Anaerobic oxidation of ammonium and short-chain gaseous alkanes coupled to nitrate reduction by a bacterial consortium

Mengxiong Wu, Xiawei Liu, J Pamela Engelberts, Gene W Tyson, Simon J McIlroy, Jianhua Guo
{"title":"Anaerobic oxidation of ammonium and short-chain gaseous alkanes coupled to nitrate reduction by a bacterial consortium","authors":"Mengxiong Wu, Xiawei Liu, J Pamela Engelberts, Gene W Tyson, Simon J McIlroy, Jianhua Guo","doi":"10.1093/ismejo/wrae063","DOIUrl":null,"url":null,"abstract":"The bacterial species ‘Candidatus Alkanivorans nitratireducens’ was recently demonstrated to mediate nitrate-dependent anaerobic oxidation of short-chain gaseous alkanes (SCGAs). In previous bioreactor enrichment studies1,2, the species appeared to reduce nitrate in two phases, switching from denitrification to dissimilatory nitrate reduction to ammonium (DNRA) in response to nitrite accumulation. The regulation of this switch or the nature of potential syntrophic partnerships with other microorganisms remains unclear. Here, we describe anaerobic multispecies cultures of bacteria which couple the oxidation of propane and butane to nitrate reduction and the oxidation of ammonium (anammox). Batch tests with 15N-isotope labelling and multi-omic analyses collectively supported a syntrophic partnership between ‘Ca. A. nitratireducens’ and anammox bacteria, with the former species mediating nitrate-driven oxidation of SCGAs, supplying the latter with nitrite for the oxidation of ammonium. The elimination of nitrite accumulation by the anammox substantially increased SCGA and nitrate consumption rates, whereas suppressing DNRA. Removing ammonium supply led to its eventual production, the accumulation of nitrite, and the upregulation of DNRA gene expression for the abundant ‘Ca. A. nitratireducens’. Increasing the supply of SCGA had a similar effect in promoting DNRA. Our results suggest that ‘Ca. A. nitratireducens’ switches to DNRA to alleviate oxidative stress caused by nitrite accumulation, giving further insight into adaptability and ecology of this microorganism. Our findings also have important implications for the understanding of the fate of nitrogen and SCGAs in anaerobic environments.","PeriodicalId":516554,"journal":{"name":"The ISME Journal","volume":null,"pages":null},"PeriodicalIF":0.0000,"publicationDate":"2024-04-16","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"The ISME Journal","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1093/ismejo/wrae063","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

Abstract

The bacterial species ‘Candidatus Alkanivorans nitratireducens’ was recently demonstrated to mediate nitrate-dependent anaerobic oxidation of short-chain gaseous alkanes (SCGAs). In previous bioreactor enrichment studies1,2, the species appeared to reduce nitrate in two phases, switching from denitrification to dissimilatory nitrate reduction to ammonium (DNRA) in response to nitrite accumulation. The regulation of this switch or the nature of potential syntrophic partnerships with other microorganisms remains unclear. Here, we describe anaerobic multispecies cultures of bacteria which couple the oxidation of propane and butane to nitrate reduction and the oxidation of ammonium (anammox). Batch tests with 15N-isotope labelling and multi-omic analyses collectively supported a syntrophic partnership between ‘Ca. A. nitratireducens’ and anammox bacteria, with the former species mediating nitrate-driven oxidation of SCGAs, supplying the latter with nitrite for the oxidation of ammonium. The elimination of nitrite accumulation by the anammox substantially increased SCGA and nitrate consumption rates, whereas suppressing DNRA. Removing ammonium supply led to its eventual production, the accumulation of nitrite, and the upregulation of DNRA gene expression for the abundant ‘Ca. A. nitratireducens’. Increasing the supply of SCGA had a similar effect in promoting DNRA. Our results suggest that ‘Ca. A. nitratireducens’ switches to DNRA to alleviate oxidative stress caused by nitrite accumulation, giving further insight into adaptability and ecology of this microorganism. Our findings also have important implications for the understanding of the fate of nitrogen and SCGAs in anaerobic environments.
查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
氨和短链气态烷烃的厌氧氧化与细菌联合体的硝酸盐还原相结合
最近证明,"Candidatus Alkanivorans nitratireducens "细菌能介导依赖硝酸盐的短链气态烷烃(SCGAs)厌氧氧化。在之前的生物反应器富集研究1,2 中,该物种似乎分两个阶段还原硝酸盐,在亚硝酸盐积累时从反硝化作用转换为异氨硝酸盐还原(DNRA)。这种转换的调控或与其他微生物潜在的合成营养伙伴关系的性质仍不清楚。在这里,我们描述了将丙烷和丁烷氧化与硝酸盐还原和氨氧化(anammox)结合起来的厌氧多物种细菌培养物。利用 15N 同位素标记和多组份分析进行的批量试验共同支持了 "Ca.A. nitratireducens "和 "Ca.A. nitratireducens "之间的合成营养伙伴关系。A.nitratireducens "和 anammox 细菌之间的综合营养伙伴关系,前者介导硝酸盐驱动的 SCGAs 氧化,为后者提供亚硝酸盐用于铵的氧化。厌氧菌消除亚硝酸盐的积累,大大提高了 SCGA 和硝酸盐的消耗率,同时抑制了 DNRA。去除氨的供应会导致氨的最终产生、亚硝酸盐的积累以及 DNRA 基因表达的上调,从而导致大量的 "Ca.A. nitratireducens'的 DNRA 基因表达上调。增加 SCGA 的供应在促进 DNRA 方面也有类似的效果。我们的研究结果表明,'Ca.A.nitratireducens'转用 DNRA 来缓解亚硝酸盐积累造成的氧化应激,从而进一步了解这种微生物的适应性和生态学。我们的发现对于了解厌氧环境中氮和 SCGAs 的归宿也有重要意义。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
自引率
0.00%
发文量
0
期刊最新文献
Chronic exposure to polycyclic aromatic hydrocarbons alters skin virome composition and virus–host interactions Marine N2-fixer Crocosphaera waterburyi Repeated horizontal acquisition of lagriamide-producing symbionts in Lagriinae beetles Trade-offs between receptor modification and fitness drive host-bacteriophage co-evolution leading to phage extinction or co-existence Metagenomic time-series reveals a western English Channel viral community dominated by members with strong seasonal signals
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1