Advertisement
JBC

HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow Submit a Letter to Editor
Right arrow Alert me when this article is cited
Right arrow Alert me when eLetters are posted
Right arrow Alert me if a correction is posted
Right arrow Citation Map
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrowRequest Permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Gao-Sheridan, H. S.
Right arrow Articles by Burgess, B. K.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Gao-Sheridan, H. S.
Right arrow Articles by Burgess, B. K.
Social Bookmarking
 Add to CiteULike   Add to Complore   Add to Connotea   Add to Del.icio.us   Add to Digg   Add to Reddit   Add to Technorati  
What's this?

J Biol Chem, Vol. 273, Issue 50, 33692-33701, December 11, 1998

A T14C Variant of Azotobacter vinelandii Ferredoxin I Undergoes Facile [3Fe-4S]0 to [4Fe-4S]2+ Conversion in Vitro but Not in Vivo

H. Samantha Gao-Sheridan, Mary A. Kemper§, Reza Khayat§, Gareth J. Tilley, Fraser A. Armstrong, Vandana Sridharparallel , G. Sridhar Prasadparallel , C. David Stoutparallel , and Barbara K. Burgess§

From the § Department of Molecular Biology and Biochemistry, University of California, Irvine, California 92697-3900, the  Department of Chemistry, Oxford University, Oxford OX1 3QR, United Kingdom, and the parallel  Department of Molecular Biology, The Scripps Research Institute, La Jolla, California 92037

[4Fe-4S]2+/+ clusters that are ligated by Cys-X-X-Cys-X-X-Cys sequence motifs share the general feature of being hard to convert to [3Fe-4S]+/0 clusters, whereas those that contain a Cys-X-X-Asp-X-X-Cys motif undergo facile and reversible cluster interconversion. Little is known about the factors that control the in vivo assembly and conversion of these clusters. In this study we have designed and constructed a 3Fe to 4Fe cluster conversion variant of Azotobacter vinelandii ferredoxin I (FdI) in which the sequence that ligates the [3Fe-4S] cluster in native FdI was altered by converting a nearby residue, Thr-14, to Cys. Spectroscopic and electrochemical characterization shows that when purified in the presence of dithionite, T14C FdI is an O2-sensitive 8Fe protein. Both the new and the indigenous clusters have reduction potentials that are significantly shifted compared with those in native FdI, strongly suggesting a significantly altered environment around the clusters. Interestingly, whole cell EPR have revealed that T14C FdI exists as a 7Fe protein in vivo. This 7Fe form of T14C FdI is extremely similar to native FdI in its spectroscopic, electrochemical, and structural features. However, unlike native FdI which does not undergo facile cluster conversion, the 7Fe form T14C FdI quickly converts to the 8Fe form with a high efficiency under reducing conditions.


Copyright © 1998 by The American Society for Biochemistry and Molecular Biology, Inc.
Add to CiteULike CiteULike   Add to Complore Complore   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us   Add to Digg Digg   Add to Reddit Reddit   Add to Technorati Technorati    What's this?


This article has been cited by other articles:


Home page
Proc. Natl. Acad. Sci. USAHome page
J. C. Crack, J. Green, M. R. Cheesman, N. E. Le Brun, and A. J. Thomson
Superoxide-mediated amplification of the oxygen-induced switch from [4Fe-4S] to [2Fe-2S] clusters in the transcriptional regulator FNR
PNAS, February 13, 2007; 104(7): 2092 - 2097.
[Abstract] [Full Text] [PDF]


Home page
J. Biol. Chem.Home page
A. Liu and A. Graslund
Electron Paramagnetic Resonance Evidence for a Novel Interconversion of [3Fe-4S]+ and [4Fe-4S]+ Clusters with Endogenous Iron and Sulfide in Anaerobic Ribonucleotide Reductase Activase in Vitro
J. Biol. Chem., April 21, 2000; 275(17): 12367 - 12373.
[Abstract] [Full Text] [PDF]


Home page
J. Biol. Chem.Home page
K. Chen, G. J. Tilley, V. Sridhar, G. S. Prasad, C. D. Stout, F. A. Armstrong, and B. K. Burgess
Alteration of the Reduction Potential of the [4Fe-4S]2+/+ Cluster of Azotobacter vinelandii Ferredoxin I
J. Biol. Chem., December 17, 1999; 274(51): 36479 - 36487.
[Abstract] [Full Text] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 All ASBMB Journals   Molecular and Cellular Proteomics 
 Journal of Lipid Research   ASBMB Today 
Copyright © 1998 by the American Society for Biochemistry and Molecular Biology.
Advertisement
spacer
Advertisement
Advertisement