ABSTRACT
Lichens are symbiotic photosynthesizing organisms with thalli formed by fungi and algae/cyanobacteria that possess high stress tolerance. One of the factors that contributes to the ability of a lichen to tolerate harsh environmental conditions is the presence of unique metabolites, including high-molecular-weight dark pigments termed melanins. The chemical composition and structure of lichen melanins remain poorly studied. We analyzed the elemental composition, the main functional groups, and the physicochemical properties of melanin extracted from Cetraria islandica and Pseudevernia furfuracea lichens. Based on the C/N ratio, this pigment is allomelanin. We also identified functional groups that provide photoprotective and antioxidant properties of melanin. Melanin synthesis might be an essential defense mechanism contributing to the survival of lichens under exposure to UV radiation.
Subject(s)
Antioxidants/pharmacology , Lichens/metabolism , Melanins/chemistry , Melanins/metabolism , Parmeliaceae/metabolism , Protein Structural Elements , Lichens/growth & development , Ultraviolet RaysABSTRACT
This is the first study to show that polyamine spermine, a low-molecular-weight nitrogen-containing compound, can induce autophagy in plants. This process is accompanied by an increased generation of reactive oxygen species and nitric oxide, which play a signal role and are required for triggering autophagy.
Subject(s)
Autophagy/drug effects , Nitric Oxide/metabolism , Reactive Oxygen Species/metabolism , Spermine/pharmacology , Triticum/metabolism , Triticum/cytologyABSTRACT
Plant cell wall is an example of a widespread natural supramolecular structure: its components are considered to be the most abundant organic compounds renewable by living organisms. Plant cell wall includes numerous components, mainly polysaccharidic; its formation is largely based on carbohydrate-carbohydrate interactions. In contrast to the extracellular matrix of most other organisms, the plant cell compartment located outside the plasma membrane is so structured that has been named "wall". The present review summarizes data on the mechanisms of formation of this supramolecular structure and considers major difficulties and results of research. Existing approaches to the study of interactions between polysaccharides during plant cell wall formation have been analyzed, including: (i) characterization of the structure of natural polysaccharide complexes obtained during cell wall fractionation; (ii) analysis of the interactions between polysaccharides "at mixing in a tube"; (iii) study of the interactions between isolated individual plant cell wall matrix polysaccharides and microfibrils formed by cellulose-synthesizing microorganisms; and (iv) investigation of cell wall formation and modification directly in plant objects. The key stages in formation of plant cell wall supramolecular structure are defined and characterized as follows: (i) formation of cellulose microfibrils; (ii) interactions between matrix polysaccharides within Golgi apparatus substructures; (iii) interaction between matrix polysaccharides, newly secreted outside the plasma membrane, and cellulose microfibrils during formation of the latter; (iv) packaging of the formed complexes and individual polysaccharides in cell wall layers; and (v) modification of deposited cell wall layers.
Subject(s)
Cell Wall/chemistry , Cell Wall/metabolism , Plant Cells , Animals , Bacteria/metabolism , Golgi Apparatus/chemistry , Golgi Apparatus/metabolism , Microfibrils/chemistry , Microfibrils/metabolism , Plants/metabolism , Polysaccharides/metabolismABSTRACT
Two active fractions of soluble oligosaccharides were isolated from pea (Pisum sativum L.) stem tissues. Both fractions are capable of affecting different phases of root development on buckwheat thin cell-layer explants (TCLs) and of inhibiting auxin-promoted growth of etiolated pea stem segments. The existence of non-wall bioactive oligosaccharides which may have a role in cell development in vivo is proposed.