| Literature DB >> 24362421 |
Karina Klevanskaa1, Nadja Bier, Kerstin Stingl, Eckhard Strauch, Stefan Hertwig.
Abstract
An efficient electroporation procedure for Vibrio vulnificus was designed using the new cloning vector pVv3 (3,107 bp). Transformation efficiencies up to 2 × 10(6) transformants per μg DNA were achieved. The vector stably replicated in both V. vulnificus and Escherichia coli and was also successfully introduced into Vibrio parahaemolyticus and Vibrio cholerae. To demonstrate the suitability of the vector for molecular cloning, the green fluorescent protein (GFP) gene and the vvhBA hemolysin operon were inserted into the vector and functionally expressed in Vibrio and E. coli.Entities:
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Year: 2013 PMID: 24362421 PMCID: PMC3911060 DOI: 10.1128/AEM.03720-13
Source DB: PubMed Journal: Appl Environ Microbiol ISSN: 0099-2240 Impact factor: 4.792