Ultraviolet radiation and cyanobacteria

Redox environment of the cell as viewed through the redox state of the glutathione disulfide/glutathione couple

Schafer, F. Q., & Buettner, G. R. (2001) · Free Radical Biology and Medicine · doi:10.1016/s0891-5849(01)00480-4 · Cited by 4,587

Architecture of the Photosynthetic Oxygen-Evolving Center

Ferreira, K. N., Iverson, T. M., Maghlaoui, K., Barber, J. P., & Iwata, S. (2004) · Science · doi:10.1126/science.1093087 · Cited by 3,330

The Ecology of Cyanobacteria

Whitton, B. A., & Potts, M. (2002) · Kluwer Academic Publishers eBooks · doi:10.1007/0-306-46855-7 · Cited by 2,323

β-Carotene: an Unusual Type of Lipid Antioxidant

Burton, G. W., & Ingold, K. U. (1984) · Science · doi:10.1126/science.6710156 · Cited by 2,150

PHOTOPROTECTION REVISITED:Genetic and Molecular Approaches

Niyogi, K. (1999) · Annual Review of Plant Physiology and Plant Molecular Biology · doi:10.1146/annurev.arplant.50.1.333 · Cited by 1,937

The Molecular Biology of Cyanobacteria

(1994) · Springer eBooks · doi:10.1007/978-94-011-0227-8 · Cited by 1,429

Desiccation tolerance of prokaryotes

Potts, M. (1994) · Microbiological Reviews · doi:10.1128/mr.58.4.755-805.1994 · Cited by 1,382

Molecular Mechanisms of Ultraviolet Radiation‐Induced DNA Damage and Repair

Rastogi, R. P., Richa, Kumar, A., Tyagi, M. B., & Sinha, R. P. (2010) · Journal of Nucleic Acids · doi:10.4061/2010/592980 · Cited by 1,329 · cited 4×

Microbial exopolymer secretions in ocean environments: their role(s) in food webs and marine processes

Decho, A. W. (1990) · Oceanography and Marine Biology/Oceanography and marine biology - an annual review · Cited by 1,199

Direct and indirect effects of UV radiation on DNA and its components

Ravanat, J.-L., Douki, T., & Cadet, J. (2001) · Journal of Photochemistry and Photobiology B: Biology · doi:10.1016/s1011-1344(01)00206-8 · Cited by 980

Toxic cyanobacteria and drinking water: Impacts, detection, and treatment

He, X., Liu, Y.-L., Conklin, A., Westrick, J. A., Weavers, L. K., Dionysiou, D. D., Lenhart, J. J., Mouser, P., Szlag, D. C., & Walker, H. W. (2016) · Harmful Algae · doi:10.1016/j.hal.2016.01.001 · Cited by 331

Cyanobacteria and the Great Oxidation Event: evidence from genes and fossils

Schirrmeister, B. E., Gugger, M., & Donoghue, P. C. J. (2015) · Palaeontology · doi:10.1111/pala.12178 · Cited by 304

Mycosporine-Like Amino Acids: Potential Health and Beauty Ingredients

Chrapusta, E., Kamiński, A., Duchnik, K., Bober, B., Adamski, M., & Białçzyk, J. (2017) · Marine Drugs · doi:10.3390/md15100326 · Cited by 204

Cyanobacterial pigments: Perspectives and biotechnological approaches

Saini, D. K., Pabbi, S., & Shukla, P. (2018) · Food and Chemical Toxicology · doi:10.1016/j.fct.2018.08.002 · Cited by 194

Ultraviolet Radiation From a Plant Perspective: The Plant-Microorganism Context

Vanhaelewyn, L., Van Der Straeten, D., De Coninck, B., & Vandenbussche, F. (2020) · Frontiers in Plant Science · doi:10.3389/fpls.2020.597642 · Cited by 188

Cyanobacterial Sunscreen Scytonemin: Role in Photoprotection and Biomedical Research

Rastogi, R. P., Sonani, R. R., & Madamwar, D. (2015) · Applied Biochemistry and Biotechnology · doi:10.1007/s12010-015-1676-1 · Cited by 135

