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Pathway Description
Lysine Biosynthesis
Escherichia coli
Metabolic Pathway
Lysine is biosynthesized from L-aspartic acid. L-Aspartic acid can be incorporated into the cell through various methods: C4 dicarboxylate/orotate:H+ symporter, glutamate/aspartate:H+ symporter GltP, dicarboxylate transporter, C4 dicarboxylate/C4 monocarboxylate transporter DauA, and glutamate/aspartate ABC transporter. L-Aspartic acid is phosphorylated by an ATP-driven aspartate kinase resulting in ADP and L-aspartyl-4-phosphate. L-Aspartyl-4-phosphate is then dehydrogenated through an NADPH-driven aspartate semialdehyde dehydrogenase resulting in a release of phosphate, NADP, and L-aspartic 4-semialdehyde (involved in methionine biosynthesis). L-Aspartic 4-semialdehyde interacts with a pyruvic acid through a 4-hydroxy-tetrahydrodipicolinate synthase resulting in a release of hydrogen ion, water, and (2S,4S)-4-hydroxy-2,3,4,5-tetrahydrodipicolinate. The latter compound is then reduced by an NADPH-driven 4-hydroxy-tetrahydrodipicolinate reductase resulting in a release of water, NADP, and (S)-2,3,4,5-tetrahydrodipicolinate, This compound interacts with succinyl-CoA and water through a tetrahydrodipicolinate succinylase resulting in a release of coenzyme A and N-succinyl-2-amino-6-ketopimelate. This compound interacts with L-glutamic acid through an N-succinyldiaminopimelate aminotransferase resulting in oxoglutaric acid and N-succinyl-L,L-2,6-diaminopimelate. The latter compound is then desuccinylated by reacting with water through an N-succinyl-L-diaminopimelate desuccinylase resulting in a succinic acid and L,L-diaminopimelate. This compound is then isomerized through a diaminopimelate epimerase resulting in a meso-diaminopimelate (involved in peptidoglycan biosynthesis I). This compound is then decarboxylated by a diaminopimelate decarboxylase resulting in a release of carbon dioxide and L-lysine. L-Lysine is then incorporated into the lysine degradation pathway. Lysine also regulates its own biosynthesis by repressing dihydrodipicolinate synthase and also by repressing lysine-sensitive aspartokinase 3. Diaminopielate is a precursor for lysine as well as other cell wall components. Synthesis of lysine starts by converting L-aspartic acid (L-aspartate) to L-Aspartyl-4-phosphate by aspartate kinase. L-Aspartyl-4-phosphate transforms to form L-aspartic 4-semialdehyde (L-aspartate semialdehyde) by aspartate semialdehyde dehydrogenase with NADPH. L-aspartic 4-semialdehyde can start the metabolic pathway of synthesis of methionine as well as synthesis of threonine. Aspartate kinase can be regulated by its end product: L-Lysine.
References
Lysine Biosynthesis References
Acord J, Masters M: Expression from the Escherichia coli dapA promoter is regulated by intracellular levels of diaminopimelic acid. FEMS Microbiol Lett. 2004 Jun 1;235(1):131-7. doi: 10.1016/j.femsle.2004.04.022.
Pubmed: 15158272
Alvarez E, Ramon F, Magan C, Diez E: L-cystine inhibits aspartate-beta-semialdehyde dehydrogenase by covalently binding to the essential 135Cys of the enzyme. Biochim Biophys Acta. 2004 Jan 14;1696(1):23-9.
Pubmed: 14726201
Angeles TS, Viola RE: The kinetic mechanisms of the bifunctional enzyme aspartokinase-homoserine dehydrogenase I from Escherichia coli. Arch Biochem Biophys. 1990 Nov 15;283(1):96-101.
Pubmed: 2241177
ANTIA M, HOARE DS, WORK E: The stereoisomers of alpha epsilon-diaminopimelic acid. III. Properties and distribution of diaminopimelic acid racemase, an enzyme causing interconversion of the LL and meso isomers. Biochem J. 1957 Mar;65(3):448-59.
Pubmed: 13412646
Baumann RJ, Bohme EH, Wiseman JS, Vaal M, Nichols JS: Inhibition of Escherichia coli growth and diaminopimelic acid epimerase by 3-chlorodiaminopimelic acid. Antimicrob Agents Chemother. 1988 Aug;32(8):1119-23.
