Streptococcus thermophilus Core Genome: Comparative Genome Hybridization Study of 47 Strains
A DNA microarray platform based on 2,200 genes from publicly available sequences was designed for Streptococcus thermophilus. We determined how single-nucleotide polymorphisms in the 65- to 75-mer oligonucleotide probe sequences affect the hybridization signals. The microarrays were then used for co...
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Published in | Applied and Environmental Microbiology Vol. 74; no. 15; pp. 4703 - 4710 |
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Main Authors | , , , , , |
Format | Journal Article Conference Proceeding |
Language | English |
Published |
Washington, DC
American Society for Microbiology
01.08.2008
American Society for Microbiology (ASM) |
Subjects | |
Online Access | Get full text |
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Summary: | A DNA microarray platform based on 2,200 genes from publicly available sequences was designed for Streptococcus thermophilus. We determined how single-nucleotide polymorphisms in the 65- to 75-mer oligonucleotide probe sequences affect the hybridization signals. The microarrays were then used for comparative genome hybridization (CGH) of 47 dairy S. thermophilus strains. An analysis of the exopolysaccharide genes in each strain confirmed previous findings that this class of genes is indeed highly variable. A phylogenetic tree based on the CGH data showed similar distances for most strains, indicating frequent recombination or gene transfer within S. thermophilus. By comparing genome sizes estimated from the microarrays and pulsed-field gel electrophoresis, the amount of unknown DNA in each strain was estimated. A core genome comprised of 1,271 genes detected in all 47 strains was identified. Likewise, a set of noncore genes detected in only some strains was identified. The concept of an industrial core genome is proposed. This is comprised of the genes in the core genome plus genes that are necessary in an applied industrial context. |
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Bibliography: | ObjectType-Article-2 SourceType-Scholarly Journals-1 ObjectType-Feature-1 content type line 23 ObjectType-Article-1 ObjectType-Feature-2 Corresponding author. Mailing address: Department of Physiology, Cultures & Enzymes Division, Chr. Hansen A/S, Bøge Alle 10-12, DK-2970 Hørsholm, Denmark. Phone: 45 45 74 84 30. Fax: 45 45 74 88 16. E-mail: dktbo@chr-hansen.com |
ISSN: | 0099-2240 1098-5336 1098-6596 |
DOI: | 10.1128/AEM.00132-08 |