z-logo
Premium
Characterization of a dual specificity aryl acid adenylation enzyme with dual function in nikkomycin biosynthesis
Author(s) -
Moon Mary,
Van Lanen Steven G.
Publication year - 2010
Publication title -
biopolymers
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.556
H-Index - 125
eISSN - 1097-0282
pISSN - 0006-3525
DOI - 10.1002/bip.21479
Subject(s) - chemistry , adenylylation , thioester , dipeptide , stereochemistry , biosynthesis , decarboxylation , aldolase a , amino acid , biochemistry , enzyme , catalysis
Nikkomycin Z is a dipeptide antifungal antibiotic characterized by two nonproteinogenic amino acids, nikkomycin C Z and 4‐(4′‐hydroxy‐2′‐pyridinyl)‐homothreonine (HPHT). The HPHT scaffold is assembled by an aldol reaction between 2‐oxobutyrate and picolinaldehyde, the latter of which is derived from picolinic acid that is activated and loaded to coenzyme A by the aryl‐activating adenylation enzyme, NikE. We now provide evidence that NikE is also involved in the activation and loading of the α‐keto acid precursor, 4‐(2′‐pyridinyl)‐2‐oxo‐4‐hydroxyisovalerate (POHIV), to a phosphopantetheinyl group of an acyl carrier protein domain of NikT. POHIV was synthesized using Escherichia coli 2‐dehydro‐3‐deoxy‐phosphogluconate aldolase, and phenylalanine dehydrogenase from Bacillus sp. NRRL B‐14911 was used to prepare the α‐amino acid, 4‐(2′‐pyridinyl)‐homothreonine (PHT). Using the carboxylic acid‐dependent, ATP‐[ 32 P]PP i exchange assay, NikE is shown to activate both picolinic acid and POHIV but not PHT. Furthermore, NikE loads POHIV to holo‐NikT to generate a new thioester‐linked intermediate, which was not observed using a NikT(S33A) mutant. Thus, NikE activates two distinct carboxylic acids to form two new thioester intermediates, one of which is subsequently reduced to the aldehyde and the other that likely serves as a substrate for the aminotransferase domain of NikT prior to condensation with nikkomycin C Z to yield the dipeptide. © 2010 Wiley Periodicals, Inc. Biopolymers 93: 791–801, 2010.

This content is not available in your region!

Continue researching here.

Having issues? You can contact us here