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Applied and Environmental Microbiology, June 2002, p. 3010-3023, Vol. 68, No. 6
0099-2240/02/$04.00+0     DOI: 10.1128/AEM.68.6.3010-3023.2002
Copyright © 2002, American Society for Microbiology. All Rights Reserved.

Bacteriophage Resistance of a {Delta}thyA Mutant of Lactococcus lactis Blocked in DNA Replication

Martin B. Pedersen,1,2* Peter R. Jensen,2 Thomas Janzen,3 and Dan Nilsson4

Department of Genomics and Strain Development,1 Phage Section,3 Research, Development, and Application, Chr. Hansen A/S, DK-2970 Hørsholm,4 Section of Molecular Microbiology, BioCentrum, Technical University of Denmark, DK-2800 Lyngby, Denmark2

Received 26 October 2001/ Accepted 12 March 2002

The thyA gene, which encodes thymidylate synthase (TS), of Lactococcus lactis CHCC373 was sequenced, including the upstream and downstream regions. We then deleted part of thyA by gene replacement. The resulting strain, MBP71 {Delta}thyA, was devoid of TS activity, and in media without thymidine, such as milk, there was no detectable dTTP pool in the cells. Hence, DNA replication was abolished, and acidification by MBP71 was completely unaffected by the presence of nine different phages tested at a multiplicity of infection (MOI) of 0.1. Nonreplicating MBP71 must be inoculated at a higher level than CHCC373 to achieve a certain pH within a specified time. For a pH of 5.2 to be reached in 6 h, the inoculation level of MBP71 must be 17-fold higher than for CHCC373. However, by adding a limiting amount of thymidine this could be lowered to just 5-fold the normal amount, while acidification was unaffected with MBP71 up to an MOI of 0.01. It was found that nonreplicating MBP71 produced largely the same products as CHCC373, though the acetaldehyde production of the former was higher.

* Corresponding author. Mailing address: Department of Genomics and Strain Development, Chr. Hansen A/S, Bøge Allé 10-12, DK-2970 Hørsholm, Denmark. Phone: 45 45 74 84 79. Fax: 45 45 74 88 16. E-mail: MartinB.Pedersen{at}dk.chr-hansen.com.

Applied and Environmental Microbiology, June 2002, p. 3010-3023, Vol. 68, No. 6
0099-2240/02/$04.00+0     DOI: 10.1128/AEM.68.6.3010-3023.2002
Copyright © 2002, American Society for Microbiology. All Rights Reserved.



This article has been cited by other articles:

  • Michelsen, O., Cuesta-Dominguez, A., Albrechtsen, B., Jensen, P. R. (2007). Detection of Bacteriophage-Infected Cells of Lactococcus lactis by Using Flow Cytometry. Appl. Environ. Microbiol. 73: 7575-7581 [Abstract] [Full Text]  
  • Bongers, R. S., Hoefnagel, M. H. N., Kleerebezem, M. (2005). High-Level Acetaldehyde Production in Lactococcus lactis by Metabolic Engineering. Appl. Environ. Microbiol. 71: 1109-1113 [Abstract] [Full Text]  
  • Pedersen, M. B., Koebmann, B. J., Jensen, P. R., Nilsson, D. (2002). Increasing Acidification of Nonreplicating Lactococcus lactis{Delta}thyA Mutants by Incorporating ATPase Activity. Appl. Environ. Microbiol. 68: 5249-5257 [Abstract] [Full Text]  


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