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Cytochrome bd-1 oxidase in Escherichia coli
ContentsIntroductionCytochrome bd oxidase is a type of quinol-dependent transmembrane (Fig. 1) terminal oxidase found exclusively in prokaryotes.[1] With a very high oxygen affinity, bd oxidases play a vital role in the oxidative phosphorylation pathway in both gram-positive and gram-negative bacteria. Cytochrome bd oxidase's responsibility in the oxidative phosphorylation pathway also allows it to act as a key survival factor in the bacterial stress response against antibacterial drugs [1], hypoxia, cyanide, nitric oxide, and H2O2[2]. Given this knowledge, bd oxidases have become an area of scientific research worth pursuing as they could serve as an ideal target for antimicrobial drug development. [3] The overall mechanism of bd oxidases involves an exergonic reduction of molecular oxygen into water (Fig. 2). During this reaction, a proton gradient is generated in order to assist in the conservation of energy. [4] Unlike other terminal oxidases, bd oxidases do not use a proton pump. Instead, bd oxidases use a form of vectorial chemistry that releases protons from the quinol oxidation into the positive, periplasmic side of the membrane. Protons that are required for the water formation are then consumed from the negative, cytoplasmic side of the membrane, thus creating the previously mentioned proton gradient. This page will be specifically focusing on the structure and overall function of the 6RX4 bd oxidase in E. coli. 6RX4 is a part of the long(L) quinol-binding domain subfamily that terminal oxidases are classified into. The L-subfamily of bd oxidases are responsible for the survival of acute infectious diseases such as E. coli and salmonella. The 6RX4's three heme groups, its periplasmically exposed Q-loop, and four protein subunits will be of primary focus when identifying the relationship between structure and function. StructureSubunitsCytochrome bd oxidase is made up of four individual subunits.[6] The two major subunits, CydA and CydB, are each composed of one peripheral helix and two bundles of four transmembrane helices. The CydA subunit plays the most important role in the oxygen reduction reaction as it contains the Q-loop as well as all three heme groups. The CydB subunit harbors the ubiquinone molecule which provides structural support to the subunit that mimics the three hemes found in CydA.[1][7] The remaining two subunits, CydS and CydX, are both single helix structures that assist in the oxygen reduction reaction. Unique to E. coli, the CydS subunit binds to CydA to block oxygen from directly binding to heme b595. The CydX subunit promotes the assembly and stability of the oxidase complex. CydX is composed of 37 mostly hydrophilic amino acid residues, including Glu25 that is exposed to the cytoplasm and prevents the helix from fully entering the membrane. [6] Q-LoopAnother significant structural feature of bd oxidase is the Q-loop which is located between TM helices 6 and 7 of the CydA subunit.[6] The periplasmic Q-loop in E. coli stretches over a length of 136 amino acid residues, making it much longer than the Q-loop in Geobacillus Thermodenitrificans.[1] The Q-loop is likely involved in quinol binding and oxidation. The N-terminal end of this Q-loop is very flexible and likely functions as the hinge that allows for quinone binding while the C-terminal end is much more rigid which provides stabilization for the enzyme.[6] Molecular FunctionH and O channelsThe hydrogen and oxygen channels (Fig. 3) are essential for H+ and O2 molecules to reach the active site of cytochrome bd oxidase. A proton motive force generated by the oxidase[1] allows protons from the cytoplasm to flow through a hydrophilic H-channel full of water (pink dots), entering at Asp119<sup>A</sup> and moving past Lys57<sup>A</sup>, Lys109<sup>B</sup>, Asp105<sup>B</sup>, Tyr379<sup>B</sup>, and Asp58<sup>B</sup>[6] where they can be transferred to the active site with the help of the conserved residues Ser108<sup>A</sup>, Glu107<sup>A</sup>, and Ser140<sup>A</sup>[1]. A smaller O-channel also exists that transitions from hydrophobic to hydrophilic as it gets