Abstract
The turnover of extracellular DNA was investigated in oligotrophic springs of the Crystal River and the eutrophic Medard Reservoir of southwest Florida. The Medard Reservoir possessed large populations of bacterioplankton and phytoplankton (6.8 × 109 cells per liter and 28.6 μg of chlorophyll a per liter, respectively), while the Crystal River springs only contained a fraction of the microbial biomass found in the Medard Reservoir. Although dissolved DNA values were greater in the Medard Reservoir, higher rates of DNA removal resulted in similar extracellular DNA turnover times in both environments (9.62 ± 3.6 h in the Crystal River and 10.5 ± 2.1 h in the Medard Reservoir). These results indicate that regardless of trophic status or microbial standing stock, extracellular DNA turns over rapidly in subtropical planktonic freshwater environments. Therefore, recombinant DNA sequences from released genetically engineered microorganisms might not be expected to survive for long periods of time in freshwater planktonic environments.
Full text
PDF





Selected References
These references are in PubMed. This may not be the complete list of references from this article.
- Aardema B. W., Lorenz M. G., Krumbein W. E. Protection of sediment-adsorbed transforming DNA against enzymatic inactivation. Appl Environ Microbiol. 1983 Aug;46(2):417–420. doi: 10.1128/aem.46.2.417-420.1983. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Deflaun M. F., Paul J. H., Davis D. Simplified method for dissolved DNA determination in aquatic environments. Appl Environ Microbiol. 1986 Oct;52(4):654–659. doi: 10.1128/aem.52.4.654-659.1986. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Lorenz M. G., Aardema B. W., Wackernagel W. Highly efficient genetic transformation of Bacillus subtilis attached to sand grains. J Gen Microbiol. 1988 Jan;134(1):107–112. doi: 10.1099/00221287-134-1-107. [DOI] [PubMed] [Google Scholar]
- Lorenz M. G., Wackernagel W. Adsorption of DNA to sand and variable degradation rates of adsorbed DNA. Appl Environ Microbiol. 1987 Dec;53(12):2948–2952. doi: 10.1128/aem.53.12.2948-2952.1987. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Paul J. H., Deflaun M. F., Jeffrey W. H. Mechanisms of DNA utilization by estuarine microbial populations. Appl Environ Microbiol. 1988 Jul;54(7):1682–1688. doi: 10.1128/aem.54.7.1682-1688.1988. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Paul J. H., Jeffrey W. H., DeFlaun M. F. Dynamics of extracellular DNA in the marine environment. Appl Environ Microbiol. 1987 Jan;53(1):170–179. doi: 10.1128/aem.53.1.170-179.1987. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Stewart G. J., Carlson C. A. The biology of natural transformation. Annu Rev Microbiol. 1986;40:211–235. doi: 10.1146/annurev.mi.40.100186.001235. [DOI] [PubMed] [Google Scholar]
- Wright R. T. Measurement and significance of specific activity in the heterotrophic bacteria of natural waters. Appl Environ Microbiol. 1978 Aug;36(2):297–305. doi: 10.1128/aem.36.2.297-305.1978. [DOI] [PMC free article] [PubMed] [Google Scholar]
