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通过已发表模型的系统比较对恶臭假单胞菌KT2440代谢网络进行重建的途径共识方法

Pathway-Consensus Approach to Metabolic Network Reconstruction for Pseudomonas putida KT2440 by Systematic Comparison of Published Models.

作者信息

Yuan Qianqian, Huang Teng, Li Peishun, Hao Tong, Li Feiran, Ma Hongwu, Wang Zhiwen, Zhao Xueming, Chen Tao, Goryanin Igor

机构信息

Key Laboratory of Systems Bioengineering (Ministry of Education), School of Chemical Engineering and Technology, Tianjin University, Tianjin, P. R. China.

Key Laboratory of Systems Microbial Biotechnology, Tianjin Institute of Industrial Biotechnology, Chinese Academy of Sciences, Tianjin, China.

出版信息

PLoS One. 2017 Jan 13;12(1):e0169437. doi: 10.1371/journal.pone.0169437. eCollection 2017.

DOI:10.1371/journal.pone.0169437
PMID:28085902
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5234801/
Abstract

Over 100 genome-scale metabolic networks (GSMNs) have been published in recent years and widely used for phenotype prediction and pathway design. However, GSMNs for a specific organism reconstructed by different research groups usually produce inconsistent simulation results, which makes it difficult to use the GSMNs for precise optimal pathway design. Therefore, it is necessary to compare and identify the discrepancies among networks and build a consensus metabolic network for an organism. Here we proposed a process for systematic comparison of metabolic networks at pathway level. We compared four published GSMNs of Pseudomonas putida KT2440 and identified the discrepancies leading to inconsistent pathway calculation results. The mistakes in the models were corrected based on information from literature so that all the calculated synthesis and uptake pathways were the same. Subsequently we built a pathway-consensus model and then further updated it with the latest genome annotation information to obtain modelPpuQY1140 for P. putida KT2440, which includes 1140 genes, 1171 reactions and 1104 metabolites. We found that even small errors in a GSMN could have great impacts on the calculated optimal pathways and thus may lead to incorrect pathway design strategies. Careful investigation of the calculated pathways during the metabolic network reconstruction process is essential for building proper GSMNs for pathway design.

摘要

近年来,已发表了100多个基因组规模的代谢网络(GSMN),并广泛用于表型预测和途径设计。然而,不同研究小组重建的特定生物体的GSMN通常会产生不一致的模拟结果,这使得难以使用GSMN进行精确的最优途径设计。因此,有必要比较和识别网络之间的差异,并构建一个针对某一生物体的共识代谢网络。在此,我们提出了一个在途径水平上系统比较代谢网络的过程。我们比较了已发表的恶臭假单胞菌KT2440的四个GSMN,并确定了导致途径计算结果不一致的差异。基于文献信息对模型中的错误进行了校正,以使所有计算出的合成和摄取途径相同。随后,我们构建了一个途径共识模型,然后用最新的基因组注释信息对其进一步更新,以获得恶臭假单胞菌KT2440的模型PpuQY1140,该模型包括1140个基因、1171个反应和1104个代谢物。我们发现,即使GSMN中存在小的误差,也可能对计算出的最优途径产生很大影响,从而可能导致错误的途径设计策略。在代谢网络重建过程中仔细研究计算出的途径对于构建适用于途径设计的合适GSMN至关重要。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e82a/5234801/dfe1b118450b/pone.0169437.g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e82a/5234801/b7e1c11a4152/pone.0169437.g001.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e82a/5234801/dfe1b118450b/pone.0169437.g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e82a/5234801/b7e1c11a4152/pone.0169437.g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e82a/5234801/a62ab29e33d3/pone.0169437.g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e82a/5234801/1276b08d5976/pone.0169437.g003.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e82a/5234801/dfe1b118450b/pone.0169437.g007.jpg

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