4. The synthesis of fatty acids and their breakdown by Boxidation occur by separate pathways. Compare the two paths by filling in the blanks below. (Some blanks may require more than one answer.) Synthesis Boxidation Thiol activating group Electron carrier coenzyme(s) Basic units added or removed Cellular location of process in mammals
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![4. The synthesis of fatty acids and their breakdown by Boxidation occur by separate pathways.
Compare the two paths by filling in the blanks below. (Some blanks may require more than one
answer.)
Synthesis
Boxidation
Thiol activating group
Electron carrier coenzyme(s)
Basic units added or removed
Cellular location of process in mammals](/v2/_next/image?url=https%3A%2F%2Fcontent.bartleby.com%2Fqna-images%2Fquestion%2Ffa4426dc-92c3-4ac7-bd5a-9ba1dd10b9af%2Fb4994a51-1c01-40e8-8dd4-961d99f88f01%2F73tn6kp.png&w=3840&q=75)
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- 8. The enzyme thiolase catalyzes one step in the ß-oxidation of saturated fats. One portion of the mechanism for this reaction is shown below. Describe the catalytic mechanism at work. (Note: "SCOA" is shorthand for the compound Acetyl-CoA) RCOCH₂COSCoA + HSCOA → H3C₂OSC0A + RCOSCOA HN NH CH₂ NH CH₂ CH₂ FS Grease NH3 H-SCO A NH CH2 CH₂ NH3 S Co A CH₂ NH 1 3 H-SCO A H3C SCO A NH3 a h-SCOA R-C S Co A CH₂ CH₂ C H₂ 0=0 HN NH + NH3 H₂C HN CH₂ NH CH₂ CH₂ 2 S Co A CH₂ NH NH4. Consider the structure shown below. Give one cycle of the reactions of the - oxidation of fatty acids. Show all the structures of the compounds involved; indicate whether the reactions are reversible or not; show the use or generation of co-factors wherever it occurs.1. Explain the reaction mechanism involved how glucogenic amino acids can yield either a pyruvic acid or an oxaloacetic acid. In what pathway will pyruvic or oxaloacetic acid be used and why is this pathway important? 2. Discuss the reaction mechanism involved how the -NH2 groups of amino acids are being metabolized. 3. Explain why gluconeogenesis under conditions of starvation or diabetes breaks down body proteins. Complete answer please. Thank you. |
- 1) Tabulate the differences and/ or similarities of the different kinds of coenzymes and cofactors. Structure Source ATP SAM COA Retinal THF- tetrahydrofolate Vitamin K NAD, NADP FMN, FAD TPP PLP Adenosylcobalamin methylcobalamin and Function/ Role/ Importance1. Outline the first round of lipid catabolism using a C18 saturated fatty acid. Indicate cofactors and type of chemistry that takes place. a. How much NADH, FADH2 and ACCOA are you getting from complete catabolism of this fatty acid? b. How many moles of ATP are you getting from the breakdown of this fatty acid? Keep in mind that in the mitochondria 1 mole FADH2 gives about 1.5 moles of ATP while 1 mole NADH yields about 2.5 moles of ATP.The function of the enzyme acyl CoA synthetase is ATP-dependent activation of fatty acids using CoA O ATP-dependent reduction prior to activation O lipolysis to release free glyceraldehyde O for UDP activation isomerization of C=C in unsaturated fatty acids
- 2. Short-chain fatty acids such as butyrate are absorbed by the mammalian intestine and used as metabolic fuels. How many ATP can be derived from the complete oxidation of butyrate? Please show me detailed solution.i. How dihydroxyacetone phosphate is formed from glycerol? Write the chemical reactions. a& ii. What product is formed by the reaction of B-glucose with ATP? OH HO Ho Hexokinase OH ATP OH OH Glucose iii. Why saturated fatty acids haye high melting points than their unsaturated counterparts? naà k7NH, This compound is directly involved in: он O=P-0-CH, H но OmP-0- O oxidizing an alcohol in the conversion of sucrose to fructose. O the synthesis of malonyl coenzyme A. reducing a ketone in gluconeogenesis. reducing a C=C double bond in fatty-acid synthesis.
- Compound A below is a key intermediate in the synthesis of keto-myo-inositol B. Suggest a synthetic route for the preparation of A from D-glucose C giving structures for all of the intermediates in your scheme. Ph3CO. Но, HO HO HO, HO 'HO. ОН ОН Ph CH3 А В(d) of glucose oxidation in diabetic human patients treated with Metformin (●) and in (nondiabetic) control human patients (0). At –150 min both groups of subjects were started on an intravenous feed of 3-(®H)-glucose, and at t = 0 min they were started on an oral glucose tolerance test whereby a measured amount of glucose in water (a syrupy mixture) was swallowed followed by measure- ment of blood glucose levels at 30 min intervals. The flux of glucose oxidation was measured by the appear- ance of 3H2O in the blood stream. While the information The diagram to the right compares the rate 8000 ORAL GLUCOSE 6000- 4000- 2000- -120 -60 60 120 180 240 300 Minutes cannot be directly extracted from the reaction mecha- nism diagrams in the textbook, the glycolytic step in which the tritium is first released into water is that catalyzed by TPI, as illustrated at the beginning of Question #3. Explain why this step is suitable for measuring the flux of glycolysis through the release of °H…3. Triose-phosphate isomerase (TPI) catalyzes the movement of a single proton to interconvert dihy- droxyacetone phosphate and glyceraldehyde 3-phosphate in glycolysis and gluconeogenesis. The enzyme, a dimer of identical subunits that are 248 amino acids in humans, has no cofactors, required metal ions, or cooperativity between subunits. The enzyme is found in all tissues. The value of Kcat/KM - 9.2 x 106 sec-'M-1 is close to the rate constant expected for a diffusion-limited reaction. The mechanism of the proton transfer is illustrated in the diagram below. Glu-165 Giu-165 Glu-165 ks HR H 20,PO HO, OH His-95 His-95 His-95 (a) ing structural formulas and naming enzymes and glycolytic intermediates, the reactions of the payoff phase. Consider only anerobic glycolysis. Remember that each glucose molecule yields two mole- cules of glyceraldehyde-3-phosphate (GAP). Indicate the net yield of ATP and NADH generated through anaerobic glycolysis per glucose molecule. The reaction catalyzed by…
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