dna

42
DNA Discovery Structure Replication 40 questions

Upload: nijole

Post on 24-Feb-2016

37 views

Category:

Documents


0 download

DESCRIPTION

DNA. DiscoveryStructure Replication. 40 questions. 1. Describe the two strains of bacteria Griffith used in his experiment with mice. S strain (deadly) -produced a protective slime coating that helped it evade the mouse immune system. -caused pneumonia (a deadly lung disease) in - PowerPoint PPT Presentation

TRANSCRIPT

Page 1: DNA

DNA Discovery Structure Replication

40 questions

Page 2: DNA

1. Describe the two strains of bacteria Griffith used in his experiment with mice.

• S strain (deadly)-produced a protective slime coating that helped it evade the mouse immune system.-caused pneumonia (a deadly lung disease) in mice.

• R strain (harmless)-did not produce a protective slime coating and therefore was easily defeated by the mouse immune system.

Page 3: DNA

2. What happened to the mice when Griffith injected them with the heat-killed S strain?

The mice lived.

Page 4: DNA

The mice died of pneumonia.

+

3. What happened to the mice when Griffith injected them with a mixture of heat-killed S strain and live R strain?

Page 5: DNA

4. A process in which one strain of bacteria is changed by a gene or genes from another strain of bacteria.

a. Transcriptionb. Replicationc. Transformationd. duplication

Page 6: DNA

5. Oswald Avery used ____ to degrade (break down) various molecules taken form heat-killed bacteria.

a. sulfurb. enzymesc. toxinsd. x-rays

Page 7: DNA

6. What types of macromolecules did Avery use enzymes on.

CarbohydratesProteins

LipidsRNADNA

Page 8: DNA

7. What kind of enzyme did Avery use to degrade bacterial proteins?

a. carbohydrasesb. lipasesc. proteasesd. DNAses

Membrane protein

Page 9: DNA

8. How did Avery ensure the validity of the results of his experiment with bacteria and mice?

a. He degraded only one type of molecule at a time. b. He used all the enzymes at the same time.c. He decided not to degrade proteins and DNA.d. He injected a mixture of degraded molecules into

mice at the same time.

Page 10: DNA

9. Bacteriophages are

a. a form of bacteriab. enzymesc. coils of DNAd. viruses

Page 11: DNA

10. What two organisms did Hershey and Chase work with in their study of DNA?

a. Bacteriophages and miceb. E. coli bacteria and micec. Bacteriophages and E. coli bacteriad. Bacteriophages and viruses

Bacteriophages

E. coli bacterium

Page 12: DNA

11. Interpret this micrograph.

Bacteriophages breaking out of a bacterium that has been infected.

BacteriophagesLysed Bacterium

Phages emerging

Page 13: DNA

12. What radioactive element did Hershey and Chase use to “tag” DNA?

32P (phosphorus)

DNA

Page 14: DNA

13. What radioactive element did Hershey and Chase use to “tag” the protein coat?

35S (sulfur)

The amino acid methionine

Page 15: DNA

14. Why can’t Hershey and Chase use to 35S to tag phage DNA?

DNA does not contain sulfur.

Page 16: DNA

15. What results did Hershey and Chase observe?

a. The protein coats were injected into the bacterial cells causing transformation.

b. Protein coats do not contain phosphorus.c. Radioactivity detected inside bacterial cells

came from 32P and not 32S.d. Bacteriophages are good at infecting bacteria.

Page 17: DNA

16. What can be concluded from the Avery and Hershey & Chase experiments?

a. DNA is the transforming molecule.b. Proteins are larger than nucleic acids.c. Enzymes are good at breaking down molecules.d. The S-strain is more deadly than the R-strain.

Page 18: DNA

17. Before DNA could be shown to be the genetic material in cells, scientists had to show that it coulda. tolerate high temperaturesb. carry, make copies of, and transmit informationc. be modified in response to environmental

conditions.d. be broken down into small subunits.

