The biochemistry of the metabolic poison propionate 3‐nitronate and its conjugate acid, 3‐nitropropionate. Issue 9 (29th July 2013)
- Record Type:
- Journal Article
- Title:
- The biochemistry of the metabolic poison propionate 3‐nitronate and its conjugate acid, 3‐nitropropionate. Issue 9 (29th July 2013)
- Main Title:
- The biochemistry of the metabolic poison propionate 3‐nitronate and its conjugate acid, 3‐nitropropionate
- Authors:
- Francis, Kevin
Smitherman, Crystal
Nishino, Shirley F.
Spain, Jim C.
Gadda, Giovanni - Abstract:
- <abstract abstract-type="main"> <title>Abstract</title> <p>3‐Nitropropionate (3‐NPA) is a nitro aliphatic compound found in numerous plants and fungi. The nitro compound exists in equilibrium with its conjugate base, propionate 3‐nitronate (P3N) and has a p<italic>K</italic><sub>a</sub> approaching the physiological range of 9.1. Since 1920, more than 30 species of plant and fungi have been identified as producing 3‐NPA as a means of defense from herbivores. Glycoside products containing moieties of 3‐NPA found in parts of the plants most accessible to herbivores can be easily hydrolyzed to free 3‐NPA by bacterial enzymes in the gut of animals. In addition to providing a defense mechanism, the nitro compound is an intermediate in the nitrification process of leguminous plants. The synthesis of 3‐NPA in these plants and fungi is poorly understood. P3N, which readily forms from 3‐NPA at physiological pH, is a potent inhibitor of the key enzyme succinate dehydrogenase in the Krebs cycle and electron transport chain. Inhibition of succinate dehydrogenase in humans and livestock causes neurotoxicity and in some cases death. Several enzymes catalyze the oxidation of 3‐NPA or P3N; all contain a noncovalently bound flavin cofactor and are found in the organisms that produce 3‐NPA. With <italic>k</italic><sub>cat</sub>/<italic>K</italic><sub>m</sub> values of &gt;10<sup>6</sup> M<sup>−1</sup> s<sup>−1</sup>, nitronate monooxygenases can quickly and efficiently oxidize P3N to malonic<abstract abstract-type="main"> <title>Abstract</title> <p>3‐Nitropropionate (3‐NPA) is a nitro aliphatic compound found in numerous plants and fungi. The nitro compound exists in equilibrium with its conjugate base, propionate 3‐nitronate (P3N) and has a p<italic>K</italic><sub>a</sub> approaching the physiological range of 9.1. Since 1920, more than 30 species of plant and fungi have been identified as producing 3‐NPA as a means of defense from herbivores. Glycoside products containing moieties of 3‐NPA found in parts of the plants most accessible to herbivores can be easily hydrolyzed to free 3‐NPA by bacterial enzymes in the gut of animals. In addition to providing a defense mechanism, the nitro compound is an intermediate in the nitrification process of leguminous plants. The synthesis of 3‐NPA in these plants and fungi is poorly understood. P3N, which readily forms from 3‐NPA at physiological pH, is a potent inhibitor of the key enzyme succinate dehydrogenase in the Krebs cycle and electron transport chain. Inhibition of succinate dehydrogenase in humans and livestock causes neurotoxicity and in some cases death. Several enzymes catalyze the oxidation of 3‐NPA or P3N; all contain a noncovalently bound flavin cofactor and are found in the organisms that produce 3‐NPA. With <italic>k</italic><sub>cat</sub>/<italic>K</italic><sub>m</sub> values of &gt;10<sup>6</sup> M<sup>−1</sup> s<sup>−1</sup>, nitronate monooxygenases can quickly and efficiently oxidize P3N to malonic semialdehyde as a means of protecting the organism from killing itself. Although it was discovered almost a century ago, the biochemistry and physiological role of 3‐NPA/P3N are just emerging. © 2013 IUBMB Life, 65(9):759–768, 2013</p> </abstract> … (more)
- Is Part Of:
- IUBMB life. Volume 65:Issue 9(2013:Sep.)
- Journal:
- IUBMB life
- Issue:
- Volume 65:Issue 9(2013:Sep.)
- Issue Display:
- Volume 65, Issue 9 (2013)
- Year:
- 2013
- Volume:
- 65
- Issue:
- 9
- Issue Sort Value:
- 2013-0065-0009-0000
- Page Start:
- 759
- Page End:
- 768
- Publication Date:
- 2013-07-29
- Subjects:
- Biochemistry -- Periodicals
Molecular biology -- Periodicals
572.8 - Journal URLs:
- http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1521-6551 ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1002/iub.1195 ↗
- Languages:
- English
- ISSNs:
- 1521-6543
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 4588.826000
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 3933.xml