Linked Life Data

9758787

Source:http://linkedlifedata.com/resource/pubmed/id/9758787

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pubmed-article:9758787pubmed:abstractTextThe differential display (DD) technique, which is widely used almost exclusively for eukaryotic gene discovery, was optimized to detect differential mRNA transcription from both pure-culture and soil-derived bacterial RNA. A model system which included toluene induction of todC1 in Pseudomonas putida F1 was used to optimize the procedure. At 24-h tod induction was determined to be approximately 8 x 10(7) transcripts/microg or 0.08% of the total mRNA. The primer concentration, primer length, annealing temperature, and template, deoxynucleoside triphosphate, and MgCl2 concentrations were varied to optimize amplification of a todC1 fragment. The limit of detection of todC1 by DD was found to be 0.015 ng of total RNA template or approximately 10(3) transcripts. Once optimized, a todC1C2 gene fragment from P. putida F1 RNA was detected by using an arbitrary primer for the reverse transcriptase step in conjunction with the same arbitrary primer and a Shine-Dalgarno primer in the PCR. To verify the results, an arbitrary primer was used to detect recovery of a new salicylate-inducible naphthalene dioxygenase in Burkholderia cepacia JS150. The method was then used to detect mRNA induction in both inoculated and uninoculated toluene-induced soil microcosms. Several putative differentially expressed partial gene sequences obtained from the uninoculated microcosms were examined, and one novel fragment was found to be differentially expressed.lld:pubmed
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pubmed-article:9758787pubmed:articleTitleOptimization of differential display of prokaryotic mRNA: application to pure culture and soil microcosms.lld:pubmed
pubmed-article:9758787pubmed:affiliationCenter for Environmental Biotechnology, The University of Tennessee, Knoxville, Tennessee 37996, USA. jtf@utk.edulld:pubmed
pubmed-article:9758787pubmed:publicationTypeJournal Articlelld:pubmed
pubmed-article:9758787pubmed:publicationTypeResearch Support, U.S. Gov't, Non-P.H.S.lld:pubmed
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