Toggle Main Menu Toggle Search

Open Access padlockePrints

Development of a viologen-based microtiter plate assay for the analysis of oxyanion reductase activity: Application to the membrane-bound selenate reductase from Enterobacter cloacae SLD1a-1

Lookup NU author(s): Dr Carys Watts, Dr Clive Butler


Full text for this publication is not currently held within this repository. Alternative links are provided below where available.


The membrane-bound selenate reductase of Enterobacter cloacae SLD1a-1 is purified in low yield and has relatively low activity in the pure form compared to that of other oxyanion reductases, such as the membrane-bound and periplasmic nitrate reductases. A microtiter plate assay based on the original quartz cuvette viologen assay of Jones and Garland (R.W. Jones, P.B. Garland, Biochem. J 164 (1977) 199-211) was developed specifically for analysis of such low-abundant, labile oxyanion reductases. The plate assay detects the enzyme-dependent reoxidation of reduced methyl viologen spectrophotometrically at 600 nm. The assay is quick, uses a minimal sample volume (<5 μl), can simultaneously test a range of alternative substrates, and permits activity measurements on multiple samples. We demonstrate the accuracy and versatility of the microtiter plate assay by application to the kinetic analysis, inhibition, and pH optimization of the membrane-bound selenate reductase from E. cloacae SLD1a-1. Results show that the membrane-bound selenate reductase has optimum activity at pH ∼ 8 and its active site is able to accommodate larger inhibitory complexes resulting in mixed-type inhibition, in the presence of selenate and potassium thiocyanate. © 2006 Elsevier Inc. All rights reserved.

Publication metadata

Author(s): Ridley H, Watts CA, Richardson DJ, Butler CS

Publication type: Article

Publication status: Published

Journal: Analytical Biochemistry

Year: 2006

Volume: 358

Issue: 2

Pages: 289-294

ISSN (print): 0003-2697

ISSN (electronic): 1096-0309

Publisher: Academic Press


DOI: 10.1016/j.ab.2006.08.028


Altmetrics provided by Altmetric