首页> 外文OA文献 >Anaerobic Respiration of Elemental Sulfur and Thiosulfate by Shewanella oneidensis MR-1 Requires psrA, a Homolog of the phsA Gene of Salmonella enterica Serovar Typhimurium LT2▿ †
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Anaerobic Respiration of Elemental Sulfur and Thiosulfate by Shewanella oneidensis MR-1 Requires psrA, a Homolog of the phsA Gene of Salmonella enterica Serovar Typhimurium LT2▿ †

机译:沙瓦氏假单胞菌MR-1对元素硫和硫代硫酸盐的无氧呼吸需要psrA,这是肠炎沙门氏菌鼠伤寒沙门氏菌LT2▿phsA基因的同源物†

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摘要

Shewanella oneidensis MR-1, a facultatively anaerobic gammaproteobacterium, respires a variety of anaerobic terminal electron acceptors, including the inorganic sulfur compounds sulfite (SO32−), thiosulfate (S2O32−), tetrathionate (S4O62−), and elemental sulfur (S0). The molecular mechanism of anaerobic respiration of inorganic sulfur compounds by S. oneidensis, however, is poorly understood. In the present study, we identified a three-gene cluster in the S. oneidensis genome whose translated products displayed 59 to 73% amino acid similarity to the products of phsABC, a gene cluster required for S0 and S2O32− respiration by Salmonella enterica serovar Typhimurium LT2. Homologs of phsA (annotated as psrA) were identified in the genomes of Shewanella strains that reduce S0 and S2O32− yet were missing from the genomes of Shewanella strains unable to reduce these electron acceptors. A new suicide vector was constructed and used to generate a markerless, in-frame deletion of psrA, the gene encoding the putative thiosulfate reductase. The psrA deletion mutant (PSRA1) retained expression of downstream genes psrB and psrC but was unable to respire S0 or S2O32− as the terminal electron acceptor. Based on these results, we postulate that PsrA functions as the main subunit of the S. oneidensis S2O32− terminal reductase whose end products (sulfide [HS−] or SO32−) participate in an intraspecies sulfur cycle that drives S0 respiration.
机译:Shewanella oneidensis MR-1是一种兼性厌氧的γ-变形杆菌,可呼吸多种厌氧末端电子受体,包括无机硫化合物亚硫酸盐(SO32-),硫代硫酸盐(S2O32-),四硫代酸盐(S4O62-)和元素硫(S0)。然而,人们对沙门氏菌对无机硫化合物进行厌氧呼吸的分子机理了解甚少。在本研究中,我们在沙门氏菌基因组中鉴定了一个三基因簇,其翻译产物与phsABC产物具有59%到73%的氨基酸相似性,而phsABC是肠炎沙门氏菌血清型鼠伤寒杆菌S0和S2O32-呼吸所必需的基因簇。 LT2。在降低S0和S2O32-的希瓦氏菌菌株的基因组中鉴定出phsA的同系物(标注为psrA),但无法还原这些电子受体的希瓦氏菌菌株的基因组中却缺失了该基因。构建了一个新的自杀载体,并用于产生无标记的框内psrA缺失,该基因编码推定的硫代硫酸盐还原酶。 psrA缺失突变体(PSRA1)保留了下游基因psrB和psrC的表达,但无法激活S0或S2O32-作为末端电子受体。根据这些结果,我们假设PsrA充当沙门氏菌S2O32-末端还原酶的主要亚基,其最终产物(硫化物[HS-]或SO32-)参与种内硫循环,从而驱动S0呼吸。

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