chlorophyll-a and artemisinin

The plastidial methylerythritol phosphate(MEP) pathway provides 5-carbon precursors to the biosynthesis of isoprenoid (including artemisinin). 2-C-Methyl-D-erythritol-4-phosphate cytidylyltransferase (MCT) is the third enzyme of the MEP pathway, which catalyzes 2-C-methyl-D-erythritol-4-phosphate to form 4-(cytidine 5’-diphospho)-2-C-methyl-D-erythritol. The full-length MCT cDNA sequence (AaMCT) was cloned and characterized for the first time from Artemisia annua L. Analysis of tissue expression pattern revealed that AaMCT was highly expressed in glandular secretory trichome and poorly expressed in leaf, flower, root and stem. AaMCT was found to be a methyl jasmonate (Me JA)-induced genes, the expression of AaMCT was significantly increased after MeJA treatment. Subcellular localization indicated that the GFP protein fused with AaMCT was targeted specifically in chloroplasts. The transgenic plants of Arabidopsis thaliana with AaMCT overexpression exhibited a significantly increase in the content of chlorophyll a, chlorophyll b and carotenoids, demonstrating that AaMCT kinase plays an influential role in isoprenoid biosynthesis.

Topics: Acetates; Arabidopsis; Artemisia annua; Artemisinins; Carotenoids; Chlorophyll; Chlorophyll A; Cloning, Molecular; Cyclopentanes; DNA, Complementary; Gene Expression Regulation, Plant; Nucleotidyltransferases; Oxylipins; Plant Proteins; Plants, Genetically Modified

Artemisinin, a potent antimalarial drug, is phytotoxic to many crops and weeds. The effects of artemisinin on stress markers, including fluorescence parameters, photosystem II photochemistry, photon energy dissipation, lipid peroxidation, reactive oxygen species generation and carbon isotope discrimination in Arabidopsis thaliana were studied. Arabidopsis ecotype Columbia (Col-0) seedlings were grown in perlite and watered with 50% Hoagland nutrient solution. Adult plants of Arabidopsis were treated with artemisinin at 0, 40, 80, 160 μM for one week. Artemisinin, in the range 40-160 μM, decreased the fresh biomass, chl a, b and leaf mineral contents. Photosynthetic efficiency, yield and electron transport rate in Arabidopsis were also reduced following exposure to 80 and 160 μM artemisinin. The ΦNPQ and NPQ were less than control. Artemisinin treatment caused an increase in root oxidizability and lipid peroxidation (MDA contents) of Arabidopsis. Calcium and nitrogen contents decreased after 80 and 160 μM artemisinin treatment compared to control. δ13C values were less negative following treatment with artemisinin as compared to the control. Artemisinin also decreased leaf protein contents in Arabidopsis. Taken together, these data suggest that artemisinin inhibits many physiological and biochemical processes in Arabidopsis.

Topics: Arabidopsis; Artemisinins; Carbon Isotopes; Chlorophyll; Electron Transport; Light; Photons; Photosynthesis; Photosystem II Protein Complex; Plant Leaves; Reactive Oxygen Species; Stress, Physiological; Xanthophylls

Artemisinin has been recognized as an allelochemical that inhibits growth of several plant species. However, its mode of action is not well clarified. In this study, the mechanism of artemisinin phytotoxicity on lettuce seedlings was investigated. Root and shoot elongation of lettuce seedlings were inhibited by artemisinin in a concentration-dependent manner. The compound effectively arrested cell division and caused loss of cell viability in root tips of lettuce. Overproduction of reactive oxygen species (ROS) was induced by artemisinin. Lipid peroxidation, proline overproduction and reduction of chlorophyll content in lettuce seedlings were found after treatments. These results suggested that artemisinin could induce ROS overproduction, which caused membrane lipids peroxidation and cell death, and impacted mitosis and physiological processes, resulting in growth inhibition of receptor plants.

