Biology Unit 4 Test 2
(149).webp "Biology Unit 4 Test 2 - Quiz")
Questions and Answers
- 1.
What is inside a bacteriophage?
- A.
Lipid
- B.
Protein
- C.
Carbohydrate
- D.
Nucleic acid
Correct Answer
D. Nucleic acidExplanation
A bacteriophage, also known as a phage, is a type of virus that infects bacteria. It consists of a protein coat, called a capsid, which protects the genetic material inside. The genetic material of a bacteriophage is composed of nucleic acids, either DNA or RNA. These nucleic acids contain the instructions for the virus to replicate and take over the host bacteria's cellular machinery. Therefore, the correct answer is nucleic acid.Rate this question:
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- 2.
What did Avery conclude caused transformation?
- A.
A carbohydrate was the transforming factor
- B.
A protein was the transforming factor
- C.
DNA was the transforming factor
- D.
A lipid was the transforming factor
Correct Answer
C. DNA was the transforming factorExplanation
Avery concluded that DNA was the transforming factor based on his experiments. He and his colleagues observed that when they destroyed the DNA in a mixture containing the transforming substance, the ability to cause transformation was lost. On the other hand, when they destroyed the proteins and carbohydrates, the transformation still occurred. This led them to conclude that DNA was responsible for the transformation process.Rate this question:
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- 3.
In which cells is the accurate transmission of information most important?
- A.
Nerve cells
- B.
Sex cells
- C.
Bone cells
- D.
Skin cells
Correct Answer
B. Sex cellsExplanation
The accurate transmission of information is most important in sex cells because they carry genetic information from one generation to the next. Any errors or inaccuracies in the transmission of this information can lead to genetic disorders or abnormalities in offspring. Nerve cells, bone cells, and skin cells do not play a direct role in transmitting genetic information, making the accurate transmission less critical in these cell types.Rate this question:
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- 4.
What structural problem prevents adenine from pairing with guanine?
- A.
The bases are both long
- B.
They lack the deoxyribose group
- C.
The bases are both short
- D.
They lack phosphate groups
Correct Answer
C. The bases are both shortExplanation
The structural problem preventing adenine from pairing with guanine is that both bases are short. In DNA, adenine pairs with thymine, while guanine pairs with cytosine. Adenine and guanine have different structures, and their respective sizes do not allow them to form a complementary base pair. Therefore, adenine cannot pair with guanine in DNA.Rate this question:
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- 5.
Which of the following statements correctly describes Chargaff's contribution to the study of DNA?
- A.
Chargaff's experiments conclusively proved that DNA was made of nucleotides, but he could not show that there four types of nitrogeonous bases
- B.
Chargaff hypothesized that DNA was a double helix, but he did not produce the image that proved this fact
- C.
Chargaff"s work proved that DNA could be made using radioactive nucleotides, but he did not show that DNA could be transferred from one organism to another.
- D.
CHargaff showed that adenine and thymine were found in equal percentages in DNA, but he did not know this was because of base-pairing.
Correct Answer
D. CHargaff showed that adenine and thymine were found in equal percentages in DNA, but he did not know this was because of base-pairing.Explanation
Chargaff's contribution to the study of DNA was that he showed that adenine and thymine were found in equal percentages in DNA. However, he did not know at the time that this was because of base-pairing.Rate this question:
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- 6.
Which of the following forms a base pair with thymine?
- A.
Deoxyribose
- B.
Guanine
- C.
Adenine
- D.
Cytosine
Correct Answer
C. AdenineExplanation
Adenine forms a base pair with thymine in DNA. Base pairing is a fundamental principle in DNA structure, where adenine always pairs with thymine, and guanine always pairs with cytosine. This pairing is based on the complementary hydrogen bonding between the nitrogenous bases. Adenine and thymine form two hydrogen bonds between them, creating a stable base pair. Deoxyribose is a sugar molecule found in DNA, but it does not directly form base pairs. Guanine and cytosine are other nitrogenous bases, but they do not pair with thymine.Rate this question:
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- 7.
Unlike DNA, RNA includes
- A.
Adenine
- B.
Phosphate groups
- C.
Uracil
- D.
