Containing Enzymes

Microemulsions or reverse micelles are composed of enzyme-containing, surfactant-stabiHzed aqueous microdroplets in a continuous organic phase. Such systems may be considered as a kind of immobilization in enzymatic synthesis reactions. 

The three most common types of inhibitors in enzymatic reactions are competitive, non-competitive, and uncompetitive. Competitive inliibition occurs when tlie substrate and inhibitor have similar molecules that compete for the identical site on the enzyme. Non-competitive inhibition results in enzymes containing at least two different types of sites. The inhibitor attaches to only one type of site and the substrate only to the other. Uncompetitive inhibition occurs when the inhibitor deactivates the enzyme substrate complex. The effect of an inhibitor is determined by measuring the enzyme velocity at various... 

This impressive reaction is catalyzed by stearoyl-CoA desaturase, a 53-kD enzyme containing a nonheme iron center. NADH and oxygen (Og) are required, as are two other proteins cytochrome 65 reductase (a 43-kD flavo-protein) and cytochrome 65 (16.7 kD). All three proteins are associated with the endoplasmic reticulum membrane. Cytochrome reductase transfers a pair of electrons from NADH through FAD to cytochrome (Figure 25.14). Oxidation of reduced cytochrome be, is coupled to reduction of nonheme Fe to Fe in the desaturase. The Fe accepts a pair of electrons (one at a time in a cycle) from cytochrome b and creates a cis double bond at the 9,10-posi-tion of the stearoyl-CoA substrate. Og is the terminal electron acceptor in this fatty acyl desaturation cycle. Note that two water molecules are made, which means that four electrons are transferred overall. Two of these come through the reaction sequence from NADH, and two come from the fatty acyl substrate that is being dehydrogenated. 

N-Heterocycles as ligands in dioxygen activation by enzymes containing binuclear nonheme iron clusters 96CRV2625. 

The metabolic breakdown of triacylglycerols begins with their hydrolysis to yield glycerol plus fatty acids. The reaction is catalyzed by a lipase, whose mechanism of action is shown in Figure 29.2. The active site of the enzyme contains a catalytic triad of aspartic acid, histidine, and serine residues, which act cooperatively to provide the necessary acid and base catalysis for the individual steps. Hydrolysis is accomplished by two sequential nucleophilic acyl substitution reactions, one that covalently binds an acyl group to the side chain -OH of a serine residue on the enzyme and a second that frees the fatty acid from the enzyme. 

Figure 29.2 MECHANISM Mechanism of action of lipase. The active site of the enzyme contains a catalytic triad of aspartic acid, histidine, and serine, which react cooperatively to carry out two nucleophilic acyl substitution reactions. Individual steps are explained in the text.

Although Zn2+ is essential to human nutrition, compounds of the two elements below zinc in the periodic table. Cd and Fig. are extremely toxic. This reflects the fact that Cd2+ and Flg2+, in contrast to Zn2+, form very stable complexes with ligands containing sulfur atoms. As a result, these two cations react with and thereby deactivate enzymes containing —SH groups. 

As early as 1908, Rosenthaler found in the ferment mixture of emulsin a u-oxynitrilase , which directed the addition of hydrocyanic acid (hydrogen cyanide) to benzaldehyde asymmetrically to give x-hydroxybenzeneacetonitrilc (mandelonitrile)9. This result was confirmed1 °, however, it was not until 1963 that Pfeil ct al. first isolated and characterized the enzyme (R)-oxyni-trilase [EC 4.1.2.101 from bitter almonds (Prunus amygdalus)1 12. The yellow-colored enzyme contains a flavin-adenine dinucleotide (FAD)11 and loses its activity by splitting off this prosthet-... 

One of the most used systems involves use of horseradish peroxidase, a 3-diketone (mosl commonly 2,4-pentandione), and hydrogen peroxide." " " Since these enzymes contain iron(II), initiation may involve decomposition of hydrogen peroxide by a redox reaction with formation of hydroxy radicals. However, the proposed initiation mechanism- involves a catalytic cycle with enzyme activation by hydrogen peroxide and oxidation of the [3-diketone to give a species which initiates polymerization. Some influence of the enzyme on tacticity and molecular... 

For an enzyme-containing detergent the enzyme is added to a detergent composition with esters and disalts of a-sulfo fatty acids. The detergent granular comprises 7 % sodium a-sulfo hardened palm oil fatty acid methyl ester, 5% disodium salt of a-sulfo hardened palm oil fatty acid, 10% sodium a-olefin (C14 18) sulfonate, 10% zeolite, 5% sodium carbonate, 5% water, and 55% sodium sulfate [82]. 

The 3D crystal structure of Dsm. baculatum [NiSeFe] hydrogenase has been solved 185), and it was indicated that the enzyme contains three [4Fe-4S] centers. A cysteine (replacing a proline usually found near the [3Fe-4S] core) provides an extra ligand, enabling the acceptance of a fourth iron site at this cluster. 

D. gigas formate dehydrogenase seems to be quite different in terms of subunit composition. It does not contain a y subunit and no heme c was detected (225). Also, two MGD were identified, but surprisingly, the enzyme contains tungsten instead of molybdenum. Mossbauer and EPR studies confirmed the presence of two [4Fe-4S] + + clusters with similar properties to the ones found in D. desulfuricans FDH (247). 

The reactions which are catalyzed by enzymes containing cobalt corrinoids can be classified into three groups. 

Isomerase Reactions Catalyzed by Enzymes Containing 5 -Deoxyadenosylcorrinoids... 

Many enzymes contain small nonprotein molecules and metal ions that participate directly in substrate binding or catalysis. Termed prosthetic groups, cofactors, and coenzymes, these extend the repertoire of catalytic capabilities beyond those afforded by the limited number of functional groups present on the aminoacyl side chains of peptides. 

Flavoprotein enzymes contain flavin mononucleotide (FMN) or flavin adenine dinucleotide (FAD) as prosthetic groups. FMN and FAD are formed in the body from the vitamin riboflavin (Chapter 45). FMN and FAD are usually tighdy—but not covalendy—bound to their respecdve apoenzyme proteins. Metalloflavopro-teins contain one or more metals as essential cofactors. 

The reduced NADH of the tespitatoty chain is in turn oxidized by a metalloflavoptotein enzyme—NADH dehydrogenase. This enzyme contains FeS and FMN, is tighdy bound to the tespitatoty chain, and passes te-ducing equivalents on to Q. 

The NHase responsible for aldoxime metabolism from the i -pyridine-3-aldoxime-degrading bacterium, Rhodococcus sp. strain YH3-3, was purified and characterized. Addition of cobalt ion was necessary for the formation of enzyme. The native enzyme had a Mr of 130000 and consisted of two subunits (a-subunit, 27 100 (3-subunit, 34500). The enzyme contained approximately 2 mol cobalt per mol enzyme. The enzyme had a wide substrate specificity it acted on aliphatic saturated and unsaturated as well as aromatic nitriles. The N-terminus of the (3-subunit showed good sequence similarities with those of other NHases. Thus, this NHase is part of the metabolic pathway for aldoximes in microorganisms. 

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