Literature DB >> 21405124

Electron transfer reactivity of type zero Pseudomonas aeruginosa azurin.

Kyle M Lancaster1, Ole Farver, Scot Wherland, Edward J Crane, John H Richards, Israel Pecht, Harry B Gray.   

Abstract

Type zero copper is a hard-ligand analogue of the classical type 1 or blue site in copper proteins that function as electron transfer (ET) agents in photosynthesis and other biological processes. The EPR spectroscopic features of type zero Cu(II) are very similar to those of blue copper, although lacking the deep blue color, due to the absence of thiolate ligation. We have measured the rates of intramolecular ET from the pulse radiolytically generated C3-C26 disulfide radical anion to the Cu(II) in both type zero C112D/M121L and type 2 C112D Pseudomonas aeruginosa azurins in pH 7.0 aqueous solutions between 8 and 45 °C. We also have obtained rate/temperature (10-30 °C) profiles for ET reactions between these mutants and the wild-type azurin. Analysis of the rates and activation parameters for both intramolecular and intermolecular ET reactions indicates that the type zero copper reorganization energy falls in a range (0.9-1.1 eV) slightly above that for type 1 (0.7-0.8 eV), but substantially smaller than that for type 2 (>2 eV), consistent with XAS and EXAFS data that reveal minimal type zero site reorientation during redox cycling.
© 2011 American Chemical Society

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Year:  2011        PMID: 21405124      PMCID: PMC3607328          DOI: 10.1021/ja1093919

Source DB:  PubMed          Journal:  J Am Chem Soc        ISSN: 0002-7863            Impact factor:   15.419


  30 in total

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Authors:  P Rosen; I Pecht
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2.  Crystal structure and electron transfer kinetics of CueO, a multicopper oxidase required for copper homeostasis in Escherichia coli.

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Journal:  Proc Natl Acad Sci U S A       Date:  2002-02-26       Impact factor: 11.205

3.  X-ray Absorption Spectra of the Oxidized and Reduced Forms of C112D Azurin from Pseudomonas aeruginosa.

Authors:  Serena DeBeer; Cynthia N. Kiser; Gary A. Mines; John H. Richards; Harry B. Gray; Edward I. Solomon; Britt Hedman; Keith O. Hodgson
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4.  Effects of folding on metalloprotein active sites.

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5.  The role of hydrogen bonding at the active site of a cupredoxin: the Phe114Pro azurin variant.

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6.  Plastocyanin is indispensable for photosynthetic electron flow in Arabidopsis thaliana.

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Authors:  B G Malmström
Journal:  Eur J Biochem       Date:  1994-08-01

8.  The introduction of a negative charge into the hydrophobic patch of Pseudomonas aeruginosa azurin affects the electron self-exchange rate and the electrochemistry.

Authors:  G Van Pouderoyen; S Mazumdar; N I Hunt; A O Hill; G W Canters
Journal:  Eur J Biochem       Date:  1994-06-01

9.  Electronic structure contributions to function in bioinorganic chemistry.

Authors:  E I Solomon; M D Lowery
Journal:  Science       Date:  1993-03-12       Impact factor: 47.728

10.  The 2.3 angstrom X-ray structure of nitrite reductase from Achromobacter cycloclastes.

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  19 in total

1.  Flexibility of the metal-binding region in apo-cupredoxins.

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2.  Design of a single protein that spans the entire 2-V range of physiological redox potentials.

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3.  Designed azurins show lower reorganization free energies for intraprotein electron transfer.

Authors:  Ole Farver; Nicholas M Marshall; Scot Wherland; Yi Lu; Israel Pecht
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4.  Tryptophan-to-heme electron transfer in ferrous myoglobins.

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5.  Catalysis of dioxygen reduction by Thermus thermophilus strain HB27 laccase on ketjen black electrodes.

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6.  Molecular dynamics simulations of apocupredoxins: insights into the formation and stabilization of copper sites under entatic control.

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Review 7.  Protein design: toward functional metalloenzymes.

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Review 8.  Metalloproteins containing cytochrome, iron-sulfur, or copper redox centers.

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9.  Spin delocalization over type zero copper.

Authors:  Alexey Potapov; Kyle M Lancaster; John H Richards; Harry B Gray; Daniella Goldfarb
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10.  Photogeneration and Quenching of Tryptophan Radical in Azurin.

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Journal:  J Phys Chem B       Date:  2015-02-17       Impact factor: 2.991

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