Temperature sensitivity of deep orange: Effects on eye pigmentation

Deep orange (dor) affects the amount of both xanthommatin and drosopterins in the eye of D. melanogaster. Our data indicate that for both of these pigments, the amount present in the eye is a temperature-sensitive phenomenon. In addition, while the distribution of the five drosopterins in dor flies is different from that found in wild-type flies, their relative distribution is not affected by temperature. We also present data which suggest that the product of dor is used throughout development.     

Analyses of absorption and fluorescence spectra of water-soluble chlorophyll proteins,pigment System II particles and chlorophyll a in diethylether solution by the curve-fitting method

Absorption and fluorescence spectra in the red region of water-soluble chlorophyll proteins, Lepidium CP661, CP663 and Brassica CP673, pigment System II particles of spinach chloroplasts and chlorophyll a in diethylether solution at 25°C were analyzed by the curve-fitting method (French, C.S., Brown, J.S. and Lawrence, M.C. (1972) Plant Physiol. 49, 421–429). It was found that each of the chlorophyll forms of the chlorophyll proteins and the pigment System II particles had a corresponding fluorescence band with the Stokes shift ranging from 0.6 to 4.0 nm.The absorption spectrum of chlorophyll a in diethylether solution was analyzed to one major band with a peak at 660.5 nm and some minor bands, while the fluorescence spectrum was analyzed to one major band with a peak at 664.9 nm and some minor bands. A mirror image was clearly demonstrated between the resolved spectra of absorption and fluorescence. The absorption spectrum of Lepidium CP661 was composed of a chlorophyll b form with a peak at 652.8 nm and two chlorophyll a forms with peaks at 662.6 and 671.9 nm. The fluorescence spectrum was analyzed to five component bands. Three of them with peaks at 654.8, 664.6 and 674.6 nm were attributed to emissions of the three chlorophyll forms with the Stokes shift of 2.0–2.7 nm. The absorption spectrum of Brassica CP673 had a chlorophyll b form with a peak at 653.7 nm and four chlorophyll a forms with peaks at 662.7, 671.3, 676.9 and 684.2 nm. The fluorescence spectrum was resolved into seven component bands. Four of them with peaks at 666.7, 673.1, 677.5 and 686.2 nm corresponded to the four chlorophyll a forms with the Stokes shift of 0.6–4.0 nm. The absorption spectrum of the pigment System II particles had a chlorophyll b form with a peak at 652.4 nm and three chlorophyll a forms with peaks at 662.9, 672.1 and 681.6 nm. The fluorescence spectrum was analyzed to four major component bands with peaks at 674.1, 682.8, 692.0 and 706.7 nm and some minor bands. The former two bands corresponded to the chlorophyll a forms with peaks at 672.1 and 681.6 nm with the Stokes shift of 2.0 and 1.2 nm, respectively.Absorption spectra at 25°C and at ?196°C of the water-soluble chlorophyll proteins were compared by the curve-fitting method. The component bands at ?196°C were blue-shifted by 0.8–4.1 nm and narrower in half widths as compared to those at 25°C.     

Shortwave light filtration effect on spectral sensitivity of two shrimp populations of <Emphasis Type="Italic">M. relicta</Emphasis> (Mysida)

Microspectrophotometric measurements of screening granules in Mysis relicta eyes showed that most of the granules have xanthommatin spectra (7n_max 455 nm) with selective absorption of blue light. We calculated spectral sensitivity of M.relicta eyes using screening granules absorption spectra and visual pigment absorption spectra. According to our computations the calculated spectral sensitivity curve appears to be in a good correspondence with the real spectral sensitivity.     

