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BL 616 (Test 4) study guide. portion of the final exam on topics since Exam 3; also the topics of ch 26-29 weren’t tested Consider questions that cross chapters and sections : Consider similarities, differences fatty acid degradation and synthesis, in terms of compartments in the cell, enzymes and energy requirement, regulation Consider need for different enzymes for synthesis vs. degradation, of glycogen, of glucose, of proteins Consider important enzymes or proteins or other molecules that have similar names: protease vs. proteasome thrombin vs. thromboxane; trypsin vs. trypsinogen glucose, glycogen, gluconeogenesis vs. glycolysis vs. glycogenolysis phosphatase, phosphorylase (ex. Glycogen phosphorylase), kinases serine proteases, tyrosine kinases Chapters 26-31 carbohydrate topics: 26: Insulin, glucagon and other hormones (see also chapter 43 for more details on this) Nature of hormones, receptors, signaling paths. What factors regulate synthesis, secretion of these two major hormones? What are effects of these hormones on cells? 27: Digestion of carbohydrates in intestine – compare/contrast with lipids, amino acids Types of transport into epithelial cells Lactose and lactose intolerance 28: glycogen synthesis, degradation use different paths Regulation of glycogen breakdown, synthesis 29: fructose and galactose are converted into intermediates of glycolysis Fig. 30.17 Blood groups are glycolipids or glycoproteins 31: gluconeogenesis makes glucose from non-carbohydrates: amino acids (alanine), lactate, glycerol Chapters 34-35 Steroid hormones, eicosanoids briefly Cholesterol from diet or synthesized – role of HMG CoA reductase – statin drugsl FH familial hypercholesterolemia – LDL receptor Steroid hormones from cholesterol – adrenal glands, gonads: progesterone Estrogen made from testosterone Work through Nuclear hormone receptors Mono-oxygenases P450 Vitamin D lipid – nuclear hormone receptor Eicosanoids from arachidonic acid include prostaglandin, thromoxanes Chapters 37-39 Nitrogen metabolism – protein digestion, amino acid absorption, urea cycle, synthesis and degradation of amino acids – in addition to iRAT Ch 39: briefly synthesis of nonessential amino acids – C skeletons from glycose, glycolysis intermediates Degradation of enzymes to gluconeogenic intermediates, ketogenic Errors of enzymes and diseases: PKU, homocystinemia