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 Lamberg, A.
Right arrow Articles by Savilahti, H.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Lamberg, A.
Right arrow Articles by Savilahti, H.
Agricola
Right arrow Articles by Lamberg, A.
Right arrow Articles by Savilahti, H.

 Previous Article  |  Next Article 

Applied and Environmental Microbiology, February 2002, p. 705-712, Vol. 68, No. 2
0099-2240/02/$04.00+0     DOI: 10.1128/AEM.68.2.705-712.2002
Copyright © 2002, American Society for Microbiology. All Rights Reserved.

Efficient Insertion Mutagenesis Strategy for Bacterial Genomes Involving Electroporation of In Vitro-Assembled DNA Transposition Complexes of Bacteriophage Mu

Arja Lamberg, Sari Nieminen, Mingqiang Qiao,,{dagger} and Harri Savilahti*

Program in Cellular Biotechnology, Institute of Biotechnology, Viikki Biocenter, University of Helsinki, 00014 Helsinki, Finland

Received 17 July 2001/ Accepted 16 November 2001

An efficient insertion mutagenesis strategy for bacterial genomes based on the phage Mu DNA transposition reaction was developed. Incubation of MuA transposase protein with artificial mini-Mu transposon DNA in the absence of divalent cations in vitro resulted in stable but inactive Mu DNA transposition complexes, or transpososomes. Following delivery into bacterial cells by electroporation, the complexes were activated for DNA transposition chemistry after encountering divalent metal ions within the cells. Mini-Mu transposons were integrated into bacterial chromosomes with efficiencies ranging from 104 to 106 CFU/µg of input transposon DNA in the four species tested, i.e., Escherichia coli, Salmonella enterica serovar Typhimurium, Erwinia carotovora, and Yersinia enterocolitica. Efficiency of integration was influenced mostly by the competence status of a given strain or batch of bacteria. An accurate 5-bp target site duplication flanking the transposon, a hallmark of Mu transposition, was generated upon mini-Mu integration into the genome, indicating that a genuine DNA transposition reaction was reproduced within the cells of the bacteria studied. This insertion mutagenesis strategy for microbial genomes may be applicable to a variety of organisms provided that a means to introduce DNA into their cells is available.


* Corresponding author. Mailing address: Institute of Biotechnology, Viikki Biocenter, P.O. Box 56, Viikinkaari 9, 00014 University of Helsinki, Finland. Phone: 358-9-191 59516. Fax: 358-9-191 59366. E-mail: harri.savilahti{at}helsinki.fi.

{dagger} Present address: Institute for Molecular Biology, Nankai University, Tianjin 300071, People’s Republic of China.


Applied and Environmental Microbiology, February 2002, p. 705-712, Vol. 68, No. 2
0099-2240/02/$04.00+0     DOI: 10.1128/AEM.68.2.705-712.2002
Copyright © 2002, American Society for Microbiology. All Rights Reserved.




This article has been cited by other articles:

  • Lanckriet, A., Timbermont, L., Happonen, L. J., Pajunen, M. I., Pasmans, F., Haesebrouck, F., Ducatelle, R., Savilahti, H., Van Immerseel, F. (2009). Generation of Single-Copy Transposon Insertions in Clostridium perfringens by Electroporation of Phage Mu DNA Transposition Complexes. Appl. Environ. Microbiol. 75: 2638-2642 [Abstract] [Full Text]  
  • Paatero, A. O., Turakainen, H., Happonen, L. J., Olsson, C., Palomaki, T., Pajunen, M. I., Meng, X., Otonkoski, T., Tuuri, T., Berry, C., Malani, N., Frilander, M. J., Bushman, F. D., Savilahti, H. (2008). Bacteriophage Mu integration in yeast and mammalian genomes. Nucleic Acids Res 36: e148-e148 [Abstract] [Full Text]  
  • Pajunen, M., Turakainen, H., Poussu, E., Peranen, J., Vihinen, M., Savilahti, H. (2007). High-precision mapping of protein protein interfaces: an integrated genetic strategy combining en masse mutagenesis and DNA-level parallel analysis on a yeast two-hybrid platform. Nucleic Acids Res 0: gkm563v1-11 [Abstract] [Full Text]  
  • Tu Quoc, P. H., Genevaux, P., Pajunen, M., Savilahti, H., Georgopoulos, C., Schrenzel, J., Kelley, W. L. (2007). Isolation and Characterization of Biofilm Formation-Defective Mutants of Staphylococcus aureus. Infect. Immun. 75: 1079-1088 [Abstract] [Full Text]  
  • Saariaho, A.-H., Savilahti, H. (2006). Characteristics of MuA transposase-catalyzed processing of model transposon end DNA hairpin substrates. Nucleic Acids Res 34: 3139-3149 [Abstract] [Full Text]  
  • Bertram, R., Kostner, M., Muller, J., Ramos, J. V., Hillen, W. (2005). Integrative elements for Bacillus subtilis yielding tetracycline-dependent growth phenotypes. Nucleic Acids Res 33: e153-e153 [Abstract] [Full Text]  
  • Poussu, E., Jantti, J., Savilahti, H. (2005). A gene truncation strategy generating N- and C-terminal deletion variants of proteins for functional studies: mapping of the Sec1p binding domain in yeast Mso1p by a Mu in vitro transposition-based approach. Nucleic Acids Res 33: e104-e104 [Abstract] [Full Text]  
  • Pajunen, M. I., Pulliainen, A. T., Finne, J., Savilahti, H. (2005). Generation of transposon insertion mutant libraries for Gram-positive bacteria by electroporation of phage Mu DNA transposition complexes. Microbiology 151: 1209-1218 [Abstract] [Full Text]  
  • Shan, Z., Xu, H., Shi, X., Yu, Y., Yao, H., Zhang, X., Bai, Y., Gao, C., Saris, P. E. J., Qiao, M. (2004). Identification of two new genes involved in twitching motility in Pseudomonas aeruginosa. Microbiology 150: 2653-2661 [Abstract] [Full Text]  
  • Vilen, H., Aalto, J.-M., Kassinen, A., Paulin, L., Savilahti, H. (2002). A Direct Transposon Insertion Tool for Modification and Functional Analysis of Viral Genomes. J. Virol. 77: 123-134 [Abstract] [Full Text]