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对来自大肠杆菌的细胞色素bd喹啉氧化酶Q环附近高度保守区域进行定点突变,会特异性地扰乱血红素b595。

Site-directed mutation of the highly conserved region near the Q-loop of the cytochrome bd quinol oxidase from Escherichia coli specifically perturbs heme b595.

作者信息

Zhang J, Hellwig P, Osborne J P, Huang H W, Moënne-Loccoz P, Konstantinov A A, Gennis R B

机构信息

Department of Biochemistry, University of Illinois at Urbana-Champaign, 600 South Mathews Avenue, Urbana, Illinois 61801, USA.

出版信息

Biochemistry. 2001 Jul 24;40(29):8548-56. doi: 10.1021/bi010469m.

Abstract

Cytochrome bd is one of the two quinol oxidases in the respiratory chain of Escherichia coli. The enzyme contains three heme prosthetic groups. The dioxygen binding site is heme d, which is thought to be part of the heme-heme binuclear center along with heme b(595), which is a high-spin heme whose function is not known. Protein sequence alignments [Osborne, J. P., and Gennis, R. B. (1999) Biochim. Biophys Acta 1410, 32--50] of cytochrome bd quinol oxidase sequences from different microorganisms have revealed a highly conserved sequence (GWXXXEXGRQPW; bold letters indicate strictly conserved residues) predicted to be on the periplasmic side of the membrane between transmembrane helices 8 and 9 in subunit I. The functional importance of this region is investigated in the current work by site-directed mutagenesis. Several mutations in this region (W441A, E445A/Q, R448A, Q449A, and W451A) resulted in a catalytically inactive enzyme with abnormal UV--vis spectra. E445A was selected for detailed analysis because of the absence of the absorption bands from heme b(595). Detailed spectroscopic and chemical analyses, indeed, show that one of the three heme prosthetic groups in the enzyme, heme b(595), is specifically perturbed and mostly missing from this mutant. Surprisingly, heme d, while known to interact with heme b(595), appears relatively unperturbed, whereas the low-spin heme b(558) shows some modification. This is the first report of a mutation that specifically affects the binding site of heme b(595).

摘要

细胞色素bd是大肠杆菌呼吸链中的两种喹啉氧化酶之一。该酶含有三个血红素辅基。双氧基结合位点是血红素d,它被认为是血红素 - 血红素双核中心的一部分,与血红素b(595)一起,血红素b(595)是一种高自旋血红素,其功能尚不清楚。来自不同微生物的细胞色素bd喹啉氧化酶序列的蛋白质序列比对[奥斯本,J.P.,和根尼斯,R.B.(1999年)《生物化学与生物物理学报》1410,32 - 50]揭示了一个高度保守的序列(GWXXXEXGRQPW;粗体字母表示严格保守的残基),预计位于亚基I中跨膜螺旋8和9之间膜的周质侧。在当前工作中通过定点诱变研究了该区域的功能重要性。该区域的几个突变(W441A、E445A/Q、R448A、Q449A和W451A)导致了一种催化无活性且具有异常紫外 - 可见光谱的酶。由于缺乏来自血红素b(595)的吸收带,选择E445A进行详细分析。详细的光谱和化学分析确实表明,该酶的三个血红素辅基之一,血红素b(595),受到特异性干扰且在该突变体中基本缺失。令人惊讶的是,已知与血红素b(595)相互作用的血红素d似乎相对未受干扰,而低自旋血红素b(558)显示出一些修饰。这是首次报道特异性影响血红素b(595)结合位点的突变。

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