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Esterase system

The ll-palm-A -THC can be hydrolyzed to II-OH-A -thc by cholesterol esterase and triacylglycerol lipase but not by phospholipase A, acetylesterase or phosphotransacetylase (16). An attempt to modify the retention of fatty acid-conjugated DDT metabolites was carried out by injecting the DDT-treated rats with sodium salt of various bile acids, heparin or lecithin of which all were known to affect the esterification or ester hydrolysis by the cholesterol esterase system. The results Indicated a significant decrease in the retention of the conjugated DDT metabolites in the rat liver and spleen (17). [Pg.216]

El-Soda, M., Abd El-Wahab, H., Ezzat, N., Desmazeaud, M. J., and Ismail, A. (1986). The esterolytic and lipolytic activities of the lactobacilli. II. Detection of esterase system of Lactobacillus helveticus, Lactobacillus bulgaricus, Lactobacillus lactis and Lactobacillus acidophilus. Lait 66, 431-443. [Pg.302]

Hayama et al.132 discussed the catalytic effects of silver ion-polyacrylic add systems toward the hydrolyses of 2,4-dinitrophenylvinylacetate 84 (DNPVA) by using the weak nudeophilicity of carboxylic groups and the change-transfer interactions between olefinie esters and silver ions133Metal complexes of basic polyelectrolytes are also stimulating as esterase models. Hatano etal. 34, 13S) reported that some copper(II)-poly-L-lysine complexes were active for the hydrolyses of amino acid esters, such as D- and L-phenylalanine methyl ester 85 (PAM). They... [Pg.167]

The microsomal fraction consists mainly of vesicles (microsomes) derived from the endoplasmic reticulum (smooth and rough). It contains cytochrome P450 and NADPH/cytochrome P450 reductase (collectively the microsomal monooxygenase system), carboxylesterases, A-esterases, epoxide hydrolases, glucuronyl transferases, and other enzymes that metabolize xenobiotics. The 105,000 g supernatant contains soluble enzymes such as glutathione-5-trans-ferases, sulfotransferases, and certain esterases. The 11,000 g supernatant contains all of the types of enzyme listed earlier. [Pg.46]

A few OP compounds cause delayed neuropathy in vertebrates because they inhibit another esterase located in the nervous system, which has been termed neuropathy target esterase (NTE). This enzyme is described in Chapter 10, Section 10.2.4. OPs that cause delayed neuropathy include diisopropyl phosphofluoridate (DFP), mipafox, leptophos, methamidophos, and triorthocresol phosphate. The delay in the appearance of neurotoxic symptoms following exposure is associated with the aging process. In most cases, nerve degeneration is not seen with initial inhibition of the esterase but appears some 2-3 weeks after commencement of exposure, as the inhibited enzyme undergoes aging (see Section 16.4.1). The condition is described as OP-induced delayed neuropathy (OPIDN). [Pg.300]

Neuropathy target esterase (NTE) An esterase of the nervous system whose inhibition by certain OPs (e.g., mipafox, leptophos) can lead to the development of delayed neuropathy. [Pg.333]

Walker, C.H. (1989). The development of an improved system of nomenclature and classification of esterases. In E. Reiner, W.N. Aldridge, and F.C.G. Hoskin (Eds.) Enzymes Elydrolysing Organophosphorous Compounds, Chichester Ellis Harwood. 53-64. [Pg.373]

Katz E, WiUner 1, Wang J (2004) Electroanalytical and bioelectroanalytical systems based on metal and semiconductor nanoparticles. Electroanalysis 16 19-44 Pardo-Yissar V, Katz E, Wasserman J, Willner 1 (2003) Acetylcholine esterase-labeled CdS nanoparticles on electrodes Photoelectrochemical sensing of the enzyme inhibitors. J Am Chem Soc 125 622-623... [Pg.348]

The pathogenicity of Erwinia chrysanthemi 3937 on African violets involves at least five pectate lyases (PelA to PelE), one methyl pectin esterase (Pern), encoded by pelA to pelE, pern genes and an iron assimilation system mediated by chiysobactin [1], (Fig. 1). [Pg.875]

Fig. 2. The intrinsic and extinsic cascade coagulation systems. activation -I, inhibition HMK, high molecular kininogen Cl-inh., complement-1 esterase inhibitor AT-III, antithrombin HI a 1 -PI, alpha-1 protein inhibitor pf-3, platelet factor 3. Fig. 2. The intrinsic and extinsic cascade coagulation systems. activation -I, inhibition HMK, high molecular kininogen Cl-inh., complement-1 esterase inhibitor AT-III, antithrombin HI a 1 -PI, alpha-1 protein inhibitor pf-3, platelet factor 3.
Syntheses of aliphatic polyesters by fermentation and chemical processes have been extensively studied from the viewpoint of biodegradable materials science. Recently, another approach to their production has been made by using an isolated lipase or esterase as catalyst via non-biosynthetic pathways under mild reaction conditions. Lipase and esterase are enzymes which catalyze hydrolysis of esters in an aqueous environment in living systems. Some of them can act as catalyst for the reverse reactions, esterifications and transesterifications, in organic media [1-5]. These catalytic actions have been expanded to... [Pg.240]

Esterases form a wide family of enzymes that catalyze the hydrolysis of ester bonds. They are ubiquitously expressed in all tissues including the intestine, and are found in both microsomal and cytosolic fractions. Prueksaritonont et al. [6] have studied the metabolism of both p-nitrophenol acetate and acetylsalicylic acid by esterases from human intestinal microsomal and cytosolic systems, and the activity values were 2.76 pmol min-1 mg-1 and 0.96 nmol min-1 mg-1, respectively. Thus, the activity for the hydrolysis of p-nitrophenol acetate in human intestine approaches that in the liver. [Pg.315]


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