Abiotic stress in algae: response, signaling and transgenic approaches

Kaur, M., Saini, K. C., Ojah, H., Sahoo, R., Gupta, K., Kumar, A., & Bast, F. (2022) · Journal of Applied Phycology · doi:10.1007/s10811-022-02746-7 · Cited by 120

Revealing the potential of cyanobacteria in cosmetics and cosmeceuticals — A new bioactive approach

Morone, J., Alfeus, A., Vasconcelos, V. M., & Martins, R. F. (2019) · Algal Research · doi:10.1016/j.algal.2019.101541 · Cited by 117

UV-Protective Compounds in Marine Organisms from the Southern Ocean

Núñez‐Pons, L., Àvila, C., Romano, G., Verde, C., & Giordano, D. (2018) · Marine Drugs · doi:10.3390/md16090336 · Cited by 115

Cyanobacteria as photoautotrophic biofactories of high-value chemicals

Noreña-Caro, D., & Benton, M. G. (2018) · Journal of CO2 Utilization · doi:10.1016/j.jcou.2018.10.008 · Cited by 117

Mechanisms of Stress Tolerance in Cyanobacteria under Extreme Conditions

Yadav, P., Singh, R. P., Rana, S., Joshi, D., Kumar, D., Bhardwaj, N., Gupta, R. K., & Kumar, A. (2022) · Stresses · doi:10.3390/stresses2040036 · Cited by 109

A perspective on ecologically relevant plant-UV research and its practical application

Robson, T. M., Aphalo, P. J., Banaś, A. K., Barnes, P. W., Brelsford, C. C., Jenkins, G. I., Kotilainen, T. K., Łabuz, J., Martínez‐Abaigar, J., Morales, L. O., et al. (2019) · Photochemical & Photobiological Sciences · doi:10.1039/c8pp00526e · Cited by 99

Pigments from UV-resistant Antarctic bacteria as photosensitizers in Dye Sensitized Solar Cells

Órdenes-Aenishanslins, N., Anziani‐Ostuni, G., Vargas-Reyes, M., Alarcón, J., Tello, A., & Perez-Donoso, J. M. (2016) · Journal of Photochemistry and Photobiology B Biology · doi:10.1016/j.jphotobiol.2016.08.004 · Cited by 105

Resilience and self-regulation processes of microalgae under UV radiation stress

Rastogi, R. P., Madamwar, D., Nakamoto, H., & Incharoensakdi, A. (2019) · Journal of Photochemistry and Photobiology C Photochemistry Reviews · doi:10.1016/j.jphotochemrev.2019.100322 · Cited by 102

Light-controlled motility in prokaryotes and the problem of directional light perception

Wilde, A., & Mullineaux, C. W. (2017) · FEMS Microbiology Reviews · doi:10.1093/femsre/fux045 · Cited by 93

Characterization and antioxidant functions of mycosporine-like amino acids in the cyanobacterium Nostoc sp. R76DM

Rastogi, R. P., Sonani, R. R., Madamwar, D., & Incharoensakdi, A. (2016) · Algal Research · doi:10.1016/j.algal.2016.03.009 · Cited by 90

Matworld – the biogeochemical effects of early life on land

Lenton, T. M., & Daines, S. J. (2016) · New Phytologist · doi:10.1111/nph.14338 · Cited by 85

Halophilic microorganism resources and their applications in industrial and environmental biotechnology

Waditee‐Sirisattha, R., Kageyama, H., & Takabe, T. (2016) · AIMS Microbiology · doi:10.3934/microbiol.2016.1.42 · Cited by 87

Mechanistic insights and applications of lignin-based ultraviolet shielding composites: A comprehensive review

Wu, X., Lian, H., Xia, C., Deng, J., Li, X., & Zhang, C. (2024) · International Journal of Biological Macromolecules · doi:10.1016/j.ijbiomac.2024.135477 · Cited by 76

Desiccation and radiation stress tolerance in cyanobacteria

Singh, H. (2018) · Journal of Basic Microbiology · doi:10.1002/jobm.201800216 · Cited by 70

UV inactivation of human infectious viruses at two full-scale wastewater treatment plants in Canada