Pubmed: 3056252
Bearer CF, Neet KE: Threonine inhibition of the aspartokinase--homoserine dehydrogenase I of Escherichia coli. A slow transient and cooperativity of inhibition of the aspartokinase activity. Biochemistry. 1978 Aug 22;17(17):3523-30.
Pubmed: 28752
Berg CM, Rossi JJ: Proline excretion and indirect suppression in Escherichia coli and Salmonella typhimurium. J Bacteriol. 1974 Jun;118(3):928-34.
Pubmed: 4598010
Berges DA, DeWolf WE Jr, Dunn GL, Newman DJ, Schmidt SJ, Taggart JJ, Gilvarg C: Studies on the active site of succinyl-CoA:tetrahydrodipicolinate N-succinyltransferase. Characterization using analogs of tetrahydrodipicolinate. J Biol Chem. 1986 May 15;261(14):6160-7.
Pubmed: 3700390
Biellmann JF, Eid P, Hirth C, Jornvall H: Aspartate-beta-semialdehyde dehydrogenase from Escherichia coli. Purification and general properties. Eur J Biochem. 1980 Feb;104(1):53-8.
Pubmed: 6102909
Biellmann JF, Eid P, Hirth C: Affinity labeling of the Escherichia coli aspartate-beta-semialdehyde dehydrogenase with an alkylating coenzyme analogue. Half-site reactivity and competition with the substrate alkylating analogue. Eur J Biochem. 1980 Feb;104(1):65-9.
Pubmed: 6102911
Billheimer JT, Shen MY, Carnevale HN, Horton HR, Jones EE: Isolation and characterization of acetylornithine delta-transaminase of wild-type Escherichia coli W. Comparison with arginine-inducible acetylornithine delta-transaminase. Arch Biochem Biophys. 1979 Jul;195(2):401-13.
Pubmed: 112925
Blickling S, Renner C, Laber B, Pohlenz HD, Holak TA, Huber R: Reaction mechanism of Escherichia coli dihydrodipicolinate synthase investigated by X-ray crystallography and NMR spectroscopy. Biochemistry. 1997 Jan 7;36(1):24-33. doi: 10.1021/bi962272d.
Pubmed: 8993314
Borthwick EB, Connell SJ, Tudor DW, Robins DJ, Shneier A, Abell C, Coggins JR: Escherichia coli dihydrodipicolinate synthase: characterization of the imine intermediate and the product of bromopyruvate treatment by electrospray mass spectrometry. Biochem J. 1995 Jan 15;305 ( Pt 2):521-4.
Pubmed: 7832769
Boughton BA, Dobson RC, Hutton CA: The crystal structure of dihydrodipicolinate synthase from Escherichia coli with bound pyruvate and succinic acid semialdehyde: unambiguous resolution of the stereochemistry of the condensation product. Proteins. 2012 Aug;80(8):2117-22. doi: 10.1002/prot.24106. Epub 2012 Jun 4.
Pubmed: 22552955
Boughton BA, Hor L, Gerrard JA, Hutton CA: 1,3-Phenylene bis(ketoacid) derivatives as inhibitors of Escherichia coli dihydrodipicolinate synthase. Bioorg Med Chem. 2012 Apr 1;20(7):2419-26. doi: 10.1016/j.bmc.2012.01.045. Epub 2012 Feb 10.
Pubmed: 22386717
Bouvier J, Stragier P, Morales V, Remy E, Gutierrez C: Lysine represses transcription of the Escherichia coli dapB gene by preventing its activation by the ArgP activator. J Bacteriol. 2008 Aug;190(15):5224-9. doi: 10.1128/JB.01782-07. Epub 2008 May 23.
Pubmed: 18502871
Bouvier J, Richaud C, Richaud F, Patte JC, Stragier P: Nucleotide sequence and expression of the Escherichia coli dapB gene. J Biol Chem. 1984 Dec 10;259(23):14829-34.
Pubmed: 6094578
Bouvier J, Richaud C, Higgins W, Bogler O, Stragier P: Cloning, characterization, and expression of the dapE gene of Escherichia coli. J Bacteriol. 1992 Aug;174(16):5265-71.
Pubmed: 1644752
Boy E, Patte JC: Multivalent repression of aspartic semialdehyde dehydrogenase in Escherichia coli K-12. J Bacteriol. 1972 Oct;112(1):84-92.
Pubmed: 4404058
Boy E, Reinisch F, Richaud C, Patte JC: Role of lysyl-tRNA in the regulation of lysine biosynthesis in Escherichia coli K12. Biochimie. 1976;58(1-2):213-8.
Pubmed: 8152
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