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Chemical Connections enzymes

Mannose-terminating compounds made in connection with glycoprotein work have the sugar either or linked through 0-4 of chitobiose. The first of these reports exemplifies the use of polymer-supported reactions. Chemical and enzymic methods were used in the production of the latter trimer. [Pg.63]

Most chemical toxicants are biotransformed and eliminated from the body in urine or bile however, some xenobiotics are not amenable to these transformations—that is, the body s enzyme systems are ineffective in transforming these compounds to more polar forms. Since these compounds are often very lipid soluble and cannot be quickly eliminated, the body stores them in our fat tissues throughout the body—a process known as bioaccumulation. In order for bioaccumulation to occur, a chemical toxicant must be absorbed faster than it is eliminated. These chemical toxicants are stored in the body s fat or lipids until a dynamic state is reached where the rates of absorption and elimination become about the same. The concentrations of these xenobiotics in fat tissues can be estimated from concentrations in blood that normally carries a small amount of circulating lipid, as reported in Incident 4.3.2.I. (See also in Section 4.2.1, Chemical Connection 4.2.1.1 Solubility, Storage, and Elimination.)... [Pg.206]

Alternatively, enzymes, which are biocatalysts, have many favorable properties compared to conventional chemical catalysts. Enzymes are large proteins that are made up of a sequence of 20 natmaUy occurring amino add residues to form a chain connected by peptide bonds, shown in Figure 1.2. As with chemical catalysts, enzymes alter the reaction by providing different pathways and operate effectively in small amounts (Lorenz and Eck, 2005). It has been reported that enzymes... [Pg.1]

Researchers at the MoneU Center (Philadelphia, Pennsylvania) are using a variety of electrophysical and biochemical techniques to characterize the ionic currents produced in taste and olfactory receptor cells by chemical stimuli. These studies are concerned with the identification and pharmacology of the active ion channels and mode of production. One of the techniques employed by the MoneU researchers is that of "patch clamp." This method aUows for the study of the electrical properties of smaU patches of the ceU membrane. The program at MoneU has determined that odors stimulate intraceUular enzymes to produce cycUc adenosine 3, 5 -monophosphate (cAMP). This production of cAMP promotes opening of the ion channel, aUowing cations to enter and excite the ceU. MoneU s future studies wiU focus on the connection of cAMP, and the production of the electrical response to the brain. The patch clamp technique also may be a method to study the specificity of receptor ceUs to different odors, as weU as the adaptation to prolonged stimulation (3). [Pg.292]

Abstract Fluorescent molecules have been widely used as biomolecular labels, enzyme substrates, environmental indicators, and cellular stains and thus constitute indispensable tools in chemistry, physics, biology, and medicinal sciences. The large variation in the photophysics of the available fluorophores connected with chemical alterations give fluorescent probe techniques an almost unlimited scope for the detection of specific molecules and the investigation of intermolecular interactions on a molecular scale. [Pg.27]

Many of the remaining problems, particularly those connected with fine structure and shape and size, cannot be completely solved by purely chemical methods of investigation, and these have to be supplemented by the use of physical methods. Furthermore, in some instances, the results from such physical measurements have to be correlated with those obtained from studying the action of highly purified enzymes on the starch. [Pg.336]

It is postulated that chemotactic agents leach from respirable cotton dust particles in the small bronchioles. AECD recruit PMNs to the lung in the following sequence connective tissue beneath the basal lamina, between airway cells, and, finally, into the lumen. Chest tightness is also correlated with leucocyte recruitment (41). Although it has been proposed that extracellular lysosomal enzymes from PMNs cause the symptoms of byssinosis by initiating release of histamine and/or other chemical mediators (25), it has not been shown that cotton dust actually liberates hist j. jjfg m j y... [Pg.147]

The primary and overriding interest of enzymes, however, is their connection with life. Of all the multitudinous chemical processes in the living cell on which its life depends, there is scarcely one which is not due to enzyme catalysis there can be no life without enzymes. [Pg.35]

Figure 2. Free energy profile for converting di hydroxy acetone phosphate, the substrate (abbreviated S) and glyceraldehyde 3-phosphate, the product (abbreviated P), with intermediate formation of the enedi-olate (abbreviated Z). Catalysis occurs either by a free carboxyl group (levels connected by dotted lines) or by triose-phosphate isomerase (levels connected by dashed lines). The vertical arrows show the limits of those states that are less well defined as a result of uncertainty in the experimental data. The transition state marked "e" refers to the exchange of protons between the solvent and the enzyme-bound enediol intermediate (EZ). Reproduced with permission of the authors and the American Chemical Society. Figure 2. Free energy profile for converting di hydroxy acetone phosphate, the substrate (abbreviated S) and glyceraldehyde 3-phosphate, the product (abbreviated P), with intermediate formation of the enedi-olate (abbreviated Z). Catalysis occurs either by a free carboxyl group (levels connected by dotted lines) or by triose-phosphate isomerase (levels connected by dashed lines). The vertical arrows show the limits of those states that are less well defined as a result of uncertainty in the experimental data. The transition state marked "e" refers to the exchange of protons between the solvent and the enzyme-bound enediol intermediate (EZ). Reproduced with permission of the authors and the American Chemical Society.

See other pages where Chemical Connections enzymes is mentioned: [Pg.323]    [Pg.2520]    [Pg.2525]    [Pg.298]    [Pg.79]    [Pg.122]    [Pg.319]    [Pg.5]    [Pg.204]    [Pg.350]    [Pg.5]    [Pg.100]    [Pg.169]    [Pg.284]    [Pg.178]    [Pg.537]    [Pg.56]    [Pg.212]    [Pg.264]    [Pg.28]    [Pg.157]    [Pg.176]    [Pg.266]    [Pg.389]    [Pg.252]    [Pg.258]    [Pg.292]    [Pg.173]    [Pg.295]    [Pg.491]    [Pg.220]    [Pg.388]    [Pg.192]    [Pg.235]    [Pg.135]    [Pg.288]    [Pg.445]    [Pg.332]    [Pg.144]    [Pg.138]   


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