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91.
92.
Non-photochemical fluorescence quenching and the diadinoxanthin cycle in a marine diatom 总被引:7,自引:0,他引:7
Miguel Olaizola Julie La Roche Zbigniew Kolber Paul G. Falkowski 《Photosynthesis research》1994,41(2):357-370
The diadinoxanthin cycle (DD-cycle) in chromophyte algae involves the interconversion of two carotenoids, diadinoxanthin (DD) and diatoxanthin (DT). We investigated the kinetics of light-induced DD-cycling in the marine diatom Phaeodactylum tricornutum and its role in dissipating excess excitation energy in PS II. Within 15 min following an increase in irradiance, DT increased and was accompanied by a stoichiometric decrease in DD. This reaction was completely blocked by dithiothreitol (DTT). A second, time-dependent, increase in DT was detected 20 min after the light shift without a concomitant decrease in DD. DT accumulation from both processes was correlated with increases in non-photochemical quenching of chlorophyll fluorescence. Stern-Volmer analyses suggests that changes in non-photochemical quenching resulted from changes in thermal dissipation in the PS II antenna and in the reaction center. The increase in non-photochemical quenching was correlated with a small decrease in the effective absorption cross section of PS II. Model calculations suggest however that the changes in cross section are not sufficiently large to significantly reduce multiple excitation of the reaction center within the turnover time of steady-state photosynthetic electron transport at light saturation. In DTT poisoned cells, the change in non-photochemical quenching appears to result from energy dissipation in the reaction center and was associated with decreased photochemical efficiency. D1 protein degradation was slightly higher in samples poisoned with DTT than in control samples. These results suggest that while DD-cycling may dynamically alter the photosynthesis-irradiance response curve, it offers limited protection against photodamage of PS II reaction centers at irradiance levels sufficient to saturate steady-state photosynthesis.Abbreviations CAP
chloramphenicol
- D1
PS II reaction center protein
- DD
diadinoxanthin
- DD
cycle-diadinoxanthin cycle
- DT
diatoxanthin
- DTT
dithiothreitol
- FCP
fucoxanthin chlorophyll a-c protein
- Fm
maximum fluorescence yield in the dark-adapted state
- Fo
minimum fluorescence yield in the dark-adapted state
- Fm and Fo
maximum and minimum fluorescence yields respectively in some light adapted state
- Fv
maximum variable fluorescence yield in the dark-adapted state
- Ik
Irradiance at the intercept of the initial slope of the photosynthesis-irradiance curve and the maximum photosynthetic rate
- kD
first order rate constant for nonradiative de-excitation of excitions in the PS II antenna
- kd
first order rate constant for non-radiative de-excitation of excitons in the PS II reaction center
- kF
first order rate constant for fluorescence
- kT
first order rate constant for exciton transfer to the reaction center
- kt
first order rate constant for exciton transfer from the reaction center to the antenna
- Rubisco
ribulose bisphosphate carboxylase
- SVm
Stern-Volmer quenching coefficient of the maximum fluorescence yield
- SVo
Stern-Volmer quenching coefficient of the miniximum fluorescence yield
- PS II
apparent absorption cross-section of PS II
- arr
average interval between exciton arrival to the PS II reaction center (ms)
- rem
average interval between electron turnover during photosynthesis in the PS II reaction center (ms)
- d
the probability that an exciton is non-radiatively dissipated in the reaction center
- T
the probability that an exciton in the antenna is transferred to the reaction center
- t
the probability that an exciton is transferred back from the reaction center to the antenna 相似文献
93.
