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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
Sridhar ,
G. Sridhar
Prasad ,
C. David
Stout , 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 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.

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Copyright © 1998 by the American Society for Biochemistry and Molecular Biology.
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