Qiu, Y., Li, Q., Lee, B. E., Ruecker, N. J., Neumann, N. F., Ashbolt, N. J., & Pang, X. (2018) · Water Research · doi:10.1016/j.watres.2018.09.057 · Cited by 70

What makes a cyanobacterial bloom disappear? A review of the abiotic and biotic cyanobacterial bloom loss factors

Harris, T. D., Reinl, K. L., Azarderakhsh, M., Berger, S. A., Berman, M. C., Bižić, M., Bhattacharya, R., Burnet, S. H., Cianci‐Gaskill, J. A., Domis, L. N. D. S., et al. (2024) · Harmful Algae · doi:10.1016/j.hal.2024.102599 · Cited by 72

Halophile, an essential platform for bioproduction

Liu, C., Baffoe, D. K., Zhan, Y., Zhang, M., Li, Y., & Zhang, G. (2019) · Journal of Microbiological Methods · doi:10.1016/j.mimet.2019.105704 · Cited by 69

Phytoplankton and anthropogenic changes in pelagic environments

Salmaso, N., & Tolotti, M. (2020) · Hydrobiologia · doi:10.1007/s10750-020-04323-w · Cited by 69

UV‐B induced biosynthesis of a novel sunscreen compound in solar radiation and desiccation tolerant cyanobacteria

Shang, J., Zhang, Z., Yin, X., Chen, M., Hao, F., Wang, K., Feng, J., Xu, H., Yin, Y., Tang, H., et al. (2017) · Environmental Microbiology · doi:10.1111/1462-2920.13972 · Cited by 65

Versatile Applications of Cyanobacteria in Biotechnology

Żymańczyk-Duda, E., Samson, S. O., Brzezińska-Rodak, M., & Klimek-Ochab, M. (2022) · Microorganisms · doi:10.3390/microorganisms10122318 · Cited by 64

Cyanobacterial biorefinery: Towards economic feasibility through the maximum valorization of biomass

Prabha, S., Vijay, A. K., Paul, R. R., & George, B. (2022) · The Science of The Total Environment · doi:10.1016/j.scitotenv.2021.152795 · Cited by 59

Resilience and Mitigation Strategies of Cyanobacteria under Ultraviolet Radiation Stress

Singh, V. K., Jha, S., Rana, P., Mishra, S., Kumari, N., Singh, S. C., Anand, S., Upadhye, V. J., & Sinha, R. P. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms241512381 · Cited by 62

DNA damage protecting and free radical scavenging properties of mycosporine-2-glycine from the Dead Sea cyanobacterium in A375 human melanoma cell lines

Cheewinthamrongrod, V., Kageyama, H., Palaga, T., Takabe, T., & Waditee‐Sirisattha, R. (2016) · Journal of Photochemistry and Photobiology B Biology · doi:10.1016/j.jphotobiol.2016.09.037 · Cited by 57

Strain Development in Microalgal Biotechnology—Random Mutagenesis Techniques

Bleisch, R., Freitag, L., Ihadjadene, Y., Sprenger, U., Steingroewer, J., Walther, T., & Krujatz, F. (2022) · Life · doi:10.3390/life12070961 · Cited by 56

Understanding the Risks of Diffusion of Cyanobacteria Toxins in Rivers, Lakes, and Potable Water

Thawabteh, A. M., Naseef, H., Karaman, D., Bufo, S. A., Scrano, L., & Karaman, R. (2023) · Toxins · doi:10.3390/toxins15090582 · Cited by 56

Identification and distribution of mycosporine-like amino acids in Brazilian cyanobacteria by UHPLC-DAD-QTOF.

Geraldes, V., Jacinavicius, F. R., Genuário, D. B., & Pinto, E. (2020) · Rapid Communications in Mass Spectrometry · doi:10.1002/rcm.8634 · Cited by 28

Quantitative analysis of mycosporine-like amino acids in marine algae by capillary electrophoresis with diode-array detection

Hartmann, A., Murauer, A., & Ganzera, M. (2017) · Journal of Pharmaceutical and Biomedical Analysis · doi:10.1016/j.jpba.2017.01.053 · Cited by 48

Lithobiontic life: “Atacama rocks are well and alive”

Gómez‐Silva, B. (2018) · Antonie van Leeuwenhoek · doi:10.1007/s10482-018-1033-9 · Cited by 48

