Evidence map›Paper›PMID 19477196›Full record

ArticlePlasmid2009

New yeast recombineering tools for bacteria.

Robert M Q Shanks, Daniel E Kadouri, Daniel P MacEachran, George A O'Toole

Abstract read
In one paragraph

Article in Plasmid, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 72 papers.

0numbers the graph read from it
0cells of the map it votes in
72citing papers in PubMed
3.1field-weighted citation impact, top 8% 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

72 citing papers in PubMed, 104 citations in OpenAlex.

  1. Article
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  6. The pGinger Family of Expression Plasmids.Microbiology spectrum · 2023
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  8. A rise in the frequency ofFrontiers in cellular and infection microbiology · 2023
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  16. Xylose-Inducible Promoter Tools forApplied and environmental microbiology · 2020
    Article
  17. Leveraging host metabolism for bisdemethoxycurcumin production inMetabolic engineering communications · 2020
    Article
  18. Article
  19. Use of Collagen Binding Domains to Deliver Molecules to the Cornea.Journal of ocular pharmacology and therapeutics : the official journal of the Association for Ocular Pharmacology and Therapeutics · 2019
    Article
  20. Article

12 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

4 authors at 3 institutions in 1 country.

Robert M Q ShanksDepartment of Ophthalmology, University of Pittsburgh Eye Center, PA 15213, USA. shanksrm@upmc.edu
Daniel E Kadouri
Daniel P MacEachran
George A O'Toole
Dartmouth College · USMassachusetts Institute of Technology · USUPMC Health System · US

Funding

Virus Production and Manipulation of Protein/Gene Expression ModuleP30EY008098 · NEI · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI Marlene Behrmann · 1989 to 2026
$17.8M
cdiGMP regulation of Biofilm FormationR01AI083256 · NIAID · DARTMOUTH COLLEGE · PI O'TOOLE, GEORGE A. · 2009 to 2013
$1.9M
Novel virulence and exoenzyme regulatorsR01AI085570 · NIAID · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI SHANKS, ROBERT M · 2010 to 2014
$1.8M
Mechanisms of Biofilm Antibiotic Resistance in StaphylococcusR21AI055774 · NIAID · DARTMOUTH COLLEGE · PI O'TOOLE, GEORGE A. · 2003 to 2004
$474k
Role of the SasAB locus in S. aureus BiofilmsF32GM066658 · NIGMS · DARTMOUTH COLLEGE · PI SHANKS, ROBERT M · 2004 to 2004
$47k
NEI NIH HHS EY08098NEI NIH HHS P30 EY008098NIAID NIH HHS R01 AI083256NIAID NIH HHS R01 AI085570NIAID NIH HHS R21 AI055774NIAID NIH HHS R21-AI055774NIGMS NIH HHS F32 GM066658NIGMS NIH HHS F32 GM66658-01A1
6 · The paper itself

Abstract

Recombineering with Saccharomyces cerevisiae is a powerful methodology that can be used to clone multiple unmarked pieces of DNA to generate complex constructs with high efficiency. Here, we introduce two new tools that utilize the native recombination enzymes of S. cerevisiae to facilitate the manipulation of DNA. First, yeast recombineering was used to make directed nested deletions in a bacteria-yeast shuttle plasmid using only one or two single stranded oligomers, thus obviating the need for a PCR step. Second, we have generated several new shuttle vectors for yeast recombineering capable of replication in a wide variety of bacterial genera. As a demonstration of utility, some of the approaches and vectors generated in this study were used to make a pigP deletion mutation in the opportunistic pathogen Serratia marcescens.

Indexed as

BacteriaGenetic EngineeringGenetic VectorsSaccharomyces cerevisiae

Identifiers

PMID19477196
PMCPMC2737453
OpenAlexW2002582075

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.