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Org Lett ; 21(2): 498-502, 2019 01 18.
Article in English | MEDLINE | ID: mdl-30601016

ABSTRACT

Nonribosomal peptide synthetase (NRPS)-like enzymes comprising A-T-TE architectures catalyze the dimerization of α-keto carboxylic acids leading to the formation of hydroxybenzoquinones or lactones. Domain change experiments with five enzymes revealed that A and A-T domains of phenyl or 4-hydroxyphenyl pyruvate-using enzymes can be effectively used by the TE domains of other enzymes. Even the A and A-T domains of an indolyl hydroxybenzoquinone synthase were successfully recombined with TE domains of a phenyl and a 4-hydroxyphenyl pyruvate-activating enzyme.


Subject(s)
Keto Acids/chemical synthesis , Lactones/chemistry , Peptide Synthases/chemistry , Catalysis , Dimerization , Keto Acids/chemistry , Molecular Structure , Recombination, Genetic
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