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Open AccessJournal ArticleDOI

Active recruitment of σ54‐RNA polymerase to the Pu promoter of Pseudomonas putida: role of IHF and αCTD

TLDR
The view that binding of σ54‐RNAP to a promoter is a step that can be subjected to regulation by factors (e.g. IHF) other than the sole intrinsic affinity of ρ54‐ RNAP for the −12/−24 site is supported.
Abstract
The sequence elements determining the binding of the sigma54-containing RNA polymerase (sigma54-RNAP) to the Pu promoter of Pseudomonas putida have been examined. Contrary to previous results in related systems, we show that the integration host factor (IHF) binding stimulates the recruitment of the enzyme to the -12/-24 sequence motifs. Such a recruitment, which is fully independent of the activator of the system, XylR, requires the interaction of the C-terminal domain of the alpha subunit of RNAP with specific DNA sequences upstream of the IHF site which are reminiscent of the UP elements in sigma70 promoters. Our data show that this interaction is mainly brought about by the distinct geometry of the promoter region caused by IHF binding and the ensuing DNA bending. These results support the view that binding of sigma54-RNAP to a promoter is a step that can be subjected to regulation by factors (e.g. IHF) other than the sole intrinsic affinity of sigma54-RNAP for the -12/-24 site.

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Journal ArticleDOI

Carbon catabolite repression in Pseudomonas : optimizing metabolic versatility and interactions with the environment

TL;DR: This review summarizes the regulatory mechanisms responsible for CCR in the bacteria of the genus Pseudomonas, which can live in many different habitats and has implications in the optimization of biotechnological processes such as biotransformations or bioremediation strategies.
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The bacterial enhancer-dependent sigma(54) (sigma(N)) transcription factor.

TL;DR: The initiation of transcription is a complex process involving many different steps, and many have been exploited by bacteria to give rise to sophisticated regulatory mechanisms that allow the cell to adapt to changing environment.
Journal ArticleDOI

UPs and downs in bacterial transcription initiation: the role of the alpha subunit of RNA polymerase in promoter recognition.

TL;DR: The current state of the understanding of the α interaction with DNA during basal transcription initiation and activated transcription initiation is reviewed.
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The black cat/white cat principle of signal integration in bacterial promoters

TL;DR: Transcriptional regulation of biodegradative genes and operons thus becomes a critical asset for the success of a newly assembled pathway to degradation, which guarantees per se the survival of a particular strain.
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Promoters in the environment: transcriptional regulation in its natural context

TL;DR: This work has shown that in vivo transcription initiation of bacterial promoters must process various physicochemical and metabolic signals to determine their output, which helps to achieve optimal bacterial fitness in extremely competitive niches.
References
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Book

Molecular Cloning: A Laboratory Manual

TL;DR: Molecular Cloning has served as the foundation of technical expertise in labs worldwide for 30 years as mentioned in this paper and has been so popular, or so influential, that no other manual has been more widely used and influential.
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Experiments in molecular genetics

TL;DR: Molecular Genetics (Biology): An Overview | Sciencing Experimental in Molecular Genetics Experiments in molecular genetics (1972 edition) | Open ...
Journal ArticleDOI

Improved M13 phage cloning vectors and host strains: nucleotide sequences of the M13mp18 and pUC19 vectors

TL;DR: New Escherichia coli host strains have been constructed for the E. coli bacteriophage M13 and the high-copy-number pUC-plasmid cloning vectors and mutations introduced into these strains improve cloning of unmodified DNA and of repetitive sequences.
Book ChapterDOI

Sequencing end-labeled DNA with base-specific chemical cleavages.

TL;DR: The chapter presents techniques for producing discrete DNA fragments, end-labeling DNA, segregating end- labeled fragments, extracting DNA from gels, and the protocols for partially cleaving it at specific bases using the chemical reactions.
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