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480<br />

Daniel Knoll and Lukas Schreiber<br />

bers are additionally sealed with adhesive tape to avoid diffusion of water<br />

through the sampling ports. Chambers are incubated upside down on dried<br />

silica gel in an air-tight polyethylene box at 25 °C. The silica gel adsorbs all<br />

free water of the air resulting in a water concentration inside the polyethylene<br />

box constantly held at 0 %. Thus, the driving force DC for the water flow across<br />

the cuticle corresponds to the density of water (10 3 kg m –3 ). The salt and sugar<br />

concentration of the nutrition solution can be neglected as it does not affect<br />

significantly the water activity a w. Control experiments showed that there was<br />

no significant change in cuticular water permeability when using deionised<br />

water or nutrition solution as the aqueous solution inside the chamber volume.<br />

Sterilisation of cuticles by UV radiation also did not significantly change<br />

water permeability.<br />

4.5.2 Effect of Bacteria on Cuticular Water Permeability<br />

Isolated cuticles are mounted in stainless steel chambers and permeability<br />

coefficients P1 for water are determined for each sample as described above.<br />

Cuticular permeability coefficients P1 determined after UV radiation ranged<br />

between 1.44◊10 –10 m/s for Vinca major leaf cuticles and 10.8x10 –9 m/s for<br />

Lycopersicon esculentum fruit cuticles (Table 1). Then cuticles are inoculated<br />

with bacteria and incubated for 12 days in the incubation box at 25 °C at air<br />

humidity close to 100 %. Control experiments are conducted by inoculating<br />

the cuticles with 200 ml PBS in place of the bacterial cell solution. After incubation<br />

with bacteria chambers are again transferred onto dried silica gel and<br />

cuticular water permeability coefficients P2 are determined after an equilibrium<br />

period of 1 day. The effects of bacteria on water permeability of the<br />

respective cuticular membrane are calculated from the permeance of the cuticle<br />

after treatment with bacteria (P2) divided by the initial permeance (P1).<br />

Effect = P2<br />

P1<br />

Table 1. Cuticular permeability coefficients for water P water (m/s) from different <strong>plant</strong><br />

species. Values are arithmetic means with 95 % confidence intervals (ci) of 14 measured<br />

permeability coefficients for each <strong>plant</strong> species<br />

Species P water ¥10 –10 (m/s) ci 95 %x10 –10 (m/s)<br />

Vinca major 1.44 1.26–1.64<br />

Hedera helix can. 2.16 1.76–2.65<br />

Prunus laurocerasus 2.93 2.34–3.68<br />

Citrus aurantium 4.53 2.97–6.92<br />

Lycopersicon esculentum 10.80 8.85–13.17

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