Heat shock induces thermotolerance and inhibition of lysis in a lysogenic strain of Lactococcus lactis

1991 ◽  
Vol 14 (1) ◽  
pp. 1-9 ◽  
Author(s):  
P. Boutibonnes ◽  
B. Gillot ◽  
Y. Auffray ◽  
B. Thammavongs
2004 ◽  
Vol 70 (10) ◽  
pp. 5929-5936 ◽  
Author(s):  
C. Desmond ◽  
G. F. Fitzgerald ◽  
C. Stanton ◽  
R. P. Ross

ABSTRACT The bacterial heat shock response is characterized by the elevated expression of a number of chaperone complexes. Two-dimensional polyacrylamide gel electrophoresis revealed that GroEL expression in probiotic Lactobacillus paracasei NFBC 338 was increased under heat adaptation conditions (52°C for 15 min). Subsequently, the groESL operon of L. paracasei NFBC 338 was PCR amplified, and by using the nisin-inducible expression system, two plasmids, pGRO1 and pGRO2, were constructed on the basis of vectors pNZ8048 and pMSP3535, respectively. These vectors were transferred into Lactococcus lactis(pGRO1) and L. paracasei(pGRO2), and after induction with nisin, overexpressed GroEL represented 15 and 20% of the total cellular protein in each strain, respectively. Following heat shock treatment of lactococci (at 54°C) and lactobacilli (at 60°C), the heat-adapted cultures maintained the highest level of viability (5-log-unit increase, approximately) in each case, while it was found that the GroESL-overproducing strains performed only moderately better (1-log-unit increase) than the controls. On the other hand, the salt tolerance of both GroESL-overproducing strains (in 5 M NaCl) was similar to that of the parent cultures. Interestingly, both strains overproducing GroESL exhibited increased solvent tolerance, most notably, the ability to grow in the presence of butanol (0.5% [vol/vol]) for 5 h, while the viability of the parent strain declined. These results confirm the integral role of GroESL in solvent tolerance, and to a lesser extent, thermotolerance of lactic acid bacteria. Furthermore, this study demonstrates that technologically sensitive cultures, including certain probiotic lactobacilli, can potentially be manipulated to become more robust for survival under harsh conditions, such as food product development and gastrointestinal transit.


Microbiology ◽  
1996 ◽  
Vol 142 (7) ◽  
pp. 1685-1691 ◽  
Author(s):  
J. Arnau ◽  
K. I. Sorensen ◽  
K. F. Appel ◽  
F. K. Vogensen ◽  
K. Hammer

2012 ◽  
Vol 11 (2) ◽  
pp. 1146-1157 ◽  
Author(s):  
M.S.P. de Azevedo ◽  
C.S. Rocha ◽  
N. Electo ◽  
D.S. Pontes ◽  
J.B. Molfetta ◽  
...  

2003 ◽  
Vol 185 (17) ◽  
pp. 5117-5124 ◽  
Author(s):  
Pekka Varmanen ◽  
Finn K. Vogensen ◽  
Karin Hammer ◽  
Airi Palva ◽  
Hanne Ingmer

ABSTRACT The heat shock response in bacterial cells is characterized by rapid induction of heat shock protein expression, followed by an adaptation period during which heat shock protein synthesis decreases to a new steady-state level. In this study we found that after a shift to a high temperature the Clp ATPase (ClpE) in Lactococcus lactis is required for such a decrease in expression of a gene negatively regulated by the heat shock regulator (CtsR). Northern blot analysis showed that while a shift to a high temperature in wild-type cells resulted in a temporal increase followed by a decrease in expression of clpP encoding the proteolytic component of the Clp protease complex, this decrease was delayed in the absence of ClpE. Site-directed mutagenesis of the zinc-binding motif conserved in ClpE ATPases interfered with the ability to repress CtsR-dependent expression. Quantification of ClpE by Western blot analysis revealed that at a high temperature ClpE is subjected to ClpP-dependent processing and that disruption of the zinc finger domain renders ClpE more susceptible. Interestingly, this domain resembles the N-terminal region of McsA, which was recently reported to interact with the CtsR homologue in Bacillus subtilis. Thus, our data point to a regulatory role of ClpE in turning off clpP gene expression following temporal heat shock induction, and we propose that this effect is mediated through CtsR.


2017 ◽  
Vol 247 ◽  
pp. 18-23 ◽  
Author(s):  
Stéphanie Weidmann ◽  
Magali Maitre ◽  
Julie Laurent ◽  
Françoise Coucheney ◽  
Aurélie Rieu ◽  
...  

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