CLONING AND ELECTROPHYSIOLOGICAL ANALYSIS OF KST1, AN INWARD RECTIFYING K+ CHANNEL EXPRESSED IN POTATO GUARD-CELLS

被引:182
作者
MULLERROBER, B [1 ]
ELLENBERG, J [1 ]
PROVART, N [1 ]
WILLMITZER, L [1 ]
BUSCH, H [1 ]
BECKER, D [1 ]
DIETRICH, P [1 ]
HOTH, S [1 ]
HEDRICH, R [1 ]
机构
[1] UNIV HANNOVER, INST BIOPHYS, D-30419 HANNOVER, GERMANY
关键词
GUARD CELLS; IN SITU HYBRIDIZATION; INWARD RECTIFYING K+ CHANNEL; POTATO (SOLANUM TUBEROSUM L); XENOPUS OOCYTES;
D O I
10.1002/j.1460-2075.1995.tb07238.x
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Potassium uptake by guard cells represents part of the osmotic motor which drives stomatal opening, Patch-clamp measurements have identified inward rectifying K+ channels capable of mediating K+ uptake in guard cells and various other plant cell types, Here we report the molecular cloning and characterization of a voltage-dependent K+ channel (KST1) from potato (Solanum tuberosum L.) guard cells. In situ hybridization shows expression of kst1 in guard cells. Two electrode voltage-clamp and patch-clamp studies of the gene product after cRNA injection into Xenopus oocytes identified KST1 as a slowly activating, voltage-dependent, inward rectifying K+ channel. The single channel current voltage curve was linear in the range -160 to +20 mV, with a deduced single channel conductance of 7 pS in symmetrical 100 mM K+. This channel type, modulated by pH changes within the physiological range, required ATP for activation. In line with the properties of a K+-selective channel, KST1 was permeable to K+, Rb+ and NH4+ and excluded Na+ and Li+. Cs+ at submillimolar concentrations blocked the channel in a voltage-dependent manner. Related studies on potato guard cell protoplasts confirmed the biophysical characteristics of the kst1 gene product (KST1) in the heterologous expression system. Therefore, KST1 represents a major K+ uptake channel in potato guard cells.
引用
收藏
页码:2409 / 2416
页数:8
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