Evidence map›Paper›PMID 27482911›Full record

ArticleLangmuir : the ACS journal of surfaces and colloids2016

Differences in Interactions of Benzoic Acid and Benzoate with Interfaces.

Benjamin J Peters, Allison S Groninger, Fabio L Fontes, Dean C Crick, Debbie C Crans

Open access · greenAbstract read
In one paragraph

Article in Langmuir : the ACS journal of surfaces and colloids, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing 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

7 citing papers in PubMed, 13 citations in OpenAlex.

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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

5 authors at 1 institution in 1 country.

Benjamin J PetersDepartment of Chemistry, ‡Department of Biochemistry, §Cell and Molecular Biology Program, and ∥Mycobacteria Research Laboratories, Department of Microbiology, Immunology, and Pathology, Colorado State University , Fort Collins, Colorado 80523, United States.
Allison S GroningerDepartment of Chemistry, ‡Department of Biochemistry, §Cell and Molecular Biology Program, and ∥Mycobacteria Research Laboratories, Department of Microbiology, Immunology, and Pathology, Colorado State University , Fort Collins, Colorado 80523, United States.
Fabio L FontesDepartment of Chemistry, ‡Department of Biochemistry, §Cell and Molecular Biology Program, and ∥Mycobacteria Research Laboratories, Department of Microbiology, Immunology, and Pathology, Colorado State University , Fort Collins, Colorado 80523, United States.
Dean C CrickDepartment of Chemistry, ‡Department of Biochemistry, §Cell and Molecular Biology Program, and ∥Mycobacteria Research Laboratories, Department of Microbiology, Immunology, and Pathology, Colorado State University , Fort Collins, Colorado 80523, United States.
Debbie C CransDepartment of Chemistry, ‡Department of Biochemistry, §Cell and Molecular Biology Program, and ∥Mycobacteria Research Laboratories, Department of Microbiology, Immunology, and Pathology, Colorado State University , Fort Collins, Colorado 80523, United States.
Colorado State University · US

Funding

Unraveling the Origin of Pyrazinamide's Synergy with other anti-TB DrugsR21AI119567 · NIAID · COLORADO STATE UNIVERSITY · PI CRICK, DEAN C · 2015 to 2016
$408k
NIAID NIH HHS R21 AI119567
6 · The paper itself

Abstract

The interaction of benzoic acid and benzoate with model membrane systems was characterized to understand the molecular interactions of the two forms of a simple aromatic acid with the components of the membrane. The microemulsion system based on bis(2-ethylhexyl)sulfosuccinate (AOT) allowed determination of the molecular positioning using 1D NMR and 2D NMR spectroscopic methods. Benzoic acid and benzoate were both found to penetrate the membrane/water interfaces; however, the benzoic acid was able to penetrate much deeper and thus is more readily able to traverse a membrane. The Langmuir monolayer model system, using dipalmitoylphosphatidylcholine, was used as a generic membrane lipid for a cell. Compression isotherms of monolayers demonstrated a pH dependent interaction with a lipid monolayer and confirming the pH dependent observations shown in the reverse micellar model system. These studies provide an explanation for the antimicrobial activity of benzoic acid while benzoate is inactive. Furthermore, these studies form the framework upon which we are investigating the mode of bacterial uptake of pyrazinoic acid, the active form of pyrazinamide, a front line drug used to combat tuberculosis.

Indexed as

Benzoic AcidHydrogen-Ion ConcentrationMagnetic Resonance SpectroscopyMembranes, ArtificialMicellesBenzoic AcidMembranes, ArtificialMicelles

Identifiers

PMID27482911
PMCPMC6168200
OpenAlexW2477345677

What OpenQuestion holds

Textmetadata
LicenceTDM
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.