Rethinking Photosynthesis: Intracellular Water Dynamics, Bicarbonate Photolysis, and Electrophysiological Coupling in Inorganic Carbon Assimilation
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Abstract
Photosynthesis is the fundamental biochemical process driving Earth's biogeochemical cycles. The traditional theory holds that water is the sole source of photosynthetic oxygen and atmospheric CO$_2$ the only inorganic carbon substrate. However, electrophysiological, isotopic, and physiological evidence from our systematic research prompts a re-examination of this paradigm, revealing an unrecognized coupling between plant inorganic carbon assimilation and intracellular water utilization. Our key findings are: (i) Intracellular water utilization rate is decoupled from atmospheric CO$_2$ assimilation, suggesting that terrestrial plants assimilate inorganic carbon from atmospheric CO$_2$, soil inorganic carbon, and internally recycled inorganic carbon derived from metabolic carbon turnover. (ii) Electrophysiologically quantified intracellular water utilization, reflecting photosynthetic water photolysis through electron transfer dynamics, may serve as a broader indicator of total photosynthetic capacity than leaf CO$_2$ flux. (iii) Bicarbonate photolysis---the first step of inorganic carbon assimilation---may contribute equally to photosynthetic oxygen evolution as water photolysis, forming a coupled chain reaction that minimizes diffusion and concentration losses to enhance efficiency. (iv) Plant growth and adaptation are jointly driven by chemical energy (ATP) and internal electrical energy stored in cellular electrical components, with energy allocation prioritizing stress responses under abiotic stressors. We propose a revised photosynthesis framework integrating bicarbonate photolysis, intracellular water--electrophysiology coupling, and multi-source inorganic carbon assimilation. This perspective highlights the theoretical significance of updating classical photosynthesis theory, its applied value for improving crop photosynthetic efficiency and stress tolerance, and outlines future directions to dissect the underlying molecular-electrophysiological mechanisms and their biotechnological translation.
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References
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Cite This Article
TY - JOUR AU - Wu, Yanyou AU - Aboueldahab, Mohamed PY - 2026 DA - 2026/05/13 TI - Rethinking Photosynthesis: Intracellular Water Dynamics, Bicarbonate Photolysis, and Electrophysiological Coupling in Inorganic Carbon Assimilation JO - Journal of Plant Electrobiology T2 - Journal of Plant Electrobiology JF - Journal of Plant Electrobiology VL - 1 IS - 2 SP - 82 EP - 93 DO - 10.62762/JPE.2026.900219 UR - https://www.icck.org/article/abs/JPE.2026.900219 KW - photosynthesis KW - bicarbonate photolysis KW - intracellular water dynamics KW - plant electrophysiology KW - inorganic carbon assimilation KW - energy allocation AB - Photosynthesis is the fundamental biochemical process driving Earth's biogeochemical cycles. The traditional theory holds that water is the sole source of photosynthetic oxygen and atmospheric CO$_2$ the only inorganic carbon substrate. However, electrophysiological, isotopic, and physiological evidence from our systematic research prompts a re-examination of this paradigm, revealing an unrecognized coupling between plant inorganic carbon assimilation and intracellular water utilization. Our key findings are: (i) Intracellular water utilization rate is decoupled from atmospheric CO$_2$ assimilation, suggesting that terrestrial plants assimilate inorganic carbon from atmospheric CO$_2$, soil inorganic carbon, and internally recycled inorganic carbon derived from metabolic carbon turnover. (ii) Electrophysiologically quantified intracellular water utilization, reflecting photosynthetic water photolysis through electron transfer dynamics, may serve as a broader indicator of total photosynthetic capacity than leaf CO$_2$ flux. (iii) Bicarbonate photolysis---the first step of inorganic carbon assimilation---may contribute equally to photosynthetic oxygen evolution as water photolysis, forming a coupled chain reaction that minimizes diffusion and concentration losses to enhance efficiency. (iv) Plant growth and adaptation are jointly driven by chemical energy (ATP) and internal electrical energy stored in cellular electrical components, with energy allocation prioritizing stress responses under abiotic stressors. We propose a revised photosynthesis framework integrating bicarbonate photolysis, intracellular water--electrophysiology coupling, and multi-source inorganic carbon assimilation. This perspective highlights the theoretical significance of updating classical photosynthesis theory, its applied value for improving crop photosynthetic efficiency and stress tolerance, and outlines future directions to dissect the underlying molecular-electrophysiological mechanisms and their biotechnological translation. SN - 3071-6268 PB - Institute of Central Computation and Knowledge LA - English ER -
@article{Wu2026Rethinking,
author = {Yanyou Wu and Mohamed Aboueldahab},
title = {Rethinking Photosynthesis: Intracellular Water Dynamics, Bicarbonate Photolysis, and Electrophysiological Coupling in Inorganic Carbon Assimilation},
journal = {Journal of Plant Electrobiology},
year = {2026},
volume = {1},
number = {2},
pages = {82-93},
doi = {10.62762/JPE.2026.900219},
url = {https://www.icck.org/article/abs/JPE.2026.900219},
abstract = {Photosynthesis is the fundamental biochemical process driving Earth's biogeochemical cycles. The traditional theory holds that water is the sole source of photosynthetic oxygen and atmospheric CO\$\_2\$ the only inorganic carbon substrate. However, electrophysiological, isotopic, and physiological evidence from our systematic research prompts a re-examination of this paradigm, revealing an unrecognized coupling between plant inorganic carbon assimilation and intracellular water utilization. Our key findings are: (i) Intracellular water utilization rate is decoupled from atmospheric CO\$\_2\$ assimilation, suggesting that terrestrial plants assimilate inorganic carbon from atmospheric CO\$\_2\$, soil inorganic carbon, and internally recycled inorganic carbon derived from metabolic carbon turnover. (ii) Electrophysiologically quantified intracellular water utilization, reflecting photosynthetic water photolysis through electron transfer dynamics, may serve as a broader indicator of total photosynthetic capacity than leaf CO\$\_2\$ flux. (iii) Bicarbonate photolysis---the first step of inorganic carbon assimilation---may contribute equally to photosynthetic oxygen evolution as water photolysis, forming a coupled chain reaction that minimizes diffusion and concentration losses to enhance efficiency. (iv) Plant growth and adaptation are jointly driven by chemical energy (ATP) and internal electrical energy stored in cellular electrical components, with energy allocation prioritizing stress responses under abiotic stressors. We propose a revised photosynthesis framework integrating bicarbonate photolysis, intracellular water--electrophysiology coupling, and multi-source inorganic carbon assimilation. This perspective highlights the theoretical significance of updating classical photosynthesis theory, its applied value for improving crop photosynthetic efficiency and stress tolerance, and outlines future directions to dissect the underlying molecular-electrophysiological mechanisms and their biotechnological translation.},
keywords = {photosynthesis, bicarbonate photolysis, intracellular water dynamics, plant electrophysiology, inorganic carbon assimilation, energy allocation},
issn = {3071-6268},
publisher = {Institute of Central Computation and Knowledge}
}
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