Katharina Schiller, Saskia Janshoff, Sanja Zenker, Prisca Viehöver, James Hartwell, Jürgen Eirich, Iris Finkemeier, Andrea Bräutigam
{"title":"Regulation of Crassulacean acid metabolism at the protein level in Kalanchoë laxiflora","authors":"Katharina Schiller, Saskia Janshoff, Sanja Zenker, Prisca Viehöver, James Hartwell, Jürgen Eirich, Iris Finkemeier, Andrea Bräutigam","doi":"10.1093/plphys/kiaf095","DOIUrl":null,"url":null,"abstract":"Crassulacean acid metabolism (CAM) is an adaptation to environments where water availability is seasonal or extremely low. It serves to ensure plant survival and/or maintain productivity in these adverse environments. CAM has repeatedly evolved in many plant lineages, although it requires a large and complex set of enzymes, transporters, and regulatory processes to control metabolite flux and pools. To test the potential levels at which CAM is regulated, we analyzed the CAM plant Kalanchoë laxiflora and compared with the genomes and transcriptomes of other CAM plants across a wide phylogenetic range. We show that CAM-associated transcripts and proteins did not exhibit a binary on/off pattern in abundance between day and night in K. laxiflora. Instead, K. laxiflora and many CAM plants displayed shared amino acid changes among proteins compared to C3 plants, especially in starch metabolism. Phosphoproteomics identified differential phosphorylation in K. laxiflora proteins between day and night. Taken together, our results demonstrate that CAM photosynthesis is regulated at both the transcript and protein levels.","PeriodicalId":20101,"journal":{"name":"Plant Physiology","volume":"96 1","pages":""},"PeriodicalIF":6.5000,"publicationDate":"2025-04-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Plant Physiology","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1093/plphys/kiaf095","RegionNum":1,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"PLANT SCIENCES","Score":null,"Total":0}
引用次数: 0
Abstract
Crassulacean acid metabolism (CAM) is an adaptation to environments where water availability is seasonal or extremely low. It serves to ensure plant survival and/or maintain productivity in these adverse environments. CAM has repeatedly evolved in many plant lineages, although it requires a large and complex set of enzymes, transporters, and regulatory processes to control metabolite flux and pools. To test the potential levels at which CAM is regulated, we analyzed the CAM plant Kalanchoë laxiflora and compared with the genomes and transcriptomes of other CAM plants across a wide phylogenetic range. We show that CAM-associated transcripts and proteins did not exhibit a binary on/off pattern in abundance between day and night in K. laxiflora. Instead, K. laxiflora and many CAM plants displayed shared amino acid changes among proteins compared to C3 plants, especially in starch metabolism. Phosphoproteomics identified differential phosphorylation in K. laxiflora proteins between day and night. Taken together, our results demonstrate that CAM photosynthesis is regulated at both the transcript and protein levels.
期刊介绍:
Plant Physiology® is a distinguished and highly respected journal with a rich history dating back to its establishment in 1926. It stands as a leading international publication in the field of plant biology, covering a comprehensive range of topics from the molecular and structural aspects of plant life to systems biology and ecophysiology. Recognized as the most highly cited journal in plant sciences, Plant Physiology® is a testament to its commitment to excellence and the dissemination of groundbreaking research.
As the official publication of the American Society of Plant Biologists, Plant Physiology® upholds rigorous peer-review standards, ensuring that the scientific community receives the highest quality research. The journal releases 12 issues annually, providing a steady stream of new findings and insights to its readership.