Demonstration of RNAN-Glycosidase Activity of a Vero Toxin (VT2 Variant) Produced byEscherichia coli091: H21 from a Patient with the Hemolytic Uremic Syndrome

Author:

Furutani Masayuki1,Ito Kiyoshi1,Oku Yuichi2,Takeda Yoshifumi23,Igarashi Kazuei1

Affiliation:

1. Faculty of Pharmaceutical Sciences; Chiba University; Chiba Chiba 260

2. Department of Bacterial Infection, The Institute of Medical Science; The University of Tokyo; Minato-ku Tokyo 108

3. Department of Microbiology, Faculty of Medicine; Kyoto University; Sakyo-ku Kyoto 606

Publisher

Wiley

Subject

Virology,Immunology,Microbiology

Reference17 articles.

1. The site of action of α-sarcin on eukaryotic ribosomes. The sequence of the α-sarcin cleavage site in 28S ribosomal ribonucleic acid;Endo;J. Biol. Chem.,1982

2. The mechanism of action of ricin and related lectins on eukaryotic ribosomes;Endo;J. Biol. Chem.,1987

3. Site of action of a Vero toxin (VT2) from Escherichia coli O157: H7 and of Shiga toxin on eukaryotic ribosomes. RNA N-glycosidase activity of the toxins;Endo;Eur. J. Biochcm.,1988

4. Inhibition of elongation factor-1 dependent aminoacyl-tRNA binding to ribosomes by Shiga-like toxin I (VTl) from Escherichia coli O157: H7 and by Shiga toxin;Igarashi;FEMS Microbiol. Lett.,1987

5. Escherichia coli strains isolated from pigs with edema disease produced a variant of Shiga-like toxin II;Marques;FEMS Microbiol. Lett.,1987

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