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Laser-flash-activated electron paramagnetic resonance studies of primary photochemical reactions in chloroplasts.

Electron paramagnetic resonance studies of the primary reactants of Photosystems I and II have been conducted at cryogenic temperatures after laser-flash activation with monochromatic light.P-700 photooxidation occurs irreversibly in chloroplasts and in Photosystem I fragments after activation with a 730 nm laser flash at a temperature of 35 degrees K. Flash activation of chloroplasts or Photosystem II chloroplast fragments with 660 nm light results in the production of a free-radical signal (g = 2.002, linewidth approximately 8 gauss) which decays with a half-time of 5.0 ms at 35 degrees K. The half-time of decay is independent of temperature in the range of 10-77 degrees K. This reversible signal can be eliminated by preillumination of the sample at 35 degrees K with 660 nm light (but not by 730 nm light), by preillumination with 660 nm light at room temperature in the presence of 3-(3',4'-dichlorophenyl)-1,1'-dimethylurea (DCMU) plus hydroxylamine, or by adjustment of the oxidation-reduction potential of the chloroplasts to - 150 mV prior to freezing. In the presence of ferricyanide (20-50 mM), two free-radical signals are photoinduced during a 660 nm flash at 35 degrees K. One signal decays with a half-time of 5 ms, whereas the second signal is formed irreversibly. These results are discussed in terms of a current model for the Photosystem II primary reaction at low temperature which postulates a back-reaction between P-680+ and the primary electron acceptor.

Ascorbic Acid↗

Anomalies in the kinetics of photosynthetic oxygen emission in sequences of flashes revealed by matrix analysis. Effects of carbonyl cyanide m-chlorophenylhydrazone and variation in time parameters.

The model of Kok et al. (Kok, B., Forbush, B. and McGloin, M. (1970) Photochem. Photobiol. 11, 457-475) is considered the best kinetic explanation of the damped oscillations of O2 evolution induced in higher plants by a sequence of brief saturating flashes. Matrix analysis applied to this model shows that the parameters involved (distribution of S states at zero time, probabilities of transition between states induced by a flash) cannot be completely known from the O2 yield sequence, Yn. However, four quantities, with limited content of information, are readily derived from data, without additional assumptions. They are sigma1, sigma2 and sigma3, three quasisymmetrical functions of the transition coefficients, and Y, a weighed average of four consecutive Yn values. The extent of misses and double hits and their variations can be qualitatively ascertained by inspection of the relative values of sigma1, sigma2and sigma3. In a regular sequence (stricly obeying Kok's model), all four quantities should be constant along the time axis. It is shown that actual sequences are seldom regular, in particular in the following conditions: (1) variable flashing frequency, (2) addition of carbonylcyanide m-chlorophenylhydrazone, (3) incomplete deactivation, (4) change of flashing frequency at steady state. In order to account for these anomalies, it is proposed to modify Kok's model by introducing, in parallel to the four state storage entity (S states), a side carrier C, which can reversibly exchange a positive charge with it. In the new model, the transition coefficients are essentially time varying, thus producing a nonregular behaviour of Yn sequences.

Carbonyl Cyanide m-Chlorophenyl Hydrazone↗

Function of three cytochromes in photosynthesis of whole cells of Rhodospirillum rubrum as studied by flash spectroscopy. Evidence for two types of reaction center.

