Abstract

Haïtham Sghaier*, Katsuya Satoh, Hirofumi Ohba and Issay Narumi

The moderately thermophilic bacterium Deinococcus geothermalis exhibits extraordinary resistance to ionizing radiation. RecA protein is considered to be one of the most important participants in radioresistance. To assess the role of the RecA protein in D. geothermalis, the recA gene was isolated from D. geothermalis and over expressed in Escherichia coli. After the D. geothermalis RecA protein (GeoRecA) was purified, the recombination activity was investigated in vitro. GeoRecA efficiently promoted the strand exchange reaction between homologous linear double-stranded DNA and circular single-stranded DNA substrates at 50°C. Like Deinococcus radiodurans RecA protein (DraRecA), GeoRecA could promote DNA strand exchange reaction through normal and inverse pathways. Furthermore, GeoRecA complemented the RecA deficiency of D. radiodurans. These results indicate that GeoRecA is a functional homologue of DraRecA and plays an important role in radioresistance. However, unlike DraRecA, GeoRecA could not complement the RecA deficiency of E. coli, suggesting that GeoRecA require more strict intracellular conditions than DraRecA does to fulfill its function. This study provides new insights into the role of deinococcal RecA protein in radioresistance.