TY - JOUR
T1 - P22-Based Challenge Phage Constructs to Study DNA-Protein Interactions between the σ54-Dependent Promoter, dctA, and Its Transcriptional Regulators
AU - Kim, Eungbin
AU - Kim, Daeyou
AU - Lee, Joon Haeng
N1 - Copyright:
Copyright 2004 Elsevier Science B.V., Amsterdam. All rights reserved.
PY - 2000
Y1 - 2000
N2 - A challenge phage system was used to study the DNA-protein interaction between C4-dicarboylic acid transport protein D (DCTD) or σ54, and a σ54-dependent promoter, dctAp. R. meliloti dctA promoter regulatory region replaced the Omnt site on the phage. S. typhimurium strains overproducing either DCTD or σ54 directed this challenge phage towards lysogeny, indicating that DCTD or Eσ54 recognized the dctA promoter on the phage and repressed transcription of the ant gene. These challenge phage constructs will be useful for examining interactions between DCTD (or σ54) and the dctA promoter region.
AB - A challenge phage system was used to study the DNA-protein interaction between C4-dicarboylic acid transport protein D (DCTD) or σ54, and a σ54-dependent promoter, dctAp. R. meliloti dctA promoter regulatory region replaced the Omnt site on the phage. S. typhimurium strains overproducing either DCTD or σ54 directed this challenge phage towards lysogeny, indicating that DCTD or Eσ54 recognized the dctA promoter on the phage and repressed transcription of the ant gene. These challenge phage constructs will be useful for examining interactions between DCTD (or σ54) and the dctA promoter region.
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M3 - Article
AN - SCOPUS:0347069855
VL - 38
SP - 176
EP - 179
JO - Journal of Microbiology
JF - Journal of Microbiology
SN - 1225-8873
IS - 3
ER -