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<front>
<journal-meta>
<journal-id journal-id-type="publisher-id">Front. Microbiol.</journal-id>
<journal-title>Frontiers in Microbiology</journal-title>
<abbrev-journal-title abbrev-type="pubmed">Front. Microbiol.</abbrev-journal-title>
<issn pub-type="epub">1664-302X</issn>
<publisher>
<publisher-name>Frontiers Media S.A.</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<article-id pub-id-type="doi">10.3389/fmicb.2021.746293</article-id>
<article-categories>
<subj-group subj-group-type="heading">
<subject>Microbiology</subject>
<subj-group>
<subject>Mini Review</subject>
</subj-group>
</subj-group>
</article-categories>
<title-group>
<article-title>Advances in Studies on Microbiota Involved in Nitrogen Removal Processes and Their Applications in Wastewater Treatment</article-title>
</title-group>
<contrib-group>
<contrib contrib-type="author">
<name>
<surname>Mai</surname>
<given-names>Wenning</given-names>
</name>
<xref rid="aff1" ref-type="aff"><sup>1</sup></xref>
<xref rid="aff2" ref-type="aff"><sup>2</sup></xref>
<xref rid="fn3" ref-type="author-notes"><sup>&#x2020;</sup></xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Chen</surname>
<given-names>Jiamin</given-names>
</name>
<xref rid="aff1" ref-type="aff"><sup>1</sup></xref>
<xref rid="aff3" ref-type="aff"><sup>3</sup></xref>
<xref rid="fn3" ref-type="author-notes"><sup>&#x2020;</sup></xref>
<uri xlink:href="https://loop.frontiersin.org/people/1440951/overview/overview"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Liu</surname>
<given-names>Hai</given-names>
</name>
<xref rid="aff4" ref-type="aff"><sup>4</sup></xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Liang</surname>
<given-names>Jiawei</given-names>
</name>
<xref rid="aff2" ref-type="aff"><sup>2</sup></xref>
<uri xlink:href="https://loop.frontiersin.org/people/1381084/overview/overview"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Tang</surname>
<given-names>Jinfeng</given-names>
</name>
<xref rid="aff5" ref-type="aff"><sup>5</sup></xref>
<uri xlink:href="https://loop.frontiersin.org/people/1226068/overview/overview"/>
</contrib>
<contrib contrib-type="author" corresp="yes">
<name>
<surname>Wei</surname>
<given-names>Yongjun</given-names>
</name>
<xref rid="aff3" ref-type="aff"><sup>3</sup></xref>
<xref rid="aff6" ref-type="aff"><sup>6</sup></xref>
<xref rid="c001" ref-type="corresp"><sup>&#x002A;</sup></xref>
<uri xlink:href="https://loop.frontiersin.org/people/685894/overview/overview"/>
</contrib>
</contrib-group>
<aff id="aff1"><sup>1</sup>
<institution>School of Ecology and Environment, Zhengzhou University</institution>, <addr-line>Zhengzhou</addr-line>, <country>China</country>
</aff>
<aff id="aff2"><sup>2</sup>
<institution>College of Public Health, Zhengzhou University</institution>, <addr-line>Zhengzhou</addr-line>, <country>China</country>
</aff>
<aff id="aff3"><sup>3</sup>
<institution>Laboratory of Synthetic Biology, Zhengzhou University</institution>, <addr-line>Zhengzhou</addr-line>, <country>China</country>
</aff>
<aff id="aff4"><sup>4</sup>
<institution>Henan Public Security Bureau</institution>, <addr-line>Zhengzhou</addr-line>, <country>China</country>
</aff>
<aff id="aff5"><sup>5</sup>
<institution>Key Laboratory for Water Quality and Conservation of Pearl River Delta, Ministry of Education, School of Environmental Science and Engineering, Link&#x00F6;ping University &#x2013; Guangzhou University Research Center on Urban Sustainable Development, Guangzhou University</institution>, <addr-line>Guangzhou</addr-line>, <country>China</country>
</aff>
<aff id="aff6"><sup>6</sup>
<institution>Key Laboratory of Advanced Drug Preparation Technologies, Ministry of Education, School of Pharmaceutical Sciences, Zhengzhou University</institution>, <addr-line>Zhengzhou</addr-line>, <country>China</country>
</aff>
<author-notes>
<fn id="fn1" fn-type="edited-by">
<p>Edited by: Tian Li, Nankai University, China</p>
</fn>
<fn id="fn2" fn-type="edited-by">
<p>Reviewed by: Chengmei Liao, Nankai University, China; Hui Wang, Xi'an University of Technology, China</p>
</fn>
<corresp id="c001">&#x002A;Correspondence: Yongjun Wei, <email>yongjunwei@zzu.edu.cn</email>
</corresp>
<fn id="fn3" fn-type="equal">
<p><sup>&#x2020;</sup>These authors have contributed equally to this work</p>
</fn>
<fn id="fn4" fn-type="other">
<p>This article was submitted to Microbiotechnology, a section of the journal Frontiers in Microbiology</p>
</fn>
</author-notes>
<pub-date pub-type="epub">
<day>28</day>
<month>09</month>
<year>2021</year>
</pub-date>
<pub-date pub-type="collection">
<year>2021</year>
</pub-date>
<volume>12</volume>
<elocation-id>746293</elocation-id>
<history>
<date date-type="received">
<day>23</day>
<month>07</month>
<year>2021</year>
</date>
<date date-type="accepted">
<day>27</day>
<month>08</month>
<year>2021</year>
</date>
</history>
<permissions>
<copyright-statement>Copyright &#x00A9; 2021 Mai, Chen, Liu, Liang, Tang and Wei.</copyright-statement>
<copyright-year>2021</copyright-year>
<copyright-holder>Mai, Chen, Liu, Liang, Tang and Wei</copyright-holder>
<license xlink:href="http://creativecommons.org/licenses/by/4.0/">
<p>This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.</p>
</license>
</permissions>
<abstract>
