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Plants use light as a resource and signal. Photons within the 400–700 nm waveband are considered photosynthetically active. Far-red photons (FR, 700–800 nm) are used by plants to detect nearby vegetation and elicit the shade avoidance syndrome. In addition, FR photons have also been shown to contribute to photosynthesis, but knowledge about these dual effects remains scarce. Here, we study shoot-architectural and photosynthetic responses to supplemental FR light during the photoperiod in several rice varieties. We observed that FR enrichment only mildly affected the rice transcriptome and shoot architecture as compared to established model species, whereas leaf formation, tillering and biomass accumulation were clearly promoted. Consistent with this growth promotion, we found that CO2-fixation in supplemental FR was strongly enhanced, especially in plants acclimated to FR-enriched conditions as compared to control conditions. This growth promotion dominates the effects of FR photons on shoot development and architecture. When substituting FR enrichment with an end-of-day FR pulse, this prevented photosynthesis-promoting effects and elicited shade avoidance responses. We conclude that FR photons can have a dual role, where effects depend on the environmental context: in addition to being an environmental signal, they are also a potent source of harvestable energy.

Plants use light as a resource and signal. Photons within the 400–700 nm waveband are considered photosynthetically active. Far-red photons (FR, 700–800 nm) are used by plants to detect nearby vegetation and elicit the shade avoidance syndrome. In addition, FR photons have also been shown to contribute to photosynthesis, but knowledge about these dual effects remains scarce. Here, we study shoot-architectural and photosynthetic responses to supplemental FR light during the photoperiod in several rice varieties. We observed that FR enrichment only mildly affected the rice transcriptome and shoot architecture as compared to established model species, whereas leaf formation, tillering and biomass accumulation were clearly promoted. Consistent with this growth promotion, we found that CO2-fixation in supplemental FR was strongly enhanced, especially in plants acclimated to FR-enriched conditions as compared to control conditions. This growth promotion dominates the effects of FR photons on shoot development and architecture. When substituting FR enrichment with an end-of-day FR pulse, this prevented photosynthesis-promoting effects and elicited shade avoidance responses. We conclude that FR photons can have a dual role, where effects depend on the environmental context: in addition to being an environmental signal, they are also a potent source of harvestable energy.

Vision is initiated by the rhodopsin family of light-sensitive G protein-coupled receptors (GPCRs). A photon is absorbed by the 11-cis retinal chromophore of rhodopsin, which isomerizes within 200 femtoseconds to the all-trans conformation, thereby initiating the cellular signal transduction processes that ultimately lead to vision. However, the intramolecular mechanism by which the photoactivated retinal induces the activation events inside rhodopsin remains experimentally unclear. Here we use ultrafast time-resolved crystallography at room temperature to determine how an isomerized twisted all-trans retinal stores the photon energy that is required to initiate the protein conformational changes associated with the formation of the G protein-binding signalling state. The distorted retinal at a 1-ps time delay after photoactivation has pulled away from half of its numerous interactions with its binding pocket, and the excess of the photon energy is released through an anisotropic protein breathing motion in the direction of the extracellular space. Notably, the very early structural motions in the protein side chains of rhodopsin appear in regions that are involved in later stages of the conserved class A GPCR activation mechanism. Our study sheds light on the earliest stages of vision in vertebrates and points to fundamental aspects of the molecular mechanisms of agonist-mediated GPCR activation.

How does a rice plant in the field fight against the weeds growing next to it? Rice feeds more than half of the world’s human population. Driven by climate change, rice farming is shifting to direct seeding, where weeds, traditionally suppressed by standing water, are becoming a major problem. In urgent need for sustainable weed-control, here we investigated how rice shoot architecture could be optimized for weed suppression. We explored the natural diversity of rice varieties and defined which traits are important for increased shade of rice shoots. In a genomic analysis, we found the genes encoding these relevant traits. In a field study, the selected rice varieties suppressed weed growth to an extent from 40 up to 70%. Insights from the field assay, and the genetic information can now be used for future rice-breeding and will help to reduce the amount of herbicide usage and enable a more sustainable and climate-change resilient rice-farming. Rice is also an interesting study object. Surprising results were found when treating rice with far-red light. Far-red light, is known to be a signal for plants for dense vegetation, to which they react with strong elongation and reduced formation of leaves. However, we observed, that rice plants were growing much faster and bushier under far-red light. Gas-exchange measurements proved that photosynthetic activity was almost doubled. This is a very new discovery in the field of photobiology, where to date, it was thought, that plants cannot use far-red light efficiently for photosynthesis. These findings open up a new field of research, in how plants balance between far-red light as a signal for dense vegetation and as energy for photosynthesis.

Light is vital for plants as it powers the photosynthesis that provides them with the energy to grow. In dense vegetation, light absorption by neighbours limits the available light to individual plants. Therefore, plants adapt their growth to optimize light capture is dense vegetation. This adaptive growth includes elongation and upward movement of stems and leaves and serves to elevate the leaves towards the light. These so-called shade avoidance responses are regulated through signalling of wavelength-specific photoreceptors. As red (R) and blue light are absorbed by leaves and used in photosynthesis, while other wavelengths such as green and far-red (FR) are not, the spectral composition changes in shade. In addition, even before actual shading occurs, the light spectrum changes through specific horizontal reflection of FR from the leaves. The specific absorption of R and reflection of FR leads to a reduction in the ratio of R/FR light in a vegetation. These changes are mimicked by changes in the activity of the phytochrome B (phyB) photoreceptor. In sunlight, where the R/FR is high, phytochrome mainly exists in it’s active, growth-repressing form. Reductions in R/FR lead to reduced phytochrome activity which alleviates the repression of growth. When rosette plants such as Arabidopsis thaliana (Arabidopsis) are grown in close proximity to their neighbours, they will first detect those neighbours at their outermost leaf tips through horizontal FR reflection. Here we describe that FR enrichment at the leaf tip of Arabidopsis leads to upward bending, or hyponasty, at the base of the leaf stalk, the petiole. The distance between the sensing and bending part of the leaf suggests long distance light signalling. We discovered that directed transport of the plant hormone auxin relays the light signal from tip to petiole base, where differential elongation between the two sides of the petiole causes the leaf to bend upwards. We reveal that auxin is synthesised in the leaf

Pigments homologous to the green fluorescent protein (GFP) have been proposed to fine-tune the internal light microclimate of corals, facilitating photoacclimation of photosynthetic coral symbionts (Symbiodiniaceae) to life in different reef habitats and environmental conditions. However, direct measurements of the in vivo light conditions inside the coral tissue supporting this conclusion are lacking. Here, we quantified the intra-tissue spectral light environment of corals expressing GFP-like proteins from widely different light regimes. We focus on: (1) photoconvertible red fluorescent proteins (pcRFPs), thought to enhance photosynthesis in mesophotic habitats via wavelength conversion, and (2) chromoproteins (CPs), which provide photoprotection to the symbionts in shallow water via light absorption. Optical microsensor measurements indicated that both pigment groups strongly alter the coral intra-tissue light environment. Estimates derived from light spectra measured in pcRFP-containing corals showed that fluorescence emission can contribute to >50% of orange-red light available to the photosynthetic symbionts at mesophotic depths. We further show that upregulation of pink CPs in shallow-water corals during bleaching leads to a reduction of orange light by 10-20% compared to low-CP tissue. Thus, screening by CPs has an important role in mitigating the light-enhancing effect of coral tissue scattering and skeletal reflection during bleaching. Our results provide the first experimental quantification of the importance of GFP-like proteins in fine-tuning the light microclimate of corals during photoacclimation.

