Questions 14-16 are based on the following. In the 1940's, Avery, Macleod, and McCarty transformed nonencapsulated bacteria into encapsulated. forms by growing the nonencapsulated cells in a culture containing an extract made from dead encapsulated cells. The transformed cells produced colonies of encapsulated bacteria. Three different procedures and their results are outlined below. Procedure I: Extract made from dead encapsulated cells added to culture medium. Nonencapsulated bacteria added to culture medium. Results: Both nonencapsulated and encapsulated bacteria grow. Procedure II: Extract made from dead encapsulated cells treated with protein-degrading enzymes before adding extract to culture medium. Nonencapsulated bacteria added to culture medium. Results: Both nonencapsulated and encapsulated bacteria grow. Procedure III: Extract made from dead encapsulated cells treated with DNAse (an enzyme that selectively destroys DNA) before adding extract to culture medium. Nonencapsulated bacteria added to culture medium. Results: Only nonencapsulated bacteria grow. 14. A reasonable conclusion to draw from the results of the experiment is that (A) DNA is the genetic material (B) DNA replication is semiconservative (C) DNA is a double helix (D) DNA is translated into protein (E) mutation is a change in the genetic material 15. What was the purpose of treating the extract with protein-degrading enzymes in Procedure II? (A) To demonstrate that the transforming factor is an enzyme (B) To demonstrate that the transforming factor is not a protein (C) To destroy nucleic acids in the extract (D) To destroy any capsules in the extract (E) To prevent the extract from being contaminated by nonencapsulated bacteria 16. What was the purpose of treating the extract with DNAse in Procedure III? (A) To remove the encapsulated bacteria from the extract (B) To serve as a positive control by demonstrating that a protein in the extract is the transforming factor (C) To serve as a negative control by demonstrating that transformation does not occur without DNA (D) To destroy enzymes in the extract (E) To destroy any capsules that might be in the extract

