2014
DOI: 10.1007/s11274-014-1663-7
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Expression of bioactive porcine interferon-alpha in Lactobacillus casei

Abstract: In this study, we constructed an expression cassette containing the inducible lac promoter and the secretion signal from an S-layer protein of Lactobacillus brevis for the expression of porcine interferon-alpha (IFN-α) in Lactobacillus casei (Lb. casei). Reverse-transcriptase PCR verified the presence of porcine IFN-α mRNA in the recombinant Lb. casei. The porcine IFN-α protein expressed in the recombinant Lb. casei was identified by both Western blot analysis and ELISA. We used various pH values and induction… Show more

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Cited by 8 publications
(3 citation statements)
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“…But there were only a few genetic tools developed in other LAB except L. lactis which were used in probiotic products. Secondly, most expression system developed in LAB were using inducible promoters, such as P nisA , P zn , P lac , P 170 which were induced by nisin, heavy metals, sugar and pH, respectively [29][30][31][32]. Inducible expression can be preferable in cases where the aim is to overproduce a desired protein at high levels, e.g.…”
Section: Resultsmentioning
confidence: 99%
“…But there were only a few genetic tools developed in other LAB except L. lactis which were used in probiotic products. Secondly, most expression system developed in LAB were using inducible promoters, such as P nisA , P zn , P lac , P 170 which were induced by nisin, heavy metals, sugar and pH, respectively [29][30][31][32]. Inducible expression can be preferable in cases where the aim is to overproduce a desired protein at high levels, e.g.…”
Section: Resultsmentioning
confidence: 99%
“…The porcine IFN-λ3 can be displayed on the surface of the membrane via a transmembrane helix anchor (the pgsA protein from Bacillus subtilis ) or attached to the cell wall anchor via a covalent link with the LPXTG motif (CWA) [ 38 ]. Hence, the use of CWA and pgsA to display porcine IFN-λ3 on the surface of L. plantarum is a promising candidate approach for the use of L. plantarum as a live oral bacterial agent [ 39 ].…”
Section: Discussionmentioning
confidence: 99%
“…In this study, pSIP expression systems were used to express FMDV-VP1 protein. Studies are currently underway to employ lactic acid bacteria vectors to produce vaccines of many viral proteins, such as the hemagglutinin (HA) gene of H9N2 avian influenza virus, anti-rotavirus protein (Llama VHH antibody fragments), and bioactive porcine interferon-alpha [48][49][50]. Two L. plantarum strains were chosen in this study to carry the pSIP plasmids.…”
Section: Discussionmentioning
confidence: 99%