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Pathway Description
Galactose Metabolism
Escherichia coli
Metabolic Pathway
Galactose can be synthesized through two pathways: melibiose degradation involving an alpha galactosidase and lactose degradation involving a beta galactosidase. Melibiose is first transported inside the cell through the melibiose:Li+/Na+/H+ symporter. Once inside the cell, melibiose is degraded through alpha galactosidase into an alpha-D-galactose and a beta-D-glucose. The beta-D-glucose is phosphorylated by a glucokinase to produce a beta-D-glucose-6-phosphate which can spontaneously be turned into a alpha D glucose 6 phosphate. This alpha D-glucose-6-phosphate is metabolized into a glucose -1-phosphate through a phosphoglucomutase-1. The glucose -1-phosphate is transformed into a uridine diphosphate glucose through UTP--glucose-1-phosphate uridylyltransferase. The product, uridine diphosphate glucose, can undergo a reversible reaction in which it can be turned into uridine diphosphategalactose through an UDP-glucose 4-epimerase.
Galactose can also be produced by lactose degradation involving a lactose permease to uptake lactose from the environment and a beta-galactosidase to turn lactose into Beta-D-galactose.
Beta-D-galactose can also be uptaken from the environment through a galactose proton symporter.
Galactose is degraded through the following process:
Beta-D-galactose is introduced into the cytoplasm through a galactose proton symporter, or it can be synthesized from an alpha lactose that is introduced into the cytoplasm through a lactose permease. Alpha lactose interacts with water through a beta-galactosidase resulting in a beta-D-glucose and beta-D-galactose. Beta-D-galactose is isomerized into D-galactose. D-Galactose undergoes phosphorylation through a galactokinase, hence producing galactose 1 phosphate. On the other side of the pathway, a gluose-1-phosphate (product of the interaction of alpha-D-glucose 6-phosphate with a phosphoglucomutase resulting in a alpha-D-glucose-1-phosphate, an isomer of Glucose 1-phosphate, or an isomer of Beta-D-glucose 1-phosphate) interacts with UTP and a hydrogen ion in order to produce a uridine diphosphate glucose. This is followed by the interaction of galactose-1-phosphate with an established amount of uridine diphosphate glucose through a galactose-1-phosphate uridylyltransferase, which in turn output a glucose-1-phosphate and a uridine diphosphate galactose. The glucose -1-phosphate is transformed into a uridine diphosphate glucose through UTP--glucose-1-phosphate uridylyltransferase. The product, uridine diphosphate glucose, can undergo a reversible reaction in which it can be turned into uridine diphosphategalactose through an UDP-glucose 4-epimerase, and so the cycle can keep going as long as more lactose or galactose is imported into the cell
References
Galactose Metabolism References
Kamogawa A, Kurahashi K: Purification and properties of uridinediphosphate glucose pyrophosphorylase from Escherichia coli K12. J Biochem. 1965 Jun;57(6):758-65.
Pubmed: 4284510
Lazarowski ER, Shea DA, Boucher RC, Harden TK: Release of cellular UDP-glucose as a potential extracellular signaling molecule. Mol Pharmacol. 2003 May;63(5):1190-7.
Pubmed: 12695547
Lerouge I, Vanderleyden J: O-antigen structural variation: mechanisms and possible roles in animal/plant-microbe interactions. FEMS Microbiol Rev. 2002 Mar;26(1):17-47.
Pubmed: 12007641
Frey PA: The Leloir pathway: a mechanistic imperative for three enzymes to change the stereochemical configuration of a single carbon in galactose. FASEB J. 1996 Mar;10(4):461-70.
Pubmed: 8647345
Abramson J, Smirnova I, Kasho V, Verner G, Kaback HR, Iwata S: Structure and mechanism of the lactose permease of Escherichia coli. Science. 2003 Aug 1;301(5633):610-5. doi: 10.1126/science.1088196.
Pubmed: 12893935
Huber RE, Lytton J, Fung EB: Efflux of beta-galactosidase products from Escherichia coli. J Bacteriol. 1980 Feb;141(2):528-33.
Pubmed: 6767683
Huber RE, Hurlburt KL: Escherichia coli growth on lactose requires cycling of beta-galactosidase products into the medium. Can J Microbiol. 1984 Mar;30(3):411-5.
Pubmed: 6426769
JACOB F, MONOD J: Genetic regulatory mechanisms in the synthesis of proteins. J Mol Biol. 1961 Jun;3:318-56.
Pubmed: 13718526
Liu JY, Miller PF, Willard J, Olson ER: Functional and biochemical characterization of Escherichia coli sugar efflux transporters. J Biol Chem. 1999 Aug 13;274(33):22977-84.
Pubmed: 10438463
Liu JY, Miller PF, Gosink M, Olson ER: The identification of a new family of sugar efflux pumps in Escherichia coli. Mol Microbiol. 1999 Mar;31(6):1845-51.
Pubmed: 10209755
Wang XG, Olsen LR, Roderick SL: Structure of the lac operon galactoside acetyltransferase. Structure. 2002 Apr;10(4):581-8.
Pubmed: 11937062
Burstein C, Kepes A: The alpha-galactosidase from Escherichia coli K12. Biochim Biophys Acta. 1971 Jan 26;230(1):52-63.
Pubmed: 5543331
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