| Entry |
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| Name |
Phosphonate and phosphinate metabolism
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| Description |
Natural products containing carbon-phosphorous bonds, so-called C-P compounds, are derivatives of phosphonate and phosphinate with substitution of alkyl group for hydrogen of phosphorus-hydrogen bonds. C-P compounds have been found in many organisms, but only protists and bacteria, mostly Actinobacteria, have biosynthetic capacity. A common reaction in the biosynthetic pathway is C-P bond forming reaction from phosphoenolpyruvate (PEP) to phosphonopyruvate (PnPy) catalyzed by PEP phosphomutase. 2-Aminoethylphosphonate (AEP) is the most abundant C-P compound in the natural world. AEP derivatives include phosphonoprotein, phosphonoglycan, and phosphonolipid. Other known C-P compounds are bioactive substances used in medicine (antibiotics) and agriculture (herbicide) such as fosfomycin, FR-33289, rhizocticin, and bialaphos.
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| Class |
Metabolism; Metabolism of other amino acids
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| Pathway map |
| Phosphonate and phosphinate metabolism |

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| Other DBs |
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| Enzyme |
| | 1.1.99.- | | | | | | | | 2.6.1.- | | | | | | | | 2.7.8.- | | | | | | | | | | | | | | | | | | | | | | 4.99.1.- | | | |
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| Compound |
| Pyruvate | | Acetate | | Phosphoenolpyruvate | | Acetaldehyde | | Ethanolamine | | D-Ribose 1,5-bisphosphate | | 3-Phosphonopyruvate | | Phosphonoacetaldehyde | | 2-Aminoethylphosphonate | | Glufosinate | | 2-Amino-3-phosphonopropanoate | | CMP-2-aminoethylphosphonate | | CMP-N-trimethyl-2-aminoethylphosphonate | | Diacylglyceryl-2-aminoethylphosphonate | | Diacylglyceryl-N-trimethyl-2-aminoethylphosphonate | | Lipophosphonoglycan | | 1-Hydroxy-2-aminoethylphosphonate | | N-Monomethyl-2-aminoethylphosphonate | | N-Dimethyl-2-aminoethylphosphonate | | Ceramide 2-aminoethylphosphonate | | Phosphonoacetate | | 2-Aminoethylphosphocholate | | 1-Carboxyvinyl carboxyphosphonate | | 3-(Hydrohydroxyphosphoryl)pyruvate | | 2-Hydroxyethylphosphonate | | (S)-2-Hydroxypropylphosphonate | | Fosfomycin | | Hydroxymethylphosphonate | | Phosphonoformate | | Bialaphos | | N-Trimethyl-2-aminoethylphosphonate | | Rhizocticin B | | 2-Oxo-4-phosphonobutanoate | | FR 900098 | | Formylphosphonate | | Rhizocticin A | | Phosphonoformyl-CMP | | Carboxyphosphonopyruvate | | 2-Phosphinomethylmalate | | Deamino-alpha-keto-demethylphosphinothricin | | N-Acetyldemethylphosphinothricin | | N-Acetyldemethylphosphinothricin tripeptide | | N-Acetylbialaphos | | N-Acetylphosphinothricin | | Rhizocticin C | | Rhizocticin D | | Demethylphosphinothricin | | Methylphosphonate | | alpha-D-Ribose 1-methylphosphonate 5-triphosphate | | alpha-D-Ribose 1-methylphosphonate 5-phosphate | | alpha-D-Ribose 1,2-cyclic phosphate 5-phosphate |
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| Reference |
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| Authors |
Metcalf WW, van der Donk WA |
| Title |
Biosynthesis of phosphonic and phosphinic acid natural products. |
| Journal |
Annu Rev Biochem 78:65-94 (2009) |
| Reference |
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| Authors |
Xiao Y, Lee K, Liu P |
| Title |
Syntheses of the P-methylase substrates of the bialaphos biosynthetic pathway. |
| Journal |
Org Lett 10:5521-4 (2008) |
| Reference |
|
| Authors |
van der Donk WA |
| Title |
Rings, radicals, and regeneration: the early years of a bioorganic laboratory. |
| Journal |
J Org Chem 71:9561-71 (2006) |
| Reference |
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| Authors |
Blodgett JA, Zhang JK, Metcalf WW |
| Title |
Molecular cloning, sequence analysis, and heterologous expression of the phosphinothricin tripeptide biosynthetic gene cluster from Streptomyces viridochromogenes DSM 40736. |
| Journal |
Antimicrob Agents Chemother 49:230-40 (2005) |
| Reference |
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| Authors |
Schwartz D, Berger S, Heinzelmann E, Muschko K, Welzel K, Wohlleben W |
| Title |
Biosynthetic gene cluster of the herbicide phosphinothricin tripeptide from Streptomyces viridochromogenes Tu494. |
| Journal |
Appl Environ Microbiol 70:7093-102 (2004) |