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C Batie

Publications and source records attributed to C Batie.

3 recordsLinked to original sources

Reaction of phthalate dioxygenase reductase with NADH and NAD: kinetic and spectral characterization of intermediates.

Phthalate dioxygenase reductase (PDR) is an electron transferase that contains FMN, which accepts a hydride from NADH, and a [2Fe-2S] center, which transfers electrons to phthalate dioxygenase. The reduction of PDR by NADH has been studied by stopped-flow spectroscopy. Data from studies using both portio- and deuterio-NADH were analyzed by nonlinear curve fitting and numerical simulation techniques. The results of these analyses indicate that the reductive half-reaction of PDR consists of five distinct kinetic phases: (a) NADH binds to form a primary Michaelis complex (MC-1) (Kd = 50 microM). (b) The enzyme undergoes a structural change (116 +/- 5 s-1) resulting in a charge-transfer complex (CT-1). (c) The next phase in the reaction shows a deuterium isotope effect of 7.0 when (4R)-[2H]NADH (NADD) is substituted for NADH, identifying this step as the one involving hydride transfer. The rate of hydride transfer from NADH to FMN is 70 s-1, and this process results in a charge-transfer intermediate between the flavin hydroquinone anion and NAD (CT). (d) Internal electron transfer from the flavin to the iron-sulfur center, which is only 35 +/- 4 s-1, then results in an intermediate consisting of a reduced [2Fe-2S] center and a neutral flavin semiquinone (SQ). It is surprising that this rate is so slow, since the shortest interatomic distance between these centers is only 4.7 A [Correll, C. C., et al. (1992) Science 258, 1604-1610]. The 2-electron-reduced form of PDR (SQ in Figure 1) binds weakly to the reaction product, NAD (Kd = 3.7 mM), but forms a tight complex with NADH (Kd = 10 microM). (e) Two molecules of the reduced iron-sulfur flavin semiquinone (SQ) form of PDR then undergo a relatively slow second-order disproportionation reaction, resulting in one molecule of 3-electron-reduced PDR and one molecule of 1-electron-reduced PDR. The latter reacts rapidly with excess NADH to form a 3-electron-reduced PDR.

Burkholderia cepacia↗

Phthalate oxygenase, a Rieske iron-sulfur protein from Pseudomonas cepacia.

Phthalate oxygenase catalyzes the oxygenation of phthalate to form a cis-dihydrodiol. It is comprised of two proteins: a flavo-iron-sulfur protein with NADH-dependent oxidoreductase activity (POR) and a nonheme iron protein with oxygenase activity (PO). The latter is a tetramer of 48 kDa units and contains a Rieske [2Fe-2S] center and one mononuclear iron per monomer. The mononuclear iron is likely the site of oxygenation. This system can be isolated in large quantities and is sufficiently stable for detailed mechanistic studies. We briefly describe some of our studies on this system which include kinetics, and visible, magnetic resonance, EXAFS, and ENDOR spectroscopies.

Electron Spin Resonance Spectroscopy↗

Paramagnetic probes of multicomponent electron-transfer systems.

Electron-transfer systems associated with steroid hormone production in the adrenals and with photosynthetic NADP+ reduction in the chloroplast share some important features. Complexes between components in both systems affect the exposure of prosthetic groups to water-soluble paramagnetic groups. The sensitivity of the components to probes of different charges suggests that electrostatic interactions are important in complex formation. Haem plane orientation in cytochrome P-450 of the adrenal system is parallel to the membrane plane in both native and reconstituted systems.

Adrenal Glands↗