{"title":"磷酸饥饿增强的紫色酸性磷酸酶GmPAP23介导大豆细胞内磷循环和产量。","authors":"Qi Guo, Shengnan Zhu, Tao Lai, Cang Tian, Meiling Hu, Xing Lu, Yingbin Xue, Cuiyue Liang, Jiang Tian","doi":"10.1111/pce.15400","DOIUrl":null,"url":null,"abstract":"<p><p>Plant internal phosphorus (P) recycling is a complex process, which is vital for improving plant P use efficiency. However, the mechanisms underlying phosphate (Pi) release from internal organic-P form remains to be deciphered in crops. Here, we functionally characterised a Pi-starvation responsive purple acid phosphatase (PAP), GmPAP23 in soybean (Glycine max). GmPAP23 could hydrolyse a series of Pi-containing compounds in vitro, such as trehalose-6-phosphate and glucose-l-phosphate. Moreover, GmPAP23 overexpression led to less P distribution in soybean source organs, including mature leaves and pod shells, but more P distribution in seeds under P sufficient conditions, although no effect was observed for transgenic soybean lines with its suppression. Metabolomic analysis found that a group of P-containing metabolites exhibited differential accumulations in mature leaves between wild type (WT) and GmPAP23 overexpression lines, such as glucose-l-phosphate and trehalose-6-phosphate. Moreover, a MYB transcription factor, GmPHR14 was subsequently found to activate the transcription of GmPAP23 via directly binding to its promoter. Collectively, these findings could highlight that the GmPHR14-GmPAP23 pathway, which controls internal P recycling in soybean, and thus affect yield.</p>","PeriodicalId":222,"journal":{"name":"Plant, Cell & Environment","volume":" ","pages":""},"PeriodicalIF":6.3000,"publicationDate":"2025-01-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"A Phosphate-Starvation Enhanced Purple Acid Phosphatase, GmPAP23 Mediates Intracellular Phosphorus Recycling and Yield in Soybean.\",\"authors\":\"Qi Guo, Shengnan Zhu, Tao Lai, Cang Tian, Meiling Hu, Xing Lu, Yingbin Xue, Cuiyue Liang, Jiang Tian\",\"doi\":\"10.1111/pce.15400\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Plant internal phosphorus (P) recycling is a complex process, which is vital for improving plant P use efficiency. However, the mechanisms underlying phosphate (Pi) release from internal organic-P form remains to be deciphered in crops. Here, we functionally characterised a Pi-starvation responsive purple acid phosphatase (PAP), GmPAP23 in soybean (Glycine max). GmPAP23 could hydrolyse a series of Pi-containing compounds in vitro, such as trehalose-6-phosphate and glucose-l-phosphate. Moreover, GmPAP23 overexpression led to less P distribution in soybean source organs, including mature leaves and pod shells, but more P distribution in seeds under P sufficient conditions, although no effect was observed for transgenic soybean lines with its suppression. Metabolomic analysis found that a group of P-containing metabolites exhibited differential accumulations in mature leaves between wild type (WT) and GmPAP23 overexpression lines, such as glucose-l-phosphate and trehalose-6-phosphate. Moreover, a MYB transcription factor, GmPHR14 was subsequently found to activate the transcription of GmPAP23 via directly binding to its promoter. Collectively, these findings could highlight that the GmPHR14-GmPAP23 pathway, which controls internal P recycling in soybean, and thus affect yield.</p>\",\"PeriodicalId\":222,\"journal\":{\"name\":\"Plant, Cell & Environment\",\"volume\":\" \",\"pages\":\"\"},\"PeriodicalIF\":6.3000,\"publicationDate\":\"2025-01-22\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Plant, Cell & Environment\",\"FirstCategoryId\":\"2\",\"ListUrlMain\":\"https://doi.org/10.1111/pce.15400\",\"RegionNum\":1,\"RegionCategory\":\"生物学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"PLANT SCIENCES\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Plant, Cell & Environment","FirstCategoryId":"2","ListUrlMain":"https://doi.org/10.1111/pce.15400","RegionNum":1,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"PLANT SCIENCES","Score":null,"Total":0}
A Phosphate-Starvation Enhanced Purple Acid Phosphatase, GmPAP23 Mediates Intracellular Phosphorus Recycling and Yield in Soybean.
Plant internal phosphorus (P) recycling is a complex process, which is vital for improving plant P use efficiency. However, the mechanisms underlying phosphate (Pi) release from internal organic-P form remains to be deciphered in crops. Here, we functionally characterised a Pi-starvation responsive purple acid phosphatase (PAP), GmPAP23 in soybean (Glycine max). GmPAP23 could hydrolyse a series of Pi-containing compounds in vitro, such as trehalose-6-phosphate and glucose-l-phosphate. Moreover, GmPAP23 overexpression led to less P distribution in soybean source organs, including mature leaves and pod shells, but more P distribution in seeds under P sufficient conditions, although no effect was observed for transgenic soybean lines with its suppression. Metabolomic analysis found that a group of P-containing metabolites exhibited differential accumulations in mature leaves between wild type (WT) and GmPAP23 overexpression lines, such as glucose-l-phosphate and trehalose-6-phosphate. Moreover, a MYB transcription factor, GmPHR14 was subsequently found to activate the transcription of GmPAP23 via directly binding to its promoter. Collectively, these findings could highlight that the GmPHR14-GmPAP23 pathway, which controls internal P recycling in soybean, and thus affect yield.
期刊介绍:
Plant, Cell & Environment is a premier plant science journal, offering valuable insights into plant responses to their environment. Committed to publishing high-quality theoretical and experimental research, the journal covers a broad spectrum of factors, spanning from molecular to community levels. Researchers exploring various aspects of plant biology, physiology, and ecology contribute to the journal's comprehensive understanding of plant-environment interactions.