Mechanisms of Photoprotection in Cyanobacteria

Pathak, J., Ahmed, H., Singh, P. R., Singh, S. P., Häder, D., & Sinha, R. P. (2018) · Elsevier eBooks · doi:10.1016/b978-0-12-814667-5.00007-6 · Cited by 51

Synthesis, Regulation and Degradation of Carotenoids Under Low Level UV-B Radiation in the Filamentous Cyanobacterium Chlorogloeopsis fritschii PCC 6912

Llewellyn, C. A., Airs, R. L., Farnham, G., & Greig, C. (2020) · Frontiers in Microbiology · doi:10.3389/fmicb.2020.00163 · Cited by 47

Multiple routes toward engineering efficient cyanobacterial photosynthetic biomanufacturing technologies

Cui, J., Sun, H., Chen, R., Sun, J., Mo, G., Luan, G., & Lü, X. (2023) · Green Carbon · doi:10.1016/j.greenca.2023.11.004 · Cited by 48

Mycosporine-like amino acid and aromatic amino acid transcriptome response to UV and far-red light in the cyanobacterium Chlorogloeopsis fritschii PCC 6912

Llewellyn, C. A., Greig, C., Silkina, A., Kultschar, B., Hitchings, M. D., & Farnham, G. (2020) · Scientific Reports · doi:10.1038/s41598-020-77402-6 · Cited by 47

Application of nano‐radiosensitizers in combination cancer therapy

Varzandeh, M., Sabouri, L., Mansouri, V., Gharibshahian, M., Beheshtizadeh, N., Hamblin, M. R., & Rezaei, N. (2023) · Bioengineering & Translational Medicine · doi:10.1002/btm2.10498 · Cited by 45

A review of microcystin and nodularin toxins derived from freshwater cyanobacterial harmful algal blooms and their impact on human health

Melaram, R., Newton, A. R., Lee, A., Herber, S., El-Khouri, A., & Chafin, J. (2024) · Toxicology and Environmental Health Sciences · doi:10.1007/s13530-024-00220-0 · Cited by 43

Mechanisms and fitness implications of photomorphogenesis during chromatic acclimation in cyanobacteria

Montgomery, B. L. (2016) · Journal of Experimental Botany · doi:10.1093/jxb/erw206 · Cited by 41

Enhanced In Situ Availability of Aphanizomenon Flos-Aquae Constituents Entrapped in Buccal Films for the Treatment of Oxidative Stress-Related Oral Diseases: Biomechanical Characterization and In Vitro/Ex Vivo Evaluation

De, V., Murgia, D., Seidita, F., Bologna, E., Alotta, G., Zingales, M., & Campisi, G. (2019) · Pharmaceutics · doi:10.3390/pharmaceutics11010035 · Cited by 40

Applications of mycosporine-like amino acids beyond photoprotection

Punchakara, A., Prajapat, G., Bairwa, H. K., Jain, S., & Agrawal, A. (2023) · Applied and Environmental Microbiology · doi:10.1128/aem.00740-23 · Cited by 42

Protein homeostasis — more than resisting a hot bath

Lee, C. D., Wigren, E., Lünsdorf, H., & Römling, U. (2016) · Current Opinion in Microbiology · doi:10.1016/j.mib.2016.02.006 · Cited by 35

Photochemistry and photophysics of mycosporine-like amino acids and gadusols, nature’s ultraviolet screens

Losantos, R., Sampedro, D., & Churio, M. S. (2015) · Pure and Applied Chemistry · doi:10.1515/pac-2015-0304 · Cited by 34

Gloeobacter and the implications of a freshwater origin of Cyanobacteria

Raven, J. A., & Sánchez‐Baracaldo, P. (2021) · Phycologia · doi:10.1080/00318884.2021.1881729 · Cited by 36

The effects of sunlight on the composition of exopolymeric substances and subsequent aggregate formation during oil spills

Sun, L., Chiu, M., Xu, C., Lin, P., Schwehr, K. A., Bacosa, H. P., Kamalanathan, M., Quigg, A. S., Chin, W., & Santschi, P. H. (2018) · Marine Chemistry · doi:10.1016/j.marchem.2018.04.006 · Cited by 34

