Evidence map›Paper›PMID 35389631›Full record

ArticleACS synthetic biology2022

OptDesign: Identifying Optimum Design Strategies in Strain Engineering for Biochemical Production.

Shouyong Jiang, Irene Otero-Muras, Julio R Banga, Yong Wang, Marcus Kaiser, Natalio Krasnogor

Abstract read
In one paragraph

Article in ACS synthetic biology, 2022. 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. Article
  2. Article
  3. Review
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.

Shouyong JiangDepartment of Computing Science, University of Aberdeen, Aberdeen AB24 3FX, U.K.ORCID 0000-0001-5099-2093
Irene Otero-MurasInstitute for Integrative Systems Biology, UV-CSIC, Valencia 46980, Spain.ORCID 0000-0003-2895-997X
Julio R BangaComputational Biology Lab, MBG-CSIC, Pontevedra 36143, Spain.
Yong WangSchool of Automation, Central South University, Changsha 410083, China.
Marcus KaiserSchool of Medicine, University of Nottingham, Nottingham NG7 2RD, U.K.
Natalio KrasnogorSchool of Computing, Newcastle University, Tyne NE4 5TG, U.K.ORCID 0000-0002-2651-4320

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Computational tools have been widely adopted for strain optimization in metabolic engineering, contributing to numerous success stories of producing industrially relevant biochemicals. However, most of these tools focus on single metabolic intervention strategies (either gene/reaction knockout or amplification alone) and rely on hypothetical optimality principles (e.g., maximization of growth) and precise gene expression (e.g., fold changes) for phenotype prediction. This paper introduces OptDesign, a new two-step strain design strategy. In the first step, OptDesign selects regulation candidates that have a noticeable flux difference between the wild type and production strains. In the second step, it computes optimal design strategies with limited manipulations (combining regulation and knockout), leading to high biochemical production. The usefulness and capabilities of OptDesign are demonstrated for the production of three biochemicals in

Indexed as

Escherichia coliMetabolic EngineeringGene Knockout TechniquesMetabolic Networks and PathwaysModels, BiologicalPhenotypeSoftwarebiotechnologyflux changegenome-scale metabolic modelgrowth-coupled designin silico strain designsystems biology

Identifiers

PMID35389631
PMCPMC9016760

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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.