-link the monomers forming the shell waU. Interfacial polymerization with isocyanates via hydrolysis is another method to form a shell wall at an organic-water interface. In this case, water acts to hydrolyze some of the polyisocyanate to an amine, which cross-links to form the polyurea microcapsule waU. [Pg.321]

Underhood electrical connectors are molded from a range of resins from thermoplastic polyesters PBT and PET to LCP, depending on property requirements, particularly temperature stability, stiffness/strength ratio, dimensional stability, and chemical resistance. Recent grades have improved toughness and higher MFR for thin-wall, complex connectors. [Pg.609]

Very thin-walled, complex parts, possibly with intricate inserts, require a more accurate weight with less variance of magnitude 1% from shot to shot. For these applications film gates in the parting line are to be preferred. [Pg.113]

Alkaline Phosphatases.—The properties of an alkaline phosphatase cell-wall complex of Pseudomonas aeruginosa have been studied in vitro. ... [Pg.403]


See other pages where Wall complex is mentioned: [Pg.386]    [Pg.52]    [Pg.71]    [Pg.73]    [Pg.167]    [Pg.235]    [Pg.354]    [Pg.233]    [Pg.200]    [Pg.148]    [Pg.62]    [Pg.381]    [Pg.385]    [Pg.386]    [Pg.136]    [Pg.12]    [Pg.387]    [Pg.53]    [Pg.72]    [Pg.150]    [Pg.276]    [Pg.108]    [Pg.237]    [Pg.607]    [Pg.188]    [Pg.296]   
See also in sourсe #XX -- [ Pg.72 ]




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