Abstract
Aerobic and microaerophilic subsurface bacteria were screened for resistance to UV light. Contrary to the hypothesis that subsurface bacteria should be sensitive to UV light, the organisms studied exhibited resistance levels as efficient as those of surface bacteria. A total of 31% of the aerobic subsurface isolates were UV resistant, compared with 26% of the surface soil bacteria that were tested. Several aerobic, gram-positive, pigmented, subsurface isolates exhibited greater resistance to UV light than all of the reference bacterial strains tested except Deinococcus radiodurans. None of the microaerophilic, gram-negative, nonpigmented, subsurface isolates were UV resistant; however, these isolates exhibited levels of sensitivity similar to those of the gram-negative reference bacteria Escherichia coli B and Pseudomonas fluorescens. Photoreactivation activity was detected in three subsurface isolates, and strain UV3 exhibited a more efficient mechanism than E. coli B. The peroxide resistance of four subsurface isolates was also examined. The aerobic subsurface bacteria resistant to UV light tolerated higher levels of H2O2 than the microaerophilic organisms. The conservation of DNA repair pathways in subsurface microorganisms may be important in maintaining DNA integrity and in protecting the organisms against chemical insults, such as oxygen radicals, during periods of slow growth.
Full text
PDF





Selected References
These references are in PubMed. This may not be the complete list of references from this article.
- Antopol S. C., Ellner P. D. Susceptibility of Legionella pneumophila to ultraviolet radiation. Appl Environ Microbiol. 1979 Aug;38(2):347–348. doi: 10.1128/aem.38.2.347-348.1979. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Balkwill D. L., Fredrickson J. K., Thomas J. M. Vertical and horizontal variations in the physiological diversity of the aerobic chemoheterotrophic bacterial microflora in deep southeast coastal plain subsurface sediments. Appl Environ Microbiol. 1989 May;55(5):1058–1065. doi: 10.1128/aem.55.5.1058-1065.1989. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Balkwill D. L., Ghiorse W. C. Characterization of subsurface bacteria associated with two shallow aquifers in oklahoma. Appl Environ Microbiol. 1985 Sep;50(3):580–588. doi: 10.1128/aem.50.3.580-588.1985. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Butler R. C., Lund V., Carlson D. A. Susceptibility of Campylobacter jejuni and Yersinia enterocolitica to UV radiation. Appl Environ Microbiol. 1987 Feb;53(2):375–378. doi: 10.1128/aem.53.2.375-378.1987. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Chapelle F. H., Lovley D. R. Rates of microbial metabolism in deep coastal plain aquifers. Appl Environ Microbiol. 1990 Jun;56(6):1865–1874. doi: 10.1128/aem.56.6.1865-1874.1990. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Colwell F. S. Microbiological comparison of surface soil and unsaturated subsurface soil from a semiarid high desert. Appl Environ Microbiol. 1989 Sep;55(9):2420–2423. doi: 10.1128/aem.55.9.2420-2423.1989. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Fliermans C. B., Phelps T. J., Ringelberg D., Mikell A. T., White D. C. Mineralization of trichloroethylene by heterotrophic enrichment cultures. Appl Environ Microbiol. 1988 Jul;54(7):1709–1714. doi: 10.2172/666263. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Harm W. Dark repair of photorepairable UV lesions in Escherichia coli. Mutat Res. 1968 Jul-Aug;6(1):25–35. doi: 10.1016/0027-5107(68)90100-0. [DOI] [PubMed] [Google Scholar]
- Hengge-Aronis R. Survival of hunger and stress: the role of rpoS in early stationary phase gene regulation in E. coli. Cell. 1993 Jan 29;72(2):165–168. doi: 10.1016/0092-8674(93)90655-a. [DOI] [PubMed] [Google Scholar]
- Hermansson M., Jones G. W., Kjelleberg S. Frequency of antibiotic and heavy metal resistance, pigmentation, and plasmids in bacteria of the marine air-water interface. Appl Environ Microbiol. 1987 Oct;53(10):2338–2342. doi: 10.1128/aem.53.10.2338-2342.1987. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Jiménez L. Molecular analysis of deep-subsurface bacteria. Appl Environ Microbiol. 1990 Jul;56(7):2108–2113. doi: 10.1128/aem.56.7.2108-2113.1990. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Krieg N. R., Hoffman P. S. Microaerophily and oxygen toxicity. Annu Rev Microbiol. 1986;40:107–130. doi: 10.1146/annurev.mi.40.100186.000543. [DOI] [PubMed] [Google Scholar]
- Linn S., Imlay J. A. Toxicity, mutagenesis and stress responses induced in Escherichia coli by hydrogen peroxide. J Cell Sci Suppl. 1987;6:289–301. doi: 10.1242/jcs.1984.supplement_6.19. [DOI] [PubMed] [Google Scholar]
- Miller R. V., Kokjohn T. A. General microbiology of recA: environmental and evolutionary significance. Annu Rev Microbiol. 1990;44:365–394. doi: 10.1146/annurev.mi.44.100190.002053. [DOI] [PubMed] [Google Scholar]
- Morton R. A., Haynes R. H. Changes in the ultraviolet sensitivity of Escherichia coli during growth in batch cultures. J Bacteriol. 1969 Mar;97(3):1379–1385. doi: 10.1128/jb.97.3.1379-1385.1969. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Stamm L. V., Charon N. W. Sensitivity of pathogenic and free-living Leptospira spp. to UV radiation and mitomycin C. Appl Environ Microbiol. 1988 Mar;54(3):728–733. doi: 10.1128/aem.54.3.728-733.1988. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Tyrrell R. M., Moss S. H., Davies D. J. The variation in UV sensitivity of four K12 strains of Escherichia coli as a function of their stage of growth. Mutat Res. 1972 Sep;16(7):1–12. doi: 10.1016/0027-5107(72)90058-9. [DOI] [PubMed] [Google Scholar]
- Van Houten B. Nucleotide excision repair in Escherichia coli. Microbiol Rev. 1990 Mar;54(1):18–51. doi: 10.1128/mr.54.1.18-51.1990. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Walker G. C. Mutagenesis and inducible responses to deoxyribonucleic acid damage in Escherichia coli. Microbiol Rev. 1984 Mar;48(1):60–93. doi: 10.1128/mr.48.1.60-93.1984. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Witkin E. M. Ultraviolet mutagenesis and inducible DNA repair in Escherichia coli. Bacteriol Rev. 1976 Dec;40(4):869–907. doi: 10.1128/br.40.4.869-907.1976. [DOI] [PMC free article] [PubMed] [Google Scholar]