Evidence map›Paper›PMID 31038200›Full record

ArticleBiotechnology and bioengineering2019

Parallel experimental evolution reveals a novel repressive control of GalP on xylose fermentation in Escherichia coli.

Gavin Kurgan, Christian Sievert, Andrew Flores, Aidan Schneider, Thomas Billings, Larry Panyon, Chandler Morris, Eric Taylor, Logan Kurgan, Reed Cartwright and 1 more

Open access · greenAbstract read
In one paragraph

Article in Biotechnology and bioengineering, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.7field-weighted citation impact, top 33% 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

4 citing papers in PubMed, 9 citations in OpenAlex.

  1. Glucose Transport inMicroorganisms · 2023
    Review
  2. Review
  3. Article
  4. 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

11 authors at 1 institution in 1 country.

Gavin KurganSchool of Life Sciences, Arizona State University, Tempe, Arizona.
Christian SievertSchool of Life Sciences, Arizona State University, Tempe, Arizona.
Andrew FloresChemical Engineering Program, School for Engineering of Matter, Transport, and Energy, Arizona State University, Tempe, Arizona.
Aidan SchneiderSchool of Life Sciences, Arizona State University, Tempe, Arizona.
Thomas BillingsSchool of Life Sciences, Arizona State University, Tempe, Arizona.
Larry PanyonSchool of Life Sciences, Arizona State University, Tempe, Arizona.
Chandler MorrisSchool of Life Sciences, Arizona State University, Tempe, Arizona.
Eric TaylorSchool of Life Sciences, Arizona State University, Tempe, Arizona.
Logan KurganSchool of Life Sciences, Arizona State University, Tempe, Arizona.
Reed CartwrightSchool of Life Sciences, Arizona State University, Tempe, Arizona.
Xuan WangSchool of Life Sciences, Arizona State University, Tempe, Arizona.ORCID 0000-0002-2910-8598
Arizona State University · US

Funding

Analysis of de novo mutation from sequencing of related individuals and cellsR01HG007178 · NHGRI · WASHINGTON UNIVERSITY · PI CONRAD, DONALD F. · 2014 to 2018
$2.6M
NHGRI NIH HHS R01 HG007178
6 · The paper itself

Abstract

Efficient xylose utilization will facilitate microbial conversion of lignocellulosic sugar mixtures into valuable products. In Escherichia coli, xylose catabolism is controlled by carbon catabolite repression (CCR). However, in E. coli such as the succinate-producing strain KJ122 with disrupted CCR, xylose utilization is still inhibited under fermentative conditions. To probe the underlying genetic mechanisms inhibiting xylose utilization, we evolved KJ122 to enhance its xylose fermentation abilities in parallel and characterized the potential convergent genetic changes shared by multiple independently evolved strains. Whole-genome sequencing revealed that convergent mutations occurred in the galactose regulon during adaptive laboratory evolution potentially decreasing the transcriptional level or the activity of GalP, a galactose permease. We showed that deletion of galP increased xylose utilization in both KJ122 and wild-type E. coli, demonstrating a common repressive role of GalP for xylose fermentation. Concomitantly, induced expression of galP from a plasmid repressed xylose fermentation. Transcriptome analysis using RNA sequencing indicates that galP inactivation increases transcription levels of many catabolic genes for secondary sugars including xylose and arabinose. The repressive role of GalP for fermenting secondary sugars in E. coli suggests that utilization of GalP as a substitute glucose transporter is undesirable for conversion of lignocellulosic sugar mixtures.

Indexed as

Catabolite RepressionEscherichia coliEscherichia coli ProteinsFermentationMetabolic EngineeringMonosaccharide Transport ProteinsMutationSuccinic AcidXyloseEscherichia coli Proteinsgalactose permeaseMonosaccharide Transport ProteinsSuccinic AcidXyloseadaptive laboratory evolutionGalPlignocellulosesuccinatetransportxylose

Identifiers

PMID31038200
PMCPMC11161036
OpenAlexW2943266569

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.