original sentence. A redox reaction (oxidation-reduction reaction) is a chemical reaction with a transfer of electrons between chemical species, resulting in a change of oxidation state for each species. A chemical species is reduced when it gains electrons and is oxidized when it loses electrons.[1] A reducing equivalent serves as the electron donor in a redox reaction and becomes oxidized (loses electrons) when it donates an electron to an electron acceptor. [2] A reducing equivalent can donate an electron in multiple ways: a lone electron, hydrogen atom, a hydride, or bond formation with an oxygen atom. Each form of reducing equivalent is characterized by the donation of at least one electron. [3]
Lone electrons edit
In redox reactions involving metal ions, lone electrons can be transferred from the electron donor to the electron acceptor. That is, no other atoms or protons are transferred along with the electron in the redox reaction[4]. For instance, consider the following reaction between iron and copper.
The iron and copper ion each begin the reaction with a double positive charge (2+). At the end of the reaction, the charge on copper decreased to a single positive charge (1+) while the charge on iron increased to a triple positive charge (3+). The alteration of charges is due to the transfer of a single electron from the iron atom to the copper atom.[4] In this reaction, iron is acting as the reducing equivalent because it donates one of its electrons to copper. As a result, iron is oxidized because it loses one of its electrons resulting in a greater positive charge.[4]
Hydrogen Atoms edit
A neutral hydrogen atom consists of one electron and one proton. Hydrogen's electronegativity value of 2.2 is less than the electronegativity of the atoms that hydrogen is commonly bound to, such as oxygen, nitrogen, carbon, or fluorine. [5] When a hydrogen atom forms a covalent bond with a more electronegative atom, the more electronegative atom will have a greater affinity for the electrons and pull the electrons away from hydrogen. [5] When a highly electronegative atom binds to a hydrogen atom it is reduced because it gains the electrons involved in the covalent bond. Conversely, when an atom loses a hydrogen atom it is oxidized because it loses electrons. [3] For example, consider the reaction involving Flavin Adenine Dinucleotide (FAD) and succinate. In this reaction FAD is reduced to FADH2 because it accepts two hydrogen atoms from succinate. Succinate serves as the reducing equivalent because it donates electrons to FAD in the form of hydrogen atoms and is itself oxidized. [6]
Hydride edit
A hydride is a hydrogen anion that carries two electrons and one proton[7]. A chemical species that donates a hydride is a reducing equivalent because it donates the equivalence of at least one electron, regardless if it is in the form of a hydride.[3] The chemical species that accepts a hydride ion will be reduced because it gains the electrons from the hydride ion. [3] The reduced form of Nicotinamide Adenine Dinucleotide (NADH) is a reducing equivalent commonly seen in biochemistry that donates a hydride ion to an electron acceptor in complex I of the electron transport chain. [8]
Bond Formation with an Oxygen Atom edit
A chemical species with a lower electronegativity than oxygen can serve as a reducing equivalent when it covalently binds to an oxygen atom. Oxygen is highly electronegative and will have a greater affinity for electrons in a covalent bond, resulting in the reduction of the oxygen atom.[3] When an atom of lower electronegativity forms a bond with oxygen it is oxidized because the electrons are pulled closer to oxygen and away from that atom.[5] [3] For instance, consider the formation of a carboxylic acid from the oxidation of an aldehyde. In this reaction, a carbon has been oxidized through the formation of a covalent bond with oxygen.[3]
Reducing Equivalents in the Mitochondrial Respiratory Chain edit
Oxidative Phosphorylation is the process by which ATP synthesis is driven by the free energy generated through the oxidation of reducing equivalents in the electron transport chain. [3][9]. The electron transport chain is located in the mitochondria and consists of transmembrane complexes that catalyze redox reactions. [10] NADH and FADH2 are reducing equivalents that donate electrons at complexes I and II respectively. These electrons are then transferred in multiple redox reactions and are carried though the complexes III and IV.[11][8] The oxidation of reducing equivalents in the electron transport chain releases protons into the intermembrane space of the mitochondria and maintains the proton electrochemical gradient. [3][8] As protons move down the electrochemical gradient the transmembrane protein (ATP Synthase) is able to generate ATP from ADP and an inorganic phosphate group [8][3]. In order to maintain the proton gradient and generate ATP, reducing equivalents are supplied to the electron transport chain from multiple processes such the TCA cycle. [12]
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References edit
- ^ Beiras, Ricardo,. Marine pollution : sources, fate and effects of pollutants in coastal ecosystems. Amsterdam, Netherlands. ISBN 9780128137376. OCLC 1045426277.
