CHEM-527 Introductory Biochemistry
Third Hourly Examination
Thursday, December 2, 1999
Dr. White Instructor
 

There are 9 pages to this examination. Put your name on each new page. The pages in the back display all of the metabolic pathways we have discussed in class. You may tear them off and refer to them. A genetic code chart is at the bottom of page 5. If you feel any question is unclear or ambiguous, clearly explain your answer or interpretation.

Do not expose your answers to the scrutiny of your neighbors. Please fold under each page before you go on to the next.

Breakdown of the exam by sections:

                                Structures                             14 Points
                                Short Answer                        20 Points
                                Multiple Choice                     21 Points
                               Problems and Short Essay     45 Points
                                Total                                  100 Points
                                (Possible Bonus                     12 Points)

                                Class Average = 55.44
                                Range 19 - 99
                                N = 50



Structure (14 Points)

1. (8 Points) Draw the structure of the deoxyribodinucleotide represented by pAT.
 

2. ( 6 Points) Identify the following molecules and indicate their respective functions.
 

 

a. ________________________ b. _______________________ c. ______________________

Function
___________________________ ________________________ ________________________

___________________________ ________________________ ________________________


Short Answer (20 points, 1 point each)

________________ 1. Number of subunits in aspartate transcarbamoylase.

________________ 2. Form in which carbon for fatty acid synthesis is exported from the             mitochondrion.

________________ 3. Human sex-linked disease associated with purine salvage.

________________ 4. A pathway that generates NADPH for reductive biosynthesis.

________________ 5. A photochemical product of UV irridation of DNA.

________________ 6. In humans during sleep, this organ consumes almost 50% of the oxygen inspired.

________________ 7. Trinucleotide sequence common to the 3' end of all tRNAs.

________________ 8. Chemical name for the bond that links an amino acid to its cognate tRNA.

________________ 9. Form in which birds excrete nitrogen.

________________ 10. Normally the exclusive energy source for brain metabolism.

________________ 11. Naturally occurring single-strand pieces of DNA that extend an RNA primer.

________________ 12. Way in which ethidium bromide binds to DNA.

________________ 13. During prolonged starvation, the primary energy source for humans is.

________________ 14. Increase in A260 absorbance of DNA when heated.

________________ 15. Kwashiorkor is a disease of humans due to a deficiency of what in the diet?

________________ 16. Antibiotic analog of p-aminobenzoate (PABA).

________________ 17. Portion of eukaryotic mRNA that doesn't hybridize with genomic DNA.

________________ 18. Noncoding segments of DNA within eukaryotic genes.

________________ 19. Major protein component of nucleosomes.

________________ 20. Inhibitor of purine and pyrimidine metabolism used in cancer chemotherapy.

Bonus (3 Points). Who was Daniel Nathans and what did he do?



Multiple Choice Questions (21 points, 3 points each)

____ 1. In a short term experiment, an 15N-labeled amino group from glutamic acid gets distributed widely among other amino acids including arginine in which 3 of the 4 nitrogens become labeled. Which of the identified nitrogens of arginine would not be labeled quickly?

____ Bonus (1 Point) True or False, 15N is a radioactive isotope.
 

____ 2. If a random RNA polymer containing equal molar amounts of A, U, and C were used as an artificial mRNA in a complete translation reaction under conditions of random initiation, Which amino acid would not be expected in the polypeptide product?
 

        A. Methionine         B. Lysine         C. Phenylalanine         D. Serine         E. Leucine
 

____3. Protein synthesis and fatty acid synthesis are both biological polymerization processes and have analogous steps. Consider the following pairs of components and identify the pair that does not correspond.

        A. Fatty Acid                                 Synthetase Ribosome

        B. Acetyl CoA                               fMet tRNA

        C. Malonyl CoA                             aminoacyl tRNA

        D. NADPH                                    ATP

        E. palmitoyl-Enz                             peptidyl-tRNA
 
 

____ 4. Which of the following is not associated with transcription?

        A. ATP         B. RNA polymerase         C. CTP         D. TTP         E. DNA
 

____ 5. The Cori Cycle is a cooperative venture between skeletal muscles and the liver, with the blood stream as the means of communication between these tissues. Select the statement that is FALSE about the Cori Cycle.
 

A. It operates primarily when muscle is actively working.

B. In muscle, glycolysis is occurring, while in liver gluconeogenesis is occurring.

C. Lactate dehydrogenase operates in the direction pyruvate to lactate in muscle, whereas in liver it   operates in the direction lactate to pyruvate.

D. The blood transports glucose from muscle to liver and then transports lactate from the liver back to muscles.

E. The Cori Cycle operates at the expense of ATP in liver


____ 6. A synthetic repeating RNA used as a messenger in an in vitro protein synthesis system produces an alternating polypeptide containing a basic amino acid and an acidic amino acid. What is the sequence of the synthetic mRNA?
 

        A. (GAA)n         B. (AAG)n         C. (AG)n         D. (CG)n         E. (CGC)n
 

____ 7. In comparing proteins among individuals of the same species, researchers commonly find variants due to a single amino acid replacement. These allelic variations are usually due to single base substitution mutations. If one observed an arginine in place of a serine in a particular pair of allelic proteins, which one of the following amino acids would be LEAST likely to be found at the same position in another variant of the same protein.

