Electronic Resource
Oxford, UK
:
Blackwell Publishing Ltd
FEMS microbiology letters
48 (1987), S. 0
ISSN:
1574-6968
Source:
Blackwell Publishing Journal Backfiles 1879-2005
Topics:
Biology
Notes:
Abstract A simple and convenient procedure that obviates the need for DNA cloning and radiolabelling is described for producing a rDNA hybridisation probe for use in bacterial strain characterisation. Bulk rRNA, comprising a mixture of 16S and 23S components, was isolated from Providencia stuartii NCTC11800 and purified by CsC1-cushion ultracentrifugation. The pure RNA was used as a template for synthesis of a single-strand copy cDNA using reverse transcriptase and random primers, with simultaneous biotin-11-dUTP labelling. EcoRI digests of chromosomal DNA from the type strain and a sample of 10 clinical isolates of P. stuartii were examined by Southern blot hybridisation on nylon membranes using the cDNA probe. All 11 strains had similar but not identical hybridisation patterns of 5–7 bands (detected colorimetrically) with sizes of about 5–19 kb. Our results indicated that the probe provided a sensitive means of detecting rRNA cistrons in P. stuartii. The method should be applicable to any group of microorganisms.
Type of Medium:
Electronic Resource
URL:
http://dx.doi.org/10.1111/j.1574-6968.1987.tb02557.x
Permalink
|
Location |
Call Number |
Expected |
Availability |
