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Molecular analysis of the distribution and phylogeny of dissimilatory adenosine-5′-phosphosulfate reductase-encoding genes (aprBA) among sulfur-oxidizing prokaryotes

机译:硫氧化原核生硫氧化氨基磺酸盐还原酶编码基因(APLBA)分子分析

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Dissimilatory adenosine-5′-phosphosulfate (APS) reductase (AprBA) is a key enzyme of the dissimilatory sulfate-reduction pathway. Homologues have been found in photo- and chemotrophic sulfur-oxidizing prokaryotes (SOP), in which they are postulated to operate in the reverse direction, oxidizing sulfite to APS. Newly developed PCR assays allowed the amplification of 92–93?% (2.1–2.3?kb) of the APS reductase locus aprBA. PCR-based screening of 116 taxonomically divergent SOP reference strains revealed a distribution of aprBA restricted to photo- and chemotrophs with strict anaerobic or at least facultative anaerobic lifestyles, including Chlorobiaceae, Chromatiaceae, Thiobacillus, Thiothrix and invertebrate symbionts. In the AprBA-based tree, the SOP diverge into two distantly related phylogenetic lineages, Apr lineages I and II, with the proteins of lineage II (Chlorobiaceae and others) in closer affiliation to the enzymes of the sulfate-reducing prokaryotes (SRP). This clustering is discordant with the dissimilatory sulfite reductase (DsrAB) phylogeny and indicates putative lateral aprBA gene transfer from SRP to the respective SOB lineages. In support of lateral gene transfer (LGT), several beta- and gammaproteobacterial species harbour both aprBA homologues, the DsrAB-congruent ‘authentic’ and the SRP-related, LGT-derived gene loci, while some relatives possess exclusively the SRP-related apr genes as a possible result of resident gene displacement by the xenologue. The two-gene state might be an intermediate in the replacement of the resident essential gene. Collected genome data demonstrate the correlation between the AprBA tree topology and the composition/arrangement of the apr gene loci (occurrence of qmoABC or aprM genes) from SRP and SOP of lineages I and II. The putative functional role of the SRP-related APS reductases in photo- and chemotrophic SOP is discussed.
机译:聚糖腺苷-5'-磷硫酸盐(APS)还原酶(APSBA)是含硫酸化硫酸盐还原途径的关键酶。已经发现在光脱色的硫氧化原核生物(SOP)中发现了同源物,其中它们被假设以在反向方向上运行,将亚硫酸盐氧化成APS。新开发的PCR测定允许扩增APS还原酶源泉APRBA的92-93?%(2.1-2.3?KB)。基于PCR的116个小位神经分歧SOP参考菌株揭示了APRBA的分布,限制性地限于与严格的厌氧或至少兼性厌氧生活方式,包括氯真菌,Chromatiaceae,Thiobacillus,Thiothrix和无脊椎动物Symbion。在基于APRBA的树中,SOP分为两种远端相关的系统发育谱系,APR谱系I和II,用血管II(氯真菌等)的蛋白质在更接近硫酸盐还原原核生物(SRP)的酶的束密度中。这种聚合物与脱胶亚硫酸盐还原酶(DSRAB)系统发育不和谐,并表明从SRP到各种呜咽物的推定的外侧APRBA基因转移。为了支持横向基因转移(LGT),几种β-和γ-和γ-和γ-和γ-γ-同源物种,DSRAB-一致的“正宗”和与SRP相关的LGT衍生的基因基因座,而一些亲属专门拥有与SRP相关的4月基因作为Xenologue居民基因位移的可能结果。双基因状态可能是替代驻留基因的中间体。收集的基因组数据证明了APRBA树拓扑和APR基因基因座(QMOABC或APRM基因)的组成/排列之间的相关性来自SRP和II和II的SRP和II。讨论了SRP相关APS还原酶在光谱和趋化性SOP中的推定功能作用。

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