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词条 Azobenzene reductase
释义

  1. Mechanism

  2. Substrate specificity

  3. Nomenclature

  4. Structural studies

  5. References

  6. Further reading

{{enzyme
| 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.

Mechanism

The 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 specificity

Most 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]

Nomenclature

The 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}}
  • azo reductase,
  • azoreductase,
  • azo-dye reductase,
  • dibromopropylaminophenylazobenzoic azoreductase,
  • dimethylaminobenzene reductase,
  • methyl red azoreductase,
  • N,N-dimethyl-4-phenylazoaniline azoreductase,
  • NAD(P)H:1-(4'-sulfophenylazo)-2-naphthol oxidoreductase,
  • NADPH2-dependent azoreductase,
  • NADPH2:4-(dimethylamino)azobenzene oxidoreductase,
  • NC-reductase,
  • new coccine (NC)-reductase,
  • nicotinamide adenine dinucleotide (phosphate) azoreductase,
  • orange I azoreductase,
  • orange II azoreductase,
  • p-aminoazobenzene reductase, and
  • p-dimethylaminoazobenzene azoreductase.
{{Div col end}}

Structural studies

As 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.

References

1. ^{{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}}
  • {{cite journal | vauthors = Suzuki Y, Yoda T, Ruhul A, Sugiura W | date = 2001 | title = Molecular cloning and characterization of the gene coding for azoreductase from Bacillus sp. OY1-2 isolated from soil | journal = J. Biol. Chem. | volume = 276 | pages = 9059–65 | pmid = 11134015 | doi = 10.1074/jbc.M008083200 | issue = 12 }}
  • {{cite journal | vauthors = Matsumoto K, Mukai Y, Ogata D, Shozui F, Nduko JM, Taguchi S, Ooi T | date = 2009 | title =Characterization of thermostable FMN-dependent NADH azoreductase from the moderate thermophile Geobacillus stearothermophilus | journal = Appl. Microbiol. Biotechnol. | pmid = 19997911 | volume = 86 | issue = 5 | pages = 1431–8 | doi = 10.1007/s00253-009-2351-7 }}
{{refend}}{{Nitrogenous donor oxidoreductases}}{{Enzymes}}{{Portal bar|Molecular and Cellular Biology|border=no}}

3 : EC 1.7.1|NADPH-dependent enzymes|Enzymes of known structure

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