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1

Geraldes, Vanessa, and Ernani Pinto. "Mycosporine-Like Amino Acids (MAAs): Biology, Chemistry and Identification Features." Pharmaceuticals 14, no. 1 (2021): 63. http://dx.doi.org/10.3390/ph14010063.

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Mycosporines and mycosporine-like amino acids are ultra-violet-absorbing compounds produced by several organisms such as lichens, fungi, algae and cyanobacteria, especially upon exposure to solar ultraviolet radiation. These compounds have photoprotective and antioxidant functions. Mycosporine-like amino acids have been used as a natural bioactive ingredient in cosmetic products. Several reviews have already been developed on these photoprotective compounds, but they focus on specific features. Herein, an extremely complete database on mycosporines and mycosporine-like amino acids, covering th
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Gorbushina, Anna A., Kenia Whitehead, Thomas Dornieden, Astrid Niesse, Anette Schulte, and John I. Hedges. "Black fungal colonies as units of survival: hyphal mycosporines synthesized by rock-dwelling microcolonial fungi." Canadian Journal of Botany 81, no. 2 (2003): 131–38. http://dx.doi.org/10.1139/b03-011.

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Microcolonial fungi, long-living modified mycelia frequently occurring on desert and pseudodesert rock surfaces, are exposed to strong ultraviolet (UV) radiation, desiccation, and nutrient scarcity. They lack ascospores; all their cells grow by mitotic cell divisions and possess a thick melanized cell wall. Colonies of several randomly selected microcolonial strains were cultured and their structure was examined by cryo-scanning and transmission electron microscopy. Extracts of nine strains were analyzed by high performance liquid chromatography interfaced with mass spectrometry for the presen
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3

Parailloux, Maroussia, Simon Godin, Susana C. M. Fernandes, and Ryszard Lobinski. "Untargeted Analysis for Mycosporines and Mycosporine-Like Amino Acids by Hydrophilic Interaction Liquid Chromatography (HILIC)—Electrospray Orbitrap MS2/MS3." Antioxidants 9, no. 12 (2020): 1185. http://dx.doi.org/10.3390/antiox9121185.

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Mycosporines and mycosporine-like amino acids have been described as natural sunscreens and antioxidant compounds presenting a great potential for health and cosmetic applications. Herein, an untargeted screening approach for mycosporines and mycosporine-like amino acids (MAAs) was developed by the coupling of zwitterionic hydrophilic interaction liquid chromatography (HILIC) with multistage electrospray mass spectrometry MS2/MS3 using an Orbitrap analyzer and fragment ion search (FISh). This method was applied to study the mycosporine and MAA contents of five algae extracted using a 50% metha
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4

Favre-Bonvin, Jean, Jacques Bernillon, Nadia Salin, and Noel Arpin. "Biosynthesis of mycosporines: Mycosporine glutaminol in Trichothecium roseum." Phytochemistry 26, no. 9 (1987): 2509–14. http://dx.doi.org/10.1016/s0031-9422(00)83866-2.

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5

Kogej, Tina, Cene Gostinčar, Marc Volkmann, Anna A. Gorbushina, and Nina Gunde-Cimerman. "Mycosporines in Extremophilic Fungi—Novel Complementary Osmolytes?" Environmental Chemistry 3, no. 2 (2006): 105. http://dx.doi.org/10.1071/en06012.

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Environmental Context.The occurrence of fungi in extreme environments, particularly in hypersaline water and in subglacial ice, is much higher than was previously assumed. When glacial ice melts as a result of calving or surface ablations, these organisms are released in the Arctic soil or sea and have a yet uninvestigated impact on the environment. Knowledge of the metabolites of these extremophilic fungi is important because they could provide signature molecules in the environment, but they can also contribute nutrients to the otherwise oligotrophic polar conditions. In the present work, we
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6

Colabella, Fernando, Martin Moline, and Diego Libkind. "UV Sunscreens of Microbial Origin: Mycosporines and Mycosporine- like Aminoacids." Recent Patents on Biotechnology 8, no. 3 (2015): 179–93. http://dx.doi.org/10.2174/1872208309666150102104520.

