How many cycles of the beta-oxidation sequence need to be executed to convert a C18 fatty acid into acetyl-CoA? Check the correct one: ( ) 7 ( ) 9 ( ) 11 ( ) 8 ( )10

(i) Consider a preparation that contains all the enzymes and cofactors necessary for fatty acid biosynthesis from acetyl-CoA and malonyl-CoA. If [2-H] acetyl-CoA labeled with deuterium, the heavy isotope of hydrogen and excess of unlabeled malonyl-CoA are added as substrates, where will you find these labeled deuterium atoms in a molecule of palmitate synthesized? Explain. S-COA (ii) Describe the steps involved in the synthesis of palmitic acid starting from acetyl-CoA and malonyl-CoA.

In the complete b-oxidation of stearic acid (18:0) How many moles of acetyl CoA are produced? How many times would the fatty acid pass through the fatty acid spiral for complete oxidation?

Based on the image below, select the correct statement HN Aspartate Rib-P Inosinate (IMP) IMP H₂O OOC-CH₂- COO NH Fumarate N 274 adenylosuccinate lyase Rib-P Adenylosuccinate GTP GDP + P₁ adenylosuccinate IMP synthetase NAD+ NADH + H+ dehydrogenase Figure 22-36 Lehninger Principles of Biochemistry, Sixth Edition ©2013 W. H. Freeman and Company H HN H -N Gin Rib P Xanthylate (XMP) NH₂ Rib P Adenylate (AMP) Glu ATP AMP + PP₁ XMP-glutamine amidotransferase HN H₂N O GTP is phosphorylated in the conversion of IMP to GMP GTP is phosphorylated in the convertion of IMP to AMP GTP is dephosphorylated in the conversion of IMP to GMP O GTP is dephosphorylated in the conversion of IMP to AMP Rib-P Guanylate (GMP) GMP

(a) Write a balanced equation for the conversion of aspartate into glucose through the intermediate oxaloacetate. Which coenzymes participate in this transformation? (b) Write a balanced equation for the conversion of aspartate into oxaloacetate through the intermediate fumarate

Most individuals with genetic defects in oxidative phosphorylation are found to have relatively high concentrations of alanine in their blood. how this in biochemical terms?  please help :)

Explain why people with a hereditary deficiency of carnitine acyltransferase II have muscle weakness. Why are the symptoms more severe during fasting? (Keep your answer to at least a paragraph)

Can u help me to explain to me, please? I stuggled my homework and i need help to understand it

The final step in the pathway for the synthesis of glucose from lactate (gluconeogenesis) is: Glucose-6-phosphate + H20 5 Glucose + Pi When glucose-6-phosphate is incubated with the proper enzyme and the reaction runs until equilibrium has been reached, the final concentrations are found to be: glucose-6-phosphate (0.035 mM), glucose (100 mM), and Pi (100 mM). Calculate AG" at 25°C and pH 7. 10:21 PM 4/21/2021 F5 F6 F7 F8 F10 F9 7 8. Backspace ー の

Explain why the option is correct and others are not