7QTH

Crystal structure of the Shewanella oneidensis MR1 MtrC mutant C453A

7QTH の概要

• エントリーDOI: 10.2210/pdb7qth/pdb
• 分子名称: Extracellular iron oxide respiratory system surface decaheme cytochrome c component MtrC, HEME C, CALCIUM ION, ... (6 entities in total)
• 機能のキーワード: electron transfer activity, oxidoreductase activity, electron transport
• 由来する生物種: Shewanella oneidensis MR-1
• タンパク質・核酸の鎖数: 1
• 化学式量合計: 78587.66

構造登録者

Edwards, M.J.,Clarke, T.A. (登録日: 2022-01-14, 公開日: 2023-01-18, 最終更新日: 2024-01-31)

主引用文献

Norman, M.P.,Edwards, M.J.,White, G.F.,Burton, J.A.J.,Butt, J.N.,Richardson, D.J.,Louro, R.O.,Paquete, C.M.,Clarke, T.A.
A Cysteine Pair Controls Flavin Reduction by Extracellular Cytochromes during Anoxic/Oxic Environmental Transitions.
Mbio, 14:e0258922-e0258922, 2023

PubMed Abstract: Many bacteria of the genus are facultative anaerobes able to reduce a broad range of soluble and insoluble substrates, including Fe(III) mineral oxides. Under anoxic conditions, the bacterium Shewanella oneidensis MR-1 uses a porin-cytochrome complex (Mtr) to mediate extracellular electron transfer (EET) across the outer membrane to extracellular substrates. However, it is unclear how EET prevents generating harmful reactive oxygen species (ROS) when exposed to oxic environments. The Mtr complex is expressed under anoxic and oxygen-limited conditions and contains an extracellular MtrC subunit. This has a conserved CXC motif that inhibits aerobic growth when removed. This inhibition is caused by an increase in ROS that kills the majority of S. oneidensis cells in culture. To better understand this effect, soluble MtrC isoforms with modified CXC were isolated. These isoforms produced increased concentrations of HO in the presence of flavin mononucleotide (FMN) and greatly increased the affinity between MtrC and FMN. X-ray crystallography revealed that the molecular structure of MtrC isoforms was largely unchanged, while small-angle X-ray scattering suggested that a change in flexibility was responsible for controlling FMN binding. Together, these results reveal that FMN reduction in S. oneidensis MR-1 is controlled by the redox-active disulfide on the cytochrome surface. In the presence of oxygen, the disulfide forms, lowering the affinity for FMN and decreasing the rate of peroxide formation. This cysteine pair consequently allows the cell to respond to changes in oxygen level and survive in a rapidly transitioning environment. Bacteria that live at the oxic/anoxic interface have to rapidly adapt to changes in oxygen levels within their environment. The facultative anaerobe Shewanella oneidensis MR-1 can use EET to respire in the absence of oxygen, but on exposure to oxygen, EET could directly reduce extracellular oxygen and generate harmful reactive oxygen species that damage the bacterium. By modifying an extracellular cytochrome called MtrC, we show how preventing a redox-active disulfide from forming causes the production of cytotoxic concentrations of peroxide. The disulfide affects the affinity of MtrC for the redox-active flavin mononucleotide, which is part of the EET pathway. Our results demonstrate how a cysteine pair exposed on the surface controls the path of electron transfer, allowing facultative anaerobic bacteria to rapidly adapt to changes in oxygen concentration at the oxic/anoxic interface.

PubMed: 36645302
DOI: 10.1128/mbio.02589-22

実験手法

X-RAY DIFFRACTION (1.9 Å)