首页> 外文期刊>Applied Microbiology >Terminal Oxidase Diversity and Function in “Metallosphaera yellowstonensis”: Gene Expression and Protein Modeling Suggest Mechanisms of Fe(II) Oxidation in the Sulfolobales
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Terminal Oxidase Diversity and Function in “Metallosphaera yellowstonensis”: Gene Expression and Protein Modeling Suggest Mechanisms of Fe(II) Oxidation in the Sulfolobales

机译:最终氧化酶多样性和功能的“黄化金丝雀”:基因表达和蛋白质建模表明Fe(II)氧化Sulfolobales的机制。

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“ Metallosphaera yellowstonensis ” is a thermoacidophilic archaeon isolated from Yellowstone National Park that is capable of autotrophic growth using Fe(II), elemental S, or pyrite as electron donors. Analysis of the draft genome sequence from M. yellowstonensis strain MK1 revealed seven different copies of heme copper oxidases (subunit I) in a total of five different terminal oxidase complexes, including doxBCEF , foxABCDEFGHIJ , soxABC , and the soxM supercomplex, as well as a novel hypothetical two-protein doxB -like polyferredoxin complex. Other genes found in M. yellowstonensis with possible roles in S and or Fe cycling include a thiosulfate oxidase ( tqoAB ), a sulfite oxidase ( som ), a cbsA cytochrome b _(558/566), several small blue copper proteins, and a novel gene sequence coding for a putative multicopper oxidase (Mco). Results from gene expression studies, including reverse transcriptase (RT) quantitative PCR (qPCR) of cultures grown autotrophically on either Fe(II), pyrite, or elemental S showed that the fox gene cluster and mco are highly expressed under conditions where Fe(II) is an electron donor. Metagenome sequence and gene expression studies of Fe-oxide mats confirmed the importance of fox genes (e.g., foxA and foxC ) and mco under Fe(II)-oxidizing conditions. Protein modeling of FoxC suggests a novel lysine-lysine or lysine-arginine heme B binding domain, indicating that it is likely the cytochrome component of a heterodimer complex with foxG as a ferredoxin subunit. Analysis of mco shows that it encodes a novel multicopper blue protein with two plastocyanin type I copper domains that may play a role in the transfer of electrons within the Fox protein complex. An understanding of metabolic pathways involved in aerobic iron and sulfur oxidation in Sulfolobales has broad implications for understanding the evolution and niche diversification of these thermophiles as well as practical applications in fields such as bioleaching of trace metals from pyritic ores.
机译:“ Metallosphaera yellowstonensis”是从黄石国家公园中分离出来的嗜热古细菌,它能够使用Fe(II),S元素或黄铁矿作为电子供体进行自养生长。对M. yellowstonensis菌株MK1的基因组序列草案进行的分析显示,在总共5种不同的终端氧化酶复合体(包括doxBCEF,foxABCDEFGHIJ,soxABC和soxM超复合体)中共有七个不同拷贝的血红素铜氧化酶(亚基I)。新型的假设的二蛋白doxB样聚铁氧还蛋白复合物。在Yellowstonensis中发现的其他基因可能在S和/或Fe循环中起作用,包括硫代硫酸盐氧化酶(tqoAB),亚硫酸盐氧化酶(som),cbsA细胞色素b _(558/566),一些小的蓝色铜蛋白和编码推定的多铜氧化酶(Mco)的新基因序列。基因表达研究的结果,包括在Fe(II),黄铁矿或元素S上自养生长的培养物的逆转录酶(RT)定量PCR(qPCR)结果表明,在Fe(II)条件下,fox基因簇和mco高度表达)是电子供体。铁氧化物垫的元基因组序列和基因表达研究证实了在Fe(II)氧化条件下fox基因(例如foxA和foxC)和mco的重要性。 FoxC的蛋白质模型表明存在新型的赖氨酸-赖氨酸或赖氨酸-精氨酸血红素B结合域,表明它可能是异二聚​​体复合物的细胞色素成分,其中foxG为铁氧还蛋白亚基。对mco的分析表明,它编码具有两个plastocyanin I型铜结构域的新型多铜蓝蛋白,该结构域可能在Fox蛋白复合物中的电子转移中起作用。对硫磺草中需氧铁和硫氧化的代谢途径的理解,对于理解这些嗜热菌的进化和生态位多样化以及在从黄铁矿中微量金属痕量生物浸提等领域的实际应用具有广泛的意义。

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