• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

相似文献

1
Microbial transformation of 2,4,6-trinitrotoluene and other nitroaromatic compounds.2,4,6-三硝基甲苯及其他硝基芳香族化合物的微生物转化
Appl Environ Microbiol. 1976 Jun;31(6):949-58. doi: 10.1128/aem.31.6.949-958.1976.
2
[Characteristics of nitroreduction as the key stage in the microbial destruction of aromatic nitro compounds].
Prikl Biokhim Mikrobiol. 1983 Jul-Aug;19(4):507-12.
3
2,4,6-trinitrotoluene reduction by an Fe-only hydrogenase in Clostridium acetobutylicum.丙酮丁醇梭菌中仅含Fe的氢化酶对2,4,6-三硝基甲苯的还原作用
Appl Environ Microbiol. 2003 Mar;69(3):1542-7. doi: 10.1128/AEM.69.3.1542-1547.2003.
4
[Bacterial reductive transformation of aromatic nitro compounds].[芳香族硝基化合物的细菌还原转化]
Mikrobiologiia. 1982;51(5):735-9.
5
Microbial degradation of nitroaromatic compounds.硝基芳香化合物的微生物降解
Adv Appl Microbiol. 1992;37:1-19. doi: 10.1016/s0065-2164(08)70250-8.
6
Biodegradation of nitroaromatic compounds.硝基芳香化合物的生物降解
Annu Rev Microbiol. 1995;49:523-55. doi: 10.1146/annurev.mi.49.100195.002515.
7
On the reduction of aliphatic and aromatic nitro compounds by Clostridia, the role of ferredoxin and its stabilization.
Hoppe Seylers Z Physiol Chem. 1983 Aug;364(8):961-75. doi: 10.1515/bchm2.1983.364.2.961.
8
Oxidative transformation of aminodinitrotoluene isomers by multicomponent dioxygenases.多组分双加氧酶对氨基二硝基甲苯异构体的氧化转化作用
Appl Environ Microbiol. 2001 Dec;67(12):5460-6. doi: 10.1128/AEM.67.12.5460-5466.2001.
9
Transformation of 2,4,6-trinitrotoluene by purified xenobiotic reductase B from Pseudomonas fluorescens I-C.荧光假单胞菌I-C中纯化的异源生物还原酶B对2,4,6-三硝基甲苯的转化
Appl Environ Microbiol. 2000 Nov;66(11):4742-50. doi: 10.1128/AEM.66.11.4742-4750.2000.
10
Reductive transformation of TNT by Escherichia coli: pathway description.大肠杆菌对三硝基甲苯的还原转化:途径描述
Appl Microbiol Biotechnol. 2005 May;67(3):397-404. doi: 10.1007/s00253-004-1736-x. Epub 2004 Oct 13.

