Cytochrome catalyst

Cytochrome P-450 — an effective catalyst of the oxidation of organic compounds by peroxides. D. I. Metelitsa, Russ. Chem. Rev. (Engl. Transl), 1981, 50,1058-1073 (147). 

Catalysis. Cytochrome P-450 model compounds catalyze the epoxidation of alkenes by hypochlorite ions.16 A typical catalyst is OMn(TMP)L+. 

In addition to their proven capacity to catalyze a highly efficient and rapid reduction of O2 under ambient conditions (e.g., cytochrome c oxidase, the enzyme that catalyzes the reduction of >90% of O2 consumed by a mammal, captures >80% of the free energy of ORR at a turnover frequency of >50 O2 molecules per second per site), metalloporphyrins are attractive candidates for Pt-free cathodes. Probably the major impetus for a search for Pt-free cathodic catalysts for low temperature fuel cells is... 

Section 18.2). The latest generation of such catalysts (1 in Fig. 18.17) reproduces the key features of the site (i) the proximal imidazole ligation of the heme (ii) the trisi-midazole ligation of distal Cu (iii) the Fe-Cu separation and (iv) the distal phenol covalently attached to one of the imidazoles. As a result, binding of O2 to compound 1 in its reduced (Fe Cu ) state appears to result in rapid reduction of O2 to the level of oxides (—2 oxidation state) without the need for outer-sphere electron transfer steps [Collman et ah, 2007b]. This reactivity is analogous to that of the heme/Cu site of cytochrome c oxidase (see Section 18.2). 

Biomimetic studies typically have one or more of the following objectives (i) to reproduce in a small synthetic molecule reactivity that was theretofore only observed in an enzyme (ii) to understand the mechanisms of an enzymatic reaction and the relationship between the stereoelectronic attributes of the catalytic site and its reactivity and (iii) to develop practical catalysts by exploiting and adopting solutions that evolved in Nature. Biomimetic studies of cytochrome c oxidase have been particularly impactfull in addressing aim (ii). On the other hand, this approach is... 

Only three steps of the proposed mechanism (Fig. 18.20) could not be carried out individually under stoichiometric conditions. At pH 7 and the potential-dependent part of the catalytic wave (>150 mV vs. NHE), the —30 mV/pH dependence of the turnover frequency was observed for both Ee/Cu and Cu-free (Fe-only) forms of catalysts 2, and therefore it requires two reversible electron transfer steps prior to the turnover-determining step (TDS) and one proton transfer step either prior to the TDS or as the TDS. Under these conditions, the resting state of the catalyst was determined to be ferric-aqua/Cu which was in a rapid equilibrium with the fully reduced ferrous-aqua/Cu form (the Fe - and potentials were measured to be within < 20 mV of each other, as they are in cytochrome c oxidase, resulting in a two-electron redox equilibrium). This first redox equilibrium is biased toward the catalytically inactive fully oxidized state at potentials >0.1 V, and therefore it controls the molar fraction of the catalytically active metalloporphyrin. The fully reduced ferrous-aqua/Cu form is also in a rapid equilibrium with the catalytically active 5-coordinate ferrous porphyrin. As a result of these two equilibria, at 150 mV (vs. NHE), only <0.1%... 

The prevalence of the heme in O2 metabolism and the discovery in the 1960s that metallophthalocyanines adsorbed on graphite catalyze four-electron reduction of O2 have prompted intense interest in metaUoporphyrins as molecular electrocatalysts for the ORR. The technological motivation behind this work is the desire for a Pt-ffee cathodic catalyst for low temperature fuel cells. To date, three types of metaUoporphyrins have attracted most attention (i) simple porphyrins that are accessible within one or two steps and are typically available commercially (ii) cofacial porphyrins in which two porphyrin macrocycles are confined in an approximately stacked (face-to-face) geometry and (iii) biomimetic catalysts, which are highly elaborate porphyrins designed to reproduce the stereoelectronic properties of the 02-reducing site of cytochrome oxidase. 

The PDMS-membrane-occluded FePcY was the first room temperature catalytic membrane and the first solid catalyst dispersed in dense organic polymer.169 The catalytic system mimics the cytochrome P-450 enzyme and can oxidize alkanes at room temperature with rates comparable to those of the... 

Fig. 6.9 The catalysts for denitrification. Nitrate is reduced by a molybdenum enzyme while nitrite and oxides of nitrogen are reduced today mainly by copper enzymes. However, there are alternatives, probably earlier iron enzymes. The electron transfer bct complex is common to that in oxidative phosphorylation and similar to the bf complex of photosynthesis, while cytochrome c2 is to be compared with cytochrome c of oxidative phosphorylation. These four processes are linked in energy capture via proton (H+) gradients see Figure 6.8(a) and (b) and the lower parts of Fig. 6.9 which show separately the active site of the all iron NO-reductase, and the active site of cytochrome oxidase (02 reductase).

Nature has had a long time to perfect her inorganic chemistry, and understanding the mechanisms of enzymatic action can suggest ways for the inorganic chemist to develop corresponding in vitro catalysts. We shall show how knowledge of cytochrome oxidase and cytochrome P-450 has led to such possibilities. 

Scup, Stenotomus chrysops injected intraperitoneally with 1,5, or 10 mg/kg BW of PCBs 77, 105, 118, 128, or 138 and examined tor increases in ethoxyresorufin O-deethylase (EROD) activity, immunodetectable cytochrome P-450E (the EROD catalyst in scup) and in vitro translatable mRNA for P-450E... 

A first application using ferroceneboronic acid as mediator [45] was described for the transformation of p-hydroxy toluene to p-hydroxy benzaldehyde which is catalyzed by the enzyme p-cresolmethyl hydroxylase (PCMH) from Pseudomonas putida. This enzyme is a flavocytochrome containing two FAD and two cytochrome c prosthetic groups. To develop a continuous process using ultrafiltration membranes to retain the enzyme and the mediator, water soluble polymer-bound ferrocenes [50] such as compounds 3-7 have been applied as redox catalysts for the application in batch electrolyses (Fig. 12) or in combination with an electrochemical enzyme membrane reactor (Fig. 13) [46, 50] with excellent results. 

Spracklin DK, Hankins DC, Fisher JM, et al. Cytochrome P450 2E1 is the principal catalyst of human oxidative halothane metabolism in vitro. J Pharmacol Exp Ther 1997 281(1) 400-411. 

The use of the reversion spectroscope enabled the position of the absorption bands to be determined accurately and to be conclusively distinguished from hemoglobin and myoglobin. It became clear that there were three different intracellular respiratory catalysts— cytochromes a,b,c—common to animals, bacteria, yeast and higher plants. In 1925 a preliminary scheme for the passage of O2 from blood to tissue was proposed ... 

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