Thymine
Correct Answer
C. UracilExplanation
RNA includes uracil instead of thymine. DNA contains adenine, guanine, cytosine, and thymine as its four nitrogenous bases. However, in RNA, thymine is replaced by uracil. This difference in the nitrogenous bases allows RNA to perform functions such as transcription and translation, which are essential for protein synthesis. Uracil pairs with adenine during RNA synthesis, forming a complementary base pair. Therefore, the presence of uracil is a characteristic feature of RNA.Rate this question:
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- 8.
Which of these are found in both DNA and RNA?
- A.
Ribose, phosphate groups, and adenine
- B.
Deoxyribose, phosphate groups,and guanine
- C.
Phosphate groups, guanine, and cytosine
- D.
Phosphate groups, guanine, and thymine
Correct Answer
C. pHospHate groups, guanine, and cytosineExplanation
Phosphate groups are found in both DNA and RNA as they are essential components of the backbone of both molecules. Guanine and cytosine are also found in both DNA and RNA as they are two of the four nitrogenous bases that make up the genetic code. Ribose and adenine are found only in RNA, while deoxyribose and thymine are found only in DNA.Rate this question:
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- 9.
What is produced during transcription?
- A.
DNA molecules
- B.
RNA molecules
- C.
RNA polymerase
- D.
Proteins
Correct Answer
B. RNA moleculesExplanation
During transcription, the process by which genetic information from DNA is copied into RNA, RNA molecules are produced. This occurs when RNA polymerase binds to a specific DNA sequence called a promoter and begins to unwind the DNA helix. It then uses one strand of the DNA as a template to synthesize a complementary RNA molecule. This RNA molecule will carry the genetic information from the DNA to the ribosomes, where it will be used as a template for protein synthesis. Therefore, the correct answer is RNA molecules.Rate this question:
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- 10.
During eukaryotic transcription, an RNA molecule is formed that is
- A.
Complementary to both strands of DNA
- B.
Identical to an entire single strand of DNA
- C.
Complementary to part of one strand of DNA
- D.
Double-stranded and inside the nucleus
Correct Answer
C. Complementary to part of one strand of DNAExplanation
During eukaryotic transcription, an RNA molecule is formed that is complementary to part of one strand of DNA. This means that the RNA molecule is synthesized using one of the DNA strands as a template, and the resulting RNA molecule will have a sequence that is complementary to a specific region of the DNA. The RNA molecule will only be complementary to a portion of the DNA strand, not the entire strand. This process allows for the synthesis of specific RNA molecules that can be used for various cellular functions.Rate this question:
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- 11.
Which of the following terms is LEAST closely related to the others?
- A.
TRNA
- B.
Spindle fibers
- C.
Polypeptide
- D.
Anticodon
Correct Answer
B. Spindle fibersExplanation
The term "spindle fibers" is least closely related to the others because it is not directly associated with protein synthesis or the genetic code. tRNA, polypeptide, and anticodon are all directly involved in the process of protein synthesis, whereas spindle fibers are structures involved in cell division and the separation of chromosomes.Rate this question:
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- 12.
During translation, the type of amino acid that is added to the growing polypeptide depends on the
- A.
Anticodon on the rRNA and the codon on the mRNA
- B.
Codon on the mRNA and the anticodon on the tRNA
- C.
Codon on the mRNA and the anticodon on the rRNA
- D.
Anticodon on the mRNA andthe anticodon on the tRNA
Correct Answer
B. Codon on the mRNA and the anticodon on the tRNAExplanation
The type of amino acid that is added to the growing polypeptide depends on the codon on the mRNA and the anticodon on the tRNA. This is because the mRNA carries the genetic code for the amino acid sequence, and the tRNA molecules have anticodons that are complementary to the codons on the mRNA. The tRNA molecules bring the corresponding amino acids to the ribosome during translation, where they are added to the growing polypeptide chain based on the codon-anticodon pairing.Rate this question:
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- 13.
Which of the following best describes the what happens during gene expression?
- A.
A cell reads the instructions in DNA and builds a protein based on those instructions
- B.
The nucleus of a cell builds cellular proteins based on the sequence of the mRNA code
- C.
A single gene leaves the nucleus of a cell and travels through the cytoplasm to the membrane
- D.
