IF 4.3 2区 生物学 Q1 BIOTECHNOLOGY & APPLIED MICROBIOLOGY
Ashley Gilliam, Natalie C Sadler, Xiaolu Li, Marci Garcia, Zachary Johnson, Marija Veličković, Young-Mo Kim, Song Feng, Wei-Jun Qian, Margaret S Cheung, Pavlo Bohutskyi
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引用次数: 0

摘要

背景:利用蓝藻平台进行光合生物生产的工业可行性仍然面临挑战,原因是产量不足,特别是由于在生长的不同时间阶段,产品形成与细胞碳需求之间存在竞争。本研究调查了昼夜节律调控如何影响细长球藻(Synechococcus elongatus PCC 7942)在储存、生长和产品合成之间的碳分配,并提供了一些见解,为增强生物生产的潜在策略提供了建议:结果:PCC 7942 培养物过渡到恒定光照后,其蔗糖生产呈现出明显的时间模式,尽管光合装置的基因中度下调,但主观夜间的生产率比主观白天高三倍。这种生产率的提高与主观夜间糖原积累减少和细胞分裂停止相吻合,表明竞争过程在时间上是分离的。转录组分析表明,昼夜节律驱动的细胞周期调整以及能量和碳代谢的重新布线是协调一致的,在四个时间点上有 300 多个基因表现出不同的表达。主观夜的特点是细胞分裂相关基因的表达发生了改变,参与糖原合成的基因表达减少,同时糖原降解途径、替代电子流成分、磷酸戊糖途径和丙酮酸氧化脱羧的表达上调。这些分子变化通过提高主要蔗糖前体(1-磷酸葡萄糖和 6-磷酸果糖)的可用性为产物的形成创造了有利条件,并通过多种机制维持了氧化还原平衡:我们对碳代谢和氧化还原平衡的昼夜节律调控重新布线的分析表明,有两种潜在方法可用于改善蓝藻的生物生产:利用自然昼夜节律优化栽培条件和途径诱导的时机;以及通过控制碳通量重新分配和氧化还原重新平衡来模拟昼夜节律驱动的代谢转变的工程菌株。虽然这些策略仍有待测试,但理论上它们可以通过更好地在细胞生长、碳储存积累和产品合成阶段之间进行时间上的分离,提高光合生物生产的效率。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Cyanobacterial circadian regulation enhances bioproduction under subjective nighttime through rewiring of carbon partitioning dynamics, redox balance orchestration, and cell cycle modulation.

Background: The industrial feasibility of photosynthetic bioproduction using cyanobacterial platforms remains challenging due to insufficient yields, particularly due to competition between product formation and cellular carbon demands across different temporal phases of growth. This study investigates how circadian clock regulation impacts carbon partitioning between storage, growth, and product synthesis in Synechococcus elongatus PCC 7942, and provides insights that suggest potential strategies for enhanced bioproduction.

Results: After entrainment to light-dark cycles, PCC 7942 cultures transitioned to constant light revealed distinct temporal patterns in sucrose production, exhibiting three-fold higher productivity during subjective night compared to subjective day despite moderate down-regulation of genes from the photosynthetic apparatus. This enhanced productivity coincided with reduced glycogen accumulation and halted cell division at subjective night time, suggesting temporal separation of competing processes. Transcriptome analysis revealed coordinated circadian clock-driven adjustment of the cell cycle and rewiring of energy and carbon metabolism, with over 300 genes showing differential expression across four time points. The subjective night was characterized by altered expression of cell division-related genes and reduced expression of genes involved in glycogen synthesis, while showing upregulation of glycogen degradation pathways, alternative electron flow components, the pentose phosphate pathway, and oxidative decarboxylation of pyruvate. These molecular changes created favorable conditions for product formation through enhanced availability of major sucrose precursors (glucose-1-phosphate and fructose-6-phosphate) and maintained redox balance through multiple mechanisms.

Conclusions: Our analysis of circadian regulatory rewiring of carbon metabolism and redox balancing suggests two potential approaches that could be developed for improving cyanobacterial bioproduction: leveraging natural circadian rhythms for optimizing cultivation conditions and timing of pathway induction, and engineering strains that mimic circadian-driven metabolic shifts through controlled carbon flux redistribution and redox rebalancing. While these strategies remain to be tested, they could theoretically improve the efficiency of photosynthetic bioproduction by enabling better temporal separation between cell growth, carbon storage accumulation, and product synthesis phases.

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来源期刊
Microbial Cell Factories
Microbial Cell Factories 工程技术-生物工程与应用微生物
CiteScore
9.30
自引率
4.70%
发文量
235
审稿时长
2.3 months
期刊介绍: Microbial Cell Factories is an open access peer-reviewed journal that covers any topic related to the development, use and investigation of microbial cells as producers of recombinant proteins and natural products, or as catalyzers of biological transformations of industrial interest. Microbial Cell Factories is the world leading, primary research journal fully focusing on Applied Microbiology. The journal is divided into the following editorial sections: -Metabolic engineering -Synthetic biology -Whole-cell biocatalysis -Microbial regulations -Recombinant protein production/bioprocessing -Production of natural compounds -Systems biology of cell factories -Microbial production processes -Cell-free systems
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