Evidence map›Paper›PMID 18667560›Full record

ArticleMicrobiology (Reading, England)2008

Shuttle expression plasmids for genetic studies in Streptococcus mutans.

Indranil Biswas, Jyoti K Jha, Nicholas Fromm

Open access · greenAbstract read
In one paragraph

Article in Microbiology (Reading, England), 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 100 papers.

0numbers the graph read from it
0cells of the map it votes in
100citing papers in PubMed
4.1field-weighted citation impact, top 6% 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

100 citing papers in PubMed, 144 citations in OpenAlex.

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  16. TheMicrobiology spectrum · 2022
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40 more citing papers are in PubMed but not listed here.

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

3 authors at 1 institution in 1 country.

Indranil BiswasDepartment of Microbiology, Molecular Genetics and Immunology, University of Kansas Medical Center, 3901 Rainbow Boulevard, Kansas City, KS 66160, USA.
Jyoti K JhaDepartment of Microbiology, Molecular Genetics and Immunology, University of Kansas Medical Center, 3901 Rainbow Boulevard, Kansas City, KS 66160, USA.
Nicholas FrommDepartment of Microbiology, Molecular Genetics and Immunology, University of Kansas Medical Center, 3901 Rainbow Boulevard, Kansas City, KS 66160, USA.
University of Kansas Medical Center · US

Funding

Mechanisms of Virulence Gene Regulation in Streptococcus mutansR01DE016686 · NIDCR · UNIVERSITY OF SOUTH DAKOTA · PI BISWAS, INDRANIL · 2007 to 2011
$1.2M
Expression of Cell Surface Proteins in Streptococcus mutansR21DE016056 · NIDCR · UNIVERSITY OF SOUTH DAKOTA · PI BISWAS, INDRANIL · 2006 to 2007
$367k
NIDCR NIH HHS DE 016056NIDCR NIH HHS DE 016686NIDCR NIH HHS R01 DE016686NIDCR NIH HHS R21 DE016056
6 · The paper itself

Abstract

A set of shuttle plasmids containing four different constitutive promoters was generated to facilitate overexpression of foreign and native genes in streptococci, such as Streptococcus mutans. The four promoters that were chosen were: P(ami), P(spac), P(23) and P(veg). These promoters are active in many Gram-positive bacteria, and allow various levels of gene expression depending on the host bacterium. Shuttle plasmids were constructed based on two types of broad-host-range replication origins: a rolling-circle replicon (pSH71) and a theta replicon (pAMbeta1). Shuttle plasmids derived from the pAMbeta1 replicon were generated to avoid the structural and segregational stability problems associated with rolling-circle replication, since these problems may be encountered during large gene cloning. In a complementation assay, we used one such plasmid to express a gene in trans to show the utility of these plasmids. In addition, a series of plasmids was generated for the expression of recombinant proteins with an N-terminal 6xHis tag or a C-terminal Strep-tag fusion, and, using a gene derived from S. mutans, we showed a high level of recombinant protein expression in S. mutans and Streptococcus pyogenes. Since these plasmids contain broad-host-range replication origins, and because the selected promoters are functional in many bacteria, they can be used for gene expression studies, such as complementation and recombinant protein expression.

Indexed as

Gene ExpressionCloning, MolecularGenetic VectorsPlasmidsPromoter Regions, GeneticRecombinant ProteinsRepliconStreptococcus mutansRecombinant Proteins

Identifiers

PMID18667560
PMCPMC4110107
OpenAlexW2148197405

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.