<p>The discharge of excess nitrogenous pollutants in rivers or other water bodies often leads to serious ecological problems and results in the collapse of aquatic ecosystems. Nitrogenous pollutants are often derived from the inefficient treatment of industrial wastewater. The biological treatment of industrial wastewater for the removal of nitrogen pollution is a green and efficient strategy. In the initial stage of the nitrogen removal process, the nitrogenous pollutants are converted to ammonia. Traditionally, nitrification and denitrification processes have been used for nitrogen removal in industrial wastewater; while currently, more efficient processes, such as simultaneous nitrification-denitrification, partial nitrification-anammox, and partial denitrification-anammox processes, are used. The microorganisms participating in nitrogen pollutant removal processes are diverse, but information about them is limited. In this review, we summarize the microbiota participating in nitrogen removal processes, their pathways, and associated functional genes. We have also discussed the design of efficient industrial wastewater treatment processes for the removal of nitrogenous pollutants and the application of microbiome engineering technology and synthetic biology strategies in the modulation of the nitrogen removal process. This review thus provides insights that would help in improving the efficiency of nitrogen pollutant removal from industrial wastewater.</p>
</abstract>
<kwd-group>
<kwd>nitrogen pollution removal</kwd>
<kwd>nitrifying bacteria</kwd>
<kwd>denitrifying bacteria</kwd>
<kwd>anammox</kwd>
<kwd>microbiome</kwd>
<kwd>wastewater</kwd>
</kwd-group>
<contract-num rid="cn1">32111530179</contract-num>
<contract-num rid="cn2">202102010401</contract-num>
<contract-sponsor id="cn1">National Natural Science Foundation of China<named-content content-type="fundref-id">10.13039/501100001809</named-content>
</contract-sponsor>
<contract-sponsor id="cn2">Science and Technology Program of Guangzhou</contract-sponsor>
<counts>
<fig-count count="1"/>
<table-count count="1"/>
<equation-count count="3"/>
<ref-count count="100"/>
<page-count count="9"/>
<word-count count="7421"/>
</counts>
</article-meta>
</front>
<body>
<sec id="sec1" sec-type="intro">
<title>Introduction</title>
<p>Industrial development improves our life quality; nevertheless, the industries, such as those producing paper and pharmaceutical products, generate large amounts of industrial wastewater (<xref ref-type="bibr" rid="ref38">Liang et al., 2021</xref>; <xref ref-type="bibr" rid="ref63">Singh et al., 2021</xref>). Nitrogen is one of the main industrial wastewater pollutants (<xref ref-type="bibr" rid="ref66">Sun et al., 2021</xref>), the spread of which pollutes the environment (<xref ref-type="bibr" rid="ref9">Chen et al., 2018</xref>), damages the ecosystem, and affects human health (<xref ref-type="bibr" rid="ref41">Liu et al., 2021</xref>). Nitrogenous pollutants in wastewater mainly comprise inorganic nitrogen and organic nitrogen (<xref ref-type="bibr" rid="ref52">Odedishemi Ajibade et al., 2021</xref>). The organic nitrogen pollutants can be catalyzed by microorganisms to form inorganic pollutants (<xref ref-type="bibr" rid="ref83">Wei et al., 2015</xref>). Thus, the primary task of wastewater treatment is the removal of inorganic nitrogen. Therefore, developing green and sustainable strategies to remove inorganic nitrogen pollutants is of great interest (<xref ref-type="bibr" rid="ref15">Deng et al., 2021</xref>).</p>
<p>Both physicochemical and biological methods are used for removing nitrogenous pollutants in wastewater. The physicochemical methods include stripping, wet oxidation technology, electrochemical technology (<xref ref-type="bibr" rid="ref47">Monfet et al., 2018</xref>), ion exchange, and adsorption methods (<xref ref-type="bibr" rid="ref48">Mook et al., 2012</xref>). While physicochemical methods require higher capital and generate solid wastes as secondary contamination, biological methods are mainly used for the efficient removal of nitrogen pollutants (<xref ref-type="bibr" rid="ref47">Monfet et al., 2018</xref>; <xref ref-type="bibr" rid="ref76">Wang et al., 2020c</xref>; <xref ref-type="bibr" rid="ref11">Chen et al., 2021b</xref>). Inorganic nitrogen pollutants are mainly available in the form of ammonia nitrogen (NH<sub>4</sub><sup>+</sup>-N), nitrite nitrogen (NO<sub>2</sub><sup>&#x2212;</sup>-N), and nitrate nitrogen (NO<sub>3</sub><sup>&#x2212;</sup>-N). Biological removal of these nitrogen pollutants in wastewater treatment plants mainly involves the process of ammonification, nitrification, denitrification, and anammox processes (<xref ref-type="bibr" rid="ref22">Guo et al., 2020</xref>; <xref ref-type="bibr" rid="ref39">Liu et al., 2020</xref>). These nitrogen removal processes convert nitrogen pollutants to several different oxidation states, and each process needs special running parameters (<xref ref-type="bibr" rid="ref55">Rahimi et al., 2020</xref>). In each process, different microorganisms function and varying metabolic reactions are involved, and the efficiency of each nitrogen removal process is divergent (<xref ref-type="bibr" rid="ref96">Zhang et al., 2021b</xref>). Hence, understanding the biological removal processes at species and molecular level is essential for the development of efficient nitrogen pollution removal strategies.</p>
<p>In this review, we aim to summarize the nitrogen removal processes and their microbiota used for the removal of nitrogen pollutants, their functional genes, metabolic pathways, and associated mechanisms. The application and optimization of nitrogen pollution removal process are systematically described, and their operating effectiveness is compared. Based on current nitrogen removal processes, we also discuss and propose the future application of these functional microorganisms and their engineering for industrial wastewater treatment <italic>via</italic> microbiota engineering and synthetic biology strategies.</p>
