Ultraviolet Radiation From a Plant Perspective: The Plant-Microorganism Context
Open accessAbstract
Ultraviolet (UV) radiation directly affects plants and microorganisms, but also alters the species-specific interactions between them. The distinct bands of UV radiation, UV-A, UV-B, and UV-C have different effects on plants and their associated microorganisms. While UV-A and UV-B mainly affect morphogenesis and phototropism, UV-B and UV-C strongly trigger secondary metabolite production. Short wave (<350 nm) UV radiation negatively affects plant pathogens in direct and indirect ways. Direct effects can be ascribed to DNA damage, protein polymerization, enzyme inactivation and increased cell membrane permeability. UV-C is the most energetic radiation and is thus more effective at lower doses to kill microorganisms, but by consequence also often causes plant damage. Indirect effects can be ascribed to UV-B specific pathways such as the UVR8-dependent upregulated defense responses in plants, UV-B and UV-C upregulated ROS accumulation, and secondary metabolite production such as phenolic compounds. In this review, we summarize the physiological and molecular effects of UV radiation on plants, microorganisms and their interactions. Considerations for the use of UV radiation to control microorganisms, pathogenic as well as non-pathogenic, are listed. Effects can be indirect by increasing specialized metabolites with plant pre-treatment, or by directly affecting microorganisms.
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Phytochemicals may operate in a variety of ways, including absorbing ultraviolet and acting as filters, stimulating the immune system, triggering gene suppression, stopping oxidative DNA damage, detoxifying carcinogens and initiating specific signaling pathways.
“Phytochemicals may operate in a variety of ways, including being capable of absorbing the ultraviolet and act as filters, stimulating the immune system, triggering gene suppression, stopping oxidative DNA damage, detoxifying carcinogens and initiating specific signaling pathways (Vanhaelewyn et al. 2020).”
From Skin protection from solar ultraviolet radiation using natural compounds: a review (2024) · cites this paper as Vanhaelewyn et al. 2020
The section on phenolics (page unavailable) says flavonoids absorb UV radiation, filter harmful UV-B rays, and act as antioxidants. It also describes antimicrobial effects and plant defense responses. It does not support the full list of mechanisms attributed to phytochemicals, particularly stimulation of the immune system, gene suppression, prevention of oxidative DNA damage, or detoxification of carcinogens; the DNA Damage section instead discusses separate DNA-repair mechanisms. (LLM, conf=0.88)
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- Aarrouf J. Urban L. (2020). Flashes of UV-C light: an innovative method for stimulating plant defences. PLoS One 15: e0235918. 10.1371/journal.pone.0235918 32645090 PMC7347194 · DOI
- Agati G. Tattini M. (2010). Multiple functional roles of flavonoids in photoprotection. New Phytol. 186 786– 793. 10.1111/j.1469-8137.2010.03269.x 20569414 · DOI
- Ahmad M. Cashmore A. R. (1993). HY4 gene of A. thaliana encodes a protein with characteristics of a blue-light photoreceptor. Nature 366 162– 166. 10.1038/366162a0 8232555 · DOI
- Ahmad M. Grancher N. Heil M. Black R. C. Giovani B. Galland P. (2002). Action spectrum for cryptochrome-dependent hypocotyl growth inhibition in Arabidopsis. Plant Physiol. 129 774– 785. 10.1104/pp.010969 12068118 PMC161700 · DOI
- Aires A. Mota V. R. Saavedra M. J. Monteiro A. A. Simoes M. Rosa E. A. S. (2009). Initial in vitro evaluations of the antibacterial activities of glucosinolate enzymatic hydrolysis products against plant pathogenic bacteria. J. Appl. Microbiol. 106 2096– 2105. 10.1111/j.1365-2672.2009.04181.x 19291239 · DOI
- Alscher R. G. Donahue J. L. Cramer C. L. (1997). Reactive oxygen species and antioxidants: relationships in green cells. Physiol. Plant. 100 224– 233. 10.1034/j.1399-3054.1997.1000203.x 11841302 · DOI
- Appalasamy S. Lo K. Y. Ch’ng S. J. Nornadia K. Othman A. S. Chan L. K. (2014). Antimicrobial activity of artemisinin and precursor derived from in vitro plantlets of Artemisia annua L. Biomed. Res. Intern. 2014: 215872. PMC3915762 24575401
- Ballare C. L. Rousseau M. C. Searles P. S. Zaller J. G. Giordano C. V. Robson T. M. (2001). Impacts of solar ultraviolet-B radiation on terrestrial ecosystems of Tierra del Fuego (southern Argentina). an overview of recent progress. J. Photochem. Photobiol. B Biol. 62 67– 77. 10.1016/s1011-1344(01)00152-x 11693368 · DOI
- Bandurska H. Cieslak M. (2013). The interactive effect of water deficit and UV-B radiation on salicylic acid accumulation in barley roots and leaves. Environ. Exp. Bot. 94 9– 18. 10.1016/j.envexpbot.2012.03.001 · DOI
- Batra P. P. Harbin T. L. Howes C. D. Bernstein S. C. (1971). A study of the relationship of structure and activity of antimycin A in the induction of carotenoid synthesis in Mycobacterium marinum. J. Biol. Chem. 246 7125– 7130. 5129724
- Bayram O. Biesemann C. Krappmann S. Galland P. Braus G. H. (2008). More than a repair enzyme: Aspergillus nidulans photolyase-like CryA is a regulator of sexual development. Mol. Biol. Cell 19 3254– 3262. 10.1091/mbc.e08-01-0061 18495868 PMC2488289 · DOI
- Berrocal T. Mesa J. L. Pizarro J. L. Bazan B. Iglesias M. Aguayo A. T. (2008). Microporous vanadyl-arsenate with the template incorporated exhibiting sorption and catalytic properties. Chem. Commun. 2008 4738– 4740. 10.1039/b807250g 18830477 · DOI
- Berrocal-Tito G. M. Esquivel-Naranjo E. U. Horwitz B. A. Herrera-Estrella A. (2007). Trichoderma atroviride PHR1, a fungal photolyase responsible for DNA repair, autoregulates its own photoinduction. Eukaryot. Cell 6 1682– 1692. 10.1128/ec.00208-06 17545314 PMC2043357 · DOI
- Binder B. Y. Peebles C. A. Shanks J. V. San K. Y. (2009). The effects of UV-B stress on the production of terpenoid indole alkaloids in Catharanthus roseus hairy roots. Biotechnol. Prog. 25 861– 865. 19479674
- Binkert M. Crocco C. D. Ekundayo B. Lau K. Raffelberg S. Tilbrook K. (2016). Revisiting chromatin binding of the Arabidopsis UV-B photoreceptor UVR8. BMC Plant Biol. 16: 42. 10.1186/s12870-016-0732-5 26864020 PMC4750278 · DOI
- Binkert M. Kozma-Bognar L. Terecskei K. De Veylder L. Nagy F. Ulm R. (2014). UV-B-responsive association of the Arabidopsis bZIP transcription factor ELONGATED HYPOCOTYL5 with target genes, including its own promoter. Plant Cell 26 4200– 4213. 10.1105/tpc.114.130716 25351492 PMC4247584 · DOI
