首页> 外文期刊>Gene: An International Journal Focusing on Gene Cloning and Gene Structure and Function >Molecular cloning and expression analysis of a new bilin lyase: The cpcT gene encoding a bilin lyase responsible for attachment of phycocyanobilin to Cys-153 on the β-subunit of phycocyanin in Arthrospira platensis FACHB314
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Molecular cloning and expression analysis of a new bilin lyase: The cpcT gene encoding a bilin lyase responsible for attachment of phycocyanobilin to Cys-153 on the β-subunit of phycocyanin in Arthrospira platensis FACHB314

机译:一种新的胆红素裂解酶的分子克隆和表达分析:编码胆红素裂解酶的pccT基因,负责将藻蓝蛋白结合到青藻FACHB314藻蓝蛋白β亚基上的Cys-153上

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摘要

To study the assembly of phycocyanin β subunit, the gene cpcT was first cloned from Arthrospira platensis FACHB314. To explore the function of cpcT, the DNA of phycocyanin β subunit and cpcT were transformed into Escherichia coli BL21 with the plasmid pET-hox1-pcyA, which contained the genes hemeoxygenase 1 (Hox1) and ferredoxin oxidoreductase (PcyA) needed to produce phycocyanobilin. The transformed strains showed specific phycocyanin fluorescence, and the fluorescence intensity was stronger than the strains with only phycocyanin β subunit, indicating that CpcT can promote the assembly of phycocyanin to generate fluorescence. To study the possible binding sites of apo-phycocyanin and phycocyanobilin, the Cys-82 and Cys-153 of the β subunit were individually mutated, giving two kinds of mutants. The results show that Cys-153 maybe the active site for β subunit binding to phycocyanobilins, which is catalyzed by CpcT in A. platensis FACHB314.
机译:为了研究藻蓝蛋白β亚基的组装,首先从白节螺旋藻FACHB314中克隆了基因cpcT。为了探索cpcT的功能,将藻蓝蛋白β亚基和cpcT的DNA用质粒pET-hox1-pcyA转化到大肠杆菌BL21中,该质粒包含产生藻蓝蛋白所需的血红素加氧酶1(Hox1)和铁氧还蛋白氧化还原酶(PcyA)基因。转化的菌株显示出特定的藻蓝蛋白荧光,并且荧光强度比仅具有藻蓝蛋白β亚基的菌株强,表明CpcT可以促进藻蓝蛋白的组装以产生荧光。为了研究载脂蛋白藻蓝蛋白和藻蓝蛋白的可能结合位点,分别突变了β亚基的Cys-82和Cys-153,给出了两种突变体。结果表明,Cys-153可能是β亚基与藻蓝蛋白结合的活性位点,这是由CpcT在A. platensis FACHB314中催化的。

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