</sec>
<sec id="sec2">
<title>Biological Denitrification Process for Nitrogen Pollutant Removal</title>
<p>The biological nitrogen pollutant removal process mainly involves partial nitrification (PN), nitrification, denitrification, and anammox (<xref ref-type="supplementary-material" rid="SM1">Supplementary Table S1</xref> and <xref ref-type="supplementary-material" rid="SM1">Supplementary information</xref>). The microbial processes and their associated genes involved in nitrogen removal have been identified in previous studies (<xref ref-type="supplementary-material" rid="SM1">Supplementary Figure S1</xref>; <xref ref-type="bibr" rid="ref79">Wang et al., 2014</xref>; <xref ref-type="bibr" rid="ref56">Rahman et al., 2018</xref>; <xref ref-type="bibr" rid="ref35">Li et al., 2021b</xref>). The nitrification process converts ammonia nitrogen into nitrate nitrogen and involves ammonia-oxidizing bacteria (AOB) and nitrite-oxidizing bacteria (NOB). AOB and NOB are autotrophic Gram-negative aerobic bacteria that use the energy released in the nitrification process for growth. First, ammonia nitrogen is transformed into nitrite nitrogen by AOB (<xref ref-type="bibr" rid="ref46">Mehrani et al., 2020</xref>) through the PN process (<xref ref-type="bibr" rid="ref75">Wang et al., 2020a</xref>), a complex biochemical process that involves electron transfer, and generates energy and diverse intermediates (<xref ref-type="bibr" rid="ref87">Xia et al., 2019</xref>; <xref ref-type="bibr" rid="ref57">Ren et al., 2020</xref>; <xref ref-type="bibr" rid="ref54">Qian et al., 2021</xref>). The process initiates by oxidation of NH<sub>4</sub><sup>+</sup>-N to hydroxylamine (NH<sub>2</sub>OH) by ammonia monooxygenase, which is then oxidized to nitrite nitrogen by hydroxylamine oxidoreductase. The nitrite nitrogen is further transformed into nitrate nitrogen by nitrite oxidoreductase of NOB (<xref ref-type="bibr" rid="ref65">Staley et al., 2018</xref>).</p>
<p>Denitrification is an important step of the biological nitrogen cycle (<xref ref-type="bibr" rid="ref92">Zhang et al., 2019</xref>); it involves several enzymes and generates various intermediate metabolites (<xref ref-type="bibr" rid="ref57">Ren et al., 2020</xref>). Four key enzymes of nitrate reductase, nitrite reductase, nitric oxide reductase, and nitrous oxide reductase catalyze the transformation of the nitrate to nitrogen gas (<xref ref-type="bibr" rid="ref16">Ding et al., 2019</xref>). Most denitrifying bacteria, being heterotrophic facultative anaerobes, carry out the reaction under anaerobic conditions in two steps using nitrate as an electron acceptor and organic matter (organic carbon) as electron donor (<xref ref-type="bibr" rid="ref61">Semedo et al., 2018</xref>).</p>
</sec>
<sec id="sec3">
<title>The Traditional Biological Nitrogen Removal Process and Simultaneous Nitrification-Denitrification Process</title>
<p>The traditional biological nitrogen removal (BNR) process involves sequential, full-scale nitrification and denitrification reactions to transform ammonia nitrogen into nitrogen gas as: NH<sub>4</sub><sup>+</sup>&#x2192;NO<sub>2</sub><sup>&#x2212;</sup>&#x2192;NO<sub>3</sub><sup>&#x2212;</sup>&#x2192;NO<sub>2</sub><sup>&#x2212;</sup>&#x2192;N<sub>2</sub>. This process has been applied for effectively removing nitrogen pollutants from the wastewater (<xref ref-type="bibr" rid="ref29">Kornaros et al., 2010</xref>; <xref ref-type="bibr" rid="ref7">Chen et al., 2021c</xref>; <xref ref-type="bibr" rid="ref94">Zhang et al., 2021a</xref>; <xref rid="fig1" ref-type="fig">Figure 1A</xref>). Based on the BNR process, simultaneous nitrification-denitrification (SND) process has been developed, wherein, the nitrification and denitrification reactions occur synchronously in the same reactor and convert ammonia nitrogen into nitrogen gas (<xref ref-type="bibr" rid="ref77">Wang et al., 2006</xref>).</p>
<fig position="float" id="fig1">
<label>Figure 1</label>
<caption>
<p>Biological nitrogen removal processes and the microorganisms involved in these processes. <bold>(A)</bold> Traditional nitrification and denitrification processes. <bold>(B)</bold> Simultaneous nitrification-denitrification process. <bold>(C)</bold> Partial nitrification-anammox process. <bold>(D)</bold> Partial denitrification-anammox process. <bold>(E)</bold> Microbiome and synthetic biology strategy used for nitrogen pollutant removal process. The natural microbiota is used for nitrogen pollutant removal; with the help of microbiome and synthetic biology strategy, new nitrogen removal strains can be isolated and engineered strains can be constructed; and these strains can be engineered for synthetic microbiota with efficient nitrogen removal ability.</p>
</caption>
<graphic xlink:href="fmicb-12-746293-g001.tif"/>
</fig>
