Hereditary fructose intolerance metabolism is the process of cellular respiration it involves three steps, 1) glycolysis, 2) the citric acid or krebs cycle and 3) electron transport system the glycolytic pathway or glycolysis is a metabolic process that leads to the formation of the energy source adenosine triphosphate (atp) in the body. Please see attached file for paper instructions write my essay | i need help with my school assignment write my essay we are the most trusted essay writing service.
Hereditary fructose intolerance (hfi) is a metabolic disease caused by the absence of an enzyme called aldolase b in people with hfi, ingestion of fructose (fruit sugar) and sucrose (cane or beet sugar, table sugar) causes severe hypoglycemia (low blood sugar) and the build up of dangerous substances in the liver.
Hereditary fructose intolerance please see attached file for paper instructions is this question part of your assignment we can help our aim is to help you get a + grades on your coursework we handle assignments in a multiplicity of subject areas including admission essays, general essays, case studies, coursework, dissertations,. Because of the ease of therapy (dietary exclusion of fructose), hfi can be effectively managed if properly diagnosed in hfi, the diagnosis of homozygotes is difficult, requiring a genomic dna screening with allele specific probes or an enzyme assay from a liver biopsy.
Hereditary fructosemia, also termed hereditary fructose intolerance, is an autosomal recessive deficiency of aldo-lase b (fructose biphosphate aldolase) in the liver, kidney, and intestines mutations occur in the aldolase b gene, located on chromosome 9q22. The hereditary fructose intolerance cases arise upon the body missing the aldolase b enzyme the enzyme is responsible for the fructose breakdown in the body (lifton, 2009) the body undergoes complicated chemical changes upon consumption of fructose of sucrose substances in the absence of the mentioned aldolase b enzyme.
Hereditary fructose intolerance caused by aldolase b deficiency (fructose-1,6-bisphosphate aldolase) is an autosomal recessive disorder characterized by vomiting shortly after fructose ingestion the disease is associated with proximal tubule dysfunction (aminoaciduria, bicarbonaturia, and phosphaturia) and lactic acidosis. Hereditary fructose intolerance is a condition that affects a person's ability to digest the sugar fructose fructose is a simple sugar found primarily in fruits affected individuals develop signs and symptoms of the disorder in infancy when fruits, juices, or other foods containing fructose are introduced into the diet. Biochemistry – metabolism task task requirements: demonstrate your understanding of the biochemical basis of hereditary fructose intolerance (hfi) by completing the following: part 1 describe two important features that make all enzymes catalysts in your written response, discuss two important features that are specific to enzymes.
In hereditary fructose intolerance (hfi), individuals have a build up of fructose 1- phosphate (f1p), due to the absence or deficiency of aldolaseb, necessary to break down f1p into the two three carbon molecules utilized in the glycolytic pathway. Our aim is to help you get a + grades on your coursework we handle papers in a multiplicity of subject areas including admission essays, general essays, case studies, coursework, dissertations, editing, research papers, and research proposals header button label: place order now get started.