State Key Laboratory of Efficient Production of Forest Resources, Key Laboratory of Tree Breeding and Cultivation of the National Forestry and Grassland Administration, Research Institute of Forestry, Chinese Academy of Forestry, Beijing, 100091, China.
State Key Laboratory of Efficient Production of Forest Resources, Key Laboratory of Tree Breeding and Cultivation of the National Forestry and Grassland Administration, Research Institute of Forestry, Chinese Academy of Forestry, Beijing, 100091, China; College of Horticulture, Jilin Agricultural University, Changchun, Jilin, 130118, China.
J Environ Manage. 2024 Apr;357:120691. doi: 10.1016/j.jenvman.2024.120691. Epub 2024 Mar 29.
Regions affected by heavy metal contamination frequently encounter phosphorus (P) deficiency. Numerous studies highlight crucial role of P in facilitating cadmium (Cd) accumulation in woody plants. However, the regulatory mechanism by which P affects Cd accumulation in roots remains ambiguous. This study aims to investigate the effects of phosphorus (P) deficiency on Cd accumulation, Cd subcellular distribution, and cell wall components in the roots of Salix caprea under Cd stress. The results revealed that under P deficiency conditions, there was a 35.4% elevation in Cd content in roots, coupled with a 60.1% reduction in Cd content in shoots, compared to the P sufficiency conditions. Under deficient P conditions, the predominant response of roots to Cd exposure was the increased sequestration of Cd in root cell walls. The sequestration of Cd in root cell walls increased from 37.1% under sufficient P conditions to 66.7% under P deficiency, with pectin identified as the primary Cd binding site under both P conditions. Among cell wall components, P deficiency led to a significant 31.7% increase in Cd content within pectin compared to P sufficiency conditions, but did not change the pectin content. Notably, P deficiency significantly increased pectin methylesterase (PME) activity by regulating the expression of PME and PMEI genes, leading to a 10.4% reduction in the degree of pectin methylesterification. This may elucidate the absence of significant changes in pectin content under P deficiency conditions and the concurrent increase in Cd accumulation in pectin. Fourier transform infrared spectroscopy (FTIR) results indicated an increase in carboxyl groups in the root cell walls under P deficiency compared to sufficient P treatment. The results provide deep insights into the mechanisms of higher Cd accumulation in root mediated by P deficiency.
受重金属污染影响的地区经常会出现磷(P)缺乏的情况。许多研究强调了 P 在促进木本植物中镉(Cd)积累方面的关键作用。然而,P 影响根系中 Cd 积累的调节机制仍不清楚。本研究旨在探讨磷(P)缺乏对 Cd 积累、Cd 亚细胞分布和细胞壁成分的影响在 Cd 胁迫下的柳属植物根中。结果表明,在 P 缺乏条件下,与 P 充足条件相比,根中 Cd 含量增加了 35.4%,而地上部分 Cd 含量减少了 60.1%。在缺乏 P 的条件下,根系对 Cd 暴露的主要反应是增加 Cd 在根细胞壁中的固定。在充足的 P 条件下,Cd 在根细胞壁中的固定率为 37.1%,在 P 缺乏条件下增加到 66.7%,果胶是两种 P 条件下的主要 Cd 结合位点。在细胞壁成分中,与 P 充足条件相比,P 缺乏导致果胶中 Cd 含量显著增加 31.7%,但不改变果胶含量。值得注意的是,P 缺乏通过调节 PME 和 PMEI 基因的表达显著增加了果胶甲酯酶(PME)活性,导致果胶甲酯化程度降低 10.4%。这可以解释在 P 缺乏条件下果胶含量没有明显变化,同时果胶中 Cd 积累增加的原因。傅里叶变换红外光谱(FTIR)结果表明,与充足的 P 处理相比,P 缺乏下根细胞壁中的羧基基团增加。研究结果深入了解了 P 缺乏介导的更高 Cd 积累在根中的机制。