Human Anatomy & Physiology (11th Edition)
11th Edition
ISBN:9780134580999
Author:Elaine N. Marieb, Katja N. Hoehn
Publisher:Elaine N. Marieb, Katja N. Hoehn
Chapter1: The Human Body: An Orientation
Section: Chapter Questions
Problem 1RQ: The correct sequence of levels forming the structural hierarchy is A. (a) organ, organ system,...
icon
Related questions
Question
100%
Questions 14-16 are based on the following.
In the 1940's, Avery, Macleod, and McCarty transformed nonencapsulated bacteria into
encapsulated. forms by growing the nonencapsulated cells in a culture containing an
extract made from dead encapsulated cells. The transformed cells produced colonies of
encapsulated bacteria. Three different procedures and their results are outlined below.
Procedure I:
Extract made from dead encapsulated cells added to culture medium.
Nonencapsulated bacteria added to culture medium.
Results: Both nonencapsulated and encapsulated bacteria grow.
Procedure II:
Extract made from dead encapsulated cells treated with protein-degrading enzymes before
adding extract to culture medium.
Nonencapsulated bacteria added to culture medium.
Results: Both nonencapsulated and encapsulated bacteria grow.
Procedure III:
Extract made from dead encapsulated cells treated with DNAse (an enzyme that selectively
destroys DNA) before adding extract to culture medium.
Nonencapsulated bacteria added to culture medium.
Results: Only nonencapsulated bacteria grow.
14. A reasonable conclusion to draw from the results of the experiment is that
(A) DNA is the genetic material
(B) DNA replication is semiconservative
(C) DNA is a double helix
(D) DNA is translated into protein
(E) mutation is a change in the genetic material
15. What
the purpose of treating the extract with protein-degrading enzymes in Procedure
II?
(A) To demonstrate that the transforming factor is an enzyme
(B) To demonstrate that the transforming factor is not a protein
(C) To destroy nucleic acids in the extract
(D) To destroy any capsules in the extract
(E) To prevent the extract from being contaminated by nonencapsulated bacteria
16. What was the purpose of treating the extract with DNAse in Procedure III?
(A) To remove the encapsulated bacteria from the extract
(B) To serve as a positive control by demonstrating that a protein in the extract is the
transforming factor
(C) To serve as a negative control by demonstrating that transformation does not occur
without DNA
(D) To destroy enzymes in the extract
(E) To destroy any capsules that might be in the extract
Transcribed Image Text:Questions 14-16 are based on the following. In the 1940's, Avery, Macleod, and McCarty transformed nonencapsulated bacteria into encapsulated. forms by growing the nonencapsulated cells in a culture containing an extract made from dead encapsulated cells. The transformed cells produced colonies of encapsulated bacteria. Three different procedures and their results are outlined below. Procedure I: Extract made from dead encapsulated cells added to culture medium. Nonencapsulated bacteria added to culture medium. Results: Both nonencapsulated and encapsulated bacteria grow. Procedure II: Extract made from dead encapsulated cells treated with protein-degrading enzymes before adding extract to culture medium. Nonencapsulated bacteria added to culture medium. Results: Both nonencapsulated and encapsulated bacteria grow. Procedure III: Extract made from dead encapsulated cells treated with DNAse (an enzyme that selectively destroys DNA) before adding extract to culture medium. Nonencapsulated bacteria added to culture medium. Results: Only nonencapsulated bacteria grow. 14. A reasonable conclusion to draw from the results of the experiment is that (A) DNA is the genetic material (B) DNA replication is semiconservative (C) DNA is a double helix (D) DNA is translated into protein (E) mutation is a change in the genetic material 15. What the purpose of treating the extract with protein-degrading enzymes in Procedure II? (A) To demonstrate that the transforming factor is an enzyme (B) To demonstrate that the transforming factor is not a protein (C) To destroy nucleic acids in the extract (D) To destroy any capsules in the extract (E) To prevent the extract from being contaminated by nonencapsulated bacteria 16. What was the purpose of treating the extract with DNAse in Procedure III? (A) To remove the encapsulated bacteria from the extract (B) To serve as a positive control by demonstrating that a protein in the extract is the transforming factor (C) To serve as a negative control by demonstrating that transformation does not occur without DNA (D) To destroy enzymes in the extract (E) To destroy any capsules that might be in the extract
Expert Solution
trending now

Trending now

This is a popular solution!

steps

Step by step

Solved in 3 steps

Blurred answer
Knowledge Booster
Violence
Learn more about
Need a deep-dive on the concept behind this application? Look no further. Learn more about this topic, biology and related others by exploring similar questions and additional content below.
Similar questions
  • SEE MORE QUESTIONS
Recommended textbooks for you
Human Anatomy & Physiology (11th Edition)
Human Anatomy & Physiology (11th Edition)
Biology
ISBN:
9780134580999
Author:
Elaine N. Marieb, Katja N. Hoehn
Publisher:
PEARSON
Biology 2e
Biology 2e
Biology
ISBN:
9781947172517
Author:
Matthew Douglas, Jung Choi, Mary Ann Clark
Publisher:
OpenStax
Anatomy & Physiology
Anatomy & Physiology
Biology
ISBN:
9781259398629
Author:
McKinley, Michael P., O'loughlin, Valerie Dean, Bidle, Theresa Stouter
Publisher:
Mcgraw Hill Education,
Molecular Biology of the Cell (Sixth Edition)
Molecular Biology of the Cell (Sixth Edition)
Biology
ISBN:
9780815344322
Author:
Bruce Alberts, Alexander D. Johnson, Julian Lewis, David Morgan, Martin Raff, Keith Roberts, Peter Walter
Publisher:
W. W. Norton & Company
Laboratory Manual For Human Anatomy & Physiology
Laboratory Manual For Human Anatomy & Physiology
Biology
ISBN:
9781260159363
Author:
Martin, Terry R., Prentice-craver, Cynthia
Publisher:
McGraw-Hill Publishing Co.
Inquiry Into Life (16th Edition)
Inquiry Into Life (16th Edition)
Biology
ISBN:
9781260231700
Author:
Sylvia S. Mader, Michael Windelspecht
Publisher:
McGraw Hill Education