High-yielding rice Takanari has superior photosynthetic response to a commercial rice Koshihikari under fluctuating light
Leaves within crop canopies experience variable light over the course of a day, which greatly affects photosynthesis and crop productivity. Little is known about the mechanisms of the photosynthetic response to fluctuating light and their genetic control. Here, we examined gas exchange, metabolite l...
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| Published in | Journal of experimental botany Vol. 70; no. 19; pp. 5287 - 5297 |
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| Main Authors | , , , , , , , , , , , , |
| Format | Journal Article |
| Language | English |
| Published |
UK
Oxford University Press
15.10.2019
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| Subjects | |
| Online Access | Get full text |
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| Abstract | Leaves within crop canopies experience variable light over the course of a day, which greatly affects photosynthesis and crop productivity. Little is known about the mechanisms of the photosynthetic response to fluctuating light and their genetic control. Here, we examined gas exchange, metabolite levels, and chlorophyll fluorescence during the photosynthetic induction response in an Oryza sativa indica cultivar with high yield (Takanari) and a japonica cultivar with lower yield (Koshihikari). Takanari had a faster induction response to sudden increases in light intensity than Koshihikari, as demonstrated by faster increases in net CO₂ assimilation rate, stomatal conductance, and electron transport rate. In a simulated light regime that mimicked a typical summer day, the faster induction response in Takanari increased daily CO₂ assimilation by 10%. The faster response of Takanari was explained in part by its maintenance of a larger pool of Calvin–Benson cycle metabolites. Together, the rapid responses of electron transport rate, metabolic flux, and stomatal conductance in Takanari contributed to the greater daily carbon gain under fluctuating light typical of natural environments. |
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| AbstractList | Leaves within crop canopies experience variable light over the course of a day, which greatly affects photosynthesis and crop productivity. Little is known about the mechanisms of the photosynthetic response to fluctuating light and their genetic control. Here, we examined gas exchange, metabolite levels, and chlorophyll fluorescence during the photosynthetic induction response in an Oryza sativa indica cultivar with high yield (Takanari) and a japonica cultivar with lower yield (Koshihikari). Takanari had a faster induction response to sudden increases in light intensity than Koshihikari, as demonstrated by faster increases in net CO2 assimilation rate, stomatal conductance, and electron transport rate. In a simulated light regime that mimicked a typical summer day, the faster induction response in Takanari increased daily CO2 assimilation by 10%. The faster response of Takanari was explained in part by its maintenance of a larger pool of Calvin-Benson cycle metabolites. Together, the rapid responses of electron transport rate, metabolic flux, and stomatal conductance in Takanari contributed to the greater daily carbon gain under fluctuating light typical of natural environments. The high-yielding rice cultivar Takanari has fast photosynthetic induction owing to a high electron transport rate, stomatal conductance, and metabolic flux, leading to high daily carbon gain under fluctuating light. The high-yielding rice cultivar Takanari has fast photosynthetic induction owing to a high electron transport rate, stomatal conductance, and metabolic flux, leading to high daily carbon gain under fluctuating light. Abstract Leaves within crop canopies experience variable light over the course of a day, which greatly affects photosynthesis and crop productivity. Little is known about the mechanisms of the photosynthetic response to fluctuating light and their genetic control. Here, we examined gas exchange, metabolite levels, and chlorophyll fluorescence during the photosynthetic induction response in an Oryza sativa indica cultivar with high yield (Takanari) and a japonica cultivar with lower yield (Koshihikari). Takanari had a faster induction response to sudden increases in light intensity than Koshihikari, as demonstrated by faster increases in net CO2 assimilation rate, stomatal conductance, and electron transport rate. In a simulated light regime that mimicked a typical summer day, the faster induction response in Takanari increased daily CO2 assimilation by 10%. The faster response of