<p>Compared with the traditional BNR process, the SND process reduces the investment in equipment and space occupation and is thus a cost-effective process for nitrogen pollutant removal from industrial wastewater (<xref ref-type="supplementary-material" rid="SM1">Supplementary Table S2</xref>; <xref ref-type="bibr" rid="ref88">Xiang et al., 2020</xref>). The microorganisms involved in the SND process are mainly nitrifying bacteria and aerobic denitrifying bacteria (<xref rid="fig1" ref-type="fig">Figure 1B</xref>). The primary factors affecting the nitrogen removal efficiency include the carbon to nitrogen ratio (COD/N), dissolved oxygen (DO) concentration, sludge concentration, and pH (<xref ref-type="bibr" rid="ref6">Chang et al., 2019</xref>). Especially, the simultaneous nitrification-denitrification process requires the simultaneous presence of aerobic and anaerobic environments within the same reactor; hence, the DO concentration directly affects the denitrification rate and efficiency (<xref ref-type="bibr" rid="ref73">Wang et al., 2018</xref>). Moreover, the SND process had been applied for the removal of phosphorus pollutants from municipal wastewater, showing the SND process is feasible in phosphorus removal (<xref ref-type="bibr" rid="ref59">Salehi et al., 2019</xref>).</p>
<p>Due to the requirements of proper DO and COD/N, the establishment of SND process and sustaining SND process at high efficiency and a stable state for industrial wastewater treatment is difficult (<xref ref-type="bibr" rid="ref31">Lai et al., 2020</xref>). Some novel microorganisms, including aerobic denitrifying bacteria, low DO nitrifying bacteria, heterotrophic denitrifying bacteria, and some autotrophic denitrifying bacteria, have been identified and used to improve the efficiency and robustness of SND process (<xref ref-type="bibr" rid="ref74">Wang et al., 2017</xref>; <xref ref-type="bibr" rid="ref5">Carneiro Fid&#x00E9;lis Silva et al., 2019</xref>). Moreover, optimization carbon-to-nitrogen ratio, DO concentration, carrier materials, and other strategies have been used for SND startup and stable running (<xref ref-type="bibr" rid="ref17">Dobbeleers et al., 2017</xref>; <xref ref-type="bibr" rid="ref24">Iannacone et al., 2019</xref>; <xref ref-type="bibr" rid="ref58">Salcedo Moyano et al., 2021</xref>). However, the denitrification process under aerobic conditions is rarely reported, and little information about the SND microbiota is available (<xref ref-type="bibr" rid="ref40">Liu et al., 2019</xref>; <xref ref-type="bibr" rid="ref34">Li et al., 2021a</xref>). In the future, giving insights into the SND process and optimizing SND startup, including the design of proper wastewater treatment plant, dynamic microbiota of the running bioreactors, and recovering the association between functional microbiota and running performance, are necessary for industrial-scale nitrogen wastewater treatment with SND process.</p>
</sec>
<sec id="sec4">
<title>Anaerobic Ammonium Oxidation Process for Nitrogen Pollutant Removal</title>
<p>In 1995, anaerobic ammonium oxidation (Anammox)&#x2014;a revolutionary process&#x2014;was identified during a denitrification process for wastewater treatment (<xref ref-type="bibr" rid="ref49">Mulder et al., 1995</xref>). This discovery provides an understanding of the available nitrogen processing in nature and is a novel applicable process for the removal of nitrogen pollutants (<xref ref-type="bibr" rid="ref64">Speth et al., 2016</xref>). Anammox process can efficiently remove nitrogen pollutants in the wastewater containing high levels of ammonia nitrogen and low levels of organic pollutants. This process is being applied these days in hundreds of large-scale wastewater treatment plants (<xref ref-type="bibr" rid="ref2">Ali and Okabe, 2015</xref>) and can potentially treat low-strength nitrogen wastewater by optimizing reactor types and operation parameters (<xref ref-type="bibr" rid="ref37">Li et al., 2021d</xref>).</p>
</sec>
<sec id="sec5">
<title>The Anammox Process for Nitrogen Removal</title>
<p>In the anammox process, anammox bacteria directly convert ammonia nitrogen and nitrite nitrogen into nitrogen gas, using ammonia nitrogen as the electron donor and nitrite nitrogen as the electron acceptor in anaerobic environments (<xref ref-type="bibr" rid="ref8">Chen et al., 2021a</xref>). First, NO<sub>2</sub><sup>&#x2212;</sup>-N is reduced to NO, which is used as the electron acceptor of NH<sub>4</sub><sup>+</sup>-N to produce N<sub>2</sub>H<sub>4</sub>. N<sub>2</sub>H<sub>4</sub> is further oxidized to form N<sub>2</sub> (<xref ref-type="bibr" rid="ref68">van de Graaf et al., 1997</xref>). The anammox process is low cost because no energy input is needed (<xref ref-type="bibr" rid="ref90">Xu et al., 2020</xref>). The bacteria involved in the anammox process are different from those in the traditional BNR process (<xref ref-type="supplementary-material" rid="SM1">Supplementary Table S2</xref>; <xref ref-type="bibr" rid="ref100">Zhu et al., 2008</xref>; <xref ref-type="bibr" rid="ref84">Wen et al., 2020</xref>).</p>
<p>The anammox process requires NO<sub>2</sub><sup>&#x2212;</sup> as an electron acceptor, but the wastewater often contains NH<sub>4</sub><sup>+</sup> and no NO<sub>2</sub><sup>&#x2212;</sup>. This NO<sub>2</sub><sup>&#x2212;</sup> can be provided by the PN process for initiation and continuation of the anammox process (<xref ref-type="bibr" rid="ref10">Chen et al., 2020</xref>). The partial nitrification-anammox (PN/A) process is a short biological denitrification method that can achieve high efficiency of denitrification at a proper temperature, DO concentration, hydraulic retention time, and pH (<xref ref-type="bibr" rid="ref67">Val Del Rio et al., 2019</xref>; <xref ref-type="bibr" rid="ref92">Zhang et al., 2019</xref>) with the help of AOB and anammox bacteria (<xref ref-type="bibr" rid="ref43">Lv et al., 2011</xref>; <xref rid="fig1" ref-type="fig">Figure 1C</xref>). This process can efficiently remove nitrogen pollutants without adding organic carbon sources and controlling wastewater COD concentration (<xref ref-type="bibr" rid="ref62">Sheng et al., 2020</xref>).</p>
