Analysis of the Structural Gene Encoding a Hemolysin inVibrio mimicus
- 1 February 1997
- journal article
- Published by Wiley in Microbiology and Immunology
- Vol. 41 (2) , 169-173
- https://doi.org/10.1111/j.1348-0421.1997.tb01183.x
Abstract
An environmental isolate of V. mimicus, strain E-33, has been reported to produce and secrete a hemolysin of 63 kDa. The hemolysin is enterotoxic in test animals. The nucleotide sequence of the structural gene of the hemolysin was determined. We found a 2,232 bp open reading frame, which codes a peptide of 744 amino acids, with a calculated molecular weight of 83,903 Da. The sequence for the structural gene was closely related to the V. cholerae el tor hlyA gene, coding an exocellular hemolysin. The amino terminal amino-acid sequence of the 63 kDa hemolysin, purified from V. mimicus, was determined by the Edman degradation method and found to be NH2-S-V-S-A-N-N-V-T-N-N-N-E-T. This sequence is identified from S-152 to T-164 predicted from the nucleotide sequence. So, it seems that the mature hemolysin in V. mimicus is processed upon deleting the first 151 amino acids, and the molecular mass is 65,972 Da. Analyzing the deduced amino-acid sequence, we also found a potential signal sequence of 24 amino acids at the amino terminal. Our results suggest that, like V. cholerae hemolysin, two-step processing also exists in V. Mimicus hemolysin.Keywords
This publication has 14 references indexed in Scilit:
- Existence of a Novel Hemagglutinin Having No Protease Activity inVibrio mimicusMicrobiology and Immunology, 1994
- Vascular Permeability Enhancement by Vibrio mimicus Protease and the Mechanisms of ActionMicrobiology and Immunology, 1991
- Basic local alignment search toolJournal of Molecular Biology, 1990
- Characterization of the hlyB gene and its role in the production of the EI Tor haemolysin of Vibrio choierae O1Molecular Microbiology, 1990
- Comparative analysis of the hemolysin genes ofVibrio choleraenon-01,V. mimicus, andV. hollisaethat are similar to thetdhgene ofV. parahaemolyticusFEMS Microbiology Letters, 1990
- [9] Sequences within ribosome binding site affecting messenger RNA translatability and method to direct ribosomes to single messenger RNA speciesPublished by Elsevier ,1990
- Extracellular proteins of Vibrio cholerae: nucleotide sequence of the structural gene (hlyA) for the haemolysin of the haemolytic El Tor strain 017 and characterization of the hlyA mutation in the non‐haemolytic classical strain 569BMolecular Microbiology, 1988
- Production and Partial Purification of a Fluid-Accumulating Factor of Non-O1Vibrio choleraeMicrobiology and Immunology, 1988
- Characterization of enterotoxin and soluble hemagglutinin fromVibrio mimicus: identity withV. choleraeO1 toxin and hemagglutininFEMS Microbiology Letters, 1985
- Portable Shine-Dalgarno Regions: A System for a Systematic Study of Defined Alterations of Nucleotide Sequences withinE. coliRibosome Binding SitesDNA, 1983