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Mário Fragata

Publications and source records attributed to Mário Fragata.

2 recordsLinked to original sources

Nonlinear enhancement of oxygen evolution in thylakoid membranes: modeling the effect of light intensity and beta-cyclodextrin concentration.

Electron transport through photosystem II, measured as oxygen evolution (OE), was investigated in isolated thylakoid membranes treated with beta-cyclodextrin (beta-CD, a cyclic oligosaccharide constituted of seven alpha-d-glucose residues linked by alpha-1,4 glycosidic bonds) and irradiated with white light of variable intensity. First, we found that the light-response curves of oxygen evolution are well fitted with a hyperbolic function, the shape of which is not affected by the beta-CD concentration. Second, we showed that under conditions of irradiation with white light of saturating intensity ( approximately 5000 mumol of photons/m(2).s) beta-CD enhances the oxygen evolution in the thylakoid membranes according to a sigmoid function displaying a sharp inflection point, or transition. Unexpectedely, this beta-CD effect is not observed at irradiances of less than approximately 300 mumol of photons/m(2).s. We attempted a theoretical analysis of the combined effect of irradiance and beta-CD concentration on oxygen evolution (OE(th)). For this purpose, the effect of irradiance (I) was modeled with a hyperbola (i) and the beta-CD concentration (C) contribution with a Hill equation, that is, a sigmoid function (ii). The mathematical simulations generated the following general expressions: (i) OE(th) = [OE(max)(0) G(1)(C)]I/[L(1/2)(0) G(2)(C) + I] and (ii) G(i)()(C) = 1 + p[C(n)()/(K(1/2)(n)() + C(n)())], where OE(max)(0) is the OE maximum (OE(max)) in the absence of beta-CD, L(1/2)(0) is the photon flux density giving OE(max)/2 in the absence of beta-CD, G(1)(C) or G(2)(C) is obtained from G(i)()(C) where i is 1 or 2, n is the Hill coefficient, p is a parameter to account for the beta-CD-mediated maximum OE increase, and K(1/2) is the beta-CD concentration giving half-maximal OE activity. The results of the calculations yielded the expression (iii) OE(th) = 151[1 + 3.3C(4.8)/(13.1(4.8) + C(4.8))]I/{97.5[1 + 5.2C(7.8)/(14.8(7.8) + C(7.8))] + I} which agrees well with the experimental data for a broad range of I and C. Note that, for C = 0, eq iii reverts to the light-response curve of oxygen evolution in the absence of beta-CD. We conclude that eq iii is a good approximation of the combined effect of irradiance and beta-CD concentration, meaning that the model has a significant value for predicting the outcome of associated photochemical and biochemical reactions.

Electron Transport↗

Photosystem II reconstitution into proteoliposomes: structure-function characterization.

This chapter discusses the photosystem II (PSII) reconstitution into proteoliposomes. In the first part of the chapter, protocols are outlined for the preparation of lipid bilayer vesicles (liposomes) constituted of individual thylakoid lipids or their mixtures for the preparation of PSII particles, and for the incorporation of the PSII particles into the liposomes. In the second part of the chapter, methodologies are described for the structure-function characterization of the PSII-lipid complexes (proteoliposomes). This includes the sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-PAGE) determination of the PSII proteins, measurement of oxygen-evolving activity of PSII in the proteoliposomes, and the study of structural changes of the PSII proteins upon their incorporation into the lipid bilayers by Fourier transform infrared (FTIR) spectroscopy.

Chloroplasts↗