José Antonio Jarillo Juan Capel Antonio Leyva José Miguel Martínez-Zapater Julio Salinas 《Plant molecular biology》1994,25(4):693-704
We have isolated two Rare Cold-Inducible (RCI1 and RCI2) cDNAs by screening a cDNA library prepared from cold-acclimated etiolated seedlings of Arabidopsis thaliana with a subtracted probe. RNA-blot hybridizations revealed that the expression of both RCI1 and RCI2 genes is induced by low temperature independently of the plant organ or the developmental stage considered. However, RCI1 mRNA accumulates faster and at higher levels than the RCI2 one indicating that these genes have differential responsiveness to cold stress. Additionally, when plants are returned to room temperature, RCI1 mRNA decreases faster than RCI2. In contrast to most of the cold-inducible plant genes characterized, the expression of RCI1 and RCI2 is not induced by ABA or water stress. The nucleotide sequences of RCI1 and RCI2 cDNAs predict two acidic polypeptides of 255 and 251 amino acids with molecular weights of 29 and 28 kDa respectively. The alignment of these polypeptides indicates that they have 181 identical amino acids suggesting that the corresponding genes have a common origin. Sequence comparisons reveal no similarities between the RCI proteins and any other cold-regulated plant protein so far described. Instead, they demonstrate that the RCI proteins are highly homologous to a family of proteins, known as 14-3-3 proteins, which are thought to be involved in the regulation of multifunctional protein kinases. 相似文献
94.
Alicia Bravo José Miguel Hermoso Margarita Salas 《Molecular & general genetics : MGG》1994,245(5):529-536
Protein p6 of the Bacillus subtilis phage ø29 is essential for in vivo viral DNA replication. This protein activates the initiation of ø29 DNA replication in vitro by forming a multimeric nucleoprotein complex at the replication origins. The N-terminal region of protein p6 is involved in DNA binding, as shown by in vitro studies with p6 proteins altered by deletions or missense mutations. We report on the development of an in vivo functional assay for protein p6. This assay is based on the ability of protein p6-producing B. subtilis non-suppressor (su
–) cells to support growth of a ø29 sus6 mutant phage. We have used this trans-complementation assay to investigate the effect on in vivo viral DNA synthesis of missense mutations introduced into the protein p6 N-terminal region. The alteration of lysine to alanine at position 2 resulted in a partially functional protein, whereas the replacement of arginine by alanine at position 6 gave rise to an inactive protein. These results indicate that arginine at position 6 is critical for the in vivo activity of protein p6. Our complementation system provides a useful genetic approach for the identification of functionally important amino acids in protein p6. 相似文献
95.
Michael A. Kron Laura Gately Janardan P. Pandey Miguel H. Jurado Jose Rumbea Guzman 《Human genetics》1994,93(5):517-519
Indigenous Indian groups comprise approximately 20% of Ecuador's population, the third largest percentage in all of Central or South America, yet immunogenetic data on these groups are lacking in the literature. In the course of population migration studies, sera collected from 65 Ecuadorians living in the northern province of Esmeraldas were typed for six GM and two KM markers. The study population consisted of 47 Cayapa Indians and 18 blacks of African origin, descendants of slaves imported into the area during the seventeenth century. The Cayapa demonstrated three GM phenotypes, two of which are common to other South American Indian tribes. The frequency of KM1 positive Cayapa Indians (63%) is similar to other South American Indian tribes, but is significantly greater than the Huaorani of eastern Ecuador (2%), the only other Ecuadorian Indian group for whom limited immunoglobulin allotype data are available (
2=35.8, P<0.0001). 相似文献
96.
Plant secondary compounds can prevent feeding by phytophagous insects or, if ingested, can be poisonous to them. Less attention has been paid to the additional effects they have on feeding behavior when they are only weakly deterrent or not deterrent at all. Experiments were carried out on the generalist grass-hopperSchistocerca americana. Individuals were presented either with two cakes of high-quality artificial food with a single deterrent compound added or with two cakes, each with a different added deterrent compound. The deterrents consisted of single plant secondary compounds that were either marginally or strongly deterrent. There were profound differences in feeding behavior between those individuals given identical and those given different cake types, including longer feeding bouts on single cakes when a choice of different cake types was available. The behavioral effects demonstrate that the presence of secondary compounds in one food can influence the patterns of feeding on other available foods and suggest that such chemicals could impact foraging activities in a complex manner. 相似文献
97.