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7

Chollet-Krugler, Marylène, Thi Nguyen, Aurelie Sauvager, Holger Thüs, and Joël Boustie. "Mycosporine-Like Amino Acids (MAAs) in Time-Series of Lichen Specimens from Natural History Collections." Molecules 24, no. 6 (2019): 1070. http://dx.doi.org/10.3390/molecules24061070.

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Mycosporine-like amino acids (MAAs) were quantified in fresh and preserved material of the chlorolichen Dermatocarpon luridum var. luridum (Verrucariaceae/Ascomycota). The analyzed samples represented a time-series of over 150 years. An HPLC coupled with a diode array detector (HPLC-DAD) in hydrophilic interaction liquid chromatography (HILIC) mode method was developed and validated for the quantitative determination of MAAs. We found evidence for substance specific differences in the quality of preservation of two MAAs (mycosporine glutamicol, mycosporine glutaminol) in Natural History Collec
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8

Waditee-Sirisattha, Rungaroon, Hakuto Kageyama, Warangkana Sopun, Yoshito Tanaka, and Teruhiro Takabe. "Identification and Upregulation of Biosynthetic Genes Required for Accumulation of Mycosporine-2-Glycine under Salt Stress Conditions in the Halotolerant Cyanobacterium Aphanothece halophytica." Applied and Environmental Microbiology 80, no. 5 (2013): 1763–69. http://dx.doi.org/10.1128/aem.03729-13.

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ABSTRACTMycosporine-like amino acids (MAAs) are valuable molecules that are the basis for important photoprotective constituents. Here we report molecular analysis of mycosporine-like amino acid biosynthetic genes from the halotolerant cyanobacteriumAphanothece halophytica, which can survive at high salinity and alkaline pH. This extremophile was found to have a unique MAA core (4-deoxygadusol)-synthesizing gene separated from three other genes.In vivoanalysis showed accumulation of the mycosporine-2-glycine but not shinorine or mycosporine-glycine. Mycosporine-2-glycine accumulation was stimu
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9

Katoch, Meenu, Rabia Mazmouz, Rocky Chau, Leanne A. Pearson, Russell Pickford, and Brett A. Neilan. "Heterologous Production of Cyanobacterial Mycosporine-Like Amino Acids Mycosporine-Ornithine and Mycosporine-Lysine in Escherichia coli." Applied and Environmental Microbiology 82, no. 20 (2016): 6167–73. http://dx.doi.org/10.1128/aem.01632-16.

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ABSTRACTMycosporine-like amino acids (MAAs) are an important class of secondary metabolites known for their protection against UV radiation and other stress factors. Cyanobacteria produce a variety of MAAs, including shinorine, the active ingredient in many sunscreen creams. Bioinformatic analysis of the genome of the soil-dwelling cyanobacteriumCylindrospermum stagnalePCC 7417 revealed a new gene cluster with homology to MAA synthase fromNostoc punctiforme. This newly identified gene cluster is unusual because it has five biosynthesis genes (mylAtomylE), compared to the four found in other MA
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Oren, Aharon, and Nina Gunde-Cimerman. "Mycosporines and mycosporine-like amino acids: UV protectants or multipurpose secondary metabolites?" FEMS Microbiology Letters 269, no. 1 (2007): 1–10. http://dx.doi.org/10.1111/j.1574-6968.2007.00650.x.

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11

Teai, Taivini, Jacqui H. Drollet, Jean-Pierre Bianchini, Aimé Cambon, and Paul M. V. Martin. "Occurrence of ultraviolet radiation-absorbing mycosporine-like amino acids in coral mucus and whole corals of French Polynesia." Marine and Freshwater Research 49, no. 2 (1998): 127. http://dx.doi.org/10.1071/mf97051.

