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Cometabolism

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Cometabolism is defined as the simultaneous degradation of two compounds, in which the degradation of the second compound (the secondary substrate) depends on the presence of the first compound (the primary substrate). [1] This is in contrast to simultaneous catabolism, where each substrate is catabolized concomitantly by different enzymes.[1][2] Cometabolism occurs when an enzyme produced by an organism to catalyze the degradation of it's growth-substrate to derive energy and carbon from it is also capable of degrading additional compounds. The fortituous degradation of these additional compounds does not support the growth of the bacteria, and some of these compounds can even be toxic in certain concentrations to the bacteria.[3][4]

The first report of this phenomena was the degredation of ethene by the species Pseudomonas methanica.[4] These bacteria degrade their growth-substrate methane with the enzyme methane monooxygenase(MMO). MMO was discovered to be capable of degrading ethene and propene, although the bacteria were unable to use these compounds as energy and carbon sources to grow. [4]

Another example is Mycobacterium vaccae, which uses an alkane monooxygenase enzyme to oxidize propane. Accidentally, this enzyme also oxidizes, at no additional cost for M. vaccaecyclohexane into cyclohexanol. Thus, cyclohexane is co-metabolized in the presence of propane. This allows for the commensal growth of Pseudomonas on cyclohexane. The latter can metabolize cyclohexanol, but not cyclohexane. [5][6]

Cometabolism in Bioremediation

Some of the molecules that are cometabolically degraded by bacteria are xenobioticpersistent compounds, such as PCETCE, and MTBE, that have harmful effects on several types of environments. Co-metabolism is thus used as an approach to biologically degrade hazardous solvents. [7][4]

Cometabolism can be used for the biodegradation of methyl-tert-butyl ether (MTBE): an aquatic environment pollutant. Some Pseudomonas members were found to be able to fully degrade MTBE cometabolically with the enzymes they produce to oxidize n-alkanes (e.g. methane, propane). [7]

Additionally, a promising method of bioremediation of chlorinated solvents involves cometabolism of the contaminants by aerobic microorganisms in groundwater and soils. Several aerobic microorganisms have been demonstrated to be capable of doing this, including n-alkanearomatic compound (e.g. toluene, phenol) and ammonium oxidizers.[4][3]One example is Pseudomonas stutzeri OX1, which can degrade a hazardous, and water-soluble compound tetrachloroethylene (PCE).[6] PCE, one of the major underground water contaminants, was regarded as being undegradable under aerobic conditions and only degraded via reductive dehalogenation to be used as a growth-substrate by organisms.[6] Reductive dehalogenation often results in the partial dechlorination of the PCE, giving rise to toxic compounds such as TCEDCE, and vinyl chloride. Pseudomonas st. OX1 can degrade PCE under aerobic conditions by using toluene-o-xylene monooxygenase (ToMO), an enzyme they produce to derive energy and carbon from toluene and several other aromatic compounds. Therefore, cometabolism is an potential pathway to remove PCE from polluted sites.[6]

However, the difficulties and high costs of maintaining the growth-substrates of the organisms capable of cometabolising these hazardous compounds and providing them an aerobic environment have led to the limited field-scale application of cometabolism for pollutant solvent degradation. Recently, this method of remediation has been proposed to be improved by the substitution of the synthetic aromatic growth-substrates (e.g. toluene) of these bacteria with cheap, non-toxic plant secondary metabolites.[8]

References

  1. ^ a b Joshua, C. J.; Dahl, R.; Benke, P. I.; Keasling, J. D. (2011). "Absence of Diauxie during Simultaneous Utilization of Glucose and Xylose by Sulfolobus acidocaldarius". J Bacteriol. 193 (6): 1293–1301. doi:10.1128/JB.01219-10. PMC 3067627. PMID 21239580.
  2. ^ Gulvik, C. A.; Buchan, A. (2013). "Simultaneous catabolism of plant-derived aromatic compounds results in enhanced growth for members of the Roseobacter lineage". Appl Environ Microbiol. 79 (12): 3716–3723. doi:10.1128/AEM.00405-13. PMC 3675927. PMID 23563956.
  3. ^ a b Qin, Ke; Struckhoff, Garrett C.; Agrawal, Abinash; Shelley, Michael L.; Dong, Hailiang (2015-01-01). "Natural attenuation potential of tricholoroethene in wetland plant roots: Role of native ammonium-oxidizing microorganisms". Chemosphere. 119 (Supplement C): 971–977. doi:10.1016/j.chemosphere.2014.09.040.
  4. ^ a b c d e Nzila, Alexis (2013-07-01). "Update on the cometabolism of organic pollutants by bacteria". Environmental Pollution. 178 (Supplement C): 474–482. doi:10.1016/j.envpol.2013.03.042.
  5. ^ Beam, H. W.; Perry, J. J. (1973-03-01). "Co-metabolism as a factor in microbial degradation of cycloparaffinic hydrocarbons". Archiv für Mikrobiologie. 91 (1): 87–90. doi:10.1007/BF00409542. ISSN 0003-9276.
  6. ^ a b c d Ryoo, D.; Shim, H.; Canada, K.; Barbieri, P.; Wood, T. K. (July 2000). "Aerobic degradation of tetrachloroethylene by toluene-o-xylene monooxygenase of Pseudomonas stutzeri OX1". Nature Biotechnology. 18 (7): 775–778. doi:10.1038/77344. ISSN 1087-0156. PMID 10888848.
  7. ^ a b Li, Shanshan; Wang, Shan; Yan, Wei (2016). "Biodegradation of Methyl tert-Butyl Ether by Co-Metabolism with a Pseudomonas sp. Strain". International Journal of Environmental Research and Public Health. 13 (9). doi:10.3390/ijerph13090883. ISSN 1661-7827. PMC 5036716. PMID 27608032.{{cite journal}}: CS1 maint: PMC format (link) CS1 maint: unflagged free DOI (link)
  8. ^ Fraraccio, Serena; Strejcek, Michal; Dolinova, Iva; Macek, Tomas; Uhlik, Ondrej (2017-08-16). "Secondary compound hypothesis revisited: Selected plant secondary metabolites promote bacterial degradation of cis-1,2-dichloroethylene (cDCE)". Scientific Reports. 7 (1): 8406. doi:10.1038/s41598-017-07760-1. ISSN 2045-2322. PMC 5559444. PMID 28814712.{{cite journal}}: CS1 maint: PMC format (link)