Chlorophylls and Bacteriochlorophylls: Biochemistry, Biophysics, Functions and Applications

Supplementary material to this book contains the following Adobe-Writer (.pdf) files: an overview of the material, the color coding for the map on the title page), and supporting information for chapter 1, 14, 20, 22 and 30. Some of the files contain further links to materials on this server, in particular is there a collection of structural formulas accessible from the material to chapter 1. Please, click on the respective files for downloading. Any reference should cite the full title of the book

Artemisinin Inhibits Chloroplast Electron Transport Activity: Mode of Action

Artemisinin, a secondary metabolite produced in Artemisia plant species, besides having antimalarial properties is also phytotoxic. Although, the phytotoxic activity of the compound has been long recognized, no information is available on the mechanism of action of the compound on photosynthetic activity of the plant. In this report, we have evaluated the effect of artemisinin on photoelectron transport activity of chloroplast thylakoid membrane. The inhibitory effect of the compound, under in vitro condition, was pronounced in loosely and fully coupled thylakoids; being strong in the former. The extent of inhibition was drastically reduced in the presence of uncouplers like ammonium chloride or gramicidin; a characteristic feature described for energy transfer inhibitors. The compound, on the other hand, when applied to plants (in vivo), behaved as a potent inhibitor of photosynthetic electron transport. The major site of its action was identified to be the QB; the secondary quinone moiety of photosystemII complex. Analysis of photoreduction kinetics of para-benzoquinone and duroquinone suggest that the inhibition leads to formation of low pool of plastoquinol, which becomes limiting for electron flow through photosystemI. Further it was ascertained that the in vivo inhibitory effect appeared as a consequence of the formation of an unidentified artemisinin-metabolite rather than by the interaction of the compound per se. The putative metabolite of artemisinin is highly reactive in instituting the inhibition of photosynthetic electron flow eventually reducing the plant growth

Growth of the C4 dicot Flaveria bidentis: photosynthetic acclimation to low light through shifts in leaf anatomy and biochemistry

In C4 plants, acclimation to growth at low irradiance by means of anatomical and biochemical changes to leaf tissue is considered to be limited by the need for a close interaction and coordination between bundle sheath and mesophyll cells. Here differences in relative growth rate (RGR), gas exchange, carbon isotope discrimination, photosynthetic enzyme activity, and leaf anatomy in the C4 dicot Flaveria bidentis grown at a low (LI; 150 μmol quanta m2 s−1) and medium (MI; 500 μmol quanta m2 s−1) irradiance and with a 12 h photoperiod over 36 d were examined. RGRs measured using a 3D non-destructive imaging technique were consistently higher in MI plants. Rates of CO2 assimilation per leaf area measured at 1500 μmmol quanta m2 s−1 were higher for MI than LI plants but did not differ on a mass basis. LI plants had lower Rubisco and phosphoenolpyruvate carboxylase activities and chlorophyll content on a leaf area basis. Bundle sheath leakiness of CO2 (ϕ) calculated from real-time carbon isotope discrimination was similar for MI and LI plants at high irradiance. ϕ increased at lower irradiances, but more so in MI plants, reflecting acclimation to low growth irradiance. Leaf thickness and vein density were greater in MI plants, and mesophyll surface area exposed to intercellular airspace (Sm) and bundle sheath surface area per unit leaf area (Sb) measured from leaf cross-sections were also both significantly greater in MI compared with LI leaves. Both mesophyll and bundle sheath conductance to CO2 diffusion were greater in MI compared with LI plants. Despite being a C4 species, F. bidentis is very plastic with respect to growth irradiance

Calibração do medidor de clorofila Minolta SPAD-502 para avaliação do conteúdo de nitrogênio do milho Calibration of a Minolta SPAD-502 chlorophyll meter for evaluation of the nitrogen nutrition of maize

O objetivo deste trabalho foi calibrar o medidor de clorofila Minolta SPAD-502 para avaliação da nutrição nitrogenada das plantas de milho, baseando-se na prévia comparação das leituras de clorofila com os teores obtidos pelos extratores N,N-dimetilformamida (DMF) e acetona 80%. No campo, foram avaliados os teores de clorofila em folhas de milho cultivado sob plantio direto após a cultura de aveia-preta e após a de tremoço-branco, por duas safras consecutivas. A extração da clorofila com a solução DMF, por 72 horas, foi a mais indicada para a calibração do medidor de clorofila SPAD502 na cultura do milho. O ajuste do modelo linear expressou melhor a relação entre o conteúdo de clorofila e as leituras do SPAD na cultura do milho, e seu uso produziu resultados coerentes com o estado nutricional da cultura.<br>The subject of this study was the calibration of a Minolta SPAD-502 chlorophyll meter for evaluation of the N nutrition of maize, firstly comparing the chlorophyll readings to the contents obtained from either 80% acetone or N,N-dimethylformamide (DMF) chlorophyll extrators. The chlorophyll of the maize leaves cultivated under zerotillage after oat and lupin for two consecutive harvests was evaluated in a field experiment. The chlorophyll extraction after 72 hours in DMF solution, was the most suitable for the calibration of the SPAD502 chlorophyll meter for maize and its use was coherent with the nutritional status of the crop