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异化亚硫酸盐还原酶的系统发育支持硫酸盐呼吸的早期起源。

Phylogeny of dissimilatory sulfite reductases supports an early origin of sulfate respiration.

作者信息

Wagner M, Roger A J, Flax J L, Brusseau G A, Stahl D A

机构信息

Department of Civil Engineering, Technological Institute, Northwestern University, Evanston, Illinois 60208-3109, USA.

出版信息

J Bacteriol. 1998 Jun;180(11):2975-82. doi: 10.1128/JB.180.11.2975-2982.1998.

Abstract

Microorganisms that use sulfate as a terminal electron acceptor for anaerobic respiration play a central role in the global sulfur cycle. Here, we report the results of comparative sequence analysis of dissimilatory sulfite reductase (DSR) genes from closely and distantly related sulfate-reducing organisms to infer the evolutionary history of DSR. A 1.9-kb DNA region encoding most of the alpha and beta subunits of DSR could be recovered only from organisms capable of dissimilatory sulfate reduction with a PCR primer set targeting highly conserved regions in these genes. All DNA sequences obtained were highly similar to one another (49 to 89% identity), and their inferred evolutionary relationships were nearly identical to those inferred on the basis of 16S rRNA. We conclude that the high similarity of bacterial and archaeal DSRs reflects their common origin from a conserved DSR. This ancestral DSR was either present before the split between the domains Bacteria, Archaea, and Eucarya or laterally transferred between Bacteria and Archaea soon after domain divergence. Thus, if the physiological role of the DSR was constant over time, then early ancestors of Bacteria and Archaea already possessed a key enzyme of sulfate and sulfite respiration.

摘要

利用硫酸盐作为厌氧呼吸终末电子受体的微生物在全球硫循环中起着核心作用。在此,我们报告了来自亲缘关系远近不同的硫酸盐还原菌的异化亚硫酸盐还原酶(DSR)基因的比较序列分析结果,以推断DSR的进化历史。仅使用靶向这些基因高度保守区域的PCR引物对,就能从能够进行异化硫酸盐还原的生物体中回收一个编码DSR大部分α和β亚基的1.9 kb DNA区域。获得的所有DNA序列彼此高度相似(同一性为49%至89%),并且它们推断的进化关系与基于16S rRNA推断的进化关系几乎相同。我们得出结论,细菌和古菌DSR的高度相似性反映了它们源自一个保守的DSR的共同起源。这种祖先DSR要么在细菌域、古菌域和真核域分化之前就已存在,要么在域分化后不久在细菌和古菌之间横向转移。因此,如果DSR的生理作用随时间保持不变,那么细菌和古菌的早期祖先就已经拥有了硫酸盐和亚硫酸盐呼吸的关键酶。

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