1. Changes in the absorption spectrum induced by 10-mus flashes and continuous light of various intensities were studied in whole cells of Rhodospirillum rubrum in the presence and absence of 2-n-heptyl-4-hydroxyquinoline-N-oxide(HOQNO) and antimycin A. 2. Three cytochromes, c-420 (cytochrome c2), c-560 (cytochrome b) and c-428 were photoactive and gamma and alpha peaks at 420 and 550, 428 and 560, and 428 and 551 nm, respectively; they were photooxidized following the flash with half times of 0.3, 0.6 and 7 ms in the approximate ratios of 1/100, 1/300 and 1/1000 (cytochrome oxidized/antenna chlorophyll) and became reduced with half times of 12 ms, 60 ms and 0.7 s, respectively. c-428 and c-560 have not been distinguished before. 3. From a detailed analysis of the kinetics of P+ (oxidized reaction center chlorophyll) and the cytochromes, we conclude that 5% of the P+ (P2+) oxidizes c-428, whereas the remaining 95% of P+ (P1+) oxidizes c-420. At actinic light intensities low enough to keep c-420 fully reduced, approx. 4-5% of P becomes oxidized, accompanied by all c-428. The P2+ -P2 difference spectrum induced by this weak light is, when corrected for a shift to longer wavelengths of the bacteriochlorophyll absorption band at 878 nm, identical to the difference spectrum caused by the photooxidation of the remaining P1. At low flash intensity, c-428 becomes preferentially photooxidized, which suggests that the reaction centers where c-428 functions as a secondary donor contain much more antenna pigments compared to the centers where c-420 serves this purpose. 4. c+-420 is reduced in a competitive way by reduced c-560 (t 1/2=7 ms), and by an electron donor pool, (t 1/2=15 ms). HOQNO inhibits both pathways; antimycin A only the first. In the presence of HOQNO, c-560 is in the oxidized state in the dark, and is reduced in a light flash (t 1/2=100 ms), indicating that c-560 acts in a cyclic electron transport chain connected to P1. 5. The ratio of numbers of molecules P1 and antenna bacteriochlorophyll, transferring excitation energy to P1, is P1/bacteriochlorophyll1=1/30 P2: bacteriochlorophyll2=1/300; c-420/P1=1:2; c-560/P1=1/6; C-428/P2=1/1; bacteriochlorophyll2=7:3. If P2 is oxidized, excitation energy is transferred from bacteriochlorophyll2 to bacteriochlorophyll1.

Anaerobiosis↗

Flash-induced changes in the in vivo bacteriochlorophyll fluorescence yield at low temperatures and low redox potentials in carotenoid-containing strains of photosynthetic bacteria.

The changes in the in vivo bacteriochlorophyll fluorescence induced by a Xenon flash at low temperatures (77--200 K) with the "primary" acceptor X chemically prereduced have been examined in whole cells of several species of photosynthetic bacteria which contain carotenoids absorbing in the visible part of the absorption spectrum. Two groups of species with different behaviour could be distinguished. In both cases a flash-induced rise of the fluorescence yield was observed with X prereduced at 77 k; as the temperature was increased the ratio of the maximum fluorescence (FM) and the basal fluorescence (F0) decreased and the kinetics of the decay of the high fluorescent state, as observed during the tail of the flash, apparently accelerated. Of the species examined the flash-induced changes in fluorescence-yield kinetics appeared to occur at higher temperatures in the members of one group (Chromatium vinosum, Rhodopseudomonas gelatinosa and Rhodopseudomonas palustris) than in the members of the other (Rhodopseudomonas palustris) than in the members of the other (Rhodopseudomonas sphaeroides and Rhodospirillum rubrum). These effects are interpreted in terms of the light-induced generation of triplet states within the reaction centre. It is suggested that the species-dependent differences may reflect differences in the molecular organisation of the reaction centre. It was found that in all species the reaction centre carotenoid triplet does not act as a fluorescence quencher under these conditions.

Bacteriochlorophylls↗

Kinetic factors limiting the synthesis of ATP by chromatophores exposed to short flash excitation.

ATP synthesis was measured after chromatophores from Rhodopseudomonas capsulata had been subjected to illumination by single turnover flashes fired at variable frequencies. Three processes were examined, which under different conditions can limit the net yield of ATP. (1) A process with an apparent relaxation time of 10-20 ms. This reaction probably limits the rate of ATP synthesis in continuous illumination. It has similar time dependence to the stimulation of the carotenoid shift decay by ADP after a single flash. (2) An active state of the ATPase only persists when the chromatophores are excited more often than once in 10 s. This state decays with similar kinetics to the entire carotenoid shift decay. Full activation is achieved after two flashes. (1) and (2) are not significantly affected by concentrations of antimycin A sufficient to block electron flow through the cytochrome b/c2 oxidoreductase and abolish phase III in the generation of the carotenoid shift. (3) In the presence of antimycin A, after the third, fourth and subsequent flashes ATP synthesis is limited by the quantity of reducing equivalents transported through the reaction centre rather than by the level of the electrochemical proton gradient.

Adenosine Triphosphate↗

Visual evoked potentials to light flash in cats: is a frontal sinus reference electrode truly indifferent?

