Liste de références Lawrence, K. P., Long, P. F. & Young, A. R. Mycosporine-Like Amino Acids for Skin Photoprotection. Curr. Med. Chem. 25 , 5512–5527 (2018) de la Coba, F. et al. UVA and UVB Photoprotective Capabilities of Topical Formulations Containing Mycosporine-like Amino Acids (MAAs) through Different Biological Effective Protection Factors (BEPFs). Mar. Drugs 17 (2019) Downs, C. A., DiNardo, J. C., Stien, D., Rodrigues, A. M. S. & Lebaron, P. Benzophenone Accumulates over Time from the Degradation of Octocrylene in Commercial Sunscreen Products. Chem. Res. Toxicol. 34 , 1046–1054 (2021) Vuckovic, D. et al. Conversion of oxybenzone sunscreen to phototoxic glucoside conjugates by sea anemones and corals. Science 376 , 644–648 (2022) Chrapusta, E. et al. Mycosporine-Like Amino Acids: Potential Health and Beauty Ingredients. Mar. Drugs 15 (2017) Woolley, J. M. et al. Unravelling the Photoprotection Properties of Mycosporine Amino Acid Motifs. J. Phys. Chem. Lett. 9 , 3043–3048 (2018) Carreto, J. I. & Carignan, M. O. Mycosporine-Like Amino Acids: Relevant Secondary Metabolites. Chemical and EcologicalAspects. Mar. Drugs 9 , 387–446 (2011) Claverie, M., McReynolds, C., Petitpas, A., Thomas, M. & Fernandes, S. C. M. Marine-Derived Polymeric Materials and Biomimetics: An Overview. Polymers 12 , 1002 (2020) La Barre, S., Roullier, C. & Boustie, J. Mycosporine-Like Amino Acids (MAAs) in Biological Photosystems. in Outstanding Marine Molecules: Chemistry, Biology, Analysis (ed. Stéphane La Barre, J.-M. K. (eds. )) 333–360 (Wiley-CH Verlag GmbH, 2014). doi:10.1002/9783527681501.ch15 Shick, J. M. & Dunlap, W. C. Mycosporine-like amino acids and related Gadusols: biosynthesis, acumulation, and UV-protective functions in aquatic organisms. Annu. Rev. Physiol. 64 , 223–262 (2002) Böhm, G. A., Pfleiderer, W., Böger, P. & Scherer, S. Structure of a novel oligosaccharide-mycosporine-amino acid ultraviolet A/B sunscreen pigment from the terrestrial cyanobacterium Nostoc commune. J. Biol. Chem. 270 , 853–8539 (1995) Matsui, K. et al. Novel glycosylated mycosporine-like amino acids with radical scavenging activity from the cyanobacterium Nostoc commune. J. Photochem. Photobiol. B 105 , 81–89 (2011) Nazifi, E. et al. Characterization of the chemical diversity of glycosylated mycosporine-like amino acids in the terrestrial cyanobacterium Nostoc commune. J. Photochem. Photobiol. B 142 , 154–168 (2015) Ishihara, K. et al. Novel glycosylated mycosporine-like amino acid, 13-O-(β-galactosyl)-porphyra-334, from the edible cyanobacterium Nostoc sphaericum-protective activity on human keratinocytes from UV light. J. Photochem. Photobiol. B 172 , 102–108 (2017) CAZy - GH70. http://www.cazy.org/GH70.html Molina, M., Cioci, G., Moulis, C., Séverac, E. & Remaud-Siméon, M. Bacterial α-Glucan and Branching Sucrases from GH70 Family: Discovery, Structure-Function Relationship Studies and Engineering. Microorganisms 9 , 1607 (2021) Vuillemin, M. et al. Characterization of the First α-(1-3) Branching Sucrases of the GH70 Family. J. Biol. Chem. 291 , 7687–7702 (2016) Malbert, Y. et al. Engineering a branching sucrase for flavonoid glucoside diversification. Sci. Rep. 8 , 15153 (2018) Fernandes, S. C. M. et al. Exploiting Mycosporines as Natural Molecular Sunscreens for the Fabrication of UV-Absorbing Green Materials. ACS Appl. Mater. Interfaces 7 , 16558–16564 (2015) Dunlap, W. C., Williams, D. M., Chalker, B. E. & Banaszak, A. T. Biochemical photoadaptation in vision : U.V.-absorbing pigments in fish eye tissues. Comp. Biochem. Physiol. Part B Comp. Biochem. 93 , 601 (1989) Wada, N., Sakamoto, T. & Matsugo, S. Mycosporine-Like Amino Acids and Their Derivatives as Natural Antioxidants. Antioxidants 4 , 603-646 (2015) Studier, F. W. Protein production by auto-induction in high density shaking cultures. Protein Expr. Purif. 41 , 207-234 (2005) Miller, G. L. Use of Dinitrosalicylic Acid Reagent for Determination of Reducing Sugar. Anal. Chem. 31 , 426-428 (1959) Claverie, M. et al. Futile Encounter Engineering of the DSR-M Dextransucrase Modifies the Resulting Polymer Length. Biochemistry 58 , 2853-2859 (2019)