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Co-metabolism 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). This shouldn’t be confused with simultaneous catabolism, where two substrates are catabolized concomitantly by different enzymes.[1]Co-metabolism occurs when an enzyme has the ability to degrade a second compound in addition to it's original, intended substrate, that is used by the organism that synthesizes the enzyme to derive energy and carbon from them. The degradation of the second compound, however, does not provide the bacteria energy or carbon, in other words, it is a non-growth-supporting substrate.[2]

As some of the molecules that are the substrates of these reactions 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.

Co-metabolism in Bioremediation

A promising method of bioremediation of chlorinated solvents involves co-metabolism of the contaminants by aerobic microorganisms in groundwater and soils. Several aerobic microorganisms have been demonstrated to be capable of doing this, including methane oxidizers, phenol-degraders, and toluene-degraders.

One of them, Pseudomonas stutzeri OX1, can degrade hazardous chlorinated solvents, such as tetrachloroethylene (PCE), with the enzyme that they originally produce with the intent of deriving energy and carbon from methane and propane. The enzyme the organism synthesize that is capable of both oxidizing methane and chlorinated solvents is methane monooxygenase. [3][2]

Another example of the use of co-metabolism to degrade pollutants would be the biodegradation of methyl-tert-butyl ether (MTBE): a chemical synthesized by the use of fossil fuels and that is toxic to both ground and underground aqueous environments. Pseudomonas aeruginosa and Pseudomonas citronellolis was shown to be able to carry out the co-metabolic degredation of MTBE and fully mineralize it by using their enzymes that has a physiological role of oxidizing short, n-alkanes to utilize them as growth sources. [4]

The difficulties and high costs of maintaining substrate and an oxic environment, have led to limited field-scale application of co-metabolism for solvent degradation. Recently, this method of remediation has been improved by the substitution of cheap, nontoxic plant secondary metabolites in the place of synthetic, toxic aromatics like toluene.[5]

  1. ^ Joshua, Chijioke J.; Dahl, Robert; Benke, Peter I.; Keasling, Jay D. (2011-3). "Absence of Diauxie during Simultaneous Utilization of Glucose and Xylose by Sulfolobus acidocaldarius". Journal of Bacteriology. 193 (6): 1293–1301. doi:10.1128/JB.01219-10. ISSN 0021-9193. PMC 3067627. PMID 21239580. {{cite journal}}: Check date values in: |date= (help)CS1 maint: PMC format (link)
  2. ^ a b Arp, Daniel J.; Yeager, Chris M.; Hyman, Michael R. (2001-03-01). "Molecular and cellular fundamentals of aerobic cometabolism of trichloroethylene". Biodegradation. 12 (2): 81–103. doi:10.1023/A:1012089908518. ISSN 0923-9820.
  3. ^ 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.
  4. ^ Li, Shanshan; Wang, Shan; Yan, Wei (2016-9). "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}}: Check date values in: |date= (help)CS1 maint: PMC format (link) CS1 maint: unflagged free DOI (link)
  5. ^ 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. doi:10.1038/s41598-017-07760-1. ISSN 2045-2322. PMC 5559444. PMID 28814712.{{cite journal}}: CS1 maint: PMC format (link)