Enzyme generation

Propose a SECM experiment for mapping the distribution of an oxidase enzyme within a carbon composite surface. (Note that the enzyme generates hydrogen peroxide in the presence of its substrate and oxygen.)... 

Metabolism of BP mediated by the cytochrome P-450 monooxygenase system forms three classes of products phenols, dihydrodiols and quinones. Formation of phenols and dihydrodiols is obtained by an initial electrophilic attack of an enzyme-generated oxygen atom. 

R.C. Bray, F.M. Pick, and D. Samuel, Oxygen-17 hyperfine splitting in the electron paramagnetic resonance spectrum of enzymically generated superoxide. Eur. J. Biochem. 15, 352-355 (1970). 

Cutting with a restriction enzyme generates two ends that are complementary to each other... 

As in the luminol case, the main role of the enhancer (EnH) seems to be related to turnover of the enzyme, generating enhancer radicals (En rad) in the process that are capable of oxidizing the acridan ester (AcH). The structure of the enhancer obviously is very important. To accelerate HRP turnover, the enhancer must on the one hand be able to rapidly react with the reactive HRP intermediates Cl and especially CII (k2 and k3 large). On the other hand, the oxidized enhancer intermediate (radical or radical cation) must be able to oxidize the acridan ester (light-generating step). This last reaction also depends on the structure of the acridan ester in a very unfavorable case, adding an enhancer for enzyme turnover could actually diminish the light production if k 4 > fct (Fig. 5), i.e., if the enhancer radical would not be able to oxidize the acridan ester. 

The interactions of NO with the iron-sulfur cluster moieties of several enzymes generate iron-sulfur-nitrosyl cluster compounds [156]. However, synthetic nitrosyl clusters such as Roussins black salt (RBS), Roussins red salt (RRS), Roussins red ester (RRE) and [FeNOS]4 (Fig. 5.3) are well known [129, 157] and can be synthesized easily [158-164]. For example, the RBS can be prepared by mixing FeS04 with NaN03 and (NH4)2S in aqueous solution [158]. RRE salts are generally insoluble in water, but recently the water soluble sulfonated derivative, Na2[Fe2(SCH2CH2S03)2(N0)4], has been prepared [165]. 

In ion-selective FETs (ISFETs), an ion-selective membrane replaces the gate electrode. When an enzyme-loaded gel is combined with the membrane, the device can be used to measure substrates which enzymically generate charged species. 

Activation of membrane-bound enzyme generating 2nd messenger following hormone binding to its receptor. 

Sarni-Manchado, P., Cheynier, V., and Moutounet, M., Reaction of enzymically generated quin-ones with malvidin-3-glucoside. Phytochemistry 45, 1365, 1997. 

Additional information about this Fc GO preparation has been reported elsewhere (112). The intramolecular electron transfer rate constant kmirn calculated using Eq. (36) equals 40 s-1 and is by a factor of 50 higher than that for the randomly modified GO (104). The distance separating the ferrocene unit and FAD in Fc GO is believed to be ca. 19 A, by 2 A shorter than in the most effective electrically contacted enzyme generated by the random modification of GO by ferrocene units. This information supports the hypothesis about the key locations of ferrocene groups that play the dominant role in the electrocatalysis (104). 

Purification of an Enzyme A biochemist discovers and purifies a new enzyme, generating the purification table below. 

The bacterial cellulose synthase from Acetobacter xylinum can be solubilized with detergents, and the resulting enzyme generates characteristic 1.7 ran cellulose fibrils (Fig. 20-4) from UDP-glucose.125/127-129 These are similar, but not identical, to the fibrils of cellulose I produced by intact bacteria.125 130 Each native fibril appears as a left-handed helix which may contain about nine parallel chains in a crystalline array. Three of these helices appear to coil together (Fig. 20-4) to form a larger 3.7-nm left-handed helical fibril. Similar fibrils are formed by plants. In both... 

The cloning and manipulation of genes usually depends upon the precise cutting of DNA into discrete fragments by restriction endonucleases. Many restriction enzymes generate cohesive ends (sticky ends). Thus, EcoRI produces DNA fragments with the single-stranded "tails" shown here at the 5 -ends of the cut duplexes ... 

Libby RD, Shedd AL, Phipps AK, Beachy TM, Gerstberger SM (1992) Defining the Involvement of HOC1 or Cl2 as Enzyme-Generated Intermediates in Chloroperoxidase-catalyzed Reactions. J Biol Chem 267 1769... 

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