Studies of Chloroplast Development in Euglena: XIV. Sequential Interactions of Ultraviolet Light and Photoreactivating Light in Green Colony Formation

Photoreactivation (PR) of green colony-forming ability in Euglena is pH-insensitive from pH 6.0 to 8.0 and temperature-sensitive with a maximum rate at 35°C. There is no PR at 0°C. The rate of PR varies with the growth stage of the cells; PR of exponential phase cells is slower than that of stationary phase cells. The reciprocity rule holds for PR over a 6-fold range of intensity. The shape of PR curves is a function of the UV dose; there appears to be a progressive increase in multiplicity until a limiting multiplicity is reached as indicated by the fact that curves for high doses are superposable. Dark-grown and light-grown cells give the same PR response for comparable UV doses. UV inactivation of cells which have been treated with UV and then with PR light shows that, if the PR dose is sufficiently large, the same UV-inactivation curve is obtained as for nonpretreated control cells. Doses of PR lower than the saturating dose produce UV-inactivation curves, the ultimate slopes of which are parallel to the slope of the control curve, but which show reduced multiplicity. The multiplicity of these curves increases with increasing PR dose. The UV inactivation of green colony-forming ability in Euglena is completely photoreactivable at the doses studied, in contrast with the UV inactivation of colony-forming ability, which occurs at considerably higher UV doses and behaves like most other photoreactivable systems, showing a photoreactivable sector of 0.32.     

Action spectra for photosynthesis in higher plants

The action and quantum yield spectra of photosynthetic CO₂ uptakeand the absorptance spectrum were determined for leaves of 33species of higher plant including 7 arbores over the wavelengthrange 344–758 nm, to interpret various curves of the spectralresponses. Almost the same curves either in the action or quantumyeild spectra were obtained for all the plants tested exceptin the ultraviolet (UV) and blue regions where the responserelative to the red maximum was significantly lower in the arboreousthan in herbaceous plants. The lower action in the UV and bluewas seen in leaves having higher absorptance in the green, anda very close correlation (r=–0.920) was found betweenthe ratio of action at 435 nm to that at 560 nm and the absorptanceat 560 nm (A560). These facts proved that the variation of actionspectra in the range from the UV to the green depended largelyon the differences in absorptance of leaves in the green, anda curve with a pronounced second peak in the blue could be obtainedwhen the A560 was less than about 0.6. (Received October 3, 1975; )     

The shape of the blacklight dose photoreactivation curve for chick embryo fibroblasts

The curves of UV (254 nm) induced pyrimidine dimers (endonuclease sensitive sites) vs. photoreactivating blacklight (365 nm) dose for cultured chick embryo fibroblasts reveal several new features. When the cells are incubated in the dark at 37 degrees following UV (254 nm) treatment, the efficiency of subsequent photorepair increases for the first few hours post-UV. The efficiency then remains approximately constant for several hours. Photorepair data obtained during this later period were plotted as the logarithm of dimer-enzyme complexes available for photoreactivation vs. blacklight (365 nm) dose. For a fixed damaging UV (254 nm) dose, the resulting curve has a shoulder of approximately 6-10 kJ/m2 followed by a straight line portion with a slope of magnitude about 1.5 X 10(-4) m2/J for UV doses up to 15 J/m2. For higher UV doses the shoulder remains about the same, but the slope decreases in magnitude. The shoulder is interpreted to indicate that a light-dependent step is necessary to activate the enzyme. The decrease in slope with increased UV dose together with some split photoreactivation dose experiments suggests that some site-to-site motion and multiple site function of the photorepair enzyme molecules may come into play at the higher levels of damage, but the evidence indicates that these complications are relatively unimportant at low UV doses.     

