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PMID: 14996794 Published · ppublish English Journal Article Research Support, U.S. Gov't, P.H.S.

Temperature regulation of the hemin storage (Hms+) phenotype of Yersinia pestis is posttranscriptional.

Journal of bacteriology ·Vol. 186 ·No. 6 ·2004-03-00 ·Pages 1638-47

Perry RD, Bobrov AG, Kirillina O, Jones HA, Pedersen L, Abney J, Fetherston JD

Abstract

In Yersinia pestis, the Congo red (and hemin) binding that is characteristic of the Hms+ phenotype occurs at temperatures up to 34 degrees C but not at higher temperatures. Manifestation of the Hms+ phenotype requires at least five proteins (HmsH, -F, -R, -S, and -T) that are organized into two separate operons: hmsHFRS and hmsT. HmsH and HmsF are outer membrane proteins, while HmsR, HmsS, and HmsT are predicted to be inner membrane proteins. We have used transcriptional reporter constructs, RNA dot blots, and Western blots to examine the expression of hms operons and proteins. Our studies indicate that transcription from the hmsHFRS and hmsT promoters is not regulated by the iron status of the cells, growth temperature, or any of the Hms proteins. In addition, the level of mRNA for both operons is not significantly affected by growth temperature. However, protein levels of HmsH, HmsR, and HmsT in cells grown at 37 degrees C are very low compared to those in cells grown at 26 degrees C, while the amounts of HmsF and HmsS show only a moderate reduction at the higher growth temperature. Neither the Pla protease nor a putative endopeptidase (Y2360) encoded upstream of hmsH is essential for temperature regulation of the Hms+ phenotype. However, HmsT at 37 degrees C is sensitive to degradation by Lon and/or ClpPX. Thus, the stability of HmsH, HmsR, and HmsT proteins likely plays a role in temperature regulation of the Hms+ phenotype of Y. pestis.

MeSH Terms
Bacterial Proteins/genetics,metabolism Culture Media Gene Expression Regulation, Bacterial Hemin/metabolism Membrane Proteins/genetics,metabolism Mutation Operon Phenotype Plasmids Temperature Transcription, Genetic Yersinia pestis/genetics,growth & development,metabolism
Chemicals
Bacterial Proteins Culture Media HMST protein, Yersinia pestis HmsR protein, Yersinia pestis Membrane Proteins Hemin
Authors & Affiliations
7 authors, click to expand affiliations / ORCID
Perry Robert D
Department of Microbiology, Immunology, and Molecular Genetics, University of Kentucky, Lexington, Kentucky 40536, USA. rperry@pop.uky.edu
Bobrov Alexander G
Kirillina Olga
Jones Heather A
Pedersen Lisa
Abney Jennifer
Fetherston Jacqueline D
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Article Info
Journal
Journal of bacteriology
Abbr.
J Bacteriol
ISSN
0021-9193
Published
2004-03-00
Pages
1638-47
Language
English
Region
United States
NLM ID
2985120R
PMCID
PMC355957
Subset
IM
Grants
NIAID NIH HHS · R01 AI025098 · United States
NIAID NIH HHS · AI25098 · United States
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