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Specimens of six scleractinian species were gathered during the austral spring (October–November) 1994 on the external slope of the barrier reef of Arue, Tahiti, and in the lagoon of Arutua, a Tuamotu island. Mucus of each specimen was collected and the optical density and volume excreted were measured. After treatment, mucus was analysed for mycosporine-like amino acids (MAAs) by high-performance liquid chromatography (HPLC). Nine UV-absorbing compounds were present in coral mucus at concentrations between 1 and 500 ng g-1 mucus. Palythine and mycosporine–gly were found in all mucus studied.
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12

Rastogi, Rajesh P., Richa, Shailendra P. Singh, Donat-P. Häder, and Rajeshwar P. Sinha. "Mycosporine-like amino acids profile and their activity under PAR and UVR in a hot-spring cyanobacterium Scytonema sp. HKAR-3." Australian Journal of Botany 58, no. 4 (2010): 286. http://dx.doi.org/10.1071/bt10004.

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The cyanobacterium Scytonema sp. HKAR-3 isolated from a hot spring in India was investigated for the presence of mycosporine-like amino acids (MAAs) and their induction under PAR and PAR+UVR. High-performance liquid-chromatograph (HPLC) analysis revealed the presence of two MAAs, mycosporine–glycine (λmax = 310 nm) and an unknown MAA-334 (λmax = 334 nm), with retention times of 4.1 and 8.7 min, respectively. This is the first report for the presence of two MAAs and, in particular, the synthesis of mycosporine–glycine in any strain of Scytonema. There was no effect of radiation type (PAR or PAR
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13

Lemoyne, F., J. Bernillon, J. Favre-Bonvin, M. L. Bouillant, and N. Arpin. "Occurrence and Characteristics of Amino Alcohols and Cyclohexenone. Components of Fungal Mycosporines." Zeitschrift für Naturforschung C 40, no. 9-10 (1985): 612–16. http://dx.doi.org/10.1515/znc-1985-9-1004.

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Abstract After determination of hydrolysis conditions which allow the best recovery of the mycosporine components (cyclohexenone 1 and the amino alcohols 2 and 3), these compounds have been searched into mycelia of several fungi. In some of them, 1 was unambiguously detected, although in minute quantities, whilst the unknown natural 2 and 3 could not be identified. So, two alternative pathways of mycosporine biogenesis are under investigation.
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14

bhatia, Saurabh, K. Sharma, A. Sharma, Arun Garg, S. Kumar, and AP Purohit. "Mycosporine and mycosporine-like amino acids: A paramount tool against ultra violet irradiation." Pharmacognosy Reviews 5, no. 10 (2011): 138. http://dx.doi.org/10.4103/0973-7847.91107.

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15

Moliné, Martín, Ernesto M. Arbeloa, María R. Flores, et al. "UVB Photoprotective Role of Mycosporines in Yeast: Photostability and Antioxidant Activity of Mycosporine-Glutaminol-Glucoside." Radiation Research 175, no. 1 (2011): 44–50. http://dx.doi.org/10.1667/rr2245.1.

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16

Patipong, Tanutcha, Takashi Hibino, Rungaroon Waditee-Sirisattha, and Hakuto Kageyama. "Efficient Bioproduction of Mycosporine-2-glycine, Which Functions as Potential Osmoprotectant, using Escherichia coli Cells." Natural Product Communications 12, no. 10 (2017): 1934578X1701201. http://dx.doi.org/10.1177/1934578x1701201017.

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Mycosporine-2-glycine (M2G) is known to be synthesized in halotolerant cyanobacterium Aphanothece halophytica. Escherichia coli cells in which the M2G synthetic genes of A. halophytica were introduced could synthesize M2G. Here, we report that M2G producing transformed E. coli cells showed salt tolerance compared to control cells. This result suggested that M2G could function as a potential osmoprotectant in E. coli. To our knowledge, this is the first report presenting the evidence that mycosporine-like amino acid confers salt tolerance on E. coli. Intracellular M2G content in the transformed
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17

Miyamoto, Kiyoko T., Mamoru Komatsu, and Haruo Ikeda. "Discovery of Gene Cluster for Mycosporine-Like Amino Acid Biosynthesis from Actinomycetales Microorganisms and Production of a Novel Mycosporine-Like Amino Acid by Heterologous Expression." Applied and Environmental Microbiology 80, no. 16 (2014): 5028–36. http://dx.doi.org/10.1128/aem.00727-14.

