PCR amplification of 16S rDNA from lyophilized cell cultures facilitates studies in molecular systematics |
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Authors: | J. D. Wisotzkey Peter Jurtshuk Jr. Dr. George E. Fox |
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Affiliation: | (1) Department of Biology, University of Houston, Houston, Texas, USA;(2) Department of Biochemical and Biophysical Sciences, University of Houston, 77204-5500 Houston, TX, USA |
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Abstract: | The sequence of the major portion of aBacillus cycloheptanicus strain SCHT 16S rRNA gene is reported. This sequence suggests thatB. cycloheptanicus is genetically quite distinct from traditionalBacillus strains (e.g.,B. subtilis) and may be properly regarded as belonging to a different genus. The sequence was determined from DNA that was produced by direct amplification of ribosomal DNA from a lyophilized cell pellet with straightforward polymerase chain reaction (PCR) procedures. By obviating the need to revive cell cultures from the lyophile pellet, this approach facilitates rapid 16S rDNA sequencing and thereby advances studies in molecular systematics.The EMBL accession number for the 16S rRNA sequence is X51928. |
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