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      The Role of Cutinsomes in Plant Cuticle Formation

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          Abstract

          The cuticle commonly appears as a continuous lipophilic layer located at the outer epidermal cell walls of land plants. Cutin and waxes are its main components. Two methods for cutin synthesis are considered in plants. One that is based on enzymatic biosynthesis, in which cutin synthase (CUS) is involved, is well-known and commonly accepted. The other assumes the participation of specific nanostructures, cutinsomes, which are formed in physicochemical self-assembly processes from cutin precursors without enzyme involvement. Cutinsomes are formed in ground cytoplasm or, in some species, in specific cytoplasmic domains, lipotubuloid metabolons (LMs), and are most probably translocated via microtubules toward the cuticle-covered cell wall. Cutinsomes may additionally serve as platforms transporting cuticular enzymes. Presumably, cutinsomes enrich the cuticle in branched and cross-linked esterified polyhydroxy fatty acid oligomers, while CUS1 can provide both linear chains and branching cutin oligomers. These two systems of cuticle formation seem to co-operate on the surface of aboveground organs, as well as in the embryo and seed coat epidermis. This review focuses on the role that cutinsomes play in cuticle biosynthesis in S. lycopersicum, O. umbellatum and A. thaliana, which have been studied so far; however, these nanoparticles may be commonly involved in this process in different plants.

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          Most cited references106

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          Building lipid barriers: biosynthesis of cutin and suberin.

          Cutin and suberin are the polymer matrices for lipophilic cell wall barriers. These barriers control the fluxes of gases, water and solutes, and also play roles in protecting plants from biotic and abiotic stresses and in controlling plant morphology. Although they are ubiquitous, cutin and suberin are the least understood of the major plant extracellular polymers. The use of forward and reverse genetic approaches in Arabidopsis has led to the identification of oxidoreductase and acyltransferase genes involved in the biosynthesis of these polymers. However, major questions about the underlying polymer structure, biochemistry, and intracellular versus extracellular assembly remain to be resolved. The analysis of plant lines with modified cutins and suberins has begun to reveal the inter-relationships between the composition and function of these polymers.
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            The Chara Genome: Secondary Complexity and Implications for Plant Terrestrialization

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              Superhydrophobic and superhydrophilic plant surfaces: an inspiration for biomimetic materials.

              The diversity of plant surface structures, evolved over 460 million years, has led to a large variety of highly adapted functional structures. The plant cuticle provides structural and chemical modifications for surface wetting, ranging from superhydrophilic to superhydrophobic. In this paper, the structural basics of superhydrophobic and superhydrophilic plant surfaces and their biological functions are introduced. Wetting in plants is influenced by the sculptures of the cells and by the fine structure of the surfaces, such as folding of the cuticle, or by epicuticular waxes. Hierarchical structures in plant surfaces are shown and further types of plant surface structuring leading to superhydrophobicity and superhydrophilicity are presented. The existing and potential uses of superhydrophobic and superhydrophilic surfaces for self-cleaning, drag reduction during moving in water, capillary liquid transport and other biomimetic materials are shown.
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                Author and article information

                Journal
                Cells
                Cells
                cells
                Cells
                MDPI
                2073-4409
                25 July 2020
                August 2020
                : 9
                : 8
                : 1778
                Affiliations
                [1 ]Faculty of Biology and Environmental Protection, Institute of Experimental Biology, Department of Cytophysiology, University of Lodz, Pomorska 141/143, 90-236 Lodz, Poland; dariusz.stepinski@ 123456biol.uni.lodz.pl (D.S.); maria.kwiatkowska@ 123456biol.uni.lodz.pl (M.K.); agnieszka.wojtczak@ 123456biol.uni.lodz.pl (A.W.); justyna.polit@ 123456biol.uni.lodz.pl (J.T.P.)
                [2 ]Instituto de Hortofruticultura Subtropical y Mediterránea “La Mayora” UMA-CSIC, Universidad de Málaga, Campus de Teatinos, 29071 Málaga, Spain; edominguez@ 123456eelm.csic.es (E.D.); heredia@ 123456uma.es (A.H.)
                Author notes
                [* ]Correspondence: katarzyna.poplonska@ 123456biol.uni.lodz.pl ; Tel.: +48-42-6354734
                [†]

                Maria Kwiatkowska (M.K.) has passed away.

                Author information
                https://orcid.org/0000-0002-9217-2883
                https://orcid.org/0000-0002-9655-001X
                https://orcid.org/0000-0001-9475-0942
                Article
                cells-09-01778
                10.3390/cells9081778
                7465133
                32722473
                df0e44ff-76ea-4bcb-a439-9e7dad87e68e
                © 2020 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
                : 07 June 2020
                : 23 July 2020
                Categories
                Review

                cuticle-synthesizing enzyme,cutin,cutinsome,electron microscopy,plant cuticle

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