scholarly journals Antagonistic Role of H-NS and GadX in the Regulation of the Glutamate Decarboxylase-dependent Acid Resistance System inEscherichia coli

2005 ◽  
Vol 280 (22) ◽  
pp. 21498-21505 ◽  
Author(s):  
Mara Giangrossi ◽  
Stefano Zattoni ◽  
Angela Tramonti ◽  
Daniela De Biase ◽  
Maurizio Falconi
2001 ◽  
Vol 64 (9) ◽  
pp. 1362-1368 ◽  
Author(s):  
PAUL D. COTTER ◽  
KAREN O'REILLY ◽  
COLIN HILL

The glutamate decarboxylase (GAD) acid resistance system of the foodborne pathogen Listeria monocytogenes plays a major role in its survival at low pH. It was found that survival of the wild-type strain, LO28, in acidified reconstituted skim milk, diluted to reduce free glutamate levels, improves in response to supplementation with monosodium glutamate. A mutant, in which the two listerial GAD homologs have been deleted (and in which there is no discernible GAD activity), did not respond to glutamate supplementation and displayed greatly enhanced sensitivity in a number of low pH foods, even when levels of free glutamate were as low as 0.22 mM. We thus show that the GAD system plays a major role in the survival of L. monocytogenes in acidic foods even when levels of free glutamate are low.


2007 ◽  
Vol 71 (1) ◽  
pp. 158-164 ◽  
Author(s):  
Ayako TAKADA ◽  
Genryou UMITSUKI ◽  
Kazuo NAGAI ◽  
Masaaki WACHI

Microbiology ◽  
2014 ◽  
Vol 160 (5) ◽  
pp. 954-961 ◽  
Author(s):  
Toshiko Aiso ◽  
Shigeru Kamiya ◽  
Hideo Yonezawa ◽  
Shinobu Gamou

The antisense RNA ArrS is complementary to a sequence in the 5′ untranslated region of the gadE T3 mRNA, the largest transcript of gadE, which encodes a transcriptional activator of the glutamate-dependent acid resistance system in Escherichia coli. Expression of arrS is strongly induced during the stationary growth phase, particularly under acidic conditions, and transcription is dependent on σS and GadE. The aim of the present study was to clarify the role of ArrS in controlling gadE expression by overexpressing arrS in E. coli. The results showed a marked increase in the survival of arrS-overexpressing cells at 2 h after a shift to pH 2.5. This was accompanied by increased expression of gadA, gadBC and gadE. The level of gadE T3 mRNA decreased markedly in response to arrS overexpression, and was accompanied by a marked increase in gadE mRNA T2. T2 mRNA had a monophosphorylated 5′ terminus, which is usually found in cleaved mRNAs, and no T2 mRNA was observed in an RNase III-deficient cell strain. In addition, T2 mRNA was not generated by a P3-deleted gadE–luc translational fusion. These results suggest strongly that T2 mRNA is generated via the processing of T3 mRNA. Moreover, the T2 mRNA, which was abundant in arrS-overexpressing cells, was more stable than T3 mRNA in non-overexpressing cells. These results suggest that overexpression of ArrS positively regulates gadE expression in a post-transcriptional manner.


Microbiology ◽  
2007 ◽  
Vol 153 (1) ◽  
pp. 238-246 ◽  
Author(s):  
Marie-Pierre Castanié-Cornet ◽  
Hélène Treffandier ◽  
Anne Francez-Charlot ◽  
Claude Gutierrez ◽  
Kaymeuang Cam

1996 ◽  
Vol 271 (2) ◽  
pp. 1022-1028 ◽  
Author(s):  
Shihong Li ◽  
N. Vinay Kumar ◽  
Umesh Varshney ◽  
Uttam L. RajBhandary

2007 ◽  
Vol 267 (1) ◽  
pp. 51-55 ◽  
Author(s):  
Dipankar Chatterji ◽  
Yoshito Ogawa ◽  
Tomohiro Shimada ◽  
Akira Ishihama

2002 ◽  
Vol 207 (1) ◽  
pp. 9-12 ◽  
Author(s):  
Ran Rosen ◽  
Dvora Biran ◽  
Eyal Gur ◽  
Dörte Becher ◽  
Michael Hecker ◽  
...  

Sign in / Sign up

Export Citation Format

Share Document