Halorespiration

The process of halorespiration, or dehalorespiration, uses reductive dehalogenation to produce energy that can be used by the respiring microorganism to carry out its growth and metabolism.[6] Halogenated organic compounds are used as the terminal electron acceptor, which results in their dehalogenation.[6] Reductive dehalogenation is the process by which this occurs.[6] It involves the reduction of halogenated compounds by removing the halogen substituents, while simultaneously adding electrons to the compound.[7] Hydrogenolysis and vicinal reduction are the two known processes of this mechanism that have been identified.[7] In both processes, the removed halogen substituents are released as anions.[7] Reductive dehalogenation is catalyzed by reductive dehalogenases, which are membrane-associated enzymes.[6][8][3] A number of not only membrane-associated but also cytoplasmic hydrogenases, in some cases as part of the protein complexes, are predicted to play roles in the dehalorespiration process.[9] Most of these enzymes contain iron-sulfur (Fe-S) clusters, and a corrinoid cofactor at their active sites.[6] Although the exact mechanism is unknown, research suggests that these two components of the enzyme may be involved in the reduction.[6]

An ecologically significant aspect of bacterial halorespiration is the reduction of tetrachloroethene (PCE) and Trichloroethene (TCE); anthropogenic pollutants with high neuro and hepatotoxicity.[11] Their presence as environmental pollutants arose from their common industrial use as metal-degreasing agents from the 1920s - 1970.[12] These xenobiotic compounds tend to form partially insoluble layers called dense non-aqueous phase liquids (DNAPLs) at the bottom of groundwater aquifers, which solubilize in a slow, reservoir-like manner, making TCE and PCE among the most common groundwater pollutants.[13]

A commonly used strategy for the removal of TCE and PCE from groundwater is the use of bioremediation via enhanced reductive dechlorination (ERD).[14] ERD involves in-situ injections of dehalorespiring bacteria, among fermentable organic substrates serving as electron donors, while the two pollutants, TCE and PCE, act as the electron acceptors.[14] This facilitates the sequential dechlorination of PCE and TCE into noxious cis-dichloroethene (DCE) and Vinyl chloride (VC), which then suit as electron acceptors for the full dechlorination into innocuous ethene.[14]

A wide array of bacteria across different genera have the capacity to partially dechlorinate PCE and TCE into cis-DCE and VC.[14] One such example of this is the Magnetospirillum bacterium, strain MS-1, which can reduce PCE into cis-DCE under aerobic conditions.[15] However, these daughter substrates have higher toxicity profiles than their parent compounds.[14] As such, effective dechlorination of cis-DCE and VC into innocuous ethene is crucial for bioremediation of PCE and TCE-contaminated aquifers.[14] Currently, bacteria of the Dehalococcoides genera are the only known organisms that can fully dechlorinate PCE into ethene. This is due to their specific transmembrane reductive dehalogenases (RDases) that metabolize the chlorine atoms on the xenobiotic pollutants for cellular energy.[16] In particular, Dehalococcoides isolates VS and BAV1 encode Vinyl Chloride RDases, which metabolize VC into innocuous ethene, making them required species in ERD systems used in bioremediation of PCE and TCE.[16]

• Reductive dechlorination
• Chloroflexota
• Dehalococcoides
• Dehalobacter