Cross-regulation between proteome reallocation and metabolic flux redistribution governs bacterial growth transition kinetics

IF 6.8 1区 生物学 Q1 BIOTECHNOLOGY & APPLIED MICROBIOLOGY
Huili Yuan , Yang Bai , Xuefei Li , Xiongfei Fu
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Abstract

Bacteria need to adjust their metabolism and protein synthesis simultaneously to adapt to changing nutrient conditions. It’s still a grand challenge to predict how cells coordinate such adaptation due to the cross-regulation between the metabolic fluxes and the protein synthesis. Here we developed a dynamic Constrained Allocation Flux Balance Analysis method (dCAFBA), which integrates flux-controlled proteome allocation and protein limited flux balance analysis. This framework can predict the redistribution dynamics of metabolic fluxes without requiring detailed enzyme parameters. We reveal that during nutrient up-shifts, the calculated metabolic fluxes change in agreement with experimental measurements of enzyme protein dynamics. During nutrient down-shifts, we uncover a switch of metabolic bottleneck from carbon uptake proteins to metabolic enzymes, which disrupts the coordination between metabolic flux and their enzyme abundance. Our method provides a quantitative framework to investigate cellular metabolism under varying environments and reveals insights into bacterial adaptation strategies.

蛋白质组重新分配与代谢通量重新分配之间的交叉调节制约着细菌的生长转换动力学
细菌需要同时调整新陈代谢和蛋白质合成,以适应不断变化的营养条件。由于新陈代谢通量和蛋白质合成之间存在交叉调节,因此预测细胞如何协调这种适应仍然是一个巨大的挑战。在这里,我们开发了一种动态受限分配通量平衡分析方法(dCAFBA),它整合了通量控制的蛋白质组分配和蛋白质受限通量平衡分析。这一框架可以预测代谢通量的再分配动态,而不需要详细的酶参数。我们发现,在养分上移过程中,计算出的代谢通量变化与酶蛋白动态的实验测量结果一致。在养分下移过程中,我们发现了代谢瓶颈从碳吸收蛋白向代谢酶的转换,这破坏了代谢通量与其酶丰度之间的协调。我们的方法为研究不同环境下的细胞代谢提供了一个定量框架,并揭示了细菌的适应策略。
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来源期刊
Metabolic engineering
Metabolic engineering 工程技术-生物工程与应用微生物
CiteScore
15.60
自引率
6.00%
发文量
140
审稿时长
44 days
期刊介绍: Metabolic Engineering (MBE) is a journal that focuses on publishing original research papers on the directed modulation of metabolic pathways for metabolite overproduction or the enhancement of cellular properties. It welcomes papers that describe the engineering of native pathways and the synthesis of heterologous pathways to convert microorganisms into microbial cell factories. The journal covers experimental, computational, and modeling approaches for understanding metabolic pathways and manipulating them through genetic, media, or environmental means. Effective exploration of metabolic pathways necessitates the use of molecular biology and biochemistry methods, as well as engineering techniques for modeling and data analysis. MBE serves as a platform for interdisciplinary research in fields such as biochemistry, molecular biology, applied microbiology, cellular physiology, cellular nutrition in health and disease, and biochemical engineering. The journal publishes various types of papers, including original research papers and review papers. It is indexed and abstracted in databases such as Scopus, Embase, EMBiology, Current Contents - Life Sciences and Clinical Medicine, Science Citation Index, PubMed/Medline, CAS and Biotechnology Citation Index.
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