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Book of Abstracts - Geyseco

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P - Posters<br />

Betaine aldehyde dehydrogenase catalyzes the last step in the<br />

synthesis <strong>of</strong> glycine betaine, a compatible solute accumulated by<br />

many plants under various abiotic stresses. Although rice (Oryza<br />

sativa L.) produces little glycine betaine, it was reported that rice<br />

has two BADH genes (OsBADH1 and OsBADH2). To characterize<br />

BADH enzyme <strong>of</strong> rice, we investigated the enzymatic properties<br />

<strong>of</strong> recombinant OsBADH1 and OsBADH2 proteins. The<br />

affinity <strong>of</strong> OsBADH2 for betaine aldehyde (Km <strong>of</strong> 231 &mu;M)<br />

was similar to that found in the BADH <strong>of</strong> other glycine betaineaccumulating<br />

plants BADHs. However OsBADH1 showed an<br />

extremely low affinity for betaine aldehyde with apparent Km<br />

<strong>of</strong> 2590 &mu;M. OsBADH1 and OsBADH2 catalyzed the oxidation<br />

<strong>of</strong> &omega;-aminoaldehydes such as 4-aminobutyraldehyde,<br />

3-aminopropionaldehyde, 4-N-trimethylaminobutyraldehyde,<br />

and 3-N-trimethylaminopropionaldehyde. We also found<br />

that both OsBADH proteins catalyzed the oxidation <strong>of</strong> acetaldehyde,<br />

but OsBADH1 showed a higher V max<br />

value for acetaldehyde<br />

than OsBADH2 did. The accumulation <strong>of</strong> OsBADH1 and<br />

OsBADH2 mRNA was decreased by submergence treatment and<br />

recovered by re-aeration. Analysis <strong>of</strong> the subcellular localization<br />

<strong>of</strong> OsBADH1 protein using green fluorescent protein indicated<br />

that OsBADH1 was localized in peroxisomes. These results suggest<br />

that OsBADHs show dehydrogenase activity for a range<br />

<strong>of</strong> aldehydes, and that OsBADH1 has a possible physiological<br />

function in the oxidation <strong>of</strong> acetaldehyde in rice plant peroxisomes.<br />

P01-019: CHANGES IN THE SALICYLIC ACID PA-<br />

THWAY IN WHEAT DURING LEAF RUST INFECTION<br />

Szalai, G.* - Vida, G. - Janda, T.<br />

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

Sciences<br />

*Corresponding author, e-mail: szalaig@mail.mgki.hu<br />

Salicylic acid (SA) has been known as a signal molecule in the<br />

induction <strong>of</strong> defence mechanisms in plants for a long time. Exogenous<br />

SA treatment may also induce the expression <strong>of</strong> pathogenesis<br />

related proteins and has been shown to establish systemic<br />

acquired resistance (SAR). Although SA is not considered to be<br />

the signal translocated from the infection site, its accumulation<br />

in distant tissues is essential for the induction <strong>of</strong> SAR. The aim<br />

<strong>of</strong> the present work was to investigate the SA pathway and the<br />

antioxidant response during leaf rust (Puccinia triticina) infection<br />

in wheat plants. Near isogenic lines containing various leaf<br />

rust resictance genes were used in the experiments. Plants were<br />

grown under field and greenhouse conditions. The activity <strong>of</strong><br />

the antioxidant enzymes (glutathione-S-transferase, ascorbate<br />

peroxidase, guaiacol peroxidase and catalase) increased after<br />

infection. The level <strong>of</strong> ortho-hydroxy-cinnamic acid decreased<br />

while the SA level increased in infected plants during the filed<br />

experiments. Further experiments were made in greenhouse to<br />

check the SA contents <strong>of</strong> various leaf levels after infection.<br />

P01-020: LIGHT-DEPENDENT REGULATORY MECHA-<br />

NISMS DURING COLD HARDENING IN WHEAT<br />

Janda, T. 1 * - Majláth, I. 1 - Szalai, G. 1 - Soós, V. 1 - Sebestyén, E.<br />

1<br />

- Balázs, E. 1 - Vanková, R. 2 - Dobrev, P. 2 - Tari, I. 3 - Tandori, J. 1<br />

1<br />

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

Sciences<br />

2<br />

Institute <strong>of</strong> Experimental Botany <strong>of</strong> the Czech Academy <strong>of</strong> Sciences<br />