<p>The PN/A process can save about 50% oxygen with low sludge generation, and no release of CO<sub>2</sub> into the air (<xref ref-type="bibr" rid="ref23">Huang et al., 2020</xref>). According to the available estimates, the PN/A process can save more than 90% of the operating cost (<xref ref-type="bibr" rid="ref98">Zhao et al., 2021</xref>). However, the low growth rate of anammox bacteria, the low robustness of anammox bacteria to environmental changes, and the nitrogen removal rate limited the application of anammox for nitrogen pollutant removal (<xref ref-type="bibr" rid="ref85">Weralupitiya et al., 2021</xref>; <xref ref-type="bibr" rid="ref69">Wang et al., 2021c</xref>). The quorum sensing strategy had been proposed for improving functions of the PN/A process, which might enhance nitrogen removal efficiency through PN/A process in the future (<xref ref-type="bibr" rid="ref98">Zhao et al., 2021</xref>).</p>
</sec>
<sec id="sec6">
<title>The Partial Denitrification Process Used for Nitrogen Removal</title>
<p>Partial denitrification (PDN) stops the reduction of Nitrite nitrogen to nitrogen and is considered to be an alternative process for providing nitrite to anammox bacteria (<xref ref-type="bibr" rid="ref21">Fu et al., 2019</xref>; <xref ref-type="bibr" rid="ref12">Cui et al., 2020</xref>). By treating wastewater with high-level nitrate nitrogen and low-level ammonia nitrogen, the PDN-anammox (PDN/A) process can reduce organic carbon source input and generate less sludge (<xref ref-type="bibr" rid="ref97">Zhang et al., 2020</xref>). The microorganisms mainly functioned in the PDN process are partial denitrifying bacteria and anammox bacteria, including <italic>Acidovorax facilis</italic>, <italic>Citrobacter diversus</italic>, and some <italic>Thauera</italic> species (<xref rid="fig1" ref-type="fig">Figure 1D</xref>; <xref ref-type="bibr" rid="ref72">Wang et al., 2020d</xref>).</p>
<p>AOB and anammox bacteria (AnAOB) are the primary functional microorganisms in the PN process and anaerobic ammonia oxidation, and they are also essential for autotrophic denitrification (<xref ref-type="bibr" rid="ref86">Wu et al., 2019</xref>). However, the PN/A process can produce more than 11% nitrate nitrogen using one-stage or two-stage PN/A processes, which needs to be processed further (<xref ref-type="bibr" rid="ref36">Li et al., 2020b</xref>). The combination of denitrification PN, and anammox processes (DN-PN/A) in a self-circulating integrated plant is a promising and efficient process to remove nitrogen pollutants from wastewater (<xref ref-type="bibr" rid="ref91">Yan et al., 2020</xref>). The primary microorganisms involved in the process are AOB, AnAOB, and denitrifying bacteria (<xref ref-type="bibr" rid="ref18">Du et al., 2021</xref>), and the reactions involved in the DN-PN/A process are as:<disp-formula id="E1">
<mml:math id="M1">
<mml:mtable columnalign="left">
<mml:mtr>
<mml:mtd>
<mml:mi mathvariant="normal">Partial nitrification</mml:mi>
<mml:mo>:</mml:mo>
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</mml:mtr>
<mml:mtr>
<mml:mtd>
<mml:msub>
<mml:mi mathvariant="normal">NH</mml:mi>
<mml:mn>4</mml:mn>
</mml:msub>
<mml:msup>
<mml:mrow>
</mml:mrow>
<mml:mo>+</mml:mo>
</mml:msup>
<mml:mo>+</mml:mo>
<mml:mn>1.5</mml:mn>
<mml:mspace width="thickmathspace"/>
<mml:msub>
<mml:mi mathvariant="normal">O</mml:mi>
<mml:mn>2</mml:mn>
</mml:msub>
<mml:mo>&#x2192;</mml:mo>
<mml:msub>
<mml:mi mathvariant="normal">NO</mml:mi>
<mml:mn>2</mml:mn>
</mml:msub>
<mml:msup>
<mml:mrow>
</mml:mrow>
<mml:mo>&#x2212;</mml:mo>
</mml:msup>
<mml:mo>+</mml:mo>
<mml:msup>
<mml:mi mathvariant="normal">2H</mml:mi>
<mml:mo>+</mml:mo>
</mml:msup>
<mml:mo>+</mml:mo>
<mml:msub>
<mml:mi mathvariant="normal">H</mml:mi>
<mml:mn>2</mml:mn>
</mml:msub>
<mml:mi mathvariant="normal">O</mml:mi>
</mml:mtd>
</mml:mtr>
</mml:mtable>
</mml:math>
<label>(1)</label>
</disp-formula>
<disp-formula id="E2">
<mml:math id="M2">
<mml:mtable columnalign="left">
<mml:mtr>
<mml:mtd>
<mml:mi mathvariant="normal">Anammox</mml:mi>
<mml:mo>:</mml:mo>
</mml:mtd>
</mml:mtr>
<mml:mtr>
<mml:mtd>
<mml:msub>
<mml:mi mathvariant="normal">NH</mml:mi>
<mml:mn>4</mml:mn>
</mml:msub>
<mml:msup>
<mml:mrow>
</mml:mrow>
<mml:mo>+</mml:mo>
</mml:msup>
<mml:mo>+</mml:mo>
<mml:mn>1.32</mml:mn>
<mml:mspace width="thickmathspace"/>
<mml:msub>
<mml:mi mathvariant="normal">NO</mml:mi>
<mml:mn>2</mml:mn>
</mml:msub>
<mml:msup>
<mml:mrow>
</mml:mrow>
<mml:mo>&#x2212;</mml:mo>
</mml:msup>
<mml:mo>&#x2192;</mml:mo>
<mml:mn>1.02</mml:mn>
<mml:mi mathvariant="normal">
</mml:mi>
<mml:msub>
<mml:mi mathvariant="normal">N</mml:mi>
<mml:mn>2</mml:mn>
</mml:msub>
<mml:mo>+</mml:mo>
<mml:mn>0.26</mml:mn>
<mml:msub>
<mml:mi mathvariant="normal">NO</mml:mi>
<mml:mn>3</mml:mn>
</mml:msub>
<mml:msup>
<mml:mrow>
</mml:mrow>
<mml:mo>&#x2212;</mml:mo>
</mml:msup>
<mml:mo>+</mml:mo>
<mml:mn>2.03</mml:mn>
<mml:msub>
<mml:mi mathvariant="normal">H</mml:mi>
<mml:mn>2</mml:mn>
</mml:msub>
<mml:mi mathvariant="normal">O</mml:mi>
</mml:mtd>
</mml:mtr>
</mml:mtable>
</mml:math>
<label>(2)</label>
</disp-formula>
<disp-formula id="E3">
<mml:math id="M3">
<mml:mtable columnalign="left">
<mml:mtr>
<mml:mtd>
<mml:mi mathvariant="normal">Denitrification reaction</mml:mi>
<mml:mo>:</mml:mo>
</mml:mtd>
</mml:mtr>
<mml:mtr>
<mml:mtd>
<mml:msub>
<mml:mi mathvariant="normal">8NO</mml:mi>
<mml:mn>3</mml:mn>
</mml:msub>
<mml:msup>
<mml:mrow>
</mml:mrow>
<mml:mo>&#x2212;</mml:mo>
</mml:msup>
