Cytochrome c oxidase inactivation in <i>Physcomitrium patens</i> reveals that respiration coordinates plant metabolism

Photosynthetic organisms use sunlight as an energy source but rely on respiration during the night and in nonphotosynthetic tissues. Respiration also occurs in photosynthetically active cells, where its role is still unclear due to the lack of viable mutants. Mutations abolishing cytochrome c oxidase (Complex IV) activity are generally lethal. In this study, we generated cytochrome c oxidase assembly protein 11 (cox11) knockout lines through vegetative propagation in the moss Physcomitrium patens. These mutants showed severely impaired growth, with an altered composition of the respiratory apparatus and increased electron transfer through alternative oxidase. The light phase of photosynthesis remained largely unaffected in cox11 plants, while the efficiency of carbon fixation was reduced. Transcriptomic and metabolomic analyses showed that disrupting the cytochrome pathway had broad consequences for carbon and nitrogen metabolism. A major alteration in nitrogen assimilation was observed, with a general reduction in amino acid abundance. Partial growth rescue was achieved by externally supplying plants with amino acids but not with sugars, demonstrating that respiration in photosynthetic plant cells plays an essential role at the interface between carbon and nitrogen metabolism and a key role in providing carbon skeletons for amino acid biosynthesis.

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Publication Details

Journal
The Plant Cell
Published
2025-05-05
DOI
https://doi.org/10.1093/plcell/koaf101
Citations
2
Primary Topic
Photosynthetic Processes and Mechanisms
Type
article
Field-Weighted Citation Impact
1.61

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article

Cytochrome c oxidase inactivation in Physcomitrium patens reveals that respiration coordinates plant metabolism

Anna Segalla, Edoardo Bizzotto, Antoni M. Vera‐Vives, Alessandro Alboresi et al.
2 citations
The Plant Cell
Photosynthetic Processes and Mechanisms
1.61
article

Cytochrome c oxidase inactivation in Physcomitrium patens reveals that respiration coordinates plant metabolism

Anna Segalla, Edoardo Bizzotto, Antoni M. Vera‐Vives, Alessandro Alboresi, Francesca Sparla, Libero Gurrieri, Andreas P.M. Weber, Stefano Campanaro, Tomas Morosinotto, Philipp Westhoff, Marco Mellon, Shun‐ling Tan
article en
2 citations

Abstract

Photosynthetic organisms use sunlight as an energy source but rely on respiration during the night and in nonphotosynthetic tissues. Respiration also occurs in photosynthetically active cells, where its role is still unclear due to the lack of viable mutants. Mutations abolishing cytochrome c oxidase (Complex IV) activity are generally lethal. In this study, we generated cytochrome c oxidase assembly protein 11 (cox11) knockout lines through vegetative propagation in the moss Physcomitrium patens. These mutants showed severely impaired growth, with an altered composition of the respiratory apparatus and increased electron transfer through alternative oxidase. The light phase of photosynthesis remained largely unaffected in cox11 plants, while the efficiency of carbon fixation was reduced. Transcriptomic and metabolomic analyses showed that disrupting the cytochrome pathway had broad consequences for carbon and nitrogen metabolism. A major alteration in nitrogen assimilation was observed, with a general reduction in amino acid abundance. Partial growth rescue was achieved by externally supplying plants with amino acids but not with sugars, demonstrating that respiration in photosynthetic plant cells plays an essential role at the interface between carbon and nitrogen metabolism and a key role in providing carbon skeletons for amino acid biosynthesis.

The Plant CellVol. 37(6)
University of Padua (IT), Cluster of Excellence on Plant Sciences (DE), Heinrich Heine University Düsseldorf (DE), University of Bologna (IT)
Deutsche Forschungsgemeinschaft, Università degli Studi di Padova, Courant Forschungszentrum Geobiologie, Georg-August-Universität Göttingen
Openalex Percentile: Top 17%
Photosynthetic Processes and Mechanisms
1.61
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