Blue light regulation of stomata in wheat seedlings. II. Action spectrum and search for action dichroism

The stomatal conductance response to low intensity blue light was studied in wheat seedlings ( Triticum aestivum L. cv. Starke II, Weibull) under red background illumination. Reciprocity was shown to be valid for illumination times from 10 s up to about 2 min. The action spectrum, constructed from fluence rate response curves, showed a maximum peak at 445–450 nm, another peak at 470 nm, a slight shoulder at 420 nm and a plateau between 370–400 nm. The relationship with action spectra for other blue light responses is discussed. The blue light response of wheat stomata did not exhibit action dichroism (the direction of the electrical vector of polarized blue light did not influence the response of the guard cells).     

Action Spectra for Phycobiliprotein Synthesis in a Chromatically Adapting Cyanophyte, Fremyella diplosiphon

The action spectra for phycocyanin production by the cyanophyte Fremyella diplosiphon shows maxima at 463 and 641 nm. The action spectrum for phycoerythrin production includes maxima at 387 and 550 nm. The maxima are based on a relative response rate well within the linear ascending portion of the dose response curves; the positions of the maxima are independent of the relative response rates chosen for reference over a 3-fold range although the comparative effectiveness of light at pairs of wavelengths varies with the standard used for comparison. These action spectra differ from those reported previously for Tolypothrix tenuis by Fujita and Hattori (Plant Cell Physiol. 3: 209-220) and by Diakoff and Scheibe (Plant Physiol. 51: 382-385) in that blue light strongly promotes phycobiliprotein synthesis in F. diphosiphon but has been reported to have little or no effect on T. tenuis.     

A Spectroscopic View of Some Recent Advances in the Study of Blue Light Photoreception*

The blue to UV-A region of the spectrum, spanning the region of about 320–520 nm, strongly influences the growth and development of plants and fungi. Photomorphogenesis in plants is, to a great extent, controlled by phytochrome, but there are unique contributions of the blue region, which cannot be duplicated by any amount of red light. Phototropism is, with few exceptions, a purely blue light response. In fungi, the blue region dominates the photocontrol of growth and development, though some red light effects have been reported. Many blue light action spectra fit the definition of cryptochrome, a pigment class defined by its UV-A and blue peaks. The action spectrum, if measured to sufficient resolution, displays several minor maxima or shoulders in the blue region which call to mind the vibrational levels of carotenoids and flavins. Recent molecular genetic studies, as well as photobiological work, have shown that some cryptochromes are related to the DNA repair enzyme photolyase, while others appear genetically and spectroscopically distinct. In this review, we have applied established criteria from photobiology, in particular, comparison of action spectra with absorption spectra, to these recent results. It is apparent that photolyase homologs such as CRY1 can explain the blue light portion of the action spectrum for hypocotyl elongation, assuming participation of the oxidized flavin. In fungi, the photoreceptor question remains open. Identification of the nph1 gene in Arabidopsis may soon lead to a photoreceptor for higher plant phototropism. Also, we present a possible solution to the most recent version of the long-standing flavin-carotenoid controversy, the zeaxanthin hypothesis for higher plant phototropism. In conclusion, there appear to be at least three classes of cryptochromes.     

The Light Requirement for Different Steps in the Development of Chloroplasts in Excised Wheat Roots

For the formation of chloroplasts in excised wheat roots blue light is necessary, but red light enhances the blue light effect. Intensity-response relationships and action spectra have been determined for the specific blue light effect as well as for the effect of red light when given before or after blue light. The longest wave length giving a blue light effect is about 500 nm. The spectrum shows a peak at about 450 nm, and a considerable effect extends down to 368 nm, the shortest wave length tested. The photoreceptor mechanism for the “blue reaction” is thought to be related to that of certain phototropisms and chloroplast movements, and to that involved in carotenoid synthesis in certain fungi. The active pigment is thought to be either a carotenoid or a flavoprotein, probably the latter. The effect of red light shows similar action spectra whether the red light is given before or after the blue, and they are consistent with protochlorophyll absorption. However, much less light is needed to produce a detectable response when the red light is given before the blue light than after. Because of the similarity of the spectra phytochrome may also be involved in the response to red light when given before blue. Far-red reversal has not been tested. The results are discussed in relation to the development of chloroplasts in leaves.     

