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Applied and Environmental Microbiology, November 2004, p. 6738-6747, Vol. 70, No. 11
0099-2240/04/$08.00+0 DOI: 10.1128/AEM.70.11.6738-6747.2004
Copyright © 2004, American Society for Microbiology. All Rights Reserved.
Lan-szu Chou,1,2,
Adele Cutler,3 and
Bart Weimer1,2,4*
Department of Nutrition and Food Sciences,1 Center for Microbe Detection and Physiology,2 Department of Mathematics and Statistics,3 Center for Integrated BioSystems, Utah State University, Logan, Utah4
Received 20 January 2004/ Accepted 12 July 2004
This report describes the use of an oligonucleotide macroarray to profile the expression of 375 genes in Lactococcus lactis subsp. lactis IL1403 during heat, acid, and osmotic stress. A set of known stress-associated genes in IL1403 was used as the internal control on the array. Every stress response was accurately detected using the macroarray, compared to data from previous reports. As a group, the expression patterns of the investigated metabolic genes were significantly altered by heat, acid, and osmotic stresses. Specifically, 13 to 18% of the investigated genes were differentially expressed in each of the environmental stress treatments. Interestingly, the methionine biosynthesis pathway genes (metA-metB1 and metB2-cysK) were induced during heat shock, but methionine utilization genes, such as metK, were induced during acid stress. These data provide a possible explanation for the differences between acid tolerance mechanisms of L. lactis strains IL1403 and MG1363 reported previously. Several groups of transcriptional responses were common among the stress treatments, such as repression of peptide transporter genes, including the opt operon (also known as dpp) and dtpT. Reduction of peptide transport due to environmental stress will have important implications in the cheese ripening process. Although stress responses in lactococci were extensively studied during the last decade, additional information about this bacterium was gained from the use of this metabolic array.
Utah Agricultural Experiment Station contribution number 7539.
Present address: Johns Hopkins University, Department of Pediatric Infectious Diseases, Baltimore, MD 21205.
Present address: ARUP Laboratories, Salt Lake City, UT 84100.
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