Acetogenesis Explained

Acetogenesis is a process through which acetate is produced by prokaryote microorganisms either by the reduction of CO2 or by the reduction of organic acids, rather than by the oxidative breakdown of carbohydrates or ethanol, as with acetic acid bacteria.[1]

The different bacterial species capable of acetogenesis are collectively termed acetogens. Reduction of CO2 to acetate by anaerobic bacteria occurs via the Wood–Ljungdahl pathway and requires an electron source (e.g., H2, CO, formate, etc.). Some acetogens can synthesize acetate autotrophically from carbon dioxide and hydrogen gas.[2] Reduction of organic acids to acetate by anaerobic bacteria occurs via fermentation.

Discovery

In 1932, organisms were discovered that could convert hydrogen gas and carbon dioxide into acetic acid. The first acetogenic bacterium species, Clostridium aceticum, was discovered in 1936 by Klaas Tammo Wieringa. A second species, Moorella thermoacetica, attracted wide interest because of its ability, reported in 1942, to convert glucose into three moles of acetic acid.[3]

Biochemistry

The precursor to acetic acid is the thioester acetyl CoA. The key aspects of the acetogenic pathway are several reactions that include the reduction of carbon dioxide to carbon monoxide (CO) and the attachment of CO to a methyl group (–CH). The first process is catalyzed by enzymes called carbon monoxide dehydrogenase. The coupling of the methyl group (provided by methylcobalamin) and CO is catalyzed by acetyl-CoA synthase.[4]

The global reduction reaction of into acetic acid by is the following:

ΔG° = −95 kJ/mol

while the conversion of one mole of glucose into 3 moles of acetic acid corresponds to a more exothermic reaction:

ΔG° = −310.9 kJ/mol

However, the energy released by mole of acetic acid produced by each reaction is about the same: −95 kJ/mol for the reduction of by, and more for the conversion of glucose into acetic acid (−104 kJ/mol).

Applications

The unique metabolism of acetogens has significant applications in biotechnology. In carbohydrate fermentations, the decarboxylation reactions end up in the conversion of organic carbon into carbon dioxide, the main greenhouse gas. This release is no longer compatible with the need to minimize the world CO2 emissions. It is not only an environmental concern but also not economically profitable in the frame of the biofuel competition with fossil fuels. Acetogens can ferment glucose without CO2 emission and convert one glucose molecule into three molecules of acetic acid, increasing the production yield of this latter by 50%. Acetogenesis does not replace glycolysis with a different pathway, but rather captures the CO2 from glycolysis and uses it to produce acetic acid. Three molecules of acetic acid can be produced in this way, while the production of three molecules of ethanol would require an additional reducing agent such as hydrogen gas.[5]

Notes and References

  1. Book: Angelidaki I, Karakashev D, Batstone DJ, Plugge CM, Stams AJ . 16. Biomethanation and Its Potential . Rosenzweig AC, Ragsdale SW . Methods in Enzymology . Methods in Methane Metabolism, Part A . Academic Press . 494 . 2011 . 327–351 . 978-0-123-85112-3 . 10.1016/B978-0-12-385112-3.00016-0 . 21402222 . http://www.sciencedirect.com/science/article/pii/B9780123851123000160.
  2. Book: Singleton . Paul . vanc . Dictionary of microbiology and molecular biology . 2006 . John Wiley . Chichester . 978-0-470-03545-0 . 3rd . Acetogenesis .
  3. Ragsdale SW, Pierce E . Acetogenesis and the Wood-Ljungdahl pathway of CO2 fixation . Biochimica et Biophysica Acta (BBA) - Proteins and Proteomics . 1784 . 12 . 1873–98 . December 2008 . 18801467 . 2646786 . 10.1016/j.bbapap.2008.08.012 .
  4. Ragsdale SW . Metals and their scaffolds to promote difficult enzymatic reactions . Chemical Reviews . 106 . 8 . 3317–37 . August 2006 . 16895330 . 10.1021/cr0503153 .
  5. Schuchmann K, Müller V . Energetics and Application of Heterotrophy in Acetogenic Bacteria . Applied and Environmental Microbiology . 82 . 14 . 4056–69 . July 2016 . 27208103 . 10.1128/AEM.00882-16 . 4959221 . 2016ApEnM..82.4056S .