<mml:mo>+</mml:mo>
<mml:msub>
<mml:mi mathvariant="normal">5CH</mml:mi>
<mml:mn>3</mml:mn>
</mml:msub>
<mml:mi mathvariant="normal">COOH</mml:mi>
<mml:mo>&#x2192;</mml:mo>
<mml:mn>10</mml:mn>
<mml:msub>
<mml:mi mathvariant="normal">CO</mml:mi>
<mml:mn>2</mml:mn>
</mml:msub>
<mml:mo>+</mml:mo>
<mml:mn>4</mml:mn>
<mml:mi mathvariant="normal">
</mml:mi>
<mml:msub>
<mml:mi mathvariant="normal">N</mml:mi>
<mml:mn>2</mml:mn>
</mml:msub>
<mml:mo>+</mml:mo>
<mml:msup>
<mml:mi mathvariant="normal">8OH</mml:mi>
<mml:mo>&#x2212;</mml:mo>
</mml:msup>
<mml:mo>+</mml:mo>
<mml:mn>6</mml:mn>
<mml:msub>
<mml:mi mathvariant="normal">H</mml:mi>
<mml:mn>2</mml:mn>
</mml:msub>
<mml:mi mathvariant="normal">O</mml:mi>
</mml:mtd>
</mml:mtr>
</mml:mtable>
</mml:math>
<label>(3)</label>
</disp-formula>
</p>
<p>In principle, the DN-PN/A process can remove 100% of ammonia nitrogen, but it is difficult to create a balance between the growth of heterotrophic microorganisms and autotrophic microorganisms (AOB, AnAOB, and other microorganisms) in one integrated reactor (<xref ref-type="bibr" rid="ref44">Ma et al., 2020</xref>). Thus, research needs to be conducted to develop or engineer optimized DN-PN/A microbiota (<xref ref-type="bibr" rid="ref25">Jiang et al., 2021</xref>).</p>
</sec>
<sec id="sec7">
<title>Industrial Application of BNR for Wastewater Treatment</title>
<p>The traditional biological denitrification process is based on three reactions, including ammonification, nitrification, and denitrification, and the associated microorganisms can be accumulated as activated sludge (<xref ref-type="supplementary-material" rid="SM1">Supplementary Figure S2</xref>). The ammoniation reaction takes place in the aeration tank and can remove organic carbon and transfer organic nitrogen to NH<sub>4</sub><sup>+</sup>-N (<xref ref-type="supplementary-material" rid="SM1">Supplementary Table S1</xref>). After precipitation, the effluent from the ammoniation process enters the nitrification tank where NH<sub>4</sub><sup>+</sup>-N is converted to NO<sub>3</sub><sup>&#x2212;</sup>-N. The nitrification reaction requires an acid to decrease the pH of the reactor. The NO<sub>3</sub><sup>&#x2212;</sup>-N is reduced to N<sub>2</sub> in the denitrification process, which requires organic carbon sources, such as methanol and glucose. In practice, original wastewater containing organic carbon is mixed with the nitrification effluent (<xref ref-type="bibr" rid="ref19">Fal&#x00E5;s et al., 2016</xref>).</p>
<p>In addition to the described processes, the anaerobic-aerobic process (A/O) or recurring denitrification process is also used for removing nitrogen pollutants. The A/O process can efficiently use original organic compounds in wastewater, reduce air input, and in the process, the intermediate tank and reflux system are removed (<xref ref-type="bibr" rid="ref93">Zhang et al., 2013</xref>). The A/O process significantly reduces construction and operation costs. Based on the A/O process, the anaerobic/anoxic/aerobic (A<sup>2</sup>/O) process is optimized to carry out the denitrification and dephosphorization processes, which can be synchronously in one reactor, and simultaneously remove the phosphorus, showing that traditional biological wastewater treatment strategy is efficient and cost-friendly (<xref ref-type="bibr" rid="ref53">Park et al., 2021</xref>).</p>
<p>To conduct operations for nitrogen removal, the microbiota of the nitrogen removal processes is examined. <italic>Nitrospira</italic>, <italic>Thauera</italic>, <italic>Dechloromonas</italic>, and <italic>Ignavibacterium</italic> are the most abundant microbial genera in the A<sup>2</sup>/O sludge (<xref ref-type="bibr" rid="ref28">Kim et al., 2013</xref>; <xref ref-type="bibr" rid="ref89">Xiang et al., 2021</xref>). Further, <italic>Nitrosomonas</italic>, <italic>Nitrospira</italic>, and <italic>Nitrobacter</italic> have been identified as the key taxa for nitrite oxidation (<xref ref-type="bibr" rid="ref71">Wang et al., 2019</xref>; <xref ref-type="bibr" rid="ref32">Li et al., 2020a</xref>; <xref ref-type="bibr" rid="ref20">Feng et al., 2021</xref>; <xref ref-type="bibr" rid="ref99">Zhou et al., 2021</xref>), and <italic>Truepera, Paracoccus</italic>, and <italic>Denitratisoma</italic> were found to primarily carry out denitrification (<xref ref-type="bibr" rid="ref71">Wang et al., 2019</xref>; <xref ref-type="bibr" rid="ref14">Deng et al., 2020</xref>; <xref ref-type="bibr" rid="ref32">Li et al., 2020a</xref>; <xref ref-type="bibr" rid="ref80">Wang et al., 2020b</xref>). Recently, the autotrophic nitrogen removal systems, including PN, anammox, and the PN/A processes in two bioreactors or in a single bioreactor, were used as cost-effective ways to treat NH<sub>4</sub><sup>+</sup> rich wastewater (<xref ref-type="bibr" rid="ref13">Dehestaniathar et al., 2021</xref>).</p>
