final Flashcards

1
Q

What are the three main stages of the cell cycle?

A

Interphase, mitosis, and cytokinesis

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2
Q

What happens during the G1 phase of interphase?

A

The cell grows, matures, and performs normal functions; some cells may enter a resting state called G0

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3
Q

What occurs during the S phase of interphase?

A

DNA replication occurs, producing identical sister chromatids; centrosomes are also duplicated

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4
Q

How do sister chromatids differ from homologous chromosomes?

A

Sister chromatids are identical copies of a chromosome joined at the centromere; homologous chromosomes are pairs of similar but non-identical chromosomes, one from each parent

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5
Q

What are the key events of prophase in mitosis?

A

Chromosomes condense, nuclear envelope breaks down, and spindle fibers begin to form

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6
Q

What happens during metaphase?

A

Chromosomes align at the metaphase plate (cell equator), attached to spindle fibers via kinetochores

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7
Q

What occurs during telophase?

A

Chromosomes decondense, nuclear envelopes reform, and the cell prepares for cytokinesis

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8
Q

What happens during translation termination?

A

Release factors bind to the ribosome, promoting release of the polypeptide and disassembly of the translation complex

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9
Q

What is the wobble hypothesis?

A

Flexibility in the third codon position allows one tRNA to recognize multiple codons

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10
Q

What is alternative splicing?

A

A process where different combinations of exons are joined to produce multiple protein variants from one gene

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11
Q

What are the three major types of RNA and their functions?

A

mRNA (carries genetic code), tRNA (transfers amino acids), and rRNA (forms ribosomes)

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12
Q

What is the function of telomerase?

A

It extends the G-rich 3’ overhang of chromosomes to prevent shortening during replication

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13
Q

Why is an RNA primer needed during DNA replication?

A

DNA polymerase cannot initiate synthesis; the RNA primer provides a starting 3’-OH group

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14
Q

What is the role of DNA polymerase III in replication?

A

It synthesizes new DNA strands by adding nucleotides to the 3’ end and has proofreading ability

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15
Q

What is semiconservative replication?

A

Each new DNA molecule consists of one original strand and one newly synthesized strand

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16
Q

What is the structure of DNA?

A

A double helix with antiparallel strands held together by complementary base pairing (A-T, G-C)

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17
Q

What are the stages of translation?

A

Initiation, elongation, and termination

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18
Q

What is the significance of codon-anticodon pairing?

A

It ensures the correct amino acid is added to the growing polypeptide chain during translation

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19
Q

What modifications occur to mRNA before it leaves the nucleus?

A

Addition of a 5’ cap and a poly-A tail, and removal of introns via splicing

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20
Q

What is the role of tRNA during translation?

A

To carry specific amino acids to the ribosome and match codons in mRNA via its anticodon

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21
Q

Q: Compare and contrast anabolic and catabolic pathways.

A

A: Anabolic pathways build complex molecules from simpler ones and consume energy; catabolic pathways break down complex molecules into simpler ones and release energy.

22
Q

Q: What makes ATP useful for conserving chemical energy in cells?

A

A: ATP has high-energy phosphoanhydride bonds whose hydrolysis releases energy that can be coupled to drive endergonic reactions.

23
Q

Q: Why is ATP hydrolysis highly exergonic?

A

A: Due to charge repulsion between phosphate groups resonance stabilization of products

24
Q

Q: What type of bonds are the “high-energy” bonds in ATP?

A

A: Phosphoanhydride bonds.

25
Q: How does ATP hydrolysis couple with endergonic reactions?
A: The exergonic hydrolysis of ATP drives otherwise unfavorable endergonic reactions making the overall coupled reaction exergonic.
26
Q: What is oxidation in biological systems?
A: Loss of electrons often accompanied by loss of protons (hydrogen ions)
27
Q: What role do NAD+ and NADH play in glycolysis?
A: NAD+ accepts electrons during glycolysis becoming NADH
28
Q: Why is an energy investment necessary in glycolysis?
A: To phosphorylate glucose and intermediates making them more reactive and enabling subsequent energy-releasing steps.
29
Q: Name the three phases of glycolysis.
A: Phase 1: Preparatory and cleavage steps; Phase 2: Oxidation and first ATP generation; Phase 3: Pyruvate formation and second ATP generation.
30
Q: How does fermentation allow continuous ATP generation?
A: By regenerating NAD+ from NADH enabling glycolysis to continue producing ATP anaerobically.
31
Q: What is the net ATP yield from fermentation per glucose molecule?
A: 2 ATP molecules.
32
Q: What are the differences between lactic acid and ethanol fermentation?
: Lactic acid fermentation produces lactic acid; ethanol fermentation produces ethanol and CO2.
33
Q: How are disaccharides like lactose and sucrose used in glycolysis?
A: They are hydrolyzed into monosaccharides which are converted into glycolytic intermediates.
34
Q: What is the role of glycogen phosphorylase in carbohydrate metabolism?
A: It catalyzes phosphorolysis of glycogen to release glucose-1-phosphate for glycolysis.
35
Q: What are the five stages of aerobic respiration?
Glycolysis
36
Q: What enzyme converts pyruvate to acetyl CoA?
A: Pyruvate dehydrogenase complex.
37
Q: Why is the citric acid cycle considered a cycle?
A: Because oxaloacetate is regenerated at the end allowing continuous processing of acetyl CoA.
38
Q: Which citric acid cycle enzyme generates ATP or GTP directly?
Succinyl CoA synthetase
39
Q: How does beta-oxidation contribute to energy metabolism?
It breaks down fatty acids into acetyl CoA units, which enter the citric acid cycle.
40
Q: What is the function of the electron transport chain (ETC)?
To transfer electrons from NADH and FADH2 to oxygen, pumping protons and creating a gradient for ATP synthesis.
41
Q: What is the role of the F0F1 ATP synthase?
To synthesize ATP using the proton gradient generated by the ETC.
42
Q: Describe the structure of DNA.
A double helix with antiparallel strands held by complementary base pairing (A-T, G-C).
43
Q: What is semiconservative replication?
Each new DNA molecule contains one parental strand and one newly synthesized strand
44
Q: What is the difference between leading and lagging strand synthesis?
Leading strand is synthesized continuously; lagging strand is synthesized discontinuously as Okazaki fragments
45
Q: Why is an RNA primer necessary in DNA replication?
DNA polymerase requires a 3’-OH group to add nucleotides; the RNA primer provides this starting point.
46
Q: How is replication fidelity maintained?
DNA polymerase proofreading removes incorrectly paired nucleotides via 3’ to 5’ exonuclease activity.
47
Q: What is the function of telomerase?
To extend telomeres, preventing chromosome shortening during replication.
48
Q: What are the main classes of RNA and their functions?
mRNA (carries genetic code), tRNA (transfers amino acids), rRNA (forms ribosomes).
49
Q: What are the components of a transcription unit?
Promoter, RNA coding region, and terminator.
50
Q: What is the role of the sigma factor in bacterial transcription?
It recognizes promoter sequences and initiates transcription by guiding RNA polymerase.
51
Q: How does bacterial transcription terminate?
Via rho-independent termination (hairpin formation) or rho-dependent termination (rho factor unwinding RNA-DNA hybrid).
52
Q: How do eukaryotic promoters differ from bacterial promoters?
Eukaryotic promoters have complex elements like the TATA box and require multiple transcription factors for initiation.