Physiological and multiomics analyses on photosynthesis and carbon utilization reveal biochemical carbon-concentrating mechanisms in Hygrophilla difformis under submergence
Abstract
Hygrophila difformis is an ornamental amphibious plant that develops distinct terrestrial (shallow-serrated) and submerged (deep-lobed) leaf forms in response to environmental conditions. Although previous studies have reported bicarbonate (HCO₃−) utilization and highlighted the involvement of carbonic anhydrase in inorganic carbon uptake, the photosynthetic strategy and carbon assimilation pathway operating under submergence remain unclear. Here, we applied an integrated framework combining physiological measurements, enzyme activity assays, transcriptomic, proteomic, and metabolomic profiling, stable carbon isotope analysis, and ultrastructural observations to compare terrestrial and submerged leaves. Submerged leaves displayed a δ 13C value of −20.068‰, indicating a substantial shift toward C₄-like photosynthetic metabolism under aquatic conditions. Consistent with this signature, activities of key carboxylation and decarboxylation enzymes were significantly elevated, supporting a transition from C₃ photosynthesis toward an NAD-malic enzyme (NAD-ME)–type C₄ pathway. Multiomics analyses revealed extensive reprogramming of photosynthetic and starch metabolic networks in response to submergence, with strong upregulation of genes and metabolites associated with the NAD-ME–type C₄ cycle, including cytosolic aspartate aminotransferase and alanine aminotransferase, accompanied by coordinated downregulation of Calvin cycle components. By contrast, terrestrial leaves retained high Rubisco activity and strong expression of Calvin cycle genes, consistent with classical C₃ photosynthesis. Reverse-transcription quantitative PCR analyses demonstrated marked induction of carbonic anhydrase genes under submerged conditions, with HdαCA9 showing a 194-fold increase in transcript abundance, highlighting its central role in underwater carbon utilization. Transmission electron microscopy further revealed dimorphic chloroplasts within submerged mesophyll cells. Collectively, results demonstrate plasticity in H. difformis and provide insights into C₄-like carbon assimilation strategies in amphibious plants.
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BibTeX
@article{kazmi2026physiological,
title = {{Physiological and multiomics analyses on photosynthesis and carbon utilization reveal biochemical carbon-concentrating mechanisms in Hygrophilla difformis under submergence}},
author = {Abeer Kazmi and Gaojie Li and Jingjing Yang and Xuyao Zhao and Md Fakhrul Islam and Xiaozhe Li and Dwi Fajar Sidhiq and Seisuke Kimura and Keiko U Torii and Hongwei Hou},
journal = {Horticulture research},
year = {2026},
month = jun,
doi = {10.1093/hr/uhag230},
url = {https://europepmc.org/article/PMC/PMC13722866},
note = {CC BY},
}
RIS
TY - JOUR
TI - Physiological and multiomics analyses on photosynthesis and carbon utilization reveal biochemical carbon-concentrating mechanisms in Hygrophilla difformis under submergence
AU - Abeer Kazmi
AU - Gaojie Li
AU - Jingjing Yang
AU - Xuyao Zhao
AU - Md Fakhrul Islam
AU - Xiaozhe Li
AU - Dwi Fajar Sidhiq
AU - Seisuke Kimura
AU - Keiko U Torii
AU - Hongwei Hou
PY - 2026
DA - 2026/06/15
JO - Horticulture research
DO - 10.1093/hr/uhag230
UR - https://europepmc.org/article/PMC/PMC13722866
AB - Hygrophila difformis is an ornamental amphibious plant that develops distinct terrestrial (shallow-serrated) and submerged (deep-lobed) leaf forms in response to environmental conditions. Although previous studies have reported bicarbonate (HCO₃−) utilization and highlighted the involvement of carbonic anhydrase in inorganic carbon uptake, the photosynthetic strategy and carbon assimilation pathway operating under submergence remain unclear. Here, we applied an integrated framework combining physiological measurements, enzyme activity assays, transcriptomic, proteomic, and metabolomic profiling, stable carbon isotope analysis, and ultrastructural observations to compare terrestrial and submerged leaves. Submerged leaves displayed a δ 13C value of −20.068‰, indicating a substantial shift toward C₄-like photosynthetic metabolism under aquatic conditions. Consistent with this signature, activities of key carboxylation and decarboxylation enzymes were significantly elevated, supporting a transition from C₃ photosynthesis toward an NAD-malic enzyme (NAD-ME)–type C₄ pathway. Multiomics analyses revealed extensive reprogramming of photosynthetic and starch metabolic networks in response to submergence, with strong upregulation of genes and metabolites associated with the NAD-ME–type C₄ cycle, including cytosolic aspartate aminotransferase and alanine aminotransferase, accompanied by coordinated downregulation of Calvin cycle components. By contrast, terrestrial leaves retained high Rubisco activity and strong expression of Calvin cycle genes, consistent with classical C₃ photosynthesis. Reverse-transcription quantitative PCR analyses demonstrated marked induction of carbonic anhydrase genes under submerged conditions, with HdαCA9 showing a 194-fold increase in transcript abundance, highlighting its central role in underwater carbon utilization. Transmission electron microscopy further revealed dimorphic chloroplasts within submerged mesophyll cells. Collectively, results demonstrate plasticity in H. difformis and provide insights into C₄-like carbon assimilation strategies in amphibious plants.
SN - 2662-6810
SN - 2052-7276
ER -