Skip to main content
. 2014 Aug 16;114(5):1023–1034. doi: 10.1093/aob/mcu170

Table 1.

Membrane potential (Em, mV) in parenchymal coleoptile cells. Data (mean ± s.e.) are means of at least seven independent experiments

Treatment A B C D E F Em at depolarization F–A
0 min 3 min 6 min 10 min 20 min 30 min
1 mm KCla –120·1 ± 4·3 –119·8 ± 3·9 –119·2 ± 4·6 –120·5 ± 5·8 –121·0 ± 5·4 –122·4 ± 6·1 –2·3ns
1 mm KCl + IAAb –120·6 ± 7·4 –121·0 ± 6·6 –116·6 ± 4·9 –117·3 ± 5·2 –126·1 ± 6·7 –131·3 ± 7·5 –115·5 ± 5·9 –10·7*
1 mm KCl + A-9-Cc + IAAb –108·4 ± 4·7 –107·9 ± 5·4 –105·4 ± 6·2 –108·1 ± 5·2 –115·8 ± 6·1 –118·5 ± 6·8 –105·3 ± 5·8 –10·1*
10 mm KCl –70·6 ± 4·1 –68·8 ± 3·9 –67·9 ± 4·3 –68·2 ± 4·5 –68·4 ± 3·8 –67·9 ± 4·2 2·7ns
10 mm KCl + IAAb –68·7 ± 4·5 –69·2 ± 4·7 –67·8 ± 3·8 –70·0 ± 3·4 –72·8 ± 4·1 –74·1 ± 4·3 –64·7 ± 4·2 –5·4*
10 mm KCl + A-9-Cc + IAAb –64·8 ± 3·9 –60·8 ± 4·2 –62·4 ± 3·6 –63·6 ± 4·5 –63·1 ± 3·3 –62·2 ± 3·5 –60·8 ± 4·2 2·6ns

aColeoptile segments were incubated in the indicated medium (the same as in growth experiments) for 110 min, after which a single segment was transferred into an electrophysiological chamber containing the same medium. Measurements of membrane potential (30 min) were carried out after insertion of a microelectrode into the cell and stabilization of the Em ( < 10 min) at 2 h (0 min).

bIAA was added after 2 h of segment preincubation in medium with 1 or 10 mm KCl (for the last 10 min the coleoptile segments were incubated in the electrophysiological chamber).

cA-9-C was added after 1 h of segment preincubation in medium with 1 or 10 mm KCl (for the last 10 min the coleoptile segments were incubated in the electrophysiological chamber).

nsNot statistically significant.

*Statistically significant at P < 0·05.