Scytonemin: Unravelling major progress and prospects

Sen, S., & Mallick, N. (2022) · Algal Research · doi:10.1016/j.algal.2022.102678 · Cited by 34

Response of Endolithic Chroococcidiopsis Strains From the Polyextreme Atacama Desert to Light Radiation

Casero, M. C., Ascaso, C., Quesada, A., Mazur‐Marzec, H., & Wierzchoś, J. (2021) · Frontiers in Microbiology · doi:10.3389/fmicb.2020.614875 · Cited by 32

Natural and anthropogenic dispersal of cyanobacteria: a review

Curren, E., & Leong, S. C. Y. (2020) · Hydrobiologia · doi:10.1007/s10750-020-04286-y · Cited by 37

Effect of ultraviolet radiation on the metabolomic profiles of potentially toxic cyanobacteria

Jacinavicius, F. R., Geraldes, V., Crnkovic, C. M., Delbaje, E., Fiore, M. F., & Pinto, E. (2020) · FEMS Microbiology Ecology · doi:10.1093/femsec/fiaa243 · Cited by 33

Colonial cell disaggregation and intracellular microcystin release following chlorination of naturally occurring Microcystis

He, X., & Wert, E. C. (2016) · Water Research · doi:10.1016/j.watres.2016.05.057 · Cited by 29

Intracellular and Extracellular Metabolites from the Cyanobacterium Chlorogloeopsis fritschii, PCC 6912, During 48 Hours of UV-B Exposure

Kultschar, B., Dudley, E., Wilson, S., & Llewellyn, C. A. (2019) · Metabolites · doi:10.3390/metabo9040074 · Cited by 28

Protection and Damage Repair Mechanisms Contributed To the Survival of Chroococcidiopsis sp. Exposed To a Mars-Like Near Space Environment

Li, C., Zhang, X., Ye, T., Li, X., & Wang, G. (2022) · Microbiology Spectrum · doi:10.1128/spectrum.03440-22 · Cited by 28

UV-Induced Oxidative Stress in Cyanobacteria: How Life is able to Survive?

Rastogi, R. P. (2015) · Biochemistry & Analytical Biochemistry · doi:10.4172/2161-1009.1000173 · Cited by 27

Surface colour: An overlooked aspect in the study of cyanobacterial biofilm formation

Gambino, M., Sanmartín, P., Longoni, M., Villa, F., Mitchell, R., & Cappitelli, F. (2018) · The Science of The Total Environment · doi:10.1016/j.scitotenv.2018.12.358 · Cited by 27

DOM production, removal, and transformation processes in marine systems

Carlson, C. A., Liu, S., Stephens, B. M., & English, C. J. (2024) · Elsevier eBooks · doi:10.1016/b978-0-443-13858-4.00013-7 · Cited by 27

Acclimation to low ultraviolet‐B radiation increases photosystem I abundance and cyclic electron transfer with enhanced photosynthesis and growth in the cyanobacterium Nostoc sphaeroides

Chen, Z., Jiang, H., Gao, K., & Qiu, B. (2019) · Environmental Microbiology · doi:10.1111/1462-2920.14836 · Cited by 25

Robust natural ultraviolet filters from marine ecosystems for the formulation of environmental friendlier bio-sunscreens

Amador-Castro, F., Rodríguez‐Martínez, V., & Carrillo-Nieves, D. (2020) · The Science of The Total Environment · doi:10.1016/j.scitotenv.2020.141576 · Cited by 28

Production of Primary and Secondary Metabolites Using Algae

Rico, M., González, A. G., Santana‐Casiano, J. M., González‐Dávila, M., Pérez-Almeida, N., & de Tangil, M. S. (2017) · Springer eBooks · doi:10.1007/978-981-10-1950-0_12 · Cited by 28

Exposure of cyanobacterium Nostoc sp. to the Mars-like stratosphere environment

Ye, T., Wang, B., Li, C., Bian, P., Chen, L., & Wang, G. (2021) · Journal of Photochemistry and Photobiology B Biology · doi:10.1016/j.jphotobiol.2021.112307 · Cited by 21

