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Chemistry
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Chemistry for Today General Organic and Biochemistry Study Set 2
Quiz 24: Lipid and Amino Acid Metabolism
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Question 61
True/False
The biosynthesis of amino acids takes place mostly in the liver.
Question 62
True/False
Chylomicrons are aggregates of triglycerides, phosphoglycerides, and cholesterol complexed with proteins.
Question 63
True/False
Nutritionists suggest that a healthy diet be low in fats and high in carbohydrates.
Question 64
True/False
If there is an excessive intake of fatty acids and\or carbohydrates, the energy is stored as triglycerides for later use.
Question 65
Multiple Choice
Consider the diagram of a mitochondrion shown below. Which of the numbered locations is where β -oxidation occurs?
Question 66
Multiple Choice
Consider the simplified diagram of the urea cycle shown below. Which species, numbered 1 through 4, is synthesized in the mitochondria?
Question 67
True/False
Glycogen that is required by brain tissue leaves the liver and is transported to the brain by means of large blood vessels used specifically for this purpose.
Question 68
True/False
The processes of fatty acid degradation and fatty acid synthesis are the chemical reverse of each other and respond to stress as predicted by Le Châtelier's principle.
Question 69
True/False
Amino acids that the body does not synthesize are termed nonessential.
Question 70
True/False
Glycerol that is liberated from fats is digested by passing through glycolysis.
Question 71
True/False
Some amino acids are synthesized from α -keto acids.
Question 72
True/False
Given the chance, a few long exercise periods will burn off more fat than will many short periods.
Question 73
True/False
If an individual does not have a sufficient level of insulin in the blood, the uptake of glucose by the cells is inhibited.
Question 74
True/False
Phenylalanine is derived from tyrosine by oxidation.
Question 75
True/False
The synthesis of amino acids and the intake of amino acids are both important in order to replace cells lost from cellular death caused by either old age of the cells or disease.
Question 76
Multiple Choice
Phenenylketonuria (PKU) is a genetic disorder where an individual is unable to produce the enzyme phenylalanine hydroxylase. This results in the inability of the body to convert phenylalanine to what substance?