首页> 外文期刊>Protoplasma: An International Journal of Cell Biology >Surface pH changes suggest a role for H+/OH- channels in salinity response of Chara australis
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Surface pH changes suggest a role for H+/OH- channels in salinity response of Chara australis

机译:表面pH变化表明Chara Australis的盐度响应中的H + / OH-通道的作用

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摘要

To understand salt stress, the full impact of salinity on plant cell physiology has to be resolved. Electrical measurements suggest that salinity inhibits the proton pump and opens putative H+/OH- channels all over the cell surface of salt sensitive Chara australis (Beilby and Al Khazaaly 2009; Al Khazaaly and Beilby 2012). The channels open transiently at first, causing a characteristic noise in membrane potential difference (PD), and after longer exposure remain open with a typical current-voltage (I/V) profile, both abolished by the addition of 1 mM ZnCl2, the main known blocker of animal H+ channels. The cells were imaged with confocal microscopy, using fluorescein isothiocyanate (FITC) coupled to dextran 70 to illuminate the pH changes outside the cell wall in artificial fresh water (AFW) and in saline medium. In the early saline exposure, we observed alkaline patches (bright fluorescent spots) appearing transiently in random spatial distribution. After longer exposure, some of the spots became fixed in space. Saline also abolished or diminished the pH banding pattern observed in the untreated control cells. ZnCl2 suppressed the alkaline spot formation in saline and the pH banding pattern in AFW. The osmotic component of the saline stress did not produce transient bright spots or affect banding. The displacement of H+ from the cell wall charges, the H+/OH- channel conductance/density, and self-organization are discussed. No homologies to animal H+ channels were found. Salinity activation of the H+/OH- channels might contribute to saline response in roots of land plants and leaves of aquatic angiosperms.
机译:为了了解盐胁迫,必须解决盐度对植物细胞生理的全部影响。电测量表明盐度抑制了质子泵,并在盐敏感的夏拉澳大利亚(Beilby和Al Khazaaly 2009; Al Khazaaly和Beilby 2012)上遍布剩余的H + / OH-通道。首先瞬时打开通道,导致膜电位差(PD)中的特征噪声,并且在更长的曝光之后用典型的电流 - 电压(I / V)轮廓保持打开,两者都通过加入1 mm ZnCl2,主要已知的动物H +通道阻滞剂。将细胞与共聚焦显微镜进行成像,使用荧光素异硫氰酸酯(FITC)偶联至葡聚糖70,以照射人造淡水(AFW)和盐培养基中的细胞壁外的pH变化。在早期的盐水暴露中,我们观察到随机空间分布瞬时出现的碱性斑块(明亮的荧光斑)。经过较长的曝光后,一些斑点在太空中固定了。盐水也消除或减少了在未处理的对照细胞中观察到的pH条带状图案。 ZnCl2抑制了盐水中的碱性点形成和AFW中的pH条带图案。盐胁迫的渗透组分没有产生瞬态亮点或影响条纹。讨论了H +从电池壁电荷,H + / OH-通道电导/密度和自组织的位移。没有发现动物H +通道的同源物。 H + / OH-通道的盐度活化可能有助于土地植物根系中的盐响应和水生性高血管植物的叶子。

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