This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrowReprints and Permissions
Right arrow Copyright Information
Right arrow Books from ASM Press
Right arrow MicrobeWorld
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Dal Bello, F.
Right arrow Articles by Hertel, C.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Dal Bello, F.
Right arrow Articles by Hertel, C.
Agricola
Right arrow Articles by Dal Bello, F.
Right arrow Articles by Hertel, C.

 Previous Article  |  Next Article 

Applied and Environmental Microbiology, October 2005, p. 5873-5878, Vol. 71, No. 10
0099-2240/05/$08.00+0     doi:10.1128/AEM.71.10.5873-5878.2005
Copyright © 2005, American Society for Microbiology. All Rights Reserved.

Inducible Gene Expression in Lactobacillus reuteri LTH5531 during Type II Sourdough Fermentation

Fabio Dal Bello,1 Jens Walter,2 Stefan Roos,3 Hans Jonsson,3 and Christian Hertel1*

Institute of Food Technology, University of Hohenheim, Stuttgart, Germany,1 Department of Microbiology and Immunology, University of Otago, Dunedin, New Zealand,2 Department of Microbiology, Swedish University of Agricultural Sciences, Uppsala, Sweden3

Received 16 December 2004/ Accepted 29 April 2005

Lactobacillus reuteri LTH5531 is a dominant member of the microbiota of type II sourdough fermentations. To investigate the genetic background of the ecological performance of LTH5531, in vivo expression technology was used to identify promoters that show elevated levels of expression during growth of this organism in a type II sourdough fermentation. Thirty-eight sourdough-induced fusions were detected, and 29 genes could be identified on the basis of the available sequence information. Four genes encoded stress-related functions (e.g., acid and general stress response), reflecting the harsh conditions prevailing during sourdough fermentation. Further, eight genes were involved in acquisition and synthesis of amino acids and nucleotides, indicating their limited availability in sourdough. The remaining genes were either part of functionally unrelated pathways or encoded hypothetical proteins. The identification of a putative proteinase and a component of the arginine deiminase pathway is of technological interest, as they are potentially involved in the formation of aroma precursors. Our study allowed insight into the transcriptional response of Lactobacillus reuteri to the dough environment, which establishes the molecular basis to investigate bacterial properties that are likely to contribute to the ecological performance of the organism and influence the final outcome of the fermentation.


* Corresponding author. Mailing address: Institute of Food Technology, University of Hohenheim, Garbenstr. 28, D-70599 Stuttgart, Germany. Phone: 49 711 459 4255. Fax: 49 711 459 4199. E-mail: hertel{at}uni-hohenheim.de.


Applied and Environmental Microbiology, October 2005, p. 5873-5878, Vol. 71, No. 10
0099-2240/05/$08.00+0     doi:10.1128/AEM.71.10.5873-5878.2005
Copyright © 2005, American Society for Microbiology. All Rights Reserved.




This article has been cited by other articles:

  • Wall, T., Bath, K., Britton, R. A., Jonsson, H., Versalovic, J., Roos, S. (2007). The Early Response to Acid Shock in Lactobacillus reuteri Involves the ClpL Chaperone and a Putative Cell Wall-Altering Esterase. Appl. Environ. Microbiol. 73: 3924-3935 [Abstract] [Full Text]  
  • Hufner, E., Markieton, T., Chaillou, S., Crutz-Le Coq, A.-M., Zagorec, M., Hertel, C. (2007). Identification of Lactobacillus sakei Genes Induced during Meat Fermentation and Their Role in Survival and Growth. Appl. Environ. Microbiol. 73: 2522-2531 [Abstract] [Full Text]