Evidence map›Paper›PMID 29374483›Full record

ArticleMicrobial cell factories2018

Engineering E. coli for simultaneous glucose-xylose utilization during methyl ketone production.

Xi Wang, Ee-Been Goh, Harry R Beller

Open access · goldAbstract read
In one paragraph

Article in Microbial cell factories, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
1.6field-weighted citation impact, top 17% 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

10 citing papers in PubMed, 38 citations in OpenAlex.

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  10. Computer-Aided Rational Design of Efficient NADPH Production System byFrontiers in bioengineering and biotechnology · 2020
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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

3 authors at 1 institution in 1 country.

Xi WangJoint BioEnergy Institute (JBEI), 5885 Hollis St., Emeryville, CA, 94608, USA.
Ee-Been GohJoint BioEnergy Institute (JBEI), 5885 Hollis St., Emeryville, CA, 94608, USA.
Harry R BellerJoint BioEnergy Institute (JBEI), 5885 Hollis St., Emeryville, CA, 94608, USA. HRBeller@lbl.gov.ORCID http://orcid.org/0000-0001-9637-3650
Lawrence Berkeley National Laboratory · US

Funding

U.S. Department of Energy DE-AC02-05CH11231U.S. Department of Energy DE-SC0015093
6 · The paper itself

Abstract

backgroundWe previously developed an E. coli strain that overproduces medium-chain methyl ketones for potential use as diesel fuel blending agents or as flavors and fragrances. To date, the strain's performance has been optimized during growth with glucose. However, lignocellulosic biomass hydrolysates also contain a substantial portion of hemicellulose-derived xylose, which is typically the second most abundant sugar after glucose. Commercialization of the methyl ketone-producing technology would benefit from the increased efficiency resulting from simultaneous, rather than the native sequential (diauxic), utilization of glucose and xylose.

resultsIn this study, genetic manipulations were performed to alleviate carbon catabolite repression in our most efficient methyl ketone-producing strain. A strain engineered for constitutive expression of xylF and xylA (involved in xylose transport and metabolism) showed synchronized glucose and xylose consumption rates. However, this newly acquired capability came at the expense of methyl ketone titer, which decreased fivefold. Further efforts were made to improve methyl ketone production in this strain, and we found that two strategies were effective at enhancing methyl ketone titer: (1) chromosomal deletion of pgi (glucose-6-phosphate isomerase) to increase intracellular NADPH supply and (2) downregulation of CRP (cAMP receptor protein) expression by replacement of the native RBS with an RBS chosen based upon mutant library screening results. Combining these strategies resulted in the most favorable overall phenotypes for simultaneous glucose-xylose consumption without compromising methyl ketone titer at both 1 and 2% total sugar concentrations in shake flasks.

conclusionsThis work demonstrated a strategy for engineering simultaneous utilization of C

Indexed as

Batch Cell Culture TechniquesCatabolite RepressionCytochrome P-450 Enzyme SystemDisaccharidesEscherichia coliEscherichia coli ProteinsFermentationGlucoseIntramolecular OxidoreductasesKetonesMetabolic EngineeringProteinsXylose2-hydroxymuconate-semialdehyde hydrolaseCytochrome P-450 Enzyme SystemDisaccharidesEscherichia coli ProteinsGlucoseIntramolecular OxidoreductasesKetonesprostacyclin synthetaseProteinsXylosexylose-glucosecAMP receptor proteinCarbon catabolite repressionMetabolic engineeringMethyl ketonesNADPH

Identifiers

PMID29374483
PMCPMC5787283
OpenAlexW2787448079

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

Registered trials

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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.