Single Ca2+ channel records were obtained from plasma membrane-enriched fractions of wheat roots incorporated into artificial planar lipid bilayers. The channel had a unitary conductance of 15 pS for a 10 to 95 mM CaCl2 gradient (cytoplasm: outside of the cell). The voltage dependence displayed by the channel agreed with that expected for Ca2+ channels in the plasma membrane. The channel gating was strongly modified by addition of 20 M extracellular verapamil (a Ca2+ channel antagonist). Extracellular AlCl3 (70 M, pH 4.9) almost completely blocked the channel. 相似文献
98.
Contrasting evidence has accumulated regarding the role of acid invertase and sucrose synthase in tomato fruit sink establishment and maintenance. In this work the relationships among the activities of sucrose synthase and acid invertase, Lycopersicon esculentum Mill cv UC-82B fruit growth, and starch accumulation were analyzed in fruit at 0 to 39 d after anthesis. Sucrose synthase, but not acid invertase, was found to be positively correlated with tomato fruit relative growth rate and with starch content in the pericarp tissue. A similar association between sucrose synthase activity and starch accumulation was also evident in the basal portion of the stem. Heat-shock treatments, which inhibited the increase in sucrose synthase activity at the beginning of the light period and had no effect on acid invertase activity, were used to examine the importance of sucrose synthase in relation to sucrose metabolism and starch synthesis. After the heat-shock treatment, concomitantly with the suppressed sucrose synthase activity relative to the controls, there was a reduction in sucrose cleavage and starch accumulation. These data substantiate the conclusion that, during the early phases of tomato fruit development, sucrose synthase rather than acid invertase is the dominant enzyme in metabolizing imported sucrose, which in turn plays a part in regulating the import of sucrose into the fruit. 相似文献
99.
Jesús Manuel de la Fuente Amalia Vázquez M. Mar González Miguel Sánchez María Molina César Nombela 《Applied microbiology and biotechnology》1993,38(6):763-769
Thermosensitive mutant strains of Saccharomyces cerevisiae that fail to generate an osmotically stable cell wall when grown at a non-permissive temperature release their cell contents upon expression of the mutation. Therefore, they may represent an alternative for the production of homologous or heterologous protein preparations. In order to analyse the expression of two of these mutations, lyt2 and slt2, we grew the corresponding strains under precisely defined conditions in batch and continuous fermentors. A switch in the temperature of batch cultures from 24° C to 37° C determined lysis of the cells with a significant release of intracellular enzymes. These include alkaline phosphatase and periplasmic proteins such as glucan-degrading enzymes, the pattern of cell lysis and protein release being maintained for about 6 h. One-stage continuous cultures of a lyt2 mutant were maintained for long periods at 37° C; a fraction of the population lysed and released the indicated proteins, but eventually a revertant of the lytic phenotype was selected. To avoid this, a two-stage continuous culture system was developed by connecting two fermentors in series, the effluent from the first one at 24°C being fed to the second one adjusted to 37° C. A steady state of cell lysis and protein liberation was reached in the second-stage fermentor without any evidence of selection of revertants. This system can be very useful for developing conditions for the use of yeast strains to produce protein preparations.
Correspondence to: C. Nombela 相似文献
100.
Miguel Lara-Aparicio Santiago López de Medrano Beatriz Fuentes-Pardo Enrique Moreno-Sáenz 《Bulletin of mathematical biology》1993,55(1):97-110
Based on experimental work on the ontogeny of the electroretinogram circadian rhythm in crayfish, we present a mathematical
model simulating changes in both frequency and amplitude of the electroretinogram oscillation during several developmental
stages until shortly before the adult age. Simultaneously, we propose a hypothetical oscillation in the hormonal release whose
frequency is imposed on the electroretinogram oscillation. The model consists of two coupled nonlinear oscillators in which
a dynamical response is obtained mainly through an Andronov-Hopf bifurcation. Through the construction of the model, a biological
hypothesis about the essential elements underlying the ERG circadian rhythm and their interrelations is formulated and discussed. 相似文献