Phototoxic Action Spectrum on a Retinal Pigment Epithelium Model of Age-Related Macular Degeneration Exposed to Sunlight Normalized Conditions

Among the identified risk factors of age-related macular degeneration, sunlight is known to induce cumulative damage to the retina. A photosensitive derivative of the visual pigment, N-retinylidene-N-retinylethanolamine (A2E), may be involved in this phototoxicity. The high energy visible light between 380 nm and 500 nm (blue light) is incriminated. Our aim was to define the most toxic wavelengths in the blue-green range on an in vitro model of the disease. Primary cultures of porcine retinal pigment epithelium cells were incubated for 6 hours with different A2E concentrations and exposed for 18 hours to 10 nm illumination bands centered from 380 to 520 nm in 10 nm increments. Light irradiances were normalized with respect to the natural sunlight reaching the retina. Six hours after light exposure, cell viability, necrosis and apoptosis were assessed using the Apotox-Glo Triplex™ assay. Retinal pigment epithelium cells incubated with A2E displayed fluorescent bodies within the cytoplasm. Their absorption and emission spectra were similar to those of A2E. Exposure to 10 nm illumination bands induced a loss in cell viability with a dose dependence upon A2E concentrations. Irrespective of A2E concentration, the loss of cell viability was maximal for wavelengths from 415 to 455 nm. Cell viability decrease was correlated to an increase in cell apoptosis indicated by caspase-3/7 activities in the same spectral range. No light-elicited necrosis was measured as compared to control cells maintained in darkness. Our results defined the precise spectrum of light retinal toxicity in physiological irradiance conditions on an in vitro model of age-related macular degeneration. Surprisingly, a narrow bandwidth in blue light generated the greatest phototoxic risk to retinal pigment epithelium cells. This phototoxic spectrum may be advantageously valued in designing selective photoprotection ophthalmic filters, without disrupting essential visual and non-visual functions of the eye.     

Isolation of phytochrome from the alga mesotaenium and liverwort sphaerocarpos

Phytochrome has been isolated from the green alga Mesotaenium and the liverwort Sphaerocarpos. The Mesotaenium pigment had absorption peaks at 649 and 710 nm for the P_R and P_FR forms, respectively. Corresponding difference spectrum maxima for the Sphaerocarpos pigment were at 655 and 720 nm. While the absorption maxima differ, the reversibility and efficiency with which red and far-red light transform the Mesotaenium pigment are very similar to that reported for phytochrome isolated from etiolated seedlings of higher plants. Methods are described which allow efficient separation of phytochrome from highly pigmented light-grown material.     

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.     

Do retinula cells trigger the screening pigment migration in the eye of the mothEphestia kuehniella?

Summary Simultaneous recordings of reflectance and the electroretinogram (ERG) of the meal moth superposition eye show a good match between the action spectrum of screening pigment migration and the spectral sensitivity curve (Fig. 5). These spectra correspond with the absorption spectrum of a xanthopsin X530 that has been evidenced in the eye. No correlation was found with the extinction spectrum of the pigment granules themselves (Fig. 7). The results suggest, that the photomechanical reaction is controlled by the visual pigment.     

Spectral sensitivity and flicker fusion frequencies of the compound eye of salmon and wild-type tsetse flies, Glossina morsitans

ABSTRACT. The spectral sensitivity and flicker fusion frequency (FFF) of wild-type and salmon Glossina morsitans morsitans Westwood (Diptera, Glossinidae) were compared electroretinographically (ERG). Spectral sensitivity curves were similar in shape for dark-adapted wild-type and salmon flies, but salmon flies were over 100 times as sensitive as wild-type flies over much of their sensitivity range. Estimation of the spectral absorption curve (from the differences in ERG sensitivities) for the pigment absent from (or present in low concentration in) the salmon eye suggests that the pigment is an ommochrome. FFF at threshold light intensities was similar in wild-type and salmon flies, but at higher light intensity (1.3 °W/cm²) the FFF of salmon flies increased c. 200–300%, due to the capacity of the salmon eye to adapt rapidly to the flicker stimulus. Body weight had little effect upon spectral sensitivity and FFF. Wild-type males were more sensitive to yellow-green light and had higher FFF than did wild-type females. Salmon males and females did not differ in spectral sensitivity, but females had higher FFF (when tested with 520-nm light) than did males. Old wild-type females did not differ from young females in either spectral sensitivity or FFF. However, old salmon females were more sensitive but had lower FFF than young salmon females. Food deprivation reduced spectral sensitivity and FFF in wild-type males but not in salmon males. Irradiation (10.5 krad) reduced spectral sensitivity ( c. 75–375%) and FFF ( c. 30%) in wild-type males. The greatly increased spectral sensitivity and FFF in salmon flies indicate that these flies may behave differently from wild-type flies in the field. Differences in the way spectral sensitivity and flicker discrimination are affected by dark and light adaptation, and by such factors as age and sex, indicate that these measurements are of two independent phenomena.     