Pigments homologous to the Green Fluorescent Protein (GFP) have been proposed to fine-tune the internal light microclimate of corals, facilitating photoacclimation of photosynthetic coral symbionts (Symbiodiniaceae) to life in different reef habitats and environmental conditions. However, direct measurements of the in vivo light conditions inside the coral tissue supporting this conclusion are lacking. Here, we quantified the intra-tissue spectral light environment of corals expressing GFP-like proteins from widely different light regimes. We focus on (1) photoconvertible red fluorescent proteins (pcRFPs), thought to enhance photosynthesis in mesophotic habitats via wavelength conversion, and (2) chromoproteins (CPs), which provide photoprotection to the symbionts in shallow water via light absorption. Optical microsensor measurements indicated that both pigment groups strongly alter the coral tissue light environment. Estimates derived from light spectra measured in pcRFP-containing corals showed that fluorescence emission can contribute to >50% of orange-red light available to the photosynthetic symbionts at mesophotic depths. We further show that upregulation of pink CPs in shallow-water corals during bleaching leads to a reduction of orange light by 10-20% compared to low-CP tissue. Thus, screening by CPs has an important role in mitigating the light-enhancing effect of coral tissue scattering during bleaching. Our results provide the first experimental quantification of the importance of GFP-like proteins in fine-tuning the light microclimate of corals during photoacclimation.

Pigments homologous to the Green Fluorescent Protein (GFP) have been proposed to fine-tune the internal light microclimate of corals, facilitating photoacclimation of photosynthetic coral symbionts (Symbiodiniaceae) to life in different reef habitats and environmental conditions. However, direct measurements of the in vivo light conditions inside the coral tissue supporting this conclusion are lacking. Here, we quantified the intra-tissue spectral light environment of corals expressing GFP-like proteins from widely different light regimes. We focus on (1) photoconvertible red fluorescent proteins (pcRFPs), thought to enhance photosynthesis in mesophotic habitats via wavelength conversion, and (2) chromoproteins (CPs), which provide photoprotection to the symbionts in shallow water via light absorption. Optical microsensor measurements indicated that both pigment groups strongly alter the coral tissue light environment. Estimates derived from light spectra measured in pcRFP-containing corals showed that fluorescence emission can contribute to >50% of orange-red light available to the photosynthetic symbionts at mesophotic depths. We further show that upregulation of pink CPs in shallow-water corals during bleaching leads to a reduction of orange light by 10-20% compared to low-CP tissue. Thus, screening by CPs has an important role in mitigating the light-enhancing effect of coral tissue scattering during bleaching. Our results provide the first experimental quantification of the importance of GFP-like proteins in fine-tuning the light microclimate of corals during photoacclimation.

The spectral distribution of light contributes to plant photosynthetic efficiency, morphology, and phytochemical content. The solar spectrum in a greenhouse can be passively modified by installing luminescent films containing quantum dots, which absorb and convert ultraviolet and blue photons into specifically designed emission peaks from green through far-red. Red romaine lettuce (Lactuca sativa L. cv. Outredgeous) was grown under six quantum dot films and a polyethylene control film. The quantum dot films were manufactured with different optical properties, including peak emissions centered at 590 nm, 600 nm, 620 nm, 660 nm, 705 nm, and a 5:1 combination of 600 nm and 705 nm. All environmental plant growth parameters, except for spectral quality, were uniform across treatments and throughout each 28-day experiment. Compared to the control, the high-concentration 660 nm quantum dot film had the highest light use efficiency (plant efficiency) (+25%), and the 620 nm, high-concentration 660 nm, and 705 nm quantum dot films had the highest radiation use efficiency (combined film and plant efficiency) (+26%, +21%, and +26%, respectively). All quantum dot films were more efficient than the polyethylene control film at manipulating the available light to promote biomass accumulation. After reviewing the data from the lettuce experiments, two films were selected for use in an experiment on fruiting plants. Dwarf cherry tomato plants (Solanum lycopersicum cv. Red Robin) were grown in a climate-controlled test stand under the two quantum dot film treatments, with peak emissions centered at 620 nm and 660 nm and compared to plants grown under a polyethylene control film. Plants grown under the 620 nm quantum dot film produced 29.7% more fruit and 14.8% more total fresh mass compared to the control, while plants under the 660 nm quantum dot film produced 10.3% percent fewer fruit and 8.6% less total fresh mass than the control. Plants grown under the 620 nm and 660 nm quantum

The light-dependent release of oxygen from plants was first discovered in the 1770s by Joseph Priestley and Jan Ingenhousz. More recently, the enzyme-catalyzed pathway of carbon assimilation was characterized by Melvin Calvin, James Bassham, and Andrew Benson in 1950, and since then, photosynthesis has been intensively studied by hundreds and thousands of other pioneers. So far, the major components of photosynthesis in different systems and the regulations over these components have been gradually revealed. Now, photosynthesis research is entering a new era, with the ambitious goal of providing new green solutions for overcoming the challenges facing our society, such as ensuring the sustainable supply of food, fiber, and fuel, as well as improving the ecological stability of our planet. We can also conceive that one day we may also leave our planet to live on others, but certainly not without photoautotrophs! Developing photosynthetic systems, both natural and artificial, with greater efficiency in using resources, such as light, nitrogen, CO2, and water, to benefit human society and our planet, is becoming a new frontier of research and a hallmark of this exciting era of photosynthesis research.

The exposure of human skin to ultraviolet-B radiation (UVBR), causes damage in skin cells, which if not repaired may lead to cell death or skin cancer. This research aimed to understand how IGF-I, a growth factor secreted by some skin cells protects adjacent cells from the damaging effects of UVBR. Using 2-dimensional cell co-cultures and 3-dimensional skin models that closely mimic cellular interactions in native skin, the molecular mechanisms of the rescue effects were investigated. The findings may have implications in the development of treatment strategies against sunburns or photodamage.

Bioluminescence—i.e., the emission of visible light by living organisms—is defined as a biochemical reaction involving, at least, a luciferin substrate, an oxygen derivative, and a specialised luciferase enzyme. In some cases, the enzyme and the substrate are durably associated and form a photoprotein. While this terminology is educatively useful to explain bioluminescence, it gives a false idea that all luminous organisms are using identical or homologous molecular tools to achieve light emission. As usually observed in biology, reality is more complex. To date, at least 11 different luciferins have indeed been discovered, and several non-homologous luciferases lato sensu have been identified which, all together, confirms that bioluminescence emerged independently multiple times during the evolution of living organisms. While some phylogenetically related organisms may use non-homologous luciferases (e.g., at least four convergent luciferases are found in Pancrustacea), it has also been observed that phylogenetically distant organisms may use homologous luciferases (e.g., parallel evolution observed in some cnidarians, tunicates and echinoderms that are sharing a homologous luciferase-based system). The evolution of luciferases then appears puzzling. The present review takes stock of the diversity of known “bioluminescent proteins,” their evolution and potential evolutionary origins. A total of 134 luciferase and photoprotein sequences have been investigated (from 75 species and 11 phyla), and our analyses identified 12 distinct types—defined as a group of homologous bioluminescent proteins. The literature review indicated that genes coding for luciferases and photoproteins have potentially emerged as new genes or have been co-opted from ancestral non-luciferase/photoprotein genes. In this latter case, the homologous gene’s co-options may occur independently in phylogenetically distant organisms.

Light represents a ubiquitous source of information for organisms to evaluate their envi ronment. The influence of light on colony growth and conidiation was determined for three Monilinia laxa isolates. The highest mycelial growth rate was observed under red light for the three M. laxa isolates, followed by green light, daylight or darkness. However, reduced sporulation levels were observed in darkness and red light, but conidiation enhancement was found under daylight, black and green light with more hours of exposure to light. Putative photoreceptors for blue (white collar and cryptochromes), green (opsins), and red light (phytochromes) were identified, and the photoresponse-related regulatory family of velvet proteins. A unique ortholog for each photoreceptor was found, and their respective domain architecture was highly conserved. Transcriptional analyses of uncovered sets of genes were performed under daylight or specific color light, and both in time course illumination, finding light-dependent triggered gene expression of MlVEL2, MlPHY2, MlOPS2, and MlCRY2, and color light as a positive inductor of MlVEL3, MlVEL4, MlPHY1, and MlCRY1 ex pression. M. laxa has a highly conserved set of photoreceptors with other light-responsive fungi. Our phenotypic analyses and the existence of this light-sensing machinery suggest transcriptional regulatory systems dedicated to modulating the development and dispersion of this pathogen.

