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A DNA chip technology, designed to provide a highly sensitive and wide-range identification of mixed microbial populations, is presented. A method for the selective identification of bacteria, most common human pathogens, from a mixture of others based on the highly conserved 16S rDNA sequence is described. Target identification is based on the differential hybridization of the organism’s specific probe(s) with DNA from the mixed culture. Microbial genotypes were detected by visualizing the hybridized target on a high density DNA chip. All target organisms were detected in a mixture of other microbes. The DNA chip-based technique is sensitive and specific. The potential of this new technology is limited only by the ability to identify the 16S rDNA sequence of an organism in the databases.Biochemical studies of purified and partially purified ribosomes from Salmonella typhimurium.
Partially purified ribosomes from Salmonella typhimurium were investigated biochemically. On sucrose density gradient centrifugation, the ribosomes exhibit the following characteristics: (i) the sucrose density profile of the ribosome fraction corresponds to the expected steady-state distribution of mRNA and r-proteins, (ii) the native molecular weights of the ribosomal components are of the order of 1.5 X 10(6) and 3.0 X 10(6) (by sucrose
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