Topics: Allelopathy; Artemisia; Artemisinins; Cell Death; Cell Membrane; Chlorophyll; Lactuca; Lipid Peroxidation; Meristem; Mitosis; Pheromones; Plant Roots; Plant Shoots; Proline; Reactive Oxygen Species; Seedlings

To study the growth effects of differing concentrations of artemisinin on green algae and to evaluate the ecological risk. The effects of artemisinin on the growth and the content change of chlorophyll, protein, oxygen, conductivity, SOD, CAT, MDA in Chlorella pyrenoidosa and Scenedesmus oblique were studied through 96 h toxicity tests. Artemisinin accelerated the growth of algae at a lower concentration ( <40 microg . L-1) with content increase of chlorophyll or protein and so on, and it inhibited the growth of algae at higher concentration ( >80 microg . L-1). The content of chlorophyll or protein in algae cells reduced with the increasing concentration of artemisinin, exhibiting the good concentration-effect relationship. SOD and CAT activity was stimulated at low concentrations ( <40 microg . L-1 ) and inhibited at high concentrations ( >80 microg . L- 1). However, MDA content increased significantly with the increase of concentration. According to the seven kinds of indicators changes, the time-response and dose-response suggested that the surfactant first hurt in Ch. pyrenoidosa was damaging membrane by changing membrane lipid molecules soluble. And primary mechanism on Chlorophyta cells might be related to the oxidation damage of lipid and other biological large molecules caused by artemisinin. The large-scale intensive planting of Artemisia annua may reduce the surrounding water productivity.

Topics: Artemisinins; Chlorophyll; Chlorophyta

Nitric oxide (NO) is an important signal molecule modulating the response of plants to environmental stress. Here we report the effects of boron (B) and aluminium (Al) contamination in soil, carried out with or without application of exogenous SNP (NO donor), on various plant processes in Artemisia annua, including changes in artemisinin content. The addition of B or Al to soil medium significantly reduced the yield and growth of plants and lowered the values of net photosynthetic rate, stomatal conductance, internal CO(2) concentration and total chlorophyll content. The follow-up treatment of NO donor favoured growth and improved the photosynthetic efficiency in stressed as well as non-stressed plants. Artemisinin content was enhanced by 24.6% and 43.8% at 1mmole of soil-applied B or Al. When SNP was applied at 2mmole concentration together with either 1mmole of B and/or Al, it further stimulated artemisinin biosynthesis compared to the control. Application of B+Al+SNP proved to be the best treatment combination for the artemisinin content in Artemisia annua leaves.

Topics: Aluminum; Antioxidants; Artemisia annua; Artemisinins; Boron; Chlorophyll; Follow-Up Studies; Nitric Oxide; Nitric Oxide Donors; Oxidative Stress; Photosynthesis; Plant Leaves; Soil Pollutants

Effects of artemisinin (derived from Artemisia annua) on the photosynthetic activity of Microcystis aeruginosa was investigated by using chlorophyll a (Chl a) fluorescence transient O-J-I-P and JIP-test after exposure to elevated artemisinin concentration. High artemisinin concentration resulted in a significant suppression in photosynthesis and respiration. Results showed that the OJIP curves flattened and the maximal fluorescence yield reached at the J step under artemisinin stress. The decreased values of the energy needed for the RCs' closure (Sm) and the number of oxidation and reduction (N) suggested that the reduction times of primary bound plastoquinone (Q(A)) was also decreased. The absorption flux (ABS/RC) per photosystem II (PSII) reaction center and the electron transport flux (ET(0)/RC) decreased with increasing artemisinin concentration. Excess artemisinin had little effect on the trapping flux (TR(0)/RC). The results showed that the decrease of photosynthesis in exposure to excess artemisinin may be a result of the inactivation of PSII reaction centers and the inhibition of electron transport in the acceptor side.

Topics: Anti-Infective Agents; Artemisinins; Chlorophyll; Fluorescence; Microcystis; Photosynthesis; Photosystem II Protein Complex; Reactive Oxygen Species; Water Pollutants, Chemical