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The V-type ATPase enhances photosynthesis in marine phytoplankton and further links phagocytosis to symbiogenesis.

Authors :
Yee DP
Samo TJ
Abbriano RM
Shimasaki B
Vernet M
Mayali X
Weber PK
Mitchell BG
Hildebrand M
Decelle J
Tresguerres M
Source :
Current biology : CB [Curr Biol] 2023 Jun 19; Vol. 33 (12), pp. 2541-2547.e5. Date of Electronic Publication: 2023 May 31.
Publication Year :
2023

Abstract

Diatoms, dinoflagellates, and coccolithophores are dominant groups of marine eukaryotic phytoplankton that are collectively responsible for the majority of primary production in the ocean. <superscript>1</superscript> These phytoplankton contain additional intracellular membranes around their chloroplasts, which are derived from ancestral engulfment of red microalgae by unicellular heterotrophic eukaryotes that led to secondary and tertiary endosymbiosis. <superscript>2</superscript> However, the selectable evolutionary advantage of these membranes and the physiological significance for extant phytoplankton remain poorly understood. Since intracellular digestive vacuoles are ubiquitously acidified by V-type H <superscript>+</superscript> -ATPase (VHA), <superscript>3</superscript> proton pumps were proposed to acidify the microenvironment around secondary chloroplasts to promote the dehydration of dissolved inorganic carbon (DIC) into CO <subscript>2</subscript> , thus enhancing photosynthesis. <superscript>4</superscript> <superscript>,</superscript> <superscript>5</superscript> We report that VHA is localized around the chloroplasts of centric diatoms and that VHA significantly contributes to their photosynthesis across a wide range of oceanic irradiances. Similar results in a pennate diatom, dinoflagellate, and coccolithophore, but not green or red microalgae, imply the co-option of phagocytic VHA activity into a carbon-concentrating mechanism (CCM) is common to secondary endosymbiotic phytoplankton. Furthermore, analogous mechanisms in extant photosymbiotic marine invertebrates <superscript>6</superscript> <superscript>,</superscript> <superscript>7</superscript> <superscript>,</superscript> <superscript>8</superscript> provide functional evidence for an adaptive advantage throughout the transition from endosymbiosis to symbiogenesis. Based on the contribution of diatoms to ocean biogeochemical cycles, VHA-mediated enhancement of photosynthesis contributes at least 3.5 Gtons of fixed carbon per year (or 7% of primary production in the ocean), providing an example of a symbiosis-derived evolutionary innovation with global environmental implications.<br />Competing Interests: Declaration of interests The authors declare no competing interests.<br /> (Copyright © 2023 The Author(s). Published by Elsevier Inc. All rights reserved.)

Details

Language :
English
ISSN :
1879-0445
Volume :
33
Issue :
12
Database :
MEDLINE
Journal :
Current biology : CB
Publication Type :
Academic Journal
Accession number :
37263270
Full Text :
https://doi.org/10.1016/j.cub.2023.05.020