Takanari was explained in part by its maintenance of a larger pool of Calvin–Benson cycle metabolites. Together, the rapid responses of electron transport rate, metabolic flux, and stomatal conductance in Takanari contributed to the greater daily carbon gain under fluctuating light typical of natural environments. The high-yielding rice cultivar Takanari has fast photosynthetic induction owing to a high electron transport rate, stomatal conductance, and metabolic flux, leading to high daily carbon gain under fluctuating light. Leaves within crop canopies experience variable light over the course of a day, which greatly affects photosynthesis and crop productivity. Little is known about the mechanisms of the photosynthetic response to fluctuating light and their genetic control. Here, we examined gas exchange, metabolite levels, and chlorophyll fluorescence during the photosynthetic induction response in an Oryza sativa indica cultivar with high yield (Takanari) and a japonica cultivar with lower yield (Koshihikari). Takanari had a faster induction response to sudden increases in light intensity than Koshihikari, as demonstrated by faster increases in net CO 2 assimilation rate, stomatal conductance, and electron transport rate. In a simulated light regime that mimicked a typical summer day, the faster induction response in Takanari increased daily CO 2 assimilation by 10%. The faster response of Takanari was explained in part by its maintenance of a larger pool of Calvin–Benson cycle metabolites. Together, the rapid responses of electron transport rate, metabolic flux, and stomatal conductance in Takanari contributed to the greater daily carbon gain under fluctuating light typical of natural environments. Leaves within crop canopies experience variable light over the course of a day, which greatly affects photosynthesis and crop productivity. Little is known about the mechanisms of the photosynthetic response to fluctuating light and their genetic control. Here, we examined gas exchange, metabolite levels, and chlorophyll fluorescence during the photosynthetic induction response in an Oryza sativa indica cultivar with high yield (Takanari) and a japonica cultivar with lower yield (Koshihikari). Takanari had a faster induction response to sudden increases in light intensity than Koshihikari, as demonstrated by faster increases in net CO2 assimilation rate, stomatal conductance, and electron transport rate. In a simulated light regime that mimicked a typical summer day, the faster induction response in Takanari increased daily CO2 assimilation by 10%. The faster response of Takanari was explained in part by its maintenance of a larger pool of Calvin-Benson cycle metabolites. Together, the rapid responses of electron transport rate, metabolic flux, and stomatal conductance in Takanari contributed to the greater daily carbon gain under fluctuating light typical of natural environments.Leaves within crop canopies experience variable light over the course of a day, which greatly affects photosynthesis and crop productivity. Little is known about the mechanisms of the photosynthetic response to fluctuating light and their genetic control. Here, we examined gas exchange, metabolite levels, and chlorophyll fluorescence during the photosynthetic induction response in an Oryza sativa indica cultivar with high yield (Takanari) and a japonica cultivar with lower yield (Koshihikari). Takanari had a faster induction response to sudden increases in light intensity than Koshihikari, as demonstrated by faster increases in net CO2 assimilation rate, stomatal conductance, and electron transport rate. In a simulated light regime that mimicked a typical summer day, the faster induction response in Takanari increased daily CO2 assimilation by 10%. The faster response of Takanari was explained in part by its maintenance of a larger pool of Calvin-Benson cycle metabolites. Together, the rapid responses of electron transport rate, metabolic flux, and stomatal conductance in Takanari contributed to the greater daily carbon gain under fluctuating light typical of natural environments. Leaves within crop canopies experience variable light over the course of a day, which greatly affects photosynthesis and crop productivity. Little is known about the mechanisms of the photosynthetic response to fluctuating light and their genetic control. Here, we examined gas exchange, metabolite levels, and chlorophyll fluorescence during the photosynthetic induction response in an Oryza sativa indica cultivar with high yield (Takanari) and a japonica cultivar with lower yield (Koshihikari). Takanari had a faster induction response to sudden increases in light intensity than Koshihikari, as demonstrated by faster increases in net CO₂ assimilation rate, stomatal conductance, and electron transport rate. In a simulated light regime that mimicked a typical summer day, the faster induction response in Takanari increased daily CO₂ assimilation by 10%. The faster response of Takanari was explained in part by its maintenance of a larger pool of Calvin–Benson cycle metabolites. Together, the rapid responses of electron transport rate, metabolic flux, and stomatal conductance in Takanari contributed to the greater daily carbon gain under fluctuating light typical of natural environments. |
