Evidence map›Paper›PMID 28349670›Full record

ArticleMicrobiologyOpen2017

Metabolic engineering to expand the substrate spectrum of Pseudomonas putida toward sucrose.

Hannes Löwe, Lukas Schmauder, Karina Hobmeier, Andreas Kremling, Katharina Pflüger-Grau

Open access · goldAbstract read
In one paragraph

Article in MicrobiologyOpen, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
2.3field-weighted citation impact, top 13% 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

15 citing papers in PubMed, 36 citations in OpenAlex.

  1. Article
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  6. D-Xylose Sensing inInternational journal of molecular sciences · 2021
    Review
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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.

Hannes LöweFachgebiet für Systembiotechnologie, Fakultät für Maschienenwesen, Technische Universität München, Garching, Germany.
Lukas SchmauderFachgebiet für Systembiotechnologie, Fakultät für Maschienenwesen, Technische Universität München, Garching, Germany.
Karina HobmeierFachgebiet für Systembiotechnologie, Fakultät für Maschienenwesen, Technische Universität München, Garching, Germany.
Andreas KremlingFachgebiet für Systembiotechnologie, Fakultät für Maschienenwesen, Technische Universität München, Garching, Germany.
Katharina Pflüger-GrauFachgebiet für Systembiotechnologie, Fakultät für Maschienenwesen, Technische Universität München, Garching, Germany.ORCID 0000-0002-8334-353X
Technical University of Munich · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Sucrose is an important disaccharide used as a substrate in many industrial applications. It is a major component of molasses, a cheap by-product of the sugar industry. Unfortunately, not all industrially relevant organisms, among them Pseudomonas putida, are capable of metabolizing sucrose. We chose a metabolic engineering approach to circumvent this blockage and equip P. putida with the activities necessary to consume sucrose. Therefore, we constructed a pair of broad-host range mini-transposons (pSST - sucrose splitting transposon), carrying either cscA, encoding an invertase able to split sucrose into glucose and fructose, or additionally cscB, encoding a sucrose permease. Introduction of cscA was sufficient to convey sucrose consumption and the additional presence of cscB had no further effect, though the sucrose permease was built and localized to the membrane. Sucrose was split extracellularly by the activity of the invertase CscA leaking out of the cell. The transposons were also used to confer sucrose consumption to Cupriavidus necator. Interestingly, in this strain, CscB acted as a glucose transporter, such that C. necator also gained the ability to grow on glucose. Thus, the pSST transposons are functional tools to extend the substrate spectrum of Gram-negative bacterial strains toward sucrose.

Indexed as

Metabolic Engineeringbeta-FructofuranosidaseCulture MediaCupriavidus necatorDNA Transposable ElementsMembrane Transport ProteinsMutagenesis, InsertionalPseudomonas putidaRecombinant ProteinsSucroseSweetening Agentsbeta-FructofuranosidaseCulture MediaDNA Transposable ElementsMembrane Transport ProteinsRecombinant ProteinsSucroseSweetening Agentsmetabolic engineeringPseudomonas putidasucrose metabolism

Identifiers

PMID28349670
PMCPMC5552902
OpenAlexW2603779769

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.