Abstract
Coccolithophores are an important group of calcifying marine phytoplankton. Although coccolithophores are not silicified, some species exhibit a requirement for Si in the calcification process. These species also possess a novel protein (SITL) that resembles the SIT family of Si transporters found in diatoms. However, the nature of Si transport in coccolithophores is not yet known, making it difficult to determine the wider role of Si in coccolithophore biology. Here, we show that coccolithophore SITLs act as Na+-coupled Si transporters when expressed in heterologous systems and exhibit similar characteristics to diatom SITs. We find that CbSITL from Coccolithus braarudii is transcriptionally regulated by Si availability and is expressed in environmental coccolithophore populations. However, the Si requirement of C. braarudii and other coccolithophores is very low, with transport rates of exogenous Si below the level of detection in sensitive assays of Si transport. As coccoliths contain only low levels of Si, we propose that Si acts to support the calcification process, rather than forming a structural component of the coccolith itself. Si is therefore acting as a micronutrient in coccolithophores and natural populations are only likely to experience Si limitation in circumstances where dissolved silicon (DSi) is depleted to extreme levels.
Original language | English |
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Pages (from-to) | 315-330 |
Number of pages | 16 |
Journal | Environmental Microbiology |
Volume | 25 |
Issue number | 2 |
DOIs | |
State | Published - Feb 2023 |
Funding
The work was supported by a NERC-NSF award to G. L. Wheeler (NE/N011708/1) and A. R. Taylor (NSF-GEO 1638838). An ERC Advanced Grant to C. Brownlee (ERC-ADG-670390) and an ERC starter grant to P. Curnow (ERC-2011-StG_20101109). Analytical electron microscopy was performed in part at UNCW Richard M. Dillaman Biological Imaging Facility (SEM supported by NSF 1828053) and at the Joint School of Nanoscience and Nanoengineering, Greensboro, North Carolina (supported by NSF ECCS-1542174). The work was supported by a NERC‐NSF award to G. L. Wheeler (NE/N011708/1) and A. R. Taylor (NSF‐GEO 1638838). An ERC Advanced Grant to C. Brownlee (ERC‐ADG‐670390) and an ERC starter grant to P. Curnow (ERC‐2011‐StG_20101109). Analytical electron microscopy was performed in part at UNCW Richard M. Dillaman Biological Imaging Facility (SEM supported by NSF 1828053) and at the Joint School of Nanoscience and Nanoengineering, Greensboro, North Carolina (supported by NSF ECCS‐1542174). H2020 European Research Council, Grant/Award Numbers: ERC‐2011‐StG_20101109, ERC‐ADG‐670390; National Science Foundation, Grant/Award Numbers: 1638838, 1828053, ECCS‐1542174; Natural Environment Research Council, Grant/Award Numbers: NE/N011708/1, NSF‐GEO 1638838 Funding information
Funders | Funder number |
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NERC-NSF | |
NERC‐NSF | |
NSF-GEO | |
NSF‐GEO | |
National Science Foundation | 1638838, 1828053 |
Horizon 2020 Framework Programme | 670390 |
H2020 European Research Council | ERC‐2011‐StG_20101109, ERC‐ADG‐670390 |
Nanoscience and Nanoengineering, Duke University | ECCS‐1542174 |
Natural Environment Research Council | NE/N011708/1 |
Neurosciences Foundation |