The archaea which populate geothermal environments are adapted to conditions that should greatly destabilize the primary structure of DNA, yet the basic biological aspects of DNA damage and repair remain unexplored for this group of prokaryotes. We used auxotrophic mutants of the extremely thermoacidophilic archaeon Sulfolobus acidocaldarius to assess genetic and physiological effects of a well-characterized DNAdamaging agent, short-wavelength UV light. Simple genetic assays enabled quantitative dose-response relationships to be determined and correlated for survival, phenotypic reversion, and the formation of genetic recombinants. Dose-response relationships were also determined for survival and phenotypic reversion of the corresponding Escherichia coli auxotrophs with the same equipment and procedures. The results showed S. acidocaldarius to be about twice as UV sensitive as E. coli and to be equally UV mutable on a surviving-cell basis. Furthermore, UV irradiation significantly increased the frequency of recombinants recovered from geneticexchange assays of S. acidocaldarius. The observed UV effects were due to the short-wavelength (i.e., UV-C) portion of the spectrum and were effectively reversed by subsequent illumination of S. acidocaldarius cells with visible light (photoreactivation). Thus, the observed responses are probably initiated by the formation of pyrimidine dimers in the S. acidocaldarius chromosome. To our knowledge, these results provide the first evidence of error-prone DNA repair and genetic recombination induced by DNA damage in an archaeon from geothermal habitats.

Exchange and recombination of chromosomal markers is an intrinsic genetic property of the thermoacidophilic archaeon Sulfolobus acidocaldarius that has not been thoroughly characterized. T o clarify the mechanism and experimental usefulness of this process, the frequency of 5. acidocaldarius prototrophs produced from mixtures of two pyrimidine auxotrophs under a variety of conditions was determined. The apparent efficiency of genetic exchange was essentially independent of the density of cells deposited on the surface of solid media. Furthermore, recombinant formation could initiate in liquid suspensions, as indieated by high recombinant frequencies resulting from mixtures plated at low cell densities, and the formation of recombinants a t equal or higher frequencies in liquid suspensions that were never plated. Apparent initiation of genetic exchange in liquid a t 22 "C was not prevented by DNase, prior digestion of parental cells with protease from Streptomyces griseus, or any other non-lethal chemical agent tested. The results support prior indications that chromosomal marker exchange in S. acidocaldarius proceeds via conjugation, and further indicate that this conjugation can initiate quickly in dilute liquid suspension. The mating system of S. acidocaldarius thus appears physiologically distinct from that of Haloferax volcanii but perhaps similar to conjugational transfer of Sulfolobus plasmid pNOB8. The frequency of recombinants formed in these assays (10'4-10'5 per c.f.u.) greatly exceeds the number of spontaneous forward mutational events per generation for biosynthetic genes in S. acidocaldarius. This suggests that chromosomal exchange has the potential to influence the genetic dynamics of natural Sulfolobus populations.

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