Some spectral properties of pea phytochrome in vivo and in vitro

The transformation difference spectrum for phytochrome (Pr spectrum minus Pfr spectrum) in pea tissue is determined below 560 nanometers and compared with similar data on phytochrome in vitro The difference spectrum in vivo between phytochrome intermediates and Pfr is also shown for comparison with the data on phytochrome solutions. These comparisons show that the peaks in the spectra occurring in the blue wave lengths are shifted to shorter wave lengths and are much enhanced when phytochrome is extracted from the cell and placed in solution. The results indicate that the physicochemical state of phytochrome in the cell may be different from that of the extracted pigment.     

Spectral absorption by screening pigment granules in the compound eye of butterflies (Heliconius)

Summary The spectral absorption by single granules, clusters and masses of granules of the screening pigment in the compound eye of the butterfly genusHeliconius was studied by microspectrophotometry. Most of the pigment granules were found to have an almost constant absorption in the wavelength region 300 to 700 nm. Other granules showed a maximal absorption either at about 450 or 560 nm. The maximum at 450 nm is suggested to be caused by xanthommatin and that at 560 nm by ommines. The pigment screen inHeliconius is concluded to be a neutral grey filter.This work was supported by the Swedish Medical Research Council, grant No. B71-14X-104 06B and 070, Sällskapet för Medicinsk Porskning and Reservationsanslaget, and the Deutsche Forschungsgemeinschaft.     

Extraction and Identification of the Pigment in the Adductor Muscle Scar of Pacific Oyster Crassostrea gigas

In this study, UV (ultraviolet) and IR (infrared radiation) spectral analysis were integrated to identify the pigment in the adductor muscle scar of the Pacific oyster Crassostrea gigas. The pigment was extracted from the adductor muscle scars of cleaned oyster shells that were pulverized, hydrolyzed in hot hydrochloric acid, purified with diethyl ether, and dissolved in 0.01 mL/L NaOH. The maximum absorption of the pigment in the UV absorption spectrum within the range of 190–500 nm was observed between 210–220 nm. The UV absorbance decreased with increasing wavelength which was consistent with the UV spectral absorption characteristics of melanin. In addition, Fourier transform infrared spectroscopy scanning revealed characteristic absorption peaks that emerged near 3440 cm^-1 and 1630 cm^-1, which was consistent with infrared scanning features of eumelanin (a type of melanin). This study has demonstrated for the first time that the pigment in the adductor muscle scar of the Pacific oyster is melanin, hinting that the adductor muscle could be another organ pigmenting the mollusc shell with melanin other than mantle.     

Microspectrophotometry of the dioptric apparatus and compound rhabdom of the moth (Manduca sexta) eye

Absorption spectra were obtained by microspectrophotometric (MSP) axial measurements of the compound rhabdom of the night moth Manduca sexta. Difference spectra derived from partial or complete bleaches revealed the evidence of four visual pigments with approximate λ_max at 350, 450, 490, and 530 nm. Upon bleaching with light of the pigment maximum at 21°C, pH 7·4–8·5, each pigment, save the u.v.-sensitive one, formed a photoproduct whose spectral maximum (ca. 370 nm) was indicative of a mixture of free and bound retinal. Rarely, small amounts of an additional photoproduct (λ_max 325–330 nm) formed, which is suggestive of retinol. The u.v.-sensitive pigment, when irradiated with u.v., formed an unknown photoproduct (λ_max 290–300 nm). Bleaching kinetics were of first order. Separate absorption determinations through lens or crystalline cones showed each component of the dioptric apparatus served as a filter effecting a sharp decrease in corneal transmission at 310 nm while being increasingly transparent from near u.v. to red. The survival benefits accruing to a largely nocturnal moth with a presumptive colour vision mechanism are discussed.     

