A plasma membrane Ca2+-dependent protein kinase PtCDPK2 promotes phosphorus starvation resilience in Phaeodactylum tricornutum

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Authors: Yasmin Meeda, E. Harrison, Susan D. Wharam, Heather O'Keefe, Andrea C. Highfield, Adam Monier, Glen L. Wheeler, Katherine E. Helliwell
Cited by: 1
References: 109

Abstract

Phosphorus (P) is an essential element limiting algal growth in aquatic ecosystems. Diatoms are abundant microalgae that thrive in nutrient-variable environments. Determining how diatoms regulate responses to P availability is thus crucial for understanding their ecological success. P-limited diatoms use Ca2+-dependent signalling to sense and coordinate responses to phosphate resupply. However, the apparatus enabling Ca2+ signal decoding in diatoms remains poorly understood. Phaeodactylum tricornutum possesses several Ca2+-dependent protein kinases (CDPKs) that are up-regulated by P starvation, although it is unknown whether they act to coordinate P starvation responses and/or transduce Ca2+ signals stimulated by P resupply. Here, we functionally characterized PtCDPK2. We show that PtCDPK2 localizes to the cell periphery, suggesting a role regulating plasma membrane processes. PtCDPK2 is co-expressed with the P starvation response regulator, PtPSR1. Increases in PtCDPK2 are also coordinated with the capacity for P-Ca2+ signalling. Quantification of extracellular phosphate indicates that the activation of P-Ca2+ signalling ability under P starvation is not controlled by external phosphate exhaustion, but decreased cellular P quota. Finally, Ptcdpk2 mutants have significantly reduced Fv/Fm and alkaline phosphatase activity under P starvation, indicating that they are impaired in their ability to cope with P depletion. Together, our findings demonstrate that Ca2+ signalling processes contribute to diatom tolerance to P limitation, alongside their established role mediating P resupply responses.

Fields of Study & Subjects

Plant nutrient uptake and metabolism Diatoms and Algae Research Photosynthetic Processes and Mechanisms

Publication details

Journal / source
Journal of Experimental Botany
Publisher
Oxford University Press (OUP)
Volume
77
Issue
10
Pages
3245–3260
Publication date
26 February 2026
Language
EN