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. 1996 Nov;62(11):3922–3928. doi: 10.1128/aem.62.11.3922-3928.1996

Denaturing gradient gel electrophoresis used to monitor the enrichment culture of aerobic chemoorganotrophic bacteria from a hot spring cyanobacterial mat.

C M Santegoeds 1, S C Nold 1, D M Ward 1
PMCID: PMC168208  PMID: 8899977

Abstract

Previous studies investigating microbial diversity in the Octopus Spring cyanobacterial mat community (Yellowstone National Park) have shown a discrepancy between bacterial populations observed by molecular retrieval and cultivation techniques. To investigate how selective enrichment culture techniques affect species composition, we used denaturing gradient gel electrophoresis (DGGE) separation of PCR-amplified 16S rRNA gene fragments to monitor the populations contained within enrichment cultures of aerobic chemoorganotrophic bacteria from the ca. 50 degrees C region of the mat community. By varying the degree of dilution of the inoculum, medium composition, and enrichment conditions and duration and by analyzing the cultures by DGGE, we detected 14 unique 16S rRNA sequence types. These corresponded to alpha-, beta-, gamma-, and delta-proteobacteria, Thermus relatives, and gram-positive bacteria with high G + C ratio and, at the highest inoculum dilutions, Chloroflexus aurantiacus relatives, which were estimated to still be approximately 300 times less abundant than cells of the mat primary producer, Synechococcus spp. Only three of these populations were previously cultivated on solidified medium after similar enrichment. Only two of these population have 16S rRNA sequences which were previously cloned directly from the mat. These results reveal a diversity of bacterial populations in enrichment culture which were not detected by either molecular retrieval or strain purification techniques.

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Selected References

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  1. Bateson M. M., Ward D. M. Photoexcretion and fate of glycolate in a hot spring cyanobacterial mat. Appl Environ Microbiol. 1988 Jul;54(7):1738–1743. doi: 10.1128/aem.54.7.1738-1743.1988. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. Brock T. D., Freeze H. Thermus aquaticus gen. n. and sp. n., a nonsporulating extreme thermophile. J Bacteriol. 1969 Apr;98(1):289–297. doi: 10.1128/jb.98.1.289-297.1969. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. Brosius J., Palmer M. L., Kennedy P. J., Noller H. F. Complete nucleotide sequence of a 16S ribosomal RNA gene from Escherichia coli. Proc Natl Acad Sci U S A. 1978 Oct;75(10):4801–4805. doi: 10.1073/pnas.75.10.4801. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. Ferris M. J., Muyzer G., Ward D. M. Denaturing gradient gel electrophoresis profiles of 16S rRNA-defined populations inhabiting a hot spring microbial mat community. Appl Environ Microbiol. 1996 Feb;62(2):340–346. doi: 10.1128/aem.62.2.340-346.1996. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. Ferris M. J., Ruff-Roberts A. L., Kopczynski E. D., Bateson M. M., Ward D. M. Enrichment culture and microscopy conceal diverse thermophilic Synechococcus populations in a single hot spring microbial mat habitat. Appl Environ Microbiol. 1996 Mar;62(3):1045–1050. doi: 10.1128/aem.62.3.1045-1050.1996. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Gray M. W., Sankoff D., Cedergren R. J. On the evolutionary descent of organisms and organelles: a global phylogeny based on a highly conserved structural core in small subunit ribosomal RNA. Nucleic Acids Res. 1984 Jul 25;12(14):5837–5852. doi: 10.1093/nar/12.14.5837. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. Maidak B. L., Larsen N., McCaughey M. J., Overbeek R., Olsen G. J., Fogel K., Blandy J., Woese C. R. The Ribosomal Database Project. Nucleic Acids Res. 1994 Sep;22(17):3485–3487. doi: 10.1093/nar/22.17.3485. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. Muyzer G., de Waal E. C., Uitterlinden A. G. Profiling of complex microbial populations by denaturing gradient gel electrophoresis analysis of polymerase chain reaction-amplified genes coding for 16S rRNA. Appl Environ Microbiol. 1993 Mar;59(3):695–700. doi: 10.1128/aem.59.3.695-700.1993. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. Nold S. C., Kopczynski E. D., Ward D. M. Cultivation of aerobic chemoorganotrophic proteobacteria and gram-positive bacteria from a hot spring microbial mat. Appl Environ Microbiol. 1996 Nov;62(11):3917–3921. doi: 10.1128/aem.62.11.3917-3921.1996. [DOI] [PMC free article] [PubMed] [Google Scholar]
  10. Nold S. C., Ward D. M. Diverse Thermus species inhabit a single hot spring microbial mat. Syst Appl Microbiol. 1995;18:274–278. doi: 10.1016/s0723-2020(11)80398-x. [DOI] [PubMed] [Google Scholar]
  11. Ramaley R. F., Hixson J. Isolation of a nonpigmented, thermophilic bacterium similar to Thermophilic bacterium similar to Thermus aquaticus. J Bacteriol. 1970 Aug;103(2):527–528. doi: 10.1128/jb.103.2.527-528.1970. [DOI] [PMC free article] [PubMed] [Google Scholar]
  12. Reysenbach A. L., Giver L. J., Wickham G. S., Pace N. R. Differential amplification of rRNA genes by polymerase chain reaction. Appl Environ Microbiol. 1992 Oct;58(10):3417–3418. doi: 10.1128/aem.58.10.3417-3418.1992. [DOI] [PMC free article] [PubMed] [Google Scholar]
  13. Ruff-Roberts A. L., Kuenen J. G., Ward D. M. Distribution of cultivated and uncultivated cyanobacteria and Chloroflexus-like bacteria in hot spring microbial mats. Appl Environ Microbiol. 1994 Feb;60(2):697–704. doi: 10.1128/aem.60.2.697-704.1994. [DOI] [PMC free article] [PubMed] [Google Scholar]
  14. Srivastava A. K., Schlessinger D. Mechanism and regulation of bacterial ribosomal RNA processing. Annu Rev Microbiol. 1990;44:105–129. doi: 10.1146/annurev.mi.44.100190.000541. [DOI] [PubMed] [Google Scholar]
  15. Weller R., Bateson M. M., Heimbuch B. K., Kopczynski E. D., Ward D. M. Uncultivated cyanobacteria, Chloroflexus-like inhabitants, and spirochete-like inhabitants of a hot spring microbial mat. Appl Environ Microbiol. 1992 Dec;58(12):3964–3969. doi: 10.1128/aem.58.12.3964-3969.1992. [DOI] [PMC free article] [PubMed] [Google Scholar]

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