(Q41478664)

English

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 O:

scientific article published on July 2000

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Europe PubMed Central

PubMed publication ID

1 October 2017

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 O: (English)

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Europe PubMed Central

PubMed publication ID

1 October 2017

Yersinia pestis

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Yersinia pseudotuberculosis

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author name string

Skurnik M

1

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Europe PubMed Central

PubMed publication ID

1 October 2017

Peippo A

2

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Europe PubMed Central

PubMed publication ID

1 October 2017

Ervelä E

3

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Europe PubMed Central

PubMed publication ID

1 October 2017

language of work or name

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publication date

1 July 2000

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1 October 2017

Molecular Microbiology

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1 October 2017

37

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Europe PubMed Central

PubMed publication ID

1 October 2017

2

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Europe PubMed Central

PubMed publication ID

1 October 2017

316-330

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Europe PubMed Central

PubMed publication ID

1 October 2017

Yersinia pestis, the cause of plague, is a recently emerged clone of Yersinia pseudotuberculosis

1 reference

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Analysis of Shigella flexneri wzz (Rol) function by mutagenesis and cross-linking: wzz is able to oligomerize.

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Overexpression and topology of the Shigella flexneri O-antigen polymerase (Rfc/Wzy).

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The activity of a putative polyisoprenol-linked sugar translocase (Wzx) involved in Escherichia coli O antigen assembly is independent of the chemical structure of the O repeat

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The JUMPstart sequence: a 39 bp element common to several polysaccharide gene clusters

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Genetic organisation and evolution of Yersinia pseudotuberculosis 3,6-dideoxyhexose biosynthetic genes

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Molecular cloning and genetic characterization of the rfb region from Yersinia pseudotuberculosis serogroup IIA, which determines the formation of the 3,6-dideoxyhexose abequose

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Molecular analysis of the 3,6-dideoxyhexose pathway genes of Yersinia pseudotuberculosis serogroup IIA

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Molecular, genetic, and topological characterization of O-antigen chain length regulation in Shigella flexneri

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Suppression of transcription polarity in the Escherichia coli haemolysin operon by a short upstream element shared by polysaccharide and DNA transfer determinants.

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Evidence for two evolutionary lineages of highly pathogenic Yersinia species

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21 January 2018

Evolution of Salmonella O antigen variation by interspecific gene transfer on a large scale

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Bacterial polysaccharide synthesis and gene nomenclature

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Increased virulence of Yersinia pseudotuberculosis by two independent mutations

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Analysis of the yopA gene encoding the Yop1 virulence determinants of Yersinia spp.

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A novel locus of Yersinia enterocolitica serotype O:3 involved in lipopolysaccharide outer core biosynthesis

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The lipopolysaccharide outer core of Yersinia enterocolitica serotype O:3 is required for virulence and plays a role in outer membrane integrity

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Studies of the biosynthesis of 3,6-dideoxyhexoses: molecular cloning and characterization of the asc (ascarylose) region from Yersinia pseudotuberculosis serogroup VA

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21 January 2018

Lipopolysaccharide from Yersinia pseudotuberculosis, Type 1B. A Structural Study of O-Specific Chains

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Biosynthesis of lipopolysaccharide O antigens

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Improved M13 phage cloning vectors and host strains: nucleotide sequences of the M13mp18 and pUC19 vectors

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The gene cluster directing O-antigen biosynthesis in Yersinia enterocolitica serotype 0:8: identification of the genes for mannose and galactose biosynthesis and the gene for the O-antigen polymerase

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Molecular and chemical characterization of the lipopolysaccharide O-antigen and its role in the virulence of Yersinia enterocolitica serotype O:8.

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21 January 2018

Identifiers

10.1046/J.1365-2958.2000.01993.X

1 reference

Europe PubMed Central

PubMed publication ID

1 October 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

1 October 2017

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