Evidence map›Paper›PMID 27542935›Full record

ArticleApplied and environmental microbiology2016

Role of Phosphate Transport System Component PstB1 in Phosphate Internalization by Nostoc punctiforme.

L Hudek, D Premachandra, W A J Webster, L Bräu

Open access · bronzeAbstract read
In one paragraph

Article in Applied and environmental microbiology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed
1.0field-weighted citation impact, top 21% 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

29 citing papers in PubMed, 60 citations in OpenAlex.

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  13. Inhibition Mechanism ofFoods (Basel, Switzerland) · 2023
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  15. Metagenome-Assembled Genome of aMicrobiology resource announcements · 2023
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  17. Review
  18. Photosynthetic and ultrastructural responses of the chlorophyte Lobosphaera to the stress caused by a high exogenic phosphate concentration.Photochemical & photobiological sciences : Official journal of the European Photochemistry Association and the European Society for Photobiology · 2022
    Article
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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

4 authors at 1 institution in 1 country.

L HudekCentre for Regional and Rural Futures, Faculty of Science Engineering and Built Environment, Deakin University, Burwood, Victoria, Australia Centre for Cellular and Molecular Biology, School of Life and Environmental Sciences, Deakin University, Burwood, Victoria, Australia.
D PremachandraCentre for Regional and Rural Futures, Faculty of Science Engineering and Built Environment, Deakin University, Burwood, Victoria, Australia Centre for Cellular and Molecular Biology, School of Life and Environmental Sciences, Deakin University, Burwood, Victoria, Australia.
W A J WebsterCentre for Regional and Rural Futures, Faculty of Science Engineering and Built Environment, Deakin University, Burwood, Victoria, Australia.
L BräuCentre for Regional and Rural Futures, Faculty of Science Engineering and Built Environment, Deakin University, Burwood, Victoria, Australia Centre for Cellular and Molecular Biology, School of Life and Environmental Sciences, Deakin University, Burwood, Victoria, Australia lambert.brau@deakin.edu.au.
Deakin University · AU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In bacteria, limited phosphate availability promotes the synthesis of active uptake systems, such as the Pst phosphate transport system. To understand the mechanisms that facilitate phosphate accumulation in the cyanobacterium Nostoc punctiforme, phosphate transport systems were identified, revealing a redundancy of Pst phosphate uptake systems that exists across three distinct operons. Four separate PstB system components were identified. pstB1 was determined to be a suitable target for creating phenotypic mutations that could result in the accumulation of excessive levels of phosphate through its overexpression or in a reduction of the capacity to accumulate phosphate through its deletion. Using quantitative real-time PCR (qPCR), it was determined that pstB1 mRNA levels increased significantly over 64 h in cells cultured in 0 mM added phosphate and decreased significantly in cells exposed to high (12.8 mM) phosphate concentrations compared to the level in cells cultured under normal (0.8 mM) conditions. Possible compensation for the loss of PstB1 was observed when pstB2, pstB3, and pstB4 mRNA levels increased, particularly in cells starved of phosphate. The overexpression of pstB1 increased phosphate uptake by N. punctiforme and was shown to functionally complement the loss of PstB in E. coli PstB knockout (PstB

Indexed as

Adenosine TriphosphatasesATP-Binding Cassette TransportersBacterial ProteinsEscherichia coliGene Knockout TechniquesMutationNostocPhosphatesReal-Time Polymerase Chain ReactionRNA, MessengerAdenosine TriphosphatasesATP-Binding Cassette TransportersBacterial Proteinsphosphate import ATP-binding protein, BacteriaPhosphatesRNA, Messenger

Identifiers

PMID27542935
PMCPMC5066351
OpenAlexW2537878094

What OpenQuestion holds

Textmetadata
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.