Characterization of the interaction between the small regulatory peptide SgrT and the EIICBGlc of the glucose- phosphotransferase system of E. coli K-12

Autor(en): Kosfeld, A.
Jahreis, K.
Stichwörter: fructose 6 phosphate, 56-83-7, 643-13-0; glucose 6 phosphate, 56-73-5; phosphoenolpyruvate sugar phosphotransferase, 56941-29-8; bacterial metabolism; bacterial protein; DNA sequence; down regulation; E. coli K-12; Escherichia coli; fluorescence analysis; fluorescence microscopy; fructose 6 phosphate; gene expression regulation; gene mutation; glucose 6 phosphate; glucose metabolism; Glucose signaling; Glucose transporter; molecular cloning; phosphoenolpyruvate sugar phosphotransferase; protein conformation; protein cross linking; protein EIICB; protein interaction; protein phosphorylation; protein SgrT; Protein-protein interaction; PTS; Regulation; SgrT; site directed mutagenesis; unclassified drug, article; Western blotting
Erscheinungsdatum: 2012
Herausgeber: MDPI AG
Journal: Metabolites
Volumen: 2
Ausgabe: 4
Startseite: 756
Seitenende: 774
Zusammenfassung: 
Escherichia coli is a widely used microorganism in biotechnological processes. An obvious goal for current scientific and technical research in this field is the search for new tools to optimize productivity. Usually glucose is the preferred carbon source in biotechnological applications. In E. coli, glucose is taken up by the phosphoenolpyruvatedependent glucose phosphotransferase system (PTS). The regulation of the ptsG gene for the glucose transporter is very complex and involves several regulatory proteins. Recently, a novel posttranscriptional regulation system has been identified which consists of a small regulatory RNA SgrS and a small regulatory polypeptide called SgrT. During the accumulation of glucose-6-phosphate or fructose-6-phosphate, SgrS is involved in downregulation of ptsG mRNA stability, whereas SgrT inhibits glucose transport activity by a yet unknown mechanism. The function of SgrS has been studied intensively. In contrast, the knowledge about the function of SgrT is still limited. Therefore, in this paper, we focused our interest on the regulation of glucose transport activity by SgrT. We identified the SgrT target sequence within the glucose transporter and characterized the interaction in great detail. Finally, we suggest a novel experimental approach to regulate artificially carbohydrate uptake in E. coli to minimize metabolic overflow in biotechnological applications.© 2012 by the authors; licensee MDPI, Basel, Switzerland.
ISSN: 22181989
DOI: 10.3390/metabo2040756
Externe URL: https://www.scopus.com/inward/record.uri?eid=2-s2.0-84902199130&doi=10.3390%2fmetabo2040756&partnerID=40&md5=52bf1229901b69e0a8dd397e6f61a52d

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