Action spectra for the photoperiodic control of polymorphism in the aphid Megoura viciae

Energy compensated action spectra are given for the photoperiodic control of polymorphism in Megoura. The production of ‘long day’ parthenogenetic virginoparae and ‘short day’ oviparae mainly depend on the night length. Light has three different effects. ‘Early’ interruptions of the dark phase in a long night cycle reverse the time-measuring dark response. The action spectrum for a 1 hr interruption placed 1.5 hr after the onset of darkness (during dark stage 1) shows a relatively narrow band of activity, mainly in the blue (450–470 nm). The threshold is ca. 0.25 μW cm^?2. ‘Late’ interruptions placed 7.5 or 8 hr after dark hour 0 (during dark stage 3) strongly promote the production of virginoparae without causing a reversal of the response. The action spectrum has the same blue maximum but sensitivity extends into the yellow and red spectral regions. The third photosensitive component, the main photoperiod itself, is required for initiating the dark timing response and has an intermediate action spectrum. Time/intensity curves for a single wavelength (471 nm) show that the responses during stages 1 and 3 depart markedly from reciprocity. Short durations cannot be compensated by high intensities. The shape of the reciprocity curve for an ‘early’ interruption suggests that the stage 1 response is complete after ca. 1.25 hr.The action spectra are believed to be compatible with the view that the photoreceptor is a caroteno-protein. It is suggested that all three pigment forms are related and that time measurement is largely a function of spontaneous ‘dark reaction’ changes in the pigment system. Stage 1 may represent the reversible conjugation phase of the protein/chromophore moieties. In Stage 2 the pigment is presumably photorefractory and is transitional to the highly sensitive broad spectrum form of stage 3.     

Action Spectrum in the Ultraviolet Region for Phototropism of Bryopsis Rhizoids

The phototropic response of the rhizoid of the marine coenocyticgreen alga Bryopsis plumosa to ultraviolet light (250–350nm) was investigated. The rhizoid exhibited negative bendingthat was due to bulging upon absorption of light in the UV region,as well as in the visible region, of the spectrum. The negativebending might not be a result of the inhibition of growth onthe irradiated side of the apical hemisphere by UV irradiationbecause growth inhibition was observed after bending had reacheda maximum within one to two hours. The action spectrum obtainedfrom fluence rate-response curves had a pronounced peak at 260nm and a small peak at 310 nm. The quantum effectiveness at260 nm was about five times that in the visible region. Phenylaceticacid (PAA), a potent inhibitor of flavin photoreactions, inhibitedthe phototropic response to both UV light and blue light withoutany obvious effect on tip growth. The inhibition of the phototropicresponse to blue light by PAA was partially overcome by rinsingthe alga with riboflavin-containing medium, which result suggeststhe involvement of flavins in the phototropism of Bryopsis rhizoids. (Received February 6, 1995; Accepted June 19, 1995)     

Dose response behaviour for polarotropism of the germ tube of the liverwort Sphaerocarpos Donnellii aust.

Summary The dose response behaviour for polarotropism of the unicellular germ tube of Sphaerocarpos was studied in blue and near UV. At constant intensities the response is proportional to the logarithm of the exposure duration, and at constant exposure durations the response is proportional to the logarithm of intensity. Neither a polarotropic response to wavelengths > 550 nm, nor a significant influence on response to blue of a pre-, post-, or simultaneous-irradiation with red or far-red could be observed. Also a dark period was without any effect on the polarotropic response to blue. Growth responses under linearly polarized light are described.     