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ABSTRACTMycosporines and mycosporine-like amino acids (MAAs), including shinorine (mycosporine-glycine-serine) and porphyra-334 (mycosporine-glycine-threonine), are UV-absorbing compounds produced by cyanobacteria, fungi, and marine micro- and macroalgae. These MAAs have the ability to protect these organisms from damage by environmental UV radiation. Although no reports have described the production of MAAs and the corresponding genes involved in MAA biosynthesis from Gram-positive bacteria to date, genome mining of the Gram-positive bacterial database revealed that two microorganisms belongi
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18

Sinha, Rajeshwar P., Shailendra P. Singh, and Donat-P. Häder. "Database on mycosporines and mycosporine-like amino acids (MAAs) in fungi, cyanobacteria, macroalgae, phytoplankton and animals." Journal of Photochemistry and Photobiology B: Biology 89, no. 1 (2007): 29–35. http://dx.doi.org/10.1016/j.jphotobiol.2007.07.006.

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19

Portwich, Anne, and Ferran Garcia-Pichel. "Biosynthetic pathway of mycosporines (mycosporine-like amino acids) in the cyanobacterium Chlorogloeopsis sp. strain PCC 6912." Phycologia 42, no. 4 (2003): 384–92. http://dx.doi.org/10.2216/i0031-8884-42-4-384.1.

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20

Drollet, Jacques H., Taivini Teai, Mizaël Faucon, and Paul M. V. Martin. "Field study of compensatory changes in UV-absorbing compounds in the mucus of the solitary coral Fungia repanda (Scleractinia: Fungiidae) in relation to solar UV radiation, sea-water temperature, and other coincident physico-chemical parameters." Marine and Freshwater Research 48, no. 4 (1997): 329. http://dx.doi.org/10.1071/mf96087.

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The relationship between coral UV-absorbing compounds (mycosporine-like amino acids, or MAAs) and solar UV radiation in the shallow coral reef environment has been much debated. The presence of these compounds in the mucus of Fungiidae allowed the measurement of weekly compensatory changes in the amount and composition of these compounds together with shifts in the wavelength of maximum absorbance (λ max. ) in the mucus of 11 specimens of Fungia repanda (Scleractinia:Fungiidae) during 18 months of monitoring in situ in Tahiti. The corals received full sunlight within a topless cage (specimen d
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Piiparinen, Jonna, Sara Enberg, Janne-Markus Rintala, et al. "The contribution of mycosporine-like amino acids, chromophoric dissolved organic matter and particles to the UV protection of sea-ice organisms in the Baltic Sea." Photochemical & Photobiological Sciences 14, no. 5 (2015): 1025–38. http://dx.doi.org/10.1039/c4pp00342j.

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22

Roullier, Catherine, Marylène Chollet-Krugler, Eva-Maria Pferschy-Wenzig, et al. "Characterization and identification of mycosporines-like compounds in cyanolichens. Isolation of mycosporine hydroxyglutamicol from Nephroma laevigatum Ach." Phytochemistry 72, no. 11-12 (2011): 1348–57. http://dx.doi.org/10.1016/j.phytochem.2011.04.002.

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23

Mishra, Sonal, Abha Pandey, Haseen Ahmed, Deepak Kumar, Vidya Singh, and Rajeshwar P. Sinha. "Mycosporine-Like Amino Acids (MAAs) Profile of cyanobacteria from Different Historical Kunds of Varanasi, India." International Journal of Applied Sciences and Biotechnology 7, no. 3 (2019): 317–26. http://dx.doi.org/10.3126/ijasbt.v7i3.25712.

