Literature DB >> 16592130

Low Temperature Electronic Absorption Spectra of Oxidized and Reduced Spinach Ferredoxins. Evidence for Nonequivalent Iron(III) Sites.

J Rawlings1, O Siiman, H B Gray.   

Abstract

The electronic absorption spectra of oxidized and reduced spinach ferredoxins have been measured between 1200 and 600 nm at low temperature in D(2)O/ethylene glycol glasses. Relatively weak absorption bands are observed at 720, 820, and 920 nm in oxidized ferredoxin, and at 652, 820, and 920 nm in reduced ferredoxin. The spectral results show that the two Fe(III) centers in oxidized ferredoxin are not equivalent, and that the 820- and 920-nm bands are associated with the nonreducible site. Assignment of the reducible site as tetrahedral Fe(III) is indicated. The 720-nm (13.9 kcm(-1)) band in oxidized ferredoxin is attributed to an intensity-enhanced (6)A(1) --> (4)T(1)d-d transition, whereas the 652-nm (15.3 kcm(-1)) feature of reduced ferredoxin could be due either to (5)E --> (3)T(1) in tetrahedral Fe(II)S(4) or an Fe(II) --> Fe(III) intervalence excitation.

Entities:  

Year:  1974        PMID: 16592130      PMCID: PMC387948          DOI: 10.1073/pnas.71.1.125

Source DB:  PubMed          Journal:  Proc Natl Acad Sci U S A        ISSN: 0027-8424            Impact factor:   11.205


  10 in total

1.  The two-iron ferredoxins in spinach, parsley, pig adrenal cortex, Azotobacter vinelandii, and Clostridium pasteurianum: studies by magnetic field Mössbauer spectroscopy.

Authors:  W R Dunham; A J Bearden; I T Salmeen; G Palmer; R H Sands; W H Orme-Johnson; H Beinert
Journal:  Biochim Biophys Acta       Date:  1971-11-02

2.  On the structure of the iron-sulfur complex in the two-iron ferredoxins.

Authors:  W R Dunham; G Palmer; R H Sands; A J Bearden
Journal:  Biochim Biophys Acta       Date:  1971-12-07

3.  The iron electron-nuclear double resonance (ENDOR) of two-iron ferredoxins from spinach, parsley, pig adrenal cortex and Pseudomonas putida.

Authors:  J Fritz; R Anderson; J Fee; G Palmer; R H Sands; J C Tsibris; I C Gunsalus; W H Orme-Johnson; H Beinert
Journal:  Biochim Biophys Acta       Date:  1971-11-02

4.  Properties of spinach ferredoxin in anaerobic urea solution: a comparison with the native protein.

Authors:  D H Petering; G Palmer
Journal:  Arch Biochem Biophys       Date:  1970-12       Impact factor: 4.013

5.  The magnetic susceptibility of spinach ferredoxin from 77-250 degrees K: a measurement of the antiferromagnetic coupling between the two iron atoms.

Authors:  G Palmer; W R Dunham; J A Fee; R H Sands; T Iizuka; T Yonetani
Journal:  Biochim Biophys Acta       Date:  1971-08-06

6.  Proton magnetic resonance, magnetic susceptibility and Mössbauer studies of Clostridium pasteurianum rubredoxin.

Authors:  W D Phillips; M Poe; J F Weiher; C C McDonald; W Lovenberg
Journal:  Nature       Date:  1970-08-08       Impact factor: 49.962

7.  Structure of rubredoxin: an x-ray study to 2.5 A resolution.

Authors:  J R Herriott; L C Sieker; L H Jensen; W Lovenberg
Journal:  J Mol Biol       Date:  1970-06-14       Impact factor: 5.469

8.  Near-infrared circular dichroism of an iron-sulfur protein. D leads to d transitions in rubredoxin.

Authors:  W A Eaton; W Lovenberg
Journal:  J Am Chem Soc       Date:  1970-12-02       Impact factor: 15.419

9.  The near infra-red electronic spectra of non-heme iron proteins at minus 196 degrees.

Authors:  D F Wilson
Journal:  Arch Biochem Biophys       Date:  1967-10       Impact factor: 4.013

10.  Mössbauer effect in Scenedesmus and spinach ferredoxins. The mechanism of electron transfer in plant-type iron-sulphur proteins.

Authors:  K K Rao; R Cammack; D O Hall; C E Johnson
Journal:  Biochem J       Date:  1971-04       Impact factor: 3.857

  10 in total
  2 in total

1.  Near-infrared in vitro measurements of photosystem I cofactors and electron-transfer partners with a recently developed spectrophotometer.

Authors:  Pierre Sétif; Alain Boussac; Anja Krieger-Liszkay
Journal:  Photosynth Res       Date:  2019-09-03       Impact factor: 3.573

2.  Escherichia coli RIC is able to donate iron to iron-sulfur clusters.

Authors:  Lígia S Nobre; Ricardo Garcia-Serres; Smilja Todorovic; Peter Hildebrandt; Miguel Teixeira; Jean-Marc Latour; Lígia M Saraiva
Journal:  PLoS One       Date:  2014-04-16       Impact factor: 3.240

  2 in total

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