Jump to content

Coenzyme M

From Wikipedia, the free encyclopedia

This is an old revision of this page, as edited by WKratts (talk | contribs) at 18:53, 3 May 2022 (Edited lead and biochemical roles section to include how coenzyme M is also used in the elimination of propylene in alkene-ozidizing bacteria. Also included some minor formatting and added a source.). The present address (URL) is a permanent link to this revision, which may differ significantly from the current revision.

Coenzyme M
Names
IUPAC name
2-Sulfanylethanesulfonate
Systematic IUPAC name
2-Sulfanylethanesulfonate
Other names
2-mercaptoethylsulfonate; 2-mercaptoethanesulfonate; coenzyme M anion; H-S-CoM; AC1L1HCY; 2-sulfanylethane-1-sulfonate; CTK8A8912
Identifiers
3D model (JSmol)
ChEBI
ChemSpider
UNII
  • InChI=1S/C2H6O3S2/c3-7(4,5)2-1-6/h6H,1-2H2,(H,3,4,5)/p-1 checkY
    Key: ZNEWHQLOPFWXOF-UHFFFAOYSA-M checkY
  • [O-]S(=O)(=O)CCS
Properties
C2H5O3S2
Molar mass 141.18 g·mol−1
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).

Coenzyme M is a coenzyme required for methyl-transfer reactions in the metabolism of archaeal methanogens,[1][2] and in the metabolism of other substrates in bacteria.[3] It is also a necessary cofactor in the metabolic pathway of alkene-oxidizing bacteria. CoM helps eliminate the toxic epoxides formed from the oxidation of alkenes such as propylene[4]. The coenzyme is an anion with the formula HSCH
2CH
2SO−
3. It is named 2-mercaptoethanesulfonate and abbreviated HS–CoM. The cation is unimportant, but the sodium salt is most available. Mercaptoethanesulfonate contains both a thiol, which is the main site of reactivity, and a sulfonate group, which confers solubility in aqueous media.

Biochemical role

Methanogenesis

The coenzyme is the C1 donor in methanogenesis. It is converted to methyl-coenzyme M thioether, the thioether CH3SCH2CH2SO−3, in the penultimate step to methane formation[5]. Methyl-coenzyme M reacts with coenzyme B, 7-thioheptanoylthreoninephosphate, to give a heterodisulfide, releasing methane:

CH3–S–CoM + HS–CoB → CH4 + CoB–S–S–CoM

This induction is catalyzed by the enzyme methyl-coenzyme M reductase, which restricts cofactor F430 as the prosthetic group.

Alkene Metabolism

Coenzyme M is also used to make acetoacetate from CO2 and propylene or ethylene in aerobic bacteria. Specifically, in bacteria that oxidize alkenes into epoxides. After the propylene (or other alkene) undergoes epoxidation and becomes epoxypropane it becomes electrophilic and toxic. These epoxides react with DNA and proteins, affecting cell function. Alkene-oxidizing bacteria like Xanthobacter autotrophicus[4] use a metabolic pathway in which CoM is conjugated with an aliphatic epoxide. This step creates a nucleophilic compound which can react with CO2. The eventual carboxylation produces acetoacetate, breaking down the propylene[4].

See also

  • Mesna – a cancer chemotherapy adjuvant with the same structure

References

  1. ^ Balch WE, Wolfe RS (1979). "Specificity and biological distribution of coenzyme M (2-mercaptoethanesulfonic acid)". J. Bacteriol. 137 (1): 256–63. doi:10.1128/JB.137.1.256-263.1979. PMC 218444. PMID 104960.
  2. ^ Taylor CD, Wolfe RS (10 August 1974). "Structure and methylation of coenzyme M(HSCH
    2    CH
    2    SO
    3    )"    . J. Biol. Chem. 249 (15): 4879–85. PMID 4367810. Archived from the original on 25 May 2009. Retrieved 29 November 2007.
  3. ^ Partovi, Sarah E.; Mus, Florence; Gutknecht, Andrew E.; Martinez, Hunter A.; Tripet, Brian P.; Lange, Bernd Markus; DuBois, Jennifer L.; Peters, John W. (2018-04-06). "Coenzyme M biosynthesis in bacteria involves phosphate elimination by a functionally distinct member of the aspartase/fumarase superfamily". The Journal of Biological Chemistry. 293 (14): 5236–5246. doi:10.1074/jbc.RA117.001234. ISSN 1083-351X. PMC 5892593. PMID 29414784.{{cite journal}}: CS1 maint: unflagged free DOI (link)
  4. ^ a b c Krishnakumar, Arathi M.; Sliwa, Darius; Endrizzi, James A.; Boyd, Eric S.; Ensign, Scott A.; Peters, John W. (2008-9). "Getting a Handle on the Role of Coenzyme M in Alkene Metabolism". Microbiology and Molecular Biology Reviews : MMBR. 72 (3): 445–456. doi:10.1128/MMBR.00005-08. ISSN 1092-2172. PMC 2546864. PMID 18772284. {{cite journal}}: Check date values in: |date= (help)
  5. ^ Thauer, Rudolf K. (1998-09-01). "Biochemistry of methanogenesis: a tribute to Marjory Stephenson:1998 Marjory Stephenson Prize Lecture". Microbiology. 144 (9): 2377–2406. doi:10.1099/00221287-144-9-2377. ISSN 1350-0872.{{cite journal}}: CS1 maint: unflagged free DOI (link)


Stub icon

This biochemistry article is a stub. You can help Wikipedia by expanding it.

Retrieved from "https://en.wikipedia.org/w/index.php?title=Coenzyme_M&oldid=1086024068"