Inactivation of a Low Temperature-Induced RNA Helicase in Synechocystis sp. PCC 6803: Physiological and Morphological Consequences
| Autor: | Meghana Ventakesh, Oxana S. Tarassova, Laura M. Patterson-Fortin, George S. Espie, Danuta Chamot, George W. Owttrim, Albert Remus R. Rosana |
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| Rok vydání: | 2012 |
| Předmět: |
chemistry.chemical_classification
Reactive oxygen species Physiology Carbon fixation Mutant Synechocystis Cell Biology Plant Science General Medicine Biology Cell morphology Photosynthesis Photosynthetic capacity RNA Helicase A Cold Temperature chemistry Biochemistry Annealing activity Biophysics Reactive Oxygen Species RNA Helicases |
| Zdroj: | Plant and Cell Physiology. 53:646-658 |
| ISSN: | 1471-9053 0032-0781 |
| DOI: | 10.1093/pcp/pcs020 |
| Popis: | Inactivation of the DEAD box RNA helicase, crhR, has dramatic effects on the physiology and morphology of the photosynthetic cyanobacterium, Synechocystis sp. PCC 6803. These effects are observed at both normal growth temperature (30°C) and under cold stress (20°C), indicating that CrhR performs crucial function(s) at all temperatures. A major physiological effect is the rapid cessation of photosynthesis upon temperature downshift from 30 to 20°C. This defect does not originate from an inability to transport or accumulate inorganic carbon or a deficiency in photosynthetic capacity as the mutant has sufficient electron transport and enzymatic capacity to sustain photosynthesis at 30°C and inorganic carbon (Ci) accumulation at 20°C. Oxygen consumption in the presence of methyl viologen indicated that while electron transport capacity is sufficient to accumulate Ci, the mutant does not possess sufficient activity to sustain carbon fixation at maximal rates. These defects are correlated with severely impaired cell growth and decreased viability, cell size and DNA content at low temperature. The ΔcrhR mutant also progressively accumulates structural abnormalities at low temperature that cannot be attributed solely to reactive oxygen species (ROS)-induced photooxidative damage, suggesting that they are manifestations of pre-existing defects that are amplified over time. The data indicate that the observed physiological and morphological effects are intimately related to crhR mutation, implying that the lack of CrhR RNA unwinding/annealing activity results in the inability to execute one or more vital steps in photosynthesis that are required at all temperatures but are crucial at low temperature. |
| Databáze: | OpenAIRE |
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