College of Horticulture, Nanjing Agricultural University, Nanjing, 21095, China.
Institute of Nanjing Agricultural Sciences, Jiangsu Academy of Agricultural Sciences, Nanjing, 210046, China.
Physiol Plant. 2019 Sep;167(1):5-20. doi: 10.1111/ppl.12967. Epub 2019 Apr 11.
To explore the mechanisms of 5-aminolevulinic acid (ALA)-improved plant salt tolerance, strawberries (Fragaria × ananassa Duch. cv. 'Benihoppe') were treated with 10 mg l ALA under 100 mmol l NaCl stress. We found that the amount of Na increased in the roots but decreased in the leaves. Laser scanning confocal microscopy (LSCM) observations showed that ALA-induced roots had more Na accumulation than NaCl alone. Measurement of the xylem sap revealed that ALA repressed Na concentrations to a large extent. The electron microprobe X-ray assay also confirmed ALA-induced Na retention in roots. qRT-PCR showed that ALA upregulated the gene expressions of SOS1 (encoding a plasma membrane Na /H antiporter), NHX1 (encoding a vacuolar Na /H antiporter) and HKT1 (encoding a protein of high-affinity K uptake), which are associated with Na exclusion in the roots, Na sequestration in vacuoles and Na unloading from the xylem vessels to the parenchyma cells, respectively. Furthermore, we found that ALA treatment reduced the H O content in the leaves but increased it in the roots. The exogenous H O promoted plant growth, increased root Na retention and stimulated the gene expressions of NHX1, SOS1 and HKT1. Diphenyleneiodonium (DPI), an inhibitor of H O generation, suppressed the effects of ALA or H O on Na retention, gene expressions and salt tolerance. Therefore, we propose that ALA induces H O accumulation in roots, which mediates Na transporter gene expression and more Na retention in roots, thereby improving plant salt tolerance.
为了探究 5-氨基乙酰丙酸(ALA)提高植物耐盐性的机制,我们用 10 mg·l-1 ALA 处理草莓(Fragaria × ananassa Duch. cv. 'Benihoppe'),同时施加 100 mmol·l-1 NaCl 胁迫。我们发现,根部的 Na 含量增加,而叶片中的 Na 含量减少。激光扫描共聚焦显微镜(LSCM)观察表明,ALA 诱导的根中 Na 积累量高于单独施加 NaCl。木质部汁液测量显示,ALA 在很大程度上抑制了 Na 浓度。电子探针 X 射线分析也证实了 ALA 诱导的根中 Na 滞留。qRT-PCR 显示,ALA 上调了 SOS1(编码质膜 Na+/H+反向转运蛋白)、NHX1(编码液泡 Na+/H+反向转运蛋白)和 HKT1(编码高亲和力 K+摄取蛋白)的基因表达,这与根中 Na 外排、液泡中 Na 螯合以及木质部导管到薄壁细胞的 Na 卸载有关。此外,我们发现 ALA 处理降低了叶片中的 H2O2 含量,但增加了根部的 H2O2 含量。外源 H2O2 促进了植物生长,增加了根中 Na 的滞留,并刺激了 NHX1、SOS1 和 HKT1 的基因表达。二苯基碘(DPI),一种 H2O2 生成抑制剂,抑制了 ALA 或 H2O2 对 Na 滞留、基因表达和耐盐性的影响。因此,我们提出 ALA 诱导根中 H2O2 积累,从而介导 Na 转运体基因表达和更多的 Na 根滞留,从而提高植物的耐盐性。