An improved Na+-selective microelectrode for intracellular measurements inplant cells

Citation
De. Carden et al., An improved Na+-selective microelectrode for intracellular measurements inplant cells, J EXP BOT, 52(359), 2001, pp. 1353-1359
Citations number
20
Categorie Soggetti
Plant Sciences","Animal & Plant Sciences
Journal title
JOURNAL OF EXPERIMENTAL BOTANY
ISSN journal
00220957 → ACNP
Volume
52
Issue
359
Year of publication
2001
Pages
1353 - 1359
Database
ISI
SICI code
0022-0957(200106)52:359<1353:AINMFI>2.0.ZU;2-O
Abstract
The high background K+ concentration in plant cells is a problem for intrac ellular measurements of Na+ using ion-selective microelectrodes, The discri mination between Na+ and K+ of the microelectrode ionophore molecule limits the usefulness of this technique. A new Na+-selective microelectrode with an ionophore incorporating a tetramethoxyethyl ester derivative of p-t-buty l calix[4]arene has been developed, Microelectrodes made with this new sens or have superior selectivity for Na+ over K+ resulting in a lower limit of detection when compared with microelectrodes made using a commercially avai lable ionophore (ETH227), Both types of microelectrodes were insensitive to changes in ionic strength and physiological ranges of pH, but only the cal ixarene-based electrodes showed no protein interference. To test the suitab ility of the calixarene-based microelectrodes for measurements in plants, t hey were used to measure Na+ in epidermal cells in the zone 10-20 mm from t he root apex of barley (Hordeum vulgare L.). Seedlings were grown in a nutr ient solution containing 200 mM NaCl for 1-6 d, The range of intracellular Na+ activity (a(Na)) measured varied from less than or equal to0.1 mM (limi t of detection) to over 100 mFA, and these values increased significantly w ith time. The membrane potential (E-m) of these cells was variable, but the values became significantly more negative with time, although there was no significant correlation between E-m and a(Na). These intracellular measure ments could not be separated into distinct populations that might be repres entative of subcellular compartments.