        A. Cysteine         B. Isoleucine         C. Asparagine         D. Tyrosine         E. Valine

                Genetic Code Table
 

UUU
PHE
UCU
SER
UAU
TYR
UGU
CYS
UUC UCC UAC UGC
UUA LEU UCA UAA
End
UGA End
UUG UCG UAG UGG TRP
CUU CCU
PRO
CAU HIS CGU
ARG
CUC CCC CAC CGC
CUA CCA CAA
GLN
CGA
CUG CCG CAG CGG
AUU
ILE
ACU
THR
AAU
ASN
AGU
SER
AUC ACC AAC AGC
AUA ACA AAA LYS AGA
ARG
AUG MET ACG AAG AGG
GUU
VAL
GCU
ALA
GAU
ASP
GGU
GLY
GUC GCC GAC GGC
GUA GCA GAA
GLU
GGA
GUG GCG GAG GGG



Thought Questions and Short Essays (45 Points)
 

1. (8 Points) While some athletes consume creatine to enhance performance, our bodies are perfectly capable of synthesizing creatine from compounds you know. From the two step pathway outlined below, provide the names of the precursors (A and B) whose structures are given and predict the structure of the intermediate (C) and byproduct (D) in the pathway. What would be the fate of D?
 
 



2. (6 Points) A number of years ago, the diagram below appeared on a seminar announcement from the Delaware Chapter of the American Chemical Society. The artist did not get good advice from the chemists. How does this representation differ significantly from the Watson and Crick model for DNA?















3. To determine the essential amino acids for the mouse, Steele (1952) fed a mouse 14C-glucose. Three days later he hydrolyzed protein from the mouse and measured the radioactivity in each of the separated amino acids. His recovery of 14C (nanoCuries/mg Carbon) in different amino acids is shown below.
 

Amino 

Acid


nCi/mgC
Amino

Acid


nCi/mgC
Amino 

Acid


nCi/mgC
Amino

Acid


nCi/mgC
Alanine 26.5 ± 3.3 Glutamate 19.0 ± 1.9 Lysine 0.0 ± 0.02 Serine 8.4 ± 0.1
Arginine  3.0 ± 0.2 Glycine 5.1 ± 0.2 Methionine 1.03 ± 0.06 Threonine 0.09 ± 0.02
Aspartate 15.8 ± 0.9 Histidine 0.07 ± 0.08 Phenylalanine 0.02 ± 0.07 Tyrosine 0.0 ± 0.07
Cysteine 3.3 ± 0.3 Isoleucine 0.06 ± 0.05 Proline 3.1 ± 0.1 Valine 0.02 ± 0.01

Your textbook lists histidine, isoleucine, leucine, lysine, methionine, threonine, phenylalanine, tryptophan, and valine as essential amino acids for mammals.

A. (4 Points) Provide a clear explanation for why alanine, aspartate, and glutamate are so highly labeled compared to the other amino acids.

B. (4 Points) Would you consider adding or removing any amino acids from the list of essential amino acids based on the Steele's results? Explain.

4. A. (4 Points) In order to determine the specificity of a new Type II restriction endonuclease, BioI, a circular 30,000 base-pair, double-stranded DNA was cleaved and its nucleotide sequence determined at both 5' ends of each restriction fragment. The consensus sequence was pTATCNNN... where N can be any deoxyribonucleotide. What hexanucleotide sequence does BioI recognize?

B. (6 Points) If the circular DNA used above contained 30% G and its nucleotide sequence were assumed to be random, how many BioI restriction sites would you expect in the entire sequence? Show your work and describe your thinking.

5. (7 Points) The diagram below is an idealized representation of the combined processes of transcription and translation as it has been observed by electron microscopy in lysed E. coli cells. Label the diagram clearly indicating the (1) DNA strand, (2) RNA Polymerase and (3) its direction of movement relative to DNA, (4) mRNA and (5) its 3' to 5' orientation, (6) a ribosome and (7) its direction of movement, and (8) the location of the promoter for the gene. Finally, put an "X" on the ribosome that would have the longest incomplete protein attached to it.


 


Bonus (2 Points) Why would this never be seen in a eukaryotic cell?
 

6. (6 Points) Essay. Describe how the human body adapts metabolically to starvation.
 

7. Bonus Question (6 Points) In 1995, Berthold et al. (Proc. Natl. Acad. Sci. 92, 10123) published a study to determine availability of dietary purines and pyrimidines for the chicken and mouse. They grew algae in the presence of 13CO2 and then isolated 13C-containing RNA from them which they fed to a hen for 4 weeks and to four mice for 6 days. They then isolated hepatic RNA and measured the 13C-enrichment of the nucleotide bases by mass spectrometry. The % 13C derived from the diet for each nucleoside for both animals is indicated in the table below. How would you interpret these data?
 

Animal Adenosine Guanosine Cytidine Uridine
Chicken 2.9 2.0 84.6 86.6
Mouse 3.6 3.6 22.8 27.4



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Last updated: 8 December 1999 by Hal White
Copyright 1999, Department of Chemistry and Biochemistry, University of Delaware, Newark, DE  19716