- Bluhm B. H. Dunkle L. D. (2008). PHL1 of Cercospora zeae-maydis encodes a member of the photolyase/cryptochrome family involved in UV protection and fungal development. Fungal Genet. Biol. 45 1364– 1372. 10.1016/j.fgb.2008.07.005 18682297 · DOI
- Blumenstein A. Vienken K. Tasler R. Purschwitz J. Veith D. Frankenberg-Dinkel N. (2005). The Aspergillus nidulans phytochrome FphA represses sexual development in red light. Curr. Biol. 15 1833– 1838. 10.1016/j.cub.2005.08.061 16243030 · DOI
- Bogatcheva E. Hanrahan C. Nikonenko B. de los Santos G. Reddy V. Chen P. (2011). Identification of SQ609 as a lead compound from a library of dipiperidines. Bioorg. Med. Chem. Lett. 21 5353– 5357. 10.1016/j.bmcl.2011.07.015 21807506 PMC3173259 · DOI
- Boubriak I. I. Grodzinsky D. M. Polischuk V. P. Naumenko V. D. Gushcha N. P. Micheev A. N. (2008). Adaptation and impairment of DNA repair function in pollen of Betula verrucosa and seeds of Oenothera biennis from differently radionuclide-contaminated sites of Chernobyl. Ann. Bot. 101 267– 276. 10.1093/aob/mcm276 17981881 PMC2711018 · DOI
- Braga G. U. Rangel D. E. Fernandes E. K. Flint S. D. Roberts D. W. (2015). Molecular and physiological effects of environmental UV radiation on fungal conidia. Curr. Genet. 61 405– 425. 10.1007/s00294-015-0483-0 25824285 · DOI
- Brandt S. von Stetten D. Gunther M. Hildebrandt P. Frankenberg-Dinkel N. (2008). The fungal phytochrome FphA from Aspergillus nidulans. J. Biol. Chem. 283 34605– 34614. 10.1074/jbc.m805506200 18931394 PMC3259886 · DOI
- Bray C. M. West C. E. (2005). DNA repair mechanisms in plants: crucial sensors and effectors for the maintenance of genome integrity. New Phytol. 168 511– 528. 10.1111/j.1469-8137.2005.01548.x 16313635 · DOI
- Briggs W. R. Beck C. F. Cashmore A. R. Christie J. M. Hughes J. Jarillo J. A. (2001). The phototropin family of photoreceptors. Plant Cell 13 993– 997. 10.2307/3871358 11424903 PMC1464709 · DOI
- Brown B. A. Cloix C. Jiang G. H. Kaiserli E. Herzyk P. Kliebenstein D. J. (2005). A UV-B-specific signaling component orchestrates plant UV protection. Proc. Natl. Acad. Sci. U.S.A. 102 18225– 18230. 10.1073/pnas.0507187102 16330762 PMC1312397 · DOI
- Bultreys A. Gheysen I. Maraite H. de Hoffmann E. (2001). Characterization of fluorescent and nonfluorescent peptide siderophores produced by Pseudomonas syringae strains and their potential use in strain identification. Appl. Environ. Microbiol. 67 1718– 1727. 10.1128/aem.67.4.1718-1727.2001 11282626 PMC92790 · DOI
- Campuzano V. Galland P. Alvarez M. I. Eslava A. P. (1996). Blue-light receptor requirement for gravitropism, autochemotropism and ethylene response in Phycomyces. Photochem. Photobiol. 63 686– 694. 10.1111/j.1751-1097.1996.tb05674.x 8628761 · DOI
- Campuzano V. Galland P. Senger H. Alvarez M. I. Eslava A. P. (1994). Isolation and characterization of phototropism mutants of Phycomyces insensitive to ultraviolet light. Curr. Genet. 26 49– 53. 10.1007/bf00326304 7954896 · DOI
- Canessa P. Schumacher J. Hevia M. A. Tudzynski P. Larrondo L. F. (2013). Assessing the effects of light on differentiation and virulence of the plant pathogen Botrytis cinerea: characterization of the white collar complex. PLoS One 8: e84223 10.1371/journal.pone.084223 PMC3877267 24391918 · DOI
- Cao Z. Buttani V. Losi A. Gartner W. (2008). A blue light inducible two-component signal transduction system in the plant pathogen Pseudomonas syringae pv. tomato. Biophys. J. 94 897– 905. 10.1529/biophysj.107.108977 17905842 PMC2186247 · DOI
- Carvalho S. D. Castillo J. A. (2018). Influence of light on plant-phyllosphere interaction. Front. Plant Sci. 9: 1482. 10.3389/fpls.2018.01482 30369938 PMC6194327 · DOI
- Castrillo M. Garcia-Martinez J. Avalos J. (2013). Light-dependent functions of the Fusarium fujikuroi CryD DASH cryptochrome in development and secondary metabolism. Appl. Environ. Microbiol. 79 2777– 2788. 10.1128/aem.03110-12 23417004 PMC3623198 · DOI
- Cazorla F. M. Codina J. C. Abad C. Arrebola E. Tores J. A. Murillo J. (2008). 62-kb plasmids harboring rulAB homologues confer UV-tolerance and epiphytic fitness to Pseudomonas syringae pv. syringae mango isolates. Microb. Ecol. 56 283– 291. 10.1007/s00248-007-9346-7 18058161 · DOI
- Cerovic Z. G. Ounis A. Cartelat A. Latouche G. Goulas Y. Meyer S. (2002). The use of chlorophyll fluorescence excitation spectra for the non-destructive in situ assessment of UV-absorbing compounds in leaves. Plant Cell Environ. 25 1663– 1676. 10.1046/j.1365-3040.2002.00942.x · DOI
- Chew F. S. (1988). Biological effects of glucosinolates. ACS Sym. Ser. 380 155– 181. 10.1021/bk-1988-0380.ch012 · DOI
- Choudhary K. K. Agrawal S. B. (2014). Cultivar specificity of tropical mung bean (Vigna radiata L.) to elevated ultraviolet-B: changes in antioxidative defense system, nitrogen metabolism and accumulation of jasmonic and salicylic acids. Environ. Exp. Bot. 99 122– 132. 10.1016/j.envexpbot.2013.11.006 · DOI
- Christie J. M. (2007). Phototropin blue-light receptors. Annu. Rev. Plant Biol. 58 21– 45. 10.1146/annurev.arplant.58.032806.103951 17067285 · DOI · Paper page
- Christie J. M. Arvai A. S. Baxter K. J. Heilmann M. Pratt A. J. O’Hara A. (2012). Plant UVR8 photoreceptor senses UV-B by tryptophan-mediated disruption of cross-dimer salt bridges. Science 335 1492– 1496. 10.1126/science.1218091 22323738 PMC3505452 · DOI
- Christie J. M. Briggs W. R. (2001). Blue light sensing in higher plants. J. Biol. Chem. 276 11457– 11460. 10.1074/jbc.r100004200 11279226 · DOI
- Christie J. M. Reymond P. Powell G. K. Bernasconi P. Raibekas A. A. Liscum E. (1998). Arabidopsis NPH1: a flavoprotein with the properties of a photoreceptor for phototropism. Science 282 1698– 1701. 10.1126/science.282.5394.1698 9831559 · DOI
- Christie J. M. Salomon M. Nozue K. Wada M. Briggs W. R. (1999). LOV (light, oxygen, or voltage) domains of the blue-light photoreceptor phototropin (nph1): binding sites for the chromophore flavin mononucleotide. Proc. Natl. Acad. Sci. U.S.A. 96 8779– 8783. 10.1073/pnas.96.15.8779 10411952 PMC17593 · DOI
- Christie J. M. Swartz T. E. Bogomolni R. A. Briggs W. R. (2002). Phototropin LOV domains exhibit distinct roles in regulating photoreceptor function. Plant J. Cell Mol. Biol. 32 205– 219. 10.1046/j.1365-313x.2002.01415.x 12383086 · DOI