β-Hydroxy-α-ketobutyric acid in Drosophila melanogaster,with reference to biosynthesis of drosopterins

A substance designated as compound D, which reacts spontaneously with 7,8-dihydropterin to give drosopterins, is found in Drosophila melanogaster. The compound was partially purified from the extract of flies by column chromatography and identified as β-hydroxy-α-ketobutyric acid by analysis of its 2,4-dinitrophenylhydrazone, mass spectrometry and reactivity with 7,8-dihydropterin. A highly significant correlation (r = 0.969, p < 0.001) was found between the amounts of the compound and drosopterins in the eye-pigment mutants of Drosophila. Changes of the compound during development of flies were also closely related to those of drosopterins. Based on these observations, a role of the compound in biosynthesis of drosopterins has been discussed.     

A comparison of electrophysiologically determined spectral responses in 35 species of Lepidoptera

Spectral responses from the compound eyes of 35 lepidopteran species representing 14 families were investigated electrophysiologically using ERG recordings. The light-stimuli used overed the range of 383–700 nm wavelengths. All species show three or four maxima in their spectral sensitivity curves. Two of these peaks were usually associated with ultraviolet and blue light (383 and 460 nm, respectively). The other maxima occurred in the 500–620 nm region. In Nymphalidae the highest peak was found in response to 560–580 nm stimuli. Of all wavelengths tested, these are the longest wavelengths to produce principal peak sensitivities.Pieridae and Lycaenidae have maxima in the UV region which represent significantly higher sensitivities than the secondary peaks to stimuli of longer wavelengths.Satyridae, Danaidae, Hesperiidae and diurnal moths except Epicopeia (Epicopeidae) generally have similar sensitivity curves with principal peaks between 500 and 520 nm.In Papilionid species except Graphium (max = 560 nm) high maxima occur in the UV and blue (460 nm) region.Noctural Sphingid moths possess the highest peak sensitivity at 540 nm. All other noctural moths tested have three or four maxima.     

Light maintains High Levels of Phytochrome Intermediates

THE plant photomorphogenetic pigment phytochrome exists in two forms, Pr and Pfr, interconvertible by light, which have peaks of absorption in the red and far-red regions of the spectrum respectively¹. Intermediates between Pr and Pfr have been demonstrated during photoconversion by Linschitz and his coworkers^2,3 using flash photolysis techniques. Low temperatures studies have also proved useful in identifying intermediates^4–8. Briggs and Fork^9,10 detected intermediates in vitro and in vivo in conditions of pigment cycling by mixed red and far-red light, but were restricted to studying the minor peaks of phytochrome absorption in the blue region of the spectrum because of the available instrumentation. In this type of measurement the problem is that actinic light has to be prevented from falling onto the photomultiplier. Briggs and Fork inserted a red cutoff filter, but this precluded measurement at the peaks of absorption of Pr and Pfr in the red and far-red regions of the spectrum. The design and construction of a sensitive quasi-continuous measuring spectrophotometer have now overcome this problem and made possible an investigation in vivo of phytochrome intermediates at any wavelength under conditions of pigment cycling, for example, in high intensity white incandescent light. The instrument can detect intermediates with a half life in excess of 0.2 ms. The longer lived intermediates between Pr and Pfr observed in the in vitro flash studies^2,3 should be readily detectable if they accumulate in conditions of cycling.     

Cone pigments in a North American marsupial, the opossum (Didelphis virginiana)

Only two of the four cone opsin gene families found in vertebrates are represented in contemporary eutherian and marsupial species. Recent genetic studies of two species of South American marsupial detected the presence of representatives from two of the classes of cone opsin genes and the structures of these genes predicted cone pigments with respective peaks in the ultraviolet and long-wavelength portions of the spectrum. The Virginia opossum (Didelphis virginiana), a profoundly nocturnal animal, is the only marsupial species found in North America. The prospects for cone-based vision in this species were examined through recordings of the electroretinogram (ERG), a commonly examined retinal response to photic stimulation. Recorded under flickering-light conditions that elicit signals from cone photoreceptors, the spectral sensitivity of the opossum eye is well accounted for by contributions from the presence of a single cone pigment having peak absorption at 561–562 nm. A series of additional experiments that employed various chromatic adaptation paradigms were conducted in a search for possible contributions from a second (short-wavelength sensitive) cone pigment. We found no evidence that such a mechanism contributes to the ERG in this marsupial.     

