Document Detail


Ralstonia eutropha H16 flagellation changes according to nutrient supply and state of poly(3-hydroxybutyrate) accumulation.
MedLine Citation:
PMID:  18502919     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
Two-dimensional polyacrylamide gel electrophoresis (2D PAGE), in combination with matrix-assisted laser desorption ionization-time of flight analysis, and the recently revealed genome sequence of Ralstonia eutropha H16 were employed to detect and identify proteins that are differentially expressed during different phases of poly(3-hydroxybutyric acid) (PHB) metabolism. For this, a modified protein extraction protocol applicable to PHB-harboring cells was developed to enable 2D PAGE-based proteome analysis of such cells. Subsequently, samples from (i) the exponential growth phase, (ii) the stationary growth phase permissive for PHB biosynthesis, and (iii) a phase permissive for PHB mobilization were analyzed. Among several proteins exhibiting quantitative changes during the time course of a cultivation experiment, flagellin, which is the main protein of bacterial flagella, was identified. Initial investigations that report on changes of flagellation for R. eutropha were done, but 2D PAGE and electron microscopic examinations of cells revealed clear evidence that R. eutropha exhibited further significant changes in flagellation depending on the life cycle, nutritional supply, and, in particular, PHB metabolism. The results of our study suggest that R. eutropha is strongly flagellated in the exponential growth phase and loses a certain number of flagella in transition to the stationary phase. In the stationary phase under conditions permissive for PHB biosynthesis, flagellation of cells admittedly stagnated. However, under conditions permissive for intracellular PHB mobilization after a nitrogen source was added to cells that are carbon deprived but with full PHB accumulation, flagella are lost. This might be due to a degradation of flagella; at least, the cells stopped flagellin synthesis while normal degradation continued. In contrast, under nutrient limitation or the loss of phasins, cells retained their flagella.
Authors:
Matthias Raberg; Frank Reinecke; Rudolf Reichelt; Ursula Malkus; Simone König; Markus Pötter; Wolfgang Florian Fricke; Anne Pohlmann; Birgit Voigt; Michael Hecker; Bärbel Friedrich; Botho Bowien; Alexander Steinbüchel
Related Documents :
11093149 - Activation-induced t cell death occurs at g1a phase of the cell cycle.
22262689 - The spermatogonial stem cell niche in the collared peccary (tayassu tajacu).
476779 - Circadian rhythms in mouse epidermal basal cell proliferation. variations in compartmen...
3908169 - Peripheral t-cell subsets in patients with alopecia areata in different clinical phases.
2475069 - Survival of vibrio anguillarum and vibrio salmonicida at different salinities.
23209539 - Convergent synthesis of the tetrasaccharide repeating unit of the cell wall lipopolysac...
24020119 - Preparation and in vitro anti-tumor properties of toad venom extract-loaded solid lipid...
925079 - Surface distribution of lets protein in relation to the cytoskeleton of normal and tran...
12114779 - Fine-needle aspiration cytology of papillary hurthle cell carcinoma with lymphocytic st...
Publication Detail:
Type:  Comparative Study; Journal Article; Research Support, Non-U.S. Gov't     Date:  2008-05-23
Journal Detail:
Title:  Applied and environmental microbiology     Volume:  74     ISSN:  1098-5336     ISO Abbreviation:  Appl. Environ. Microbiol.     Publication Date:  2008 Jul 
Date Detail:
Created Date:  2008-07-14     Completed Date:  2008-07-31     Revised Date:  2013-06-05    
Medline Journal Info:
Nlm Unique ID:  7605801     Medline TA:  Appl Environ Microbiol     Country:  United States    
Other Details:
Languages:  eng     Pagination:  4477-90     Citation Subset:  IM    
Affiliation:
Institut für Molekulare Mikrobiologie und Biotechnologie, Westfälische Wilhelms-Universität, D-48149 Münster, Germany.
Export Citation:
APA/MLA Format     Download EndNote     Download BibTex
MeSH Terms
Descriptor/Qualifier:
Bacterial Proteins / isolation & purification*
Culture Media
Electrophoresis, Gel, Pulsed-Field
Fermentation
Flagella / physiology*
Gene Expression Regulation, Bacterial
Hydroxybutyrates / metabolism*
Microscopy, Electron
Polyesters / metabolism*
Proteome
Ralstonia / growth & development,  physiology*
Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization
Chemical
Reg. No./Substance:
0/Bacterial Proteins; 0/Culture Media; 0/Hydroxybutyrates; 0/Polyesters; 0/Proteome; 26063-00-3/poly-beta-hydroxybutyrate
Comments/Corrections

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine


Previous Document:  Genetic tools for allelic replacement in Burkholderia species.
Next Document:  Diversity surveys and evolutionary relationships of aoxB genes in aerobic arsenite-oxidizing bacteri...