引用本文的文献

1
Comparative study of NiO/CuO/Ag doped graphene based materials for reduction of nitroaromatic compounds and degradation of dye with statistical study.基于NiO/CuO/Ag掺杂石墨烯材料用于还原硝基芳香族化合物及降解染料的比较研究与统计分析
Sci Rep. 2024 Jan 24;14(1):2077. doi: 10.1038/s41598-024-51342-x.
2
Hemicyanine-Based Near-Infrared Fluorescence Off-On Probes for Imaging Intracellular and In Vivo Nitroreductase Activity.基于半花菁的近红外荧光开启型探针用于检测细胞内和体内硝基还原酶活性。
Int J Mol Sci. 2023 Mar 23;24(7):6074. doi: 10.3390/ijms24076074.
3
Fabrication of Bimetallic Cu-Ag Nanoparticle-Decorated Poly(cyclotriphosphazene--4,4'-sulfonyldiphenol) and Its Enhanced Catalytic Activity for the Reduction of 4-Nitrophenol.双金属铜 - 银纳米粒子修饰的聚(环三磷腈 - 4,4'-磺酰二苯酚)的制备及其对4-硝基苯酚还原的增强催化活性
ACS Omega. 2022 Feb 15;7(8):7096-7102. doi: 10.1021/acsomega.1c06786. eCollection 2022 Mar 1.
4
Degradation of High Energy Materials Using Biological Reduction: A Rational Way to Reach Bioremediation.高能材料的生物还原降解:实现生物修复的合理途径。
Int J Mol Sci. 2019 Nov 7;20(22):5556. doi: 10.3390/ijms20225556.
5
Method development and laboratory intercomparison of an RP-HPLC-UV method for energetic chemicals in marine tissues.建立海洋组织中爆炸物类化合物的反相高效液相色谱-紫外检测法并进行实验室间比对。
Talanta. 2019 Jun 1;198:284-294. doi: 10.1016/j.talanta.2019.02.005. Epub 2019 Feb 6.
6
Systems Biology Approach to Bioremediation of Nitroaromatics: Constraint-Based Analysis of 2,4,6-Trinitrotoluene Biotransformation by Escherichia coli.系统生物学方法在硝基芳烃生物修复中的应用:基于约束的大肠杆菌 2,4,6-三硝基甲苯生物转化分析。
Molecules. 2017 Aug 14;22(8):1242. doi: 10.3390/molecules22081242.
7
Multiple environmental stressors elicit complex interactive effects in the western fence lizard (Sceloporus occidentalis).多种环境胁迫因素会在西部壁蜥(Sceloporus occidentalis)中引发复杂的交互作用。
Ecotoxicology. 2012 Nov;21(8):2372-90. doi: 10.1007/s10646-012-0993-1. Epub 2012 Sep 14.
8
Aerobic growth of Escherichia coli with 2,4,6-trinitrotoluene (TNT) as the sole nitrogen source and evidence of TNT denitration by whole cells and cell-free extracts.以2,4,6-三硝基甲苯(TNT)作为唯一氮源时大肠杆菌的需氧生长以及全细胞和无细胞提取物对TNT进行脱硝的证据。
Appl Environ Microbiol. 2006 Dec;72(12):7945-8. doi: 10.1128/AEM.01052-06. Epub 2006 Sep 29.
9
Transformation of 2,4,6-Trinitrotoluene by Pseudomonas pseudoalcaligenes JS52.假单胞菌 JS52 对 2,4,6-三硝基甲苯的转化。
Appl Environ Microbiol. 1997 May;63(5):2007-15. doi: 10.1128/aem.63.5.2007-2015.1997.
10
Reduction and Acetylation of 2,4-Dinitrotoluene by a Pseudomonas aeruginosa Strain.铜绿假单胞菌还原和乙酰化 2,4-二硝基甲苯。
Appl Environ Microbiol. 1996 Jul;62(7):2257-63. doi: 10.1128/aem.62.7.2257-2263.1996.

本文引用的文献

1
The metabolism of 2:4:6-trinitrotoluene (alpha-T.N.T.).2,4,6-三硝基甲苯(α-梯恩梯)的代谢
Biochem J. 1944;38(1):70-85. doi: 10.1042/bj0380070.
2
DEGRADATION OF PYRUVATE BY MICROCOCCUS LACTILYTICUS II. : Studies of Cofactors in the Formate-Exchange Reaction.乳酸微球菌对丙酮酸的降解作用II:甲酸交换反应中辅助因子的研究
J Bacteriol. 1962 Apr;83(4):899-906. doi: 10.1128/jb.83.4.899-906.1962.
3
DEGRADATION OF PYRUVATE BY MICROCOCCUS LACTILYTICUS I. : General Properties of the Formate-Exchange Reaction.乳酸溶球菌对丙酮酸的降解作用I:甲酸交换反应的一般特性
J Bacteriol. 1962 Apr;83(4):887-98. doi: 10.1128/jb.83.4.887-898.1962.
4
Protein measurement with the Folin phenol reagent.使用福林酚试剂进行蛋白质测定。
J Biol Chem. 1951 Nov;193(1):265-75.
5
Evidence for oxidative phosphorylation during the reduction of sulfate with hydrogen by Desulfovibrio desulfuricans.脱硫脱硫弧菌利用氢气还原硫酸盐过程中氧化磷酸化的证据。
J Biol Chem. 1960 Sep;235:2734-8.
6
DISC ELECTROPHORESIS. II. METHOD AND APPLICATION TO HUMAN SERUM PROTEINS.圆盘电泳。II. 方法及其在人血清蛋白中的应用。
Ann N Y Acad Sci. 1964 Dec 28;121:404-27. doi: 10.1111/j.1749-6632.1964.tb14213.x.
7
THE PURIFICATION OF A NITRO-REDUCTASE OF NOCARDIA V.诺卡氏菌V型硝基还原酶的纯化
J Biol Chem. 1964 Mar;239:773-6.
8
Bacterial degradation of the nitrobenzoic acids.硝基苯甲酸的细菌降解
Biochem J. 1959 Feb;71(2):248-61. doi: 10.1042/bj0710248.
9
A new procedure for assay of bacterial hydrogenases.一种测定细菌氢化酶的新方法。
J Bacteriol. 1956 Jan;71(1):70-80. doi: 10.1128/jb.71.1.70-80.1956.
10
The inhibition of organiz nitro reductase by aureomycin in cell-free extracts. II. Cofactor requirements for the nitro reductase enzyme complex.金霉素对无细胞提取物中微生物硝基还原酶的抑制作用。II. 硝基还原酶复合物的辅因子需求
Arch Biochem Biophys. 1954 Jul;51(1):5-16. doi: 10.1016/0003-9861(54)90447-6.