In flaxedilized cats, visual cortex evoked potentials (VEPs) to an intensity series of brief light flashes were recorded differentially using either a screw over frontal sinus or an insect pin in neck muscle as the reference electrode. At the same time EPs from the cornea (the ERG) and frontal sinus were recorded differentially against the neck muscle electrode. The EP recorded from the frontal sinus screw was a miniature of the ERG recorded from the cornea, with the same latencies and shape as the ERG but only 10-30% of its amplitude. At a fast presentation rate (1/sec) the amplitude of the ERG, and consequently the frontal sinus potential, decreased with increasing intensity of light flash, whereas at a slow presentation rate (1/3 or 1/5 sec) the ERG and frontal sinus potential increased in response to all but the highest intensities. The location of the reference electrode and the rate of light flash presentation had the following effects on visual cortex EP amplitudes. A frontal sinus reference increased the amplitudes of early components (less than 100 msec) of the VEP. Also, VEP amplitudes as a function of flash intensity yielded slopes which tended to be positive at a slow presentation rate and negative at a fast presentation rate. This effect is in accord with the rate dependent slopes of the frontal sinus potential.

Animals↗

The influence of intermittent light stimulation on potentials evoked by single flashes in photosensitive and non-photosensitive Papio papio.

The effects of intermittent light stimulation (ILS) on visual potentials (VEPs), evoked in different cortical areas, were statistically studied in baboons either naturally photosensitive or made photosensitive by allylglycine at a subconvulsant dose, as well as in non-photosensitive animals. VEPs were induced by single flashes (paradigm a) or by flashes preceded by trains of ILS (paradigm b). In every baboon, photosensitive or not, the VEPs induced by paradigm b in the striate area show a decrease of amplitude compared to VEPs induced by paradigm a. The ERG evolves in the same way. Therefore, these effects do not depend on photosensitivity; they depend on the intensity of stimulation. In photosensitive animals the single flash in paradigm b can induce a paroxysmal VEP in the fronto-rolandic (FR) area. In parietal and peristriate areas the VEPs induced by paradigm b show new late components when compared to those induced by paradigm a. These changes are observed even if no FR paroxysmal VEP is induced; they depend on the presence of a train of ILS preceding the single flash and on the predisposition to epilepsy (both natural and due to allylglycine); in the non-photosensitive animals the VEPs recorded in the same areas do not show such differences. We consider that among afferents which could act in inducing FR paroxysmal activities some cortico-cortical visual afferents can come from non-specific cortical areas (parietal or peristriate), but would not directly originate in the striate cortex; anatomical data in this species may support such a hypothesis.

Afferent Pathways↗

Effect of roll and pitch on flash-induced nystagmus: support for involvement of retinal direction-selective elements?

The direction of eye movement (i.e., the angle of the resultant velocity vector calculated from the horizontal and vertical components) during flash-induced nystagmus was evaluated in static roll and pitch positions. It appeared that this direction coincided with the orientation of the visual streak, as influenced by the ocular countertorsion which is known to occur in the various body positions. This supports the hypothesis that flash-induced nystagmus results from stimulation of direction-selective retinal elements. The intensity of flash-induced nystagmus, evaluated either by measuring slow-phase velocity (i.e., magnitude of resultant vector) or by beat frequency, was minimal in approximately 90 and 270 degrees roll or pitch positions, presumably because the total combined (utricular and saccular, left and right) excitatory otolith stimulation was maximal in these positions, the effect of this stimulation being inhibitory to the flash-induced nystagmus.

Animals↗

Flash induced XANES spectroscopy for the Ca-depleted Mn-cluster in the photosynthetic O2-evolving enzyme.

Flash-induced changes of the Mn K-edge absorption spectra have been studied in the oxygen-evolving complex depleted of Ca. The Mn K-edge energy for the Ca-depleted S1-state was lower by 1.5 eV than that for the normal S1-state. The K-edge energy upshifted by 1 eV after one flash, indicative of an oxidation of Mn. After two flashes, the K-edge was elevated as well by 0.4 eV, and then reached a steady-state high level after continuous illumination where the K-edge energy was higher by 0.9 eV than that after one flash. The results indicate that the Mn-cluster and/or its direct ligand could be oxidized up to two electrons but further events are blocked.

Calcium↗

Analysis of photoenzymatic repair of UV lesions in DNA by single light flashes. XII. Evidence for enhanced photolysis enzyme-substrate complexes by a 2-photon reaction.

