Evidence map›Paper›PMID 31306566›Full record

ArticleBiotechnology progress2019

Engineering Escherichia coli for enhanced sensitivity to the autoinducer-2 quorum sensing signal.

Kristina Stephens, Amin Zargar, Milad Emamian, Nadia Abutaleb, Erica Choi, David N Quan, Gregory Payne, William E Bentley

Abstract read
In one paragraph

Article in Biotechnology progress, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact
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

3 citing papers in PubMed.

  1. Auxin (Indole-3-acetic acid) modulation of quorum sensing enhances phage susceptibility in Klebsiella pneumoniae.European journal of clinical microbiology & infectious diseases : official publication of the European Society of Clinical Microbiology · 2026
    Article
  2. Article
  3. 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.

Kristina StephensFischell Department of Bioengineering, University of Maryland, College Park, Maryland.
Amin ZargarFischell Department of Bioengineering, University of Maryland, College Park, Maryland.
Milad EmamianFischell Department of Bioengineering, University of Maryland, College Park, Maryland.
Nadia AbutalebFischell Department of Bioengineering, University of Maryland, College Park, Maryland.
Erica ChoiFischell Department of Bioengineering, University of Maryland, College Park, Maryland.
David N QuanFischell Department of Bioengineering, University of Maryland, College Park, Maryland.
Gregory PayneInstitute for Bioscience and Biotechnology Research, University of Maryland, College Park, Maryland.
William E BentleyFischell Department of Bioengineering, University of Maryland, College Park, Maryland.ORCID 0000-0002-4855-7866

Funding

Training in Host-pathogens interactionsT32AI089621 · NIAID · UNIV OF MARYLAND, COLLEGE PARK · PI LEE, VINCENT T, MCIVER, KEVIN S. · 2010 to 2025
$2.1M
Accessing molecular communication via synthetic biology and microelectronics – gut on a chip modelR21EB024102 · NIBIB · UNIV OF MARYLAND, COLLEGE PARK · PI BENTLEY, WILLIAM E. · 2017 to 2018
$412k
FDA HHS U01 FD005946NIAID NIH HHS T32 AI089621NIBIB NIH HHS R21 EB024102
6 · The paper itself

Abstract

The autoinducer-2 (AI-2) quorum sensing system is involved in a range of population-based bacterial behaviors and has been engineered for cell-cell communication in synthetic biology systems. Investigation into the cellular mechanisms of AI-2 processing has determined that overexpression of uptake genes increases AI-2 uptake rate, and genomic deletions of degradation genes lowers the AI-2 level required for activation of reporter genes. Here, we combine these two strategies to engineer an Escherichia coli strain with enhanced ability to detect and respond to AI-2. In an E. coli strain that does not produce AI-2, we monitored AI-2 uptake and reporter protein expression in a strain that overproduced the AI-2 uptake or phosphorylation units LsrACDB or LsrK, a strain with the deletion of AI-2 degradation units LsrF and LsrG, and an "enhanced" strain with both overproduction of AI-2 uptake and deletion of AI-2 degradation elements. By adding up to 40 μM AI-2 to growing cell cultures, we determine that this "enhanced" AI-2 sensitive strain both uptakes AI-2 more rapidly and responds with increased reporter protein expression than the others. This work expands the toolbox for manipulating AI-2 quorum sensing processes both in native environments and for synthetic biology applications.

Indexed as

BioengineeringEscherichia coliHomoserineLactonesQuorum SensingHomoserineLactonesN-octanoylhomoserine lactoneAI-2autoinductionquorum sensing

Identifiers

PMID31306566
PMCPMC7025430

What OpenQuestion holds

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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.