Search PubMed⌕ Search

Biomedical subjects

E F DeLong

Publications and source records attributed to E F DeLong.

39 records · Page 3Linked to original sources

Phylogenetic stains: ribosomal RNA-based probes for the identification of single cells.

Rapid phylogenetic identification of single microbial cells was achieved with a new staining method. Formaldehyde-fixed, intact cells were hybridized with fluorescently labeled oligodeoxynucleotides complementary to 16S ribosomal RNA (rRNA) and viewed by fluorescence microscopy. Because of the abundance of rRNA in cells, the binding of the fluorescent probes to individual cells is readily visualized. Phylogenetic identification is achieved by the use of oligonucleotides (length 17 to 34 nucleotides) that are complementary to phylogenetic group-specific 16S rRNA sequences. Appropriate probes can be composed of oligonucleotide sequences that distinguish between the primary kingdoms (eukaryotes, eubacteria, archaebacteria) and between closely related organisms. The simultaneous use of multiple probes, labeled with different fluorescent dyes, allows the identification of different cell types in the same microscopic field. Quantitative microfluorimetry shows that the amount of an rRNA-specific probe that binds to Escherichia coli varies with the ribosome content and therefore reflects growth rate.

Bacillus megaterium↗

Phylogenetic group-specific oligodeoxynucleotide probes for identification of single microbial cells.

Examination of collections of 16S rRNA sequences revealed sequence domains that were unique to (and invariant within) the three primary lines of cellular descent: the archaebacteria, the eubacteria, and the eucaryotes. Oligodeoxynucleotides complementary to these conserved sequence domains were synthesized and used as hybridization probes. Each of the radiolabeled probes specifically hybridized to nylon membrane-bound 16S rRNA from the targeted kingdom. A probe complementary to a universally conserved sequence in 16S rRNAs was used as a positive control, while its complement provided a negative control for nonspecific binding. The abilities of the probes to bind specifically to whole, fixed cells representing a broad array of phylogenetic diversity were tested in whole-cell dot blot assays. Again, all of the probes specifically bound the targeted groups. By microautoradiography, the method was extended to permit phylogenetic identification of single cells microscopically.

Animals↗

Adaptation of the membrane lipids of a deep-sea bacterium to changes in hydrostatic pressure.

The fatty acid composition of the cell membrane of the barophilic marine bacterium CNPT3 was found to vary as a function of pressure. Greater amounts of unsaturated fatty acids were present in bacteria growing at higher pressures. The results suggest adaptations in the membrane lipids to environmentally relevant pressures. This response to pressure appears to be analogous to temperature-induced membrane adaptations observed in other organisms.

Adaptation, Biological↗