Light represents a ubiquitous source of information for organisms to evaluate their environment. The influence of light on colony growth and conidiation was determined for three Monilinia laxa isolates. The highest mycelial growth rate was observed under red light for the three M. laxa isolates, followed by green light, daylight or darkness. However, reduced sporulation levels were observed in darkness and red light, but conidiation enhancement was found under daylight, black and green light with more hours of exposure to light. Putative photoreceptors for blue (white-collar and cryptochromes), green (opsins), and red light (phytochromes) were identified, and the photoresponse-related regulatory family of velvet proteins. A unique ortholog for each photoreceptor was found, and their respective domain architecture was highly conserved. Transcriptional analyses of uncovered sets of genes were performed under daylight or specific color light, and both in time course illumination, finding light-dependent triggered gene expression of MlVEL2, MlPHY2, MlOPS2, and MlCRY2, and color light as a positive inductor of MlVEL3, MlVEL4, MlPHY1, and MlCRY1 expression. M. laxa has a highly conserved set of photoreceptors with other light-responsive fungi. Our phenotypic analyses and the existence of this light-sensing machinery suggest transcriptional regulatory systems dedicated to modulating the development and dispersion of this pathogen.

The constitutively active missense allele of Arabidopsis phytochrome B, AtPHYBY276H or AtYHB, encodes a polypeptide that adopts a light-insensitive, physiologically active conformation capable of sustaining photomorphogenesis in darkness. Here, we show that the orthologous OsYHB allele of rice phytochrome B (OsPHYBY283H ) also encodes a dominant "constitutively active" photoreceptor through comparative phenotypic analyses of AtYHB and OsYHB transgenic lines of four eudicot species, Arabidopsis thaliana, Nicotiana tabacum (tobacco), Nicotiana sylvestris and Solanum lycopersicum cv. MicroTom (tomato), and of two monocot species, Oryza sativa ssp. japonica and Brachypodium distachyon. Reciprocal transformation experiments show that the gain-of-function constitutive photomorphogenic (cop) phenotypes by YHB expression are stronger in host plants within the same class than across classes. Our studies also reveal additional YHB-dependent traits in adult plants, which include extreme shade tolerance, both early and late flowering behaviors, delayed leaf senescence, reduced tillering, and even viviparous seed germination. However, the strength of these gain-of-function phenotypes depends on the specific combination of YHB allele and species/cultivar transformed. Flowering and tillering of OsYHB- and OsPHYB-expressing lines of rice Nipponbare and Kitaake cultivars were compared, also revealing differences in YHB/PHYB allele versus genotype interaction on the phenotypic behavior of the two rice cultivars. In view of recent evidence that the regulatory activity of AtYHB is not only light insensitive but also temperature insensitive, selective YHB expression is expected to yield improved agronomic performance of both dicot and monocot crop plant species not possible with wild-type PHYB alleles.

This study investigates shading panels’ (SPs) impacts on daylighting features in a lab scale model in terms of parameters representing potential human eyes’ biological responses identified as image forming (IF) and non-image forming (NIF). IF responses enable vision and NIF responses regulate internal body clocks known as circadian clocks. Human-centric lighting evaluates photopic units, representing IF responses, and melanopic units representing NIF responses, combined with correlated color temperature (CCT) of light for potential biological effects. SPs’ impacts on such parameters of daylighting have not yet been studied. Previous research mostly studied panels’ impacts on visual comfort and glare related to IF responses. This research explores the impact of SPs’ color, reflectance, orientation, and openness on photopic and melanopic units and CCT of daylighting inside a 1:50 physical scale model of a space. Approximately prototypes of SPs were evaluated. An experimental setup was designed under outdoor daylighting conditions to capture high dynamic range (HDR) images inside the model. HDR images were post processed to calculate and render the distribution of photopic and melanopic units, melanopic/photopic (M/P) ratios and CCTs in the captured viewpoint of the model. Results reveal the behavior of SPs’ color, reflectance, orientation, and openness in modifying daylighting parameters related to biological responses. Bluish panels, in particular, increase daylighting melanopic units and CCTs whereas reddish panels increase photopic units and reduce CCTs. The research results were discussed to provide an outline for future developments of panels to adapt daylighting to occupants' IF and NIF responses.

This work analyzes the effects of red LED light on mammalian sperm mitochondrial function, using the pig as an animal model. Liquid-stored pig semen was stimulated with red-light for 1, 5 and 10 min in the presence or absence of oligomycin A, a specific inhibitor of mitochondrial ATP synthase, or carbonyl cyanide 4-(trifluoromethoxy)phenylhydrazone (FCCP), a specific disruptor of mitochondrial electron chain. Whereas exposure for 1 and 5 min significantly (p < 0.05) decreased total motility and intracellular ATP levels, irradiation for 10 min induced the opposite effect. Oligomycin A abolished the light-effects on intracellular ATP levels, O2 consumption and mitochondrial membrane potential, whereas compared to non-irradiated samples, FCCP significantly (p < 0.05) increased O2 consumption when sperm were irradiated for 1 min. Both oligomycin A and FCCP significantly (p < 0.05) decreased total motility. Red-light increased cytochrome c oxidase activity with a maximal effect after 5 min of irradiation, which was abolished by both oligomycin A and FCCP. In conclusion, red-light modulates sperm mitochondrial function via electron chain activity in an exposition, time-dependent manner.

To become self-sustaining, human habitats in extreme environments such as the moon and Mars will require bioregenerative life support systems (BLSS) involving controlled environment agriculture (CEA) technology. CEA is an enabling technology for growing plants in an enclosed space with optimal conditions, and plants facilitate human survival in space. Just as on Earth, plants provide important ecosystem services, including atmospheric revitalization, water purification, and food production. To demonstrate the feasibility of plants to provide all the oxygen and water as well as half the caloric requirements of one astronaut, the Prototype Mars-Lunar Greenhouse (MLGH) was developed as BLSS in which plants could be grown hydroponically. Previous experiments in the MLGH approached these goals, but plant productivity needed to be improved to satisfy life-support requirements. Plant growth is rate-limited by quantity and quality of light radiation; thus, a novel agricultural application of colloidal semiconductor nanocrystals, or quantum dots (QDs), was investigated to optimize the spectral quality provided to the plants. Two types of CuInS2/ZnS core-shell QDs were manufactured and embedded as fluorophores into plastic nanocomposite films. The QDs absorbed ultraviolet and blue light and exhibited peak emissions at wavelengths of either 600 nm (Orange) or 660 nm (Red) within the photosynthetically active radiation range. For 28 days, these QD films and a QD-free, polyethylene control film were positioned between solar spectrum-mimicking lamps and lettuce (Lactuca sativa L. cv. ‘Outredgeous’ red romaine) grown under uniform environmental conditions in a laboratory setting. Compared with the lettuce grown under the control film, crop yield increases under the Orange and Red films were respectively observed: edible dry mass (13% and 9%), edible fresh mass (11% and 11%), and total leaf area (8% and 13%). These crop yield enhancements demonstrate the potential for spectral qual

