Stress responses in lactic acid bacteria

被引:596
作者
van de Guchte, M [1 ]
Serror, P [1 ]
Chervaux, C [1 ]
Smokvina, T [1 ]
Ehrlich, SD [1 ]
Maguin, E [1 ]
机构
[1] INRA, Genet Microbienne, F-78352 Jouy En Josas, France
来源
ANTONIE VAN LEEUWENHOEK INTERNATIONAL JOURNAL OF GENERAL AND MOLECULAR MICROBIOLOGY | 2002年 / 82卷 / 1-4期
关键词
lactic acid bacteria; stress response; adaptive response; cross protection; gene regulation;
D O I
10.1023/A:1020631532202
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Lactic acid bacteria (LAB) constitute a heterogeneous group of bacteria that are traditionally used to produce fermented foods. The industrialization of food bio-transformations increased the economical importance of LAB, as they play a crucial role in the development of the organoleptique and hygienic quality of fermented products. Therefore, the reliability of starter strains in terms of quality and functional properties (important for the development of aroma and texture), but also in terms of growth performance and robustness has become essential. These strains should resist to adverse conditions encountered in industrial processes, for example during starter handling and storage (freeze-drying, freezing or spray-drying). The development of new applications such as life vaccines and probiotic foods reinforces the need for robust LAB since they may have to survive in the digestive tract, resist the intestinal flora, maybe colonize the digestive or uro-genital mucosa and express specific functions under conditions that are unfavorable to growth (for example, during stationary phase or storage). Also in nature, the ability to quickly respond to stress is essential for survival and it is now well established that LAB, like other bacteria, evolved defense mechanisms against stress that allow them to withstand harsh conditions and sudden environmental changes. While genes implicated in stress responses are numerous, in LAB the levels of characterization of their actual role and regulation differ widely between species. The functional conservation of several stress proteins (for example, HS proteins, Csp, etc) and of some of their regulators (for example, HrcA, CtsR) renders even more striking the differences that exist between LAB and the classical model micro-organisms. Among the differences observed between LAB species and B. subtilis, one of the most striking is the absence of a sigma(B) orthologue in L. lactis ssp. lactis as well as in at least two streptococci and probably E. faecalis. The overview of LAB stress responses also reveals common aspects of stress responses. As in other bacteria, adaptive responses appear to be a usual mode of stress protection in LAB. However, the cross-protection to other stress often induced by the expression of a given adaptive response, appears to vary between species. This observation suggests that the molecular bases of adaptive responses are, at least in part, species (or even subspecies) specific. A better understanding of the mechanisms of stress resistance should allow to understand the bases of the adaptive responses and cross protection, and to rationalize their exploitation to prepare LAB to industrial processes. Moreover, the identification of crucial stress related genes will reveal targets i) for specific manipulation (to promote or limit growth), ii) to develop tools to screen for tolerant or sensitive strains and iii) to evaluate the fitness and level of adaptation of a culture. In this context, future genome and transcriptome analyses will undoubtedly complement the proteome and genetic information available today, and shed a new light on the perception of, and the response to, stress by lactic acid bacteria.
引用
收藏
页码:187 / 216
页数:30
相关论文
共 315 条
[61]   Identification of genes encoding conjugated bile salt hydrolase and transport in Lactobacillus johnsonii 100-100 [J].
Elkins, CA ;
Savage, DC .
JOURNAL OF BACTERIOLOGY, 1998, 180 (17) :4344-4349
[62]   NONHEME CATALASE ACTIVITY OF LACTIC-ACID BACTERIA [J].
ENGESSER, DM ;
HAMMES, WP .
SYSTEMATIC AND APPLIED MICROBIOLOGY, 1994, 17 (01) :11-19
[63]   Phosphate-starvation-inducible proteins in Bacillus subtilis: A two-dimensional gel electrophoresis study [J].
Eymann, C ;
Mach, H ;
Harwood, CR ;
Hecker, M .
MICROBIOLOGY-UK, 1996, 142 :3163-3170
[64]  
Fabret C, 1998, J BACTERIOL, V180, P6375
[65]   Promoter-independent cold-shock induction of cspA and its derepression at 37 degrees C by mRNA stabilization [J].
Fang, L ;
Jiang, WN ;
Bae, WH ;
Inouye, M .
MOLECULAR MICROBIOLOGY, 1997, 23 (02) :355-364
[66]   MOLECULAR-BASIS OF TBE OPTOCHIN-SENSITIVE PHENOTYPE OF PNEUMOCOCCUS - CHARACTERIZATION OF THE GENES ENCODING THE F-0 COMPLEX OF THE STREPTOCOCCUS-PNEUMONIAE AND STREPTOCOCCUS-ORALIS H+-ATPASES [J].
FENOLL, A ;
MUNOZ, R ;
GARCIA, E ;
DELACAMPA, AG .
MOLECULAR MICROBIOLOGY, 1994, 12 (04) :587-598
[67]   Complete genome sequence of an M1 strain of Streptococcus pyogenes [J].
Ferretti, JJ ;
McShan, WM ;
Ajdic, D ;
Savic, DJ ;
Savic, G ;
Lyon, K ;
Primeaux, C ;
Sezate, S ;
Suvorov, AN ;
Kenton, S ;
Lai, HS ;
Lin, SP ;
Qian, YD ;
Jia, HG ;
Najar, FZ ;
Ren, Q ;
Zhu, H ;
Song, L ;
White, J ;
Yuan, XL ;
Clifton, SW ;
Roe, BA ;
McLaughlin, R .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2001, 98 (08) :4658-4663
[68]   Evolutionary genomics of pathogenic bacteria [J].
Fitzgerald, JR ;
Musser, JM .
TRENDS IN MICROBIOLOGY, 2001, 9 (11) :547-553
[69]   Comparison of the bile salts and sodium dodecyl sulfate stress responses in Enterococcus faecalis [J].
Flahaut, S ;
Frere, J ;
Boutibonnes, P ;
Auffray, Y .
APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 1996, 62 (07) :2416-2420
[70]  
Flahaut S, 1996, FEMS MICROBIOL LETT, V138, P49, DOI 10.1016/0378-1097(96)00080-8