首页> 外文会议>International Biohydrometallurgy Symposium >Regulation of the iron and sulfur oxidation pathways in the acidophilic A cidithiobacillus ferrooxidans
【24h】

Regulation of the iron and sulfur oxidation pathways in the acidophilic A cidithiobacillus ferrooxidans

机译:在嗜酸性嗜酸性嗜酸性嗜酸性的铁氧化物中的铁和硫氧化途径

获取原文

摘要

The acidophilic and strictly chemolithoautotrophic bacterium Acidithiobacillus ferrooxidans oxidizes ferrous (Fe(II)) to ferric (Fe(III)) iron and reduced inorganic sulfur compounds (RISC) to sulfuric acid, in oxic conditions. The redox proteins involved in the electron transfer between Fe(II) and oxygen are encoded in the same transcriptional unit, the rus operon. The expression of this operon is induced in the presence of Fe(II), but not Fe(III), and is not repressed in the presence of sulfur (S°). A number of genes differentially expressed in iron or sulfur conditions have been identified by microarrays transcript profiling. We show here that the presence of Fe(II) induced the expression of the genes involved in iron oxidation and repressed the expression of the genes involved in RISC oxidation. Identification of the regulator(s) involved in this transcriptional regulation is underway. Two genes encoding putative regulators belonging to two transcriptional units located downstream from the rus operon have been cloned. One regulator with a putative iron-sulfur cluster belongs to the IscR family and the other belongs to the two component sensor/regulator family. Expression of both genes is induced in the presence of Fe(II) and is not repressed by S°. The recombinant proteins have been purified and gel shift assays with the target regulatory regions are in progress.
机译:嗜酸性和严格的培养基脱硫酸酐酸脱氧氧化物在氧化物条件下将铁(Fe(II))氧化铁(Fe(II))铁(Fe(II))铁和减少的无机硫化合物(RISC)。参与Fe(II)和氧气之间的电子传递的氧化还原蛋白在相同的转录单元中被编码,Rus操纵子。该操纵子的表达在Fe(II)存在下诱导,但不是Fe(III),并且在硫(S°)存在下没有压制。通过微阵列转录物分析鉴定了许多在铁或硫条件中表达的许多基因。我们在此展示Fe(II)的存在诱导参与铁氧化的基因的表达并抑制参与RISC氧化的基因的表达。正在进行鉴定参与该转录调节的调节剂。已经克隆了编码属于来自RUS操纵子下游的两个转录单位的推定调节器的两个基因。一个带有推定的铁硫簇的调节器属于ISCR系列,另一个属于两个组件传感器/调节器系列。在Fe(II)存在下,诱导两个基因的表达,并且不被S°压制。已经纯化了重组蛋白质,并正在进行靶调节区域的凝胶移位测定。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号