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First published online April 15, 2009; 10.1104/pp.108.134601 Plant Physiology 150:825-833 (2009) © 2009 American Society of Plant Biologists OPEN ACCESS ARTICLE
Manganese Deficiency Leads to Genotype-Specific Changes in Fluorescence Induction Kinetics and State Transitions1,[C],[OA]Plant and Soil Science Laboratory, Department of Agriculture and Ecology (S.H., K.H.L., C.A.H., S.B.S., P.P.), and The Villum Kann Rasmussen Research Center "Pro-Active Plants," Department of Plant Biology and Biotechnology, Faculty of Life Sciences, University of Copenhagen, DK–1871 Frederiksberg C, Copenhagen, Denmark (A.H., P.E.J.)
Barley (Hordeum vulgare) genotypes display a marked difference in their ability to tolerate growth at low manganese (Mn) concentrations, a phenomenon designated as differential Mn efficiency. Induction of Mn deficiency in two genotypes differing in Mn efficiency led to a decline in the quantum yield efficiency for both, although faster in the Mn-inefficient genotype. Leaf tissue and thylakoid Mn concentrations were reduced under Mn deficiency, but no difference between genotypes was observed and no visual Mn deficiency symptoms were developed. Analysis of the fluorescence induction kinetics revealed that in addition to the usual O-J-I-P steps, clear K and D steps were developed in the Mn-inefficient genotype under Mn deficiency. These marked changes indicated damages to photosystem II (PSII). This was further substantiated by state transition measurements, indicating that the ability of plants to redistribute excitation energy was reduced. The percentage change in state transitions for control plants with normal Mn supply of both genotypes was 9% to 11%. However, in Mn-deficient leaves of the Mn-inefficient genotypes, state transitions were reduced to less than 1%, whereas no change was observed for the Mn-efficient genotypes. Immunoblotting and the chlorophyll a/b ratio confirmed that Mn deficiency in general resulted in a significant reduction in abundance of PSII reaction centers relative to the peripheral antenna. In addition, PSII appeared to be significantly more affected by Mn limitation than PSI. However, the striking genotypic differences observed in Mn-deficient plants, when analyzing state transitions and fluorescence induction kinetics, could not be correlated with specific changes in photosystem proteins. Thus, there is no simple linkage between protein expression and the differential reduction in state transition and fluorescence induction kinetics observed for the genotypes under Mn deficiency.
1 This work was supported by the Ministry of Science, Technology, and Innovation (contract nos. 53–00–0234 and 274–06–0325), the Danish Grain Breeding Foundation, the Danish National Research Foundation, the Villum Kann Rasmussen Foundation, and the Danish Natural Science Research Council (contract no. 272–05–0360). The author responsible for distribution of materials integral to the findings presented in this article in accordance with the policy described in the Instructions for Authors (www.plantphysiol.org) is: Søren Husted (shu{at}life.ku.dk). [C] Some figures in this article are displayed in color online but in black and white in the print edition. [OA] Open Access articles can be viewed online without a subscription. www.plantphysiol.org/cgi/doi/10.1104/pp.108.134601 * Corresponding author; e-mail shu{at}life.ku.dk. Received December 18, 2008; accepted April 4, 2009; published April 15, 2009.
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