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First published online September 7, 2007; 10.1104/pp.107.105023 Plant Physiology 145:1018-1030 (2007) © 2007 American Society of Plant Biologists OPEN ACCESS ARTICLE
Transcriptional Regulation of the Respiratory Genes in the Cyanobacterium Synechocystis sp. PCC 6803 during the Early Response to Glucose Feeding1,[C],[W],[OA]Laboratory of Plant Genomics, Korea Research Institute of Bioscience and Biotechnology, Daejeon 305–806, Korea (S.L., J.-H.J.); Department of Biology, Chungnam National University, Daejeon 305–764, Korea (J.-Y.R., S.Y.K., J.Y.S., H.-T.C., Y.-I.P.); Department of Biological Sciences, Myongji University, Yongin, Kyunggi-do 449–728, Korea (S.-B.C.); Department of Plant Science, Seoul National University, Seoul 151–742, Korea (D.C.); and Institut Pasteur, Unité des Cyanobactéries (CNRS URA 2172) 28, F–75724 Paris cedex 15, France (N.T.d.M.)
The coordinated expression of the genes involved in respiration in the photosynthetic cyanobacterium Synechocystis sp. PCC 6803 during the early period of glucose (Glc) treatment is poorly understood. When photoautotrophically grown cells were supplemented with 10 mM Glc in the light or after a dark adaptation period of 14 h, significant increases in the respiratory activity, as determined by NAD(P)H turnover, respiratory O2 uptake rate, and cytosolic alkalization, were observed. At the same time, the transcript levels of 18 genes coding for enzymes associated with respiration increased with differential induction kinetics; these genes were classified into three groups based on their half-rising times. Transcript levels of the four genes gpi, zwf, pdhB, and atpB started to increase along with a net increase in NAD(P)H, while the onset of net NAD(P)H consumption coincided with an increase in those of the genes tktA, ppc, pdhD, icd, ndhD2, ndbA, ctaD1, cydA, and atpE. In contrast, the expression of the atpI/G/D/A/C genes coding for ATP synthase subunits was the slowest among respiratory genes and their expression started to accumulate only after the establishment of cytosolic alkalization. These differential effects of Glc on the transcript levels of respiratory genes were not observed by inactivation of the genes encoding the Glc transporter or glucokinase. In addition, several Glc analogs could not mimic the effects of Glc. Our findings suggest that genes encoding some enzymes involved in central carbon metabolism and oxidative phosphorylation are coordinately regulated at the transcriptional level during the switch of nutritional mode.
1 This work was supported by grants from the Crop Functional Genomics Center (CG2122) and KOSEF (R01–2004–000010246–0) funded by the Ministry of Science and Technology, Korea. S.Y.K. is a recipient of a BK21 Fellowship from the Ministry of Education, Korea. 2 These authors contributed equally to the article. 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: Youn-Il Park (yipark{at}cnu.ac.kr). [C] Some figures in this article are displayed in color online but in black and white in the print edition. [W] The online version of this article contains Web-only data. [OA] Open Access articles can be viewed online without a subscription. www.plantphysiol.org/cgi/doi/10.1104/pp.107.105023 * Corresponding author; e-mail yipark{at}cnu.ac.kr. Received July 2, 2007; accepted September 4, 2007; published September 7, 2007.
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