2,4,6-三硝基甲苯及其他硝基芳香族化合物的微生物转化

Microbial transformation of 2,4,6-trinitrotoluene and other nitroaromatic compounds.

作者信息

McCormick N G, Feeherry F E, Levinson H S

出版信息

Appl Environ Microbiol. 1976 Jun;31(6):949-58. doi: 10.1128/aem.31.6.949-958.1976.

DOI:10.1128/aem.31.6.949-958.1976
PMID:779650
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC169861/
Abstract

A variety of nitroaromatic compounds, including 2,4,6-trinitrotoluene (TNT), were reduced by hydrogen in the presence of enzyme preparations from Veillonella alkalescens. Consistent with the proposed reduction pathway, R-NO2 H2 leads to R-NO H2 leads to R-NHOH H2 leads to R-NH2, 3 mol of H2 was utilized per mol of nitro group. The rates of reduction of 40 mono-, di-, and trinitroaromatic compounds by V. alkalescens extract were determined. The reactivity of the nitro groups depended on other substituents and on the position of the nitro groups relative to these substituents. In the case of the nitrotoluenes, the para-nitro group was the most readily reduced, the 4-nitro position of 2,4-dinitrotulene being reduced first. The pattern of reduction of TNT (disappearance of TNT and reduction products formed) depended on the type of preparation (cell-free extract, resting cells, or growing culture), on the species, and on the atmosphere (air or H2). The "nitro-reductase" activity of V. alkalescens extracts was associated with protein fractions, one having some ferredoxin-like properties and the other possessing hydrogenase activity. Efforts to eliminate hydrogenase from the reaction have thus far been unsuccessful. The question of whether ferredoxin acts as a nonspecific reductase for nitroaromatic compounds remains unresolved.

摘要

在来自产碱韦荣球菌的酶制剂存在下,多种硝基芳香族化合物,包括2,4,6-三硝基甲苯(TNT),被氢气还原。与提出的还原途径一致,R-NO₂ + H₂ 生成 R-NO + H₂,进而生成 R-NHOH + H₂,最终生成 R-NH₂,每摩尔硝基消耗3摩尔氢气。测定了产碱韦荣球菌提取物对40种单、二和三硝基芳香族化合物的还原速率。硝基的反应活性取决于其他取代基以及硝基相对于这些取代基的位置。就硝基甲苯而言,对硝基最容易被还原,2,4-二硝基甲苯的4-硝基位置首先被还原。TNT的还原模式(TNT的消失以及形成的还原产物)取决于制剂类型(无细胞提取物、静止细胞或生长培养物)、菌种以及气氛(空气或氢气)。产碱韦荣球菌提取物的“硝基还原酶”活性与蛋白质组分相关,一种具有一些铁氧化还原蛋白样特性,另一种具有氢化酶活性。迄今为止,在反应中消除氢化酶的努力尚未成功。铁氧化还原蛋白是否作为硝基芳香族化合物的非特异性还原酶这一问题仍未解决。