Full Text Available

Note: Clicking the button above will open the full text document at the original institutional repository in a new window.

The Mycobacterium smegmatis "Proteome" : effects of growth phase on total protein synthesis and on the response to heat shock

As an initial step towards characterisation of the molecular processes that define the phenotype of the mycobacterial stationary phase, the effect of growth phase of Mycobacterium smegmatis on total protein synthesis and on the heat shock response was investigated. De novo protein synthesis was moni...

Full description

Saved in:
Bibliographic Details
Main Author: Ntolosi, Bongi Audrey
Other Authors: Steyn, Lafras M
Format: Thesis
Language:English
Published: Division of Medical Microbiology 2017
Subjects:
Tags: Add Tag
No Tags, Be the first to tag this record!
_version_ 1867613219944660992
access_status_str Open Access
author Ntolosi, Bongi Audrey
author2 Steyn, Lafras M
author_browse Ntolosi, Bongi Audrey
Steyn, Lafras M
author_facet Steyn, Lafras M
Ntolosi, Bongi Audrey
author_sort Ntolosi, Bongi Audrey
collection Thesis
description As an initial step towards characterisation of the molecular processes that define the phenotype of the mycobacterial stationary phase, the effect of growth phase of Mycobacterium smegmatis on total protein synthesis and on the heat shock response was investigated. De novo protein synthesis was monitored by labelling with 35 [S]methionine and the protein expression profiles analysed using one- and/two-dimensional polyacrylamide gel electrophoresis, autoradiography, and/or immunoblot analysis. The ATP content of the culture was found to be a more accurate indicator that cells were entering stationary phase than the number of colony forming units (CFU). A plateau in the ATP growth curve preceded several stationary phase-induced events : a transitory cessation in the increase in number of CFU ; a decrease in the rate of accumulation of the cell division protein FtsZ; inhibition of the synthesis of 58, 30.5, and 20 kDa exponential phase proteins; induction of the 48, 46, 32, 31, 25, and 20 kDa stationary phase (postexponential phase) proteins ; and the highest induction of the 95 kDa, 75 kDa (DnaK), 66 kDa ( GroEL ), and - 17 kDa (doublet) proteins in response to heat shock. Identification of the stationary phase-induced proteins should enable their roles in the multigenic processes that occur during transition into stationary phase to be determined. The amino acid sequence of one of the - 17 kDa heat shock proteins (with an apparent molecular weight of 16.8 kDa, named Hspl7-2) showed significant homology to open reading frame 28 of M tuberculosis cosmid MTCY01B2. This is the first time a functional characteristic has been assigned to this open reading frame, and it remains to be seen if Hspl 7-2 represents a new family of heat shock proteins. Synthesis and secretion of the antigen (Ag)-85 complex proteins was demonstrated for the first time in M smegmatis. Heat shock resulted in increased release of Ag85A and Ag85B but not of Ag85C in M smegmatis. No heat-induction of the Ag85 complex could be demonstrated in My cobacterium bovis BCG. Whereas heat shock resulted in increased release of the 19 kDa lipoprotein antigen in both M bovis BCG and M tuberculosis H37Rv, its presence in M smegmatis could not be demonstrated. This study presents an experimental approach which may prove useful in investigating the effect of various environmental stresses on the profile, and hence the function of secreted proteins.
format Thesis
id oai:open.uct.ac.za:11427/25661
institution University of Cape Town (South Africa)
language eng
last_indexed 2026-06-10T12:32:39.476Z
license_str Not specified — see source repository
provenance_str_mv Harvested via OAI-PMH from UCTD — University of Cape Town Open Access Repository
publishDate 2017
publishDateRange 2017
publishDateSort 2017
publisher Division of Medical Microbiology
publisherStr Division of Medical Microbiology
record_format dspace
source_str UCTD — University of Cape Town Open Access Repository