Effects of elevated ultraviolet radiation on primary metabolites in selected alpine algae and cyanobacteria

Hartmann, A., Albert, A., & Ganzera, M. (2015) · Journal of Photochemistry and Photobiology B Biology · doi:10.1016/j.jphotobiol.2015.05.016 · Cited by 24

Short-term interactive effects of ultraviolet radiation, carbon dioxide and nutrient enrichment on phytoplankton in a shallow coastal lagoon

Domingues, R. B., Guerra, C. C., Galvão, H. M., Brotas, V., & Barbosa, A. B. (2016) · Aquatic Ecology · doi:10.1007/s10452-016-9601-4 · Cited by 23

Identification, biochemical composition and phycobiliproteins production of Chroococcidiopsis sp. from arid environment

Montero, Z., Fuentes, J. L., Garbayo, I., Ascaso, C., Wierzchoś, J., Vega, J. M., & Vı́lchez, C. (2020) · Process Biochemistry · doi:10.1016/j.procbio.2020.07.005 · Cited by 23

Biologically-Based and Physiochemical Life Support and In Situ Resource Utilization for Exploration of the Solar System—Reviewing the Current State and Defining Future Development Needs

Keller, R. J., Porter, W., Goli, K., Rosenthal, R., Butler, N., & Jones, J. A. (2021) · Life · doi:10.3390/life11080844 · Cited by 23

Aquatic Productivity under Multiple Stressors

Häder, D., & Gao, K. (2023) · Water · doi:10.3390/w15040817 · Cited by 27

Impacts of disinfected wastewater irrigation on soil characteristics, microbial community composition, and crop yield

Leonel, L. P., Bize, A., Mariadassou, M., Midoux, C., Schneider, J., & Tonetti, A. L. (2022) · Blue-Green Systems · doi:10.2166/bgs.2022.126 · Cited by 25

Ultraviolet-screening compound mycosporine-like amino acids in cyanobacteria: biosynthesis, functions, and applications

Singh, D. K., Pathak, J., Pandey, A., Singh, V., Ahmed, H., Rajneesh, Kumar, D., & Sinha, R. P. (2020) · Elsevier eBooks · doi:10.1016/b978-0-12-819311-2.00015-2 · Cited by 22

Ultraviolet light and ozone controls Cryptocaryon irritans infection in factory aquaculture

Lu, G., Jiang, B., Li, Z.-C., & Li, A. (2021) · Aquaculture · doi:10.1016/j.aquaculture.2021.737598 · Cited by 21

Proteomic profiling of Nostoc flagelliforme reveals the common mechanism in promoting polysaccharide production by different light qualities

Han, P.-P., Guo, R., Shen, S.-G., Yan, R.-R., Wu, Y.-K., Yao, S., Wang, H., & Jia, S. (2017) · Biochemical Engineering Journal · doi:10.1016/j.bej.2017.12.006 · Cited by 21

Nostoc entophytum cell response to cadmium exposure: A possible role of chaperon proteins GroEl and HtpG in cadmium-induced stress

Alidoust, L., Zahiri, H. S., Maleki, H., Soltani, N., Vali, H., & Noghabi, K. A. (2018) · Ecotoxicology and Environmental Safety · doi:10.1016/j.ecoenv.2018.10.104 · Cited by 21

Life’s Critical Role in the Long-term Carbon Cycle: the Biotic Enhancement of Weathering

SCHWARTZMAN, D. W. (2017) · AIMS Geosciences · doi:10.3934/geosci.2017.2.216 · Cited by 20

Interactions between ultraviolet radiation exposure and phosphorus limitation in the marine nitrogen‐fixing cyanobacteria Trichodesmium and Crocosphaera

Zhu, Z., Fu, F., Qu, P., Mak, E. W. K., Jiang, H., Zhang, R., Zhu, ⎜., Gao, K., & Hutchins, D. A. (2019) · Limnology and Oceanography · doi:10.1002/lno.11304 · Cited by 20

Genetic and biochemical evidence for redundant pathways leading to mycosporine-like amino acid biosynthesis in the cyanobacterium Sphaerospermopsis torques-reginae ITEP-024