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Copious facts have demonstrated that UV radiation is harmful to cyanobacteria. Sun-screening compounds such as mycosporine-like amino acids (MAAs) protect these organisms from deleterious UV radiation. MAAs absorb UV radiation in the range of 310 to 362 nm. These natural sunscreens obtained from cyanobacteria are excellent alternative to present day synthetic UV filters. In the present study, several cyanobacteria were collected from six historical Kunds of Varanasi, India. MAAs profile of these cyanobacteria was recorded with the help of UV-Vis spectroscopy, High performance liquid chromatogr
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Llewellyn, C. A., and D. S. Harbour. "A temporal study of mycosporine-like amino acids in surface water phytoplankton from the English Channel and correlation with solar irradiation." Journal of the Marine Biological Association of the United Kingdom 83, no. 1 (2003): 1–9. http://dx.doi.org/10.1017/s0025315403006726h.

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A seasonal survey was undertaken, over a year, of phytoplankton from surface water in the western English Channel (Station L4) measuring mycosporine-like amino acids (MAAs), photosynthetic pigments and microscopic counts. Ground level solar radiation (ultraviolet-B, ultraviolet-A and photosynthetically active radiation; UV-B, UV-A and PAR) was measured at a nearby site. From this we estimated in situ solar irradiance received by phytoplankton using measurements of the mixed layer depth and calculations of the 50% light level cut-off. The MAAs occurred year round, with concentrations increasing
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Hylander, Samuel. "Mycosporine-Like Amino Acids (MAAs) in Zooplankton." Marine Drugs 18, no. 2 (2020): 72. http://dx.doi.org/10.3390/md18020072.

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Organisms have different adaptations to avoid damage from ultraviolet radiation and one such adaptation is the accumulation of mycosporine-like amino acids (MAAs). These compounds are common in aquatic taxa but a comprehensive review is lacking on their distribution and function in zooplankton. This paper shows that zooplankton MAA concentrations range from non-detectable to ~13 µg mgDW−1. Copepods, rotifers, and krill display a large range of concentrations, whereas cladocerans generally do not contain MAAs. The proposed mechanisms to gain MAAs are via ingestion of MAA-rich food or via symbio
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Figueroa, Félix L. "Mycosporine-Like Amino Acids from Marine Resource." Marine Drugs 19, no. 1 (2021): 18. http://dx.doi.org/10.3390/md19010018.

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In the last 10 years, a great number of publications (both regular papers and reviews) have been published on the interesting molecules—mycosporine-like amino acids (MAAs). Despite significant advances in the research of MAAs, current overviews in the recent publications involving MAA research still need reporting. The aim of this Special Issue is to join, as an interdisciplinary approach, the photochemical and photobiological aspects, with emphasis on new natural resources to obtain both algae and zooplankton MAAs, advances in methodology of extraction and chemical identification of new MAAs.
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Lawrence, Karl P., Paul F. Long, and Antony R. Young. "Mycosporine-Like Amino Acids for Skin Photoprotection." Current Medicinal Chemistry 25, no. 40 (2019): 5512–27. http://dx.doi.org/10.2174/0929867324666170529124237.

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Background: Excessive human exposure to solar ultraviolet radiation (UVR) continues to be a major public health concern, with skin cancer rates increasing year on year. The major protective measure is the use of synthetic UVR filters formulated into sunscreens, but there is a growing concern that some of these chemicals cause damage to delicate marine ecosystems. One alternative is the use of biocompatible mycosporine-like amino acids (MAA), which occur naturally in a wide range of marine species. Their role within nature is mainly thought to be photoprotective. However, their potential for hu
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Kulkarni, Atul, Jeong Hun Lee, Hyo Hyun Seo, et al. "Photoinduced conductivity in mycosporine-like amino acids." Materials Chemistry and Physics 151 (February 2015): 1–4. http://dx.doi.org/10.1016/j.matchemphys.2014.11.056.

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Rosic, Nedeljka N., and Sophie Dove. "Mycosporine-Like Amino Acids from Coral Dinoflagellates." Applied and Environmental Microbiology 77, no. 24 (2011): 8478–86. http://dx.doi.org/10.1128/aem.05870-11.

