Kinraide TB
Appalachian Soil and Water Conservation Research Laboratory, Agricultural Research Service, United States Department of Agriculture, Beaver, West Virginia 25813-0400, USA.
Plant Physiol. 1998 Oct;118(2):513-20. doi: 10.1104/pp.118.2.513.
Ca2+ in rooting medium is essential for root elongation, even in the absence of added toxicants. In the presence of rhizotoxic levels of Al3+, H+, or Na+ (or other cationic toxicants), supplementation of the medium with higher levels of Ca2+ alleviates growth inhibition. Experiments to determine the mechanisms of alleviation entailed measurements of root elongation in wheat (Triticum aestivum L. cv Scout 66) seedlings in controlled medium. A Gouy-Chapman-Stern model was used to compute the electrical potentials and the activities of ions at the root-cell plasma membrane surfaces. Analysis of root elongation relative to the computed surface activities of ions revealed three separate mechanisms of Ca2+ alleviation. Mechanism I is the displacement of cell-surface toxicant by the Ca2+-induced reduction in cell-surface negativity. Mechanism II is the restoration of Ca2+ at the cell surface if the surface Ca2+ has been reduced by the toxicant to growth-limiting levels. Mechanism III is the collective ameliorative effect of Ca2+ beyond mechanisms I and II, and may involve Ca2+-toxicant interactions at the cell surface other than the displacement interactions of mechanisms I and II. Mechanism I operated in the alleviation of all of the tested toxicities; mechanism II was generally a minor component of alleviation; and mechanism III was toxicant specific and operated strongly in the alleviation of Na+ toxicity, moderately in the alleviation of H+ toxicity, and not at all in the alleviation of Al3+ toxicity.
即使在不添加有毒物质的情况下,生根培养基中的Ca2+对于根的伸长也是必不可少的。在存在根毒性水平的Al3+、H+或Na+(或其他阳离子毒物)的情况下,向培养基中补充更高水平的Ca2+可减轻生长抑制。为确定缓解机制而进行的实验涉及在受控培养基中测量小麦(Triticum aestivum L. cv Scout 66)幼苗的根伸长。使用Gouy-Chapman-Stern模型计算根细胞质膜表面的电势和离子活性。相对于计算出的离子表面活性对根伸长进行分析,揭示了Ca2+缓解的三种不同机制。机制I是Ca2+诱导的细胞表面负电性降低所导致的细胞表面毒物的置换。机制II是如果表面Ca2+已被毒物降低到限制生长的水平,则在细胞表面恢复Ca2+。机制III是Ca2+超出机制I和II的集体改善作用,可能涉及细胞表面的Ca2+-毒物相互作用,而不是机制I和II的置换相互作用。机制I在缓解所有测试毒性中起作用;机制II通常是缓解的次要组成部分;机制III具有毒物特异性,在缓解Na+毒性方面作用强烈,在缓解H+毒性方面作用中等,而在缓解Al3+毒性方面完全不起作用。