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J. Biol. Chem., Vol. 265, Issue 22, 12761-12762, Aug, 1990
L Mauch, V Bichler and R Brandsch
The requirements for FAD-attachment to His71 of 6-hydroxy-D-nicotine
oxidase (6-HDNO) were investigated by site-directed mutagenesis. The
following amino acid replacements were introduced into the sequence
Arg67-Ser68-Gly69-Gly70-His71 of the 6-HDNO-polypeptide: 1) Arg67 was
replaced with Ala (A1 mutant); 2) Ser68 was replaced with Ala (A2 mutant);
and 3) Arg67 was replaced with Lys (K mutant). The substitution in mutant
A2 had no effect on flavinylation, measured as [14C]FAD incorporation into
apo-6-HDNO. Replacement of Arg67 with Ala prevented, but replacement with
Lys permitted the flavinylation of His71. Mutant A1 showed no 6-HDNO
activity, whereas the replacement of Ser with Ala in mutant A2 had only a
slight effect on 6-HDNO activity. The substitution of Lys for Arg67,
however, reduced the specific 6-HDNO activity in extracts of Escherichia
coli cells expressing the mutant polypeptide from 50.3 to 17.5
milliunits/mg protein. It is concluded that a basic amino acid residue
(Arg67 or Lys67) is required to mediate the attachment of FAD to His71, and
while Lys can substitute for Arg67 in this function, it can only partially
replace Arg67 in the enzyme reaction mechanism of 6-HDNO.
Lysine can replace arginine 67 in the mediation of covalent attachment of FAD to histidine 71 of 6-hydroxy-D-nicotine oxidase
Biochemisches Institut, Universitat Freiburg, Federal Republic of Germany.
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