The Redox Potential of the Plastoquinone Pool of the Cyanobacterium Synechocystis Species Strain PCC 6803 Is under Strict Homeostatic Control
| Autor: | J. Merijn Schuurmans, Martijn Bekker, Jacco C. Kromkamp, R. Milou Schuurmans, Klaas J. Hellingwerf, Hans C. P. Matthijs |
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| Přispěvatelé: | Molecular Microbial Physiology (SILS, FNWI), Aquatic Microbiology (IBED, FNWI) |
| Jazyk: | angličtina |
| Rok vydání: | 2014 |
| Předmět: |
Chlorophyll
Light Plastoquinone Physiology Analytical chemistry chemistry.chemical_element Plant Science Chemostat Redox Oxygen Electron Transport chemistry.chemical_compound Phycobilisomes Genetics Homeostasis Photosynthesis Chromatography High Pressure Liquid Photosystem I Protein Complex biology Strain (chemistry) Chlorophyll A Synechocystis Extraction (chemistry) Photosystem II Protein Complex Articles biology.organism_classification Fluorescence Spectrometry Fluorescence chemistry Batch Cell Culture Techniques Biophysics Oxidation-Reduction Half-Life |
| Zdroj: | Plant Physiology, 165(1), 463-475. American Society of Plant Biologists |
| ISSN: | 0032-0889 |
| DOI: | 10.1104/pp.114.237313 |
| Popis: | A method is presented for rapid extraction of the total plastoquinone (PQ) pool from Synechocystis sp. strain PCC 6803 cells that preserves the in vivo plastoquinol (PQH2) to -PQ ratio. Cells were rapidly transferred into ice-cold organic solvent for instantaneous extraction of the cellular PQ plus PQH2 content. After high-performance liquid chromatography fractionation of the organic phase extract, the PQH2 content was quantitatively determined via its fluorescence emission at 330 nm. The in-cell PQH2-PQ ratio then followed from comparison of the PQH2 signal in samples as collected and in an identical sample after complete reduction with sodium borohydride. Prior to PQH2 extraction, cells from steady-state chemostat cultures were exposed to a wide range of physiological conditions, including high/low availability of inorganic carbon, and various actinic illumination conditions. Well-characterized electron-transfer inhibitors were used to generate a reduced or an oxidized PQ pool for reference. The in vivo redox state of the PQ pool was correlated with the results of pulse-amplitude modulation-based chlorophyll a fluorescence emission measurements, oxygen exchange rates, and 77 K fluorescence emission spectra. Our results show that the redox state of the PQ pool of Synechocystis sp. strain PCC 6803 is subject to strict homeostatic control (i.e. regulated between narrow limits), in contrast to the more dynamic chlorophyll a fluorescence signal. |
| Databáze: | OpenAIRE |
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