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Book of Abstracts - Geyseco

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FESPB 2010 - XVII Congress <strong>of</strong> the Federation <strong>of</strong> European Societies <strong>of</strong> Plant Biology<br />

mutants under controlled sodium and potassium conditions.<br />

When grown under low potassium levels, sos1 growth was severely<br />

affected but only if the medium contained sodium. Removal<br />

<strong>of</strong> sodium abrogated the potassium phenotype.<br />

Growth <strong>of</strong> akt1 mutant was reduced at low potassium levels but<br />

not affected by sodium at the low concentration <strong>of</strong> this cation<br />

used in the experiment. Moreover, an akt1 sos1 double mutant<br />

behaved like akt1 single mutant in normal conditions but, when<br />

sodium was added to the medium, growth was reduced compared<br />

to that <strong>of</strong> sos1 and akt1 single mutants in all the potassium<br />

concentrations tested. Our results shed light on the interaction <strong>of</strong><br />

both SOS1 and AKT1 in potassium nutrition.<br />

S08-001: EFFECTS OF SALICYLIC ACID ON PHOTOS-<br />

YNTHESIS<br />

Janda, K.¹* - Hideg, É.² - Janda, T.³ - Szalai, G.³ - Kovács, L.²<br />

¹University <strong>of</strong> Szeged<br />

²Biological Research Center <strong>of</strong> the Hungarian Academy <strong>of</strong> Sciences<br />

³Agricultural Research Institute <strong>of</strong> the Hungarian Academy <strong>of</strong><br />

Sciences<br />

*Corresponding author e-mail: gumimacihu@yahoo.co.uk<br />

Salicylic acid (SA) is a phenolic phytohormone with important<br />

roles in plant development, transpiration, endogenous signalling<br />

and defence against pathogens.<br />

One <strong>of</strong> the pathways <strong>of</strong> SA biosynthesis is located in the chloroplasts.<br />

The aim <strong>of</strong> the present work was to investigate the<br />

possible regulatory effects <strong>of</strong> SA on the photosynthetic electron<br />

transport processes. Here we show that SA also affects leaf photosynthesis,<br />

via inducing stomatal closure and also by slowing<br />

down Photosystem (PS) II electron transport. Photosynthetic<br />

CO 2<br />

incorporation, and stomatal conductivity (measured with an<br />

infrared gas analyser) were much lower in SA-infiltrated tobacco<br />

leaves than in untreated or water-infiltrated controls.<br />

Data <strong>of</strong> tobacco and pea leaves show that PS II electron transport<br />

(calculated from PAM chlorophyll fluorescence data) was more<br />

sensitive to SA than PS I (measured with far red absorption). Direct<br />

probing <strong>of</strong> PS II charge separation and stabilization (measured<br />

with thermoluminescence), however, showed that these<br />

events were less affected in isolated thylakoid membranes than<br />

in leaves, suggesting that the effect <strong>of</strong> SA on PS II is indirect and<br />

different from that <strong>of</strong> phenolic herbicides.<br />

Our data also suggest that the effects <strong>of</strong> SA may differ in different<br />

plant species.<br />

S08-002: MONITORING CHLOROPHYLL A FLUORES-<br />

CENCE IN ARABIDOPSIS PLANTS AFTER CITRAL<br />

TREATMENT<br />

Sotelo Pérez, T. * - Graña, E. - Reigosa, M.J. - Sánchez-Moreiras,<br />

A.M.<br />

University <strong>of</strong> Vigo<br />

*Corresponding author e-mail: tamaras@uvigo.es<br />

Imaging <strong>of</strong> chlorophyll a fluorescence has been recognized as a<br />

valuable, non-invasive technique for the investigation <strong>of</strong> photosynthesis<br />

and the detection <strong>of</strong> stress in plants1.<br />

Fluorescence emission allows to estimate effective PSII quantum<br />

yield Y(II); quantum yield <strong>of</strong> regulated energy dissipation<br />

Y(NPQ), quantum yield <strong>of</strong> non-regulated energy dissipation<br />

Y(NO), coefficient <strong>of</strong> photochemical quenching (qL), coefficient<br />

<strong>of</strong> nonphotochemical quenching (qN), maximal PSII quantum<br />

yield (Fv/Fm) and electron transport rate (ETR).<br />

The knowledge <strong>of</strong> these parameters allows estimate how plant<br />

metabolism copes with environmental constrains.<br />

Citral is an essential oil known to show anti-microbial, anti-insecticide<br />

and anti-tumoral activity. The previously demonstrated<br />

toxicity on other organisms suggests the potential <strong>of</strong> this compound<br />

on weed control. However, this plant secondary metabolite<br />

has been never assayed on plants. Therefore we decided<br />

to investigate the phytotoxic activity and the mode <strong>of</strong> action <strong>of</strong><br />

