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      A Method for the Isolation and Characterization of Mycosporine-Like Amino Acids from Cyanobacteria

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          Abstract

          This report provides a broadly applicable and cost-effective method for the purification of mycosporine-like amino acids (MAAs) from cyanobacteria. As MAAs are known to have multiple bioactivities for health and beauty, a universal isolation method of MAAs from biomass is attractive. In particular, the biomass of photosynthetic microorganisms such as cyanobacteria is of interest as a natural source of useful compound production, because of their photoautotrophic property. The method presented here is applicable for the isolation of mycosporine-2-glycine (M2G), which is a rare MAA produced in a halotolerant cyanobacterium. This method also allowed for the isolation of two of the most common MAAs, shinorine (SHI) and porphyra-334 (P334). A three-step separation process using low pressure liquid chromatography yielded purified MAAs, which were characterized by nuclear magnetic resonance (NMR) and liquid chromatography-mass spectrometry (LC/MS) analyses. The purified MAAs exhibited free radical scavenging activity in the 2,2′-azino- bis(3-ethylbenzothiazoline-6-sulfonic acid) (ABTS) assay. The experimental parameters obtained in this report may allow for a scale-up of the MAA purification process for future industrial applications.

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          Antioxidant activity of mycosporine-like amino acids isolated from three red macroalgae and one marine lichen

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            Mycosporine-Like Amino Acids: Potential Health and Beauty Ingredients

            Human skin is constantly exposed to damaging ultraviolet radiation (UVR), which induces a number of acute and chronic disorders. To reduce the risk of UV-induced skin injury, people apply an additional external protection in the form of cosmetic products containing sunscreens. Nowadays, because of the use of some chemical filters raises a lot of controversies, research focuses on exploring novel, fully safe and highly efficient natural UV-absorbing compounds that could be used as active ingredients in sun care products. A promising alternative is the application of multifunctional mycosporine-like amino acids (MAAs), which can effectively compete with commercially available filters. Here, we outline a complete characterization of these compounds and discuss their enormous biotechnological potential with special emphasis on their use as sunscreens, activators of cells proliferation, anti-cancer agents, anti-photoaging molecules, stimulators of skin renewal, and functional ingredients of UV-protective biomaterials.
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              A broadly applicable method for extraction and characterization of mycosporines and mycosporine-like amino acids of terrestrial, marine and freshwater origin.

              A universal method allowing simultaneous extraction and analysis of diverse ultraviolet-B-absorbing compounds belonging to mycosporines and mycosporine-like amino acids (MAAs) is presented. Mycosporines and MAAs are found both in prokaryotes and eukaryotes and possess photoprotective properties. Our method was successfully tested by screening 31 cyanobacterial, 11 actinomycete and 45 fungal strains for their mycosporine and MAA content. The majority of the isolates tested originated from subaerial rock surfaces and were inherently protected from excessive sun irradiation. The new method includes a solid-liquid extraction procedure, followed by a reversed phase liquid chromatography/mass spectrometry. Eight different mycosporines and five MAAs were efficiently separated and identified by their retention times, absorption maxima and fragmentation patterns. Mycosporines were found both in rock-inhabiting fungi and cyanobacteria and consequently may render an ecological marker of these peculiar terrestrial environments.
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                Author and article information

                Journal
                Methods Protoc
                Methods Protoc
                mps
                Methods and Protocols
                MDPI
                2409-9279
                03 December 2018
                December 2018
                : 1
                : 4
                : 46
                Affiliations
                [1 ]Department of Microbiology, Faculty of Science, Chulalongkorn University, Payathai Road, Pathumwan, Bangkok 10330, Thailand; siripat.ngoennet@ 123456gmail.com
                [2 ]Faculty of Pharmacy, Meijo University, 150 Yagotoyama, Tenpaku-ku, Nagoya, Aichi 468-8503, Japan; yasuhiro@ 123456meijo-u.ac.jp
                [3 ]Faculty of Science and Technology, Meijo University, 1-501 Shiogamaguchi, Tenpaku-ku, Nagoya, Aichi 468-8502, Japan; hibino@ 123456meijo-u.ac.jp
                Author notes
                [* ]Correspondence: Rungaroon.W@ 123456chula.ac.th (R.W.-S.); kageyama@ 123456meijo-u.ac.jp (H.K.); Tel.: +66-2-218-5091 (R.W.-S.); +81-52-838-2609 (H.K.)
                Author information
                https://orcid.org/0000-0002-7741-7408
                Article
                mps-01-00046
                10.3390/mps1040046
                6481085
                9de1590c-5386-411f-9aeb-77663b66835e
                © 2018 by the authors.

                Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license ( http://creativecommons.org/licenses/by/4.0/).

                History
                : 26 October 2018
                : 30 November 2018
                Categories
                Protocol

                mycosporine-like amino acids,mycosporine-2-glycine,shinorine,porphyra-334

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