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ABSTRACTCoral reefs are one of the most important marine ecosystems, providing habitat for approximately a quarter of all marine organisms. Within the foundation of this ecosystem, reef-building corals form mutualistic symbioses with unicellular photosynthetic dinoflagellates of the genusSymbiodinium. Exposure to UV radiation (UVR) (280 to 400 nm) especially when combined with thermal stress has been recognized as an important abiotic factor leading to the loss of algal symbionts from coral tissue and/or a reduction in their pigment concentration and coral bleaching. UVR may damage biological
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Serban, Radu, and Gheorghe Stoian. "Mycosporine like amino acids in brown algae." Balneo Research Journal 4, no. 4 (2013): 158–61. http://dx.doi.org/10.12680/balneo.2013.1057.

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Oda, Yuta, Quang Zhang, Satoko Matsunaga, Masaki J. Fujita, and Ryuichi Sakai. "Two New Mycosporine-like Amino Acids LC-343 and Mycosporine-ethanolamine from the Micronesian Marine Sponge Lendenfeldia chondrodes." Chemistry Letters 46, no. 8 (2017): 1272–74. http://dx.doi.org/10.1246/cl.170490.

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Orfanoudaki, Maria, Anja Hartmann, Helena Miladinovic, Hieu Nguyen Ngoc, Ulf Karsten, and Markus Ganzera. "Bostrychines A–F, Six Novel Mycosporine-Like Amino-Acids and a Novel Betaine from the Red Alga Bostrychia scorpioides." Marine Drugs 17, no. 6 (2019): 356. http://dx.doi.org/10.3390/md17060356.

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Various red algae have repeatedly been reported to produce a variety of UV-absorbing mycosporine-like amino acids (MAAs), compounds that are well-known as natural sun-screens, as well as a plethora of betaines, metabolites which contribute to the osmotic balance under salt stress. Among other Rhodophyta, Bostrychia scorpioides, which is thriving as epiphyte on salt marsh plants in Europe and hence experiences extreme environmental conditions such as desiccation, UV-stress and osmotic stress, has barely been investigated for its secondary metabolites. In the present study, seven mycosporine lik
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Orfanoudaki, Maria, Anja Hartmann, Mostafa Alilou, et al. "Absolute Configuration of Mycosporine-Like Amino Acids, Their Wound Healing Properties and In Vitro Anti-Aging Effects." Marine Drugs 18, no. 1 (2019): 35. http://dx.doi.org/10.3390/md18010035.

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Mycosporine-like amino acids (MAAs) are water-soluble metabolites, reported to exhibit strong UV-absorbing properties. They have been found in a wide range of marine organisms, especially those that are exposed to extreme levels of sunlight, to protect them against solar radiation. In the present study, the absolute configuration of 14 mycosporine-like-amino acids was determined by combining the results of electronic circular dichroism (ECD) experiments and that of advanced Marfey’s method using LC-MS. The crystal structure of a shinorine hydrate was determined from single crystal X-ray diffra
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Carignan, Mario O., and José I. Carreto. "Characterization of mycosporine-serine-glycine methyl ester, a major mycosporine-like amino acid from dinoflagellates: a mass spectrometry study." Journal of Phycology 49, no. 4 (2013): 680–88. http://dx.doi.org/10.1111/jpy.12076.

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Laurion, I., F. Blouin, and S. Roy. "Packaging of mycosporine-like amino acids in dinoflagellates." Marine Ecology Progress Series 279 (2004): 297–303. http://dx.doi.org/10.3354/meps279297.

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Whitehead, Kenia, and John I. Hedges. "Photodegradation and photosensitization of mycosporine-like amino acids." Journal of Photochemistry and Photobiology B: Biology 80, no. 2 (2005): 115–21. http://dx.doi.org/10.1016/j.jphotobiol.2005.03.008.

