Product inhibition

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Product inhibition is a type of enzyme inhibition where the product of an enzyme reaction inhibits its production.[1] Cells utilize product inhibition to regulate of metabolism as a form of negative feedback controlling metabolic pathways.[2] Product inhibition is also an important topic in biotechnology, as overcoming this effect can increase the yield of a product, such as an antibiotic.[3] Product inhibition can be competitive, non-competitive or uncompetitive.

Mitigation of product inhibition

Reactor design

One method to reduce product inhibition is the use of a membrane reactor.[4] These bioreactors uses a membrane to separate products from the rest of the reactor, limiting their inhibition. If the product differs greatly in size from the cells producing it, and the substrate feeding the cells, then the reactor can utilize a semipermeable membrane allowing to products to exit the reactor while leaving the cells and substrate behind to continue reacting making more product. Other reactor systems use chemical potential to separate products from the reactor, such as solubility of different compounds allowing one to pass through the membrane. Electrokinetic bioreactor systems have been developed which use electrolysis, a process that uses electrical charge to remove the product from the bioreactor system.[5]

External loop reactor uses current created by air bubbles flowing through the reactor to create a flow that brings the reactor contents through an external loop. A separating membrane can be placed in the external loop to collect product, and reduce product inhibition. A downside to external loop reactors is they create additional shear stress.[6] Submerged membrane bioreactors have the membrane contained within the main chamber of the bioreactor.[6]

A separative bioreactor is a type of continuous reactor where the producing cells are mounted on a resin membrane as to not flow out of the reactor as substrate is passed over them. The continuous flow of the reactor takes the product downstream as it is produced.[7]

Other methods of mitigating product inhibition

Integrated liquid-liquid extraction can be used to remove products that have a density that differs from the rest of the bioreactors contents.[8] This is done by adding a solvent downstream of the bioreactor and letting the product separate out in a settling tank before the bioreactor effluent is moved to a secondary reactor or returned to its initial reactor to continue its cultivation. This process can be done in batch or continuous operation.

Vacuum extraction[9] can be used in fermentation to remove ethanol from a reactor. When the liquid in the vessel is placed in vacuum conditions the ethanol begins to evaporate because its more volatile than the rest of the reactor contents. This technique requires an acclimation period for the yeast in the reactor to adapt to the lower pressure environment.[citation needed]

Product neutralization if a products inhibition due to its pH then it can be neutralized in the reactor and further processed downstream back into its original form.[citation needed]

References

  1. ^ Walter, Charles; Frieden, Earl (1963). "The Prevalence and Significance of the Product Inhibition of Enzymes". In Nord, F.F. (ed.). Advances in Enzymology and Related Subjects of Biochemistry. Vol. 25. pp. 167–274. doi:10.1002/9780470122709.ch4. ISBN 978-0-470-12270-9. PMID 14149677.
  2. ^ Hutson, NJ; Kerbey, AL; Randle, PJ; Sugden, PH (1979). "Regulation of pyruvate dehydrogenase by insulin action". Progress in Clinical and Biological Research. 31: 707–719. PMID 231784. NAID 10010916605.
  3. ^ Schügerl, Karl; Hubbuch, Jürgen (June 2005). "Integrated bioprocesses". Current Opinion in Microbiology. 8 (3): 294–300. doi:10.1016/j.mib.2005.01.002. PMID 15939352.
  4. ^ Fan, Rong; Ebrahimi, Mehrdad; Czermak, Peter (3 May 2017). "Anaerobic Membrane Bioreactor for Continuous Lactic Acid Fermentation". Membranes. 7 (2): 26. doi:10.3390/membranes7020026. PMC 5489860. PMID 28467384.
  5. ^ Li, Hong; Mustacchi, Roberta; Knowles, Christopher J; Skibar, Wolfgang; Sunderland, Garry; Dalrymple, Ian; Jackman, Simon A (January 2004). "An electrokinetic bioreactor: using direct electric current for enhanced lactic acid fermentation and product recovery". Tetrahedron. 60 (3): 655–661. doi:10.1016/j.tet.2003.10.110.
  6. ^ a b Carstensen, Frederike; Apel, Andreas; Wessling, Matthias (March 2012). "In situ product recovery: Submerged membranes vs. external loop membranes". Journal of Membrane Science. 394–395: 1–36. doi:10.1016/j.memsci.2011.11.029.
  7. ^ Arora, M. B.; Hestekin, J. A.; Snyder, S. W.; St. Martin, E. J.; Lin, Y. J.; Donnelly, M. I.; Millard, C. Sanville (July 2007). "The Separative Bioreactor: A Continuous Separation Process for the Simultaneous Production and Direct Capture of Organic Acids". Separation Science and Technology. 42 (11): 2519–2538. doi:10.1080/01496390701477238. PMC 3662075. PMID 23723533.
  8. ^ Kaur, Guneet; Srivastava, A.K.; Chand, Subhash (December 2015). "Debottlenecking product inhibition in 1,3-propanediol fermentation by In-Situ Product Recovery". Bioresource Technology. 197: 451–457. doi:10.1016/j.biortech.2015.08.101. PMID 26356117.
  9. ^ Tavares, Bruna; Felipe, Maria das Graças de Almeida; dos Santos, Júlio César; Pereira, Félix Monteiro; Gomes, Simone Damasceno; Sene, Luciane (February 2019). "An experimental and modeling approach for ethanol production by Kluyveromyces marxianus in stirred tank bioreactor using vacuum extraction as a strategy to overcome product inhibition". Renewable Energy. 131: 261–267. doi:10.1016/j.renene.2018.07.030.