| Author | Tanaka, Yu Nagano, Atsushi J. Adachi, Shunsuke Tezuka, Ayumi Toya, Yoshihiro Ohkubo, Satoshi Kawai-Yamada, Maki Kobayashi, Shunzo Kashima, Makoto Miyagi, Atsuko Shimizu, Hiroshi Sage, Rowan F. Yamori, Wataru |
| AuthorAffiliation | 3 Graduate School of Agriculture, Kyoto University , Kitashirakawa Oiwake-cho, Sakyo-ku, Kyoto, Japan 5 Research Institute for Food and Agriculture, Ryukoku University , Yokotani, Seta Oe-cho, Otsu, Shiga, Japan 9 Department of Biological Sciences, Graduate School of Science, The University of Tokyo , Hongo, Bunkyo-ku, Tokyo, Japan 10 University of Essex , UK 8 Faculty of Agriculture, Ryukoku University , Yokotani, Seta Oe-cho, Otsu, Shiga, Japan 2 Japan Science and Technology Agency, Precursory Research for Embryonic Science and Technology , Kawaguchi, Japan 7 Department of Ecology and Evolutionary Biology, University of Toronto , Toronto, ON, Canada 4 Graduate School of Science and Engineering, Saitama University , Shimo-Okubo, Sakura-ku, Saitama, Japan 1 Institute of Global Innovation Research, Tokyo University of Agriculture and Technology , Saiwaicho, Fuchu, Tokyo, Japan 6 Department of Bioinformatic Engineering, Graduate School of Information Science and Technology, Osaka University , Yam |
| AuthorAffiliation_xml | – name: 7 Department of Ecology and Evolutionary Biology, University of Toronto , Toronto, ON, Canada – name: 3 Graduate School of Agriculture, Kyoto University , Kitashirakawa Oiwake-cho, Sakyo-ku, Kyoto, Japan – name: 5 Research Institute for Food and Agriculture, Ryukoku University , Yokotani, Seta Oe-cho, Otsu, Shiga, Japan – name: 10 University of Essex , UK – name: 4 Graduate School of Science and Engineering, Saitama University , Shimo-Okubo, Sakura-ku, Saitama, Japan – name: 1 Institute of Global Innovation Research, Tokyo University of Agriculture and Technology , Saiwaicho, Fuchu, Tokyo, Japan – name: 2 Japan Science and Technology Agency, Precursory Research for Embryonic Science and Technology , Kawaguchi, Japan – name: 6 Department of Bioinformatic Engineering, Graduate School of Information Science and Technology, Osaka University , Yamadaoka, Suita, Osaka, Japan – name: 9 Department of Biological Sciences, Graduate School of Science, The University of Tokyo , Hongo, Bunkyo-ku, Tokyo, Japan – name: 8 Faculty of Agriculture, Ryukoku University , Yokotani, Seta Oe-cho, Otsu, Shiga, Japan |
| Author_xml | – sequence: 1 givenname: Shunsuke surname: Adachi fullname: Adachi, Shunsuke – sequence: 2 givenname: Yu surname: Tanaka fullname: Tanaka, Yu – sequence: 3 givenname: Atsuko surname: Miyagi fullname: Miyagi, Atsuko – sequence: 4 givenname: Makoto surname: Kashima fullname: Kashima, Makoto – sequence: 5 givenname: Ayumi surname: Tezuka fullname: Tezuka, Ayumi – sequence: 6 givenname: Yoshihiro surname: Toya fullname: Toya, Yoshihiro – sequence: 7 givenname: Shunzo surname: Kobayashi fullname: Kobayashi, Shunzo – sequence: 8 givenname: Satoshi surname: Ohkubo fullname: Ohkubo, Satoshi – sequence: 9 givenname: Hiroshi surname: Shimizu fullname: Shimizu, Hiroshi – sequence: 10 givenname: Maki surname: Kawai-Yamada fullname: Kawai-Yamada, Maki – sequence: 11 givenname: Rowan F. surname: Sage fullname: Sage, Rowan F. – sequence: 12 givenname: Atsushi J. surname: Nagano fullname: Nagano, Atsushi J. – sequence: 13 givenname: Wataru surname: Yamori fullname: Yamori, Wataru |
| BackLink | https://www.ncbi.nlm.nih.gov/pubmed/31257443$$D View this record in MEDLINE/PubMed |
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| Snippet | Leaves within crop canopies experience variable light over the course of a day, which greatly affects photosynthesis and crop productivity. Little is known... The high-yielding rice cultivar Takanari has fast photosynthetic induction owing to a high electron transport rate, stomatal conductance, and metabolic flux,... |
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| Title | High-yielding rice Takanari has superior photosynthetic response to a commercial rice Koshihikari under fluctuating light |
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