College of Horticulture, China Agricultural University, Beijing, 100193, P.R. China.
Key Laboratory of Biology and Genetic Improvement of Horticultural (Nutrition and Physiology), The Ministry of Agriculture and Rural Affairs, Beijing, P.R. China.
Plant J. 2024 Aug;119(4):1880-1899. doi: 10.1111/tpj.16893. Epub 2024 Jun 25.
Due to the chelation of phosphorus in the soil, it becomes unavailable for plant growth and development. The mechanisms by which phosphorus-solubilizing bacteria activate immobilized phosphorus to promote the growth and development of woody plants, as well as the intrinsic molecular mechanisms, are not clear. Through the analysis of microbial communities in the rhizosphere 16S V3-V4 and a homologous gene encoding microbial alkaline phosphomonoesterase (phoD) in phosphate-efficient (PE) and phosphate-inefficient apple rootstocks, it was found that PE significantly enriched beneficial rhizobacteria. The best phosphorus-solubilizing bacteria, Bacillus sp. strain 7DB1 (B2), was isolated, purified, and identified from the rhizosphere soil of PE rootstocks. Incubating with Bacillus B2 into the rhizosphere of apple rootstocks significantly increased the soluble phosphorus and flavonoid content in the rhizosphere soil. Simultaneously, this process stimulates the root development of the rootstocks and enhances plant phosphorus uptake. After root transcriptome sequencing, candidate transcription factor MhMYB15, responsive to Bacillus B2, was identified through heatmap and co-expression network analysis. Yeast one-hybrid, electrophoretic mobility shift assay, and LUC assay confirmed that MhMYB15 can directly bind to the promoter regions of downstream functional genes, including chalcone synthase MhCHS2 and phosphate transporter MhPHT1;15. Transgenic experiments with MhMYB15 revealed that RNAi-MhMYB15 silenced lines failed to induce an increase in flavonoid content and phosphorus levels in the roots under the treatment of Bacillus B2, and plant growth was slower than the control. In conclusion, MhMYB15 actively responds to Bacillus B2, regulating the accumulation of flavonoids and the uptake of phosphorus, thereby influencing plant growth and development.
由于土壤中磷的螯合作用,它变得无法被植物生长和发育所利用。溶磷细菌激活固定磷以促进木本植物生长和发育的机制,以及内在的分子机制尚不清楚。通过分析高效磷(PE)和低效磷苹果砧木根际的 16S V3-V4 微生物群落和编码微生物碱性磷酸单酯酶(phoD)的同源基因,发现 PE 显著富集了有益的根际细菌。从 PE 砧木根际土壤中分离、纯化和鉴定出最好的溶磷细菌,芽孢杆菌属菌株 7DB1(B2)。将芽孢杆菌 B2 接种到苹果砧木根际土壤中,显著增加了根际土壤中的可溶性磷和类黄酮含量。同时,这一过程刺激了砧木的根系发育,增强了植物对磷的吸收。对根转录组进行测序后,通过热图和共表达网络分析,鉴定出对芽孢杆菌 B2 有响应的候选转录因子 MhMYB15。酵母单杂交、电泳迁移率变动分析和 LUC 分析证实,MhMYB15 可以直接结合到下游功能基因的启动子区域,包括查尔酮合酶 MhCHS2 和磷酸盐转运蛋白 MhPHT1;15。MhMYB15 的转基因实验表明,RNAi-MhMYB15 沉默系在芽孢杆菌 B2 处理下未能诱导根中类黄酮含量和磷水平的增加,且植物生长速度比对照慢。综上所述,MhMYB15 对芽孢杆菌 B2 积极响应,调节类黄酮的积累和磷的吸收,从而影响植物的生长和发育。