The Spectral Sensitivities of Single Receptor Cells in the Lateral, Median, and Ventral Eyes of Normal and White-Eyed Limulus

Spectral sensitivity curves can be distorted by screening pigments. We have determined whether this is true for Limulus polyphemus by determining, from receptor potentials recorded using intracellular microelectrodes, spectral sensitivity curves for normal animals and for white-eyed animals (which lack screening pigment). Our results show: (a) In median ocelli, the curve for UV-sensitive receptor cells peaks at 360 nm and does not depend on the presence of screening pigment, (b) The curve for ventral eye photoreceptors is identical to that for retinular cells from the lateral eyes of white-eyed animals and peaks at 520–525 nm. (c) In normal lateral eyes, when the stimulating light passes through screening pigment, the curve indicates relatively more sensitivity in the red region of the spectrum than does the curve for white-eyed animals. Therefore, the screening pigment is probably red-transmitting, (d) In median ocelli, the curve for visible-sensitive cells peaks at 525 nm and is approximately the same whether the ocelli are from normal or white-eyed animals. However, the curve is significantly broader than that for ventral eyes and for lateral eyes from white-eyed animals.     

The pigment system of the photoreceptor 7 yellow in the fly,a complex photoreceptor

Summary The 7y photoreceptor in the fly (Musca, Calliphora) retina harbours an unusually complex pigment system consisting of a bistable visual pigment (xanthopsin, X and metaxanthopsin, M), a blue-absorbing C₄₀-carotenoid (zeaxanthin and/or lutein) and a uv sensitizing pigment (3-OH retinol).The difference spectrum and photoequilibrium spectrum in single 7y rhabdomeres were determined microspectrophotometrically (Fig. 2).The extinction spectrum of the C₄₀-carotenoid has a pronounced vibrational structure, with peaks at 430, 450 and 480 nm (Fig. 3). The off-axis spectral sensitivity, determined electrophysiologically with 1 nm resolution shows no trace of this fine structure thus excluding the possibility that the C₄₀-carotenoid is a second sensitizing pigment (Fig. 4).The absorption spectra of X and M are derived by fitting nomogram spectra (based on fly R1–6 xanthopsin) to the difference spectrum. max for X is 425 nm, and for M 510 nm (Fig. 5). It is shown that the photoequilibrium spectrum and the difference spectrum can be used to derive the relative photosensitivity spectra of X and M using the analytical method developed by Stavenga (1975). The result (Fig. 6) shows a pronounced uv sensitivity for both, X and M, indicating that the uv sensitizing pigment transfers energy to both X and M. A value of 0.7 for, the relative efficiency of photoconversion for X and M, is obtained by fitting the analytically derived relative photosensitivity spectra to the absorption spectra at wavelengths beyond 420 nm.     

Xanthommatin biosynthesis in wild-type and mutant strains of the Australian sheep blowfly Lucilia cuprina

The synthesis of eye pigments has been studied in the seven eye color mutants of the Australian sheep blowfly, Lucilia cuprina. Six appear to be affected primarily in the synthesis of xanthommatin. In wild type, the onset of xanthommatin biosynthesis occurs midway through metamorphosis. Developmental patterns of accumulation of the xanthommatin precursors tryptophan, kynurenine, and 3-hydroxykynurenine have also been established for wild type. By determining the levels of these precursors in late pupae of the mutants, it has been shown that the mutant yellowish accumulates excess tryptophan and the mutant yellow accumulates excess kynurenine. The implications of these results—that yellowish lacks tryptophan oxygenase, thus failing to convert tryptophan to kynurenine, and that yellow lacks kynurenine hydroxylase (blocked in the conversion of kynurenine to 3-hydroxykynurenine)—have been confirmed. This has involved in vitro assays of tryphophan oxygenase and precursor feeding experiments. The precursor accumulation patterns are less clear for the other mutants.