2013
DOI: 10.1186/1472-6750-13-3
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Cloning, overexpression, purification, and characterization of a polyextremophilic β-galactosidase from the Antarctic haloarchaeon Halorubrum lacusprofundi

Abstract: BackgroundHalorubrum lacusprofundi is a cold-adapted halophilic archaeon isolated from Deep Lake, a perennially cold and hypersaline lake in Antarctica. Its genome sequencing project was recently completed, providing access to many genes predicted to encode polyextremophilic enzymes active in both extremely high salinity and cold temperatures.ResultsAnalysis of the genome sequence of H. lacusprofundi showed a gene cluster for carbohydrate utilization containing a glycoside hydrolase family 42 β-galactosidase g… Show more

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Cited by 84 publications
(81 citation statements)
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“…NRC-1Δ ura 3Δ gvp C deletion strain, constructed using the ura 3-based gene deletion method 54 , showed a partially gas vesicle-deficient phenotype with small, mainly lemon-shaped gas vesicles. We next constructed a gvp C expression vector series using pMC2, an expression plasmid with the cold-inducible csp D2 promoter, and pDRK, an expression plasmid incorporating the higher-level gvpA promoter 55,56 . A series of PCR amplified gvp C gene fragments (C-series) were then inserted into the expression plasmids to test their ability to bind to GVNPs and complement nanoparticle production.…”
Section: Experimental Approach and Findingsmentioning
confidence: 99%
“…NRC-1Δ ura 3Δ gvp C deletion strain, constructed using the ura 3-based gene deletion method 54 , showed a partially gas vesicle-deficient phenotype with small, mainly lemon-shaped gas vesicles. We next constructed a gvp C expression vector series using pMC2, an expression plasmid with the cold-inducible csp D2 promoter, and pDRK, an expression plasmid incorporating the higher-level gvpA promoter 55,56 . A series of PCR amplified gvp C gene fragments (C-series) were then inserted into the expression plasmids to test their ability to bind to GVNPs and complement nanoparticle production.…”
Section: Experimental Approach and Findingsmentioning
confidence: 99%
“…The expression vector is based on the pHV2 origin which maintains the plasmid at a copy number of approximately 6 per genome equivalent (Allers 2010 ). To date, the H. volcanii expression system has been successfully applied for heterologous protein expressions on a shaker-flask scale (Karan et al 2013 ;Timpson et al 2012Timpson et al , 2013.…”
Section: Introductionmentioning
confidence: 99%
“…NRC-1Δ ura 3Δ gvp C strain, we constructed a derivative of the previously described pDRK expression plasmid containing a fragment of the gvp C gene (Fig. 1B) [20]. This pDRK-C3 plasmid contains a sequence encoding the C3 fragment of GvpC (280 out of 382 amino acids) downstream of the gvp A promoter and His 6 coding region.…”
Section: Resultsmentioning
confidence: 99%