Veränderung der Lichtabsorption eines Carotinoids im Enzym (De-epoxidase)-Substrat(Violaxanthin)-Komplex

Summary The enzyme violaxanthin de-epoxidase catalysing the transformation of the xanthophyll violaxanthin to zeaxanthin has been isolated from spinach chloroplasts.Special properties of the enzyme make it possible for the carotenoid to be bound without initiation of any catalytic reaction; the isolation of an enzyme-substratecomplex is thereby greatly facilitated. After addition of cofactors to this complex the transformation of violaxanthin to zeaxanthin takes place.In this complex the light-absorption of violaxanthin is changed drastically: the normal three-peak absorption curve in the blue region of the spectrum is strongly decreased but in the uv-region around 380 nm a new absorption maximum appears.Recently a similar spectrum has been determined in vivo in the phototropic sensitive region of the sporangiophores of Phycomyces (Wolken, 1969) with the aid of microspectrophotometry.From these results it is concluded that part of the carotenoids occurring in plants is present in a protein-bound form and that these pigments show a considerably changed light absorption in comparison with the isolated pigment. The simultaneous occurrence of differently bound carotenoids may lead to the formation of 4-peak absorption curves (similar to those of flavines) with 3 maxima in the blue region and 1 maximum in the UV around 370–380 nm. These 4-peak curves are characteristic for many action spectra.It is emphasized that the strong absorption changes of carotenoids occurring during the binding of these pigments to proteins should be considered in analyzing difference spectra.     

Blue–green opponency and trichromatic vision in the greenhouse whitefly (Trialeurodes vaporariorum) explored using light emitting diodes

Visual orientation in the greenhouse whitefly (Trialeurodes vaporariorum Westwood, Hemiptera: Aleyrodidae) is the result of “wavelength‐specific behaviours.” Green–yellow elicits “settling behaviour” while ultraviolet (UV) radiation initiates “migratory behaviour.” The only available physiological study of the photoreceptors' spectral efficiency showed peaks in the green and the UV range and whitefly vision was said to be dichromatic so far. In order to study the visual behaviour of T. vaporariorum, 19 narrow‐bandwidth light emitting diodes (LEDs) covering the UV‐A and visible range were used in combination with light scattering acrylic glass screens in a small‐scale choice arena under greenhouse conditions. Multiple‐choice and dual‐choice assays were performed, resulting in LED‐based behavioural action spectra of settling (green) and migratory behaviour (UV). A potential inhibitory blue–green chromatic mechanism was studied by combining yellow with different bluish LEDs. Intensity dependencies were illustrated by changing LED intensities. Regarding the “settling response,” highest attraction was achieved by a green LED with a centroid wavelength of 550 nm, while a blue LED with 469 nm proved to be most inhibitory. Besides this inhibitory interaction, an intensity dependence was observed within the action spectrum in the green–yellow range. “Migratory behaviour” was elicited the most by the UV LED with the shortest available wavelength of 373 nm. The results provide compelling behavioural evidence for the presence of a green and a yet undescribed blue sensitive photoreceptor and a blue–green opponent mechanism. Furthermore, empirical colour choice models were built and receptor peaks were estimated around 510–520 nm (green), 480–490 nm (blue) and 340–370 nm (UV). Consequently, a trichromatic receptor setup is suggested for T. vaporariorum.     

Photobiological properties of the inhibition of etiolated Arabidopsis seedling growth by ultraviolet-B irradiation

Alteration of 'normal' levels of ultraviolet-B light (UV-B, 280–320 nm) can affect plant chemical composition as well as growth; however, little is known about how plants perceive UV-B light. We have carried out fluence response curves, and demonstrated that the growth inhibition of etiolated Arabidopsis thaliana seedlings by low fluence UV light is specific to UV-B and not UV-A (320–390 nm). The response shows reciprocity between duration and intensity, at least over a limited range, and thus depends only on photon fluence and not on photon flux. The action spectrum for this response indicates a peak of maximum effectiveness at 290 nm, and response spectra at different fluences indicate that the most effective wavelength at 30 000  µ mol m^–2 is 290 nm, whereas 300 nm light was the most effective at 100 000  µ mol m^–2. This response occurs in mutant seedlings deficient in cryptochrome, phytochrome or phototropin, suggesting that none of the known photoreceptors is the major UV-B photoreceptor. Some null mutants in DNA repair enzymes show hypersensitivity to UV-B, suggesting that even at low fluence rates, direct damage to DNA may be one component of the response to UV-B.     

