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First published online June 28, 2007; 10.1104/pp.107.103341

Plant Physiology 144:1946-1959 (2007)
© 2007 American Society of Plant Biologists

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BIOENERGETICS AND PHOTOSYNTHESIS

Long-Term Response toward Inorganic Carbon Limitation in Wild Type and Glycolate Turnover Mutants of the Cyanobacterium Synechocystis sp. Strain PCC 68031,[W]

Marion Eisenhut, Eneas Aguirre von Wobeser, Ludwig Jonas, Hendrik Schubert, Bas W. Ibelings, Hermann Bauwe, Hans C.P. Matthijs and Martin Hagemann*

Universität Rostock, Institut für Biowissenschaften, Abteilung Pflanzenphysiologie (M.E., H.B., M.H.) und Ökologie (H.S.), D–18059 Rostock, Germany; University of Amsterdam, Institute for Biodiversity and Ecosystem Dynamics, NL–1018WS Amsterdam, The Netherlands (E.A.v.W., H.C.P.M.); Universität Rostock, Institut für Pathologie, Elektronenmikroskopisches Zentrum, D–18055 Rostock, Germany (L.J.); Netherlands Institute of Ecology, Centre for Limnology, Department of Foodweb Studies, NL–3631AC Nieuwersluis, The Netherlands (B.W.I.); and Eawag, Swiss Federal Institute of Aquatic Sciences and Technology, Centre of Ecology, Evolution, and Biogeochemistry, CH–6047 Kastanienbaum, Switzerland (B.W.I.)

Concerted changes in the transcriptional pattern and physiological traits that result from long-term (here defined as up to 24 h) limitation of inorganic carbon (Ci) have been investigated for the cyanobacterium Synechocystis sp. strain PCC 6803. Results from reverse transcription-polymerase chain reaction and genome-wide DNA microarray analyses indicated stable up-regulation of genes for inducible CO2 and HCO3 uptake systems and of the rfb cluster that encodes enzymes involved in outer cell wall polysaccharide synthesis. Coordinated up-regulation of photosystem I genes was further found and supported by a higher photosystem I content and activity under low Ci (LC) conditions. Bacterial-type glycerate pathway genes were induced by LC conditions, in contrast to the genes for the plant-like photorespiratory C2 cycle. Down-regulation was observed for nitrate assimilation genes and surprisingly also for almost all carboxysomal proteins. However, for the latter the observed elongation of the half-life time of the large subunit of Rubisco protein may render compensation. Mutants defective in glycolate turnover ({Delta}glcD and {Delta}gcvT) showed some transcriptional changes under high Ci conditions that are characteristic for LC conditions in wild-type cells, like a modest down-regulation of carboxysomal genes. Properties under LC conditions were comparable to LC wild type, including the strong response of genes encoding inducible high-affinity Ci uptake systems. Electron microscopy revealed a conspicuous increase in number of carboxysomes per cell in mutant {Delta}glcD already under high Ci conditions. These data indicate that an increased level of photorespiratory intermediates may affect carboxysomal components but does not intervene with the expression of majority of LC inducible genes.


1 This work was supported by a scholarship from Consejo Nacional para la Ciencia y Tecnología (Mexico) and by a grant from the Earth and Life Sciences Foundation (to E.A.v.W.), which is subsidized by the Netherlands Organization for Scientific Research (grant to Dr. Jef Huisman, University of Amsterdam). Financial support for setting up the array facility and for purchase of the arrays used in this study was provided by the Bootsma fonds at the Royal Academy of Arts and Sciences (grant to B.W.I.). This work was also supported by a grant from the Deutsche Forschungsgemeinschaft (to M.H.).

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: Martin Hagemann (martin.hagemann{at}uni-rostock.de).

[W] The online version of this article contains Web-only data.

www.plantphysiol.org/cgi/doi/10.1104/pp.107.103341

* Corresponding author; e-mail martin.hagemann{at}uni-rostock.de; fax 49–0–3814986112.

Received June 4, 2007; accepted June 24, 2007; published June 28, 2007.




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