Kanalrhodopsine (ChRs) sind lichtgesteuerte Ionenkanäle aus einzelligen Grünalgen, die in der Optogenetik verwendet werden. Photonabsorption führt zur Isomerisierung des Retinal-Kofaktors, was eine Reihe von Reaktionen auslöst, die als Photozyklus bezeichnet werden und die Bildung des leitenden Zustands umfassen. In dieser Arbeit wurde der Photozyklus-Mechanismus ausgewählter ChRs mittels FTIR (Fourier Transform Infrarot)- und UV-Vis-Spektroskopie, sowie Retinalextraktion und HPLC (Hochleistungsflüssigkeitschromatographie)-Analyse untersucht. Photorezeptoren sind dafür optimiert, Lichtenergie zu nutzen, um Konformationsänderungen des Proteins hervorzurufen. Dafür wird ein Teil der Lichtenergie durch eine transiente Verdrillung des Chromophors gespeichert. In dieser Arbeit wird gezeigt, dass der Transfer der gespeicherten Energie zum Protein in ReaChR stark vom Protonierungszustand von Glu163 beeinflusst wird; er wird durch eine erhöhte Rigidität des aktiven Zentrums bei protoniertem Glu163 verlangsamt. In Chrimson hingegen relaxiert der Chromophor nach Photoisomerisierung, was auf einen verdrillten Chromophor im Dunkelzustand hinweist, was vermutlich für die bathochrome Verschiebung von Bedeutung ist. Zusätzlich zur Chromophorgeometrie beeinflusst der Protonierungszustand von Glu163 in ReaChR und dem homologen Glu165 in Chrimson die Stereoselektivität der Photoreaktion. Ein weiterer Faktor der Stereoselektivität ist Asp196 in ReaChR (Asp195 in C1C2), welches im Photozyklus deprotoniert. Die Bildung des leitenden Zustands in C1C2 und ReaChR geht mit einem Wassereinstrom ins Protein einher, welcher den Transport größerer Kationen erleichtert. Die Deprotonierung von Glu130 in ReaChR (Glu129 in C1C2) verändert die Ionenselektivität des Kanals, wie aus elektrophysiologischen Messungen bekannt ist. In Chrimson ist das Ausmaß des Wassereinstroms deutlich reduziert, was – in Übereinstimmung mit elektrophysiologischen Experimenten – den Transport von Protonen begünstigt., Channelrhodopsins (ChRs) are light-gated ion channels found in single-cell algae and used in optogenetics. Photon absorption leads to isomerization of the retinal cofactor, initiating a number of reactions that are referred to as photocycle and involve formation of the ion-conducting state. In this thesis, the photocycle mechanism of selected ChRs was investigated using FTIR (Fourier Transform Infrared) and UV-Vis spectroscopy, as well as retinal extraction and subsequent HPLC (High Performance Liquid Chromatography) analysis. Photoreceptors are optimized to use photon energy to drive conformational changes of the protein. Therefore, a fraction of the photon energy is stored by a transient distortion of the chromophore. In this thesis, it is shown that in ReaChR the transfer of the stored energy to the protein is largely affected by the protonation state of Glu163, being decelerated by protonated Glu163 due to an enhanced rigidity of the active site. In contrast, the chromophore in Chrimson relaxes upon photoisomerization, hinting at a distorted retinal geometry in the dark state, which is probably essential for its unprecedented bathochromic absorption. In addition to the chromophore geometry, the protonation state of Glu163 in ReaChR and the homologue Glu165 in Chrimson affects the stereoselectivity of the photoreaction. Another factor for stereoselectivity is Asp196 in ReaChR (Asp195 in C1C2) which deprotonates in the photocycle. Formation of the ion-conducting state in C1C2 and ReaChR involves water influx into the protein, facilitating transport of larger cations. Deprotonation of Glu130 in ReaChR (Glu129 in C1C2) alters the ion selectivity of the channel as known from electrophysiological experiments. In Chrimson, the extent of water influx is drastically reduced which favors the conductance of protons in agreement with electrophysiological characterization.

Kanalrhodopsine (ChRs) sind lichtgesteuerte Ionenkanäle aus einzelligen Grünalgen, die in der Optogenetik verwendet werden. Photonabsorption führt zur Isomerisierung des Retinal-Kofaktors, was eine Reihe von Reaktionen auslöst, die als Photozyklus bezeichnet werden und die Bildung des leitenden Zustands umfassen. In dieser Arbeit wurde der Photozyklus-Mechanismus ausgewählter ChRs mittels FTIR (Fourier Transform Infrarot)- und UV-Vis-Spektroskopie, sowie Retinalextraktion und HPLC (Hochleistungsflüssigkeitschromatographie)-Analyse untersucht. Photorezeptoren sind dafür optimiert, Lichtenergie zu nutzen, um Konformationsänderungen des Proteins hervorzurufen. Dafür wird ein Teil der Lichtenergie durch eine transiente Verdrillung des Chromophors gespeichert. In dieser Arbeit wird gezeigt, dass der Transfer der gespeicherten Energie zum Protein in ReaChR stark vom Protonierungszustand von Glu163 beeinflusst wird; er wird durch eine erhöhte Rigidität des aktiven Zentrums bei protoniertem Glu163 verlangsamt. In Chrimson hingegen relaxiert der Chromophor nach Photoisomerisierung, was auf einen verdrillten Chromophor im Dunkelzustand hinweist, was vermutlich für die bathochrome Verschiebung von Bedeutung ist. Zusätzlich zur Chromophorgeometrie beeinflusst der Protonierungszustand von Glu163 in ReaChR und dem homologen Glu165 in Chrimson die Stereoselektivität der Photoreaktion. Ein weiterer Faktor der Stereoselektivität ist Asp196 in ReaChR (Asp195 in C1C2), welches im Photozyklus deprotoniert. Die Bildung des leitenden Zustands in C1C2 und ReaChR geht mit einem Wassereinstrom ins Protein einher, welcher den Transport größerer Kationen erleichtert. Die Deprotonierung von Glu130 in ReaChR (Glu129 in C1C2) verändert die Ionenselektivität des Kanals, wie aus elektrophysiologischen Messungen bekannt ist. In Chrimson ist das Ausmaß des Wassereinstroms deutlich reduziert, was – in Übereinstimmung mit elektrophysiologischen Experimenten – den Transport von Protonen begünstigt., Channelrhodopsins (ChRs) are light-gated ion channels found in single-cell algae and used in optogenetics. Photon absorption leads to isomerization of the retinal cofactor, initiating a number of reactions that are referred to as photocycle and involve formation of the ion-conducting state. In this thesis, the photocycle mechanism of selected ChRs was investigated using FTIR (Fourier Transform Infrared) and UV-Vis spectroscopy, as well as retinal extraction and subsequent HPLC (High Performance Liquid Chromatography) analysis. Photoreceptors are optimized to use photon energy to drive conformational changes of the protein. Therefore, a fraction of the photon energy is stored by a transient distortion of the chromophore. In this thesis, it is shown that in ReaChR the transfer of the stored energy to the protein is largely affected by the protonation state of Glu163, being decelerated by protonated Glu163 due to an enhanced rigidity of the active site. In contrast, the chromophore in Chrimson relaxes upon photoisomerization, hinting at a distorted retinal geometry in the dark state, which is probably essential for its unprecedented bathochromic absorption. In addition to the chromophore geometry, the protonation state of Glu163 in ReaChR and the homologue Glu165 in Chrimson affects the stereoselectivity of the photoreaction. Another factor for stereoselectivity is Asp196 in ReaChR (Asp195 in C1C2) which deprotonates in the photocycle. Formation of the ion-conducting state in C1C2 and ReaChR involves water influx into the protein, facilitating transport of larger cations. Deprotonation of Glu130 in ReaChR (Glu129 in C1C2) alters the ion selectivity of the channel as known from electrophysiological experiments. In Chrimson, the extent of water influx is drastically reduced which favors the conductance of protons in agreement with electrophysiological characterization.

Ultraviolet B radiation (UVBR) induces the formation of photolesions in epidermal keratinocytes, potentially affecting cellular function and contributing towards malignant transformation. Insulin-like growth factor-I (IGF-I) contributes to protection of keratinocytes against UVBR-induced damage. Studies have shown that exogenous IGF-I or dermal fibroblast conditioned media pre-UVBR contributes to protection in primary keratinocytes by preventing apoptosis, modulating cell cycle progression and affecting photolesion removal through its damage preventative effects, however, the efficacy of IGF-I post-UVBR has not been sufficiently addressed. Using 2D and 3D photobiology skin models, the ability of IGF-I post-UVBR to rescue primary keratinocytes from photodamage was investigated. The photoprotective effect of IGF-I, both pre- and post-UVBR on cellular functions of irradiated keratinocytes was examined. IGF-I application, either pre- or post-UVBR, was found to alter keratinocyte survival, apoptosis, cell cycle progression and damage removal responses to UVBR. In particular, IGF-I application post-UVBR was found to promote increased keratinocyte survival, prevent apoptosis, shift cell cycle progression and reduce photodamage in all the skin models. Furthermore, marked differences were observed in activation of signalling cascades upon IGF-I treatment post-UVBR. Taken together, these findings indicate that in addition to a previously known photodamage preventative effect, IGF-I treatment post-UVBR has a photoreparative role suggesting it may hold potential in the development of effective remedial strategies against sunburns and photodamage.

