EVIDENCE THAT THE TYPE-2 COPPER CENTERS ARE THE SITE OF NITRITE REDUCTION BY ACHROMOBACTER-CYCLOCLASTES NITRITE REDUCTASE

被引:96
|
作者
LIBBY, E [1 ]
AVERILL, BA [1 ]
机构
[1] UNIV VIRGINIA,DEPT CHEM,CHARLOTTESVILLE,VA 22901
基金
美国国家科学基金会;
关键词
D O I
10.1016/0006-291X(92)90476-2
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Methods have been developed for selective depletion and reconstitution of the Type 2 Cu (non-blue) sites in the nitrite reductase from A. cycloclastes, resulting in preparations ranging from 0.5 to 2.6 Type Cu per trimer; the Type 1 Cu content is invariant at 3.0 per trimer. The activity of the enzyme is directly proportional to the Type 2 content as measured by direct metal determination or by analysis of the EPR spectra. These results indicate that an earlier report that the A. cycloclastes enzyme contains only Type 1 Cu sites is incorrect, and that the Type 2 Cu centers constitute the site at which NO2- is reduced. Furthermore, they suggest that other Cu nitrite reductases that are reported to contain only Type 1 Cu sites and exhibit relatively low activity may actually be largely Type 2 Cu-depleted forms of the enzymes. © 1992.
引用
收藏
页码:1529 / 1535
页数:7
相关论文
共 50 条
  • [41] EPR AND ELECTRON-NUCLEAR DOUBLE-RESONANCE (ENDOR) STUDIES SHOW NITRITE BINDING TO THE TYPE-2 COPPER CENTERS OF THE DISSIMILATORY NITRITE REDUCTASE OF ALCALIGENES XYLOSOXIDANS (NCIMB-11015)
    HOWES, BD
    ABRAHAM, ZHL
    LOWE, DJ
    BRUSER, T
    EADY, RR
    SMITH, BE
    BIOCHEMISTRY, 1994, 33 (11) : 3171 - 3177
  • [42] PURIFICATION AND CHARACTERIZATION OF THE DISSIMILATORY NITRITE REDUCTASE FROM ALCALIGENES-XYLOSOXIDANS SUBSP XYLOSOXIDANS (NCIMB 11015) - EVIDENCE FOR THE PRESENCE OF BOTH TYPE-1 AND TYPE-2 COPPER CENTERS
    ABRAHAM, ZHL
    LOWE, DJ
    SMITH, BE
    BIOCHEMICAL JOURNAL, 1993, 295 : 587 - 593
  • [43] CuI and CuII complexes containing nitrite and tridentate aromatic amine ligand as models for the substrate-binding type-2 Cu site of nitrite reductase
    Yokoyama, H
    Yamaguchi, K
    Sugimoto, M
    Suzuki, S
    EUROPEAN JOURNAL OF INORGANIC CHEMISTRY, 2005, (08) : 1435 - 1441
  • [44] The covalent structure of the blue copper-containing nitrite reductase from Achromobacter xylosoxidans
    Vandenberghe, IHM
    Meyer, TE
    Cusanovich, MA
    Van Beeumen, JJ
    BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1998, 247 (03) : 734 - 740
  • [45] ENDOR study of the catalytic type 2 copper of nitrite reductase.
    Scholes, CP
    Lukoyanov, D
    Zhao, YW
    Shapleigh, JP
    ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY, 2002, 223 : A31 - A32
  • [46] Biomimetic catalysis of nitrite reductase enzyme using copper complexes in chemical and electrochemical reduction of nitrite
    Ferreira, Millena P. P.
    Castro, Caio B. B.
    Honorato, Joao
    He, Sheng
    Guimaraes, Walber Goncalves
    Esmieu, Charlene
    Castellano, Eduardo E. E.
    de Moura, Andre F.
    Truzzi, Daniela R.
    Nascimento, Otaciro R.
    Simonneau, Antoine
    Netto, Caterina G. C. Marques
    DALTON TRANSACTIONS, 2023, 52 (32) : 11254 - 11264
  • [47] STRUCTURAL-CHANGE IN THE ONE-ELECTRON OXIDATION REDUCTION AT THE COPPER SITE IN NITRITE REDUCTASE - EVIDENCE FROM EXAFS
    SANO, M
    MATSUBARA, T
    INORGANICA CHIMICA ACTA-BIOINORGANIC CHEMISTRY, 1988, 152 (01): : 53 - 54
  • [48] Theoretical study of structure of catalytic copper site in nitrite reductase
    Källrot, N
    Nilsson, K
    Rasmussen, T
    Ryde, U
    INTERNATIONAL JOURNAL OF QUANTUM CHEMISTRY, 2005, 102 (05) : 520 - 541
  • [49] Elucidating the mechanism for the reduction of nitrite by copper nitrite reductase - A contribution from quantum chemical studies
    De Marothy, S. A.
    Blomberg, M. R. A.
    Siegbahn, P. E. M.
    JOURNAL OF COMPUTATIONAL CHEMISTRY, 2007, 28 (02) : 528 - 539
  • [50] Reduction of nitrite to NO at a mononuclear copper(II)-phenolate site
    Maria, S.
    Chattopadhyay, Taraknath
    Ananya, S.
    Kundu, Subrata
    INORGANICA CHIMICA ACTA, 2020, 506