Book of Abstracts - Geyseco
Book of Abstracts - Geyseco
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