Chronic exposure of human skin to solar ultraviolet radiation (UVR) induces a range of biological reactions which may directly or indirectly lead to the development of skin cancer. In order to overcome these damaging effects of UVR and to reduce photodamage, the skin's endogenous defence system functions in concert with the various exogenous photoprotectors. Growth factors, particularly insulin-like growth factor-I (IGF-I), produced within the body as a result of cellular interaction in response to UVR demonstrates photoprotective properties in human skin. This review summarises the impact of UVR-induced photolesions on human skin, discusses various endogenous as well as exogenous approaches of photoprotection described to date and explains how IGF-I mediates UVR photoprotective responses at the cellular and mitochondrial level. Further, we describe the current interventions using growth factors and propose how the knowledge of the IGF-I photoprotection signalling cascades may direct the development of improved UVR protection and remedial strategies.

The constitutively active missense allele of Arabidopsis phytochrome B, AtPHYBY276H or AtYHB, encodes a polypeptide that adopts a light-insensitive, physiologically active conformation capable of sustaining photomorphogenesis in darkness. Here, we show that the orthologous OsYHB allele of rice phytochrome B (OsPHYBY283H ) also encodes a dominant "constitutively active" photoreceptor through comparative phenotypic analyses of AtYHB and OsYHB transgenic lines of four eudicot species, Arabidopsis thaliana, Nicotiana tabacum (tobacco), Nicotiana sylvestris and Solanum lycopersicum cv. MicroTom (tomato), and of two monocot species, Oryza sativa ssp. japonica and Brachypodium distachyon. Reciprocal transformation experiments show that the gain-of-function constitutive photomorphogenic (cop) phenotypes by YHB expression are stronger in host plants within the same class than across classes. Our studies also reveal additional YHB-dependent traits in adult plants, which include extreme shade tolerance, both early and late flowering behaviors, delayed leaf senescence, reduced tillering, and even viviparous seed germination. However, the strength of these gain-of-function phenotypes depends on the specific combination of YHB allele and species/cultivar transformed. Flowering and tillering of OsYHB- and OsPHYB-expressing lines of rice Nipponbare and Kitaake cultivars were compared, also revealing differences in YHB/PHYB allele versus genotype interaction on the phenotypic behavior of the two rice cultivars. In view of recent evidence that the regulatory activity of AtYHB is not only light insensitive but also temperature insensitive, selective YHB expression is expected to yield improved agronomic performance of both dicot and monocot crop plant species not possible with wild-type PHYB alleles.

This study investigates shading panels’ (SPs) impacts on daylighting features in a lab scale model in terms of parameters representing potential human eyes’ biological responses identified as image forming (IF) and non-image forming (NIF). IF responses enable vision and NIF responses regulate internal body clocks known as circadian clocks. Human-centric lighting evaluates photopic units, representing IF responses, and melanopic units representing NIF responses, combined with correlated color temperature (CCT) of light for potential biological effects. SPs’ impacts on such parameters of daylighting have not yet been studied. Previous research mostly studied panels’ impacts on visual comfort and glare related to IF responses. This research explores the impact of SPs’ color, reflectance, orientation, and openness on photopic and melanopic units and CCT of daylighting inside a 1:50 physical scale model of a space. Approximately prototypes of SPs were evaluated. An experimental setup was designed under outdoor daylighting conditions to capture high dynamic range (HDR) images inside the model. HDR images were post processed to calculate and render the distribution of photopic and melanopic units, melanopic/photopic (M/P) ratios and CCTs in the captured viewpoint of the model. Results reveal the behavior of SPs’ color, reflectance, orientation, and openness in modifying daylighting parameters related to biological responses. Bluish panels, in particular, increase daylighting melanopic units and CCTs whereas reddish panels increase photopic units and reduce CCTs. The research results were discussed to provide an outline for future developments of panels to adapt daylighting to occupants' IF and NIF responses.

Cyanobacteriochromes (CBCRs) are small, bistable linear tetrapyrrole (bilin)-binding light sensors which are typically found as modular components in multidomain cyanobacterial signaling proteins. The CBCR family has been categorized into many lineages that roughly correlate with their spectral diversity, but CBCRs possessing a conserved DXCF motif are found in multiple lineages. DXCF CBCRs typically possess two conserved Cys residues: a first Cys that remains ligated to the bilin chromophore and a second Cys found in the DXCF motif. The second Cys often forms a second thioether linkage, providing a mechanism to sense blue and violet light. DXCF CBCRs have been described with blue/green, blue/orange, blue/teal, and green/teal photocycles, and the molecular basis for some of this spectral diversity has been well established. We here characterize AM1_1499g1, an atypical DXCF CBCR that lacks the second cysteine residue and exhibits an orange/green photocycle. Based on prior studies of CBCR spectral tuning, we have successfully engineered seven AM1_1499g1 variants that exhibit robust yellow/teal, green/teal, blue/teal, orange/yellow, yellow/green, green/green, and blue/green photocycles. The remarkable spectral diversity generated by modification of a single CBCR provides a good template for multiplexing synthetic photobiology systems within the same cellular context, thereby bypassing the time-consuming empirical optimization process needed for multiple probes with different protein scaffolds.

Kanalrhodopsine (ChRs) sind lichtgesteuerte Ionenkanäle aus einzelligen Grünalgen, die in der Optogenetik verwendet werden. Photonabsorption führt zur Isomerisierung des Retinal-Kofaktors, was eine Reihe von Reaktionen auslöst, die als Photozyklus bezeichnet werden und die Bildung des leitenden Zustands umfassen. In dieser Arbeit wurde der Photozyklus-Mechanismus ausgewählter ChRs mittels FTIR (Fourier Transform Infrarot)- und UV-Vis-Spektroskopie, sowie Retinalextraktion und HPLC (Hochleistungsflüssigkeitschromatographie)-Analyse untersucht. Photorezeptoren sind dafür optimiert, Lichtenergie zu nutzen, um Konformationsänderungen des Proteins hervorzurufen. Dafür wird ein Teil der Lichtenergie durch eine transiente Verdrillung des Chromophors gespeichert. In dieser Arbeit wird gezeigt, dass der Transfer der gespeicherten Energie zum Protein in ReaChR stark vom Protonierungszustand von Glu163 beeinflusst wird; er wird durch eine erhöhte Rigidität des aktiven Zentrums bei protoniertem Glu163 verlangsamt. In Chrimson hingegen relaxiert der Chromophor nach Photoisomerisierung, was auf einen verdrillten Chromophor im Dunkelzustand hinweist, was vermutlich für die bathochrome Verschiebung von Bedeutung ist. Zusätzlich zur Chromophorgeometrie beeinflusst der Protonierungszustand von Glu163 in ReaChR und dem homologen Glu165 in Chrimson die Stereoselektivität der Photoreaktion. Ein weiterer Faktor der Stereoselektivität ist Asp196 in ReaChR (Asp195 in C1C2), welches im Photozyklus deprotoniert. Die Bildung des leitenden Zustands in C1C2 und ReaChR geht mit einem Wassereinstrom ins Protein einher, welcher den Transport größerer Kationen erleichtert. Die Deprotonierung von Glu130 in ReaChR (Glu129 in C1C2) verändert die Ionenselektivität des Kanals, wie aus elektrophysiologischen Messungen bekannt ist. In Chrimson ist das Ausmaß des Wassereinstroms deutlich reduziert, was – in Übereinstimmung mit elektrophysiologischen Experimenten – den Transport von Protonen begünstigt., Channelrhodopsins (ChRs) are light-gated ion channels found in single-cell algae and used in optogenetics. Photon absorption leads to isomerization of the retinal cofactor, initiating a number of reactions that are referred to as photocycle and involve formation of the ion-conducting state. In this thesis, the photocycle mechanism of selected ChRs was investigated using FTIR (Fourier Transform Infrared) and UV-Vis spectroscopy, as well as retinal extraction and subsequent HPLC (High Performance Liquid Chromatography) analysis. Photoreceptors are optimized to use photon energy to drive conformational changes of the protein. Therefore, a fraction of the photon energy is stored by a transient distortion of the chromophore. In this thesis, it is shown that in ReaChR the transfer of the stored energy to the protein is largely affected by the protonation state of Glu163, being decelerated by protonated Glu163 due to an enhanced rigidity of the active site. In contrast, the chromophore in Chrimson relaxes upon photoisomerization, hinting at a distorted retinal geometry in the dark state, which is probably essential for its unprecedented bathochromic absorption. In addition to the chromophore geometry, the protonation state of Glu163 in ReaChR and the homologue Glu165 in Chrimson affects the stereoselectivity of the photoreaction. Another factor for stereoselectivity is Asp196 in ReaChR (Asp195 in C1C2) which deprotonates in the photocycle. Formation of the ion-conducting state in C1C2 and ReaChR involves water influx into the protein, facilitating transport of larger cations. Deprotonation of Glu130 in ReaChR (Glu129 in C1C2) alters the ion selectivity of the channel as known from electrophysiological experiments. In Chrimson, the extent of water influx is drastically reduced which favors the conductance of protons in agreement with electrophysiological characterization.

