DOI: 10.1016/s0928-8244(03)00181-0. A rapid and simple method for inactivating chromosomal genes in<i>Yersinia</i>

A rapid and simple method for inactivating chromosomal genes inYersinia

10.1016/s0928-8244(03)00181-0

Crossref journal-article

Oxford University Press (OUP)

FEMS Immunology & Medical Microbiology (286)

Bibliography

Derbise, A., Lesic, B., Dacheux, D., Ghigo, J. M., & Carniel, E. (2003). A rapid and simple method for inactivating chromosomal genes inYersinia. FEMS Immunology & Medical Microbiology, 38(2), 113â116.

Authors 5

Anne Derbise (first)
Biliana Lesic (additional)
Denis Dacheux (additional)
Jean Marc Ghigo (additional)
Elisabeth Carniel (additional)

References 10 Referenced 205

[1] Chaveroche, M.K., Ghigo, J.M., d'Enfert, C. A rapid method for efficient gene replacement in the filamentous fungus Aspergillus nidulans Nucleic Acids Res. 28 2000 E97 (10.1093/nar/28.22.e97)
10.1073/pnas.120163297 / Proc. Natl. Acad. Sci. USA / One-step inactivation of chromosomal genes in Escherichia coli K-12 using PCR products by Datsenko (2000)
10.1128/JB.180.8.2063-2071.1998 / J. Bacteriol. / Use of bacteriophage lambda recombination functions to promote gene replacement in Escherichia coli by Murphy (1998)
10.1128/IAI.59.12.4310-4317.1991 / Infect. Immun. / Construction of an eae deletion mutant of enteropathogenic Escherichia coli by using a positive-selection suicide vector by Donnenberg (1991)
[5] Taylor, L.A., Rose, R.E. A correction in the nucleotide sequence of the Tn 903 kanamycin resistance determinant in pUC4K Nucleic Acids Res. 16 1988 358 (10.1093/nar/16.1.358)
10.1002/(SICI)1097-0061(19960315)12:3<259::AID-YEA901>3.0.CO;2-C / Yeast / PCR-synthesis of marker cassettes with long flanking homology regions for gene disruptions in S. cerevisiae by Wach (1996)
10.1016/0378-1119(89)90359-4 / Gene / Engineering hybrid genes without the use of restriction enzymes: gene splicing by overlap extension by Horton (1989)
10.1016/0378-1119(90)90505-L / Gene / A highly efficient electroporation system for transformation of Yersinia by Conchas (1990)
10.1046/j.1365-2958.1998.01124.x / Mol. Microbiol. / The high-pathogenicity island of Yersinia pseudotuberculosis can be inserted into any of the three chromosomal asn tRNA genes by Buchrieser (1998)
10.1046/j.1365-2958.2000.01993.x / Mol. Microbiol. / Characterization of the O-antigen gene clusters of Yersinia pseudotuberculosis and the cryptic O-antigen gene cluster of Yersinia pestis shows that the plague bacillus is most closely related to and has evolved from Y. pseudotuberculosis serotype O1b by Skurnik (2000)

Dates

Type	When
Created	22 years, 1 month ago (July 7, 2003, 9:47 a.m.)
Deposited	5 years, 5 months ago (March 24, 2020, 1:15 p.m.)
Indexed	1 month ago (July 30, 2025, 10:31 a.m.)
Issued	22 years ago (Sept. 1, 2003)
Published	22 years ago (Sept. 1, 2003)
Published Print	22 years ago (Sept. 1, 2003)

Funders 0

None

BibTeX

@article{Derbise_2003, title={A rapid and simple method for inactivating chromosomal genes inYersinia}, volume={38}, ISSN={1574-695X}, url={http://dx.doi.org/10.1016/s0928-8244(03)00181-0}, DOI={10.1016/s0928-8244(03)00181-0}, number={2}, journal={FEMS Immunology & Medical Microbiology}, publisher={Oxford University Press (OUP)}, author={Derbise, Anne and Lesic, Biliana and Dacheux, Denis and Ghigo, Jean Marc and Carniel, Elisabeth}, year={2003}, month=sep, pages={113–116} }

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