Differential effects of bromination on substrates and inhibitors of kynureninase from Pseudomonas fluorescens

Organic & Biomolecular Chemistry Pub Date: 2002-12-09 DOI: 10.1039/B208910F

Abstract

A series of brominated compounds has been synthesized and evaluated as substrates and inhibitors of kynureninase from Pseudomonas fluorescens. Both 3-bromo-L-kynurenine and 5-bromo-L-kynurenine were found to be substrates with similar kcat values to L-kynurenine, but the Km value for 3-bromo-L-kynurenine is very high (ca. 2 mM) compared to that for 5-bromo-L-kynurenine (11 μM) and L-kynurenine (25 μM). Both isomers of bromokynurenine react with kynureninase within the dead time of the stopped-flow instrument (ca. 1 ms) to form quinonoid intermediates with a λmax of 494 nm that decay with rate constants of 300–600 s?1, similar to L-kynurenine. The two diastereomers of 5-bromodihydro-L-kynurenine were also prepared, and are more potent inhibitors than dihydro-L-kynurenines. (4R)-5-Bromodihydro-L-kynurenine is one of the most potent inhibitors of P. fluorescens kynureninase found to date (Ki = 55 nM) and also acts as a slow substrate; the (4S)-epimer, on the other hand, shows no measurable substrate activity, but it is a potent competitive inhibitor with a Ki value of 170 nM. In contrast, brominated analogs of (S)-(2-aminophenyl)-L-cysteine S,S-dioxide, (S)-(2-amino-4-bromophenyl)-L-cysteine S,S-dioxide and (S)-(2-amino-5-bromophenyl)-L-cysteine S,S-dioxide are competitive inhibitors of kynureninase, with Ki values of about 300 and 400 nm, respectively, about ten-fold higher than the value of 27 nM obtained for the parent compound. These results suggest that the binding modes of substrates and the various classes of inhibitors in the active site of kynureninase are different.

Graphical abstract: Differential effects of bromination on substrates and inhibitors of kynureninase from Pseudomonas fluorescens
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