Kanalrhodopsine (ChRs) sind lichtgesteuerte Ionenkanäle aus einzelligen Grünalgen, die in der Optogenetik verwendet werden. Photonabsorption führt zur Isomerisierung des Retinal-Kofaktors, was eine Reihe von Reaktionen auslöst, die als Photozyklus bezeichnet werden und die Bildung des leitenden Zustands umfassen. In dieser Arbeit wurde der Photozyklus-Mechanismus ausgewählter ChRs mittels FTIR (Fourier Transform Infrarot)- und UV-Vis-Spektroskopie, sowie Retinalextraktion und HPLC (Hochleistungsflüssigkeitschromatographie)-Analyse untersucht. Photorezeptoren sind dafür optimiert, Lichtenergie zu nutzen, um Konformationsänderungen des Proteins hervorzurufen. Dafür wird ein Teil der Lichtenergie durch eine transiente Verdrillung des Chromophors gespeichert. In dieser Arbeit wird gezeigt, dass der Transfer der gespeicherten Energie zum Protein in ReaChR stark vom Protonierungszustand von Glu163 beeinflusst wird; er wird durch eine erhöhte Rigidität des aktiven Zentrums bei protoniertem Glu163 verlangsamt. In Chrimson hingegen relaxiert der Chromophor nach Photoisomerisierung, was auf einen verdrillten Chromophor im Dunkelzustand hinweist, was vermutlich für die bathochrome Verschiebung von Bedeutung ist. Zusätzlich zur Chromophorgeometrie beeinflusst der Protonierungszustand von Glu163 in ReaChR und dem homologen Glu165 in Chrimson die Stereoselektivität der Photoreaktion. Ein weiterer Faktor der Stereoselektivität ist Asp196 in ReaChR (Asp195 in C1C2), welches im Photozyklus deprotoniert. Die Bildung des leitenden Zustands in C1C2 und ReaChR geht mit einem Wassereinstrom ins Protein einher, welcher den Transport größerer Kationen erleichtert. Die Deprotonierung von Glu130 in ReaChR (Glu129 in C1C2) verändert die Ionenselektivität des Kanals, wie aus elektrophysiologischen Messungen bekannt ist. In Chrimson ist das Ausmaß des Wassereinstroms deutlich reduziert, was – in Übereinstimmung mit elektrophysiologischen Experimenten – den Transport von Protonen begünstigt., Channelrhodopsins (ChRs) are light-gated ion channels found in single-cell algae and used in optogenetics. Photon absorption leads to isomerization of the retinal cofactor, initiating a number of reactions that are referred to as photocycle and involve formation of the ion-conducting state. In this thesis, the photocycle mechanism of selected ChRs was investigated using FTIR (Fourier Transform Infrared) and UV-Vis spectroscopy, as well as retinal extraction and subsequent HPLC (High Performance Liquid Chromatography) analysis. Photoreceptors are optimized to use photon energy to drive conformational changes of the protein. Therefore, a fraction of the photon energy is stored by a transient distortion of the chromophore. In this thesis, it is shown that in ReaChR the transfer of the stored energy to the protein is largely affected by the protonation state of Glu163, being decelerated by protonated Glu163 due to an enhanced rigidity of the active site. In contrast, the chromophore in Chrimson relaxes upon photoisomerization, hinting at a distorted retinal geometry in the dark state, which is probably essential for its unprecedented bathochromic absorption. In addition to the chromophore geometry, the protonation state of Glu163 in ReaChR and the homologue Glu165 in Chrimson affects the stereoselectivity of the photoreaction. Another factor for stereoselectivity is Asp196 in ReaChR (Asp195 in C1C2) which deprotonates in the photocycle. Formation of the ion-conducting state in C1C2 and ReaChR involves water influx into the protein, facilitating transport of larger cations. Deprotonation of Glu130 in ReaChR (Glu129 in C1C2) alters the ion selectivity of the channel as known from electrophysiological experiments. In Chrimson, the extent of water influx is drastically reduced which favors the conductance of protons in agreement with electrophysiological characterization.

To become self-sustaining, human habitats in extreme environments such as the moon and Mars will require bioregenerative life support systems (BLSS) involving controlled environment agriculture (CEA) technology. CEA is an enabling technology for growing plants in an enclosed space with optimal conditions, and plants facilitate human survival in space. Just as on Earth, plants provide important ecosystem services, including atmospheric revitalization, water purification, and food production. To demonstrate the feasibility of plants to provide all the oxygen and water as well as half the caloric requirements of one astronaut, the Prototype Mars-Lunar Greenhouse (MLGH) was developed as BLSS in which plants could be grown hydroponically. Previous experiments in the MLGH approached these goals, but plant productivity needed to be improved to satisfy life-support requirements. Plant growth is rate-limited by quantity and quality of light radiation; thus, a novel agricultural application of colloidal semiconductor nanocrystals, or quantum dots (QDs), was investigated to optimize the spectral quality provided to the plants. Two types of CuInS2/ZnS core-shell QDs were manufactured and embedded as fluorophores into plastic nanocomposite films. The QDs absorbed ultraviolet and blue light and exhibited peak emissions at wavelengths of either 600 nm (Orange) or 660 nm (Red) within the photosynthetically active radiation range. For 28 days, these QD films and a QD-free, polyethylene control film were positioned between solar spectrum-mimicking lamps and lettuce (Lactuca sativa L. cv. ‘Outredgeous’ red romaine) grown under uniform environmental conditions in a laboratory setting. Compared with the lettuce grown under the control film, crop yield increases under the Orange and Red films were respectively observed: edible dry mass (13% and 9%), edible fresh mass (11% and 11%), and total leaf area (8% and 13%). These crop yield enhancements demonstrate the potential for spectral qual

Studying carbon dynamics in the coral holobiont provides essential knowledge of nutritional strategies and is thus central to understanding coral ecophysiology. In this study, we assessed the carbon budget in Pocillopora damicornis (using H13CO3) as a function of feeding status and temperature stress. We also compared dissolved oxygen (O2) fluxes measured at the colony scale and at the polyp scale. At both scales, O2 production rates were enhanced for fed vs. unfed corals, and unfed corals exhibited higher bleaching and reduced photosynthetic activity at high temperature. Unfed corals exclusively respired autotrophically acquired carbon, while fed corals mostly respired heterotrophically acquired carbon. As a consequence, fed corals excreted on average > 5 times more organic carbon than unfed corals. Photosynthate translocation was higher under thermal stress, but most of the carbon was lost via respiration and/or mucus release (42−46 % and 57−75 % of the fixed carbon for unfed and fed corals, respectively). Such high loss of translocated carbon, coupled to low assimilation rates in the coral tissue and symbionts, suggests that P. damicornis was nitrogen and/or phosphorus limited. Heterotrophy might thus cover a larger portion of the nutritional demand for P. damicornis than previously assumed. Our results suggest that active feeding plays a fundamental role in metabolic dynamics and bleaching susceptibility of corals.

