A phosphor converted RED light for automotive LED rear lamp and compliance with ECE light regulation

Optik ◽  
2021 ◽  
Vol 234 ◽  
pp. 166590
Author(s):  
Seok-Ho Jeong ◽  
Jung-Young Kim ◽  
Xiao Xiao ◽  
Young-Suk Kim
Keyword(s):  
2018 ◽  
Vol 56 (1) ◽  
pp. 41-66 ◽  
Author(s):  
Gwyn A. Beattie ◽  
Bridget M. Hatfield ◽  
Haili Dong ◽  
Regina S. McGrane

Plants collect, concentrate, and conduct light throughout their tissues, thus enhancing light availability to their resident microbes. This review explores the role of photosensing in the biology of plant-associated bacteria and fungi, including the molecular mechanisms of red-light sensing by phytochromes and blue-light sensing by LOV (light-oxygen-voltage) domain proteins in these microbes. Bacteriophytochromes function as major drivers of the bacterial transcriptome and mediate light-regulated suppression of virulence, motility, and conjugation in some phytopathogens and light-regulated induction of the photosynthetic apparatus in a stem-nodulating symbiont. Bacterial LOV proteins also influence light-mediated changes in both symbiotic and pathogenic phenotypes. Although red-light sensing by fungal phytopathogens is poorly understood, fungal LOV proteins contribute to blue-light regulation of traits, including asexual development and virulence. Collectively, these studies highlight that plant microbes have evolved to exploit light cues and that light sensing is often coupled with sensing other environmental signals.


1999 ◽  
Vol 47 (4) ◽  
pp. 225-229 ◽  
Author(s):  
Anat Katz ◽  
David Weiss

We have previously shown that light is essential for anthocyanin synthesis in detached petunia flowers. In this study, we examined the effect of light quality on anthocyanin accumulation and on the expression of the anthocyanin biosynthetic gene chalcone synthase (chs) in the attached petunia flowers. When plants were kept for 48 h in the dark,chsexpression could not be detected. Blue light and red light promoted the expression of the gene to similar levels, whereas the effect of green light was slightly smaller. Neither UV-A nor UV-B radiation were required for anthocyanin accumulation, or for the induction and maintenance ofchsexpression. The results of this study show that light is essential for anthocyanin synthesis in petunia flowers and that its active spectrum includes most of the visible part but not UV radiation.


2004 ◽  
Vol 43 (2) ◽  
pp. 117-125 ◽  
Author(s):  
C.L. Steed ◽  
L.K. Taylor ◽  
M.A. Harrison

1994 ◽  
Vol 49 (11-12) ◽  
pp. 757-762 ◽  
Author(s):  
Gudrun Meya ◽  
Wolfgang Kowallik

Glutamine synthetase (EC 6.3.1.2) activity of a non-photosynthetic mutant of Chlorella kessleri is markedly enhanced under blue and slightly increased under red light. In both cases, the effect is largest after 6 h of irradiation. In blue light, saturation is reached at about 10 μEm-2 s-1; in red light, it is not even indicated at 62 μE m-2 s-1.Semilogarithmic plots of both intensity dependencies reveal different slopes, indicating envolvement of two separate photoreceptors. This feature is supported by different effects of pulse irradiation: The response to 15 min of red light irradiation (λmax 650 nm) increases in subsequent darkness. It reaches the same value as in continuous light after 6 h. The response to 15 min of blue light irradiation (λmax 441 nm) increases also in subsequent darkness. However, after 6 h it reaches only 30% of the value obtained by continuous irradiation.It is concluded that, glutamine synthetase of Chlorella is controlled by two different photoreceptors both independent of photosynthesis. There is evidence of two forms of glutamine synthetase, the intracellular distribution and specific light regulations of these are discussed.


2019 ◽  
Author(s):  
Alexandra-Madelaine Tichy ◽  
Elliot J. Gerrard ◽  
Julien M.D. Legrand ◽  
Robin M. Hobbs ◽  
Harald Janovjak

ABSTRACTOptogenetics enables the spatio-temporally precise control of cell and animal behaviour. Many optogenetic tools are driven by light-controlled protein-protein-interactions (PPIs) that are repurposed from natural light-sensitive domains (LSDs). Applying light-controlled PPI to new target proteins is challenging because it is difficult to predict whether one the many available LSDs will yield robust light regulation. As a consequence, fusion protein libraries need to be prepared and tested, but methods and platforms to facilitate this process are currently not available. Here, we developed a genetic engineering strategy and vector library for the rapid generation of light-controlled PPIs. The strategy permits fusing a target protein to LSDs efficiently and in two orientations. The public and expandable library contains 29 vectors with blue, green or red light-responsive LSDs many of which have been previously applied ex vivo and in vivo. We demonstrate the versatility of the approach and the necessity for sampling LSDs by generating light-activated caspase-9 (casp9) enzymes. Collectively, this work provides a new resource for optical regulation of a broad range of target proteins in cell and developmental biology.


2019 ◽  
Vol 46 (10) ◽  
pp. 916 ◽  
Author(s):  
Zhiqiang Liu ◽  
Chunyu Cao ◽  
Yawen Li ◽  
Guangdong Yang ◽  
Yanxi Pei

Signal transduction mediated by photoreceptors regulates many physiological processes during plant growth and development including seed germination, flowering and photosynthesis, which are also regulated by hydrogen sulfide (H2S). However, studies of the connection between the vital environmental factors – light and the significant endogenous gasotransmitter – H2S, is lacking. Here, the seedlings of foxtail millet were used to reveal the mechanism of light regulation in H2S generation. Results showed that seedling hypocotyl elongation was promoted by H2S, but inhibited by HA under dark or white light condition. H2S contents in hypocotyl increased at first under red, blue or white light then decreased, and the duration of increase under white light was longer than under red or blue light. The activity of cysteine desulfhydrases, which catalyse H2S generation, was increased by red light but decreased by blue and white light. The expressions of cysteine desulfhydrases coding genes LCD1 and LCD2 were promoted by red or white light, but inhibited by blue light. In contrast, DES gene was promoted by white light but inhibited by red or blue light. In addition, the activities of LCDs were regulated by the phosphorylation mediated by photoreceptors PHYB and CRY1/CRY2. Finally, there are two pathways of light regulating H2S production, including a rapid process that involves the modification of phosphorylation on LCDs protein mediated by photoreceptors directly or indirectly, as well as a slower process that involves in regulating the expressions of LCDs and DES genes. This discovery has potential value for the application of H2S in agricultural production protecting the crops from unsuited light condition.


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