Molecular mechanisms, metabolic remodeling, and energy reallocation underlying calcification in the coccolithophore <i>Gephyrocapsa huxleyi</i>

extrusion during calcification in the calcified strain, along with their associated proteins, including signal molecules and chaperones. Furthermore, an energy-intensive process was observed in calcifying cells, and this process was principally sustained by enhanced photosynthetic efficiency, supplemented by glucose accumulation as an energy reserve and COX6B translational upregulation, providing nocturnal energy. Notably, calcifying cells employed an energy conservation strategy characterized by transcriptional downregulation yet translational maintenance of photosynthesis and carbon metabolism genes while simultaneously upregulating protein biosynthesis and trafficking pathways to probably meet calcification demands, a process potentially facilitated by increased glutamine biosynthesis. Through multiomic technology, our findings provide insights into the molecular adaptations in the calcified coccolithophorid cells, revealing critical physiological trade-offs, carbon metabolism, and energy allocation that can inform predictions of their acclimation capacity under changing oceanic conditions.

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Publication Details

Journal
Journal of Phycology
Published
2026-04-30
DOI
https://doi.org/10.1111/jpy.70170
Primary Topic
Photosynthetic Processes and Mechanisms
Type
article
Field-Weighted Citation Impact
0.00

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article

Molecular mechanisms, metabolic remodeling, and energy reallocation underlying calcification in the coccolithophore Gephyrocapsa huxleyi

Senjie Lin, Ying Liu, Cong Wang, Xinyu Deng et al.
Journal of Phycology
Photosynthetic Processes and Mechanisms
article

Molecular mechanisms, metabolic remodeling, and energy reallocation underlying calcification in the coccolithophore Gephyrocapsa huxleyi

Senjie Lin, Ying Liu, Cong Wang, Xinyu Deng, Guanjia Lin, Nianzhi Jiao
article en

Abstract

extrusion during calcification in the calcified strain, along with their associated proteins, including signal molecules and chaperones. Furthermore, an energy-intensive process was observed in calcifying cells, and this process was principally sustained by enhanced photosynthetic efficiency, supplemented by glucose accumulation as an energy reserve and COX6B translational upregulation, providing nocturnal energy. Notably, calcifying cells employed an energy conservation strategy characterized by transcriptional downregulation yet translational maintenance of photosynthesis and carbon metabolism genes while simultaneously upregulating protein biosynthesis and trafficking pathways to probably meet calcification demands, a process potentially facilitated by increased glutamine biosynthesis. Through multiomic technology, our findings provide insights into the molecular adaptations in the calcified coccolithophorid cells, revealing critical physiological trade-offs, carbon metabolism, and energy allocation that can inform predictions of their acclimation capacity under changing oceanic conditions.

Journal of Phycology
University of Connecticut (US), Xiamen University (CN), Ministry of Natural Resources (CN), Fujian Institute of Oceanography (CN)
National Natural Science Foundation of China
Openalex Percentile: Top 13%
Photosynthetic Processes and Mechanisms
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