Cargando…
Noninvasive imaging of hollow structures and gas movement revealed the gas partial‐pressure‐gradient‐driven long‐distance gas movement in the aerenchyma along the leaf blade to submerged organs in rice
Rice (Oryza sativa) plants have porous or hollow organs consisting of aerenchyma, which is presumed to function as a low‐resistance diffusion pathway for air to travel from the foliage above the water to submerged organs. However, gas movement in rice plants has yet to be visualized in real time. In...
Autores principales: | , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9293169/ https://www.ncbi.nlm.nih.gov/pubmed/34498274 http://dx.doi.org/10.1111/nph.17726 |
_version_ | 1784749555737165824 |
---|---|
author | Yin, Yong‐Gen Mori, Yoshinao Suzui, Nobuo Kurita, Keisuke Yamaguchi, Mitsutaka Miyoshi, Yuta Nagao, Yuto Ashikari, Motoyuki Nagai, Keisuke Kawachi, Naoki |
author_facet | Yin, Yong‐Gen Mori, Yoshinao Suzui, Nobuo Kurita, Keisuke Yamaguchi, Mitsutaka Miyoshi, Yuta Nagao, Yuto Ashikari, Motoyuki Nagai, Keisuke Kawachi, Naoki |
author_sort | Yin, Yong‐Gen |
collection | PubMed |
description | Rice (Oryza sativa) plants have porous or hollow organs consisting of aerenchyma, which is presumed to function as a low‐resistance diffusion pathway for air to travel from the foliage above the water to submerged organs. However, gas movement in rice plants has yet to be visualized in real time. In this study involving partially submerged rice plants, the leaves emerging from the water were fed nitrogen‐13‐labeled nitrogen ([(13)N]N(2)) tracer gas, and the gas movement downward along the leaf blade, leaf sheath, and internode over time was monitored. The [(13)N]N(2) gas arrived at the bottom of the plant within 10 min, which was 20 min earlier than carbon‐11 photoassimilates. The [(13)N]N(2) gas movement was presumably mediated by diffusion along the aerenchyma network from the leaf blade to the root via nodes functioning as junctions, which were detected by X‐ray computed tomography. These findings imply the diffusion of gas along the aerenchyma, which does not consume energy, has enabled plants to adapt to aquatic environments. Additionally, there were no major differences in [(13)N]N(2) gas movement between paddy rice and deepwater rice plants, indicative of a common aeration mechanism in the two varieties, despite the difference in their response to flooding. |
format | Online Article Text |
id | pubmed-9293169 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-92931692022-07-20 Noninvasive imaging of hollow structures and gas movement revealed the gas partial‐pressure‐gradient‐driven long‐distance gas movement in the aerenchyma along the leaf blade to submerged organs in rice Yin, Yong‐Gen Mori, Yoshinao Suzui, Nobuo Kurita, Keisuke Yamaguchi, Mitsutaka Miyoshi, Yuta Nagao, Yuto Ashikari, Motoyuki Nagai, Keisuke Kawachi, Naoki New Phytol Research Rice (Oryza sativa) plants have porous or hollow organs consisting of aerenchyma, which is presumed to function as a low‐resistance diffusion pathway for air to travel from the foliage above the water to submerged organs. However, gas movement in rice plants has yet to be visualized in real time. In this study involving partially submerged rice plants, the leaves emerging from the water were fed nitrogen‐13‐labeled nitrogen ([(13)N]N(2)) tracer gas, and the gas movement downward along the leaf blade, leaf sheath, and internode over time was monitored. The [(13)N]N(2) gas arrived at the bottom of the plant within 10 min, which was 20 min earlier than carbon‐11 photoassimilates. The [(13)N]N(2) gas movement was presumably mediated by diffusion along the aerenchyma network from the leaf blade to the root via nodes functioning as junctions, which were detected by X‐ray computed tomography. These findings imply the diffusion of gas along the aerenchyma, which does not consume energy, has enabled plants to adapt to aquatic environments. Additionally, there were no major differences in [(13)N]N(2) gas movement between paddy rice and deepwater rice plants, indicative