Department of Soil and Environmental Sciences, University of California, Riverside, California 92521.
Plant Physiol. 1992 Sep;100(1):309-18. doi: 10.1104/pp.100.1.309.
Knowledge of the mechanistic basis of differential aluminum (Al) tolerance depends, in part, on an improved ability to quantify Al located in the apoplastic and symplastic compartments of the root apex. Using root tips excised from seedlings of an Al-tolerant wheat cultivar (Triticum aestivum L. cv Yecora Rojo) grown in Al solutions for 2 d, we established an operationally defined apoplastic Al fraction determined with six sequential 30-min washes using 5 mm CaCl(2) (pH 4.3). Soluble symplastic Al was eluted by freezing root tips to rupture cell membranes and performing four additional 30-min CaCl(2) washes, and a residual fraction was determined via digestion of root tips with HNO(3). The three fractions were then determined in Yecora Rojo and a sensitive wheat cultivar (Tyler) grown at 18, 55, or 140 mum total solution Al (Al(T)). When grown at equal Al(T), Tyler contained more Al than Yecora Rojo in all fractions, but both total Al and fractional distribution were similar in the two cultivars grown at Al(T) levels effecting a 50% reduction in root growth. Residual Al was consistently 50 to 70% of the total, and its location was elucidated by staining root tips with the fluorophore morin and examining them using fluorescence and confocal laser scanning microscopy. Wall-associated Al was only observed in tips prior to any washing, and the residual fraction was manifested as distinct staining of the cytoplasm and nucleus but not of the apoplastic space. Accordingly, the residual fraction was allocated to the symplastic compartment for both cultivars, and recalculated apoplastic Al was consistently approximately 30 to 40% of the total. Distributions of Al in the two cultivars did not support a symplastic detoxification hypothesis, but the role of cytoplasmic exclusion remains unsettled.
对铝(Al)耐性差异的机制基础的了解,部分依赖于提高定量分析根尖质外体和共质体中 Al 含量的能力。我们从在 Al 溶液中培养 2 天的耐 Al 小麦品种(Triticum aestivum L. cv Yecora Rojo)幼苗中切取根尖,建立了一个用 5mm CaCl₂(pH 4.3)进行 6 次 30 分钟洗涤操作定义的质外体 Al 分数。通过冷冻根尖以破坏细胞膜并进行另外 4 次 30 分钟的 CaCl₂洗涤来洗脱可溶的共质体 Al,然后通过用 HNO₃消化根尖来测定残余分数。然后在 Yecora Rojo 和敏感小麦品种(Tyler)中测定这三个分数,这两个品种在 18、55 或 140 µm 总溶液 Al(Al(T))下生长。当在相等的 Al(T)下生长时,Tyler 比 Yecora Rojo 在所有分数中含有更多的 Al,但在 Al(T)水平下对根生长抑制 50%的两个品种中,总 Al 和分数分布都相似。残余 Al 始终占总 Al 的 50%到 70%,通过用荧光染料 morin 染色根尖并使用荧光和共焦激光扫描显微镜观察来阐明其位置。仅在进行任何洗涤之前在根尖上观察到与细胞壁结合的 Al,残余分数表现为细胞质和核的明显染色,但不染色质外体空间。因此,将残余分数分配给两个品种的共质体,重新计算的质外体 Al 始终约占总 Al 的 30%到 40%。这两个品种中 Al 的分布不支持共质体解毒假说,但细胞质排除的作用仍未解决。