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. 1996 Feb;178(3):931–935. doi: 10.1128/jb.178.3.931-935.1996

Efficient insertional mutagenesis in lactococci and other gram-positive bacteria.

E Maguin 1, H Prévost 1, S D Ehrlich 1, A Gruss 1
PMCID: PMC177749  PMID: 8550537

Abstract

In lactococci, the study of chromosomal genes and their regulation is limited by the lack of an efficient transposon mutagenesis system. We associated the insertion sequence ISS1 with the thermosensitive replicon pG+ host to generate a mutagenic tool that can be used even in poorly transformable strains. ISS1 transposition is random in different lactococcal strains as well as in Enterococcus faecalis and Streptococcus thermophilus. High-frequency random insertion (of about 1%) obtained with this system in Lactococcus lactis allows efficient mutagenesis, with typically one insertion per cell. After ISS1 replicative transposition, the chromosome contains duplicated ISS1 sequences flanking pG+ host. This structure allows cloning of the interrupted gene. In addition, efficient excision of the plasmid leaves a single ISS1 copy at the mutated site, thus generating a stable mutant strain with no foreign markers. Mutants obtained by this transposition system are food grade and can thus be used in fermentation processes.

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Selected References

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  1. Araya T., Ishibashi N., Shimamura S., Tanaka K., Takahashi H. Genetic and molecular analysis of the rpoD gene from Lactococcus lactis. Biosci Biotechnol Biochem. 1993 Jan;57(1):88–92. doi: 10.1271/bbb.57.88. [DOI] [PubMed] [Google Scholar]
  2. Bardowski J., Ehrlich S. D., Chopin A. BglR protein, which belongs to the BglG family of transcriptional antiterminators, is involved in beta-glucoside utilization in Lactococcus lactis. J Bacteriol. 1994 Sep;176(18):5681–5685. doi: 10.1128/jb.176.18.5681-5685.1994. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. Bardowski J., Ehrlich S. D., Chopin A. Tryptophan biosynthesis genes in Lactococcus lactis subsp. lactis. J Bacteriol. 1992 Oct;174(20):6563–6570. doi: 10.1128/jb.174.20.6563-6570.1992. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. Biswas I., Gruss A., Ehrlich S. D., Maguin E. High-efficiency gene inactivation and replacement system for gram-positive bacteria. J Bacteriol. 1993 Jun;175(11):3628–3635. doi: 10.1128/jb.175.11.3628-3635.1993. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. Biswas I., Maguin E., Ehrlich S. D., Gruss A. A 7-base-pair sequence protects DNA from exonucleolytic degradation in Lactococcus lactis. Proc Natl Acad Sci U S A. 1995 Mar 14;92(6):2244–2248. doi: 10.1073/pnas.92.6.2244. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Chopin M. C., Chopin A., Rouault A., Galleron N. Insertion and amplification of foreign genes in the Lactococcus lactis subsp. lactis chromosome. Appl Environ Microbiol. 1989 Jul;55(7):1769–1774. doi: 10.1128/aem.55.7.1769-1774.1989. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. Dabert P., Ehrlich S. D., Gruss A. Chi sequence protects against RecBCD degradation of DNA in vivo. Proc Natl Acad Sci U S A. 1992 Dec 15;89(24):12073–12077. doi: 10.1073/pnas.89.24.12073. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. Delorme C., Ehrlich S. D., Renault P. Histidine biosynthesis genes in Lactococcus lactis subsp. lactis. J Bacteriol. 1992 Oct;174(20):6571–6579. doi: 10.1128/jb.174.20.6571-6579.1992. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. Duwat P., Ehrlich S. D., Gruss A. A general method for cloning recA genes of gram-positive bacteria by polymerase chain reaction. J Bacteriol. 1992 Aug;174(15):5171–5175. doi: 10.1128/jb.174.15.5171-5175.1992. [DOI] [PMC free article] [PubMed] [Google Scholar]
  10. Eaton T., Shearman C., Gasson M. Cloning and sequence analysis of the dnaK gene region of Lactococcus lactis subsp. lactis. J Gen Microbiol. 1993 Dec;139(12):3253–3264. doi: 10.1099/00221287-139-12-3253. [DOI] [PubMed] [Google Scholar]
