Pseudomonas stutzeri soluble nitrate reductase αβ‐subunit is a soluble enzyme with a similar electronic structure at the active site as the inner membrane‐bound αβγ holoenzyme

FEBS Letters

Diekmann, Stephan¹  Steinrücke, Peter¹  Mathé, Lutz¹  Anemüller, Stefan²  Borcherding, Heike¹  Hettmann, Thomas¹ 

[1]Department of Molecular Biology, IMB, Beutenbergstr. 11, D-07745 Jena, Germany

[2]Institut für Biochemie, Medizinische Universität zu Lübeck, Ratzeburger Allee 160, D-23538 Lübeck, Germany

关键词: Nitrate reductase;    Molybdenum;    Electron paramagnetic resonance;    Oxidoreductase;    Enzymology;    Pseudomonas stutzeri;   

DOI  :  10.1016/S0014-5793(02)03837-1

学科分类：生物化学/生物物理

来源: John Wiley & Sons Ltd.

【 摘 要 】

A two-subunit (αβ) form of dissimilatory nitrate reductase from Pseudomonas stutzeri strain ZoBell was separated from the membrane-residing γ-subunit by a heat solubilization step. Here we present an optimized purification protocol leading to a soluble αβ form with high specific activity (70 U/mg). The soluble form has the stoichiometry α₁β₁ consisting of the 130 kDa α-subunit and the 58 kDa β-subunit. We did not observe any proteolytic cleavage in the course of the heat solubilization. The enzyme is competively inhibited by azide, but not by chlorate. It exhibits a K _M value of 3.2 mM for nitrate. We compare the enzymatic and electron paramagnetic resonance (EPR) spectroscopic properties of the αβ form with the αβγ holoenzyme which resides in the membrane and can be prepared by detergent extraction. The nearly identical EPR spectra for the Mo(V) signal of both enzyme preparations show that the active site is unaffected by the heat step. The factors influencing the binding of the α- and β-subunit to the γ-subunit are discussed.

【 授权许可】

Unknown