- Chun L. Kawakami A. Christopher D. A. (2001). Phytochrome A mediates blue light and UV-A-dependent chloroplast gene transcription in green leaves. Plant Physiol. 125 1957– 1966. 10.1104/pp.125.4.1957 11299375 PMC88851 · DOI
- Clayton W. A. Albert N. W. Thrimawithana A. H. McGhie T. K. Deroles S. C. Schwinn K. E. (2018). UVR8-mediated induction of flavonoid biosynthesis for UVB tolerance is conserved between the liverwort Marchantia polymorpha and flowering plants. Plant J. 96 503– 517. 10.1111/tpj.14044 30044520 · DOI
- Cody Y. S. Gross D. C. (1987). Characterization of pyoverdin(pss), the fluorescent siderophore produced by Pseudomonas syringae pv. syringae. Appl. Environ. Microbiol. 53 928– 934. 10.1128/aem.53.5.928-934.1987 16347352 PMC203788 · DOI
- Cohrs K. C. Schumacher J. (2017). The two cryptochrome/photolyase family proteins fulfill distinct roles in DNA photorepair and regulation of conidiation in the gray mold fungus Botrytis cinerea. Appl. Environ. Microbiol. 83: e00812-17. PMC5561282 28667107
- Cushnie T. P. T. Cushnie B. Lamb A. J. (2014). Alkaloids: an overview of their antibacterial, antibiotic-enhancing and antivirulence activities. Int. J. Antimicrob. Agents 44 377– 386. 10.1016/j.ijantimicag.2014.06.001 25130096 · DOI
- Cushnie T. P. T. Lamb A. J. (2005). Antimicrobial activity of flavonoids. Int. J. Antimicrob. Agents 26 343– 356. 10.1016/j.ijantimicag.2005.09.002 16323269 PMC7127073 · DOI
- Demkura P. V. Abdala G. Baldwin I. T. Ballare C. L. (2010). Jasmonate-dependent and -independent pathways mediate specific effects of solar ultraviolet b radiation on leaf phenolics and antiherbivore defense. Plant Physiol. 152 1084– 1095. 10.1104/pp.109.148999 20007446 PMC2815854 · DOI
- Demkura P. V. Ballare C. L. (2012). UVR8 mediates UV-B-induced Arabidopsis defense responses against Botrytis cinerea by controlling sinapate accumulation. Mol. Plant 5 642– 652. 10.1093/mp/sss025 22447155 · DOI
- Dinh S. T. Galis I. Baldwin I. T. (2013). UVB radiation and 17-hydroxygeranyllinalool diterpene glycosides provide durable resistance against mirid (Tupiocoris notatus) attack in field-grown Nicotiana attenuata plants. Plant Cell Environ. 36 590– 606. 10.1111/j.1365-3040.2012.02598.x 22897424 · DOI
- Favory J. J. Stec A. Gruber H. Rizzini L. Oravecz A. Funk M. (2009). Interaction of COP1 and UVR8 regulates UV-B-induced photomorphogenesis and stress acclimation in Arabidopsis. EMBO J. 28 591– 601. 10.1038/emboj.2009.4 19165148 PMC2657586 · DOI
- Fedina I. Nedeva D. Georgieva K. Velitchkova M. (2009). Methyl jasmonate counteract UV-B stress in barley seedlings. J. Agron. Crop Sci. 195 204– 212. 10.1111/j.1439-037x.2008.00358.x · DOI
- Feher B. Kozma-Bognar L. Kevei E. Hajdu A. Binkert M. Davis S. J. (2011). Functional interaction of the circadian clock and UV RESISTANCE LOCUS 8-controlled UV-B signaling pathways in Arabidopsis thaliana. Plant J. 67 37– 48. 10.1111/j.1365-313x.2011.04573.x 21395889 · DOI
- Fofana B. McNally D. J. Labbe C. Boulanger R. Benhamou N. Seguin A. (2002). Milsana-induced resistance in powdery mildew-infected cucumber plants correlates with the induction of chalcone synthase and chalcone isomerase. Physiol. Mol. Plant 61 121– 132. 10.1006/pmpp.2002.0420 · DOI
- Froehlich A. C. Chen C. H. Belden W. J. Madeti C. Roenneberg T. Merrow M. (2010). Genetic and molecular characterization of a cryptochrome from the filamentous fungus Neurospora crassa. Eukaryot. Cell 9 738– 750. 10.1128/ec.00380-09 20305004 PMC2863965 · DOI
- Froehlich A. C. Liu Y. Loros J. J. Dunlap J. C. (2002). White Collar-1, a circadian blue light photoreceptor, binding to the frequency promoter. Science 297 815– 819. 10.1126/science.1073681 12098706 · DOI · Paper page
- Frohnmeyer H. Loyall L. Blatt M. R. Grabov A. (1999). Millisecond UV-B irradiation evokes prolonged elevation of cytosolic-free Ca2+ and stimulates gene expression in transgenic parsley cell cultures. Plant J. 20 109– 117. 10.1046/j.1365-313x.1999.00584.x 10571870 · DOI
- Fuglevand G. Jackson J. A. Jenkins G. I. (1996). UV-B, UV-A, and blue light signal transduction pathways interact synergistically to regulate chalcone synthase gene expression in Arabidopsis. Plant Cell 8 2347– 2357. 10.2307/3870473 8989887 PMC161357 · DOI
- Fujibe T. Watanabe K. Nakajima N. Ohashi Y. Mitsuhara I. Yamamoto K. T. (2000). Accumulation of pathogenesis-related proteins in tobacco leaves irradiated with UV-B. J. Plant Res. 113 387– 394. 10.1007/pl00013946 · DOI
- Fuller K. K. Loros J. J. Dunlap J. C. (2015). Fungal photobiology: visible light as a signal for stress, space and time. Curr. Genet. 61 275– 288. 10.1007/s00294-014-0451-0 25323429 PMC4401583 · DOI
- Gachomo E. W. Seufferheld M. J. Kotchoni S. O. (2010). Melanization of appressoria is critical for the pathogenicity of Diplocarpon rosae. Mol. Biol. Rep. 37 3583– 3591. 10.1007/s11033-010-0007-4 20204524 · DOI
- Galal A. M. Ross S. A. Jacob M. ElSohly M. A. (2005). Antifungal activity of artemisinin derivatives. J. Nat. Prod. 68 1274– 1276. 10.1021/np050074u 16124777 · DOI · Paper page
- Gangappa S. N. Botto J. F. (2016). The multifaceted roles of HY5 in plant growth and development. Mol. Plant 9 1353– 1365. 10.1016/j.molp.2016.07.002 27435853 · DOI
- Garcia-Esquivel M. Esquivel-Naranjo E. U. Hernandez-Onate M. A. Ibarra-Laclette E. Herrera-Estrella A. (2016). The Trichoderma atroviride cryptochrome/photolyase genes regulate the expression of blr1-independent genes both in red and blue light. Fungal Biol. 120 500– 512. 10.1016/j.funbio.2016.01.007 27020152 · DOI
- Gayan E. Manas P. Alvarez I. Condon S. (2013). Mechanism of the synergistic inactivation of Escherichia coli by UV-C light at mild temperatures. Appl. Environ. Microbiol. 79 4465– 4473. 10.1128/aem.00623-13 23686270 PMC3697489 · DOI
- Gill S. S. Anjum N. A. Gill R. Jha M. Tuteja N. (2015). DNA damage and repair in plants under ultraviolet and ionizing radiations. Sci. World J. 2015: 250158. PMC4333283 25729769
- Goldman G. H. McGuire S. L. Harris S. D. (2002). The DNA damage response in filamentous fungi. Fungal Genet. Biol. 35 183– 195. 10.1006/fgbi.2002.1344 11929209 · DOI
- Goncalves R. C. Lisboa H. C. Pombeiro-Sponchiado S. R. (2012). Characterization of melanin pigment produced by Aspergillus nidulans. World J. Microbiol. Biotechnol. 28 1467– 1474. 10.1007/s11274-011-0948-3 22805928 · DOI
- Gonzalez-Lamothe R. Mitchell G. Gattuso M. Diarra M. S. Malouin F. Bouarab K. (2009). Plant antimicrobial agents and their effects on plant and human pathogens. Intern. J. Mol. Sci. 10 3400– 3419. 10.3390/ijms10083400 20111686 PMC2812829 · DOI