Geraldes, V., de Medeiros, L. S., de Lima, S. T., Alvarenga, D. O., Gaćeša, R., Long, P. F., Fiore, M. F., & Pinto, E. (2020) · ALGAE · doi:10.4490/algae.2020.35.5.19 · Cited by 20

Extruded polysaccharide/protein matrix from Arthrospira platensis cultures mediated silver nanoparticles biosynthesis and capping

Hamouda, R. A., Hussein, M. H., Elhadary, A. M. A., & Abuelmagd, M. A. (2020) · Applied Nanoscience · doi:10.1007/s13204-020-01490-z · Cited by 22

Harmful Cyanobacterial Blooms (HCBs): innovative green bioremediation process based on anti-cyanobacteria bioactive natural products

Zerrifi, S. E. A., Mugani, R., Redouane, E. M., Khalloufi, F. E., Campos, A. M. O., Vasconcelos, V. M., & Oudra, B. (2020) · Archives of Microbiology · doi:10.1007/s00203-020-02015-6 · Cited by 19

Photoprotective and antioxidant properties of scytonemin isolated from Antarctic cyanobacterium Nostoc commune Vaucher ex Bornet & Flahault and its potential as sunscreen ingredient

Ručová, D., Vilková, M., Sovová, S., Vargová, Z., Kostecká, Z., Frenák, R., Routray, D., & Bačkor, M. (2023) · Journal of Applied Phycology · doi:10.1007/s10811-023-03109-6 · Cited by 21

New types of ATP ‐grasp ligase are associated with the novel pathway for complicated mycosporine‐like amino acid production in desiccation‐tolerant cyanobacteria

Zhang, Z., Wang, K., Hao, F., Shang, J., Tang, H., & Qiu, B. (2021) · Environmental Microbiology · doi:10.1111/1462-2920.15732 · Cited by 19

Dark blue-green: Cave-inhabiting cyanobacteria as a model for astrobiology

Jung, P., Harion, F., Wu, S., Nürnberg, D. J., Bellamoli, F., Guillén, A., Leira, M., & Lakatos, M. (2023) · Frontiers in Astronomy and Space Sciences · doi:10.3389/fspas.2023.1107371 · Cited by 20

Photosynthetic microorganisms, an overview of their biostimulant effects on plants and perspectives for space agriculture

Renaud, C., Leys, N., & Wattiez, R. (2023) · Journal of Plant Interactions · doi:10.1080/17429145.2023.2242697 · Cited by 19

UV Photoprotectants From Algae—Synthesis and Bio-Functionalities

Rastogi, R. P., Sonani, R. R., & Madamwar, D. (2017) · Elsevier eBooks · doi:10.1016/b978-0-444-63784-0.00002-3 · Cited by 20

Involvement of glycogen metabolism in circadian control of UV resistance in cyanobacteria

Kawasaki, K., & Iwasaki, H. (2020) · PLoS Genetics · doi:10.1371/journal.pgen.1009230 · Cited by 18

Color Sensing and Signal Transmission Diversity of Cyanobacterial Phytochromes and Cyanobacteriochromes.

Villafani, Y., Yang, H. W., & Park, Y. (2020) · PubMed Central · doi:10.14348/molcells.2020.0077 · Cited by 17

Effects of changes in UV-B radiation levels on biofilm-forming organisms commonly found in cultural heritage surfaces

Fuentes, E., Pérez-Velón, D., & Prieto, B. (2022) · Environmental Research · doi:10.1016/j.envres.2022.114061 · Cited by 17

Decoding the photoprotection strategies and manipulating cyanobacterial photoprotective metabolites, mycosporine-like amino acids, for next-generation sunscreens

Mishra, R., Kaur, P., Soni, R., Madan, A., Agarwal, P., & Singh, G. (2024) · Plant Physiology and Biochemistry · doi:10.1016/j.plaphy.2024.108744 · Cited by 17

Restoration of damaged drylands through acceleration of biocrust development

Malešević, T. P., Meriluoto, J. A. O., Mihalj, I., Važić, T., Marković, R. S., Jurca, T., Codd, G. A., & Svirčev, Z. B. (2024) · CATENA · doi:10.1016/j.catena.2024.108265 · Cited by 15

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