硝基还原酶激活荧光探针检测细菌感染。

IF 4.3 3区 化学 Q2 CHEMISTRY, MULTIDISCIPLINARY
ACS Omega Pub Date : 2025-05-06 eCollection Date: 2025-05-20 DOI:10.1021/acsomega.5c00194
Tawanya Kamthong, Onnicha Khaikate, Narathip Naradun, Piyasiri Chueakwon, James R Ketudat Cairns, Anyanee Kamkaew, Rung-Yi Lai
{"title":"硝基还原酶激活荧光探针检测细菌感染。","authors":"Tawanya Kamthong, Onnicha Khaikate, Narathip Naradun, Piyasiri Chueakwon, James R Ketudat Cairns, Anyanee Kamkaew, Rung-Yi Lai","doi":"10.1021/acsomega.5c00194","DOIUrl":null,"url":null,"abstract":"<p><p>Nitroreductase (NTR), found in various bacteria, plays a crucial role in the detoxification of nitro-containing compounds, making it a valuable target for bacterial detection. In this study, we developed an NTR-responsive fluorescent probe (<b>IND-NO<sub>2</sub></b> ) for the selective detection of NTR activity in microorganisms. In preliminary tests, Escherichia coli NTR (<i>Ec</i>NfsB) was used as a model enzyme, and it effectively converted the probe's nitro group to an amino group in the presence of reduced nicotinamide adenine dinucleotide (NADH), resulting in a significant increase in fluorescence at 564 nm. To confirm the product identity, <b>IND-OH</b>, the reaction was analyzed by fluorescence spectroscopy and high-performance liquid chromatography (HPLC). Kinetic parameters for probe reduction were determined, revealing a limit of detection of 6.21 nM (0.16 μg/mL). The probe demonstrated high specificity for NTR, with the control experiments showing no reduction by various biological reductants. Furthermore, the probe successfully detected NTR activities in the bacteria E. coli TISTR780, Pseudomonas aeruginosa TISTR781, and Staphylococcus aureus TISTR1466, representing ESKAPE pathogens, by fluorescence spectroscopy and the naked eye, demonstrating its potential for real-time bacterial detection.</p>","PeriodicalId":22,"journal":{"name":"ACS Omega","volume":"10 19","pages":"19564-19573"},"PeriodicalIF":4.3000,"publicationDate":"2025-05-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12096206/pdf/","citationCount":"0","resultStr":"{\"title\":\"Nitroreductase-Activated Fluorescence Probe for Detection of Bacterial Infections.\",\"authors\":\"Tawanya Kamthong, Onnicha Khaikate, Narathip Naradun, Piyasiri Chueakwon, James R Ketudat Cairns, Anyanee Kamkaew, Rung-Yi Lai\",\"doi\":\"10.1021/acsomega.5c00194\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Nitroreductase (NTR), found in various bacteria, plays a crucial role in the detoxification of nitro-containing compounds, making it a valuable target for bacterial detection. In this study, we developed an NTR-responsive fluorescent probe (<b>IND-NO<sub>2</sub></b> ) for the selective detection of NTR activity in microorganisms. In preliminary tests, Escherichia coli NTR (<i>Ec</i>NfsB) was used as a model enzyme, and it effectively converted the probe's nitro group to an amino group in the presence of reduced nicotinamide adenine dinucleotide (NADH), resulting in a significant increase in fluorescence at 564 nm. To confirm the product identity, <b>IND-OH</b>, the reaction was analyzed by fluorescence spectroscopy and high-performance liquid chromatography (HPLC). Kinetic parameters for probe reduction were determined, revealing a limit of detection of 6.21 nM (0.16 μg/mL). The probe demonstrated high specificity for NTR, with the control experiments showing no reduction by various biological reductants. Furthermore, the probe successfully detected NTR activities in the bacteria E. coli TISTR780, Pseudomonas aeruginosa TISTR781, and Staphylococcus aureus TISTR1466, representing ESKAPE pathogens, by fluorescence spectroscopy and the naked eye, demonstrating its potential for real-time bacterial detection.</p>\",\"PeriodicalId\":22,\"journal\":{\"name\":\"ACS Omega\",\"volume\":\"10 19\",\"pages\":\"19564-19573\"},\"PeriodicalIF\":4.3000,\"publicationDate\":\"2025-05-06\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12096206/pdf/\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"ACS Omega\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://doi.org/10.1021/acsomega.5c00194\",\"RegionNum\":3,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"2025/5/20 0:00:00\",\"PubModel\":\"eCollection\",\"JCR\":\"Q2\",\"JCRName\":\"CHEMISTRY, MULTIDISCIPLINARY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"ACS Omega","FirstCategoryId":"92","ListUrlMain":"https://doi.org/10.1021/acsomega.5c00194","RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/5/20 0:00:00","PubModel":"eCollection","JCR":"Q2","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
引用次数: 0

摘要

硝基还原酶(Nitroreductase, NTR)存在于多种细菌中,在含硝基化合物的解毒过程中起着至关重要的作用,使其成为细菌检测的重要靶点。在这项研究中,我们开发了一种NTR响应荧光探针(IND-NO2),用于选择性检测微生物中NTR的活性。在初步实验中,以大肠杆菌NTR (EcNfsB)作为模型酶,在还原的烟酰胺腺嘌呤二核苷酸(NADH)存在下,能有效地将探针的硝基转化为氨基,在564 nm处荧光显著增强。通过荧光光谱和高效液相色谱对反应进行了分析,以确定产物IND-OH的身份。测定探针还原动力学参数,检测限为6.21 nM (0.16 μg/mL)。该探针对NTR具有很高的特异性,对照实验显示各种生物还原剂对NTR没有还原作用。此外,该探针还成功地通过荧光光谱和肉眼检测了代表ESKAPE病原体的大肠杆菌TISTR780、铜绿假单胞菌TISTR781和金黄色葡萄球菌TISTR1466中NTR的活性,显示了其实时细菌检测的潜力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Nitroreductase-Activated Fluorescence Probe for Detection of Bacterial Infections.

Nitroreductase (NTR), found in various bacteria, plays a crucial role in the detoxification of nitro-containing compounds, making it a valuable target for bacterial detection. In this study, we developed an NTR-responsive fluorescent probe (IND-NO2 ) for the selective detection of NTR activity in microorganisms. In preliminary tests, Escherichia coli NTR (EcNfsB) was used as a model enzyme, and it effectively converted the probe's nitro group to an amino group in the presence of reduced nicotinamide adenine dinucleotide (NADH), resulting in a significant increase in fluorescence at 564 nm. To confirm the product identity, IND-OH, the reaction was analyzed by fluorescence spectroscopy and high-performance liquid chromatography (HPLC). Kinetic parameters for probe reduction were determined, revealing a limit of detection of 6.21 nM (0.16 μg/mL). The probe demonstrated high specificity for NTR, with the control experiments showing no reduction by various biological reductants. Furthermore, the probe successfully detected NTR activities in the bacteria E. coli TISTR780, Pseudomonas aeruginosa TISTR781, and Staphylococcus aureus TISTR1466, representing ESKAPE pathogens, by fluorescence spectroscopy and the naked eye, demonstrating its potential for real-time bacterial detection.

求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
ACS Omega
ACS Omega Chemical Engineering-General Chemical Engineering
CiteScore
6.60
自引率
4.90%
发文量
3945
审稿时长
2.4 months
期刊介绍: ACS Omega is an open-access global publication for scientific articles that describe new findings in chemistry and interfacing areas of science, without any perceived evaluation of immediate impact.
×
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