of a common aeration mechanism in the two varieties, despite the difference in their response to flooding. John Wiley and Sons Inc. 2021-09-30 2021-12 /pmc/articles/PMC9293169/ /pubmed/34498274 http://dx.doi.org/10.1111/nph.17726 Text en © 2021 The Authors. New Phytologist © 2021 New Phytologist Foundation https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Yin, Yong‐Gen Mori, Yoshinao Suzui, Nobuo Kurita, Keisuke Yamaguchi, Mitsutaka Miyoshi, Yuta Nagao, Yuto Ashikari, Motoyuki Nagai, Keisuke Kawachi, Naoki Noninvasive imaging of hollow structures and gas movement revealed the gas partial‐pressure‐gradient‐driven long‐distance gas movement in the aerenchyma along the leaf blade to submerged organs in rice |
title | Noninvasive imaging of hollow structures and gas movement revealed the gas partial‐pressure‐gradient‐driven long‐distance gas movement in the aerenchyma along the leaf blade to submerged organs in rice |
title_full | Noninvasive imaging of hollow structures and gas movement revealed the gas partial‐pressure‐gradient‐driven long‐distance gas movement in the aerenchyma along the leaf blade to submerged organs in rice |
title_fullStr | Noninvasive imaging of hollow structures and gas movement revealed the gas partial‐pressure‐gradient‐driven long‐distance gas movement in the aerenchyma along the leaf blade to submerged organs in rice |
title_full_unstemmed | Noninvasive imaging of hollow structures and gas movement revealed the gas partial‐pressure‐gradient‐driven long‐distance gas movement in the aerenchyma along the leaf blade to submerged organs in rice |
title_short | Noninvasive imaging of hollow structures and gas movement revealed the gas partial‐pressure‐gradient‐driven long‐distance gas movement in the aerenchyma along the leaf blade to submerged organs in rice |
title_sort | noninvasive imaging of hollow structures and gas movement revealed the gas partial‐pressure‐gradient‐driven long‐distance gas movement in the aerenchyma along the leaf blade to submerged organs in rice |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9293169/ https://www.ncbi.nlm.nih.gov/pubmed/34498274 http://dx.doi.org/10.1111/nph.17726 |
work_keys_str_mv | AT yinyonggen noninvasiveimagingofhollowstructuresandgasmovementrevealedthegaspartialpressuregradientdrivenlongdistancegasmovementintheaerenchymaalongtheleafbladetosubmergedorgansinrice AT moriyoshinao noninvasiveimagingofhollowstructuresandgasmovementrevealedthegaspartialpressuregradientdrivenlongdistancegasmovementintheaerenchymaalongtheleafbladetosubmergedorgansinrice AT suzuinobuo noninvasiveimagingofhollowstructuresandgasmovementrevealedthegaspartialpressuregradientdrivenlongdistancegasmovementintheaerenchymaalongtheleafbladetosubmergedorgansinrice AT kuritakeisuke noninvasiveimagingofhollowstructuresandgasmovementrevealedthegaspartialpressuregradientdrivenlongdistancegasmovementintheaerenchymaalongtheleafbladetosubmergedorgansinrice AT yamaguchimitsutaka noninvasiveimagingofhollowstructuresandgasmovementrevealedthegaspartialpressuregradientdrivenlongdistancegasmovementintheaerenchymaalongtheleafbladetosubmergedorgansinrice AT miyoshiyuta noninvasiveimagingofhollowstructuresandgasmovementrevealedthegaspartialpressuregradientdrivenlongdistancegasmovementintheaerenchymaalongtheleafbladetosubmergedorgansinrice AT nagaoyuto noninvasiveimagingofhollowstructuresandgasmovementrevealedthegaspartialpressuregradientdrivenlongdistancegasmovementintheaerenchymaalongtheleafbladetosubmergedorgansinrice AT ashikarimotoyuki noninvasiveimagingofhollowstructuresandgasmovementrevealedthegaspartialpressuregradientdrivenlongdistancegasmovementintheaerenchymaalongtheleafbladetosubmergedorgansinrice AT nagaikeisuke noninvasiveimagingofhollowstructuresandgasmovementrevealedthegaspartialpressuregradientdrivenlongdistancegasmovementintheaerenchymaalongtheleafbladetosubmergedorgansinrice AT kawachinaoki noninvasiveimagingofhollowstructuresandgasmovementrevealedthegaspartialpressuregradientdrivenlongdistancegasmovementintheaerenchymaalongtheleafbladetosubmergedorgansinrice |