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      The cell wall polysaccharides of a photosynthetic relative of apicomplexans, Chromera velia

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          Abstract

          Chromerids are a group of alveolates, found in corals, that show peculiar morphological and genomic features. These organisms are evolutionary placed in‐between symbiotic dinoflagellates and parasitic apicomplexans. There are two known species of chromerids: Chromera velia and Vitrella brassicaformis. Here, the biochemical composition of the C.  velia cell wall was analyzed. Several polysaccharides adorn this structure, with glucose being the most abundant monosaccharide (approx. 80%) and predominantly 4‐linked (approx. 60%), suggesting that the chromerids cell wall is mostly cellulosic. The presence of cellulose was cytochemically confirmed with calcofluor white staining of the algal cell. The remaining wall polysaccharides, assuming structures are similar to those of higher plants, are indicative of a mixture of galactans, xyloglucans, heteroxylans, and heteromannans. The present work provides, for the first time, insights into the outermost layers of the photosynthetic alveolate C.  velia.

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          A photosynthetic alveolate closely related to apicomplexan parasites.

          Many parasitic Apicomplexa, such as Plasmodium falciparum, contain an unpigmented chloroplast remnant termed the apicoplast, which is a target for malaria treatment. However, no close relative of apicomplexans with a functional photosynthetic plastid has yet been described. Here we describe a newly cultured organism that has ultrastructural features typical for alveolates, is phylogenetically related to apicomplexans, and contains a photosynthetic plastid. The plastid is surrounded by four membranes, is pigmented by chlorophyll a, and uses the codon UGA to encode tryptophan in the psbA gene. This genetic feature has been found only in coccidian apicoplasts and various mitochondria. The UGA-Trp codon and phylogenies of plastid and nuclear ribosomal RNA genes indicate that the organism is the closest known photosynthetic relative to apicomplexan parasites and that its plastid shares an origin with the apicoplasts. The discovery of this organism provides a powerful model with which to study the evolution of parasitism in Apicomplexa.
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            Determining the polysaccharide composition of plant cell walls.

            The plant cell wall is a chemically complex structure composed mostly of polysaccharides. Detailed analyses of these cell wall polysaccharides are essential for our understanding of plant development and for our use of plant biomass (largely wall material) in the food, agriculture, fabric, timber, biofuel and biocomposite industries. We present analytical techniques not only to define the fine chemical structures of individual cell wall polysaccharides but also to estimate the overall polysaccharide composition of cell wall preparations. The procedure covers the preparation of cell walls, together with gas chromatography-mass spectrometry (GC-MS)-based methods, for both the analysis of monosaccharides as their volatile alditol acetate derivatives and for methylation analysis to determine linkage positions between monosaccharide residues as their volatile partially methylated alditol acetate derivatives. Analysis time will vary depending on both the method used and the tissue type, and ranges from 2 d for a simple neutral sugar composition to 2 weeks for a carboxyl reduction/methylation linkage analysis.
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              Evolution and diversity of plant cell walls: from algae to flowering plants.

              All photosynthetic multicellular Eukaryotes, including land plants and algae, have cells that are surrounded by a dynamic, complex, carbohydrate-rich cell wall. The cell wall exerts considerable biological and biomechanical control over individual cells and organisms, thus playing a key role in their environmental interactions. This has resulted in compositional variation that is dependent on developmental stage, cell type, and season. Further variation is evident that has a phylogenetic basis. Plants and algae have a complex phylogenetic history, including acquisition of genes responsible for carbohydrate synthesis and modification through a series of primary (leading to red algae, green algae, and land plants) and secondary (generating brown algae, diatoms, and dinoflagellates) endosymbiotic events. Therefore, organisms that have the shared features of photosynthesis and possession of a cell wall do not form a monophyletic group. Yet they contain some common wall components that can be explained increasingly by genetic and biochemical evidence.
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                Author and article information

                Contributors
                giadatortorelli@gmail.com
                Journal
                J Phycol
                J Phycol
                10.1111/(ISSN)1529-8817
                JPY
                Journal of Phycology
                John Wiley and Sons Inc. (Hoboken )
                0022-3646
                1529-8817
                07 October 2021
                December 2021
                : 57
                : 6 ( doiID: 10.1111/jpy.v57.6 )
                : 1805-1809
                Affiliations
                [ 1 ] School of Biosciences The University of Melbourne Parkville 3010 Victoria Australia
                [ 2 ] CSIRO Agriculture and Food Canberra 2601 Australian Capital Territory Australia
                [ 3 ] State Key Laboratory of Biocontrol Center for Parasitic Organisms School of Life Sciences Sun Yat‐Sen University Guangzhou 510275 China
                [ 4 ] Institute of Parasitology, Biology Centre Czech Academy of Sciences 370 05 České Budějovice Czech Republic
                [ 5 ] Department of Animal, Plant & Soil Sciences La Trobe Institute for Agriculture and Food La Trobe University AgriBio Building Bundoora Victoria Australia
                [ 6 ] Faculty of Science University of South Bohemia 37005 České Budějovice Czech Republic
                Author notes
                [*] [* ] Author for correspondence: email giadatortorelli@ 123456gmail.com .

                Author information
                https://orcid.org/0000-0001-6854-8070
                Article
                JPY13211
                10.1111/jpy.13211
                9293442
                34491587
                e0dd2438-05ca-4cc7-b10c-e773364ac446
                © 2021 The Authors. Journal of Phycology published by Wiley Periodicals LLC on behalf of Phycological Society of America

                This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.

                History
                : 09 August 2021
                : 13 May 2021
                : 24 August 2021
                Page count
                Figures: 2, Tables: 1, Pages: 5, Words: 2589
                Funding
                Funded by: ERDF/ESF
                Award ID: CZ.02.1.01/0.0/0.0/16_019/0000759
                Funded by: Czech Science Foundation , doi 10.13039/501100001824;
                Award ID: 21‐03224S
                Funded by: Australian Research Council , doi 10.13039/501100000923;
                Award ID: DP210100639
                Categories
                Note
                Note
                Custom metadata
                2.0
                December 2021
                Converter:WILEY_ML3GV2_TO_JATSPMC version:6.1.7 mode:remove_FC converted:18.07.2022

                alveolata,calcofluor white,cell wall,cellulose,chromera velia,chromerids,monosaccharide linkage analysis

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