closer to the active site. This channel allows oxygen to reach the active site, starting near Trp63 in CydB and passing by Ile144<sup>A</sup>, Leu101<sup>A</sup>, and Glu99<sup>A</sup>[1], which assists with the binding of oxygen to the active site. The O-channel channel is approximately 1.5 Å in diameter[6], which may help with selectivity. Interestingly, the O-channel does not exist in the cytochrome bd oxidase of Geobacillus thermodenitrificans; instead, oxygen binds directly to the active site[7]. The CydS subunit found in E. coli blocks this alternate oxygen entry site, which allows oxygen to travel through the O-channel[1][6]. The presence of an O-channel affects oxidase activity, as the E. coli oxidase acts as a "true" oxidase, while the G. thermodenitrificans bd oxidase contributes more to detoxification[6]. HemesThree hemes are present in the CydA subunit. These three hemes form a triangle to maximize subunit stability[1][6][7], which is an evolutionary conserved feature across bd oxidases[1]. Heme b558 acts as the primary electron acceptor by catalyzing the oxidation of quinol[6]. Conserved His186 and Met393 help to stabilize heme b558[6]. Heme b558 transfers the electrons to heme b595, which transfers them to the active site heme d[1]. Multiple residues help stabilzie this electron trasnfer including a conserved Trp441 that assists heme b595 in transferring electrons to heme d[7]. A conserved Glu445 is also essential for charge stabilization of heme b595[6], while His19 stabilizes heme d[7]. As heme d collects the electrons from heme b595, Glu99 in the O-channel facilities the binding of oxygen to heme d, and Ser108, Glu107, and Ser140 in the H-channel facilitate proton transfer to heme d[1]. Similar to the three hemes, the ubiquinone-8 (UQ-8) molecule found in the CydB subunit mimics the triangular formation to stabilize the subunit[1]. MechanismQuinol transfers two electrons to heme b558 and releases two protons into the periplasmic space as the initial electron donor. Heme b558 transfers the electrons to heme b595, which transfers the electrons to heme d. Concurrently, the H-channel collects protons from the cytoplasmic side using the proton gradient and the O-channel collects oxygen atoms. The protons and oxygen flow to the active site heme d (Fig. 3). With electrons, oxygen, and protons available, heme d can successfully reduce dioxygen to water (Fig. 2, 4). RelevanceThe cytochrome bd oxidase is essential for pathogenic bacteria to thrive in the human body because it enhances bacterial growth and colonization. Any alteration of the bd oxidase Cyd subunits will most likely produce a nonfunctional mutant cytochrome bd oxidase[8], which inhibits bacterial growth. If E. coli are missing or possess ineffective CydA and B subunits, bacterial growth ceases.[9]. With colitis, E. coli mutants that were missing CydAB colonized poorly in comparison to the wild type levels of colonization[9]. The cytochrome bd oxidase is the main component in nitric oxide (NO) tolerance in bacteria, which is released by neutrophils and macrophages when the host is infected[10]. E. coli growth seen in urinary tract infections is mainly due to the NO resistant bd oxidase. Without the CydA and CydB subunits, bacteria could not colonize in high NO conditions[10]. Cytochrome bd oxidases are essential for life in other pathogenic bacteria such as M. tuberculosis. Deletion of the CydA and CydB subunits dramatically decreased the growth of M. tb compared to the wild type when exposed to imidazo[1,2-]pyridine, a known inhibitor of respiratory enzymes[11]. Upregulation of the cytochrome bd oxidase Cyd genes resulted in a mutant strain of M. tb that was resistant to imidazo[1,2-α]pyridine[11]. Since cytochrome bd oxidases are only found in prokaryotes and are required for pathogenic bacterial infections, inhibitors that target cytochrome bd oxidase are promising antibacterial agents. Compounds that target heme b558[2], create unusable forms of oxygen[12], and target the o-channel [13] have shown potential in halting bacterial growth.
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References
Student Contributors
- Grace Bassler
- Emily Neal
- Marisa Villarreal



