Department of Biology, Indiana University-Purdue University at Indianapolis, 1201 East 38th Street, Indianapolis, Indiana 46205.
Plant Physiol. 1978 Jul;62(1):94-6. doi: 10.1104/pp.62.1.94.
Segments of oat (Avena sativa L.) roots which had been exposed to 1 millimolar CdSO(4) in quarter-strength Hoagland No. 1 solution exhibited decreased respiratory rates, ATP levels, membrane-bound ATPase activity, and reduced K(+) fluxes. Respiration and ATP levels were decreased after a 2-hour treatment with 1 millimolar CdSO(4) to 65 and 75%, respectively, of control rates. A membrane-bound, Mg(2+)-dependent, K(+)-stimulated acid ATPase was rapidly inhibited to 12% of control activity in the presence of 1 millimolar CdSO(4). Potassium uptake into root segments was inhibited to 80% of control values after 30 minutes in the presence of CdSO(4). A 2-hour pretreatment of root segments with CdSO(4) inhibited K(+) uptake to 15% of control values. Cytoplasmic K(+) efflux was inhibited with 1 millimolar CdSO(4).The rates and the degree of Cd(2+) inhibition of the parameters listed above suggest that one of the first sites of Cd(2+) action is the plasmalemma K(+) carrier (ATPase) in oat roots.
在四分之一强度 Hoagland No.1 溶液中,暴露于 1mM CdSO4 的燕麦(Avena sativa L.)根段表现出呼吸速率、ATP 水平、膜结合 ATP 酶活性降低以及 K+通量减少。暴露于 1mM CdSO4 2 小时后,呼吸速率和 ATP 水平分别下降至对照的 65%和 75%。在 1mM CdSO4 存在下,快速抑制了膜结合的 Mg2+依赖的 K+刺激的酸 ATP 酶,活性降至对照的 12%。在 CdSO4 存在下 30 分钟后,根段对钾的摄取抑制至对照值的 80%。用 CdSO4 预处理根段 2 小时,抑制 K+摄取至对照值的 15%。用 1mM CdSO4 抑制细胞质 K+外排。上述参数的速率和 Cd2+抑制程度表明,Cd2+作用的最初部位之一是燕麦根的质膜 K+载体(ATP 酶)。