Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 1990 Jul;56(7):2108-13.
doi: 10.1128/aem.56.7.2108-2113.1990.

Molecular analysis of deep-subsurface bacteria

Affiliations

Molecular analysis of deep-subsurface bacteria

L Jiménez. Appl Environ Microbiol. 1990 Jul.

Abstract

Bacterial isolates from deep-sediment samples from three sites at the Savannah River site, near Aiken, S.C., were studied to determine their microbial community composition and DNA structure by using total DNA hybridization and moles percent G + C. Standard phenotypic identification underestimated the bacterial diversity at the three sites, since isolates with the same phenotype had different DNA structures in terms of moles percent G + C and DNA homology. The G + C content of deep-subsurface bacteria ranged from 20 to 77 mol%. More than 60% of the isolates tested had G + C values similar to those of Pseudomonas spp., and 12% had values similar to those of Acinetobacter spp. No isolates from deeper formations showed the same DNA composition as isolates from upper formations. Total-DNA hybridization and DNA base composition analysis provided a better resolution than phenotypic tests for the understanding of the diversity and structure of deep-subsurface bacterial communities. On the basis of the moles percent G + C values, deep-subsurface isolates tested seemed to belong to the families Pseudomonadaceae and Neisseriaceae, which might reflect a long period of adaptation to the environmental conditions of the deep subsurface.

PubMed Disclaimer

References

    1. Appl Environ Microbiol. 1989 Jun;55(6):1578-83 - PubMed
    1. Appl Environ Microbiol. 1989 Sep;55(9):2420-3 - PubMed
    1. Appl Environ Microbiol. 1988 Apr;54(4):979-83 - PubMed
    1. Appl Environ Microbiol. 1988 Dec;54(12):2916-23 - PubMed
    1. Appl Environ Microbiol. 1988 Aug;54(8):2049-53 - PubMed

Publication types

LinkOut - more resources