Intermittent oxygenation is essential for modulating nitrite ammonifiers in an agricultural upland soil to minimize nitrogen loss

IF 5 2区 农林科学 Q1 SOIL SCIENCE
Xiaogang Wu , Siyu Yu , Weikang Sui , Xinyu Zhang , Ji Li , Qiaoyu Wu , Xiaojun Zhang
{"title":"Intermittent oxygenation is essential for modulating nitrite ammonifiers in an agricultural upland soil to minimize nitrogen loss","authors":"Xiaogang Wu ,&nbsp;Siyu Yu ,&nbsp;Weikang Sui ,&nbsp;Xinyu Zhang ,&nbsp;Ji Li ,&nbsp;Qiaoyu Wu ,&nbsp;Xiaojun Zhang","doi":"10.1016/j.apsoil.2025.106386","DOIUrl":null,"url":null,"abstract":"<div><div>Denitrification and dissimilatory nitrate reduction to ammonium (DNRA), two divergent nitrogen metabolism pathways, share nitrite as a common intermediate during anaerobic reduction. Unlike denitrification, which involves nitrogen loss through gaseous nitrogen emission and nitrate leaching, DNRA is beneficial for the conservation of nitrogen. Previous studies have reported factors such as carbon and oxygen can independently affect DNRA. Nevertheless, the key mechanism underlying the joint regulation of aerobic carbon metabolism to nitrite ammonifiers in soil is still unclear. Here, microcosm experiments with agricultural upland soil were conducted under different aeration conditions supplemented with labile carbon to analyze the process of denitrification and DNRA. The results indicated that denitrification exclusively dominated nitrite reduction when the soil was directly placed in an anaerobic environment. Nonetheless, a significant increase in DNRA activity and the attenuation of denitrification were detected when the soil was incubated aerobically with the addition of glucose prior to anaerobic incubation. Specifically, up to 55.8 % of nitrite reduction switched to nitrogen conservation mainly via DNRA under high‑carbon conditions. Quantitative assays of the <em>nrfA</em> gene showed that aerobic incubation with 1000 mg·kg<sup>−1</sup> carbon addition increased DNRA by 3.74 ± 0.24 fold. Sequence analysis of <em>nrfA</em> gene indicated a marked shift in nitrite ammonifiers, with Firmicutes being the most altered phylum. These results intriguingly indicate that nitrate/nitrite metabolic flux in the soil could be regulated to enhance DNRA by stimulating facultative anaerobic nitrite ammonifiers such as <em>Sedimentibacter</em> under alternating aerobic and anaerobic environments with carbon metabolism.</div></div>","PeriodicalId":8099,"journal":{"name":"Applied Soil Ecology","volume":"214 ","pages":"Article 106386"},"PeriodicalIF":5.0000,"publicationDate":"2025-08-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Applied Soil Ecology","FirstCategoryId":"97","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0929139325005244","RegionNum":2,"RegionCategory":"农林科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"SOIL SCIENCE","Score":null,"Total":0}
引用次数: 0

Abstract

Denitrification and dissimilatory nitrate reduction to ammonium (DNRA), two divergent nitrogen metabolism pathways, share nitrite as a common intermediate during anaerobic reduction. Unlike denitrification, which involves nitrogen loss through gaseous nitrogen emission and nitrate leaching, DNRA is beneficial for the conservation of nitrogen. Previous studies have reported factors such as carbon and oxygen can independently affect DNRA. Nevertheless, the key mechanism underlying the joint regulation of aerobic carbon metabolism to nitrite ammonifiers in soil is still unclear. Here, microcosm experiments with agricultural upland soil were conducted under different aeration conditions supplemented with labile carbon to analyze the process of denitrification and DNRA. The results indicated that denitrification exclusively dominated nitrite reduction when the soil was directly placed in an anaerobic environment. Nonetheless, a significant increase in DNRA activity and the attenuation of denitrification were detected when the soil was incubated aerobically with the addition of glucose prior to anaerobic incubation. Specifically, up to 55.8 % of nitrite reduction switched to nitrogen conservation mainly via DNRA under high‑carbon conditions. Quantitative assays of the nrfA gene showed that aerobic incubation with 1000 mg·kg−1 carbon addition increased DNRA by 3.74 ± 0.24 fold. Sequence analysis of nrfA gene indicated a marked shift in nitrite ammonifiers, with Firmicutes being the most altered phylum. These results intriguingly indicate that nitrate/nitrite metabolic flux in the soil could be regulated to enhance DNRA by stimulating facultative anaerobic nitrite ammonifiers such as Sedimentibacter under alternating aerobic and anaerobic environments with carbon metabolism.

Abstract Image

间歇性氧合是必不可少的调节亚硝酸盐氨化在农业旱地土壤,以尽量减少氮的损失
反硝化和异化硝酸还原成铵(DNRA)是两种不同的氮代谢途径,在厌氧还原过程中,亚硝酸盐是共同的中间体。与通过气态氮排放和硝酸盐浸出导致氮损失的反硝化作用不同,DNRA有利于氮的保存。先前的研究已经报道了碳和氧等因素可以独立影响DNRA。然而,土壤中好氧碳代谢对亚硝酸盐氨化物联合调控的关键机制尚不清楚。本研究以农业旱地土壤为研究对象,在不同曝气条件下,通过添加活性碳的微观环境试验,分析土壤反硝化和DNRA的过程。结果表明,当土壤直接置于厌氧环境时,反硝化作用完全主导了亚硝酸盐的还原。尽管如此,当土壤在厌氧培养之前添加葡萄糖进行好氧培养时,可以检测到DNRA活性的显著增加和反硝化作用的衰减。具体来说,在高碳条件下,高达55.8%的亚硝酸盐还原主要通过DNRA转换为氮保护。nrfA基因的定量分析表明,添加1000 mg·kg−1碳的好氧培养使DNRA增加了3.74±0.24倍。nrfA基因序列分析表明,亚硝酸盐氨化菌发生了明显的变化,其中厚壁菌门变化最大。这些结果表明,在碳代谢交替的好氧和厌氧环境下,通过刺激沉积杆菌等兼性厌氧亚硝酸盐氨化菌,可以调节土壤中硝酸盐/亚硝酸盐的代谢通量,从而提高DNRA。
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 求助全文
来源期刊
Applied Soil Ecology
Applied Soil Ecology 农林科学-土壤科学
CiteScore
9.70
自引率
4.20%
发文量
363
审稿时长
5.3 months
期刊介绍: Applied Soil Ecology addresses the role of soil organisms and their interactions in relation to: sustainability and productivity, nutrient cycling and other soil processes, the maintenance of soil functions, the impact of human activities on soil ecosystems and bio(techno)logical control of soil-inhabiting pests, diseases and weeds.
×
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
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
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 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信