Abstract

A multitude of biological functions relies on iron-sulfur clusters. The formation of photosynthetic complexes goes along with an additional demand for iron-sulfur clusters for bacteriochlorophyll synthesis and photosynthetic electron transport. However, photooxidative stress leads to the destruction of iron-sulfur clusters, and the released iron promotes the formation of further reactive oxygen species. A balanced regulation of iron-sulfur cluster synthesis is required to guarantee the supply of this cofactor, on the one hand, but also to limit stress, on the other hand. The phototrophic alpha-proteobacterium Rhodobacter sphaeroides harbors a large operon for iron-sulfur cluster assembly comprising the iscRS and suf genes. IscR (iron-sulfur cluster regulator) is an iron-dependent regulator of isc-suf genes and other genes with a role in iron metabolism. We applied reporter gene fusions to identify promoters of the isc-suf operon and studied their activity alone or in combination under different conditions. Gel-retardation assays showed the binding of regulatory proteins to individual promoters. Our results demonstrated that several promoters in a sense and antisense direction influenced isc-suf expression and the binding of the IscR, Irr, and OxyR regulatory proteins to individual promoters. These findings demonstrated a complex regulatory network of several promoters and regulatory proteins that helped to adjust iron-sulfur cluster assembly to changing conditions in Rhodobacter sphaeroides.

Highlights

  • Proteins containing iron-sulfur (Fe-S) clusters are present in almost all living organisms

  • Organisms have to develop multicomponent systems that promote the biogenesis of Fe-S proteins while protecting the cellular surrounding from the deleterious effects of free iron

  • Prediction of Promoters for the isc-suf Operon of R. sphaeroides Based on dRNA-Seq Analysis

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Summary

Introduction

Proteins containing iron-sulfur (Fe-S) clusters are present in almost all living organisms. They have diverse and often essential functions, for example, electron carriers in redox reactions, in redox sensing, oxidative stress defense, biosynthesis of metal-containing cofactors, DNA replication and repair, regulation of gene expression, and tRNA modification. With the appearance of oxygenic photosynthesis, increasing oxygen levels drastically decrease iron availability [3]. Different reactive oxygen species (ROS) appear, which are very harmful to living cells since they can damage proteins, lipids, and nucleic acids. Molecular oxygen and ROS destabilize Fe-S clusters, leading to the release of Fe2+ ions that, in turn, potentiate oxygen toxicity by the production of hydroxyl radicals in the Fenton reaction [4]. Organisms have to develop multicomponent systems that promote the biogenesis of Fe-S proteins while protecting the cellular surrounding from the deleterious effects of free iron

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