Studying carbon dynamics in the coral holobiont provides essential knowledge of nutritional strategies and is thus central to understanding coral ecophysiology. In this study, we assessed the carbon budget in Pocillopora damicornis (using H13CO3) as a function of feeding status and temperature stress. We also compared dissolved oxygen (O2) fluxes measured at the colony scale and at the polyp scale. At both scales, O2 production rates were enhanced for fed vs. unfed corals, and unfed corals exhibited higher bleaching and reduced photosynthetic activity at high temperature. Unfed corals exclusively respired autotrophically acquired carbon, while fed corals mostly respired heterotrophically acquired carbon. As a consequence, fed corals excreted on average > 5 times more organic carbon than unfed corals. Photosynthate translocation was higher under thermal stress, but most of the carbon was lost via respiration and/or mucus release (42−46 % and 57−75 % of the fixed carbon for unfed and fed corals, respectively). Such high loss of translocated carbon, coupled to low assimilation rates in the coral tissue and symbionts, suggests that P. damicornis was nitrogen and/or phosphorus limited. Heterotrophy might thus cover a larger portion of the nutritional demand for P. damicornis than previously assumed. Our results suggest that active feeding plays a fundamental role in metabolic dynamics and bleaching susceptibility of corals.

Introduction: Actinic prurigo is a chronic photodermatosis. It affects the Latin American population more frequently, predominantly women, and involves the sun-exposed areas of the skin, conjunctiva, and lips.Objective: To update the information on the clinical-epidemiological characteristics and treatment of patients with actinic prurigo in Colombia.Materials and methods: We conducted a cross-sectional study including the medical records of patients with actinic prurigo treated in the Photodermatology Service of Hospital Universitario Centro Dermatológico Federico Lleras Acosta between 2011 and 2016. We described the demographic, clinical, histopathological, and treatment characteristics of the patients.Results: We included 108 patients, 77 (71.3%) were women and 31 (28.7%) men, mainly with phototypes III-IV (70%). The disease had begun during the first decade of life in 66.4% of the cases and 25% of the patients had a family history with the condition. The lesions predominated on the face (93.5%), forearms (79.6%), and back of the hands (70.4%). Ocular (87.9%) and lip (88.8%) involvement was also documented. A photo-provocation test with UVA was performed in 25% of the cases and skin biopsies in 19.4%. Physical and chemical photoprotection was indicated in all patients. Mild to moderate cases were treated with topical corticosteroids (91.7%) and calcineurin inhibitors (65.7%) while severe cases received thalidomide (33.3%) and pentoxifylline (14.8%).Conclusion: The characteristics of actinic prurigo patients in Colombia are similar to those reported in other Latin American countries: early onset of the disease, predominance in women, frequent involvement of conjunctiva and lips, and adequate response to topical and systemic treatment., Introducción. El prurigo actínico es una fotodermatosis crónica. Afecta con mayor frecuencia a la población latinoamericana, predomina en mujeres y compromete la piel expuesta al sol, las conjuntivas y los labios.Objetivo. Actualizar la información sobre las características clínico-epidemiológicas y el tratamiento de pacientes con prurigo actínico en Colombia.Materiales y métodos. Se hizo un estudio de corte transversal que incluyó los registros clínicos de pacientes con prurigo actínico atendidos en el Servicio de Fotodermatología del Hospital Universitario Centro Dermatológico Federico Lleras Acosta entre el 2011 y el 2016, y se describieron sus características demográficas, clínicas e histopatológicas, así como su tratamiento.Resultados. Se incluyeron 108 pacientes, el 71,3 % de ellos mujeres y el 28,7% hombres, con predominio de los fototipos III-IV (70 %). La enfermedad se había iniciado durante la primera década de vida en el 66,4% de los casos y el 25 % de los pacientes tenía antecedentes familiares de la enfermedad. Las lesiones predominaban en el rostro (93,5 %), los antebrazos (79,6 %) y el dorso de las manos (70,4 %). También, se documentó compromiso ocular (87,9 %) y de los labios (88,8 %). Se hizo la prueba de fotoprovocación con radiación ultravioleta A en el 25 % de los casos y biopsia cutánea en el 19,4 %. Todos los pacientes se trataron con protección solar química y física. En los casos leves a moderados, se formularon corticoides tópicos (91,7 %) e inhibidores de la calcineurina (65,7 %), y en los graves, talidomida (33,3 %) y pentoxifilina (14,8 %).Conclusión. Las características de los pacientes colombianos con prurigo actínico son similares a las reportadas en otros países latinoamericanos: inicio temprano de la enfermedad, predominio en mujeres, compromiso frecuente de conjuntivas y labios, y adecuada respuesta al tratamiento tópico y sistémico.

miniSOG is the first flavin-binding protein that has been developed with the specific aim of serving as a genetically-encodable light-induced source of singlet oxygen (1O2). We have determined its 1.17 Å resolution structure, which has allowed us to investigate its mechanism of photosensitization using an integrated approach combining spectroscopic and structural methods. Our results provide a structural framework to explain the ability of miniSOG to produce 1O2 as a competition between oxygen- and protein quenching of its triplet state. In addition, a third excited-state decay pathway has been identified that is pivotal for the performance of miniSOG as 1O2 photosensitizer, namely the photo-induced transformation of flavin mononucleotide (FMN) into lumichrome, which increases the accessibility of oxygen to the flavin FMN chromophore and makes protein quenching less favourable. The combination of the two effects explains the increase in the 1O2 quantum yield by one order of magnitude upon exposure to blue light. Besides, we have identified several surface electron-rich residues that are progressively photo-oxidized, further contributing to facilitate the production of 1O2. Our results help reconcile the apparent poor level of 1O2 generation by miniSOG and its excellent performance in correlative light and electron microscopy experiments.

In his celebrated 1974 essay “What Is It Like to Be a Bat?” Thomas Nagel stages a human-bat encounter to illustrate and support his claim that “subjective experience” is irreducible to “objective fact”: because Nagel cannot experience the world as a bat does, he will never know what it is like to be one. In Nagel’s account, heterogeneity is figured negatively— as a failure or lack of resemblance—and functions to constrain his knowledge of bats. Today, as white-nose syndrome threatens bat populations across North America, might figuring heterogeneity positively, as a condition of creativity, open up new modes of receptivity and responsiveness to species extinctions? This essay turns to philosophies of becoming and to recent research in the biological sciences to explore this possibility. I suggest that attending to the heterogeneity of experience alerts us to more public dimensions of our being and may thereby work against the tendency to understand and experience ourselves as self-contained and closed off from one another and the world we share in common. This may in turn enhance our sense of entanglement with the events, bodies, and forces on the “outside” of experience, including bats and the white-nose syndrome with which they are afflicted today. Such an affirmation of heterogeneity as a condition of creativity holds the greatest promise for multispecies ethics today, I propose, when it is joined to an affirmation of incompatibilities within and between things as a real force of suffering and destruction in a heterogeneous world., info:eu-repo/semantics/published

Plants can deal with shade in different ways. Sun-adapted species express a set of growth traits to reach for light; the so-called shade avoidance syndrome (SAS). However, shade-tolerant species from the forest understory are not able to outgrow surrounding trees and adopt a tolerance strategy including suppression of shade avoidance. All plants sense the drop in the ratio between red (R) and far-red (FR) light via specialized photoreceptors, the phytochromes, but unlike the molecular pathways promoting SAS, virtually nothing is known about the regulation of shade tolerance. We selected two wild Geranium species with opposite growth responses to FR light enrichment; the shade avoiding G. pyrenaicum and shade tolerant G. robertianum. RNA sequencing of these species revealed contrasting transcriptomic changes treated upon FR light and in the first place showed how differential regulation of phytohormone synthesis and –perception could correlate to the species growth patterns in shade. Analysis of the hormone levels and growth responses to auxin, gibberellic acid and brassinosteroid application or –inhibition confirmed a role for these hormones in the Geranium shade responses. Secondly, the transcriptome analysis revealed a striking difference in FR induced regulation of pathogen defences. G. pyrenaicum showed far-red-mediated down-regulation of defence genes and increased susceptibility to the fungal pathogen Botrytis cinerea, similar to model species Arabidopsis. Interestingly, G. robertianum seems to boost its defences and becomes more resistant when exposed to FR-enriched light. Furthermore, the RNAseq analysis identified genes of which the expression patterns match growth data and give an insight into novel possible players and pathways responsible for the opposite light responses; two receptor-like kinases and a bHLH transcription factor. The importance of these novel candidates was verified in heterologous functional studies in Arabidopsis.

