词条 | Azobenzene reductase |
释义 |
| Name = azobenzene reductase (azoreductase) | EC_number = 1.7.1.6 | CAS_number = 9029-31-6 | IUBMB_EC_number = 1/7/1/6 | GO_code = 0050446 | image = | width = | caption = }} Azobenzene reductase also known as azoreductase ({{EC number|1.7.1.6}}) is an enzyme that catalyzes the chemical reaction: N,N-dimethyl-1,4-phenylenediamine + aniline + NADP+ 4-(dimethylamino)azobenzene + NADPH + H+ The 3 substrates of this enzyme are N,N-dimethyl-1,4-phenylenediamine, aniline, and nicotinamide adenine dinucleotide phosphate ion, whereas its 3 products are 4-(dimethylamino)azobenzene, nicotinamide adenine dinucleotide phosphate, and hydrogen ion.[1] This enzyme belongs to the family of oxidoreductases, specifically those acting on other nitrogenous compounds as donors with NAD+ or NADP+ as acceptor. MechanismThe reaction catalyzed by this enzyme proceeds via a ping-pong mechanism[2] by using 2 equivalents of NAD(P)H to reduce one equivalent of the azo compound substrate (for example methyl red where Ar = p-dimethylaniline and Ar' = o-benzoic acid) into two equivalents of aniline product: Ar–N=N–Ar' + 2(NAD(P)H + H+) Ar–NH2 + NH2–Ar' + 2NAD(P)+ Substrate specificityMost azoreductase isoenzymes can reduce methyl red, but are not able to reduce sulfonated azo dyes. The unique azoreductase isozyme from Bacillus sp. B29 has the ability to reduce sulfonated azo dyes however.[3] NomenclatureThe systematic name of this enzyme class is N,N-dimethyl-1,4-phenylenediamine, aniline:NADP+ oxidoreductase. Other names in common use include: {{div col|colwidth=30em}}
Structural studiesAs of late 2007, 3 structures have been solved for this class of enzymes, with PDB accession codes {{PDB link|1NNI}}, {{PDB link|1V4B}}, and {{PDB link|2D5I}}. Please check the last updated data on RCSB PDB site. References1. ^{{cite journal |author1 = Mueller GC |author2 =Miller JA | title = The reductive cleavage of 4-dimethylaminoazobenzene by rat liver; the intracellular distribution of the enzyme system and its requirement for triphosphopyridine nucleotide | journal = J. Biol. Chem. | volume = 180 | issue = 3 | pages = 1125–36 |date=October 1949 | pmid = 18139207 | doi = | url = | issn = }} 2. ^{{cite journal | vauthors = Ooi T, Shibata T, Sato R, Ohno H, Kinoshita S, Thuoc TL, Taguchi S | title = An azoreductase, aerobic NADH-dependent flavoprotein discovered from Bacillus sp.: functional expression and enzymatic characterization | journal = Appl. Microbiol. Biotechnol. | volume = 75 | issue = 2 | pages = 377–86 |date=May 2007 | pmid = 17546472 | doi = 10.1007/s00253-006-0836-1 | url = | issn = }} 3. ^{{cite journal | vauthors = Ooi T, Shibata T, Matsumoto K, Kinoshita S, Taguchi S | title = Comparative enzymatic analysis of azoreductases from Bacillus sp. B29 | journal = Biosci. Biotechnol. Biochem. | volume = 73 | issue = 5 | pages = 1209–11 |date=May 2009 | pmid = 19420689 | doi = 10.1271/bbb.80872 | url = | issn = }} Further reading{{refbegin}}
3 : EC 1.7.1|NADPH-dependent enzymes|Enzymes of known structure |
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