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PQQ Pyrroloquinoline quinone

C. PQQ-Dependent Dehydrogenases (PQQ, Pyrroloquinoline Quinone) Properties of Mediators... [Pg.201]

All potentials vs. screen-printed Ag/AgCl pseudo-reference, except values marked with asterisk ( ), which are vs. Ag/3M AgCl double-junction reference electrode, and values marked with dagger CfO, which are vs. saturated calomel. Abbreviations CoPC cobalt phthalocyanine, SPCE screen-printed carbon electrode, GOD glucose oxidase, MWCNT multi-walled carbon nanotubes, NAD nicotinamide adenine dinucleotide, PQQ pyrroloquinoline quinone, FIA flow injection analysis. [Pg.501]

PQQ = pyrroloquinoline quinone). The synthesis of its triester J is achieved by the following sequence based on 2-methoxy-5-nitroaniline (X) ... [Pg.536]

Abbreviations PP, pyridoxal phosphate PQQ, pyrroloquinoline quinone SAM, 5-adenosyl-L-methionine. A. Ramos et al, manuscript in preparation. [Pg.229]

The other less common type of phenol biosensor involves enzymes like PQQ (pyrroloquinoline quinone)-dependent glucose dehydrogenase (GDH) (9-12) or... [Pg.114]

Conversion of methanol into formaldehyde by methanol dehydrogenase. A complex array of genes is involved in this oxidation and the dehydrogenase contains pyrroloquinoline quinone (PQQ) as a cofactor (references in Ramamoorthi and Lidstrom 1995). Details of its function must, however, differ from that of methylamine dehydrogenase that also contains a quinoprotein—tryptophan tryptophylquinone (TTQ). [Pg.297]

Fructose dehydrogenase (FDH) having pyrroloquinoline quinone (PQQ) as a prosthetic group is an redox enzyme to catalyze the oxidation of fructose. A... [Pg.340]

Fig. 1. Prosthetic groups in oxidases (A FAD B Thio-Tyrosine C NAD(P) + D 6-Hydroxy-DOPA E Methoxanthin (Pyrroloquinoline quinone PQQ) F Tryptophane-Tryptophan quinone)... Fig. 1. Prosthetic groups in oxidases (A FAD B Thio-Tyrosine C NAD(P) + D 6-Hydroxy-DOPA E Methoxanthin (Pyrroloquinoline quinone PQQ) F Tryptophane-Tryptophan quinone)...
Examples of surface-immobilized mediators are electropolymerized azines for electro-oxidation of The extreme form of this approach is formation of biocatalytic monolayer, comprising a surface-bound mediator species that is itself bound to a single enzyme molecule. Katz et al. report a complete cell based on novel architecture at both electrodes (Figure 7). On the anode side, the FAD center of glucose oxidase is removed from the enzyme shell and covalently attached to a pyrroloquinoline quinone (PQQ) mediator species previously immobilized on a gold surface. The GOx apoenzyme (enzyme with active center removed) is reintroduced in solution and selectively binds to FAD, resulting in a PQQ-... [Pg.638]

Pyrroloquinoline quinone (PQQ) (or methoxatin) 6 is a coenzyme, responsible for the oxidation of methanol [7]. It has been found that cyclopropanol 4 inactivates the enzyme from M. methanica [8], the dimeric methanol dehydrogenase and the monomeric enzyme from a Pseudomonas PQQ-dependent methanol dehydrogenase [9] by forming adducts such as 7, through a one-electron oxidation process and the ready ring opening of a cyclopropyloxonium radical, Eq. (3) [8,9]. [Pg.3]

Oxidation by direct H transfer from the a-carbon of alcohols to the pyrroloquinoline quinone (PQQ) cofactor of alcohol dehydrogenases was studied using ab initio quantum mechanical methods <2001JCC1732>. Energies and geometries were calculated at the 6-31G(d,p) level of theory, results were compared to available structural and spectroscopic data, and the role of calcium in the enzymatic reaction was explored. Transition state searches at the semi-empirical and STO-3G(d) level of theory provided evidence that direct transfer from the alcohol to C-5 of PQQ is energetically feasible. [Pg.1202]

Pyrroloquinoline Quinone Isomers A Prelude to Studies of PQQ Analogs as Pharmaceuticals... [Pg.117]

In studies of analogs of the redox cofactor pyrroloquinoline quinone (PQQ), synthetic efforts have focused initially on isosteric, isomeric structures that reflect on important mechanisms of electron-transfer catalysis mediated by PQQ. These studies provide insight into the choice of PQQ as an electron-transfer catalyst in nature, and bear directly on pharmaceutical applications of this vitamin-like nutritional factor. [Pg.117]


See other pages where PQQ Pyrroloquinoline quinone is mentioned: [Pg.1480]    [Pg.146]    [Pg.57]    [Pg.707]    [Pg.541]    [Pg.400]    [Pg.245]    [Pg.10]    [Pg.73]    [Pg.118]    [Pg.172]    [Pg.219]    [Pg.414]    [Pg.443]    [Pg.1480]    [Pg.146]    [Pg.57]    [Pg.707]    [Pg.541]    [Pg.400]    [Pg.245]    [Pg.10]    [Pg.73]    [Pg.118]    [Pg.172]    [Pg.219]    [Pg.414]    [Pg.443]    [Pg.106]    [Pg.571]    [Pg.45]    [Pg.157]    [Pg.161]    [Pg.203]    [Pg.337]    [Pg.338]    [Pg.122]    [Pg.127]   
See also in sourсe #XX -- [ Pg.170 , Pg.171 ]




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