Kosegarten H, Grolig F, Esch A, Glusenkamp KH, Mengel K
Institut fur Pflanzenernahrung, Justus-Liebig Universitat Giessen, Sudanlage 6, D-35390 Giessen, Germany.
Planta. 1999 Oct;209(4):444-52. doi: 10.1007/s004250050747.
A fluorimetric ratio technique was elaborated to measure apoplastic pH in the outer root cortex of maize (Zea mays L.) grown hydroponically. A newly synthesized fluorescent probe, fluorescein boronic acid (pK(a) = 5.48), which covalently binds to the cell wall of the outer cell layers, was used. Under conditions of saturating ion concentrations the apoplastic pH was determined along the root axis ranging from 1 to 30 mm behind the root tip. Apoplastic pH was recorded for root segment areas (1 mm(2)), and pH values of high statistical significance were obtained. With an external solution of pH 5, the apoplastic pH was about pH 5.1 in the division zone, between pH 4.8 and 4.9 in the elongation region and about pH 4.9 in the root hair zone. At an external pH of 8.6, the difference between the external pH and the apoplastic pH was considerably more, with a pH of 5.2-5.3 in all root zones. Addition of 1 mM NH(4)(+) caused a small apoplastic pH decrease (0.05 of a pH unit) in all root zones. Apoplastic alkalization upon application of 6 mM NO(3)(-) was highest (0.3 of a pH unit) in the zone where root hairs emerge; in the division and early elongation zones, apoplastic pH increased only transiently. In the presence of 10 mM HCO(3)(-), NO(3)(-) elicited a higher and persistent alkalization (0.06-0.25 of a pH unit) in all root zones. Application of fusicoccin reduced apoplastic pH from 4.85 to 4.75 in the elongation zone, while inhibition of the H(+)-ATPase with vanadate alkalized the apoplast in the root hair zone from pH 5.4 to 5.6. The observed pH differences along the root axis upon differential N supply and application of HCO(3)(-) provide evidence that this new pH technique is a useful tool with which to measure apoplastic pH, and in future may permit measurements at microsites at the cell level by use of microscope imaging.
构建了一种荧光比率技术,用于测量水培生长的玉米(Zea mays L.)外根皮层的质外体pH值。使用了一种新合成的荧光探针——荧光素硼酸(pK(a)=5.48),它能与外层细胞的细胞壁共价结合。在离子浓度饱和的条件下,测定了根尖后方1至30毫米范围内根轴上的质外体pH值。记录了根段区域(1平方毫米)的质外体pH值,并获得了具有高度统计学意义的pH值。在外源溶液pH值为5时,分生区的质外体pH值约为5.1,伸长区为4.8至4.9,根毛区约为4.9。在外源pH值为8.6时,外源pH值与质外体pH值之间的差异更大,所有根区的pH值为5.2至5.3。添加1 mM NH(4)(+)会导致所有根区的质外体pH值略有下降(0.05个pH单位)。施加6 mM NO(3)(-)时,根毛出现区域的质外体碱化程度最高(0.3个pH单位);在分生区和早期伸长区,质外体pH值仅短暂升高。在存在10 mM HCO(3)(-)的情况下,NO(3)(-)在所有根区引发了更高且持续的碱化(0.06至0.25个pH单位)。施加壳梭孢菌素使伸长区的质外体pH值从4.85降至4.75,而用钒酸盐抑制H(+)-ATP酶则使根毛区的质外体从pH 5.4碱化至5.6。在不同氮供应和施加HCO(3)(-)时沿根轴观察到的pH差异表明,这种新的pH技术是测量质外体pH值的有用工具,未来可能通过显微镜成像在细胞水平的微位点进行测量。