4.3 Article

Transcription analysis of rpoH in Pseudomonas putida

Journal

FEMS MICROBIOLOGY LETTERS
Volume 205, Issue 2, Pages 165-169

Publisher

OXFORD UNIV PRESS
DOI: 10.1111/j.1574-6968.2001.tb10942.x

Keywords

transcriptional start site; E sigma(70); E sigma(E)

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We previously determined the complete DNA sequence of the rpoH gene encoding the heat-shock a factor (sigma (H)) of Pseudomonas putida. In the present study, the transcriptional start sites of rpoH were determined to be 41 nucleotides (T1), 153 nucleotides (T2) and 157 nucleotides (T3) upstream from the translational start codon (AUG) of rpoH by rapid amplification of cDNA 5'-ends. Based on the locations of T2 and T3, a sigma (70)-type promoter (P2) was determined to be located in the open reading frame region of upstream ftsX in addition to the sigma (F)-type promoter (P1; DNA Res. 6 (1999) 241). In the in vitro transcription assay with reconstituted RNA polymerases (E sigma (70), E sigma (E), E sigma (H) and E sigma (S)) of Pseudomonas aeruginosa, E sigma (F) transcribed rpoH from T1 and E sigma (70) transcribed it from T2 and T3. In both cases, the level of transcription was higher at 42 degreesC than at 30 degreesC. No transcript was detected when E sigma (H) or E sigma (S) was used. These results indicate that E sigma (E) and E sigma (70) recognize P1 promoter and P2 promoter, respectively, and also prove that the synthesis of rpoH mRNA is inducible upon heat shock. (C) 2001 Federation of European Microbiological Societies. Published by Elsevier Science BY. All rights reserved.

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