Events Surrounding the Early Development of Euglena Chloroplasts: VI. Action Spectra for the Formation of Chlorophyll, Lag Elimination in Chlorophyll Synthesis, and Appearance of TPN-dependent Triose Phosphate Dehydrogenase and Alkaline DNase Activities

Action spectra derived from dose-response curves measured for various processes associated with chloroplast development in Euglena gracilis var. bacillaris are presented. The action spectrum for chlorophyll synthesis during the first 36 hours of continuous illumination of dark-grown resting cells resembles the absorption spectrum of protochlorophyll(ide). The action spectrum for the preillumination phase of potentiation, during which preillumination followed by a dark period brings about lag elimination in chlorophyll synthesis when the cells are subsequently exposed to postilluminating light, shows a high peak in the blue region (at about 433 nm) with a small peak in the yellow-orange region (at about 597 nm); the postillumination phase yields an action spectrum very similar to that obtained for chlorophyll synthesis in continuous light in normal, unpotentiated cells, with peaks at 433 and 631 nm. Alkaline DNase and TPN-linked triose phosphate dehydrogenase, two plastid enzymes which are synthesized outside the chloroplast, yield action spectra which are consistent with protochlorophyll(ide) being the major light receptor. The action spectra which implicate pigments resembling protochlorophyll(ide) holochrome have blue to red peak ratios in the vicinity of 5:1 as does the absorption spectrum of the protochlorophyllide holochrome from beans; the action spectrum is not identical with the holochrome spectrum indicating that the Euglena holochrome may differ from the bean pigment in details of its absorption spectrum. The action spectrum for preillumination, shows a ratio of the blue peak to the red effectiveness of about 24:1. This suggests that preillumination is controlled by a photoreceptor different from the protochlorophyll(ide) holochrome.     

Analysis of substances issuing from Zajdela ascitic hepatoma cells after exposure to UV radiation of different wave-lengths. I. Relationship to dose]

The release of substances from the Zaidela ascitic hepatoma cells after irradiation with physiological doses of short-wave (254 nm) and long-wave (300-380 nm) UV light (far and near UV light) has been studied spectrophotometrically. Within the range of 200-520 nm, the absorption spectra of releasing substances show maxima at 215 and 260 nm and are identical to spectra of non-irradiated cells. The amount of substances increases with dose making up, at the maximal alteration, 180-220%, of the amount releasing from non-irradiated cells. Irradiation with far UV light exceeds by one order that with near UV light. The effect of minimum doses is opposite to the action of high doses: the release of substances from irradiated cells is much less.     

Photoperiodism and the photic environment of the pitcher-plant mosquito,Wyeomyia smithii

Summary Wyeomyia smithii Coq. (Diptera: Culicidae) overwinters as a larva in a state of diapause which is initiated, maintained, and terminated by photoperiod. Both in the dawn and in the dusk, diapausing larvae are photoperiodically most sensitive to blue light (390–450 nm) with a shoulder in response in the bluegreen and green (480–540 nm) region of the spectrum. The saturation curves for response to blue light in the dusk has a steeper slope than for response to blue-green and green light in the dusk, suggesting two distinct pigments or pigment complexes underly photoperiodic response in W. smithii.The photic environment of W. smithii during twilight is rich in yellow-green light but sufficient light is available at 390–540 nm to trigger photoperiodic response early during morning civil twilight and to sustain response until late in evening civil twilight. Comparison of action spectra with spectra of available light indicates that the zenith angles of the sun which would result in 50% response are 95°48 and 94°52 in the dawn and dusk, respectively. Using these zenith angles to approximate daylength in nature provides a resonable prediction of development in the field.The flux density of photons necessary to elicit 50% development a 454 nm is about 9×10⁷ photons/cm² s in the dawn and 3×10⁸ photons/cm² s in the dusk. This high degree of sensitivity enables W. smithii to cue to the rapidly changing light intensity which occurs around the nautical-civil twilight transition. At the same time, the chromophore is not likely to be stimulated by the light of the full moon.     

