Learning metabolic dynamics from irregular observations by Bidirectional Time-Series State Transfer Network.

IF 5 2区 生物学 Q1 MICROBIOLOGY mSystems Pub Date : 2024-08-20 Epub Date: 2024-07-26 DOI:10.1128/msystems.00697-24
Shaohua Xu, Ting Xu, Yuping Yang, Xin Chen
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Abstract

Modeling microbial metabolic dynamics is important for the rational optimization of both biosynthetic systems and industrial processes to facilitate green and efficient biomanufacturing. Classical approaches utilize explicit equation systems to represent metabolic networks, enabling the quantification of pathway fluxes to identify metabolic bottlenecks. However, these white-box models, despite their diverse applications, have limitations in simulating metabolic dynamics and are intrinsically inaccurate for industrial strains that lack information on network structures and kinetic parameters. On the other hand, black-box models do not rely on prior mechanistic knowledge of strains but are built upon observed time-series trajectories of biosynthetic systems in action. In practice, these observations are typically irregular, with discontinuously observed time points across multiple independent batches, each time point potentially containing missing measurements. Learning from such irregular data remains challenging for existing approaches. To address this issue, we present the Bidirectional Time-Series State Transfer Network (BTSTN) for modeling metabolic dynamics directly from irregular observations. Using evaluation data sets derived from both ideal dynamic systems and a real-world fermentation process, we demonstrate that BTSTN accurately reconstructs dynamic behaviors and predicts future trajectories. This approach exhibits enhanced robustness against missing measurements and noise, as compared to the state-of-the-art methods.IMPORTANCEIndustrial biosynthetic systems often involve strains with unclear genetic backgrounds, posing challenges in modeling their distinct metabolic dynamics. In such scenarios, white-box models, which commonly rely on inferred networks, are thereby of limited applicability and accuracy. In contrast, black-box models, such as statistical models and neural networks, are directly fitted or learned from observed time-series trajectories of biosynthetic systems in action. These methods typically assume regular observations without missing time points or measurements. If the observations are irregular, a pre-processing step becomes necessary to obtain a fully filled data set for subsequent model training, which, at the same time, inevitably introduces errors into the resulting models. BTSTN is a novel approach that natively learns from irregular observations. This distinctive feature makes it a unique addition to the current arsenal of technologies modeling metabolic dynamics.

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通过双向时间序列状态转移网络从不规则观测中学习代谢动力学
建立微生物代谢动力学模型对于合理优化生物合成系统和工业流程以促进绿色高效的生物制造非常重要。经典方法利用显式方程系统来表示代谢网络,从而量化途径通量,找出代谢瓶颈。然而,这些白盒模型尽管应用广泛,但在模拟代谢动力学方面存在局限性,而且对于缺乏网络结构和动力学参数信息的工业菌株来说,本质上并不准确。另一方面,黑盒模型并不依赖于菌株的先验机理知识,而是建立在观察到的生物合成系统运行的时间序列轨迹上。在实践中,这些观测数据通常是不规则的,在多个独立批次中的观测时间点是不连续的,每个时间点都可能包含缺失的测量数据。对于现有方法来说,从这种不规则数据中学习仍然具有挑战性。为了解决这个问题,我们提出了双向时间序列状态转移网络(BTSTN),用于直接从不规则观测数据中建立代谢动态模型。通过使用来自理想动态系统和真实世界发酵过程的评估数据集,我们证明了 BTSTN 能准确重建动态行为并预测未来轨迹。与最先进的方法相比,这种方法对缺失测量和噪声具有更强的鲁棒性。 重要意义工业生物合成系统通常涉及遗传背景不明确的菌株,这给它们独特的代谢动力学建模带来了挑战。在这种情况下,通常依赖于推断网络的白盒模型的适用性和准确性都很有限。与此相反,统计模型和神经网络等黑箱模型则是直接从观察到的生物合成系统的时间序列轨迹中拟合或学习的。这些方法通常假定观测结果是有规律的,没有缺失的时间点或测量值。如果观测结果不规则,则需要进行预处理,以获得完整的数据集,用于后续的模型训练。BTSTN 是一种从不规则观测数据中学习的新方法。这一显著特点使其成为当前新陈代谢动力学建模技术中独一无二的新成员。
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来源期刊
mSystems
mSystems Biochemistry, Genetics and Molecular Biology-Biochemistry
CiteScore
10.50
自引率
3.10%
发文量
308
审稿时长
13 weeks
期刊介绍: mSystems™ will publish preeminent work that stems from applying technologies for high-throughput analyses to achieve insights into the metabolic and regulatory systems at the scale of both the single cell and microbial communities. The scope of mSystems™ encompasses all important biological and biochemical findings drawn from analyses of large data sets, as well as new computational approaches for deriving these insights. mSystems™ will welcome submissions from researchers who focus on the microbiome, genomics, metagenomics, transcriptomics, metabolomics, proteomics, glycomics, bioinformatics, and computational microbiology. mSystems™ will provide streamlined decisions, while carrying on ASM''s tradition of rigorous peer review.
期刊最新文献
Announcing the mSystems special collection on microbial dormancy L-tryptophan and copper interactions linked to reduced colibactin genotoxicity in pks+ Escherichia coli Characterization of the carbapenem-resistant Acinetobacter baumannii clinical reference isolate BAL062 (CC2:KL58:OCL1): resistance properties and capsular polysaccharide structure The occurrence of Aerococcus urinaeequi and non-aureus staphylococci in raw milk negatively correlates with Escherichia coli clinical mastitis The predicted secreted proteome of activated sludge microorganisms indicates distinct nutrient niches
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