- Gould K. S. McKelvie J. Markham K. R. (2002). Do anthocyanins function as antioxidants in leaves? Imaging of H2O2 in red and green leaves after mechanical injury. Plant Cell Environ. 25 1261– 1269. 10.1046/j.1365-3040.2002.00905.x · DOI
- Guimaraes A. C. Meireles L. M. Lemos M. F. Guimaraes M. C. C. Endringer D. C. Fronza M. (2019). Antibacterial activity of terpenes and terpenoids present in essential oils. Molecules 24: 2471. 10.3390/molecules24132471 31284397 PMC6651100 · DOI
- Gunasekera T. S. Paul N. D. (2007). Ecological impact of solar ultraviolet-B (UV-B: 320-290 nm) radiation on Corynebacterium aquaticum and Xanthomonas sp. colonization on tea phyllosphere in relation to blister blight disease incidence in the field. Lett. Appl. Microbiol. 44 513– 519. 10.1111/j.1472-765x.2006.02102.x 17451518 · DOI
- Gunasekera T. S. Sundin G. W. (2006). Role of nucleotide excision repair and photoreactivation in the solar UVB radiation survival of Pseudomonas syringae pv. syringae B728a. J. Appl. Microbiol. 100 1073– 1083. 10.1111/j.1365-2672.2006.02841.x 16630008 · DOI
- Halkier B. A. Gershenzon J. (2006). Biology and biochemistry of glucosinolates. Annu. Rev. Plant Biol. 57 303– 333. 10.1146/annurev.arplant.57.032905.105228 16669764 · DOI
- Han I. S. Cho H. Y. Moni A. Lee A. Y. Briggs W. R. (2013). Investigations on the photoregulation of chloroplast movement and leaf positioning in Arabidopsis. Plant Cell Physiol. 54 48– 56. 10.1093/pcp/pcs098 22782888 PMC3539441 · DOI
- Han K. Y. Chae S. K. Han D. M. (1998). The uvsI gene of Aspergillus nidulans required for UV-mutagenesis encodes a homolog to REV3, a subunit of the DNA polymerase zeta of yeast involved in translesion DNA synthesis. FEMS Microbiol. Lett. 164 13– 19. 10.1016/s0378-1097(98)00185-2 9675845 · DOI
- Harborne J. B. Williams C. A. (2000). Advances in flavonoid research since 1992. Phytochemistry 55 481– 504. 10.1016/s0031-9422(00)00235-1 11130659 · DOI · Paper page
- Hatakeyama S. Ito Y. Shimane A. Ishii C. Inoue H. (1998). Cloning and characterization of the yeast RAD1 homolog gene (mus-38) from Neurospora crassa: evidence for involvement in nucleotide excision repair. Curr. Genet. 33 276– 283. 10.1007/s002940050337 9560435 · DOI
- He Q. Cheng P. Yang Y. Wang L. Gardner K. H. Liu Y. (2002). White collar-1, a DNA binding transcription factor and a light sensor. Science 297 840– 843. 10.1126/science.1072795 12098705 · DOI · Paper page
- He Q. Liu Y. (2005). Molecular mechanism of light responses in Neurospora: from light-induced transcription to photoadaptation. Genes Dev. 19 2888– 2899. 10.1101/gad.1369605 16287715 PMC1315395 · DOI
- Heijde M. Ulm R. (2012). UV-B photoreceptor-mediated signalling in plants. Trends Plant Sci. 17 230– 237. 10.1016/j.tplants.2012.01.007 22326562 · DOI
- Heinze M. Hanschen F. S. Wiesner-Reinhold M. Baldermann S. Grafe J. Schreiner M. (2018). Effects of developmental stages and reduced UVB and Low UV conditions on plant secondary metabolite profiles in Pak Choi (Brassica rapa subsp. chinensis). J. Agric. Food Chem. 66 1678– 1692. 10.1021/acs.jafc.7b03996 29397716 · DOI
- Herrera-Vasquez A. Carvallo L. Blanco F. Tobar M. Villarroel-Candia E. Vicente-Carbajosa J. (2015). Transcriptional control of glutaredoxin GRXC9 expression by a salicylic acid-dependent and NPR1-independent pathway in Arabidopsis. Plant Mol. Biol. Rep. 33 624– 637. 10.1007/s11105-014-0782-5 26696694 PMC4677692 · DOI
- Hideg E. Jansen M. A. Strid A. (2013). UV-B exposure, ROS, and stress: inseparable companions or loosely linked associates? Trends Plant Sci. 18 107– 115. 10.1016/j.tplants.2012.09.003 23084465 · DOI
- Hirano S. S. Upper C. D. (2000). Bacteria in the leaf ecosystem with emphasis on Pseudomonas syringae-a pathogen, ice nucleus, and epiphyte. Microbiol. Mol. Biol. Rev. 64 624– 653. 10.1128/mmbr.64.3.624-653.2000 10974129 PMC99007 · DOI
- Hohm T. Preuten T. Fankhauser C. (2013). Phototropism: translating light into directional growth. Am. J. Bot. 100 47– 59. 10.3732/ajb.1200299 23152332 · DOI
- Hollosy F. (2002). Effects of ultraviolet radiation on plant cells. Micron 33 179– 197. 10.1016/s0968-4328(01)00011-7 11567887 · DOI
- Holtkotte X. Ponnu J. Ahmad M. Hoecker U. (2017). The blue light-induced interaction of cryptochrome 1 with COP1 requires SPA proteins during Arabidopsis light signaling. PLoS Genet. 13: e1007044 10.1371/journal.pone.1007044 PMC5648270 28991901 · DOI
- Hraiech S. Bregeon F. Brunel J. M. Rolain J. M. Lepidi H. Andrieu V. (2012). Antibacterial efficacy of inhaled squalamine in a rat model of chronic Pseudomonas aeruginosa pneumonia. J. Antimicrob. Chemother. 67 2452– 2458. 10.1093/jac/dks230 22744759 · DOI
- Idnurm A. Rodriguez-Romero J. Corrochano L. M. Sanz C. Iturriaga E. A. Eslava A. P. (2006). The Phycomyces madA gene encodes a blue-light photoreceptor for phototropism and other light responses. Proc. Natl. Acad. Sci. U.S.A. 103 4546– 4551. 10.1073/pnas.0600633103 16537433 PMC1450208 · DOI
- Inoue H. (2011). Exploring the processes of DNA repair and homologous integration in Neurospora. Mutat. Res. 728 1– 11. 10.1016/j.mrrev.2011.06.003 21757027 · DOI
- Isman M. B. (2006). Botanical insecticides, deterrents, and repellents in modern agriculture and an increasingly regulated world. Annu. Rev. Entomol. 51 45– 66. 10.1146/annurev.ento.51.110104.151146 16332203 · DOI
- Izaguirre M. M. Mazza C. A. Svatos A. Baldwin I. T. Ballare C. L. (2007). Solar ultraviolet-B radiation and insect herbivory trigger partially overlapping phenolic responses in Nicotiana attenuata and Nicotiana longiflora. Ann. Bot. 99 103– 109. 10.1093/aob/mcl226 17210605 PMC2802969 · DOI
- Izaguirre M. M. Scopel A. L. Baldwin I. T. Ballare C. L. (2003). Convergent responses to stress. Solar ultraviolet-B radiation and Manduca sexta herbivory elicit overlapping transcriptional responses in field-grown plants of Nicotiana longiflora. Plant Physiol. 132 1755– 1767. 10.1104/pp.103.024323 12913133 PMC181263 · DOI
- Jenkins G. I. (2017). Photomorphogenic responses to ultraviolet-B light. Plant Cell Environ. 40 2544– 2557. 10.1111/pce.12934 28183154 · DOI
- Jenkins G. I. Long J. C. Wade H. K. Shenton M. R. Bibikova T. N. (2001). UV and blue light signalling: pathways regulating chalcone synthase gene expression in Arabidopsis. New Phytol. 151 121– 131. 10.1046/j.1469-8137.2001.00151.x 33873370 · DOI
- Jiang L. Wang Y. Olof Bjorn L. He J. X. Li S. (2012). Sensing of UV-B radiation by plants. Plant Signal. Behav. 7 999– 1003. 22751358 PMC3474703
