A simplified approach for measuring Rubisco carbon isotope fractionation and the first determination in marine haptophyte <i>Gephyrocapsa oceanica</i>

Abstract. Rubisco is the central photosynthetic enzyme that catalyzes the fixation of CO2 to RuBP, initiating the most dominant carbon assimilation pathway on Earth that supports nearly all trophic chains in the biosphere. The CO2 fixation reaction expresses a strong kinetic isotope effect, producing biomass depleted in 13C and leaving characteristic imprints in sediments and sedimentary rocks, which are widely used to reconstruct past biological activity and environmental conditions, including ancient atmospheric CO2 levels. Despite its importance, carbon isotope fractionation of Rubisco (ϵRubisco) has been measured in only a limited number of organisms, with most studies focusing on land plants rather than on major contributors to the sedimentary record, such as cyanobacteria and coccolithophores. This scarcity reflects the complexity of existing experimental procedures and the high cost of instrumentation. Here, we present a simplified method that overcomes these limitations, eliminating the need for complex purification protocols, specialized equipment, and experimental designs that yield little CO2 fixation and high uncertainties. We use a simplified purification procedure yielding semi-purified Rubisco extracts, together with an Apollo–Picarro δ13C-DIC analyzer capable of simultaneously measuring DIC concentration and 13C isotope ratios. Using this protocol, we accurately determined ϵRubisco for the model plant Spinacia oleracea, the cyanobacterium Synechococcus sp., and provide the first determination for the coccolithophore Gephyrocapsa oceanica. The measured values span a striking range, from 13.1 ‰ to 30 ‰, highlighting both the variability of Rubisco fractionation and the versatility of our approach for studying carbon isotope discrimination across diverse biological systems. This study establishes a method that enables reliable determination of ϵRubisco across phylogenetically diverse groups, thereby supports research that provides new insights into the mechanisms of Rubisco fractionation, and improves interpretation of environmental carbon isotope records.

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Journal
Biogeosciences
Published
2026-02-27
DOI
https://doi.org/10.5194/bg-23-1591-2026
Primary Topic
Photosynthetic Processes and Mechanisms
Type
article
Field-Weighted Citation Impact
0.00

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article

A simplified approach for measuring Rubisco carbon isotope fractionation and the first determination in marine haptophyte Gephyrocapsa oceanica

Jeroni Galmés, Heather Stoll, Reto S. Wijker, Pere Aguiló Nicolau et al.
Biogeosciences
Photosynthetic Processes and Mechanisms
article

A simplified approach for measuring Rubisco carbon isotope fractionation and the first determination in marine haptophyte Gephyrocapsa oceanica

Jeroni Galmés, Heather Stoll, Reto S. Wijker, Pere Aguiló Nicolau, Madalina Jaggi
article en

Abstract

Abstract. Rubisco is the central photosynthetic enzyme that catalyzes the fixation of CO2 to RuBP, initiating the most dominant carbon assimilation pathway on Earth that supports nearly all trophic chains in the biosphere. The CO2 fixation reaction expresses a strong kinetic isotope effect, producing biomass depleted in 13C and leaving characteristic imprints in sediments and sedimentary rocks, which are widely used to reconstruct past biological activity and environmental conditions, including ancient atmospheric CO2 levels. Despite its importance, carbon isotope fractionation of Rubisco (ϵRubisco) has been measured in only a limited number of organisms, with most studies focusing on land plants rather than on major contributors to the sedimentary record, such as cyanobacteria and coccolithophores. This scarcity reflects the complexity of existing experimental procedures and the high cost of instrumentation. Here, we present a simplified method that overcomes these limitations, eliminating the need for complex purification protocols, specialized equipment, and experimental designs that yield little CO2 fixation and high uncertainties. We use a simplified purification procedure yielding semi-purified Rubisco extracts, together with an Apollo–Picarro δ13C-DIC analyzer capable of simultaneously measuring DIC concentration and 13C isotope ratios. Using this protocol, we accurately determined ϵRubisco for the model plant Spinacia oleracea, the cyanobacterium Synechococcus sp., and provide the first determination for the coccolithophore Gephyrocapsa oceanica. The measured values span a striking range, from 13.1 ‰ to 30 ‰, highlighting both the variability of Rubisco fractionation and the versatility of our approach for studying carbon isotope discrimination across diverse biological systems. This study establishes a method that enables reliable determination of ϵRubisco across phylogenetically diverse groups, thereby supports research that provides new insights into the mechanisms of Rubisco fractionation, and improves interpretation of environmental carbon isotope records.

BiogeosciencesVol. 23(4)
ETH Zurich (CH), Universitat de les Illes Balears (ES)
Eidgenössische Technische Hochschule Zürich, Universitat de les Illes Balears, Govern de les Illes Balears, Agencia Estatal de Investigación
Openalex Percentile: Top 40%
Photosynthetic Processes and Mechanisms
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