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Unveiling Unusual Features of Formation of Septal Partition and Constriction in Mycobacteria—an Ultrastructural Study
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ABSTRACT
The ultrastructural functions of the electron-dense glycopeptidolipid-containing outermost layer (OL), the arabinogalactan-mycolic acid-containing electron-transparent layer (ETL), and the electron-dense peptidoglycan layer (PGL) of the mycobacterial cell wall in septal growth and constriction are not clear. Therefore, using transmission electron microscopy, we studied the participation of the three layers in septal growth and constriction in the fast-growing saprophytic species
Mycobacterium smegmatis
and the slow-growing pathogenic species
Mycobacterium xenopi
and
Mycobacterium tuberculosis
in order to document the processes in a comprehensive and comparative manner and to find out whether the processes are conserved across different mycobacterial species. A complete septal partition is formed first by the fresh synthesis of the septal PGL (S-PGL) and septal ETL (S-ETL) from the envelope PGL (E-PGL) in
M. smegmatis
and
M. xenopi
. The S-ETL is not continuous with the envelope ETL (E-ETL) due to the presence of the E-PGL between them. The E-PGL disappears, and the S-ETL becomes continuous with the E-ETL, when the OL begins to grow and invaginate into the S-ETL for constriction. However, in
M. tuberculosis
, the S-PGL and S-ETL grow from the E-PGL and E-ETL, respectively, without a separation between the E-ETL and S-ETL by the E-PGL, in contrast to the process in
M. smegmatis
and
M. xenopi
. Subsequent growth and invagination of the OL into the S-ETL of the septal partition initiates and completes septal constriction in
M. tuberculosis
. A model for the conserved sequential process of mycobacterial septation, in which the formation of a complete septal partition is followed by constriction, is presented. The probable physiological significance of the process is discussed. The ultrastructural features of septation and constriction in mycobacteria are unusually different from those in the well-studied organisms
Escherichia coli
and
Bacillus subtilis
.
American Society for Microbiology
Title: Unveiling Unusual Features of Formation of Septal Partition and Constriction in Mycobacteria—an Ultrastructural Study
Description:
ABSTRACT
The ultrastructural functions of the electron-dense glycopeptidolipid-containing outermost layer (OL), the arabinogalactan-mycolic acid-containing electron-transparent layer (ETL), and the electron-dense peptidoglycan layer (PGL) of the mycobacterial cell wall in septal growth and constriction are not clear.
Therefore, using transmission electron microscopy, we studied the participation of the three layers in septal growth and constriction in the fast-growing saprophytic species
Mycobacterium smegmatis
and the slow-growing pathogenic species
Mycobacterium xenopi
and
Mycobacterium tuberculosis
in order to document the processes in a comprehensive and comparative manner and to find out whether the processes are conserved across different mycobacterial species.
A complete septal partition is formed first by the fresh synthesis of the septal PGL (S-PGL) and septal ETL (S-ETL) from the envelope PGL (E-PGL) in
M.
smegmatis
and
M.
xenopi
.
The S-ETL is not continuous with the envelope ETL (E-ETL) due to the presence of the E-PGL between them.
The E-PGL disappears, and the S-ETL becomes continuous with the E-ETL, when the OL begins to grow and invaginate into the S-ETL for constriction.
However, in
M.
tuberculosis
, the S-PGL and S-ETL grow from the E-PGL and E-ETL, respectively, without a separation between the E-ETL and S-ETL by the E-PGL, in contrast to the process in
M.
smegmatis
and
M.
xenopi
.
Subsequent growth and invagination of the OL into the S-ETL of the septal partition initiates and completes septal constriction in
M.
tuberculosis
.
A model for the conserved sequential process of mycobacterial septation, in which the formation of a complete septal partition is followed by constriction, is presented.
The probable physiological significance of the process is discussed.
The ultrastructural features of septation and constriction in mycobacteria are unusually different from those in the well-studied organisms
Escherichia coli
and
Bacillus subtilis
.
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