- Jones L. A. Worobo R. W. Smart C. D. (2014). UV light inactivation of human and plant pathogens in unfiltered surface irrigation water. Appl. Environ. Microbiol. 80 849– 854. 10.1128/aem.02964-13 24242253 PMC3911201 · DOI
- Kadivar H. Stapleton A. E. (2003). Ultraviolet radiation alters maize phyllosphere bacterial diversity. Microb. Ecol. 45 353– 361. 10.1007/s00248-002-1065-5 12704563 · DOI
- Kaiserli E. Jenkins G. I. (2007). UV-B promotes rapid nuclear translocation of the Arabidopsis UV-B specific signaling component UVR8 and activates its function in the nucleus. Plant Cell 19 2662– 2673. 10.1105/tpc.107.053330 17720867 PMC2002606 · DOI
- Kasahara M. Swartz T. E. Olney M. A. Onodera A. Mochizuki N. Fukuzawa H. (2002). Photochemical properties of the flavin mononucleotide-binding domains of the phototropins from Arabidopsis, rice, and Chlamydomonas reinhardtii. Plant Physiol. 129 762– 773. 10.1104/pp.002410 12068117 PMC161699 · DOI
- Keller N. P. (2019). Fungal secondary metabolism: regulation, function and drug discovery. Nat. Rev. Microbiol. 17 167– 180. 10.1038/s41579-018-0121-1 30531948 PMC6381595 · DOI
- Kelner A. (1949). Photoreactivation of ultraviolet-irradiated Escherichia Coli, with special reference to the dose-reduction principle and to ultraviolet-induced mutation. J. Bacteriol. 58 511– 522. 10.1128/jb.58.4.511-522.1949 16561813 PMC385659 · DOI
- Kim B. C. Tennessen D. J. Last R. L. (1998). UV-B-induced photomorphogenesis in Arabidopsis thaliana. Plant J. 15 667– 674. 10.1046/j.1365-313x.1998.00246.x 9778848 · DOI
- Kim J. J. Sundin G. W. (2000). Regulation of the rulAB mutagenic DNA repair operon of Pseudomonas syringae by UV-B (290 to 320 nanometers) radiation and analysis of rulAB-mediated mutability in vitro and in planta. J. Bacteriol. 182 6137– 6144. 10.1128/jb.182.21.6137-6144.2000 11029435 PMC94749 · DOI
- Kim J. J. Sundin G. W. (2001). Construction and analysis of photolyase mutants of Pseudomonas aeruginosa and Pseudomonas syringae: contribution of photoreactivation, nucleotide excision repair, and mutagenic DNA repair to cell survival and mutability following exposure to UV-B radiation. Appl. Environ. Microbiol. 67 1405– 1411. 10.1128/aem.67.4.1405-1411.2001 11282583 PMC92747 · DOI
- Kim W. Y. Fujiwara S. Suh S. S. Kim J. Kim Y. Han L. (2007). ZEITLUPE is a circadian photoreceptor stabilized by GIGANTEA in blue light. Nature 449 356– 360. 10.1038/nature06132 17704763 · DOI
- Koru O. Toksoy F. Acikel C. H. Tunca Y. M. Baysallar M. Uskudar Guclu A. (2007). In vitro antimicrobial activity of propolis samples from different geographical origins against certain oral pathogens. Anaerobe 13 140– 145. 10.1016/j.anaerobe.2007.02.001 17475517 · DOI
- Kovacs V. Gondor O. K. Szalai G. Majlath I. Janda T. Pal M. (2014). UV-B radiation modifies the acclimation processes to drought or cadmium in wheat. Environ. Exp. Bot. 100 122– 131. 10.1016/j.envexpbot.2013.12.019 · DOI
- Kraiselburd I. Moyano L. Carrau A. Tano J. Orellano E. G. (2017). Bacterial photosensory proteins and their role in plant-pathogen interactions. Photochem. Photobiol. 93 666– 674. 10.1111/php.12754 28500702 · DOI
- Kubo Y. Furusawa I. (1991). “ Melanin biosynthesis,” in The Fungal Spore and Disease Initiation in Plants and Animals, eds Cole G. T. Hoch H. C. (Boston, MA: Springer), 205– 218.
- Kytridis V. P. Manetas Y. (2006). Mesophyll versus epidermal anthocyanins as potential in vivo antioxidants: evidence linking the putative antioxidant role to the proximity of oxy-radical source. J. Exp. Bot. 57 2203– 2210. 10.1093/jxb/erj185 16714309 · DOI
- Larson R. A. Marley K. A. (1984). Quenching of singlet oxygen by alkaloids and related nitrogen-heterocycles. Phytochemistry 23 2351– 2354. 10.1016/s0031-9422(00)80550-6 · DOI
- Li J. Ou-Lee T. M. Raba R. Amundson R. G. Last R. L. (1993). Arabidopsis flavonoid mutants are hypersensitive to UV-B irradiation. Plant Cell 5 171– 179. 10.1105/tpc.5.2.171 12271060 PMC160260 · DOI
- Li N. Teranishi M. Yamaguchi H. Matsushita T. Watahiki M. K. Tsuge T. (2015). UV-B-induced CPD photolyase gene expression is regulated by UVR8-dependent and -independent pathways in Arabidopsis. Plant Cell Physiol. 56 2014– 2023. 10.1093/pcp/pcv121 26272552 · DOI
- Liang T. Mei S. Shi C. Yang Y. Peng Y. Ma L. (2018). UVR8 interacts with BES1 and BIM1 to regulate transcription and photomorphogenesis in Arabidopsis. Dev. Cell 44 512– 523.e515. 29398622
- Liu C. C. Chi C. Jin L. J. Zhu J. Yu J. Q. Zhou Y. H. (2018). The bZip transcription factor HY5 mediates CRY1a-induced anthocyanin biosynthesis in tomato. Plant Cell Environ. 41 1762– 1775. 10.1111/pce.13171 29566255 · DOI
- Liu H. Cao X. Liu X. Xin R. Wang J. Gao J. (2017). UV-B irradiation differentially regulates terpene synthases and terpene content of peach. Plant Cell Environ. 40 2261– 2275. 10.1111/pce.13029 28722114 · DOI
- López-Gresa M. P. Torres C. Campos L. Lisón P. Rodrigo I. Bellés J. M. (2011). Identification of defence metabolites in tomato plants infected by the bacterial pathogen Pseudomonas syringae. Environ. Exp. Bot. 74 216– 228. 10.1016/j.envexpbot.2011.06.003 · DOI
- Lu Y. Chen Q. Bu Y. Luo R. Hao S. Zhang J. (2017). Flavonoid accumulation plays an important role in the rust resistance of Malus plant leaves. Front. Plant Sci. 8: 1286. 10.3389/fpls.2017.01286 28769974 PMC5514348 · DOI
- Lu Y. K. Sun K. H. Shen W. C. (2005). Blue light negatively regulates the sexual filamentation via the Cwc1 and Cwc2 proteins in Cryptococcus neoformans. Mol. Microbiol. 56 480– 491. 10.1111/j.1365-2958.2005.04549.x 15813738 · DOI
- Luque E. M. Gutierrez G. Navarro-Sampedro L. Olmedo M. Rodriguez-Romero J. Ruger-Herreros C. (2012). A relationship between carotenoid accumulation and the distribution of species of the fungus Neurospora in spain. PLoS One 7: e33658. 10.1371/journal.pone.0033658 22448263 PMC3309001 · DOI
- Ma Y. Ding S. Fei Y. Liu G. Jang H. Fang J. (2019). Antimicrobial activity of anthocyanins and catechins against foodborne pathogens Escherichia coli and Salmonella. Food Control 106: 106712 10.1016/j.foodcont.2019.106712 · DOI
- Mackerness S. A. H. Surplus S. L. Blake P. John C. F. Buchanan-Wollaston V. Jordan B. R. (1999). Ultraviolet-B-induced stress and changes in gene expression in Arabidopsis thaliana: role of signalling pathways controlled by jasmonic acid, ethylene and reactive oxygen species. Plant Cell Environ. 22 1413– 1423. 10.1046/j.1365-3040.1999.00499.x · DOI
