Evidence map›Paper›PMID 37087502›Full record

ArticleThe ISME journal2023

Marine picocyanobacterial PhnD1 shows specificity for various phosphorus sources but likely represents a constitutive inorganic phosphate transporter.

Bhumika S Shah, Benjamin A Ford, Deepa Varkey, Halina Mikolajek, Christian Orr, Vitaliy Mykhaylyk, Raymond J Owens, Ian T Paulsen

Open access · hybridAbstract read
In one paragraph

Article in The ISME journal, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.7field-weighted citation impact, top 41% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

5 citing papers in PubMed, 9 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Molecular mechanism of a coastal cyanobacteriumMarine life science & technology · 2024
    Article
  5. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors at 4 institutions in 2 countries.

Bhumika S ShahSchool of Natural Sciences, Macquarie University, Sydney, NSW, Australia. bhumika.shah@mq.edu.au.ORCID 0000-0001-8968-440X
Benjamin A FordSchool of Natural Sciences, Macquarie University, Sydney, NSW, Australia.
Deepa VarkeySchool of Natural Sciences, Macquarie University, Sydney, NSW, Australia.ORCID 0000-0002-9540-5638
Halina MikolajekDiamond Light Source Ltd., Harwell Science and Innovation Campus, Didcot, UK.
Christian OrrDiamond Light Source Ltd., Harwell Science and Innovation Campus, Didcot, UK.ORCID 0000-0002-6137-8969
Vitaliy MykhaylykDiamond Light Source Ltd., Harwell Science and Innovation Campus, Didcot, UK.
Raymond J OwensDivision of Structural Biology, The Wellcome Centre for Human Genetics, University of Oxford, Oxford, UK.ORCID 0000-0002-3705-2993
Ian T PaulsenSchool of Natural Sciences, Macquarie University, Sydney, NSW, Australia. ian.paulsen@mq.edu.au.ORCID 0000-0001-9015-9418
Diamond Light Source · GBARC Centre of Excellence in Synthetic Biology · AUMacquarie University · AUCentre for Human Genetics · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Despite being fundamental to multiple biological processes, phosphorus (P) availability in marine environments is often growth-limiting, with generally low surface concentrations. Picocyanobacteria strains encode a putative ABC-type phosphite/phosphate/phosphonate transporter, phnDCE, thought to provide access to an alternative phosphorus pool. This, however, is paradoxical given most picocyanobacterial strains lack known phosphite degradation or carbon-phosphate lyase pathway to utilise alternate phosphorus pools. To understand the function of the PhnDCE transport system and its ecological consequences, we characterised the PhnD1 binding proteins from four distinct marine Synechococcus isolates (CC9311, CC9605, MITS9220, and WH8102). We show the Synechococcus PhnD1 proteins selectively bind phosphorus compounds with a stronger affinity for phosphite than for phosphate or methyl phosphonate. However, based on our comprehensive ligand screening and growth experiments showing Synechococcus strains WH8102 and MITS9220 cannot utilise phosphite or methylphosphonate as a sole phosphorus source, we hypothesise that the picocyanobacterial PhnDCE transporter is a constitutively expressed, medium-affinity phosphate transporter, and the measured affinity of PhnD1 to phosphite or methyl phosphonate is fortuitous. Our MITS9220_PhnD1 structure explains the comparatively lower affinity of picocyanobacterial PhnD1 for phosphate, resulting from a more limited H-bond network. We propose two possible physiological roles for PhnD1. First, it could function in phospholipid recycling, working together with the predicted phospholipase, TesA, and alkaline phosphatase. Second, by having multiple transporters for P (PhnDCE and Pst), picocyanobacteria could balance the need for rapid transport during transient episodes of higher P availability in the environment, with the need for efficient P utilisation in typical phosphate-deplete conditions.

Indexed as

OrganophosphonatesPhosphitesSynechococcusMembrane Transport ProteinsPhosphatesPhosphate Transport ProteinsPhosphorusMembrane Transport ProteinsOrganophosphonatesPhosphatesPhosphate Transport ProteinsPhosphitesPhosphorus

Identifiers

PMID37087502
PMCPMC10284923
OpenAlexW4366768584

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.