Page 19: DNA

18. A nucleotide does NOT contain a

a. 5-carbon sugar.b. nitrogen basec. proteind. phosphate group

Phosphate group

Sugar (deoxyribose)

Nitrogenous base

Page 20: DNA

19. According to Chargaff’s rule of base pairing, which of the following is true about DNA?

a. A = T, and C = Gb. A = C, and T = Gc. A = G, and T = Cd. A = T = C = G

Erwin Chargaff (1905 – 2002)

A

C

T

G

=

=

Page 21: DNA

Thymine Guanine_____________ Cytosine

20. Name the missing nitrogenous base.

Adenine

Page 22: DNA

21. Use Chargaff’s rule to complete the table below.

Organism % Adenine % Cytosine % Guanine % Thymine

Human 30 30

60100

+ ?

Page 23: DNA

21. Use Chargaff’s rule to complete the table below.

Organism % Adenine % Cytosine % Guanine % Thymine

Human 30 3020 20

60100

+40

Page 24: DNA

22. The bonds that hold the two strands of DNA together come from

a. The attraction of phosphate groups for each other.

b. Strong bonds between nitrogenous bases and the sugar-phosphate backbone.

c. Hydrogen bonds between nitrogenous bases.

d. Carbon-to-carbon bonds in the sugar portion of the nucleotides.

T GA C

Page 25: DNA

23. What is the term that describes how the two strands in DNA run in opposite directions?

AntiparallelC A T G

T AG C

Page 26: DNA

24. Who took this photo?

Rosalind Franklin

Photo 51

(1920 – 1958)

Page 27: DNA

25. What is this a photo ofand what technique was used to make it?

Photo 51

• The photo shows the structure of DNA

• Rosalind used X-ray diffraction to take the picture

Page 28: DNA

26. List two things this Rosalind Franklin learnedfrom her photo?

• DNA has a double helix shape

• DNA is made of two strands.

• The nitrogenous bases are near the center.

Photo 51

Page 29: DNA

27. Who are these two men and what are they famous for?

• James Watson and Francis Crick.

• They won the Nobel prize for building the first accurate model of DNA.

James Watson(1928 - )

Francis Crick(1916 - 2004 )

Page 30: DNA

28. Name the three parts of the nucleotide shown below?

C

B

A

A. phosphate groupB. sugar (deoxyribose)C. nitrogenous base

Page 31: DNA

29. The process of copying DNA prior to cell division is called

a. cytokinesisb. Interphasec. Base pairingd. replication

Page 32: DNA

30. The diagram below shows the process of DNA

a. replicationb. digestionc. transformationd. transpiration

Page 33: DNA

31. The enzyme that “unzips” DNA during replication is called

a. DNA polymeraseb. carbohydrasec. helicased. replicase

Page 34: DNA

32. The enzyme that “fastens” new nucleotides to the original DNA strand is called.

a. carbohydraseb. DNA polymerasec. helicased. replicase

Page 35: DNA

33. In which direction is the circled DNA polymerase moving?

Right to left

Page 36: DNA

34. From left to right, identify the missing bases.

TG

AC

Page 37: DNA

35. Is the chromosome shown below from a prokaryote or eukaryote? How do you know?

• It is from a prokaryote• The DNA forms a loop or ring like this one

Page 38: DNA

36. The micrograph below shows DNA in fruit flies. What are the “bubbles” (as indicated by the arrows) caused by?

The bubbles are where DNA replication is taking place.

Page 39: DNA

37. Interpret the following sequence of diagrams?

The diagrams demonstrate prokaryote replication, which involves only one replication bubble. Replication

proceeds within the bubble in opposite directions.

Replication bubble

Replication nearly

complete

Two identical

chromosomes result

Replication in two

directions

Page 40: DNA

38. How many replication forks are shown in this micrograph?

There are two forks. One at each end of the bubble.

Replication forks

Page 41: DNA

39. Is this a prokaryotic or eukaryotic chromosome? How can you tell?

• Eukaryotic• The chromosome is rod shaped

instead of circular.

Human chromatids

Page 42: DNA

40. What are the tips of chromosomes called and what enzyme replicates them.

• The tips are called telomeres• The enzyme is telomerase

TelomeresTelomeres