<p>The anammox process for industrial wastewater treatment was developed in China more than a decade ago (<xref ref-type="bibr" rid="ref50">Ni et al., 2010</xref>). For synthetic wastewater treatment, the primary functional anammox microbes were identified to be <italic>Nitrosomonas</italic>, <italic>Stuttgartiensis</italic>, and <italic>Candidatus Kuenenia</italic> (<xref ref-type="bibr" rid="ref93">Zhang et al., 2013</xref>). The anammox process has also been used for the treatment of vitamin B<sub>2</sub> production wastewater, and <italic>Ca. Kuenenia</italic> and <italic>Nanaocystis</italic> were found to be the main functional microorganisms (<xref rid="tab1" ref-type="table">Table 1</xref>; <xref ref-type="bibr" rid="ref45">Mai et al., 2020</xref>). Besides, new anammox bacterial species and sulfate-dependent anammox bacteria, such as <italic>Anammoxoglobus sulfate</italic> (<xref ref-type="bibr" rid="ref42">Liu et al., 2008</xref>) and <italic>Bacillus benzoevorans</italic> (<xref ref-type="bibr" rid="ref4">Cai et al., 2010</xref>), were found to assist in removing ammonium and sulfate simultaneously during wastewater treatment (<xref ref-type="bibr" rid="ref51">Nie et al., 2021</xref>). Currently, with the aid of molecular techniques, at least five genera of anammox bacterial have been identified, including <italic>Ca. Brocadia</italic> (<xref ref-type="bibr" rid="ref26">Kartal et al., 2008</xref>), <italic>Ca. Kuenenia</italic> (<xref ref-type="bibr" rid="ref60">Schmid et al., 2000</xref>), <italic>Ca. Scalindua</italic> (<xref ref-type="bibr" rid="ref3">Ali et al., 2020</xref>), <italic>Ca. Anammoxoglobus</italic> (<xref ref-type="bibr" rid="ref27">Kartal et al., 2007</xref>), and <italic>Ca. Jettenia asiatica</italic> (<xref ref-type="bibr" rid="ref1">Ali et al., 2013</xref>). However, no pure culture of these anammox has been obtained yet. In the future, culturomics may contribute to the isolation of anammox bacteria and help unravel nitrogen metabolic pathways of anammox (<xref ref-type="bibr" rid="ref30">Lagier et al., 2018</xref>).</p>
<table-wrap position="float" id="tab1">
<label>Table 1</label>
<caption>
<p>Biological nitrogen removal processes for different wastewater types.</p>
</caption>
<table frame="hsides" rules="groups">
<thead>
<tr>
<th align="center" valign="top">Wastewater types</th>
<th align="center" valign="top">Main process</th>
<th align="center" valign="top">Nitrogen removal microorganisms in the microbiota</th>
<th align="center" valign="top">References</th>
</tr>
</thead>
<tbody>
<tr>
<td align="left" valign="middle">Domestic wastewater</td>
<td align="left" valign="middle">anaerobic/anoxic/aerobic (A<sup>2</sup>/O)</td>
<td align="left" valign="middle">
<italic>Dechloromonas; Nitrospira; Arcobacter; Dokdonella</italic>
</td>
<td align="left" valign="middle">
<xref ref-type="bibr" rid="ref89">Xiang et al., 2021</xref>
</td>
</tr>
<tr>
<td align="left" valign="middle">Campus wastewater</td>
<td align="left" valign="middle">Synchronous nitration denitrification (SND)</td>
<td align="left" valign="middle">
<italic>Nitrospira; Thermomicrobia; Denitratisoma; Rhodocyclaceae</italic>
</td>
<td align="left" valign="middle">
<xref ref-type="bibr" rid="ref88">Xiang et al., 2020</xref>
</td>
</tr>
<tr>
<td align="left" valign="middle">Synthetic wastewater</td>
<td align="left" valign="middle">Anammox</td>
<td align="left" valign="middle">
<italic>Candidatus</italic> Scalindua; <italic>Actinomarinales</italic>
</td>
<td align="left" valign="middle">
<xref ref-type="bibr" rid="ref93">Zhang et al., 2013</xref>
</td>
</tr>
<tr>
<td align="left" valign="middle">Sewage</td>
<td align="left" valign="middle">Partial denitrification-anammox (PDN/A)</td>
<td align="left" valign="middle">
<italic>Thauera; Candidatus Brocadia</italic>
</td>
<td align="left" valign="middle">
<xref ref-type="bibr" rid="ref80">Wang et al., 2020b</xref>
</td>
</tr>
<tr>
<td align="left" valign="middle">Landfill leachate</td>
<td align="left" valign="middle">Partial nitrification-denitrification (PND)</td>
<td align="left" valign="middle">
<italic>Nitrosomonas; Nitrospira; Ottowia; Pseudomonas; Thermomonas; Thiobacillus; Paracoccus; Thauera; Arenimonas</italic>
</td>
<td align="left" valign="middle">
<xref ref-type="bibr" rid="ref32">Li et al., 2020a</xref>
</td>
</tr>
<tr>
<td align="left" valign="middle">Mature landfill leachate</td>
<td align="left" valign="middle">Simultaneous partial nitrification, anammox and denitrification (SNAD)</td>
<td align="left" valign="middle">
<italic>Nitrosomonas; Chloroflexi; Ignavibacteria; Candidatus Brocadia; Candidatus Jettenia</italic>
</td>
<td align="left" valign="middle">
<xref ref-type="bibr" rid="ref71">Wang et al., 2019</xref>
</td>
</tr>
<tr>
<td align="left" valign="middle">Municipal wastewater</td>
<td align="left" valign="middle">Partial nitrification-simultaneous anammox and denitrification (PN-SAD)</td>
<td align="left" valign="middle">
<italic>Limnobacter; Ignavibacter; Thauera; Denitration; Candidatus Brocadia</italic>
</td>
<td align="left" valign="middle">
<xref ref-type="bibr" rid="ref14">Deng et al., 2020</xref>
</td>
</tr>
<tr>
<td align="left" valign="middle">Piggery wastewater</td>
<td align="left" valign="middle">Heterotrophic nitrification-anammox</td>
<td align="left" valign="middle">
<italic>Candidatus Kuenenia; Planctomyces; Pirellula; Hyphomicrobium; Rhodobacter; Ignavibacterium</italic>
</td>
<td align="left" valign="middle">
<xref ref-type="bibr" rid="ref99">Zhou et al., 2021</xref>
</td>
</tr>
<tr>
<td align="left" valign="middle">Vitamin B<sub>2</sub> production wastewater</td>
<td align="left" valign="middle">Anammox</td>
<td align="left" valign="middle">
<italic>Candidatus Kuenenia; Nanaocystis</italic>
</td>
<td align="left" valign="middle">
<xref ref-type="bibr" rid="ref45">Mai et al., 2020</xref>
</td>
</tr>
<tr>
<td align="left" valign="middle">Domestic sewage</td>
<td align="left" valign="middle">Anaerobic/Aerobic/Anoxic/Aerobic process (AOAO)</td>
<td align="left" valign="middle">
<italic>Dechloromonas; Candidatus Competibacter</italic>; <italic>Nitrospira; Nitrosomonas</italic>
</td>
<td align="left" valign="middle">
<xref ref-type="bibr" rid="ref20">Feng et al., 2021</xref>
</td>
</tr>
</tbody>
</table>