- Mageroy M. H. Kowalik E. H. Folta K. M. Shinkle J. (2010). Evidence of physiological phototropin1 (phot1) action in response to UV-C illumination. Plant Signal. Behav. 5 1204– 1210. 10.4161/psb.5.10.12413 20861684 PMC3115349 · DOI
- Mahdavian K. Ghorbanli M. Kalantari K. M. (2008). Role of salicylic acid in regulating ultraviolet radiation-induced oxidative stress in pepper leaves. Russ. J. Plant Phys. 55 560– 563. 10.1134/s1021443708040195 · DOI
- Mandalari C. Losi A. Gartner W. (2013). Distance-tree analysis, distribution and co-presence of bilin- and flavin-binding prokaryotic photoreceptors for visible light. Photochem. Photobiol. Sci. 12 1144– 1157. 10.1039/c3pp25404f 23467500 · DOI
- Martin-Rojas V. Greiner H. Wagner T. Fukshansky L. Cerda-Olmedo E. (1995). Specific tropism caused by ultraviolet C radiation in Phycomyces. Planta 197 63– 68. 11540146
- Mayer R. Stecher G. Wuerzner R. Silva R. C. Sultana T. Trojer L. (2008). Proanthocyanidins: target compounds as antibacterial agents. J. Agric. Food Chem. 56 6959– 6966. 10.1021/jf800832r 18636738 · DOI
- McNally D. J. Wurms K. V. Labbe C. Belanger R. R. (2003). Synthesis of C-glycosyl flavonoid phytoalexins as a site-specific response to fungal penetration in cucumber. Physiol. Mol. Plant 63 293– 303. 10.1016/j.pmpp.2004.03.005 · DOI
- Mewis I. Appel H. M. Hom A. Raina R. Schultz J. C. (2005). Major signaling pathways modulate Arabidopsis glucosinolate accumulation and response to both phloem-feeding and chewing insects. Plant Physiol. 138 1149– 1162. 10.1104/pp.104.053389 15923339 PMC1150428 · DOI
- Mewis I. Schreiner M. Nguyen C. N. Krumbein A. Ulrichs C. Lohse M. (2012). UV-B irradiation changes specifically the secondary metabolite profile in Broccoli sprouts: induced signaling overlaps with defense response to biotic stressors. Plant Cell Physiol. 53 1546– 1560. 10.1093/pcp/pcs096 22773681 PMC3439869 · DOI
- Mewis I. Tokuhisa J. G. Schultz J. C. Appel H. M. Ulrichs C. Gershenzon J. (2006). Gene expression and glucosinolate accumulation in Arabidopsis thaliana in response to generalist and specialist herbivores of different feeding guilds and the role of defense signaling pathways. Phytochemistry 67 2450– 2462. 10.1016/j.phytochem.2006.09.004 17049571 · DOI
- Michaelakis A. Papachristos D. Kimbaris A. Koliopoulos G. Giatropoulos A. Polissiou M. G. (2009). Citrus essential oils and four enantiomeric pinenes against Culex pipiens (Diptera: Culicidae). Parasitol. Res. 105 769– 773. 10.1007/s00436-009-1452-7 19424721 · DOI
- Mintoff S. J. L. Rookes J. E. Cahill D. M. (2015). Sub-lethal UV-C radiation induces callose, hydrogen peroxide and defence-related gene expression in Arabidopsis thaliana. Plant Biol. 17 703– 711. 10.1111/plb.12286 25381714 · DOI
- Mithen R. F. (2001). Glucosinolates and their degradation products. Adv. Bot. Res. 35 213– 262. 10.1016/s0065-2296(01)35008-5 · DOI
- Molnar P. Deli J. Tanaka T. Kann Y. Tani S. Gyemant N. (2010). Carotenoids with anti-Helicobacter pylori activity from golden delicious apple. Phytother. Res. 24 644– 648. 19591126
- Moon Y. J. Kim S. I. Chung Y. H. (2012). Sensing and responding to UV-A in Cyanobacteria. Intern. J. Mol. Sci. 13 16303– 16332. 10.3390/ijms131216303 23208372 PMC3546692 · DOI
- Morales L. O. Brosche M. Vainonen J. Jenkins G. I. Wargent J. J. Sipari N. (2013). Multiple roles for UV RESISTANCE LOCUS8 in regulating gene expression and metabolite accumulation in Arabidopsis under solar ultraviolet radiation. Plant Physiol. 161 744– 759. 10.1104/pp.112.211375 23250626 PMC3561016 · DOI
- Moreira-Rodriguez M. Nair V. Benavides J. Cisneros-Zevallos L. Jacobo-Velazquez D. A. (2017). UVA, UVB light, and methyl jasmonate, alone or combined, redirect the biosynthesis of Glucosinolates, Phenolics, Carotenoids, and chlorophylls in Broccoli sprouts. Intern. J. Mol. Sci. 18: 2330. 10.3390/ijms18112330 29113068 PMC5713299 · DOI
- Nsa I. Y. Karunarathna N. Liu X. Huang H. Boetteger B. Bell-Pedersen D. (2015). A novel cryptochrome-dependent oscillator in Neurospora crassa. Genetics 199 233– 245. 10.1534/genetics.114.169441 25361899 PMC4286687 · DOI
- Nuutinen T. (2018). Medicinal properties of terpenes found in Cannabis sativa and Humulus lupulus. Eur. J. Med. Chem. 157 198– 228. 10.1016/j.ejmech.2018.07.076 30096653 · DOI
- Oelmuller R. Mohr H. (1985). Mode of coaction between blue/UV light and light absorbed by phytochrome in light-mediated anthocyanin formation in the milo (Sorghum vulgare Pers.) seedling. Proc. Natl. Acad. Sci. U.S.A. 82 6124– 6128. 10.1073/pnas.82.18.6124 16593604 PMC390712 · DOI
- O’Hara A. Headland L. R. Diaz-Ramos L. A. Morales L. O. Strid A. Jenkins G. I. (2019). Regulation of Arabidopsis gene expression by low fluence rate UV-B independently of UVR8 and stress signaling. Photochem. Photobiol. Sci. 18 1675– 1684. 10.1039/c9pp00151d 31218318 · DOI
- Okajima K. Matsuoka D. Tokutomi S. (2011). LOV2-linker-kinase phosphorylates LOV1-containing N-terminal polypeptide substrate via photoreaction of LOV2 in Arabidopsis phototropin1. FEBS Lett. 585 3391– 3395. 10.1016/j.febslet.2011.10.003 22001205 · DOI
- Oppezzo O. J. (2012). Contribution of UVB radiation to bacterial inactivation by natural sunlight. J. Photochem. Photobiol. B Biol. 115 58– 62. 10.1016/j.jphotobiol.2012.06.011 22819168 · DOI
- Oravecz A. Baumann A. Máté Z. Brzezinska A. Molinier J. Oakeley E. J. (2006). CONSTITUTIVELY PHOTOMORPHOGENIC1 is required for the UV-B response in Arabidopsis. Plant Cell 18 1975– 1990. 10.1105/tpc.105.040097 16829591 PMC1533968 · DOI
- Ozcelik B. (2007). Fungi/bactericidal and static effects of ultraviolet light in 254 and 354 nm Wavelengths. Res. J. Microbiol. 2 42– 49. 10.3923/jm.2007.42.49 · DOI
- Parhi A. Kelley C. Kaul M. Pilch D. S. LaVoie E. J. (2012). Antibacterial activity of substituted 5-methylbenzo[c]phenanthridinium derivatives. Bioorg. Med. Chem. Lett. 22 7080– 7083. 10.1016/j.bmcl.2012.09.097 23084900 PMC3947833 · DOI
- Pereira J. A. Oliveira I. Sousa A. Valentāo P. Andrade P. B. Ferreira I. C. F. R. (2007). Walnut (Juglans regia L.) leaves: Phenolic compounds, antibacterial activity and antioxidant potential of different cultivars. Food Chem. Toxicol. 45 2287– 2295. 10.1016/j.fct.2007.06.004 17637491 · DOI
- Rai N. O’Hara A. Farkas D. Safronov O. Ratanasopa K. Wang F. (2020). The photoreceptor UVR8 mediates the perception of both UV-B and UV-A wavelengths up to 350 nm of sunlight with responsivity moderated by cryptochromes. Plant Cell Environ. 43 1513– 1527. 10.1111/pce.13752 32167576 · DOI