{{cite book}}: CS1 maint: extra punctuation (link) CS1 maint: multiple names: authors list (link) - ^ Voet, Donald, (2011). Biochemistry. Voet, Judith G., (4th edition ed.). Hoboken, NJ: John Wiley & Sons. p. 584. ISBN 9780470570951. OCLC 690489261.
{{cite book}}:|edition=has extra text (help)CS1 maint: extra punctuation (link) CS1 maint: multiple names: authors list (link) - ^ a b c d e f g h i j Nelson, David L. (David Lee), 1942-. Lehninger principles of biochemistry. Cox, Michael M.,, Lehninger, Albert L. (Seventh edition ed.). New York, NY. pp. 519, 711–712. ISBN 9781464126116. OCLC 986827885.
{{cite book}}:|edition=has extra text (help)CS1 maint: multiple names: authors list (link) CS1 maint: numeric names: authors list (link) - ^ a b c Damm, Henry C.; Goldwyn, Alvin J.; Thomas, Carolyn A. (1966). The handbook of biochemistry and biophysics. Cleveland, Ohio: The World Publishing Company. pp. 400–415.
- ^ a b c Atkins, P. W. (Peter William), 1940- (2013). Chemical principles : the quest for insight. Jones, Loretta., Laverman, Leroy, 1971- (6th ed ed.). New York: W H Freeman. pp. 90–92. ISBN 1429288973. OCLC 819816793.
{{cite book}}:|edition=has extra text (help)CS1 maint: multiple names: authors list (link) CS1 maint: numeric names: authors list (link) - ^ Stryer, Lubert; Tymoczko, John L.; Berg, Jeremy M. (2002). "The Citric Acid Cycle Oxidizes Two-Carbon Units". Biochemistry. 5th edition: Section 17.1.8.
- ^ Stenesh, J., 1927- (1975). Dictionary of biochemistry. New York: Wiley. ISBN 0471821055. OCLC 1530913.
{{cite book}}: CS1 maint: multiple names: authors list (link) CS1 maint: numeric names: authors list (link) - ^ a b c d Voet, Donald. (2013). Fundamentals of biochemistry : life at the molecular level. Voet, Judith G., Pratt, Charlotte W. (Fourth edition ed.). Hoboken, NJ: Wiley. pp. 456, 588, 603–604. ISBN 9780470547847. OCLC 738349533.
{{cite book}}:|edition=has extra text (help) - ^ "ScienceDirect". www.sciencedirect.com. doi:10.1016/0891-5849(94)90008-6. Retrieved 2019-05-14.
- ^ Begley, Tadhg P., ed. (2009). Wiley encyclopedia of chemical biology. John Wiley & Sons. pp. 161–166. ISBN 9780471754770. OCLC 928719683.
{{cite book}}:|last=has generic name (help)CS1 maint: multiple names: authors list (link) - ^ Ahern, Kevin; Rajagopal, Indira; Tan, Taralyn (2018). Biochemistry Free for All. Creative Commons. p. 432.
- ^ Pratt, Steven; Werker, Alan; Laycock, Bronwyn; Montano-Herrera, Liliana (2017). "The Evolution of Polymer Composition during PHA Accumulation: The Significance of Reducing Equivalents". Bioengineering. 4 (1): 20. doi:10.3390/bioengineering4010020. PMC 5590436. PMID 28952499.
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