Evidence map›Paper›PMID 34193117›Full record

ArticleMicrobial cell factories2021

Integration of enzyme constraints in a genome-scale metabolic model of Aspergillus niger improves phenotype predictions.

Jingru Zhou, Yingping Zhuang, Jianye Xia

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Article in Microbial cell factories, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

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0cells of the map it votes in
11citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

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3 · Its place in the literature

Who cites it

11 citing papers in PubMed.

  1. Review
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  9. Enzyme-constrained metabolic model andComputational and structural biotechnology journal · 2023
    Article
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  11. Review
4 · The record

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5 · Who and what money

Authors and funding

3 authors.

Jingru ZhouState Key Laboratory of Bioreactor Engineering, East China University of Science and Technology, Shanghai, 200237, China.
Yingping ZhuangState Key Laboratory of Bioreactor Engineering, East China University of Science and Technology, Shanghai, 200237, China.
Jianye XiaState Key Laboratory of Bioreactor Engineering, East China University of Science and Technology, Shanghai, 200237, China. jyxia@ecust.edu.cn.ORCID http://orcid.org/0000-0003-2114-5770

Funding

National Key R&D Program of China No.2019YFA0904300
6 · The paper itself

Abstract

backgroundGenome-scale metabolic model (GSMM) is a powerful tool for the study of cellular metabolic characteristics. With the development of multi-omics measurement techniques in recent years, new methods that integrating multi-omics data into the GSMM show promising effects on the predicted results. It does not only improve the accuracy of phenotype prediction but also enhances the reliability of the model for simulating complex biochemical phenomena, which can promote theoretical breakthroughs for specific gene target identification or better understanding the cell metabolism on the system level.

resultsBased on the basic GSMM model iHL1210 of Aspergillus niger, we integrated large-scale enzyme kinetics and proteomics data to establish a GSMM based on enzyme constraints, termed a GEM with Enzymatic Constraints using Kinetic and Omics data (GECKO). The results show that enzyme constraints effectively improve the model's phenotype prediction ability, and extended the model's potential to guide target gene identification through predicting metabolic phenotype changes of A. niger by simulating gene knockout. In addition, enzyme constraints significantly reduced the solution space of the model, i.e., flux variability over 40.10% metabolic reactions were significantly reduced. The new model showed also versatility in other aspects, like estimating large-scale [Formula: see text] values, predicting the differential expression of enzymes under different growth conditions.

conclusionsThis study shows that incorporating enzymes' abundance information into GSMM is very effective for improving model performance with A. niger. Enzyme-constrained model can be used as a powerful tool for predicting the metabolic phenotype of A. niger by incorporating proteome data. In the foreseeable future, with the fast development of measurement techniques, and more precise and rich proteomics quantitative data being obtained for A. niger, the enzyme-constrained GSMM model will show greater application space on the system level.

Indexed as

Aspergillus nigerEnzymesGene Knockout TechniquesGenome, FungalKineticsMetabolic EngineeringModels, BiologicalPhenotypeProteomeEnzymesProteomeAspergillus nigerDifferential expression of enzymesGenome-scale metabolic modelProteome constraint GSMM

Identifiers

PMID34193117
PMCPMC8247156

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