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Light-harvesting Complex (light-harvesting + complex)
Selected AbstractsDifferential expression of antenna and core genes in Prochlorococcus PCC 9511 (Oxyphotobacteria) grown under a modulated light,dark cycleENVIRONMENTAL MICROBIOLOGY, Issue 3 2001Laurence Garczarek The continuous changes in incident solar light occurring during the day oblige oxyphototrophs, such as the marine prokaryote Prochlorococcus, to modulate the synthesis and degradation rates of their photosynthetic components finely. How this natural phenomenon influences the diel expression of photosynthetic genes has never been studied in this ecologically important oxyphotobacterium. Here, the high light-adapted strain Prochlorococcus sp. PCC 9511 was grown in large-volume continuous culture under a modulated 12 h,12 h light,dark cycle mimicking the conditions found in the upper layer of equatorial oceans. The pcbA gene encoding the major light-harvesting complex showed strong diel variations in transcript levels with two maxima, one before the onset of illumination and the other near the end of the photoperiod. In contrast, the mRNA level of psbA (encoding the reaction centre II subunit D1), the monocistronic transcript of psbD (encoding D2) and the dicistronic transcript of psbDC were all tightly correlated with light irradiance, with a minimum at night and a maximum at noon. The occurrence of a second peak during the dark period for the monocistronic transcript of psbC (encoding one of the PS II core Chl a antenna proteins) suggested the involvement of post-transcriptional regulation. Differential expression of the external antenna and core genes may constitute a mechanism of regulation of the antenna size to cope with the excess photon fluxes that Prochlorococcus cells experience in the upper layer of oceans around midday. The 5, ends of all transcripts were mapped, and a conserved motif, 5,-TTGATGA-3,, was identified within the putative psbA and pcbA promoters. [source] THE ANTARCTIC PSYCHROPHILE, CHLAMYDOMONAS RAUDENSIS ETTL (UWO241) (CHLOROPHYCEAE, CHLOROPHYTA), EXHIBITS A LIMITED CAPACITY TO PHOTOACCLIMATE TO RED LIGHT,JOURNAL OF PHYCOLOGY, Issue 4 2005Rachael M. Morgan-Kiss The psychrophilic Antarctic alga, Chlamydomonas raudensis Ettl (UWO241), grows under an extreme environment of low temperature and low irradiance of a limited spectral quality (blue-green). We investigated the ability of C. raudensis to acclimate to long-term imbalances in excitation caused by light quality through adjustments in photosystem stoichiometry. Log-phase cultures of C. raudensis and C. reinhardtii grown under white light were shifted to either blue or red light for 12 h. Previously, we reported that C. raudensis lacks the ability to redistribute light energy via the short-term mechanism of state transitions. However, similar to the model of mesophilic alga, C. reinhardtii, the psychrophile retained the capacity for long-term adjustment in energy distribution between PSI and PSII by modulating the levels of PSI reaction center polypeptides, PsaA/PsaB, with minimal changes in the content of the PSII polypeptide, D1, in response to changes in light quality. The functional consequences of the modulation in PSI/PSII stoichiometry in the psychrophile were distinct from those observed in C. reinhardtii. Exposure of C. raudensis to red light caused 1) an inhibition of growth and photosynthetic rates, 2) an increased reduction state of the intersystem plastoquinone pool with concomitant increases in nonphotochemical quenching, 3) an uncoupling of the major light-harvesting complex from the PSII core, and 4) differential thylakoid protein phosphorylation profiles compared with C. reinhardtii. We conclude that the characteristic low levels of PSI relative to PSII set the limit in the capacity of C. raudensis to photoacclimate to an environment enriched in red light. [source] Effects of long-term chilling on growth and photosynthesis of the C4 gramineae Paspalum dilatatumPHYSIOLOGIA PLANTARUM, Issue 1 2003Ana M. Cavaco Dallis grass (Paspalum dilatatum Poir.) is a C4/NADP-ME gramineae, previously classified as semi-tolerant to cold, although a complete study on this species acclimation process under a long-term chilling and controlled environmental conditions has never been conducted. In the present work, plants of the variety Raki maintained at 25/18°C (day/night) (control) were compared with plants under a long-term chilling at 10/8°C (day/night) (cold-acclimated) in order to investigate how growth and carbon assimilation mechanisms are engaged in P. dilatatum chilling tolerance. Although whole plant mean relative growth rate (mean RGR) and leaf growth were significantly decreased by cold exposure, chilling did not impair plant development nor favour the investment in biomass below ground. Cold-acclimated P. dilatatum cv. Raki had a lower leaf chlorophyll content, but a higher photosynthetic capacity at optimal temperatures, its range being shifted to lower values. Associated with this higher capacity to use the reducing power in CO2 assimilation, cold-acclimated plants further showed a higher capacity to oxidize the primary stable quinone electron acceptor of PSII, QA. The activity and activation of phosphoenolpyruvate carboxylase (PEPC; EC 4.1.1.31) and ribulose-1,5-bisphosphate carboxylase/oxygenase (Rubisco; EC 4.1.1.39) were not significantly affected by the long-term chilling. Cold-acclimated P. dilatatum cv. Raki apparently showed a lower transfer of excitation energy from the light-harvesting complex of photosystem II to the respective reaction centre and enhancement of radiationless energy-dissipating mechanisms at suboptimal temperatures. Overall, long-term chilling resulted in several effects that comprise responses with an intermediate character of both chilling-tolerant and ,sensitive plants, which seem to play a significant role in the survival and acclimation of P. dilatatum cv. Raki at low temperature. [source] Self-interaction chromatography as a tool for optimizing conditions for membrane protein crystallizationACTA CRYSTALLOGRAPHICA SECTION D, Issue 1 2010Mads Gabrielsen The second virial coefficient, or B value, is a measurement of how well a protein interacts with itself in solution. These interactions can lead to protein crystallization or precipitation, depending on their strength, with a narrow range of B values (the `crystallization slot') being known to promote crystallization. A convenient method of determining the B value is by self-interaction chromatography. This paper describes how the light-harvesting complex 1,reaction centre core complex from Allochromatium vinosum yielded single straight-edged crystals after iterative cycles of self-interaction chromatography and crystallization. This process allowed the rapid screening of small molecules and detergents as crystallization additives. Here, a description is given of how self-interaction chromatography has been utilized to improve the crystallization conditions of a membrane protein. [source] |