Abstract

The cysteine desulfurase enzymes NifS and IscS provide sulfur for the biosynthesis of Fe/S proteins. NifU and IscU have been proposed to serve as template or scaffold proteins in the initial Fe/S cluster assembly events, but the mechanism of sulfur transfer from NifS or IscS to NifU or IscU has not been elucidated. We have employed [(35)S]cysteine radiotracer studies to monitor sulfur transfer between IscS and IscU from Escherichia coli and have used direct binding measurements to investigate interactions between the proteins. IscS catalyzed transfer of (35)S from [(35)S]cysteine to IscU in the absence of additional thiol reagents, suggesting that transfer can occur directly and without involvement of an intermediate carrier. Surface plasmon resonance studies and isothermal titration calorimetry measurements further revealed that IscU binds to IscS with high affinity (K(d) approximately 2 microm) in support of a direct transfer mechanism. Transfer was inhibited by treatment of IscU with iodoacetamide, and (35)S was released by reducing reagents, suggesting that transfer of persulfide sulfur occurs to cysteinyl groups of IscU. A deletion mutant of IscS lacking C-terminal residues 376-413 (IscSDelta376-413) displayed cysteine desulfurase activity similar to the full-length protein but exhibited lower binding affinity for IscU, decreased ability to transfer (35)S to IscU, and reduced activity in assays of Fe/S cluster assembly on IscU. The findings with IscSDelta376-413 provide additional support for a mechanism of sulfur transfer involving a direct interaction between IscS and IscU and suggest that the C-terminal region of IscS may be important for binding IscU.

Highlights

  • Cysteine desulfurase enzymes play important roles in biological sulfur mobilization and provide inorganic sulfur for incorporation into Fe/S proteins

  • Previous studies have shown that the cysteine desulfurase enzymes NifS and IscS can provide sulfur for assembly of Fe/S proteins, but the mechanism of sulfur transfer to the acceptor proteins was not determined

  • By employing 35S-labeled cysteine, we were able to measure sulfur transfer independent of Fe/S protein formation and avoid the use of added reducing reagents required for Fe/S cluster assembly

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Summary

Introduction

Cysteine desulfurase enzymes play important roles in biological sulfur mobilization and provide inorganic sulfur for incorporation into Fe/S proteins. The peptide region containing the cysteine residue presumed to be involved in sulfur transfer was disordered and could not be resolved in the crystal structure, and it was suggested that this may reflect the requirement for this segment to be flexible in order to both accept sulfur at the active site and transfer it to acceptor proteins [16]. Evidence is presented that complex formation is mediated in part by a region of IscS not required for cysteine desulfurase activity and that this region is required for efficient Fe/S cluster formation

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