  11. Gansel X., Hartke A., Boutibonnes P., Auffray Y. Nucleotide sequence of the Lactococcus lactis NCDO 763 (ML3) rpoD gene. Biochim Biophys Acta. 1993 Oct 19;1216(1):115–118. doi: 10.1016/0167-4781(93)90045-f. [DOI] [PubMed] [Google Scholar]
  12. Godon J. J., Chopin M. C., Ehrlich S. D. Branched-chain amino acid biosynthesis genes in Lactococcus lactis subsp. lactis. J Bacteriol. 1992 Oct;174(20):6580–6589. doi: 10.1128/jb.174.20.6580-6589.1992. [DOI] [PMC free article] [PubMed] [Google Scholar]
  13. Gruss A., Ehrlich S. D. Insertion of foreign DNA into plasmids from gram-positive bacteria induces formation of high-molecular-weight plasmid multimers. J Bacteriol. 1988 Mar;170(3):1183–1190. doi: 10.1128/jb.170.3.1183-1190.1988. [DOI] [PMC free article] [PubMed] [Google Scholar]
  14. Haandrikman A. J., van Leeuwen C., Kok J., Vos P., de Vos W. M., Venema G. Insertion elements on lactococcal proteinase plasmids. Appl Environ Microbiol. 1990 Jun;56(6):1890–1896. doi: 10.1128/aem.56.6.1890-1896.1990. [DOI] [PMC free article] [PubMed] [Google Scholar]
  15. Hill C., Daly C., Fitzgerald G. F. Development of High-Frequency Delivery System for Transposon Tn919 in Lactic Streptococci: Random Insertion in Streptococcus lactis subsp. diacetylactis 18-16. Appl Environ Microbiol. 1987 Jan;53(1):74–78. doi: 10.1128/aem.53.1.74-78.1987. [DOI] [PMC free article] [PubMed] [Google Scholar]
  16. Holo H., Nes I. F. High-Frequency Transformation, by Electroporation, of Lactococcus lactis subsp. cremoris Grown with Glycine in Osmotically Stabilized Media. Appl Environ Microbiol. 1989 Dec;55(12):3119–3123. doi: 10.1128/aem.55.12.3119-3123.1989. [DOI] [PMC free article] [PubMed] [Google Scholar]
  17. Horinouchi S., Weisblum B. Nucleotide sequence and functional map of pE194, a plasmid that specifies inducible resistance to macrolide, lincosamide, and streptogramin type B antibodies. J Bacteriol. 1982 May;150(2):804–814. doi: 10.1128/jb.150.2.804-814.1982. [DOI] [PMC free article] [PubMed] [Google Scholar]
  18. Huang D. C., Huang X. F., Novel G., Novel M. Two genes present on a transposon-like structure in Lactococcus lactis are involved in a Clp-family proteolytic activity. Mol Microbiol. 1993 Mar;7(6):957–965. doi: 10.1111/j.1365-2958.1993.tb01187.x. [DOI] [PubMed] [Google Scholar]
  19. Huang D. C., Novel M., Huang X. F., Novel G. Nonidentity between plasmid and chromosomal copies of ISS1-like sequences in Lactococcus lactis subsp. lactis CNRZ270 and their possible role in chromosomal integration of plasmid genes. Gene. 1992 Sep 1;118(1):39–46. doi: 10.1016/0378-1119(92)90246-l. [DOI] [PubMed] [Google Scholar]
  20. Israelsen H., Hansen E. B. Insertion of Transposon Tn917 Derivatives into the Lactococcus lactis subsp. lactis Chromosome. Appl Environ Microbiol. 1993 Jan;59(1):21–26. doi: 10.1128/aem.59.1.21-26.1993. [DOI] [PMC free article] [PubMed] [Google Scholar]
  21. Khan S. A., Novick R. P. Complete nucleotide sequence of pT181, a tetracycline-resistance plasmid from Staphylococcus aureus. Plasmid. 1983 Nov;10(3):251–259. doi: 10.1016/0147-619x(83)90039-2. [DOI] [PubMed] [Google Scholar]
  22. Kim S. G., Batt C. A. Cloning and sequencing of the Lactococcus lactis subsp. lactis groESL operon. Gene. 1993 May 15;127(1):121–126. doi: 10.1016/0378-1119(93)90626-e. [DOI] [PubMed] [Google Scholar]
  23. Kok J., van der Vossen J. M., Venema G. Construction of plasmid cloning vectors for lactic streptococci which also replicate in Bacillus subtilis and Escherichia coli. Appl Environ Microbiol. 1984 Oct;48(4):726–731. doi: 10.1128/aem.48.4.726-731.1984. [DOI] [PMC free article] [PubMed] [Google Scholar]
  24. Le Bourgeois P., Lautier M., Mata M., Ritzenthaler P. New tools for the physical and genetic mapping of Lactococcus strains. Gene. 1992 Feb 1;111(1):109–114. doi: 10.1016/0378-1119(92)90610-2. [DOI] [PubMed] [Google Scholar]
  25. Maguin E., Duwat P., Hege T., Ehrlich D., Gruss A. New thermosensitive plasmid for gram-positive bacteria. J Bacteriol. 1992 Sep;174(17):5633–5638. doi: 10.1128/jb.174.17.5633-5638.1992. [DOI] [PMC free article] [PubMed] [Google Scholar]
