Degradation of normal glycogen results to 97.2% glucose 1-phosphate and 7.2% glucose. Assuming a ratio of glucose 1-phosphate to glucose recorded in a glycogen sample from a patient with a liver disease was 100, The patient’s most likely enzymatic deficiency is _________
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Degradation of normal glycogen results to 97.2% glucose 1-phosphate and 7.2% glucose. Assuming a ratio of glucose 1-phosphate to glucose recorded in a glycogen sample from a patient with a liver disease was 100,
The patient’s most likely enzymatic deficiency is _________
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- During glycolysis, fructose 1,6-biphosphate splits into two compounds: ______________ after reacting with aldolase and _____________Cori’s disease, is an autosomal recessive metabolic disorder that is characterized by defects in the glycogen debranching enzyme amylo-1,6-glucosidase,4-α-glucanotransferase (AGL). It primarily effects the Liver, heart and skeletal muscle. Symptoms can include hyperlipidemia, ketoacidosis, and hypoglycemia. The possible dietary recommendations are as follows:1. A high protein diet to facilitate gluconeogenesis2. A ketogenic diet to provide an alternate source of energy3. Small frequent meals to prevent hypoglycemia4. A high fat dietWhich dietary recommendations can be used to treat this disorder? a) 2 and 4 b) 1 and 2 c) 2 and 3 d) 1 and 3 e) None of the above recommendations would be effective f) 3 and 4 g) 1 and 4You have a crude lysate sample (CL) containing a mixture of six proteins (1, 2, 3, 4, 5, ẞ- galactosidase), and your goal is to obtain purified ẞ-gal. Some characteristics of these proteins are shown in the table below. Protein Alcohol dehydrogenase Carbonic anhydrase Insulin B chain Phosphorylase B Glutamic dehydrogenase B-galactosidase 45% Concentration of ammonium sulfate (AS) required for precipitation Molecular Weight (kDa) Isoelectric point (pl) 38 3.7 80% 65% 20% 30% 45% 28 4.8 4 5.3 98 6.8 49 9.5 115 5.3 You begin your purification by performing an ammonium sulfate (AS) precipitation. You add the appropriate concentration of AS to your CL sample, incubate overnight at 4°C, then centrifuge to generate a supernatant (AS-S) and pellet (AS-P). What concentration of AS will you use to precipitate Glutamic dehydrogenase? © 20% O 30% 45% 65% 80%
- In 2-3 paragraphs (must be typed) explain: Discuss the regulation of cholesterol synthesis.Metabolic disorders are due to a LACK OF A PARTICULAR ENZYME OR ONE THAT is defective. Select a metabolis disorder/disease Describe the defect, identifying the enzyme(s) and discuss the therapy available treatment. Does the therapy treat the symptoms or the meatbolic nature of the disease? Explain.The major enzymatic defense against oxidative stress is provided by superoxide dismutase, glutathione, peroxidase, peroxiredoxin, and _____________
- Calculate the free energy change for glucose entry into cells when the extracellular concentration is 4.5 mM and the intracellular concentration is 2.1 mM at 37oC. Express your answer in kJ/mol. ___KJ/mol+ edu.au/courses/26618/quizzes/67364/take The image below shows the urea cycle. Based on the information in the image, which of the following is the most effective way of reducing the production of urea? CNH, Fumarate Arginine H₂O Arginase NH3+ C=N Arginino- succinate AMP + PP₁ NH₂ Arginino- succinase UREA CYCLE Urea ATP Argininosuccinate synthetase Ornithine H₂N H₂N 2 Citrulline Rate- limiting Ornithine 1. Carbamoyl phosphate synthase 1 N-acetyl glutamate H+ADP P₁ NH3 HCO3 ATP Carbamoyl Phosph. NH₂C-PO4 Ornithine 2. Citrulline formation P Citrulline C-NH₂ transcarbamoylase Aspartate NH₂ CYTOSOL MITOCHONDRIAL MATRIX https://canvas.uts.edu.au/assessment questions/356957/files/1562677/download? verifier=gRMPoy7VCgDrvn6QNfkZxDSsbLUwP1gRxFB3dLPjIdentify if True or False The activated form of glucose that serves as glucose donor for glycogen synthesis is formed by the reaction of UTP and glucose 1-phosphate. True False
- Hello good day, I am having a problem answering this question and I need your help on this. Hoping for a response and thank you In each chosen disease, pls. supply the information below: So I've chosen "Glucose-6-Phosphate Dehydrogenase (G6PD)", so I need a short description, its pathophysiology, laboratory diagnosis, and Treatment and Prevention of my chosen disease. Thank you. a. Short Description b. Pathophysiology c. Laboratory Diagnosis d. Treatment and PreventionThe activated form of glucose that serves as glucose donor for glycogen synthesis is formed by the reaction of UTP and glucose 6-phosphate. True FalseA sample of glycogen from a patient with liver disease is incubated with orthophosphate, phosphorylase, the transferase, and the debranching enzyme ( α -1,6- glucosidase). The ratio of glucose 1- phosphate to glucose formed in this mixture is 100. What is the most likely enzymatic deficiency in this patient?