In situ probing of gram-positive bacteria with high DNA G + C content using 23S rRNA-targeted oligonucleotides.
暂无分享,去创建一个
R Amann | M Wagner | K. Schleifer | R. Amann | W. Ludwig | M. Wagner | W Ludwig | K H Schleifer | C Roller | C. Roller | Wolfgang Ludwig | Rudolf Amann | Carsten Roller | Michael Wagner | R. Amann
[1] K. Schleifer,et al. Identification of Whole Fixed Bacterial Cells with Nonradioactive 23S rRNA-Targeted Polynucleotide Probes , 1994, Applied and environmental microbiology.
[2] G. Fox,et al. Rapid in situ hybridization technique using 16S rRNA segments for detecting and differentiating the closely related gram-positive organisms Bacillus polymyxa and Bacillus macerans , 1992, Applied and environmental microbiology.
[3] K. Schleifer,et al. Gram-positive bacteria with a high DNA G+C content are characterized by a common insertion within their 23S rRNA genes. , 1992, Journal of general microbiology.
[4] N. Pace,et al. The excision of intervening sequences from salmonella 23S ribosomal RNA , 1990, Cell.
[5] M. Skurnik,et al. Intervening sequences (IVSs) in the 23S ribosomal RNA genes of pathogenic Yersinia enterocolitica strains. The IVSs in Y enterocolitica and Salmonella typhimurium have a common origin , 1991, Molecular microbiology.
[6] K. Schleifer,et al. The 23S ribosomal RNA higher-order structure of Pseudomonas cepacia and other prokaryotes. , 1989, European journal of biochemistry.
[7] R. Amann,et al. Molecular and microscopic identification of sulfate-reducing bacteria in multispecies biofilms , 1992, Applied and environmental microbiology.
[8] K. Schleifer,et al. In situ Identification of Lactococci, Enterococci and Streptococci , 1993 .
[9] P. Greenfield,et al. Foaming in activated sludge plants: a survey in Queensland, Australia and an evaluation of some control strategies , 1991 .
[10] C. Woese,et al. Bacterial evolution , 1987, Microbiological reviews.
[11] D. Minnikin,et al. Nocardia pinensis sp. nov., an Actinomycete Found in Activated Sludge Foams in Australia , 1989 .
[12] B Flesher,et al. Use of phylogenetically based hybridization probes for studies of ruminal microbial ecology , 1988, Applied and environmental microbiology.
[13] K. Schleifer,et al. Phylogenetic Oligodeoxynucleotide Probes for the Major Subclasses of Proteobacteria: Problems and Solutions , 1992 .
[14] E. Delong,et al. Phylogenetic stains: ribosomal RNA-based probes for the identification of single cells. , 1989, Science.
[15] K. Schleifer,et al. Identification of single bacterial cells using digoxigenin-labelled, rRNA-targeted oligonucleotides. , 1991, Journal of General Microbiology.
[16] A. Steinbüchel,et al. Isolation of prokaryotic RNA and detection of specific mRNA with biotinylated probes , 1990 .
[17] K. Schleifer,et al. Bacterial phylogeny based on 16S and 23S rRNA sequence analysis. , 1994, FEMS microbiology reviews.
[18] D. Sá,et al. Development of a rapid method for detecting bacterial cells in situ using 16S rRNA-targeted probes. , 1992 .
[19] D A Stahl,et al. Fluorescent-oligonucleotide probing of whole cells for determinative, phylogenetic, and environmental studies in microbiology , 1990, Journal of bacteriology.
[20] K. Schleifer,et al. In situ characterization of the microbial consortia active in two wastewater treatment plants , 1994 .
[21] R. Amann,et al. Combination of 16S rRNA-targeted oligonucleotide probes with flow cytometry for analyzing mixed microbial populations , 1990, Applied and environmental microbiology.
[22] K. Schleifer,et al. Probing activated sludge with oligonucleotides specific for proteobacteria: inadequacy of culture-dependent methods for describing microbial community structure , 1993, Applied and environmental microbiology.
[23] K. Schleifer,et al. Detection of micro-organisms in soil after in situ hybridization with rRNA-targeted, fluorescently labelled oligonucleotides. , 1992, Journal of general microbiology.
[24] W. Liesack,et al. Complete nucleotide sequence of the Mycobacterium leprae 23 S and 5 S rRNA genes plus flanking regions and their potential in designing diagnostic oligonucleotide probes , 1991, FEBS letters.
[25] R. Amann,et al. Optimizing fluorescent in situ hybridization with rRNA-targeted oligonucleotide probes for flow cytometric identification of microorganisms. , 1993, Cytometry.
[26] N. Larsen,et al. Higher order interactions in 23s rRNA. , 1992, Proceedings of the National Academy of Sciences of the United States of America.
[27] H. Lemmer,et al. Chemotaxonomy and Physiology of Some Actinomycetes Isolated from Scumming Activated Sludge , 1984 .
[28] P Simonet,et al. Frankia genus-specific characterization by polymerase chain reaction , 1991, Applied and environmental microbiology.
[29] D. Stahl,et al. Genus- and group-specific hybridization probes for determinative and environmental studies of sulfate-reducing bacteria , 1992 .
[30] H. Noller,et al. Gene organization and primary structure of a ribosomal RNA operon from Escherichia coli. , 1981, Journal of molecular biology.