| Literature DB >> 23792095 |
Satoshi Inouye1, Jun-ichi Sato, Yuiko Sahara-Miura, Suguru Yoshida, Hajime Kurakata, Takamitsu Hosoya.
Abstract
The codon-optimized gene for the mutated 19 kDa protein (nanoKAZ), which is the catalytic component of Oplophorus luciferase, was expressed in Escherichia coli cells and the recombinant protein was highly purified. The secretory expression of nanoKAZ from CHO-K1 cells was performed by fusing the secretory signal peptide sequence of Gaussia luciferase to the amino-terminus of nanoKAZ. The substrate specificity for the purified nanoKAZ and the nanoKAZ secreted into the cultured medium was determined, indicating that bis-coelenterazine (bis-CTZ) and newly synthesized 6h-f-coelenterazine (6h-f-CTZ) are an efficient substrate for the glow luminescence reaction of nanoKAZ.Entities:
Keywords: 19kOLase; CTZ; Codon-optimized gene; Coelenterazine; FWHM; Furimazine; GLase; Gaussia; Gaussia luciferase; I(max); Reporter assay; coelenterazine; full width at half maximum; maximum intensity of luminescence; nanoKAZ; relative light units; rlu; the catalytic 19kDa protein of Oplophorus luciferase; the mutated 19kOLase
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Year: 2013 PMID: 23792095 DOI: 10.1016/j.bbrc.2013.06.026
Source DB: PubMed Journal: Biochem Biophys Res Commun ISSN: 0006-291X Impact factor: 3.575