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J. Biol. Chem., Vol. 276, Issue 44, 40457-40463, November 2, 2001
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From the Department of Molecular Biology and Functional Genomics,
Stockholm University, SE-10691 Stockholm, Sweden
Class III ribonucleotide reductase is
an anaerobic enzyme that uses a glycyl radical to catalyze the
reduction of ribonucleotides to deoxyribonucleotides and formate as
ultimate reductant. The reaction mechanism of class III ribonucleotide
reductases requires two cysteines within the active site, Cys-79 and
Cys-290 in bacteriophage T4 NrdD numbering. Cys-290 is believed to
form a transient thiyl radical that initiates the reaction with
substrate and Cys-79 to take part as a transient thiyl radical in later
steps of the reductive reaction. The recently solved three-dimensional
structure of class III ribonucleotide reductase (RNR) from
bacteriophage T4 shows that two highly conserved asparagines, Asn-78
and Asn-311, are positioned close to the essential Cys-79. We have
investigated the function of Asn-78 and Asn-311 by site-directed
mutagenesis and measured enzyme activity and glycyl radical formation
in five single (N78(A/C/D) and N311(A/C)) and one double (N78A/N311A) mutant proteins. Our results suggest that both asparagines are important for the catalytic mechanism of class III RNR and that one
asparagine can partially compensate for the lack of the other functional group in the single Asn
Two Active Site Asparagines Are Essential for the Reaction
Mechanism of the Class III Anaerobic Ribonucleotide Reductase from
Bacteriophage T4*
§,
,
Ala mutant proteins. A
plausible role for these two asparagines could be in positioning
formate in the active site to orient it toward the proposed thiyl
radical of Cys-79. This would also control the highly reactive carbon dioxide radical anion form of formate within the active site before it
is released as carbon dioxide. A detailed reaction scheme including the
function of the two asparagines and two formate molecules is proposed
for class III RNRs.
*
The costs of publication of this
article were defrayed in part by the
payment of page charges. The article
must therefore be hereby marked
"advertisement" in
accordance with 18 U.S.C. Section
1734 solely to indicate this fact.
These authors have contributed equally to this work.
§
Present address: Dept. of Biological Chemistry and Molecular
Pharmacology, Harvard Medical School, 240 Longwood Ave., Boston, MA 02115.
¶
To whom correspondence should be addressed. Tel.: 46-8-164150;
Fax: 46-8-152350; E-mail: bitte@molbio.su.se.
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