Microbial domestication and response of low C/N ammonia nitrogen wastewater treated by zonal influent micro-pressure internal circulation reactor

IF 3.7 3区 生物学 Q2 BIOTECHNOLOGY & APPLIED MICROBIOLOGY
Fan Wang, Fangyuan Zhang, Wenai Liu, Yuying Fan, Kailun Yang, Jinhao Pu, Dejun Bian
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Abstract

In this study, by distributing the influent in a micro-pressure internal circulation reactor (MPR) at a flow rate ratio of 1:2:1 to the anaerobic zone, anoxic zone, and aerobic zone, efficient denitrification of low C/N ammonia nitrogen wastewater was successfully achieved without the need for additional carbon sources or nitrified liquid reflux. Compared with the traditional treatment method of adding carbon sources, the treatment cost was reduced. By regulating the dissolved oxygen (DO) content in the growth environment of microbial flora, the nitrifying flora was first enriched, followed by the denitrifying and simultaneous nitrification-denitrification (SND) bacteria flora. During this process, the diversity of microbial populations decreased with the increase of DO concentration. The removal efficiency of COD, NH4+ -N and TN reached 95 %, 85 % and 80 % respectively. The 16S rRNA amplicon sequencing showed that the increase of dissolved oxygen during domestication promoted the proliferation of nitrifying bacteria, the relative abundance of nitrifying genes increased, while the secretion of extracellular polymers increased, and the activities of dehydrogenase activity and specific aerobic rate increased. Then, with the decrease of DO concentration, the relative abundance of nitrifying bacteria at the genus level wasn′t affected. However, the denitrifying functional bacteria increased significantly, especially the abundance of bacteria with SND functions, and the TN removal amount in the aerobic zone reached 21.24 % of the total removal amount.
分区进水微压内循环反应器处理低碳氮比氨氮废水的微生物驯化及响应
在本研究中,通过在微压内循环反应器(MPR)中以1:2:1的流量比将进水分配到厌氧区、缺氧区和好氧区,成功地实现了低C/N氨氮废水的高效反硝化,而不需要额外的碳源或硝化液回流。与传统的添加碳源的处理方法相比,降低了处理成本。通过调节微生物菌群生长环境中的溶解氧(DO)含量,首先使硝化菌群富集,其次是反硝化菌群和同时硝化-反硝化菌群。在此过程中,微生物种群的多样性随着DO浓度的增加而降低。对COD、NH4+ -N和TN的去除率分别达到95 %、85 %和80 %。16S rRNA扩增子测序结果表明,驯化过程中溶解氧的增加促进了硝化细菌的增殖,硝化基因的相对丰度增加,同时胞外聚合物的分泌增加,脱氢酶活性和特定好氧速率的活性增加。因此,随着DO浓度的降低,属水平上的硝化细菌相对丰度不受影响。但反硝化功能菌显著增加,尤其是SND功能菌丰度增加,好氧区TN去除率达到总去除率的21.24 %。
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来源期刊
Biochemical Engineering Journal
Biochemical Engineering Journal 工程技术-工程:化工
CiteScore
7.10
自引率
5.10%
发文量
380
审稿时长
34 days
期刊介绍: The Biochemical Engineering Journal aims to promote progress in the crucial chemical engineering aspects of the development of biological processes associated with everything from raw materials preparation to product recovery relevant to industries as diverse as medical/healthcare, industrial biotechnology, and environmental biotechnology. The Journal welcomes full length original research papers, short communications, and review papers* in the following research fields: Biocatalysis (enzyme or microbial) and biotransformations, including immobilized biocatalyst preparation and kinetics Biosensors and Biodevices including biofabrication and novel fuel cell development Bioseparations including scale-up and protein refolding/renaturation Environmental Bioengineering including bioconversion, bioremediation, and microbial fuel cells Bioreactor Systems including characterization, optimization and scale-up Bioresources and Biorefinery Engineering including biomass conversion, biofuels, bioenergy, and optimization Industrial Biotechnology including specialty chemicals, platform chemicals and neutraceuticals Biomaterials and Tissue Engineering including bioartificial organs, cell encapsulation, and controlled release Cell Culture Engineering (plant, animal or insect cells) including viral vectors, monoclonal antibodies, recombinant proteins, vaccines, and secondary metabolites Cell Therapies and Stem Cells including pluripotent, mesenchymal and hematopoietic stem cells; immunotherapies; tissue-specific differentiation; and cryopreservation Metabolic Engineering, Systems and Synthetic Biology including OMICS, bioinformatics, in silico biology, and metabolic flux analysis Protein Engineering including enzyme engineering and directed evolution.
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