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Glc 6 p

Manufactured by Merck Group
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Glc-6-P is a chemical compound that serves as an intermediate in the glycolysis pathway, which is the process of converting glucose into energy for cellular processes. It is formed by the phosphorylation of glucose, a key step in the initial stages of glucose metabolism. Glc-6-P is a central molecule in cellular energy production and carbohydrate metabolism.

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Lab products found in correlation

Adenosine triphosphate (atp), by Merck Group (3 mentions) Glc 1 p, by Merck Group (2 mentions) Pyruvate kinase, by Merck Group (2 mentions) L malic dehydrogenase, by Merck Group (2 mentions) L lactate dehydrogenase, by Roche (2 mentions) Adenosine diphosphate (adp), by Merck Group (2 mentions) L malic acid, by Merck Group (2 mentions) Isopropyl β d 1 thiogalactopyranoside (iptg), by Merck Group (1 mentions) Oligonucleotide, by Merck Group (1 mentions) D glucuronic acid, by Merck Group (1 mentions) D mannose, by Merck Group (1 mentions) D galactose, by Merck Group (1 mentions) D glucose, by Merck Group (1 mentions) Glcn6p, by Merck Group (1 mentions)

5 protocols using glc 6 p

1

Preparation of Biochemical Reagents

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Protein standards, antibiotics, IPTG, Glc-1P, Glc-6P, glucosamine-1P (GlcN-1P), galactose-1P (Gal-1P), N-acetylglucosamine-1P (GlcNAc-1P), 6-phosphogluconate (6-PGlcA), ATP, UTP, GTP, CTP, fructose-6P (Fru-6P), ribose-5P (Rib-5P), phosphoenolpyruvate (PEP), pyruvate (Pyr), NADPH, and oligonucleotides were obtained from Sigma-Aldrich (St. Louis, MO, USA). All other reagents were of the highest quality available.
Cereijo A.E., Asencion Diez M.D., Dávila Costa J.S., Alvarez H.M, & Iglesias A.A. (2016). On the Kinetic and Allosteric Regulatory Properties of the ADP-Glucose Pyrophosphorylase from Rhodococcus jostii: An Approach to Evaluate Glycogen Metabolism in Oleaginous Bacteria. Frontiers in Microbiology, 7, 830.
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2

Sulfoquinovose Biosynthesis Assay

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d-Glucose (Glc), d-mannose (Man), d-galactose (Gal), d-glucuronic acid (GlcA), and Glc-6-P were purchased from Sigma–Aldrich. d-Sulfoquinovose was purchased from MCAT GmbH (Germany, http://www.MCAT.de). 4-Nitrophenyl α-d-sulfoquinovoside and Escherichia coli YihQ sulfoquinovosidase have been described recently [4 (link)].
Abayakoon P., Lingford J.P., Jin Y., Bengt C., Davies G.J., Yao S., Goddard-Borger E.D, & Williams S.J. (2018). Discovery and characterization of a sulfoquinovose mutarotase using kinetic analysis at equilibrium by exchange spectroscopy. Biochemical Journal, 475(7), 1371-1383.
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3

Enzymatic Phosphate Compound Acquisition

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Glc-1-P, Glc-6-P, glucose-1,6-bisphosphate (Glc-1,6-2P) and GlcN-6-P were purchased from Sigma-Aldrich. GlcNAc-6-P, GlcNAc-1-P and GlcN-1-P were purchased from Santa Cruz Biotechnology. Double distilled water was used for HPLC, and all other solvents and chemicals were HPLC grade.
Jia X., Kang J, & Yin H. (2016). A simple and rapid method for measuring α-D-phosphohexomutases activity by using anion-exchange chromatography coupled with an electrochemical detector. PeerJ, 4, e1517.
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4

Enzymatic Assay for Metabolic Intermediates

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ATP, ADP, PEP, OAA, NADH, Glc6P, L-malic acid, pyruvate kinase, and L-malic dehydrogenase were from Sigma Aldrich. L-lactate dehydrogenase was from Roche. All other reagents were of the highest available quality.
Rojas B.E., Hartman M.D., Figueroa C.M., & Iglesias A.Á. (2020). Proteolytic cleavage ofArabidopsis thalianaphosphoenolpyruvate carboxykinase-1 modifies its allosteric regulation.
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5

Enzyme-Coupled Metabolite Assay

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ATP, ADP, PEP, OAA, NADH, Glc6P, L-malic acid, pyruvate kinase, and L-malic dehydrogenase were from Sigma Aldrich. L-Lactate dehydrogenase was from Roche. All other reagents were of the highest available quality.
Rojas B.E., Hartman M.D., Figueroa C.M, & Iglesias A.A. (2021). Proteolytic cleavage of Arabidopsis thaliana phosphoenolpyruvate carboxykinase-1 modifies its allosteric regulation. Journal of experimental botany, 72(7).
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