The dual-specific active site of 7,8-diaminopelargonic acid synthase and the effect of the R391A mutation.

Abstract:

:7,8-diaminopelargonic acid (DAPA) synthase (EC 2.6.1.62) is a pyridoxal phosphate (PLP)-dependent transaminase that catalyzes the transfer of the alpha-amino group from S-adenosyl-L-methionine (SAM) to 7-keto-8-aminopelargonic acid (KAPA) to form DAPA in the antepenultimate step in the biosynthesis of biotin. The wild-type enzyme has a steady-state kcat value of 0.013 s(-1), and the K(m) values for SAM and KAPA are 150 and <2 microM, respectively. The k(max) and apparent K(m) values for the half-reaction of the PLP form of the enzyme with SAM are 0.016 s(-1) and 300 microM, respectively, while those for the reaction with DAPA are 0.79 s(-1) and 1 microM. The R391A mutant enzyme exhibits near wild-type kinetic parameters in the reaction with SAM, while the apparent K(m) for DAPA is increased 180-fold. The 2.1 A crystal structure of the R391A mutant enzyme shows that the mutation does not significantly alter the structure. These results indicate that the conserved arginine residue is not required for binding the alpha-amino acid SAM, but it is important for recognition of DAPA.

journal_name

Biochemistry

journal_title

Biochemistry

authors

Eliot AC,Sandmark J,Schneider G,Kirsch JF

doi

10.1021/bi026339a

subject

Has Abstract

pub_date

2002-10-22 00:00:00

pages

12582-9

issue

42

eissn

0006-2960

issn

1520-4995

pii

bi026339a

journal_volume

41

pub_type

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