荧光素酶
基质(水族馆)
化学
大肠杆菌
重组DNA
分子生物学
信号肽
催化作用
生物化学
生物发光
发光
肽
酶
基因
生物
转染
材料科学
光电子学
生态学
作者
S Inouye,Junichi Sato,Yuiko Sahara‐Miura,Suguru Yoshida,Hajime Kurakata,Takamitsu Hosoya
标识
DOI:10.1016/j.bbrc.2013.06.026
摘要
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.
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