α-cyanobacteria possessing form IA RuBisCO globally dominate aquatic habitats

Author:

Cabello-Yeves Pedro J.,Scanlan David J.ORCID,Callieri Cristiana,Picazo Antonio,Schallenberg Lena,Huber PaulaORCID,Roda-Garcia Juan J.,Bartosiewicz Maciej,Belykh Olga I.,Tikhonova Irina V.,Torcello-Requena AlbertoORCID,De Prado Paula MartinORCID,Millard Andrew D.,Camacho AntonioORCID,Rodriguez-Valera FranciscoORCID,Puxty Richard J.ORCID

Abstract

AbstractRuBisCO (ribulose 1,5-bisphosphate carboxylase/oxygenase) is one the most abundant enzymes on Earth. Virtually all food webs depend on its activity to supply fixed carbon. In aerobic environments, RuBisCO struggles to distinguish efficiently between CO2 and O2. To compensate, organisms have evolved convergent solutions to concentrate CO2 around the active site. The genetic engineering of such inorganic carbon concentrating mechanisms (CCMs) into plants could help facilitate future global food security for humankind. In bacteria, the carboxysome represents one such CCM component, of which two independent forms exist: α and β. Cyanobacteria are important players in the planet’s carbon cycle and the vast majority of the phylum possess a β-carboxysome, including most cyanobacteria used as laboratory models. The exceptions are the exclusively marine Prochlorococcus and Synechococcus that numerically dominate open ocean systems. However, the reason why marine systems favor an α-form is currently unknown. Here, we report the genomes of 58 cyanobacteria, closely related to marine Synechococcus that were isolated from freshwater lakes across the globe. We find all these isolates possess α-carboxysomes accompanied by a form 1A RuBisCO. Moreover, we demonstrate α-cyanobacteria dominate freshwater lakes worldwide. Hence, the paradigm of a separation in carboxysome type across the salinity divide does not hold true, and instead the α-form dominates all aquatic systems. We thus question the relevance of β-cyanobacteria as models for aquatic systems at large and pose a hypothesis for the reason for the success of the α-form in nature.

Publisher

Springer Science and Business Media LLC

Subject

Ecology, Evolution, Behavior and Systematics,Microbiology

Reference94 articles.

1. Martin WF, Bryant DA, Beatty JT. A physiological perspective on the origin and evolution of photosynthesis. FEMS Microbiol Rev. 2018;42:205–31.

2. Partensky F, Blanchot J, Vaulot D. Differential distribution and ecology of Prochlorococcus and Synechococcus in oceanic waters: a review. Bull Oceanogr Monaco, no Spec. 1999;19:457–76.

3. Zwirglmaier K, Jardillier L, Ostrowski M, Mazard S, Garczarek L, Vaulot D, et al. Global phylogeography of marine Synechococcus and Prochlorococcus reveals a distinct partitioning of lineages among oceanic biomes. Environ Microbiol. 2008;10:147–61.

4. Callieri C. Picophytoplankton in freshwater ecosystems: the importance of small-sized phototrophs. Freshw Rev. 2008;1:1–28.

5. Stal LJ. Physiological ecology of cyanobacteria in microbial mats and other communities. New Phytol. 1995;131:1–32.

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