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MCBD Exam 2
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delta-tennessee-fruit-yankee-colorado-tennis
Status
Last Update
Fields
Published
11/16/2023
Sucrose
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Lactose
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Maltose
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How many monosaccarides do oligosaccharides contain?
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How many monosaccharides do polysaccharides contain?
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Starch is a polysaccharide polymer of glucose with what linkages?
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What is starch catabolized by?
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Glycogen is a polymer of glucose with what linkages and where is it located?
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Inulin is a polymer of what and is used for what?
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Glycosaminoglycans(mucopolysaccharides, GAGs) contain repeating disaccharide units and are located where?
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Glycosaminoglycans are highly negatively charged...
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Proteoglycans are a core protein meaning they are rich in _______. They are attached to GAGS. and are located in the ECM.
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Cellulose is a structural polysaccharide with glucose monomers with ______ glycosidic linkages.
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Describe starch digestion.
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What enzyme catalyses glucose being added to sucrose, making glucans?
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What enzyme is responsible for catalyzing the addition of fructose to sucrose, making fructan polymers?
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______ comprises 10–20% dry weight of dental plaque
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________ is branched glucan that modulates bacterial adhesion.
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_________ is a bacterial polysaccharide that contributes to the formation of extracellular polysaccharide matrix and promotes plaque formation
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Structual molecule, lubrication, transport, immune function, hormone, and enzyme are all functions of...
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sIgA lysozyme, bicarbonate, water, a-amylase, glycoproteins, calcium phosphate, and mucin are all components of what?
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_________ are a complex carbohydrate derived from ceramide. They are found of the outer cell membrane and are sphingolipids with attached carbohydrate…
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When fed glucose is stored as what and where?
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Between meals the _____ converts glycogen into glucose.
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Low level of insulin signals ___________ to begin.
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What is released in response to high blood glucose?
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Glycolysis is achieved by breaking down glucose into 2 ________ molecules.
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Thiamine deficiency causes __________.
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Abnormalities in the peripheral nervous system , weakness, enlarged heart, alcoholics, elderly, glucose administration does nothing.
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apathy, loss of memory, abnormal eye movement, treatable with thiamine supplementation
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Point where carbohydrates, amino acids, & fatty acids catabolism converge. •Provides energy to produce ATP •Provides intermediates for biosyntheti…
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The citric acid cycle occurs where?
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The Citric Acid Cycle is linked to amino acid metabolism via...
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-Alternative metabolism of glucose -Operates in parallel with glycolysis but have a different biological role -To generate NADPH (irreversible) -To pr…
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Entner-Doudoroff Pathway
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Gluconeogenesis is produced by...
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In gluconeogenesis, lactate is oxidized to pyruvate by _____________.
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In gluconeogenesis, alanine is converted to pyruvate by _____________.
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Gluconeogenesis produces glucose from what?
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_______________ converts pyruvate to oxaloacetate in gluconeogenesis.
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The ________ is the source of rapid ATP production during muscle activity.
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Prevents lactic acidosis by moving lactate out of muscle into liver
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The brain can't do what?
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Cyanide binds irreversibly to ____________, which inhibits electron transfer to oxygen in the ETC.
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CO binds to cytochrome a. It also binds to hemoglobin and displaces oxygen. This does what?
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________ (Aspirin, 2,4-dinitrophenol) decrease the H+ gradient in the ETC.
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Humans cannot digest cellulose as we cannot break down what linkage?
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-Deficiency of glucose-6-phosphatase (type A) or glucose-6-phosphate translocase (type B) Symptoms - Hypoglycemia and a swollen belly Treatment - Diet…
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-Aka GSD II -Defects in alpha-glucosidase, leading to glycogen buildup Symptoms - Muscles impaired, hepatomegaly, heart defects Treatment: Supportive …
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11/16/2023
-Aka GSD III, Forbes -Mutations in the AGL gene coding for glycogen debranching enzyme Symptoms - Enlarged liver, delayed growth, muscle weakness Trea…
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-Aka GSD IV -Deficiency in glycogen branching enzyme Symptoms - Enlarged liver, cirrhosis, failure to thrive Treatment: No specific treatment availabl…
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-Aka GSD V -Deficient muscle glycogen phosphorylase Symptoms - Muscle fatigue, exercise intolerance Treatment: No specific treatment available
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-Aka GSD VI -Deficient hepatic glycogen phosphorylase -Hypoglycemia, hepatomegaly, lactic acidosis Symptoms are generally mild Treatment: …
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Inborn errors of carb metabolism and glycogen storage inherited as...
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Inborn Errors of Carbohydrate Metabolism - Glycogen Storage Diseases(Notice the pattern in the disease names)
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Mucopolysaccharide storage diseases include what two diseases?
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During aerobic metabolism, pyruvate is converted into _________ before entering Citric Acid Cycle
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The conversion of pyruvate to acetyl CoA is mediated by __________ complex.
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11/16/2023
During Vit B1 deficiency, PDH complex cannot carry out its function, leading to this condition characterized by abnormalities in the peripheral nervou…
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11/16/2023
In a state of fasting when glucose is needed by the brain, pyruvate will be converted to _______, the first product in the pathway of gluconeogenesis
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11/16/2023
Carbohydrate, amino acid, & fatty acid metabolisms all converge at this metabolic pathway.
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11/16/2023
As lactate accumulates in muscle tissue during intense exercise, it eventually diffuses into the bloodstream and is transported to the _____ to be con…
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11/16/2023
Conversion of lactate to pyruvate to glucose in the liver is accomplished via _____________ before glucose is released back into circulation.
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11/16/2023
The cyclic conversion of glucose to pyruvate to lactate and back to pyruvate and glucose is called the ______.
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11/16/2023
The Cori Cycle takes the product of anaerobic metabolism(______) from the muscles and turns it into pyruvate then back to glucose in the liver.
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G6PD/NADPH in _________ pathway is the only source of reduced glutathione in RBCs.
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11/16/2023
Another important function of Pentose Phosphate Pathway is to provide intermediates for _____________.
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11/16/2023
Status
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Fields