- Rai R. Meena R. P. Smita S. S. Shukla A. Rai S. K. Pandey-Rai S. (2011). UV-B and UV-C pre-treatments induce physiological changes and artemisinin biosynthesis in Artemisia annua L. - an antimalarial plant. J. Photochem. Photobiol. B Biol. 105 216– 225. 10.1016/j.jphotobiol.2011.09.004 22019553 · DOI
- Ramani S. Chelliah J. (2007). UV-B-induced signaling events leading to enhanced-production of catharanthine in Catharanthus roseus cell suspension cultures. BMC Plant Biol. 7: 61. 10.1186/1471-2229-7-61 17988378 PMC2213653 · DOI
- Rao B. K. Kumar P. Rao S. Gurung B. (2011). Bactericidal effect of ultraviolet C (UVC), direct and filtered through transparent plastic, on gram-positive cocci: an in vitro study. Ostomy Wound Manag. 57 46– 52. 21904015
- Rauha J. P. Remes S. Heinonen M. Hopia A. Kahkonen M. Kujala T. (2000). Antimicrobial effects of Finnish plant extracts containing flavonoids and other phenolic compounds. Int. J. Food Microbiol. 56 3– 12. 10.1016/s0168-1605(00)00218-x 10857921 · DOI
- Ricci A. Dramis L. Shah R. Gartner W. Losi A. (2015). Visualizing the relevance of bacterial blue- and red-light receptors during plant-pathogen interaction. Environ. Microbiol. Rep. 7 795– 802. 10.1111/1758-2229.12320 26147514 · DOI
- Rigonato J. Alvarenga D. O. Andreote F. D. Dias A. C. Melo I. S. Kent A. (2012). Cyanobacterial diversity in the phyllosphere of a mangrove forest. FEMS Microbiol. Ecol. 80 312– 322. 10.1111/j.1574-6941.2012.01299.x 22611551 · DOI
- Robson T. M. Klem K. Urban O. Jansen M. A. (2015). Re-interpreting plant morphological responses to UV-B radiation. Plant Cell Environ. 38 856– 866. 10.1111/pce.12374 24890713 · DOI
- Rombouts S. Volckaert A. Venneman S. Declercq B. Vandenheuvel D. Allonsius C. N. (2016). Characterization of novel bacteriophages for biocontrol of bacterial blight in leek caused by Pseudomonas syringae pv. porri. Front. Microbiol. 7: 279. 10.3389/fmicb.2016.00279 27014204 PMC4791379 · DOI
- Sakai T. Kagawa T. Kasahara M. Swartz T. E. Christie J. M. Briggs W. R. (2001). Arabidopsis nph1 and npl1: blue light receptors that mediate both phototropism and chloroplast relocation. Proc. Natl. Acad. Sci. U.S.A. 98 6969– 6974. 10.1073/pnas.101137598 11371609 PMC34462 · DOI · Paper page
- Saladino F. Bordin K. Luciano F. B. Franzón M. F. Mañes J. Meca G. (2016). “ Antimicrobial Activity of the glucosinolates,” in Glucosinolates, eds Mérillon J.-M. Ramawat K. G. (Cham: Springer International Publishing), 1– 26. 10.1007/978-3-319-26479-0_18-1 · DOI
- Salehi B. Upadhyay S. Erdogan O. I. Kumar J. A. Rad J. S. Cho W. C. (2019). Therapeutic potential of alpha- and beta-pinene: a miracle gift of nature. Biomolecules 9: 738. 10.3390/biom9110738 31739596 PMC6920849 · DOI
- Sancar A. (1996). DNA excision repair. Annu. Rev. Biochem. 65 43– 81. 8811174
- Sancar A. (2003). Structure and function of DNA photolyase and cryptochrome blue-light photoreceptors. Chem. Rev. 103 2203– 2237. 10.1021/cr0204348 12797829 · DOI
- Sancar G. B. Sancar A. (1987). Structure and function of DNA photolyases. Trends Biochem. Sci. 12 259– 261. 10.1016/0968-0004(87)90130-7 · DOI
- Sang Y. Li Q. H. Rubio V. Zhang Y. C. Mao J. Deng X. W. (2005). N-terminal domain-mediated homodimerization is required for photoreceptor activity of Arabidopsis CRYPTOCHROME 1. Plant Cell 17 1569– 1584. 10.1105/tpc.104.029645 15805487 PMC1091775 · DOI
- Sanz C. Rodriguez-Romero J. Idnurm A. Christie J. M. Heitman J. Corrochano L. M. (2009). Phycomyces MADB interacts with MADA to form the primary photoreceptor complex for fungal phototropism. Proc. Natl. Acad. Sci. U.S.A. 106 7095– 7100. 10.1073/pnas.0900879106 19380729 PMC2678449 · DOI
- Saxena C. Wang H. Kavakli I. H. Sancar A. Zhong D. (2005). Ultrafast dynamics of resonance energy transfer in cryptochrome. J. Am. Chem. Soc. 127 7984– 7985. 10.1021/ja0421607 15926801 · DOI
- Schäfer E. Nagy F. (2006). Photomorphogenesis in Plants and Bacteria: Function and Signal Transduction Mechanisms. Dordrecht: Springer.
- Schenke D. Utami H. P. Zhou Z. Gallegos M. T. Cai D. (2019). Suppression of UV-B stress induced flavonoids by biotic stress: is there reciprocal crosstalk? Plant Physiol. Biochem. 134 53– 63. 10.1016/j.plaphy.2018.06.026 30558728 · DOI
- Schmoll M. Esquivel-Naranjo E. U. Herrera-Estrella A. (2010). Trichoderma in the light of day–physiology and development. Fungal Genet. Biol. 47 909– 916. 10.1016/j.fgb.2010.04.010 20466064 PMC2954361 · DOI
- Schumacher J. (2016). DHN melanin biosynthesis in the plant pathogenic fungus Botrytis cinerea is based on two developmentally regulated key enzyme (PKS)-encoding genes. Mol. Microbiol. 99 729– 748. 10.1111/mmi.13262 26514268 · DOI · Paper page
- Selby C. P. Sancar A. (2006). A cryptochrome/photolyase class of enzymes with single-stranded DNA-specific photolyase activity. Proc. Natl. Acad. Sci. U.S.A. 103 17696– 17700. 10.1073/pnas.0607993103 17062752 PMC1621107 · DOI
- Sharma A. Sharma B. Hayes S. Kerner K. Hoecker U. Jenkins G. I. (2019). UVR8 disrupts stabilisation of PIF5 by COP1 to inhibit plant stem elongation in sunlight. Nat. Commun. 10: 4417. PMC6764944 31562307
- Sharma C. Al Kaabi J. M. Nurulain S. M. Goyal S. N. Kamal M. A. Ojha S. (2016). Polypharmacological properties and therapeutic potential of beta-caryophyllene: a dietary phytocannabinoid of pharmaceutical promise. Curr. Pharm. Des. 22 3237– 3264. 10.2174/1381612822666160311115226 26965491 · DOI
- Sharrock R. A. (2008). The phytochrome red/far-red photoreceptor superfamily. Genome Biol. 9: 230. 10.1186/gb-2008-9-8-230 18771590 PMC2575506 · DOI
- Shimura M. Ito Y. Ishii C. Yajima H. Linden H. Harashima T. (1999). Characterization of a Neurospora crassa photolyase-deficient mutant generated by repeat induced point mutation of the phr gene. Fungal Genet. Biol. 28 12– 20. 10.1006/fgbi.1999.1158 10512668 · DOI
- Shin D. H. Choi M. Kim K. Bang G. Cho M. Choi S. B. (2013). HY5 regulates anthocyanin biosynthesis by inducing the transcriptional activation of the MYB75/PAP1 transcription factor in Arabidopsis. FEBS Lett. 587 1543– 1547. 10.1016/j.febslet.2013.03.037 23583450 · DOI
- Shinomura T. Nagatani A. Hanzawa H. Kubota M. Watanabe M. Furuya M. (1996). Action spectra for phytochrome A- and B-specific photoinduction of seed germination in Arabidopsis thaliana. Proc. Natl. Acad. Sci. U.S.A. 93 8129– 8133. 10.1073/pnas.93.15.8129 8755615 PMC38887 · DOI
- Silva F. Torres-Martinez S. Garre V. (2006). Distinct white collar-1 genes control specific light responses in Mucor circinelloides. Mol. Microbiol. 61 1023– 1037. 10.1111/j.1365-2958.2006.05291.x 16879651 · DOI