</table-wrap>
</sec>
<sec id="sec8">
<title>The Application of Microbiome and Synthetic Biology for Nitrogen Removal</title>
<p>High-throughput sequencing techniques, metagenomics, and other microbiome strategies are being applied to analyze microbiota with the ability to remove nitrogen pollutants (<xref ref-type="bibr" rid="ref89">Xiang et al., 2021</xref>). There is a great diversity in the dominant microorganisms functioned in different nitrogen pollutant removal processes. Nevertheless, most microorganisms are assigned to the phyla of Proteobacteria, Bacteroidetes, Nitrospirae, and Chloroflexiphyla (<xref rid="tab1" ref-type="table">Table 1</xref>), and some bacteria in the ammonification, nitrification, and denitrification processes have already been isolated (<xref rid="tab1" ref-type="table">Table 1</xref>). Although several anammox bacteria have been identified using molecular techniques, no pure culture of the anammox bacteria has yet been obtained (<xref rid="tab1" ref-type="table">Table 1</xref>; <xref ref-type="bibr" rid="ref95">Zhang and Okabe, 2020</xref>).</p>
<p>In the future, microbiome strategies can be used to discover anammox genomes and the functional genes in the PN/A microbiota and other microbiota. Based on metabolic information inferred from the microbiome data, a proper medium can be designed for the isolation or enrichment of anammox bacteria (<xref ref-type="bibr" rid="ref82">Wei et al., 2020</xref>). Besides, the functional genes and pathways discovered in the microorganisms that can remove nitrogen pollutants can be expressed in the model organisms, such as <italic>Escherichia coli</italic> (<xref ref-type="bibr" rid="ref70">Wang et al., 2021a</xref>), <italic>Clostridium perfringens</italic> (<xref ref-type="bibr" rid="ref81">Wang et al., 2011</xref>), <italic>Klebsiella pneumoniae</italic> (<xref ref-type="bibr" rid="ref78">Wang et al., 2021b</xref>), and others (<xref ref-type="bibr" rid="ref76">Wang et al., 2020c</xref>), to build genetically engineered strains for nitrogen pollutant removal (<xref rid="fig1" ref-type="fig">Figure 1E</xref>). These isolated strains, engineered strains, and enriched microbiota can be used for the construction of a series of synthetic microbiota with nitrogen removal ability, as well as those that can accomplish different nitrogen removal processes (<xref ref-type="bibr" rid="ref25">Jiang et al., 2021</xref>; <xref ref-type="bibr" rid="ref33">Li et al., 2021c</xref>). Based on the nitrogen pollutant types and concentration, proper synthetic microbiota can be selected and developed for nitrogen pollutant removal (<xref rid="fig1" ref-type="fig">Figure 1E</xref>).</p>
</sec>
<sec id="sec9">
<title>Perspectives</title>
<p>In this review, current biological denitrification processes and associated functional microorganisms have been summarized. The advantages and limitations of current mainstream denitrification processes in wastewater treatment have also been reviewed, and PN/A, PDN/A, DN-PN/A, and other anammox processes might be the main nitrogen removal strategies in the next few years. In order to enhance nitrogen removal efficiency, proposing novel integrated process for nitrogen removal and giving insight into the molecular mechanisms of each nitrogen removal process are essential for nitrogen pollutant removal in the industrial-scale wastewater. Moreover, some primary nitrogen pollutant removal bacteria have not yet been cultured in the laboratory, and microbiome should be implemented for the recovery of microorganisms functioned in the nitrogen pollutant removal process. In the future, synthetic biology strategies would help construct/synthesize microbiota for the efficient treatment of nitrogen pollutants in wastewater based on the nitrogen removal isolates and engineered microbial strains.</p>
</sec>
<sec id="sec10">
<title>Author Contributions</title>
<p>YW conceived the study. JC, YW, WM, JT, HL, and JL drafted the manuscript. JC and YW prepared the figures. HL and JT revised the manuscript. All the authors read, revised, and approved the manuscript.</p>
</sec>
<sec id="sec11" sec-type="funding-information">
<title>Funding</title>
<p>This work was supported by the National Natural Science Foundation of China (no. 32111530179), and the Science and Technology Program of Guangzhou, China (no. 202102010401).</p>
</sec>
<sec id="conf1" sec-type="coi">
<title>Conflict of Interest</title>
<p>The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.</p>
</sec>
<sec id="sec12" sec-type="disclaimer">
<title>Publisher&#x2019;s Note</title>
<p>All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article, or claim that may be made by its manufacturer, is not guaranteed or endorsed by the publisher.</p>
</sec>
</body>
<back>
<ack>
<p>We would like to thank TopEdit (<ext-link xlink:href="http://www.topeditsci.com" ext-link-type="uri">www.topeditsci.com</ext-link>) for the English language editing of this manuscript.</p>
</ack>
<sec id="sec13" sec-type="supplementary-material">
<title>Supplementary Material</title>
<p>The Supplementary Material for this article can be found online at: <ext-link xlink:href="https://www.frontiersin.org/articles/10.3389/fmicb.2021.746293/full#supplementary-material" ext-link-type="uri">https://www.frontiersin.org/articles/10.3389/fmicb.2021.746293/full#supplementary-material</ext-link></p>
<supplementary-material xlink:href="Data_Sheet_1.doc" id="SM1" mimetype="application/msword" xmlns:xlink="http://www.w3.org/1999/xlink"/>
</sec>
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