Exogenous putrescine plays a switch-like influence on the pH stress adaptability of biofilm-based activated sludge.

IF 3.9 2区 生物学 Q2 BIOTECHNOLOGY & APPLIED MICROBIOLOGY
Applied and Environmental Microbiology Pub Date : 2024-07-24 Epub Date: 2024-06-25 DOI:10.1128/aem.00569-24
Guanyu Jiang, Can Wang, Yongchao Wang, Jiayi Wang, Yimei Xue, Yuting Lin, Xurui Hu, Yahui Lv
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引用次数: 0

Abstract

Microbial community adaptability to pH stress plays a crucial role in biofilm formation. This study aims to investigate the regulatory mechanisms of exogenous putrescine on pH stress, as well as enhance understanding and application for the technical measures and molecular mechanisms of biofilm regulation. Findings demonstrated that exogenous putrescine acted as a switch-like distributor affecting microorganism pH stress, thus promoting biofilm formation under acid conditions while inhibiting it under alkaline conditions. As pH decreases, the protonation degree of putrescine increases, making putrescine more readily adsorbed. Protonated exogenous putrescine could increase cell membrane permeability, facilitating its entry into the cell. Subsequently, putrescine consumed intracellular H+ by enhancing the glutamate-based acid resistance strategy and the γ-aminobutyric acid metabolic pathway to reduce acid stress on cells. Furthermore, putrescine stimulated ATPase expression, allowing for better utilization of energy in H+ transmembrane transport and enhancing oxidative phosphorylation activity. However, putrescine protonation was limited under alkaline conditions, and the intracellular H+ consumption further exacerbated alkali stress and inhibits cellular metabolic activity. Exogenous putrescine promoted the proportion of fungi and acidophilic bacteria under acidic stress and alkaliphilic bacteria under alkali stress while having a limited impact on fungi in alkaline biofilms. Increasing Bdellovibrio under alkali conditions with putrescine further aggravated the biofilm decomposition. This research shed light on the unclear relationship between exogenous putrescine, environmental pH, and pH stress adaptability of biofilm. By judiciously employing putrescine, biofilm formation could be controlled to meet the needs of engineering applications with different characteristics.IMPORTANCEThe objective of this study is to unravel the regulatory mechanism by which exogenous putrescine influences biofilm pH stress adaptability and understand the role of environmental pH in this intricate process. Our findings revealed that exogenous putrescine functioned as a switch-like distributor affecting the pH stress adaptability of biofilm-based activated sludge, which promoted energy utilization for growth and reproduction processes under acidic conditions while limiting biofilm development to conserve energy under alkaline conditions. This study not only clarified the previously ambiguous relationship between exogenous putrescine, environmental pH, and biofilm pH stress adaptability but also offered fresh insights into enhancing biofilm stability within extreme environments. Through the modulation of energy utilization, exerting control over biofilm growth and achieving more effective engineering goals could be possible.

外源腐胺对基于生物膜的活性污泥的 pH 压力适应性具有类似开关的影响。
微生物群落对 pH 值应激的适应性在生物膜形成过程中起着至关重要的作用。本研究旨在探讨外源腐胺对pH应激的调控机制,并加深对生物膜调控技术措施和分子机制的理解和应用。研究结果表明,外源腐胺可作为影响微生物pH应激的开关样分配器,从而在酸性条件下促进生物膜的形成,而在碱性条件下抑制生物膜的形成。随着 pH 值的降低,腐胺的质子化程度增加,使腐胺更容易被吸附。质子化的外源腐胺可增加细胞膜的通透性,促进其进入细胞。随后,腐胺通过增强以谷氨酸为基础的抗酸策略和γ-氨基丁酸代谢途径消耗细胞内的H+,从而减轻对细胞的酸应激。此外,腐胺还能刺激 ATP 酶的表达,从而更好地利用 H+ 跨膜运输中的能量,并增强氧化磷酸化活性。然而,在碱性条件下,腐胺质子化受到限制,细胞内 H+ 的消耗进一步加剧了碱应激,抑制了细胞的代谢活动。在酸性应激条件下,外源腐胺促进了真菌和嗜酸性细菌的比例;在碱性应激条件下,外源腐胺促进了嗜碱性细菌的比例,但对碱性生物膜中真菌的影响有限。在碱性条件下,用腐霉利增加Bdellovibrio进一步加剧了生物膜的分解。这项研究揭示了外源腐霉利、环境酸碱度和生物膜的酸碱应激适应性之间的不明确关系。本研究旨在揭示外源腐霉利影响生物膜 pH 应力适应性的调控机制,并了解环境 pH 在这一复杂过程中的作用。我们的研究结果表明,外源腐胺可作为一种类似开关的分配器,影响生物膜型活性污泥的 pH 压力适应性,在酸性条件下促进生长和繁殖过程中的能量利用,而在碱性条件下限制生物膜的发展以节约能量。这项研究不仅澄清了外源腐胺、环境 pH 值和生物膜 pH 值应激适应性之间先前模糊不清的关系,还为增强生物膜在极端环境中的稳定性提供了新的见解。通过调节能量利用,可以控制生物膜的生长,实现更有效的工程目标。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Applied and Environmental Microbiology
Applied and Environmental Microbiology 生物-生物工程与应用微生物
CiteScore
7.70
自引率
2.30%
发文量
730
审稿时长
1.9 months
期刊介绍: Applied and Environmental Microbiology (AEM) publishes papers that make significant contributions to (a) applied microbiology, including biotechnology, protein engineering, bioremediation, and food microbiology, (b) microbial ecology, including environmental, organismic, and genomic microbiology, and (c) interdisciplinary microbiology, including invertebrate microbiology, plant microbiology, aquatic microbiology, and geomicrobiology.
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