Evidence map›Paper›PMID 30439494›Full record

ArticleMetabolic engineering2019

Predicting the metabolic capabilities of Synechococcus elongatus PCC 7942 adapted to different light regimes.

Jared T Broddrick, David G Welkie, Denis Jallet, Susan S Golden, Graham Peers, Bernhard O Palsson

Open access · greenAbstract read
In one paragraph

Article in Metabolic engineering, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
1.7field-weighted citation impact, top 15% 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

19 citing papers in PubMed, 45 citations in OpenAlex.

  1. Intrinsic period stability of the cyanobacterial circadian oscillator across in vitro and in vivo conditions.Proceedings of the National Academy of Sciences of the United States of America · 2026
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  7. Highlighting the potential ofFrontiers in microbiology · 2023
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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

6 authors at 2 institutions in 2 countries.

Jared T BroddrickDivision of Biological Sciences, University of California San Diego, 9500 Gilman Dr., La Jolla, CA 92093, USA; Department of Bioengineering, University of California San Diego, 9500 Gilman Dr., La Jolla, CA 92093, USA.
David G WelkieDivision of Biological Sciences, University of California San Diego, 9500 Gilman Dr., La Jolla, CA 92093, USA.
Denis JalletDepartment of Biology, Colorado State University, 251 W. Pitkin St., Fort Collins, CO 80521, USA.
Susan S GoldenDivision of Biological Sciences, University of California San Diego, 9500 Gilman Dr., La Jolla, CA 92093, USA.
Graham PeersDepartment of Biology, Colorado State University, 251 W. Pitkin St., Fort Collins, CO 80521, USA.
Bernhard O PalssonDepartment of Bioengineering, University of California San Diego, 9500 Gilman Dr., La Jolla, CA 92093, USA. Electronic address: palsson@ucsd.edu.
Colorado State University · USUniversity of California, San Diego · US

Funding

Undergraduate Summer Research Experience: Molecular and cellular mechanisms of circadian timekeeping in a prokaryote modelR35GM118290 · NIGMS · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI GOLDEN, SUSAN S · 2016 to 2025
$6.7M
NIGMS NIH HHS R35 GM118290
6 · The paper itself

Abstract

There is great interest in engineering photoautotrophic metabolism to generate bioproducts of societal importance. Despite the success in employing genome-scale modeling coupled with flux balance analysis to engineer heterotrophic metabolism, the lack of proper constraints necessary to generate biologically realistic predictions has hindered broad application of this methodology to phototrophic metabolism. Here we describe a methodology for constraining genome-scale models of photoautotrophy in the cyanobacteria Synechococcus elongatus PCC 7942. Experimental photophysiology parameters coupled to genome-scale flux balance analysis resulted in accurate predictions of growth rates and metabolic reaction fluxes at low and high light conditions. Additionally, by constraining photon uptake fluxes, we characterized the metabolic cost of excess excitation energy. The predicted energy fluxes were consistent with known light-adapted phenotypes in cyanobacteria. Finally, we leveraged the modeling framework to characterize existing photoautotrophic and photomixtotrophic engineering strategies for 2,3-butanediol production in S. elongatus. This methodology, applicable to genome-scale modeling of all phototrophic microorganisms, can facilitate the use of flux balance analysis in the engineering of light-driven metabolism.

Indexed as

LightAcclimatizationButylene GlycolsChlorophyllComputer SimulationEnergy MetabolismGenomeMetabolic EngineeringMetabolic Flux AnalysisOxygenPhotosynthesisPigmentationSynechococcus2,3-butylene glycolButylene GlycolsChlorophyllOxygenConstraint based modelingCyanobacteria engineeringFlux balance analysisGenome-scale modelingPhotosynthesisSynechococcus elongatus

Identifiers

PMID30439494
PMCPMC6407710
OpenAlexW2901268380

What OpenQuestion holds

Textmetadata
LicenceTDM
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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.