Citation
Abstract
A vector that drives the expression of the reporter gusA gene in both Lactobacillus plantarum and Lactococcus lactis was constructed in this study. This vector contained a newly characterized heat shock promoter (Phsp), amplified from an Enterococcus faecium plasmid, pAR6. Functionality and characterization of this promoter was initially performed by cloning Phsp into pNZ8008, a commercial lactococcal plasmid used for screening of putative promoters which utilizes gusA as a reporter. It was observed that Phsp was induced under heat, salinity and alkaline stresses or a combination of all three stresses. The newly characterized Phsp promoter was then used to construct a novel Lactobacillus vector, pAR1801 and its ability to express the gusA under stress-induced conditions was reproducible in both Lb. plantarum Pa21 and L. lactis M4 hosts.
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Additional Metadata
Item Type: | Article |
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Divisions: | Faculty of Biotechnology and Biomolecular Sciences Institute of Bioscience |
DOI Number: | https://doi.org/10.1016/j.plasmid.2014.05.003 |
Publisher: | Elsevier |
Keywords: | Heat shock promoter; LAB; Lactococcus lactis; Lactobacillus plantarum |
Depositing User: | Nabilah Mustapa |
Date Deposited: | 12 Jan 2016 00:26 |
Last Modified: | 12 Jan 2016 00:26 |
Altmetrics: | http://www.altmetric.com/details.php?domain=psasir.upm.edu.my&doi=10.1016/j.plasmid.2014.05.003 |
URI: | http://psasir.upm.edu.my/id/eprint/36892 |
Statistic Details: | View Download Statistic |
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