Probing lethal damage expression in cytochalasin B-induced polykaryons by radiation quality

The polykaryon-forming unit (PFU) cell survival assay is based on the postirradiation flow cytometric analysis of the DNA content accumulated in high-ploidy cells (polykaryons) induced by the cytokinesis inhibitor cytochalasin B and can provide a meaningful measure of cell radiosensitivity. In this assay, cell survival is defined as the ability to form a polykaryon of a given ploidy after irradiation. The slope of the polykaryon dose response has been shown to be highly correlated with the initial slope of the clonogenic survival curves after gamma irradiation, which implies a common subset of lethal lesions. We reported previously on an apoptotic mode of cell death in the polykaryon system and on the heritability of small variations in polykaryon radioresponse. We now show that exposure of PFUs to a given dose of alpha particles results in a greater reduction in the proportion of cells able to reach at least 16C when compared to the same dose of low-LET radiation. This reduction is less than that observed in the low-dose (alpha term) region of the clonogenic curve. On the basis of published LET-dependent spectra of radiation-induced DNA damage, we suggest that this behavior reflects a differential expression of lethal damage that can be probed by varying the LET of the radiation and that base damages contributing additional complexity to clustered DNA lesions may be more deleterious in PFUs than in clonogens.     

Light-stimulated respiration in the green algaDunaliella tertiolecta: Involvement of the ultraviolet/blue-light photoreceptor(s) and phytochrome?

Starch breakdown and respiratory O₂ uptake in the green algaDunaliella tertiolecta (Butcher) are stimulated not only by blue, but also by red light. In the present study, attempts are described to identify the photoreceptor(s) involved. Fluence rate-response curves with different slopes in the ultraviolet (UV)/blue and in the red spectral region as well as differences in the kinetics and in the unfluence of dark pre-incubation on the stimulation of respiratory O₂ uptake by blue and red light strongly indicate the action of two photoreceptors. Since the effect of red light shows some far-red reversibility, and since simultaneous irradiation with red and far-red light decreases the effectiveness of red light, the involvement of phytochrome — in addition to the UV/blue photoreceptor(s) — is suggested in the light-stimulated respiration inDunaliella.Abbreviation UV ultraviolet     

Light-induced absorbance changes in the fungus Verticillium agaricinum

Light-induced absorbance changes were investigated in vivo in the fungus Verticillium agaricinum (Link) Corda. There was a broad light-induced absorbance decrease in the blue and near UV with a maximum at 384 nm. An action spectrum indicated that the absorbance changes were due to photo-bleaching of a pigment with an absorption spectrum that was similar to the action spectrum. Neither redox reactions nor energy metabolism were involved in the photo-bleaching process. A direct comparison of action spectra for light-induced absorbance changes and photo-induction of carotenogenesis suggests that the photo-bleaching may not be related to photo-induction of carotenogenesis.     

A computer simulation of aggregated phytochrome photoconversion

In order to check the relevance of possible phytochrome aggregation forms for the diversity of action spectra and dose-response curves for light sensing by plants, a model for phytochrome photoconversion was produced for different aggregates. Under saturating light treatments, a computer simulation of dimer and aggregated dimer (tetramers and hexamers) photoconversion provided similar compositions of various aggregates in red and green light, which differed from blue and far-red light. These aggregates could account for the variable action spectra only if the nature of the primary transducing components is taken into account. The initial kinetics of aggregated phytochrome appear to be slower in comparison to the monomeric form, and there were transient peaks of certain aggregates in red and green light. A single peak occurred under blue light, but not in far-red, only if dimers are aggregated into tetramers and hexamers. This finding suggests that the initial kinetics of aggregated phytochrome are not sufficient to account for the variable dose-response curves in light-mediated responses by plants, so again the feature of signal transduction components may play a decisive role.