Citral on plant metabolism.<br />

Arabidopsis plants were sprayed or watered for 21 days with different<br />

citral concentrations. Our results showed a decrease for<br />

the two treatments in effective PSII quantum yield confirmed by<br />

an increase in Y(NO), while no significant change occurred in<br />

Y(NPQ). However, spraying affected Fv/Fm and ETR in a very<br />

effectiveway.<br />

The results <strong>of</strong> photosynthetic activity, growth rate, pigment content<br />

and total proteins suggest a general reduction <strong>of</strong> the metabolism<br />

in citral-watered plants, while the results obtained for<br />

spraying could be suggesting more direct by-contact damage. In<br />

conclusion, citral appears as a plant growth regulator with potential<br />

as bioherbicide.<br />

1 Oxborough K (2004) J. Exp. Bot., 55:1195-1205.<br />

S08-003: IN VIVO CYTOCHROME AND ALTERNATIVE<br />

PATHWAY RESPIRATION IN ARABIDOPSIS THALIANA<br />

PLANTS WITH ALTERED ALTERNATIVE PATHWAY<br />

CAPACITY UNDER LOW AND HIGH LIGHT CONDI-<br />

TIONS<br />

Florez-Sarasa, I.¹* - Flexas, J.¹ - Umbach, A.L.² - Siedow, J.N.² -<br />

Gallé, A.¹ - Ribas-Carbo, M.¹<br />

¹Universitat de les Illes Balears<br />

²Duke University<br />

*Corresponding author e-mail : igor.florez@uib.es<br />

Plant respiration is characterised by the existence <strong>of</strong> a cyanideinsensitive<br />

respiratory pathway, alternative to the cytochrome<br />

respiratory pathway. Alternative oxidase (AOX) activity is<br />

thought to be regulated by several factors: a) inter-disulfide bond,<br />

b) α-ketoacids interaction c) AOX protein expression.<br />

Arabidopsis thaliana plants with altered levels <strong>of</strong> AOX protein<br />

(AtAOX1a antisense, AS-12 and overexpressor, XX-2) as well<br />

as wild type Columbia 0 plants (Col-0) were grown under low<br />

light conditions (80 μmol quanta m-2 s-1) and moved to high<br />

light (800 μmol quanta m-2 s-1) for 2 hours. The alternative pathway<br />

capacity was different between lines while no differences<br />

were observed on total respiration neither on electron partitioning<br />

through alternative pathway (τa) under low light. However,<br />

when plants were exposed to high light for 2 hours, τa in AS-12<br />

plants decreased while no changes were observed in Col-0 and<br />

XX-2 plants. Despite changes on τa in AS-12 under high light<br />

conditions, effects on photosynthesis and chlorophyll fluorescence<br />

parameters were similar in all 3 lines.<br />

In vivo regulation <strong>of</strong> the mitochondrial electron partitioning in<br />

relation to AOX expression levels under photoinhibitory conditions<br />

will be discussed.<br />

S08-004: STOMATAL DENSITY LINKED TO LEAF IN-<br />

TERNAL CO 2<br />

CONCENTRATION<br />

Santrucek, J.¹ - Vaskova, M.¹ - Tomsickova, J.¹ - Simkova, M. -<br />

Hronkova, M.² - Kveton, J.¹ - Vrabl, D.¹ - Schreiber, L.³<br />

¹Univ. South Bohemia<br />

²BC, Inst. Plant Mol. Biol.<br />

³Univ. Bonn, ICMB<br />

Stomata are hydraulically controlled pores between two guard<br />

cells in epidermis allowing gas, primarily water vapor and CO 2<br />

,<br />

exchange between plants and atmosphere. It was recently shown<br />

that number <strong>of</strong> stomata per unit <strong>of</strong> leaf area, stomatal density SD,<br />

changed with changing atmospheric CO 2<br />

concentration, c a<br />

, over<br />

geologic time. SD is used as a proxy for paleo-CO 2<br />

reconstructions.<br />

However the SD/c a<br />

proportionality factor, estimated from<br />

glasshouse cultivation data or leaf remains, is affected also by<br />

light, air humidity, drought and other environmental factors. Moreover,<br />

stomata evolve in an early stage when the folded leaf is<br />

sheathed or covered by other leaves primordia evolving local<br />

massive flux <strong>of</strong> respiratory CO 2<br />

.<br />

This doubts the role <strong>of</strong> ambient CO 2<br />

as an exclusive environmental<br />

factor controlling SD. Here, we show results <strong>of</strong> cultivation

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