Literature DB >> 11302167

LysR-type transcriptional regulator ChiR is essential for production of all chitinases and a chitin-binding protein, CBP21, in Serratia marcescens 2170.

K Suzuki1, T Uchiyama, M Suzuki, N Nikaidou, M Regue, T Watanabe.   

Abstract

To identify the genes required for chitinase production by Serratia marcescens 2170, various Tn5 mutants somehow defective in chitinase production were isolated in a previous study. In order to identify the mutated gene in one of the chitinase-deficient mutants, N1, DNA regions flanking the Tn5 insertion were cloned and sequenced. Sequence comparison showed that the mutation occurred in the ORF located between chiB and cbp, which encode chitinase B and chitin-binding protein CBP21, respectively. The ORF encodes a 313-amino acid polypeptide which has significant similarity with various LysR-type transcriptional regulators, and thus the gene was designated chiR. Targeted mutagenesis confirmed that disruption of the chiR gene results in the phenotype of N1. Gel mobility shift assays using partially purified ChiR protein demonstrated that this protein specifically binds to the intergenic region between chiR and cbp. These results strongly suggest that ChiR is a LysR-type transcriptional regulator which is essential for production of all chitinases and CBP21.

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Year:  2001        PMID: 11302167     DOI: 10.1271/bbb.65.338

Source DB:  PubMed          Journal:  Biosci Biotechnol Biochem        ISSN: 0916-8451            Impact factor:   2.043


  7 in total

1.  Virulence factors of the human opportunistic pathogen Serratia marcescens identified by in vivo screening.

Authors:  C Léopold Kurz; Sophie Chauvet; Emmanuel Andrès; Marianne Aurouze; Isabelle Vallet; Gérard P F Michel; Mitch Uh; Jean Celli; Alain Filloux; Sophie De Bentzmann; Ivo Steinmetz; Jules A Hoffmann; B Brett Finlay; Jean-Pierre Gorvel; Dominique Ferrandon; Jonathan J Ewbank
Journal:  EMBO J       Date:  2003-04-01       Impact factor: 11.598

2.  Uptake of N,N'-diacetylchitobiose [(GlcNAc)2] via the phosphotransferase system is essential for chitinase production by Serratia marcescens 2170.

Authors:  Taku Uchiyama; Ryousuke Kaneko; Junko Yamaguchi; Akane Inoue; Takahiro Yanagida; Naoki Nikaidou; Miguel Regue; Takeshi Watanabe
Journal:  J Bacteriol       Date:  2003-03       Impact factor: 3.490

3.  Diversity and specificity in the interaction between Caenorhabditis elegans and the pathogen Serratia marcescens.

Authors:  Hinrich Schulenburg; Jonathan J Ewbank
Journal:  BMC Evol Biol       Date:  2004-11-22       Impact factor: 3.260

4.  Metabolic characterization of the chitinolytic bacterium Serratia marcescens using a genome-scale metabolic model.

Authors:  Qiang Yan; Seth Robert; J Paul Brooks; Stephen S Fong
Journal:  BMC Bioinformatics       Date:  2019-05-06       Impact factor: 3.169

5.  The requirement for the LysR-type regulator PtrA for Pseudomonas chlororaphis PA23 biocontrol revealed through proteomic and phenotypic analysis.

Authors:  Natasha Klaponski; Carrie Selin; Kelly Duke; Vic Spicer; Dilantha W G Fernando; Mark F Belmonte; Teresa R de Kievit
Journal:  BMC Microbiol       Date:  2014-04-17       Impact factor: 3.605

6.  A holin and an endopeptidase are essential for chitinolytic protein secretion in Serratia marcescens.

Authors:  Jaeger J Hamilton; Victoria L Marlow; Richard A Owen; Marília de Assis Alcoforado Costa; Manman Guo; Grant Buchanan; Govind Chandra; Matthias Trost; Sarah J Coulthurst; Tracy Palmer; Nicola R Stanley-Wall; Frank Sargent
Journal:  J Cell Biol       Date:  2014-12-08       Impact factor: 10.539

7.  Chitinase Expression in Listeria monocytogenes Is Influenced by lmo0327, Which Encodes an Internalin-Like Protein.

Authors:  Dafni Katerina Paspaliari; Vicky Gaedt Kastbjerg; Hanne Ingmer; Magdalena Popowska; Marianne Halberg Larsen
Journal:  Appl Environ Microbiol       Date:  2017-10-31       Impact factor: 4.792

  7 in total

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