Vitamin C targets (p)ppGpp synthesis leading to stalling of long-term survival and biofilm formation in Mycobacterium smegmatis
Abstract Earlier, vitamin C was demonstrated to sterilize Mycobacterium tuberculosis culture via Fenton's reaction at high concentration. It alters the regulatory pathways associated with stress response and dormancy. Since (p)ppGpp is considered to be the master regulator of stress response an...
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Veröffentlicht in: | FEMS microbiology letters 2017-01, Vol.364 (1), p.fnw282 |
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Zusammenfassung: | Abstract
Earlier, vitamin C was demonstrated to sterilize Mycobacterium
tuberculosis culture via Fenton's reaction at high concentration.
It alters the regulatory pathways associated with stress response and dormancy.
Since (p)ppGpp is considered to be the master regulator of stress response and
is responsible for bacterial survival under stress, we tested the effect of
vitamin C on the formation of (p)ppGpp. In vivo estimation of
(p)ppGpp showed a decrease in (p)ppGpp levels in vitamin C-treated M.
smegmatis cells in comparison to the untreated cells. Furthermore,
in vitro (p)ppGpp synthesis using RelMSM enzyme
was conducted in order to confirm the specificity of the inhibition in the
presence of variable concentrations of vitamin C. We observed that vitamin C at
high concentration can inhibit the synthesis of (p)ppGpp. We illustrated binding
of vitamin C to RelMSM by isothermal titration calorimetry. Enzyme
kinetics was followed where K0.5 was found to be increased with the
concomitant reduction of Vmax value suggesting mixed inhibition. Both
long-term survival and biofilm formation were inhibited by vitamin C. The
experiments suggest that vitamin C has the potential to be developed as the
inhibitor of (p)ppGpp synthesis and stress response, at least in the
concentration range used here.
Vitamin C inhibits (p)ppGpp synthesis and stress response in
Mycobacterium smegmatis.
Graphical Abstract Figure.
Vitamin C inhibits (p)ppGpp synthesis and stress response in
Mycobacterium smegmatis. |
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ISSN: | 0378-1097 1574-6968 1574-6968 |
DOI: | 10.1093/femsle/fnw282 |