Chapter 17
Biochemistry · 10 exercises
Problem 1
Describe three processes by which nitrogen gas \(\left(\mathrm{N}_{2}\right)\) is incorporated into the biosphere.
3 step solution
Problem 3
What three mechanisms have evolved in nitrogen-fixing microorganisms to limit the inhibitory effects of \(\mathrm{O}_{2}\) on the nitrogenase reaction?
3 step solution
Problem 4
Describe how the nitrogen cycle works to redistribute nitrogen in Earth's biosphere.
6 step solution
Problem 5
How does the combined activity of glutamine synthetase and glutamate synthase assimilate \(\mathrm{NH}_{4}^{+}\) into amino acids? Why doesn't the glutamate dehydrogenase reaction contribute much to ammonia assimilation under normal physiologic conditions?
3 step solution
Problem 6
Describe the biochemical function of the \(\mathrm{E} 1, \mathrm{E} 2,\) and E3 enzymes in the ubiquitinating system. Why are there -500 E3 genes in the human genome but only two E1 genes?
5 step solution
Problem 8
What is the difference between a glucogenic and a ketogenic amino acid? Which amino acids fit the description of both a glucogenic and a ketogenic amino acid?
3 step solution
Problem 9
What is meant by the term "inborn errors of metabolism"? Give three examples of inborn errors that are directly related to the metabolism of phenylalanine and tyrosine.
5 step solution
Problem 10
What is the functional definition of essential and nonessential amino acids in the human diet? How might this functional definition be explained in evolutionary terms?
2 step solution
Problem 11
Glyphosate (Roundup) is a very effective herbicide that is toxic to almost all types of plants. a. Why is glyphosate considered an animal-safe herbicide? b. Why does it take up to 7 days before there is any noticeable herbicidal effect of glyphosate? c. Why don't Roundup Ready soybean plants die when they are sprayed with glyphosate?
3 step solution
Problem 12
Phenylketonuria is caused by a recessive genetic mutation, whereas acute intermittent porphyria is caused by a dominant genetic mutation. a. What is the biochemical difference in terms of protein function that distinguishes most recessive mutations from dominant mutations? b. What is the probability that a father with phenylketonuria and a homozygous normal mother will have a child that is a phenylketonuria carrier? c. What is the probability that a heterozygous mother with acute intermittent porphyria will have a child with the disease if the father is disease free?
3 step solution