Yeast photoreactivating enzyme (PRE), preilluminated with wavelengths ranging from the near-UV to the red spectral region, forms with 254 nm-irradiated transforming DNA of Haemophilus influenzae enzyme-substrate complexes that are more efficiently photorepaired than complexes formed from non-preilluminated PRE. The action spectrum for this "preillumination effect", previously shown to have a maximum in the near-UV region, has another maximum near 577 nm. In complexes formed from non-preilluminated PRE the repair probability per incident photon is only about 25% of that in complexes formed from preilluminated PRE, if low-intensity photoreactivating light is applied continuously or as a sequence of flashes. However, photoreactivating light in the form of a single, high-intensity flash of 1 msec duration raises the repair probability to greater than 50%. Two light flashes, discharged with a delay of slightly more than a millisecond, may already achieve less photorepair than the same energy given as a single flash. These results are explained by the assumption that the great majority of PRE molecules in a non-preilluminated preparation have reduced activity (of the order of 1/4 of maximal activity). These less reactive molecules form enzyme-substrate complexes ("non-activated complexes") in which the repair probability per incident photon is considerably increased if 2 or more photons are absorbed within a time period of the order of milliseconds. This phenomenon, tentatively termed "2-photon photolysis" does not occur in "activated complexes" (i.e. those formed form preilluminated enzyme). The data are compatible with suggestion that the first absorption leads to a metastable excited state of the complex, during which the repair probability is increased by absorption of another photon. The generally observed heterogeneity of the photolytic response of enzyme-substrate complexes can be partly explained by heterogeneity of PRE molecules regarding their activity. In particular, uncontrolled exposure of enzyme to almost any kind of room light before its experimental use can enhance the heterogeneity.

DNA↗

Propagating inhibition as a function of flash diameter and duration.

Van der Wildt and Vrolijk (1981) Vision Res. 21, 1765-1771, detected propagation of inhibition with small and short flashes, separated in time and space. In this paper, the results measured with flashes of longer duration and/or larger diameter are described and discussed. A model, describing inhibition arising on the flanks of the stimulus; luminance distribution and acting at the top luminance of the probe flash, gives a good description of the results. When non-identical flashes are used, the inhibition proves to be backwards. The propagating inhibition described also seems to give a possible explanation of metacontrast.

Humans↗

A polychromatic flash photolysis apparatus (PFPA).

A wide variety of biologically relevant chemical intermediates have been identified and characterised by their spectral properties. When rapid kinetics, i.e. rapid changes in these spectral properties are studied, the equipment designed for these studies (flash photolysis-, T-jump apparatus) usually allows only the registration of intensity changes of the monitoring light beam at one particular wavelength. Quite frequently, however, particularly in biological systems, the reactions of interest are too complex to be fully understood using single wavelength techniques. We have therefore designed and built a flash photolysis apparatus which permits the simultaneous recording of absorbance changes at 32 wavelengths, freely selectable between 300 and 1000 nm, as well as changes in fluorescence, luminescence, birefringence and light scattering. The apparatus, which we have called Polychromatic Flash Photolysis Apparatus (PFPA), acquires up to 8000 difference spectra per second with an amplitude resolution of better than 0.0001 absorbance unit. Data acquisition and activation of an actinic xenon flash unit occurs under computer control. The same computer is responsible for data storage, handling and graphic display. This communication describes the PFPA, its performance, and, as a demonstration of its potential usefulness, its application to the measurement of the light driven photocycle of bacterial rhodopsin, the proton pumping protein of Halobacterium halobium.

Photolysis↗

Changes in flash but not pattern evoked cortical potentials after subchronic application of a monoamine oxidase (MAO) type A inhibitor in man.

Changes in flash but not pattern evoked cortical potentials after subchronic application of the MAO type A inhibitor pirlindole in man are reported. Pirlindole affects the deamination of serotonin and noradrenaline in the central nervous system and has serotonin reuptake inhibiting properties. Flash and pattern evoked cortical potentials were recorded in 6 healthy men before and after a 7 day period of treatment with 3 X 75 mg/day of pirlindole. After drug treatment, an increase in P100 latency to flash stimuli was seen without a change in the latency to pattern stimuli. This indicates that different neuronal systems process flash and pattern stimuli.

Adult↗

A high-intensity, goggle-mounted flash stimulator for short-latency visual evoked potentials.

The few studies that have been done on short-latency, subcortical visual evoked potentials (SVEPs) have all used stroboscopic flashes as the evoking stimulus. The dimensions of the stimulator, the acoustical artifacts and the photic spread to the examination room limited the use of SVEPs to research laboratories. With the advent of high-efficiency light-emitting diodes (LEDs), high-intensity flashes can now be generated from goggle-mounted LEDs. In this study, a goggle-mounted high-intensity stimulator was constructed and its flashes used to evoke SVEPs. The reproducibility of SVEPs across subjects and the ease of using the high-intensity LED flash stimulator make them a promising candidate for testing subcortical visual pathway function in the operating room.

