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Pathway Description
Operon: Sugar Uptake
Escherichia coli
Signaling Pathway
The ptsHI-crr operon in E. coli contains three genes which encode proteins that are part of the phosphoenolpyruvate-dependent sugar phosphotransferase system (PEP group translocation or sugar PTS). This is an active transport system used to bring sugars such as glucose and mannose into the cell. The operon can be activated by the cAMP-activated global transcriptional regulator CRP (CAP), which binds upstream of the promoter region and interacts with RNA polymerase, activating transcription of the operon. The operon can also be inhibited in several locations by various proteins. The catabolite repressor/activator protein Cra can bind to the promoter region, and depending on the binding of CRP, can either activate the operon's transcription if CRP is not bound, or can inhibit it if CRP is bound.
Protein mlc is a repressor that can bind to the promoter region of the operon, repressing transcription. It is involved in the repression and regulation of other proteins involved in the sugar PTS. Finally, the N-acetylglucosamine repressor can bind to the promoter region after being activated by the binding of N-acetyl-D-glucosamine 6-phosphate, allowing it to inhibit transcription of the operon.
The first gene in the operon, ptsH, encodes the phosphocarrier protein HPr, which is a general carrier protein in the sugar PTS that is not specific to the sugar being transported by the system. It takes a phosphoryl group from phosphoenolpyruvate (PEP) and transfers it to the EIIA domain of the carrier.
The second gene, ptsI, encodes phosphoenolpyruvate-protein phosphotransferase, another component of the sugar PTS that is not specific to the sugar. This enzyme is responsible for transferring the phosphoryl group from PEP to the protein HPr.
The final gene in the operon, crr, encodes theglucose-specific phosphotransferase enzyme IIA component, which combines with the PTS system N-acetylmuramic acid-specific EIIBC component to form the Enzyme E II protein. First, EIIA takes the phosphoryl group from HPr and transfers it to EIIB. Then EIIB transfers it across the cell membrane to EIIC via glucose, forming glucose-6-phosphate, which does not exit the cell naturally, allowing more glucose to be pumped into the cell forming a gradient.
References
Operon: Sugar Uptake References
Oberto J: FITBAR: a web tool for the robust prediction of prokaryotic regulons. BMC Bioinformatics. 2010 Nov 11;11:554. doi: 10.1186/1471-2105-11-554.
Pubmed: 21070640
Ryu S, Ramseier TM, Michotey V, Saier MH Jr, Garges S: Effect of the FruR regulator on transcription of the pts operon in Escherichia coli. J Biol Chem. 1995 Feb 10;270(6):2489-96.
Pubmed: 7852310
Ryu S, Garges S: Promoter switch in the Escherichia coli pts operon. J Biol Chem. 1994 Feb 18;269(7):4767-72.
Pubmed: 8106445
De Reuse H, Danchin A: The ptsH, ptsI, and crr genes of the Escherichia coli phosphoenolpyruvate-dependent phosphotransferase system: a complex operon with several modes of transcription. J Bacteriol. 1988 Sep;170(9):3827-37.
Pubmed: 2457575
Zheng D, Constantinidou C, Hobman JL, Minchin SD: Identification of the CRP regulon using in vitro and in vivo transcriptional profiling. Nucleic Acids Res. 2004 Nov 1;32(19):5874-93. doi: 10.1093/nar/gkh908. Print 2004.
Pubmed: 15520470
Plumbridge J: DNA binding sites for the Mlc and NagC proteins: regulation of nagE, encoding the N-acetylglucosamine-specific transporter in Escherichia coli. Nucleic Acids Res. 2001 Jan 15;29(2):506-14.
Pubmed: 11139621
Shimada T, Yamamoto K, Ishihama A: Novel members of the Cra regulon involved in carbon metabolism in Escherichia coli. J Bacteriol. 2011 Feb;193(3):649-59. doi: 10.1128/JB.01214-10. Epub 2010 Nov 29.
Pubmed: 21115656
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