Chandra Bellasio, Hilary Stuart‐Williams, Graham D. Farquhar, Jaume Flexas
{"title":"Fast dehydration reduces bundle sheath conductance in C4 maize and sorghum","authors":"Chandra Bellasio, Hilary Stuart‐Williams, Graham D. Farquhar, Jaume Flexas","doi":"10.1111/nph.20167","DOIUrl":null,"url":null,"abstract":"Summary<jats:list list-type=\"bullet\"> <jats:list-item>In the face of anthropogenic warming, drought poses an escalating threat to food production. C<jats:sub>4</jats:sub> plants offer promise in addressing this threat. C<jats:sub>4</jats:sub> leaves operate a biochemical CO<jats:sub>2</jats:sub> concentrating mechanism that exchanges metabolites between two partially isolated compartments (mesophyll and bundle sheath), which confers high‐productivity potential in hot climates boosting water use efficiency. However, when C<jats:sub>4</jats:sub> leaves experience dehydration, photosynthesis plummets. This paper explores the physiological mechanisms behind this decline.</jats:list-item> <jats:list-item>In a fast dehydration experiment, we measured the fluxes and isotopic composition of water and CO<jats:sub>2</jats:sub> in the gas exchanged by leaves, and we interpreted results using a novel biochemical model and analysis of elasticity.</jats:list-item> <jats:list-item>Our findings show that, while CO<jats:sub>2</jats:sub> supply to the mesophyll and to the bundle sheath persisted during dehydration, there was a decrease in CO<jats:sub>2</jats:sub> conductance at the bundle sheath‐mesophyll interface.</jats:list-item> <jats:list-item>We interpret this as causing a slowdown of intercellular metabolite exchange – an essential feature of C<jats:sub>4</jats:sub> photosynthesis. This would impede the supply of reducing power to the bundle sheath, leading to phosphoglycerate accumulation and feedback inhibition of Rubisco carboxylation. The interplay between this rapid sensitivity and the effectiveness of coping strategies that C<jats:sub>4</jats:sub> plants deploy may be an overlooked driver of their competitive performance.</jats:list-item> </jats:list>","PeriodicalId":214,"journal":{"name":"New Phytologist","volume":"236 1","pages":""},"PeriodicalIF":8.3000,"publicationDate":"2024-10-26","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"New Phytologist","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1111/nph.20167","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
SummaryIn the face of anthropogenic warming, drought poses an escalating threat to food production. C4 plants offer promise in addressing this threat. C4 leaves operate a biochemical CO2 concentrating mechanism that exchanges metabolites between two partially isolated compartments (mesophyll and bundle sheath), which confers high‐productivity potential in hot climates boosting water use efficiency. However, when C4 leaves experience dehydration, photosynthesis plummets. This paper explores the physiological mechanisms behind this decline.In a fast dehydration experiment, we measured the fluxes and isotopic composition of water and CO2 in the gas exchanged by leaves, and we interpreted results using a novel biochemical model and analysis of elasticity.Our findings show that, while CO2 supply to the mesophyll and to the bundle sheath persisted during dehydration, there was a decrease in CO2 conductance at the bundle sheath‐mesophyll interface.We interpret this as causing a slowdown of intercellular metabolite exchange – an essential feature of C4 photosynthesis. This would impede the supply of reducing power to the bundle sheath, leading to phosphoglycerate accumulation and feedback inhibition of Rubisco carboxylation. The interplay between this rapid sensitivity and the effectiveness of coping strategies that C4 plants deploy may be an overlooked driver of their competitive performance.
期刊介绍:
New Phytologist is an international electronic journal published 24 times a year. It is owned by the New Phytologist Foundation, a non-profit-making charitable organization dedicated to promoting plant science. The journal publishes excellent, novel, rigorous, and timely research and scholarship in plant science and its applications. The articles cover topics in five sections: Physiology & Development, Environment, Interaction, Evolution, and Transformative Plant Biotechnology. These sections encompass intracellular processes, global environmental change, and encourage cross-disciplinary approaches. The journal recognizes the use of techniques from molecular and cell biology, functional genomics, modeling, and system-based approaches in plant science. Abstracting and Indexing Information for New Phytologist includes Academic Search, AgBiotech News & Information, Agroforestry Abstracts, Biochemistry & Biophysics Citation Index, Botanical Pesticides, CAB Abstracts®, Environment Index, Global Health, and Plant Breeding Abstracts, and others.