Cerebral Cortex↗

Hydrogen peroxide mediated photodegradation of phenol as studied by a flash photolysis/HPLC technique.

The technique of flash photolysis followed by high-performance liquid chromatography has been applied to the study of the photodegradation of phenol (I) in the presence of hydrogen peroxide. Progress of the reaction of I (0.1 mM) in undegassed aqueous solution ([H2O2]/[I] = 200/l) was observed by using multiple flashes (16 J). Analysis after a single flash indicated that catechol and hydroquinone were the primary products of the reaction. The reaction was found to be independent of pH in the range 7.0-9.0, but the yield of degradation decreased at pH > 9.0 and at pH < 7.0. The effects of the hydrogen peroxide concentration and flash energy on the chemical yield of the pollutant degradation, and product formation, were investigated as well. The mechanism of the reaction is discussed. A possibility of the application of flashlamps as powerful sources of the UV irradiation in industrial reactors for wastewater treatment is suggested.

Journal Article↗

Dynamic magnetic resonance imaging of the temporomandibular joint using FLASH sequences.

Magnetic resonance imaging (MRI) is a suitable modality for the visualization of the temporomandibular joint (TMJ) in both normal and pathologic conditions. Until recently, MRI had been unable to provide diagnostic dynamic images of the TMJ during opening. A series of 30 TMJ MRI examinations of 17 symptomatic patients and two normal volunteers (15 to 43 years old; 14 men and five women) was performed. Fast low angle shot (FLASH) sequences were used to provide a series of dynamic images of the TMJ in various phases of opening. In 30% of the joint examined, FLASH sequences contributed clinically significant information not available with standard T1-weighted sequences. These results suggest that FLASH images are particularly useful in distinguishing normal disc variants from pathologic conditions in which the disc is displaced anteriorly to a mild extent. The short imaging time of FLASH sequences decreases motion artifact in patients who have difficulty remaining still during the examination.

Adolescent↗

Obesity and fat distribution in relation to hot flashes in Dutch women from the DOM-project.

The authors studied obesity and fat distribution in relation to the occurrence of hot flashes in a population-based study comprising 2904 women aged 40-44 and 569 women aged 54-69 presenting for mammographic screening (the DOM-project). Women aged 40-44 in the upper tertiles of Quetelet's index and waist/hip ratio reported hot flashes significantly more often than women in the respective lower tertiles. These associations were independent of each other and independent of age. After adjustment for age, waist/hip ratio and menopausal status, the odds ratio comparing the upper tertile of Quetelet's index to the lower tertile was 1.70 (95% confidence interval, 1.30-2.21). After adjustment for age, Quetelet's index and menopausal status, the odds ratio comparing the upper tertile of waist/hip ratio to the lower tertile was 1.37 (95% CI, 1.05-1.78). In women aged 54-69 no significant associations between Quetelet's index and complaints of hot flashes were observed. Women in the upper tertile of waist/hip ratio reported hot flashes more often than women in the lower tertile, but this result was not significant (OR 1.38; 95% CI, 0.87-2.22).

Adult↗

A long-lived transient resulting from flash photolysis of hematoporphyrin in aqueous solution.

A long-lived transient with a lifetime of several hundred microseconds was observed following the flash photolysis of aqueous solutions of hematoporphyrin buffered at pH 7.5. The transient-ground state difference absorption spectrum was determined 500 microseconds after flash photolysis. The yield of this species was found to increase with increasing hematoporphyrin concentration and it was also found to depend on the excitation wavelength. The lifetime of the species is not significantly affected by the presence of oxygen. Because the triplet state of hematoporphyrin is not the only long-lived species produced by flash photolysis of aqueous hematoporphyrin solutions, the observed triplet state extinction coefficients will be lower than the true value and hence the triplet state yields of hematoporphyrin determined by the flash photolysis, "complete conversion" technique, are only upper limits. The formation of the long-lived species is discussed in terms of electron transfer between the monomer partners in hematoporphyrin dimer and aggregates which are present in aqueous solutions of hematoporphyrin, particularly in concentrated solutions.

Hematoporphyrins↗