Abstract

Interfering RNA was used to suppress the expression of two genes that encode the manganese-stabilizing protein of photosystem II in Arabidopsis thaliana, MSP-1 (encoded by psbO-1, At5g66570), and MSP-2 (encoded by psbO-2, At3g50820). A phenotypic series of transgenic plants was recovered that expressed high, intermediate, and low amounts of these two manganese-stabilizing proteins. Chlorophyll fluorescence induction and decay analyses were performed. Decreasing amounts of expressed protein led to the progressive loss of variable fluorescence and a marked decrease in the fluorescence quantum yield (F(v)/F(m)) in both the absence and the presence of dichloromethylurea. This result indicated that the amount of functional photosystem II reaction centers was compromised in the plants that exhibited intermediate and low amounts of the manganese-stabilizing proteins. An analysis of the decay of the variable fluorescence in the presence of dichlorophenyldimethylurea indicated that charge recombination between Q ((A-)) and the S(2) state of the oxygen-evolving complex was seriously retarded in the plants that expressed low amounts of the manganese stabilizing proteins. This may have indicated a stabilization of the S(2) state in the absence of the extrinsic component. Immunological analysis of the photosystem II protein complement indicated that significant losses of the CP47, CP43, and D1 proteins occurred upon the loss of the manganese-stabilizing proteins. This indicated that these extrinsic proteins were required for photosystem II core assembly/stability. Additionally, although the quantity of the 24-kDa extrinsic protein was only modestly affected by the loss of the manganese-stabilizing proteins, the 17-kDa extrinsic protein dramatically decreased. The control proteins ribulose bisphosphate carboxylase and cytochrome f were not affected by the loss of the manganese-stabilizing proteins; the photosystem I PsaB protein, however, was significantly reduced in the low expressing transgenic plants. Finally, it was determined that the transgenic plants that expressed low amounts of the manganese-stabilizing proteins could not grow photoautotrophically.

Highlights

  • In higher plants and cyanobacteria, at least six intrinsic proteins appear to be required for oxygen evolution by photosystem II (PS II)1 [1,2,3]

  • The results showed that 11% of the plants had expression levels similar to wild type for manganese-stabilizing protein (MSP)-1 and MSP-2, 49% of the transgenic plants expressed only MSP-1, and 14% of the transgenic plants showed differential suppression of MSP-1 and MSP-2

  • In Synechocystis 6803, a strong correlation exists (r ϭ 0.94) between the total yield of variable fluorescence (Fm Ϫ Fo) and the PS II content [25] of wild type and mutant strains. Since such a correlation has never been established in either green algae or higher plants, we view such an analysis as being only semiquantitative when applied to the higher plant system. With this caveat in mind, our results indicated that there appeared to be a dramatic decrease in the quantity of fully functional PS II reaction centers as the amounts of the MSPs in the transgenic plants decreased

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Summary

Introduction

In higher plants and cyanobacteria, at least six intrinsic proteins appear to be required for oxygen evolution by photosystem II (PS II)1 [1,2,3]. Three extrinsic proteins, with apparent molecular masses of 33, 24, and 17 kDa, are required for high rates of oxygen evolution at physiological inorganic cofactor concentrations [7]. The 24- and 17-kDa proteins appear to modulate the calcium and chloride requirements for efficient oxygen evolution These three extrinsic components interact with intrinsic membrane proteins and possibly with each other to yield fully functional oxygen-evolving complexes. A point mutation in the psbO-1 gene was recovered that led to the introduction of a premature stop codon and the loss of the MSP-1 protein [12]. This mutant exhibited slow growth, aberrant fluorescence induction characteristics, and an increased expression of MSP-2

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