3<br />

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

*Corresponding author, e-mail: jandat@mail.mgki.hu<br />

Frost tolerance is the result <strong>of</strong> a wide range <strong>of</strong> physical and biochemical<br />

processes that allow functioning at low temperatures.<br />

Earlier results showed that frost hardening at low temperature<br />

under low light conditions is much less effective than under normal<br />

light conditions, and several processes, including the lipid,<br />

polyamine, or salicylic acid metabolism and antioxidant activity,<br />

may contribute to the light-induced freezing tolerance. The aim<br />

<strong>of</strong> the present work was to discover what other changes in the<br />

regulatory processes were responsible for the light-enhanced<br />

freezing tolerance <strong>of</strong> wheat plants. Young winter and spring<br />

wheat varieties were cold hardened under medium or low light<br />

conditions. Microarray and RT-PCR analyses show that the light<br />

intensity during the hardening period significantly affected the<br />

expression <strong>of</strong> several genes, which may have role in the development<br />

<strong>of</strong> frost hardiness <strong>of</strong> wheat plants. In order to get more<br />

information about the regulatory processes during cold hardening<br />

period, the changes in the levels <strong>of</strong> plant hormones were<br />

also detected. While the abscisic acid level was lower in the 12-d<br />

cold hardened plants than in the controls in both genotypes, independently<br />

on the light intensity, changes in the plant growth<br />

regulator cytokinins, signal transducer NO, ethylene precursor<br />

ACC, and proline levels showed a strong light and variety dependencies.<br />

Results suggest that temperature and light regulate the<br />

development <strong>of</strong> frost hardiness in a complex way.<br />

P01-021: A TRUNCATED FORM OF A Β-ADAPTIN CON-<br />

FERS WEAK ACID RESISTANCE IN ARABIDOPSIS<br />

Niñoles, R. 1 * - Alejandro, S. 2 - Fernández, J.A 3 - García-Sánchez,<br />

M.J. 3 - Serrano, R. 1<br />

1<br />

IBMCP<br />

2<br />

Institute <strong>of</strong> Plant Biology University <strong>of</strong> Zurich<br />

3<br />

Universidad de Málaga<br />

*Corresponding author, e-mail: renioro@ibmcp.upv.es<br />

The homeostasis <strong>of</strong> intracellular pH is a fundamental activity <strong>of</strong><br />

living cells. In order to identify new components <strong>of</strong> the Arabidopsis<br />

pH regulation system, an activation-tagged mutant seed<br />

collection was screened using acetic acid as a selection agent.<br />

The dominant mutant wat1-1D (Weak Acid Tolerant) is more resistant<br />

to the acid stress generated by weak acids such as acetic,<br />

propionic and sorbic acid, and this tolerance correlates with its<br />

T-DNA insertion. Wat1-1D also shows lithium sensitivity and<br />

ABA resistance during the germination stage. Measurements <strong>of</strong><br />

intracellular pH show that during acid stress mutant plants maintain<br />

a higher cytosolic pH than the wild type, although their acetate<br />

uptake is normal. The plasma membrane (PM) H+ATPase<br />

activity and the PM potential are similar in the wild type and<br />

the mutant in normal conditions. However, under acid stress the<br />

wild type undergoes a higher PM hiperpolarization. The T-DNA<br />

insertion <strong>of</strong> wat1-1D interrupts the At3g55480 gene, an adaptin<br />

family protein, and causes an induction <strong>of</strong> the adjacent gene<br />

At3g55470. Surprisingly it is the expression <strong>of</strong> a truncated form<br />

<strong>of</strong> the adaptin and not the overexpression <strong>of</strong> At3g55470 what<br />

causes the observed phenotypes, as transgenic plants expressing<br />

the truncated adaptin or the antisense gene have similar phenotypes<br />

to those <strong>of</strong> the wat1-1D mutant. In adition, a SAIL T-DNA<br />

insertion mutant in At3g55480 also shows the same phenotypes.<br />

Our working hypothesis is that under acid stress this mutant introduces<br />

the excess <strong>of</strong> protons into the vacuole.<br />

P01-022: THE ROLE OF PROLINE AND ITS METABO-<br />

LISM ENZYMES IN CUCUMBER CELL CULTURES DU-<br />

RING ACCLIMATION TO SALINITY<br />

Naliwajski, M.* - Sklodowska, M.<br />

Department <strong>of</strong> Plant Physiology and Biochemistry, University <strong>of</strong><br />

Lodz, Poland,<br />

*Corresponding author, e-mail: nalmar@biol.uni.lodz.pl<br />

Proline is one <strong>of</strong> the most widely distributed osmolytes and<br />

acts as a reservoir <strong>of</strong> nitrogen and carbon source for post stress<br />

growth, a stabilizer <strong>of</strong> the membranes and as a sink <strong>of</strong> energy to<br />

regulate redox potential. The aim <strong>of</strong> this study was to investigate<br />

the role <strong>of</strong> the activities <strong>of</strong> pyrroline-5-carboxylate: synthetase<br />

(P5CS), reductase (P5CR), proline dehydrogenase (PDH) and<br />

proline level in salinity adaptation in cell cultures. All biochemical<br />

analyses were carried out in two cucumber cell cultures:<br />

P

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