A gene is copied many times so that all of a cell's daughter cells will have their own copy
Correct Answer
A. A cell reads the instructions in DNA and builds a protein based on those instructionsExplanation
During gene expression, a cell reads the instructions in DNA and uses them to synthesize a protein. This process involves the transcription of DNA into mRNA and the translation of mRNA into a protein. The DNA sequence contains the genetic code that provides instructions for the sequence of amino acids in the protein. The cell's machinery reads this code and assembles the corresponding amino acids to build the protein according to the instructions encoded in the DNA.Rate this question:
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- 14.
A mutation that involves one or a few nucleotides is called
- A.
A mutagen
- B.
An inversion
- C.
A point mutation
- D.
A translocation
Correct Answer
C. A point mutationExplanation
A mutation that involves one or a few nucleotides is called a point mutation. This type of mutation occurs when a single nucleotide is substituted, inserted, or deleted in the DNA sequence. Point mutations can lead to changes in the amino acid sequence during protein synthesis, which can have various effects on the organism's phenotype.Rate this question:
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- 15.
The virus in Figure 12-6 is made of two parts: the _____ _____ on the outside, and the genetic material inside.
Correct Answer
protein coatExplanation
The virus in Figure 12-6 consists of two main components: the protein coat on the outside and the genetic material inside. The protein coat, also known as the capsid, surrounds and protects the genetic material, which can be DNA or RNA. This protein coat plays a crucial role in the virus's ability to infect host cells and replicate. It helps in recognizing and attaching to specific receptors on the host cell surface, facilitating the entry of the virus into the cell. Additionally, the protein coat provides stability and structural integrity to the virus particle.Rate this question:
- 16.
The Watson and Crick model of DNA is a ______ _____, in which two strands are wound around each other.
Correct Answer
double helixExplanation
The Watson and Crick model of DNA is a structure called a double helix, which refers to the two strands of DNA that are twisted around each other in a spiral shape. This model accurately represents the way DNA is organized and provides a clear understanding of its structure and function. The term "double helix" describes the specific shape and arrangement of the DNA molecule, with the two strands forming a twisted ladder-like structure.Rate this question:
- 17.
A prokaryotic cell replicates its ___ before it splits to form new cells, so that each new cell can have genetic material.
Correct Answer
DNAExplanation
A prokaryotic cell replicates its DNA before it splits to form new cells, so that each new cell can have genetic material. DNA replication is an essential process in cell division, ensuring that each daughter cell receives a complete set of genetic instructions. Prokaryotic cells lack a nucleus, so their DNA is found in the cytoplasm. Replication involves unwinding and separating the DNA strands, followed by the synthesis of new complementary strands. This ensures that the genetic material is faithfully passed on to the next generation of cells.Rate this question:
- 18.
Eukaryotic DNA has more replication forks than prokaryotic DNA, because it has more starting places, or _____ __ _________.
Correct Answer
origins of replicationExplanation
Eukaryotic DNA has more replication forks than prokaryotic DNA because it has more starting places, known as origins of replication. In eukaryotes, the DNA molecules are much larger and more complex than in prokaryotes. Therefore, they require multiple origins of replication to ensure efficient and timely replication of the entire genome. This allows for faster DNA synthesis and ensures that the replication process is completed in a timely manner.Rate this question:
- 19.
The order of nitrogeonous bases in DNA determines the order of ______ ______ in proteins.
Correct Answer
amino acidsExplanation
The order of nitrogenous bases in DNA determines the order of amino acids in proteins. This is because DNA carries the genetic information that codes for the synthesis of proteins. The sequence of nitrogenous bases in DNA is transcribed into mRNA, which is then translated into a sequence of amino acids during protein synthesis. The specific order of amino acids determines the structure and function of the protein. Therefore, the correct answer is amino acids.Rate this question:
- 20.
Mutant 1 in Figure 13-7 is the result of an _________ because part of the chromosome reverses direction.
Correct Answer
inversionExplanation
Mutant 1 in Figure 13-7 is the result of an inversion because part of the chromosome reverses direction.Rate this question:
- 21.
A mutation in a series of genes called ___ _____ can change the organs that develop in specific parts of an embryo.
Correct Answer
Hox genesExplanation
Hox genes are responsible for controlling the development of body structures in specific regions of an embryo. Mutations in these genes can lead to changes in the organs that form in those specific parts of the embryo. Therefore, the given answer, Hox genes, accurately explains how mutations in these genes can affect organ development.Rate this question:
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Mar 08, 2024Quiz Edited by
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Dec 08, 2015Quiz Created by
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