"Glucose6phosphate dehydrogenase deficiency" Essays and Research Papers

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    The Citric Acid Cycle

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    succinate in a multistep process that includes two other oxidation reactions. Pyruvate + 4NAD+ + FAD + GDP + Pi + 2H2O  3CO2 + 4NADH + FADH2 + GTP + 4H+ • The cycle is strongly exergonic. Pyruvate is Converted to Acetyl-CoA  Pyruvate dehydrogenase complex is responsible for the conversion of pyruvate to CO2 and the acetyl portion of acetyl-CoA. Five enzymes in complex: 1. 2. 3. 4. 5. 

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    What precautions and actions will you teach her about this drug therapy? As a precautionary measure‚ metabolism inhibitors should be avoided in any person who has a genetic disorder called glucose-6-phosphate dehydrogenase (G6PD) deficiency‚ which causes red blood cells to break. G6PD is most common among males of African-Americans and or Mediterranean decent. In addition‚ thiazide diuretics should not be prescribed with trimethoprim/sulfamethoxazole (Bactrim). Combining

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    Jaundice

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    1 Hepatic events • 4 Diagnostic approach • 5 Complications • 6 References • 7 External links Signs and symptoms A 4-year-old boy with icteric (jaundiced) sclera which later proved to be a manifestation of hemolytic anemia due to G6PD deficiency following fava bean consumption. The main symptom of jaundice is a yellow discoloration of the white part of the eyes and of the skin. The conjunctiva of the eye are one of the first tissues to change color as bilirubin levels rise in jaundice

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    Biology

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    Influence of Malonate and Sodium Fluoride on the Activity of Enzyme Succinate Dehydrogenase to Assess Inhibitors of Cellular Respiration Thaovy Mai Tran BI 151.5233 (Winter 2013) Todd Tiano 03/25/2013 Introduction Most organisms produce adenosine triphosphate (ATP) as a source of energy for cellular work‚ using cellular respiration. Cellular respiration

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    molecule of ATP by substrate-level phosphorylation‚ and reduces three molecules of NAD and one molecule of FAD for use in Oxidative Phosphorylation. The cycle is preceded by Glycolysis‚ which also occurs in anaerobic respiration‚ and the pyruvate dehydrogenase complex‚ which occur in the cytoplasm and the mitochondrial matrix respectively. In aerobic respiration‚ glycolysis breaks down one molecule of glucose and two molecules of pyruvate‚ and gives a net product

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    pyruvate is changed over to acetyl CoA. This transformation step is irreversible in numerous living beings and controls how much acetyl CoA "fuel" enters the citrus extract. The compound that catalyses the transformation response is called pyruvate dehydrogenase. ATP and NADH make this protein less dynamic‚ while ADP makes it more

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    1954 by John Hans Menkes‚ a pediatric neurologist who would also discover Menkes Disease. People with this condition lack specific enzymes required to metabolize certain amino acids. It is also commonly known as BCKD deficiency‚ branched chain alpha-ketoacid dehydrogenase deficiency‚ branched chain ketonuria I‚ classical maple syrup urine disease or MSUD. There are several subtypes each with varying levels of severity and symptoms. Because it is inherited prevention is impossible.

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    case-controlled studies‚ research showed that children with the African variant of G6PD deficiency had twice the resistance to P. falciparum malaria compared to children to children who didn’t have the mutation. Laboratory experiments have also shown that malarial-causing parasites preferred “normal” red blood cells compared to the G6PD-deficient red blood cells. Question: Did favism‚ or G6PD enzyme deficiency‚ help humanity survive through malaria? Research: Favism and malaria are found in areas

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    Biochemistry-Metabolism

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    References: Energy‚ ATP‚ and Enzymes. Retrieved on February 28‚ 2013 from http://www.uic.edu/classes/bios/bios100/lectures/enzymes.htm Genetic People. (2011). Fructose 1-Phosphate Aldolase Deficiency (Fructose Intolerance). Retrieved on February 26‚ 2013 from http://geneticpeople.com/?p=882. Hudon-Miller‚ Sarah. 2012. Cori Cycle. Video retrieved from http://www.youtube.com/watch?v=gWXDNBiLva4&feature=youtu.be. Hudon-Miller‚ Sarah. 2012. Enzymes

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    with mitochondria and active dehydrogenases we found a color change supporting the fact of active mitochondria. Raw kernels have active dehydrogenation because of the colorless tetrazolium turning red. We can understand that boiled kernels were absent mitochondrial activity as well as active dehydrogenases due to the absence of any pink areas coincided with our understanding. Overall‚ the purpose of this lab was to find mitochondrial activity and/or active dehydrogenase using differential centrifugation

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