Xi L, Cho K W, Tu S C
Department of Biochemical and Biophysical Sciences, University of Houston, Texas 77204-5500.
J Bacteriol. 1991 Feb;173(4):1399-405. doi: 10.1128/jb.173.4.1399-1405.1991.
Xenorhabdus luminescens HW is the only known luminous bacterium isolated from a human (wound) source. A recombinant plasmid was constructed that contained the X. luminescens HW luxA and luxB genes, encoding the luciferase alpha and beta subunits, respectively, as well as luxC, luxD, and a portion of luxE. The nucleotide sequences of these lux genes, organized in the order luxCDABE, were determined, and overexpression of the cloned luciferase genes was achieved in Escherichia coli host cells. The cloned luciferase was indistinguishable from the wild-type enzyme in its in vitro bioluminescence kinetic properties. Contrary to an earlier report, our findings indicate that neither the specific activity nor the size of the alpha (362 amino acid residues, Mr 41,389) and beta (324 amino acid residues, Mr 37,112) subunits of the X. luminescens HW luciferase was unusual among known luminous bacterial systems. Significant sequence homologies of the alpha and beta subunits of the X. luminescens HW luciferase with those of other luminous bacteria were observed. However, the X. luminescens HW luciferase was unusual in the high stability of the 4a-hydroperoxyflavin intermediate and its sensitivity to aldehyde substrate inhibition.
发光光杆状菌HW是唯一已知的从人类(伤口)源分离出的发光细菌。构建了一种重组质粒,其中包含发光光杆状菌HW的luxA和luxB基因,分别编码荧光素酶的α和β亚基,以及luxC、luxD和部分luxE。确定了这些按luxCDABE顺序排列的lux基因的核苷酸序列,并在大肠杆菌宿主细胞中实现了克隆的荧光素酶基因的过表达。克隆的荧光素酶在其体外生物发光动力学特性方面与野生型酶没有区别。与早期报告相反,我们的研究结果表明,发光光杆状菌HW荧光素酶的α(362个氨基酸残基,Mr 41,389)和β(324个氨基酸残基,Mr 37,112)亚基的比活性和大小在已知的发光细菌系统中都没有异常。观察到发光光杆状菌HW荧光素酶的α和β亚基与其他发光细菌的α和β亚基有显著的序列同源性。然而,发光光杆状菌HW荧光素酶在4a-氢过氧黄素中间体的高稳定性及其对醛底物抑制的敏感性方面是不同寻常的。