  26. Mierau I., Tan P. S., Haandrikman A. J., Mayo B., Kok J., Leenhouts K. J., Konings W. N., Venema G. Cloning and sequencing of the gene for a lactococcal endopeptidase, an enzyme with sequence similarity to mammalian enkephalinase. J Bacteriol. 1993 Apr;175(7):2087–2096. doi: 10.1128/jb.175.7.2087-2096.1993. [DOI] [PMC free article] [PubMed] [Google Scholar]
  27. Nardi M., Chopin M. C., Chopin A., Cals M. M., Gripon J. C. Cloning and DNA sequence analysis of an X-prolyl dipeptidyl aminopeptidase gene from Lactococcus lactis subsp. lactis NCDO 763. Appl Environ Microbiol. 1991 Jan;57(1):45–50. doi: 10.1128/aem.57.1.45-50.1991. [DOI] [PMC free article] [PubMed] [Google Scholar]
  28. Nilsson D., Lauridsen A. A., Tomoyasu T., Ogura T. A Lactococcus lactis gene encodes a membrane protein with putative ATPase activity that is homologous to the essential Escherichia coli ftsH gene product. Microbiology. 1994 Oct;140(Pt 10):2601–2610. doi: 10.1099/00221287-140-10-2601. [DOI] [PubMed] [Google Scholar]
  29. Noirot P., Petit M. A., Ehrlich S. D. Plasmid replication stimulates DNA recombination in Bacillus subtilis. J Mol Biol. 1987 Jul 5;196(1):39–48. doi: 10.1016/0022-2836(87)90509-2. [DOI] [PubMed] [Google Scholar]
  30. Otto R., de Vos W. M., Gavrieli J. Plasmid DNA in Streptococcus cremoris Wg2: Influence of pH on Selection in Chemostats of a Variant Lacking a Protease Plasmid. Appl Environ Microbiol. 1982 Jun;43(6):1272–1277. doi: 10.1128/aem.43.6.1272-1277.1982. [DOI] [PMC free article] [PubMed] [Google Scholar]
  31. Polzin K. M., Romero D., Shimizu-Kadota M., Klaenhammer T. R., McKay L. L. Copy number and location of insertion sequences ISS1 and IS981 in lactococci and several other lactic acid bacteria. J Dairy Sci. 1993 May;76(5):1243–1252. doi: 10.3168/jds.S0022-0302(93)77453-6. [DOI] [PubMed] [Google Scholar]
  32. Polzin K. M., Shimizu-Kadota M. Identification of a new insertion element, similar to gram-negative IS26, on the lactose plasmid of Streptococcus lactis ML3. J Bacteriol. 1987 Dec;169(12):5481–5488. doi: 10.1128/jb.169.12.5481-5488.1987. [DOI] [PMC free article] [PubMed] [Google Scholar]
  33. Renault P. P., Heslot H. Selection of Streptococcus lactis Mutants Defective in Malolactic Fermentation. Appl Environ Microbiol. 1987 Feb;53(2):320–324. doi: 10.1128/aem.53.2.320-324.1987. [DOI] [PMC free article] [PubMed] [Google Scholar]
  34. Romero D. A., Klaenhammer T. R. Characterization of insertion sequence IS946, an Iso-ISS1 element, isolated from the conjugative lactococcal plasmid pTR2030. J Bacteriol. 1990 Aug;172(8):4151–4160. doi: 10.1128/jb.172.8.4151-4160.1990. [DOI] [PMC free article] [PubMed] [Google Scholar]
  35. Romero D. A., Klaenhammer T. R. IS946-mediated integration of heterologous DNA into the genome of Lactococcus lactis subsp. lactis. Appl Environ Microbiol. 1992 Feb;58(2):699–702. doi: 10.1128/aem.58.2.699-702.1992. [DOI] [PMC free article] [PubMed] [Google Scholar]
  36. Romero D. A., Klaenhammer T. R. Transposable elements in Lactococci: a review. J Dairy Sci. 1993 Jan;76(1):1–19. doi: 10.3168/jds.S0022-0302(93)77318-X. [DOI] [PubMed] [Google Scholar]
  37. Schäfer A., Jahns A., Geis A., Teuber M. Distribution of the IS elements ISS1 and IS904 in lactococci. FEMS Microbiol Lett. 1991 May 15;64(2-3):311–317. doi: 10.1111/j.1574-6968.1991.tb04681.x. [DOI] [PubMed] [Google Scholar]
  38. Simon D., Chopin A. Construction of a vector plasmid family and its use for molecular cloning in Streptococcus lactis. Biochimie. 1988 Apr;70(4):559–566. doi: 10.1016/0300-9084(88)90093-4. [DOI] [PubMed] [Google Scholar]
  39. de Vos W. M., Vos P., de Haard H., Boerrigter I. Cloning and expression of the Lactococcus lactis subsp. cremoris SK11 gene encoding an extracellular serine proteinase. Gene. 1989 Dec 21;85(1):169–176. doi: 10.1016/0378-1119(89)90477-0. [DOI] [PubMed] [Google Scholar]
  40. van Asseldonk M., Simons A., Visser H., de Vos W. M., Simons G. Cloning, nucleotide sequence, and regulatory analysis of the Lactococcus lactis dnaJ gene. J Bacteriol. 1993 Mar;175(6):1637–1644. doi: 10.1128/jb.175.6.1637-1644.1993. [DOI] [PMC free article] [PubMed] [Google Scholar]

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