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细胞色素bd氧化酶的序列分析表明亚基I的拓扑结构有所修订。

Sequence analysis of cytochrome bd oxidase suggests a revised topology for subunit I.

作者信息

Osborne J P, Gennis R B

机构信息

School of Chemical Sciences, University of Illinois, Urbana, IL 61801, USA.

出版信息

Biochim Biophys Acta. 1999 Jan 27;1410(1):32-50. doi: 10.1016/s0005-2728(98)00171-6.

Abstract

Numerous sequences of the cytochrome bd quinol oxidase (cytochrome bd) have recently become available for analysis. The analysis has revealed a small number of conserved residues, a new topology for subunit I and a phylogenetic tree involving extensive horizontal gene transfer. There are 20 conserved residues in subunit I and two in subunit II. Algorithms utilizing multiple sequence alignments predicted a revised topology for cytochrome bd, adding two transmembrane helices to subunit I to the seven that were previously indicated by the analysis of the sequence of the oxidase from E. coli. This revised topology has the effect of relocating the N-terminus and C-terminus to the periplasmic and cytoplasmic sides of the membrane, respectively. The new topology repositions I-H19, the putative ligand for heme b595, close to the periplasmic edge of the membrane, which suggests that the heme b595/heme d active site of the oxidase is located near the outer (periplasmic) surface of the membrane. The most highly conserved region of the sequence of subunit I contains the sequence GRQPW and is located in a predicted periplasmic loop connecting the eighth and ninth transmembrane helices. The potential importance of this region of the protein was previously unsuspected, and it may participate in the binding of either quinol or heme d. There are two very highly conserved glutamates in subunit I, E99 and E107, within the third transmembrane helix (E. coli cytochrome bd-I numbering). It is speculated that these glutamates may be part of a proton channel leading from the cytoplasmic side of the membrane to the heme d oxygen-reactive site, now placed near the periplasmic surface. The revised topology and newly revealed conserved residues provide a clear basis for further experimental tests of these hypotheses. Phylogenetic analysis of the new sequences of cytochrome bd reveals considerable deviation from the 16sRNA tree, suggesting that a large amount of horizontal gene transfer has occurred in the evolution of cytochrome bd.

摘要

细胞色素bd喹啉氧化酶(细胞色素bd)的众多序列最近已可用于分析。分析揭示了少量保守残基、亚基I的新拓扑结构以及涉及广泛水平基因转移的系统发育树。亚基I中有20个保守残基,亚基II中有2个。利用多序列比对的算法预测了细胞色素bd的修订拓扑结构,在亚基I中增加了两个跨膜螺旋,使其从之前对大肠杆菌氧化酶序列分析所表明的七个增加到九个。这种修订后的拓扑结构的作用是将N端和C端分别重新定位到膜的周质侧和细胞质侧。新拓扑结构将I-H19(推测为血红素b595的配体)重新定位到靠近膜周质边缘的位置,这表明氧化酶的血红素b595/血红素d活性位点位于膜的外(周质)表面附近。亚基I序列中最保守的区域包含序列GRQPW,位于预测的连接第八和第九个跨膜螺旋的周质环中。该蛋白区域的潜在重要性此前未被怀疑,它可能参与喹啉或血红素d的结合。亚基I中有两个高度保守的谷氨酸,E99和E107,位于第三个跨膜螺旋内(大肠杆菌细胞色素bd-I编号)。据推测,这些谷氨酸可能是质子通道的一部分,该通道从膜的细胞质侧通向现在位于周质表面附近的血红素d氧反应位点。修订后的拓扑结构和新揭示的保守残基为这些假设的进一步实验测试提供了明确的基础。细胞色素bd新序列系统发育分析显示与16sRNA树有相当大的偏差,这表明在细胞色素bd的进化过程中发生了大量水平基因转移。

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