首页> 美国卫生研究院文献>International Journal of Molecular Sciences >Effect of Auxin (IAA) on the Fast Vacuolar (FV) Channels in Red Beet (Beta vulgaris L.) Taproot Vacuoles
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Effect of Auxin (IAA) on the Fast Vacuolar (FV) Channels in Red Beet (Beta vulgaris L.) Taproot Vacuoles

机译:蟾蜍素(IAA)对红甜菜(Beta Vulgaris L.)Taproot真空的快速真空(FV)通道的影响

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摘要

In contrast to the well-studied effect of auxin on the plasma membrane K channel activity, little is known about the role of this hormone in regulating the vacuolar K channels. Here, the patch-clamp technique was used to investigate the effect of auxin (IAA) on the fast-activating vacuolar (FV) channels. It was found that the macroscopic currents displayed instantaneous currents, which at the positive potentials were about three-fold greater compared to the one at the negative potentials. When auxin was added to the bath solution at a final concentration of 1 µM, it increased the outward currents by about 60%, but did not change the inward currents. The imposition of a ten-fold vacuole-to-cytosol KCl gradient stimulated the efflux of K from the vacuole into the cytosol and reduced the K current in the opposite direction. The addition of IAA to the bath solution with the 10/100 KCl gradient decreased the outward current and increased the inward current. Luminal auxin reduced both the outward and inward current by approximately 25% compared to the control. The single channel recordings demonstrated that cytosolic auxin changed the open probability of the FV channels at the positive voltages to a moderate extent, while it significantly increased the amplitudes of the single channel outward currents and the number of open channels. At the positive voltages, auxin did not change the unitary conductance of the single channels. We suggest that auxin regulates the activity of the fast-activating vacuolar (FV) channels, thereby causing changes of the K fluxes across the vacuolar membrane. This mechanism might serve to tightly adjust the volume of the vacuole during plant cell expansion.
机译:与植物蛋白的良好效果相比,血管膜K通道活动的良好作用,关于该激素在调节真空K通道方面的作用几乎是已知的。这里,使用蛋白钳技术来研究蟾蜍蛋白(IAA)对快激活真空(FV)通道的影响。结果发现,与负电位的一个相比,宏观电流显示在正电位的瞬时电流上大约三倍。当以1μm的终浓度加入浴溶液的浴溶液中时,它将向外电流增加约60%,但没有改变向内电流。施加十倍芳瓦芳啉醇KCl梯度刺激从芳瓦尔进入胞浆中的k的流出,并在相反方向上降低k电流。用10/100kcl梯度加入浴液溶液的浴溶液降低了向外电流并增加了向内电流。与对照相比,腔湿润率将向外和向内电流降低约25%。单通道录制表明,细胞骨制氮在正电压下改变了FV通道的开放概率,以适度的程度,而它显着增加了单通道向外电流的幅度和打开通道的数量。在阳性电压下,养蛋白没有改变单个通道的整体电导。我们建议养肝素调节快激活真空(FV)通道的活性,从而导致血管膜穿过k助熔剂的变化。该机制可能有助于在植物细胞膨胀期间紧密调节液泡的体积。

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