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聚(3-羟基丁酸酯)在炭疽芽孢杆菌孢子形成过程中为三羧酸循环和从头脂质生物合成提供能量。

Poly(3-hydroxybutyrate) fuels the tricarboxylic acid cycle and de novo lipid biosynthesis during Bacillus anthracis sporulation.

作者信息

Sadykov Marat R, Ahn Jong-Sam, Widhelm Todd J, Eckrich Valerie M, Endres Jennifer L, Driks Adam, Rutkowski Gregory E, Wingerd Kevin L, Bayles Kenneth W

机构信息

Department of Pathology and Microbiology, University of Nebraska Medical Center, Omaha, NE, 68198, USA.

Department of Microbiology and Immunology, Loyola University Chicago, Stritch School of Medicine, Maywood, IL, 60153, USA.

出版信息

Mol Microbiol. 2017 Jun;104(5):793-803. doi: 10.1111/mmi.13665. Epub 2017 Mar 30.

Abstract

Numerous bacteria accumulate poly(3-hydroxybutyrate) (PHB) as an intracellular reservoir of carbon and energy in response to imbalanced nutritional conditions. In Bacillus spp., where PHB biosynthesis precedes the formation of the dormant cell type called the spore (sporulation), the direct link between PHB accumulation and efficiency of sporulation was observed in multiple studies. Although the idea of PHB as an intracellular carbon and energy source fueling sporulation was proposed several decades ago, the mechanisms underlying PHB contribution to sporulation have not been defined. Here, we demonstrate that PHB deficiency impairs Bacillus anthracis sporulation through diminishing the energy status of the cells and by reducing carbon flux into the tricarboxylic acid (TCA) cycle and de novo lipid biosynthesis. Consequently, this metabolic imbalance decreased biosynthesis of the critical components required for spore integrity and resistance, such as dipicolinic acid (DPA) and the spore's inner membrane. Supplementation of the PHB deficient mutant with exogenous fatty acids overcame these sporulation defects, highlighting the importance of the TCA cycle and lipid biosynthesis during sporulation. Combined, the results of this work reveal the molecular mechanisms of PHB contribution to B. anthracis sporulation and provide valuable insight into the metabolic requirements for this developmental process in Bacillus species.

摘要

许多细菌在营养条件失衡时会积累聚(3-羟基丁酸酯)(PHB)作为细胞内的碳和能量储备。在芽孢杆菌属中,PHB生物合成先于称为孢子(孢子形成)的休眠细胞类型的形成,多项研究观察到了PHB积累与孢子形成效率之间的直接联系。尽管几十年前就有人提出PHB作为为孢子形成提供燃料的细胞内碳和能量来源的观点,但PHB对孢子形成的贡献机制尚未明确。在此,我们证明PHB缺乏会通过降低细胞的能量状态以及减少进入三羧酸(TCA)循环和从头脂质生物合成的碳通量来损害炭疽芽孢杆菌的孢子形成。因此,这种代谢失衡减少了孢子完整性和抗性所需的关键成分的生物合成,如吡啶二羧酸(DPA)和孢子的内膜。用外源脂肪酸补充PHB缺陷突变体克服了这些孢子形成缺陷,突出了TCA循环和脂质生物合成在孢子形成过程中的重要性。综合来看,这项工作的结果揭示了PHB对炭疽芽孢杆菌孢子形成的贡献的分子机制,并为芽孢杆菌属中这一发育过程的代谢需求提供了有价值的见解。

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