Document Detail


Autoregulator protein PhaR for biosynthesis of polyhydroxybutyrate [P(3HB)] possibly has two separate domains that bind to the target DNA and P(3HB): Functional mapping of amino acid residues responsible for DNA binding.
MedLine Citation:
PMID:  17122335     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
PhaR from Paracoccus denitrificans functions as a repressor or autoregulator of the expression of genes encoding phasin protein (PhaP) and PhaR itself, both of which are components of polyhydroxyalkanoate (PHA) granules (A. Maehara, S. Taguchi, T. Nishiyama, T. Yamane, and Y. Doi, J. Bacteriol. 184:3992-4002, 2002). PhaR is a unique regulatory protein in that it also has the ability to bind tightly to an effector molecule, PHA polyester. In this study, by using a quartz crystal microbalance, we obtained direct evidence that PhaR binds to the target DNA and poly[(R)-3-hydroxybutyrate] [P(3HB)], one of the PHAs, at the same time. To identify the PhaR amino acid residues responsible for DNA binding, deletion and PCR-mediated random point mutation experiments were carried out with the gene encoding the PhaR protein. PhaR point mutants with decreased DNA-binding abilities were efficiently screened by an in vivo monitoring assay system coupled with gene expression of green fluorescent protein in Escherichia coli. DNA-binding abilities of the wild-type and mutants of recombinant PhaR expressed in E. coli were evaluated using a gel shift assay and a surface plasmon resonance analysis. These experiments revealed that basic amino acids and a tyrosine in the N-terminal region, which is highly conserved among PhaR homologs, are responsible for DNA binding. However, most of the mutants with decreased DNA-binding abilities were unaffected in their ability to bind P(3HB), strongly suggesting that PhaR has two separate domains capable of binding to the target DNA and P(3HB).
Authors:
Miwa Yamada; Koichi Yamashita; Akiko Wakuda; Kazuyoshi Ichimura; Akira Maehara; Michihisa Maeda; Seiichi Taguchi
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Publication Detail:
Type:  Journal Article; Research Support, Non-U.S. Gov't     Date:  2006-11-22
Journal Detail:
Title:  Journal of bacteriology     Volume:  189     ISSN:  0021-9193     ISO Abbreviation:  J. Bacteriol.     Publication Date:  2007 Feb 
Date Detail:
Created Date:  2007-01-19     Completed Date:  2007-06-11     Revised Date:  2010-09-16    
Medline Journal Info:
Nlm Unique ID:  2985120R     Medline TA:  J Bacteriol     Country:  United States    
Other Details:
Languages:  eng     Pagination:  1118-27     Citation Subset:  IM    
Affiliation:
Graduate School of Engineering, Hokkaido University, N13W8, Sapporo, Hokkaido 060-8628, Japan.
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MeSH Terms
Descriptor/Qualifier:
Amino Acid Motifs
Amino Acid Sequence
Bacterial Proteins / chemistry,  genetics,  metabolism*
Circular Dichroism
DNA-Binding Proteins / chemistry,  genetics,  metabolism*
Gene Deletion
Genetic Vectors / genetics
Hydroxybutyrates / metabolism*
Molecular Sequence Data
Paracoccus denitrificans / genetics,  metabolism*
Polyesters / metabolism*
Polymerase Chain Reaction
Protein Binding
Protein Structure, Tertiary
Repressor Proteins / chemistry,  genetics,  metabolism*
Sequence Alignment
Sequence Analysis, DNA
Chemical
Reg. No./Substance:
0/Bacterial Proteins; 0/DNA-Binding Proteins; 0/Hydroxybutyrates; 0/Polyesters; 0/Repressor Proteins; 26063-00-3/poly-beta-hydroxybutyrate
Comments/Corrections

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