- Singh P. Santoni S. Weber A. This P. Peros J. P. (2019). Understanding the phyllosphere microbiome assemblage in grape species (Vitaceae) with amplicon sequence data structures. Sci. Rep. 9: 14294. PMC6778096 31586145
- Sinha R. P. Hader D. P. (2002). UV-induced DNA damage and repair: a review. Photochem. Photobiol. Sci. 1 225– 236. 12661961
- Sinha R. P. Singh S. P. Hader D. P. (2007). Database on mycosporines and mycosporine-like amino acids (MAAs) in fungi, cyanobacteria, macroalgae, phytoplankton and animals. J. Photochem. Photobiol. B Biol. 89 29– 35. 10.1016/j.jphotobiol.2007.07.006 17826148 · DOI · Paper page
- Steiner U. Oerke E. C. (2007). Localized melanization of appressoria is required for pathogenicity of Venturia inaequalis. Phytopathology 97 1222– 1230. 10.1094/phyto-97-10-1222 18943680 · DOI
- Stevenson P. C. Haware M. P. (1999). Maackiain in Cicer bijugum Rech. f. associated with resistance to Botrytis grey mould. Biochem. Syst. Ecol. 27 761– 767. 10.1016/s0305-1978(99)00023-x · DOI
- Stracke R. Favory J. J. Gruber H. Bartelniewoehner L. Bartels S. Binkert M. (2010a). The Arabidopsis bZIP transcription factor HY5 regulates expression of the PFG1/MYB12 gene in response to light and ultraviolet-B radiation. Plant Cell Environ. 33 88– 103. 10.1111/j.1365-313x.2011.04670.x 19895401 · DOI
- Stracke R. Jahns O. Keck M. Tohge T. Niehaus K. Fernie A. R. (2010b). Analysis of PRODUCTION OF FLAVONOL GLYCOSIDES-dependent flavonol glycoside accumulation in Arabidopsis thaliana plants reveals MYB11-, MYB12- and MYB111-independent flavonol glycoside accumulation. New Phytol. 188 985– 1000. 10.1111/j.1469-8137.2010.03421.x 20731781 · DOI
- Stratmann J. W. Stelmach B. A. Weller E. W. Ryan C. A. (2000). UVB/UVA radiation activates a 48 kDa myelin basic protein kinase and potentiates wound signaling in tomato leaves. Photochem. Photobiol. 71 116– 123. 10.1562/0031-8655(2000)0710116sipuur2.0.co2 10687382 · DOI
- Sundin G. W. Jacobs J. L. (1999). Ultraviolet radiation (UVR) sensitivity analysis and UVR survival strategies of a bacterial community from the phyllosphere of field-grown peanut (Arachis hypogeae L.). Microb. Ecol. 38 27– 38. 10.1007/s002489900152 10384007 · DOI
- Sundin G. W. Murillo J. (1999). Functional analysis of the Pseudomonas syringae rulAB determinant in tolerance to ultraviolet B (290-320 nm) radiation and distribution of rulAB among P. syringae pathovars. Environ. Microbiol. 1 75– 87. 10.1046/j.1462-2920.1999.00008.x 11207720 · DOI
- Suthaparan A. Stensvand A. Solhaug K. A. Torre S. Telfer K. H. Ruud A. K. (2014). Suppression of cucumber powdery mildew by supplemental UV-B radiation in greenhouses can be augmented or reduced by background radiation quality. Plant Dis. 98 1349– 1357. 10.1094/pdis-03-13-0222-re 30703932 · DOI
- Tagua V. G. Pausch M. Eckel M. Gutierrez G. Miralles-Duran A. Sanz C. (2015). Fungal cryptochrome with DNA repair activity reveals an early stage in cryptochrome evolution. Proc. Natl. Acad. Sci. U.S.A. 112 15130– 15135. 10.1073/pnas.1514637112 26578805 PMC4679004 · DOI
- Takahashi M. Teranishi M. Ishida H. Kawasaki J. Takeuchi A. Yamaya T. (2011). Cyclobutane pyrimidine dimer (CPD) photolyase repairs ultraviolet-B-induced CPDs in rice chloroplast and mitochondrial DNA. Plant J. Cell Mol. Biol. 66 433– 442. 10.1111/j.1365-313x.2011.04500.x 21251107 · DOI
- Takano H. (2016). The regulatory mechanism underlying light-inducible production of carotenoids in nonphototrophic bacteria. Biosci. Biotechnol. Biochem. 80 1264– 1273. 10.1080/09168451.2016.1156478 26967471 · DOI
- Tang C. Xie B. J. Sun Z. D. (2017). Antibacterial activity and mechanism of B-type oligomeric procyanidins from lotus seedpod on enterotoxigenic Escherichia coli. J. Funct. Foods 38 454– 463. 10.1016/j.jff.2017.09.046 · DOI
- Tavridou E. Pireyre M. Ulm R. (2020). Degradation of the transcription factors PIF4 and PIF5 under UV-B promotes UVR8-mediated inhibition of hypocotyl growth in Arabidopsis. Plant J. Cell Mol. Biol. 101 507– 517. 10.1111/tpj.14556 31571300 PMC7027837 · DOI
- Teranishi M. Taguchi T. Ono T. Hidema J. (2012). Augmentation of CPD photolyase activity in japonica and indica rice increases their UVB resistance but still leaves the difference in their sensitivities. Photochem. Photobiol. Sci. 11 812– 820. 10.1039/c2pp05392f 22362193 · DOI
- Terashima K. Yuki K. Muraguchi H. Akiyama M. Kamada T. (2005). The dst1 gene involved in mushroom photomorphogenesis of Coprinus cinereus encodes a putative photoreceptor for blue light. Genetics 171 101– 108. 10.1534/genetics.104.040048 15956671 PMC1456503 · DOI
- Thind T. S. Schilder A. C. (2018). Understanding photoreception in fungi and its role in fungal development with focus on phytopathogenic fungi. Indian Phytopathol. 71 169– 182. 10.1007/s42360-018-0025-z · DOI
200 of 232 shown
- Authors
- Vanhaelewyn, L., Van Der Straeten, D., De Coninck, B., & Vandenbussche, F.
- Affiliations
- Ghent University (BE)
- Corresponding author
- Vanhaelewyn, Lucas
- Vandenbussche, Filip
- Venue
- Frontiers in Plant Science
- Publisher
- Frontiers Media SA
- Published
- 2020-12-15
- Volume
- 11
- Pages
- 597642-597642
- ISSN
- 1664-462X (ISSN-L)
- PMC
- PMC7769811
- OpenAlex
- W3112361604
- Cited by
- 188
- References
- 251
- Citations by year
- 2026: 34 · 2025: 45 · 2024: 49 · 2023: 29 · 2022: 24 · 2021: 7
- FWCI
- 1.27
- Type
- journal article
- Language
- en
- Open access
- gold
- doi.org
- Licence
- Locations
- Frontiers in Plant Science (publishedVersion, cc-by)
- PubMed Central (publishedVersion, cc-by)
- PubMed (publishedVersion)
- Ghent University Academic Bibliography (Ghent University) (submittedVersion, cc-by)
- Lirias (KU Leuven) (submittedVersion, other-oa)
- DOAJ (DOAJ: Directory of Open Access Journals) (submittedVersion, cc-by-sa)
- Funders
- Fonds Wetenschappelijk Onderzoek (G000515N)
- Universiteit Gent
- Vlaamse regering
- Bijzonder Onderzoeksfonds UGent
- Topics
- Life Sciences › Agricultural and Biological Sciences › Plant Science › Light effects on plants
- Life Sciences › Agricultural and Biological Sciences › Plant Science › Plant-Microbe Interactions and Immunity
- Life Sciences › Agricultural and Biological Sciences › Plant Science › Plant Disease Management Techniques
- Keywords
- ultraviolet radiation, UV-B radiation, UV-C, UVA, plant-microbe interactions, plant pathogens, secondary metabolite production, UVR8, reactive oxygen species, phenolic compounds, DNA damage, photomorphogenesis, phototropism
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