Evidence map›Paper›PMID 25047076›Full record

ArticlePloS one2014

Differential Bees Flux Balance Analysis with OptKnock for in silico microbial strains optimization.

Yee Wen Choon, Mohd Saberi Mohamad, Safaai Deris, Rosli Md Illias, Chuii Khim Chong, Lian En Chai, Sigeru Omatu, Juan Manuel Corchado

Abstract read
In one paragraph

Article in PloS one, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing 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

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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

6 citing papers in PubMed.

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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

8 authors.

Yee Wen ChoonArtificial Intelligence and Bioinformatics Group, Faculty of Computing, Universiti Teknologi Malaysia, Johor, Malaysia.
Mohd Saberi MohamadArtificial Intelligence and Bioinformatics Group, Faculty of Computing, Universiti Teknologi Malaysia, Johor, Malaysia.
Safaai DerisArtificial Intelligence and Bioinformatics Group, Faculty of Computing, Universiti Teknologi Malaysia, Johor, Malaysia.
Rosli Md IlliasDepartment of Bioprocess Engineering, Faculty of Chemical Engineering, Universiti Teknologi Malaysia, Skudai, Johor, Malaysia.
Chuii Khim ChongArtificial Intelligence and Bioinformatics Group, Faculty of Computing, Universiti Teknologi Malaysia, Johor, Malaysia.
Lian En ChaiArtificial Intelligence and Bioinformatics Group, Faculty of Computing, Universiti Teknologi Malaysia, Johor, Malaysia.
Sigeru OmatuDepartment of Electronics, Information and Communication Engineering, Osaka Institute of Technology, Osaka, Japan.
Juan Manuel CorchadoBiomedical Research Institute of Salamanca/BISITE Research Group, University of Salamanca, Salamanca, Spain.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Microbial strains optimization for the overproduction of desired phenotype has been a popular topic in recent years. The strains can be optimized through several techniques in the field of genetic engineering. Gene knockout is a genetic engineering technique that can engineer the metabolism of microbial cells with the objective to obtain desirable phenotypes. However, the complexities of the metabolic networks have made the process to identify the effects of genetic modification on the desirable phenotypes challenging. Furthermore, a vast number of reactions in cellular metabolism often lead to the combinatorial problem in obtaining optimal gene deletion strategy. Basically, the size of a genome-scale metabolic model is usually large. As the size of the problem increases, the computation time increases exponentially. In this paper, we propose Differential Bees Flux Balance Analysis (DBFBA) with OptKnock to identify optimal gene knockout strategies for maximizing the production yield of desired phenotypes while sustaining the growth rate. This proposed method functions by improving the performance of a hybrid of Bees Algorithm and Flux Balance Analysis (BAFBA) by hybridizing Differential Evolution (DE) algorithm into neighborhood searching strategy of BAFBA. In addition, DBFBA is integrated with OptKnock to validate the results for improving the reliability the work. Through several experiments conducted on Escherichia coli, Bacillus subtilis, and Clostridium thermocellum as the model organisms, DBFBA has shown a better performance in terms of computational time, stability, growth rate, and production yield of desired phenotypes compared to the methods used in previous works.

Indexed as

Models, BiologicalAcetivibrio thermocellusAlgorithmsBacillus subtilisComputational BiologyComputer SimulationEscherichia coliGene Knockout TechniquesPhenotypeReproducibility of Results

Identifiers

PMID25047076
PMCPMC4105462

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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.