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The Global Mass and Average Rate of Rubisco

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Specialty Science
Date 2019 Feb 21
PMID 30782794
Citations 74
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Abstract

Photosynthetic carbon assimilation enables energy storage in the living world and produces most of the biomass in the biosphere. Rubisco (d-ribulose 1,5-bisphosphate carboxylase/oxygenase) is responsible for the vast majority of global carbon fixation and has been claimed to be the most abundant protein on Earth. Here we provide an updated and rigorous estimate for the total mass of Rubisco on Earth, concluding it is ≈0.7 Gt, more than an order of magnitude higher than previously thought. We find that >90% of Rubisco enzymes are found in the ≈2 × 10 m of leaves of terrestrial plants, and that Rubisco accounts for ≈3% of the total mass of leaves, which we estimate at ≈30 Gt dry weight. We use our estimate for the total mass of Rubisco to derive the effective time-averaged catalytic rate of Rubisco of ≈0.03 s on land and ≈0.6 s in the ocean. Compared with the maximal catalytic rate observed in vitro at 25 °C, the effective rate in the wild is ≈100-fold slower on land and sevenfold slower in the ocean. The lower ambient temperature, and Rubisco not working at night, can explain most of the difference from laboratory conditions in the ocean but not on land, where quantification of many more factors on a global scale is needed. Our analysis helps sharpen the dramatic difference between laboratory and wild environments and between the terrestrial and marine environments.

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References
1.
Young J, Goldman J, Kranz S, Tortell P, Morel F . Slow carboxylation of Rubisco constrains the rate of carbon fixation during Antarctic phytoplankton blooms. New Phytol. 2014; 205(1):172-81. DOI: 10.1111/nph.13021. View

2.
MacKenzie T, Burns R, Campbell D . Carbon status constrains light acclimation in the cyanobacterium Synechococcus elongatus. Plant Physiol. 2004; 136(2):3301-12. PMC: 523389. DOI: 10.1104/pp.104.047936. View

3.
Brading P, Warner M, Smith D, Suggett D . Contrasting modes of inorganic carbon acquisition amongst Symbiodinium (Dinophyceae) phylotypes. New Phytol. 2013; 200(2):432-442. DOI: 10.1111/nph.12379. View

4.
Halsey K, Milligan A, Behrenfeld M . Physiological optimization underlies growth rate-independent chlorophyll-specific gross and net primary production. Photosynth Res. 2010; 103(2):125-37. DOI: 10.1007/s11120-009-9526-z. View

5.
Levitan O, Kranz S, Spungin D, Prasil O, Rost B, Berman-Frank I . Combined effects of CO2 and light on the N2-fixing cyanobacterium Trichodesmium IMS101: a mechanistic view. Plant Physiol. 2010; 154(1):346-56. PMC: 2938161. DOI: 10.1104/pp.110.159285. View