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

机译:在曲霉尼日尔的基因组级代谢模型中的酶限制集成改善了表型预测

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Genome-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. Based 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 $$k_{{cat}}$$ values, predicting the differential expression of enzymes under different growth conditions. This 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.
机译:基因组级代谢模型(GSMM)是研究细胞代谢特性的强大工具。随着近年来多OMICS测量技术的发展,将多个OMICS数据集成到GSMM中的新方法显示了对预测结果的有希望的影响。它不仅提高了表型预测的准确性,而且还提高了模拟复杂生物化学现象的模型的可靠性,这可以促进特定基因靶标识的理论突破或更好地理解系统水平对细胞代谢。基于Aspergillus Niger的基本GSMM模型IHL1210,我们集成了大规模酶动力学和蛋白质组学数据,以基于酶限制建立GSMM,使用动力学和常规数据(GECKO)称为酶促约束的宝石。结果表明,酶约束有效提高了模型的表型预测能力,并通过模拟基因敲除来通过预测尼日尔的代谢表型变化来引导靶基因鉴定的模型。此外,酶限制显着降低了模型的溶液空间,即,超过40.10%的助焊剂可变性显着降低。新模型在其他方面显示出多功能性,例如估计大规模$$ k {{cat}} $$值,预测不同生长条件下酶的差异表达。本研究表明,将酶的丰度信息纳入GSMM对于改善与尼日尔的模型性能非常有效。酶约束模型可用作通过掺入蛋白质组数据来预测A. Niger的代谢表型的强大工具。在可预见的未来,随着测量技术的快速发展,对于A.Niger获得的更精确且富含富蛋白质组学的定量数据,酶受约束的GSMM模型将在系统水平上显示更大的应用空间。

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