A highly efficient photochromic hydrogel was successfully fabricated via casting precursor, which is based on amorphous tungsten oxide and poly (ethylene oxide)-block-poly (propylene oxide)-block-poly (ethylene oxide). Under simulated solar illumination, the hydrogel has a rapid and controlled temperature increasing ratio as its coloration degree. Localized electrons in the amorphous tungsten oxide play a vital role in absorption over a broad range of wavelengths from 400 nm to 1100 nm, encompassing the entire visible light and infrared regions in the solar spectrum. More importantly, the material exhibits sustainable released H2O2 induced by localized electrons, which has a synergistic effect with the rapid surface temperature increase. The amount of H2O2 released by each film can be tuned by the light irradiation, and the film coloration can indicate the degree of oxidative stress. The ability of the H2O2-releasing gels in vitro study was investigated to induce apoptosis in melanoma tumor cells and NIH 3T3 fibroblasts. The in vivo experimental results indicate that these gels have a greater healing effect than the control in the early stages of tumor formation. © The Author(s) 2016.

A highly efficient photochromic hydrogel was successfully fabricated via casting precursor, which is based on amorphous tungsten oxide and poly (ethylene oxide)-block-poly (propylene oxide)-block-poly (ethylene oxide). Under simulated solar illumination, the hydrogel has a rapid and controlled temperature increasing ratio as its coloration degree. Localized electrons in the amorphous tungsten oxide play a vital role in absorption over a broad range of wavelengths from 400 nm to 1100 nm, encompassing the entire visible light and infrared regions in the solar spectrum. More importantly, the material exhibits sustainable released H2O2 induced by localized electrons, which has a synergistic effect with the rapid surface temperature increase. The amount of H2O2 released by each film can be tuned by the light irradiation, and the film coloration can indicate the degree of oxidative stress. The ability of the H2O2-releasing gels in vitro study was investigated to induce apoptosis in melanoma tumor cells and NIH 3T3 fibroblasts. The in vivo experimental results indicate that these gels have a greater healing effect than the control in the early stages of tumor formation. © The Author(s) 2016.

Light-driven ion-pumping rhodopsins are widely distributed in microorganisms and are now classified into the categories of outward H+ and Na+ pumps and an inward Cl- pump. These different types share a common protein architecture and utilize the photoisomerization of the same chromophore, retinal, to evoke photoreactions. Despite these similarities, successful pump-to-pump conversion had been confined to only the H+ pump bacteriorhodopsin, which was converted to a Cl- pump in 1995 by a single amino acid replacement. In this study we report the first success of the reverse conversion from a Cl- pump to a H+ pump. A novel microbial rhodopsin (MrHR) from the cyanobacterium Mastigocladopsis repens functions as a Cl- pump and belongs to a cluster that is far distant from the known Cl- pumps. With a single amino acid replacement, MrHR is converted to a H+ pump in which dissociable residues function almost completely in the H+ relay reactions. MrHR most likely evolved from a H+ pump, but it has not yet been highly optimized into a mature Cl- pump.

Light-driven ion-pumping rhodopsins are widely distributed in microorganisms and are now classified into the categories of outward H+ and Na+ pumps and an inward Cl- pump. These different types share a common protein architecture and utilize the photoisomerization of the same chromophore, retinal, to evoke photoreactions. Despite these similarities, successful pump-to-pump conversion had been confined to only the H+ pump bacteriorhodopsin, which was converted to a Cl- pump in 1995 by a single amino acid replacement. In this study we report the first success of the reverse conversion from a Cl- pump to a H+ pump. A novel microbial rhodopsin (MrHR) from the cyanobacterium Mastigocladopsis repens functions as a Cl- pump and belongs to a cluster that is far distant from the known Cl- pumps. With a single amino acid replacement, MrHR is converted to a H+ pump in which dissociable residues function almost completely in the H+ relay reactions. MrHR most likely evolved from a H+ pump, but it has not yet been highly optimized into a mature Cl- pump.

A highly efficient photochromic hydrogel was successfully fabricated via casting precursor, which is based on amorphous tungsten oxide and poly (ethylene oxide)-block-poly (propylene oxide)-block-poly (ethylene oxide). Under simulated solar illumination, the hydrogel has a rapid and controlled temperature increasing ratio as its coloration degree. Localized electrons in the amorphous tungsten oxide play a vital role in absorption over a broad range of wavelengths from 400 nm to 1100 nm, encompassing the entire visible light and infrared regions in the solar spectrum. More importantly, the material exhibits sustainable released H2O2 induced by localized electrons, which has a synergistic effect with the rapid surface temperature increase. The amount of H2O2 released by each film can be tuned by the light irradiation, and the film coloration can indicate the degree of oxidative stress. The ability of the H2O2-releasing gels in vitro study was investigated to induce apoptosis in melanoma tumor cells and NIH 3T3 fibroblasts. The in vivo experimental results indicate that these gels have a greater healing effect than the control in the early stages of tumor formation. © The Author(s) 2016.

Diatoms are ubiquitous organisms in aquatic environments and are estimated to be responsible for 20–25 % of the total global primary production. A unique feature of diatomsis the silica wall, called the frustule. The frustule is characterized by species-specific intricate nanopatterning in the same size range as wave lengths of visible and ultraviolet (UV) light. This has prompted research into the possible role of the frustule in mediating light for the diatoms’ photosynthesis as well as into possible photonic applications of the diatom frustule. One of the possible biological roles, as well as area of potential application, is UV protection. In this review, we explore the possible adaptive value of the silica frustule with focus on research on the effect of UV radiation ondiatoms. We also explore the possible effect of the frustules on UV radiation, from a theoretical, biological, and applied perspective, including recent experimental data on UV transmission of diatom frustules.

Drosophila phototransduction is the fastest G-protein coupled signaling pathway known to date. Several key proteins including TRP, NORPA and ePKC, are assembled into a large complex by a master scaffold protein, INAD, which contains five PDZ domains. Previous study in our lab discovered that INAD PDZ2 binds to eye PKC and INAD PDZ3 binds to TRP. However, the binding partners of INAD PDZ5 and the molecular mechanism governing their interactions are unknown. Here, we discovered that NORPA CTD binds to INAD PDZ45 strongly with a dissociation constant of 20 nM, more than 100-fold stronger than canonical PDZ-PBM interactions. Apo-form NORPA crystal structures, combined with NMR and ITC data, reveal a supramodule binding model for NORPA/INAD interaction. In addition, we discovered that NORPA CTD undergoes pH-dependent changes of structural stability and membrane binding, which may represent another evidence for proton as a general second messenger in PLC/PIP2 signaling processes.

Drosophila phototransduction is the fastest G-protein coupled signaling pathway known to date. Several key proteins including TRP, NORPA and ePKC, are assembled into a large complex by a master scaffold protein, INAD, which contains five PDZ domains. Previous study in our lab discovered that INAD PDZ2 binds to eye PKC and INAD PDZ3 binds to TRP. However, the binding partners of INAD PDZ5 and the molecular mechanism governing their interactions are unknown. Here, we discovered that NORPA CTD binds to INAD PDZ45 strongly with a dissociation constant of 20 nM, more than 100-fold stronger than canonical PDZ-PBM interactions. Apo-form NORPA crystal structures, combined with NMR and ITC data, reveal a supramodule binding model for NORPA/INAD interaction. In addition, we discovered that NORPA CTD undergoes pH-dependent changes of structural stability and membrane binding, which may represent another evidence for proton as a general second messenger in PLC/PIP2 signaling processes.

The quenching of Chlorophyll triplets by triplet energy transfer (TET) to carotenoids is one of the photoprotection strategies in photosynthetic organisms, and prevents singlet oxygen formation. Here we present the study of TET rates in a minor light-harvesting complex (LHC) of higher plants, using a fully atomistic strategy that combines a molecular dynamic simulation a polarizable quantum/classical calculation. We find that structural fluctuations of the LHC can largely enhance the TET rates, which are in the sub-nanosecond scale, in agreement with experimental findings.