Organic Letters · 2019 · 54 citations · 27 references
Life SciencesBiochemistryMolecular BiologyEnzyme TechnologyEnzymologyProtein EngineeringCatalytic MechanismsEnzyme FunctionNonribosomal Peptide BiosynthesisCatalytic DomainsEnzymatic Reaction MechanismsEnzyme Domain RecombinationEnzyme Reaction MechanismsNonribosomal Peptide Synthetase ArchitectureNonribosomal Peptides
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.
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