chlorophyll-a and 2-aminoindan-2-phosphonic-acid

Effects of methyl jasmonate (MeJA), salicylic acid (SA) or 2-aminoindane-2-phosphonic acid (AIP) pre-treatments on the sensitivity of Xanthoria parietina exposed to UV-A were studied. UV decreased chlorophylls and stimulated increase in hydrogen peroxide and superoxide level. Accumulation of soluble phenols and flavonoids increased in response to UV treatment. Metabolic modulators had negligible impact on these UV-induced changes. Within free amino acids, AIP (-UV variant) and SA and MeJA (+UV variants) altered their accumulation. AIP had no effect on the amount of phenylalanine. Benzoic and cinnamic acids were elevated by UV and mainly MeJA influenced their accumulations. Among lichen specific metabolites, vulpinic acid and ergosterol increased while usnic acid and atranorin decreased after exposure to UV; accumulation of parietin was not affected. Applied modulators showed a different effect on these lichen metabolites but biosynthetic pathway-specific trend of alteration was visible. Overall, MeJA showed the most pronounced effect among studied parameters. Accumulation of selected phenolics in response to UV-A seems to be an important feature of Xanthoria tolerance. Present finding in the context of phenolic metabolism in non-vascular plants and with respect to limited data about effect of studied modulators on non-vascular plants are discussed.

Topics: Acetates; Amino Acids; Ascomycota; Benzoic Acid; Chlorophyll; Cinnamates; Cyclopentanes; Flavonoids; Indans; Lichens; Organophosphonates; Oxylipins; Phenols; Reactive Oxygen Species; Salicylic Acid; Ultraviolet Rays

Lettuce (Lactuca sativa) plants grown in a protective environment, similar to in vitro conditions, were acclimated in a growth chamber and subjected to water stress to examine the activation of genes involved in secondary metabolism and biosynthesis of antioxidants. The expression of phenylalanine ammonia-lyase (PAL), gamma-tocopherol methyl transferase (gamma-TMT) and l-galactose dehydrogenase (l-GalDH) genes involved in the biosynthesis of phenolic compounds, alpha-tocopherol and ascorbic acid, respectively, were determined during plant adaptation. These genes were activated in tender plants, grown under protective conditions, when exposed to normal growing conditions in a growth chamber. A large increase in transcript level for PAL, a key gene in the phenylpropanoid pathway leading to the biosynthesis of a wide array of phenolics and flavonoids, was observed within 1h of exposure of tender plants to normal growing conditions. Plant growth, especially the roots, was retarded in tender plants when exposed to normal growing conditions. Furthermore, exposure of both protected and unprotected plants to water stress resulted in the activation of PAL. PAL inhibition by 2-aminoindan-2-phosphonic acid (AIP) rendered these plants more sensitive to chilling and heat shock treatments. These results suggest that activation of secondary metabolism as well as the antioxidative metabolism is an integral part of plant adaptation to normal growing conditions in lettuce plants.

Topics: Adaptation, Physiological; Antioxidants; Chlorophyll; Electrolytes; Environment; Fluorescence; Gene Expression Regulation, Plant; Indans; Lactuca; Organophosphonates; Photosynthesis; Plant Leaves; Plant Roots; Plant Shoots; Stress, Physiological; Water

Duckweed (Spirodela intermedia) was grown axenically on 1/2 strength Hutner's nutrient solution plus 1% sucrose, with the l-phenylalanine ammonia-lyase (PAL) inhibitor 2-aminoindan-2-phosphonic acid (AIP) at 0.0, 0.05, or 10 microM, at constant 25 degrees C and a light intensity of 300 micromol m(-2) s(-1) photosynthetically active radiation from CW fluorescent lamps. Growth with 10 microM AIP led to decreased frond area and fresh weight, but dry weight was unchanged. Microscopic examination of fronds revealed increased frond thickness and a lack of reticulate aerenchyma. Ultraviolet epifluorescence microscopy and UV-Vis spectroscopy of methanolic extracts confirmed the dose-dependent inhibition of secondary phenolic synthesis with the near total elimination of secondary phenolic accumulation at the 10 microM level. AIP-treated plants showed increased sensitivity to UV-B as shown by a reduced F(v)/F(m). The results provided direct evidence of the working hypothesis that phenols function to screen UV radiation from reaching photosynthetic tissues or damaging other sensitive tissues. A novel histochemical method employing zirconyl chloride to visualize phenols is discussed.

Topics: Araceae; Chlorophyll; Enzyme Inhibitors; Indans; Microscopy, Electron, Scanning; Organophosphonates; Phenols; Phenylalanine Ammonia-Lyase; Photosynthesis; Plant Leaves; Ultraviolet Rays