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Wulff, A., and M. Appelgren. "Mycosporine-Like Amino Acids in Harmful Marine Microalgae." Journal of Phycology 38, s1 (2002): 37–38. http://dx.doi.org/10.1046/j.1529-8817.38.s1.107.x.

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Orfanoudaki, Maria, Anja Hartmann, Mitsunobu Kamiya, John West, and Markus Ganzera. "Chemotaxonomic Study of Bostrychia spp. (Ceramiales, Rhodophyta) Based on Their Mycosporine-Like Amino Acid Content." Molecules 25, no. 14 (2020): 3273. http://dx.doi.org/10.3390/molecules25143273.

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This study presents a chemotaxonomic investigation of the genus Bostrychia through the quantitation of the major mycosporine-like amino acids (MAAs). The presence of some cryptic species had been suggested in the B. moritziana/B. radicans complex and MAA-profiling in respective samples revealed different chemotypes within this species complex. Another possibly polyphyletic species is Bostrychia simpliciuscula; previous molecular phylogenetic analyses showed four genetic lineages within this species, one of which was recently distinguished as a new species. Phytochemical profiling of those samp
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Rastogi, Rajesh P., Sunita Kumari, Richa, Taejun Han, and Rajeshwar P. Sinha. "Molecular characterization of hot spring cyanobacteria and evaluation of their photoprotective compounds." Canadian Journal of Microbiology 58, no. 6 (2012): 719–27. http://dx.doi.org/10.1139/w2012-044.

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Phylogenetic analysis of 4 cyanobacterial strains isolated from hot springs in Rajgir, India, was carried out using the 16S rRNA gene (1400 bp). These strains were identified as members of Chroococcales ( Cyanothece sp. strain HKAR-1) and Nostocales ( Nostoc sp. strain HKAR-2, Scytonema sp. strain HKAR-3, and Rivularia sp. strain HKAR-4). Furthermore, we evaluated the presence of ultraviolet-screening and (or) photoprotective compounds, such as mycosporine-like amino acids (MAAs) and scytonemin, in these cyanobacteria by using high-performance liquid chromatography. Well-characterized MAAs, in
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Saha, Subarna, Animesh Sen, Sikha Mandal, Siba Prasad Adhikary, and Jnanendra Rath. "Mycosporine-alanine, an oxo-mycosporine, protect Hassallia byssoidea from high UV and solar irradiation on the stone monument of Konark." Journal of Photochemistry and Photobiology B: Biology 224 (November 2021): 112302. http://dx.doi.org/10.1016/j.jphotobiol.2021.112302.

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Ritchie, Raymond J., Adrienne J. Grant, Kylie Eltringham, and Rosalind Hinde. "Clotrimazole, a Model Compound for the Host Release Factor of the Coral Plesiastrea versipora." Functional Plant Biology 24, no. 3 (1997): 283. http://dx.doi.org/10.1071/pp96106.

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Crude homogenates of animal host tissues stimulate the release of photosynthetic products from symbiotic dinoflagellates isolated from corals and several other invertebrates. It is believed that specific ‘host release factors’ stimulate the symbiotic algae to release water-soluble compounds, chiefly glycerol and amino acids, to the host. Crude host homogenates also contain compounds which sometimes inhibit photosynthesis in isolated algal cells, although this inhibition is not apparent in the intact association. Therefore, use of crude homogenates in translocation experiments may sometimes lea
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Hirose, Euichi, Kaori Ohtsuka, Masaharu Ishikura, and Tadashi Maruyama. "Ultraviolet absorption in ascidian tunic and ascidian-Prochloron symbiosis." Journal of the Marine Biological Association of the United Kingdom 84, no. 4 (2004): 789–94. http://dx.doi.org/10.1017/s0025315404009956h.

