Re-discussing the synergistic mechanisms in dual metabolism of microalgae and N-cycling bacteria on joint N removal

IF 13.2 1区 工程技术 Q1 ENGINEERING, CHEMICAL Chemical Engineering Journal Pub Date : 2025-02-04 DOI:10.1016/j.cej.2025.160276
Xue Li, Xi Chen, Yuhao Chu, Nanqi Ren, Jo-Shu Chang, Shih-Hsin Ho
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Abstract

Nitrogen (N) removal in microalgal-bacterial system (MBS) depends on the dual metabolism of microalgae and N-cycling bacteria. However, the effect of specific synergistic mechanisms involved in the dual metabolism on N removal remains unclear. Here, N removal performance, community compositions, N-cycling related metabolism, and biosynthesis and transport of cofactors were explored to clarify the synergistic mechanism between microalgae and N-cycling bacteria. Results indicated that microalgae hindered the N removal capability of dissimilatory nitrate reducing (DNR) bacteria, denitrifying bacteria, nitrifying bacteria, and assimilating bacteria by suppressing the electron transport chain of N-cycling bacteria. Fortunately, although the N removal ability of N-cycling bacteria decreased, the N-cycling bacterial community collaborative mode among multiple N-cycling pathways could drive microalgal growth and assimilation via providing the essential vitamins B1, B2, and B7, thus enhancing the synergistic effects of microalgae and N-cycling bacteria on N removal. Compared with the control, the removal efficiencies of TN and NH4+-N in MBS increased by 6.64-fold and 7.46-fold. Meanwhile, microalgal growth and chlorophyll a increased by 1.53-fold and 1.52-fold in MBS. But, the NO3-N removal efficiency decreased by 0.94-fold in MBS, the abundance of denitrifying bacteria was higher than DNR bacteria in MBS, suggesting that NO3-N removal capacity in MBS was predominantly associated with denitrifying bacteria, while microalgae exhibit a tendency to prefer absorbing NH4+-N rather than NO3-N. Together, this work improves our understanding of N removal mechanisms in MBS and provides valuable insights for the effective design and operation of MBS in real wastewater.

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再论微藻和氮循环细菌双重代谢对共同去除氮的协同机制
微藻-细菌系统(MBS)的脱氮依赖于微藻和氮循环细菌的双重代谢。然而,双重代谢所涉及的特定协同机制对氮去除的影响尚不清楚。本文通过对微藻脱氮性能、群落组成、氮循环相关代谢以及辅因子的生物合成和转运等方面的研究,阐明微藻与氮循环细菌的协同作用机制。结果表明,微藻通过抑制氮循环菌的电子传递链,抑制了异同化硝酸还原菌(DNR)、反硝化菌、硝化菌和同化菌的脱氮能力。幸运的是,虽然N循环细菌的N去除能力下降,但N循环细菌群落在多个N循环途径之间的协同模式可以通过提供必需维生素B1、B2和B7来驱动微藻的生长和同化,从而增强微藻和N循环细菌对N去除的协同效应。与对照相比,MBS对TN和NH4+-N的去除率分别提高了6.64倍和7.46倍。同时,微藻生长和叶绿素a分别提高了1.53倍和1.52倍。但MBS对NO3——N的去除效率降低了0.94倍,反硝化细菌的丰度高于DNR细菌,说明MBS对NO3——N的去除能力主要与反硝化细菌有关,而微藻则倾向于吸收NH4+-N而不是NO3——N。总之,这项工作提高了我们对MBS中N去除机制的理解,并为MBS在实际废水中的有效设计和运行提供了有价值的见解。
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来源期刊
Chemical Engineering Journal
Chemical Engineering Journal 工程技术-工程:化工
CiteScore
21.70
自引率
9.30%
发文量
6781
审稿时长
2.4 months
期刊介绍: The Chemical Engineering Journal is an international research journal that invites contributions of original and novel fundamental research. It aims to provide an international platform for presenting original fundamental research, interpretative reviews, and discussions on new developments in chemical engineering. The journal welcomes papers that describe novel theory and its practical application, as well as those that demonstrate the transfer of techniques from other disciplines. It also welcomes reports on carefully conducted experimental work that is soundly interpreted. The main focus of the journal is on original and rigorous research results that have broad significance. The Catalysis section within the Chemical Engineering Journal focuses specifically on Experimental and Theoretical studies in the fields of heterogeneous catalysis, molecular catalysis, and biocatalysis. These studies have industrial impact on various sectors such as chemicals, energy, materials, foods, healthcare, and environmental protection.
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