CloR, a bifunctional non-heme iron oxygenase involved in clorobiocin biosynthesis.

J Biol Chem

Universität Tübingen, Pharmazeutische Biologie, Auf der Morgenstelle 8, 72076 Tübingen, Germany.

Published: August 2003

AI Article Synopsis

  • The aminocoumarin antibiotics novobiocin and clorobiocin have a specific structural component called 3-dimethylallyl-4-hydroxybenzoate (3DMA-4HB), whose biosynthesis had been investigated.
  • The enzyme CloQ, identified in the clorobiocin biosynthetic gene cluster, works as a transferase, while CloR is characterized as a bifunctional enzyme that catalyzes the conversion of key intermediates through oxidative decarboxylation.
  • Distinct from known oxygenases, CloR introduces a new mechanism in the formation of benzoic acids, incorporating oxygen in a unique way during its biochemical reactions.

Article Abstract

The aminocoumarin antibiotics novobiocin and clorobiocin contain a 3-dimethylallyl-4-hydroxybenzoate (3DMA-4HB) moiety. The biosynthesis of this moiety has now been identified by biochemical and molecular biological studies. CloQ from the clorobiocin biosynthetic gene cluster in Streptomyces roseochromogenes DS 12976 has recently been identified as a 4-hydroxyphenylpyruvate-3-dimethylallyltransferase. In the present study, the enzyme CloR was overexpressed in Escherichia coli, purified, and identified as a bifunctional non-heme iron oxygenase, which converts 3-dimethylallyl-4-hydroxyphenylpyruvate (3DMA-4HPP) via 3-dimethylallyl-4-hydroxymandelic acid (3DMA-4HMA) to 3DMA-4HB by two consecutive oxidative decarboxylation steps. In 18O2 labeling experiments we showed that two oxygen atoms are incorporated into the intermediate 3DMA-4HMA in the first reaction step, but only one further oxygen is incorporated into the final product 3DMA-4HB during the second reaction step. CloR does not show sequence similarity to known oxygenases. It apparently presents a novel member of the diverse family of the non-heme iron (II) and alpha-ketoacid-dependent oxygenases, with 3DMA-4HPP functioning both as an alpha-keto acid and as a hydroxylation substrate. The reaction catalyzed by CloR represents a new pathway for the formation of benzoic acids in nature.

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http://dx.doi.org/10.1074/jbc.M303190200DOI Listing

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