spelling oai:open.uct.ac.za:11427/25661 The Mycobacterium smegmatis "Proteome" : effects of growth phase on total protein synthesis and on the response to heat shock Ntolosi, Bongi Audrey Steyn, Lafras M Zappe, Harold Medical Microbiology As an initial step towards characterisation of the molecular processes that define the phenotype of the mycobacterial stationary phase, the effect of growth phase of Mycobacterium smegmatis on total protein synthesis and on the heat shock response was investigated. De novo protein synthesis was monitored by labelling with 35 [S]methionine and the protein expression profiles analysed using one- and/two-dimensional polyacrylamide gel electrophoresis, autoradiography, and/or immunoblot analysis. The ATP content of the culture was found to be a more accurate indicator that cells were entering stationary phase than the number of colony forming units (CFU). A plateau in the ATP growth curve preceded several stationary phase-induced events : a transitory cessation in the increase in number of CFU ; a decrease in the rate of accumulation of the cell division protein FtsZ; inhibition of the synthesis of 58, 30.5, and 20 kDa exponential phase proteins; induction of the 48, 46, 32, 31, 25, and 20 kDa stationary phase (postexponential phase) proteins ; and the highest induction of the 95 kDa, 75 kDa (DnaK), 66 kDa ( GroEL ), and - 17 kDa (doublet) proteins in response to heat shock. Identification of the stationary phase-induced proteins should enable their roles in the multigenic processes that occur during transition into stationary phase to be determined. The amino acid sequence of one of the - 17 kDa heat shock proteins (with an apparent molecular weight of 16.8 kDa, named Hspl7-2) showed significant homology to open reading frame 28 of M tuberculosis cosmid MTCY01B2. This is the first time a functional characteristic has been assigned to this open reading frame, and it remains to be seen if Hspl 7-2 represents a new family of heat shock proteins. Synthesis and secretion of the antigen (Ag)-85 complex proteins was demonstrated for the first time in M smegmatis. Heat shock resulted in increased release of Ag85A and Ag85B but not of Ag85C in M smegmatis. No heat-induction of the Ag85 complex could be demonstrated in My cobacterium bovis BCG. Whereas heat shock resulted in increased release of the 19 kDa lipoprotein antigen in both M bovis BCG and M tuberculosis H37Rv, its presence in M smegmatis could not be demonstrated. This study presents an experimental approach which may prove useful in investigating the effect of various environmental stresses on the profile, and hence the function of secreted proteins. 2017-10-13T07:45:25Z 2017-10-13T07:45:25Z 1998 2017-07-13T11:17:29Z Doctoral Thesis Doctoral PhD http://hdl.handle.net/11427/25661 eng application/pdf Division of Medical Microbiology Faculty of Health Sciences University of Cape Town
spellingShingle Medical Microbiology
Ntolosi, Bongi Audrey
The Mycobacterium smegmatis "Proteome" : effects of growth phase on total protein synthesis and on the response to heat shock
thesis_degree_str Doctoral
title The Mycobacterium smegmatis "Proteome" : effects of growth phase on total protein synthesis and on the response to heat shock
title_full The Mycobacterium smegmatis "Proteome" : effects of growth phase on total protein synthesis and on the response to heat shock
title_fullStr The Mycobacterium smegmatis "Proteome" : effects of growth phase on total protein synthesis and on the response to heat shock
title_full_unstemmed The Mycobacterium smegmatis "Proteome" : effects of growth phase on total protein synthesis and on the response to heat shock
title_short The Mycobacterium smegmatis "Proteome" : effects of growth phase on total protein synthesis and on the response to heat shock
title_sort mycobacterium smegmatis proteome effects of growth phase on total protein synthesis and on the response to heat shock
topic Medical Microbiology
url http://hdl.handle.net/11427/25661
work_keys_str_mv AT ntolosibongiaudrey themycobacteriumsmegmatisproteomeeffectsofgrowthphaseontotalproteinsynthesisandontheresponsetoheatshock
AT ntolosibongiaudrey mycobacteriumsmegmatisproteomeeffectsofgrowthphaseontotalproteinsynthesisandontheresponsetoheatshock