{"title":"两个一氧化二氮还原酶的故事:一个警世的观点","authors":"Sukhwan Yoon , Min Joon Song , Michele Laureni","doi":"10.1016/j.mib.2025.102631","DOIUrl":null,"url":null,"abstract":"<div><div>Nitrous oxide reductases (N2OR) are the sole sink of the potent greenhouse gas nitrous oxide (N<sub>2</sub>O) in the environment. Having been studied for decades, N2OR have attracted renewed attention following the discovery of a previously unrecognized clade, now termed clade II. This clade exhibits unexpectedly widespread taxonomic distribution and prevalence across diverse environments, prompting research efforts to define and assign distinct clade-specific traits. In this perspective, we aim to critically review and evaluate dichotomous clade-based classifications, addressing oversimplifications and unresolved ambiguities in linking clade identity to physiological traits like substrate affinity, acid tolerance, and aerotolerance. Growing experimental evidence from N<sub>2</sub>O-reducing isolates and enrichments suggests a general difference in substrate affinity between the clades. Recent discoveries of N<sub>2</sub>O reduction at pH < 5.0 attribute the long-sought acidophilic N<sub>2</sub>O reduction exclusively to organisms possessing clade II <em>nosZ</em>, and attempts have also been made to relate clade separation to aerotolerant N<sub>2</sub>O reduction. However, it is important to note that such binary characterizations are based on limited observations and lack a solid understanding of the underlying mechanisms, exposing them to bias and oversimplification risks. We emphasize the need for a balanced research effort to establish a robust link between ecophysiology and biochemistry, enabling a more accurate evaluation of clade-based characterizations and, ultimately, a deeper understanding and effective harnessing of N<sub>2</sub>O-reducing organisms.</div></div>","PeriodicalId":10921,"journal":{"name":"Current opinion in microbiology","volume":"86 ","pages":"Article 102631"},"PeriodicalIF":5.9000,"publicationDate":"2025-07-05","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"A tale of two nitrous oxide reductases: a cautionary perspective\",\"authors\":\"Sukhwan Yoon , Min Joon Song , Michele Laureni\",\"doi\":\"10.1016/j.mib.2025.102631\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>Nitrous oxide reductases (N2OR) are the sole sink of the potent greenhouse gas nitrous oxide (N<sub>2</sub>O) in the environment. Having been studied for decades, N2OR have attracted renewed attention following the discovery of a previously unrecognized clade, now termed clade II. This clade exhibits unexpectedly widespread taxonomic distribution and prevalence across diverse environments, prompting research efforts to define and assign distinct clade-specific traits. In this perspective, we aim to critically review and evaluate dichotomous clade-based classifications, addressing oversimplifications and unresolved ambiguities in linking clade identity to physiological traits like substrate affinity, acid tolerance, and aerotolerance. Growing experimental evidence from N<sub>2</sub>O-reducing isolates and enrichments suggests a general difference in substrate affinity between the clades. Recent discoveries of N<sub>2</sub>O reduction at pH < 5.0 attribute the long-sought acidophilic N<sub>2</sub>O reduction exclusively to organisms possessing clade II <em>nosZ</em>, and attempts have also been made to relate clade separation to aerotolerant N<sub>2</sub>O reduction. However, it is important to note that such binary characterizations are based on limited observations and lack a solid understanding of the underlying mechanisms, exposing them to bias and oversimplification risks. We emphasize the need for a balanced research effort to establish a robust link between ecophysiology and biochemistry, enabling a more accurate evaluation of clade-based characterizations and, ultimately, a deeper understanding and effective harnessing of N<sub>2</sub>O-reducing organisms.</div></div>\",\"PeriodicalId\":10921,\"journal\":{\"name\":\"Current opinion in microbiology\",\"volume\":\"86 \",\"pages\":\"Article 102631\"},\"PeriodicalIF\":5.9000,\"publicationDate\":\"2025-07-05\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Current opinion in microbiology\",\"FirstCategoryId\":\"99\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S1369527425000530\",\"RegionNum\":2,\"RegionCategory\":\"生物学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"MICROBIOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Current opinion in microbiology","FirstCategoryId":"99","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S1369527425000530","RegionNum":2,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"MICROBIOLOGY","Score":null,"Total":0}
A tale of two nitrous oxide reductases: a cautionary perspective
Nitrous oxide reductases (N2OR) are the sole sink of the potent greenhouse gas nitrous oxide (N2O) in the environment. Having been studied for decades, N2OR have attracted renewed attention following the discovery of a previously unrecognized clade, now termed clade II. This clade exhibits unexpectedly widespread taxonomic distribution and prevalence across diverse environments, prompting research efforts to define and assign distinct clade-specific traits. In this perspective, we aim to critically review and evaluate dichotomous clade-based classifications, addressing oversimplifications and unresolved ambiguities in linking clade identity to physiological traits like substrate affinity, acid tolerance, and aerotolerance. Growing experimental evidence from N2O-reducing isolates and enrichments suggests a general difference in substrate affinity between the clades. Recent discoveries of N2O reduction at pH < 5.0 attribute the long-sought acidophilic N2O reduction exclusively to organisms possessing clade II nosZ, and attempts have also been made to relate clade separation to aerotolerant N2O reduction. However, it is important to note that such binary characterizations are based on limited observations and lack a solid understanding of the underlying mechanisms, exposing them to bias and oversimplification risks. We emphasize the need for a balanced research effort to establish a robust link between ecophysiology and biochemistry, enabling a more accurate evaluation of clade-based characterizations and, ultimately, a deeper understanding and effective harnessing of N2O-reducing organisms.
期刊介绍:
Current Opinion in Microbiology is a systematic review journal that aims to provide specialists with a unique and educational platform to keep up-to-date with the expanding volume of information published in the field of microbiology. It consists of 6 issues per year covering the following 11 sections, each of which is reviewed once a year:
Host-microbe interactions: bacteria
Cell regulation
Environmental microbiology
Host-microbe interactions: fungi/parasites/viruses
Antimicrobials
Microbial systems biology
Growth and development: eukaryotes/prokaryotes