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To characterize the ultraviolet (UV) light-absorbing function of the ascidian tunic, the light absorption spectrum was compared in 22 ascidian species collected from tropical and temperate waters. Non-photosymbiotic ascidians (17 species) had transparent tunics transmitting both visible and UV light, or pigmented or opaque tunics equally absorb both UV and visible light. However, a prominent absorption peak around 320 nm was exclusively found in the colonial ascidians hosting the algal symbiont Prochloron sp., and this absorption peak corresponded to absorption of UV-A (320–400 nm) and UV-B (2
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Bhatia, Saurabh, Satish Sardana, Ajay Sharma, Celia Bertha Vargas De La Cruz, Bhupal Chaugule, and Laleh Khodaie. "Development of broad spectrum mycosporine loaded sunscreen formulation from Ulva fasciata delile." BioMedicine 9, no. 3 (2019): 17. http://dx.doi.org/10.1051/bmdcn/2019090317.

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Ba.ckground: Sunscreen formulations primarily offer protection against UV induced damages however nowadays it also maintains skin natural physiological conditions. Current global market is flooded with numerous sunscreen products which offer protection to skin against several UV induced damages. However most of these sunscreen formulations offers narrow spectrum protection against UV and also suffer from stability as well as toxicity related issues. Methods: Present work aims to isolate mycosporine amino acid (Mgy) from green alga namely Ulva fasciata (U. fasciata) and study its sunscreen pote
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Chrapusta, Ewelina, Ariel Kaminski, Kornelia Duchnik, Beata Bober, Michal Adamski, and Jan Bialczyk. "Mycosporine-Like Amino Acids: Potential Health and Beauty Ingredients." Marine Drugs 15, no. 10 (2017): 326. http://dx.doi.org/10.3390/md15100326.

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Al-Utaibi, Ahmad A., Gul Raze Niaz, and Ahmad A. Al-UtaibiSultan S. Al-Lihaibi. "Mycosporine-like amino acids in six scleractinian coral species." OCEANOLOGIA 51, no. 1 (2009): 93–104. http://dx.doi.org/10.5697/oc.51-1.093.

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Woolley, Jack M., Michael Staniforth, Michael D. Horbury, Gareth W. Richings, Martin Wills, and Vasilios G. Stavros. "Unravelling the Photoprotection Properties of Mycosporine Amino Acid Motifs." Journal of Physical Chemistry Letters 9, no. 11 (2018): 3043–48. http://dx.doi.org/10.1021/acs.jpclett.8b00921.

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Kim, Hyeong-U., Soohyun Ha, Dinesh Amalnerkar, et al. "MoS2-Graphene-Mycosporine-Like Amino Acid Nanocomposite as Photocatalyst." Nano 12, no. 02 (2017): 1750019. http://dx.doi.org/10.1142/s1793292017500199.

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In the quest of extending isostructural hybridization approach to organic–inorganic nanocomposite-based photocatalytic systems, a unique strategy of replacing the traditional inorganic semiconductors with naturally produced mycosporine-like amino acids (MAA) is proposed. The main motivation of incorporating MAA in symbiotically configured nanocomposites is with regard to MAA green, nontoxic nature, UV absorption and photostability. Our facile one-pot solvothermal method is to facilitate the amalgamation of MAA and molybdenum disulfide-graphene (MG) composite at the molecular/nanoscale level to
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Zimba, P. V., and S. Boue. "Mycosporine-Like Amino Acid Intercalibration Effort Using Replicate Samples." Journal of Phycology 38, s1 (2002): 41. http://dx.doi.org/10.1046/j.1529-8817.38.s1.11.x.

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Jain, Shikha, Ganshyam Prajapat, Mustari Abrar, Lalita Ledwani, Anoop Singh, and Akhil Agrawal. "Cyanobacteria as efficient producers of mycosporine-like amino acids." Journal of Basic Microbiology 57, no. 9 (2017): 715–27. http://dx.doi.org/10.1002/jobm.201700044.

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Řezanka, T., M. Temina, A. G. Tolstikov, and V. M. Dembitsky. "Natural microbial UV radiation filters — Mycosporine-like amino acids." Folia Microbiologica 49, no. 4 (2004): 339–52. http://dx.doi.org/10.1007/bf03354663.

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