Exam 5 Flashcards

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1
Q

Initiator proteins and Helicase

A

The initial proteins in T-A regions that bind to DNA so helicase can also bind and break the hydrogen bonds between two nucleotides.

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2
Q

Primase

A

Adds RNA primers as a starting point for new strands of DNA

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3
Q

Single strand binding proteins

A

Holds single strands of DNA apart to prevent the DNA from rebinding to each other.

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4
Q

Sliding clamp

A

Assists in holding polymerase III to the template strand of DNA

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5
Q

Clamp Loader

A

Loads the sliding clamp onto DNA template strands and connects the polymerase III of the lagging and leading strands together

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6
Q

Polymerase III

A

Bonds new nucleotides forming new phosphodiester bonds with the free hydroxyl group of growing strands of new DNA.

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7
Q

Polymerase I

A

Removes the RNA primers that assisted in DNA replication and adds DNA nucleotides, creating phosphodiester bonds

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8
Q

Ligase

A

Forms new phosphodiester bonds where new nucleotides have been placed (gaps where primer was removed, sections in circular DNA where the lagging and leading strands connect, etc).

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9
Q

Explain the fundamental principles of base pairing in DNA replication

A

One purine is bonded with one pyrimidine and the nucleotide placed should match the correct number of hydrogen bonds possible. For example, A-T can create two hydrogen bonds and C-G as they can create three hydrogen bonds. Adenine and guanine are purines and cytosine, thymine and uracil are pyrimidines

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10
Q

Identify and describe the origin of replication and the formation of replication forks including how the replication process proceeds bidirectionally from the origin, leading to the synthesis of leading and lagging strands.

Distinguish between the synthesis of the leading and lagging strands during DNA replication

A

The origin of replication is a region thick of thymine nucleotides bonded to adenine as they contain only two hydrogen bonds and are easier to break apart. As this section of DNA is broken apart by helicase, a small bubble forms and single stranded binding proteins hold individual strands apart to prevent rebinding. This allows helicases to continue unzipping and breaking the hydrogen bonds of DNA in two different directions. This allows forms two replication forks in each direction of the original bubble. The strands that form, the leading strands, oriented 5’ to 3’ ends, are ones that are replicated continuously with polymerase III. The lagging strands, oriented 3’ to 5’, are replicated in discontinuous jumps with polymerase III as the enzyme can only add new nucleotides to existing free hydroxyl groups on the 3’ end.

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11
Q

Outer membrane of the mitochondrion

A

A membrane that contains large porins or transport channels

Pyruvate enters the mitochondria through porins

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12
Q

Intermembrane space of the mitochondrion

A

The space between the two membranes that contains enzymes capable of phosphorylation

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13
Q

Inner membrane of the mitochondrion

A

Numerous cristae folds that contain proteins for oxidative phosphorylation (ETC, ATPase) as well as transport proteins

Pyruvate is transported through the membrane by mitochondrial pyruvate carrier

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14
Q

Matrix of the mitochondrion

A

The space that contains highly concentrated mixture of 100’s of enzymes required for oxidation of pyruvate and fatty acids of the CAC

Pyruvate is converted into fatty acids and acetyl CoA with pyruvate hydrogenase

Citric Acid Cycle occurs here

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15
Q

Understand the citric acid cycle’s role in cellular metabolism, including its major inputs and outputs.

A

Requires two acetyl CoA

Provides 6 NAHD, 2 GTP, 4 CO2 and 2 FADH

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16
Q

Master the mechanics of the electron transport chain, recognizing its critical role in cellular respiration as it facilitates the transfer of electrons to generate a proton gradient

A

Electron carriers such as FADH2 and NAHD provide electrons to the electron transport chain, a series of protein complexes in the inner mitochondrial membrane. This charges the membrane as protons (H+ ions) are pumped into the intermembrane space, creating a proton gradient. At the end of the electron transport chain, an electron bonds with a proton and oxygen to form H2O.

17
Q

ATP synthesis based off the ETC

A

Protons were pumped out of the mitochondrial matrix and into the intermembrane space by the electron transport chain which created an electrochemical gradient. Hydrogens in the intermembrane space want to move down their chemical gradients and inter the matrix.

This movement is couple with the ATP synthase protein which uses this flow of hydrogens to power the motor of ATPase. This provides the energy to phosphorylate ADP to ATP as conformation changes are made to ADP with the center shaft rotation of ATP synthase. ATP is made in the matrix.

18
Q

Elucidate the mechanism by which ATP synthase harnesses the proton gradient established by the electron transport chain to synthesize ATP, emphasizing the enzyme’s role in converting electrochemical energy into the cellular energy currency.

A

H+ ions or protons flow from high to low gradients through the rotor subunit (F0) of ATP synthase in the inner membrane to the matrix. This charges the motor and allows the center shaft (F1) of the protein to rotate. ADP and inorganic phosphate bind to the enzyme causing conformational changes bringing them closer that allow them to be phosphorylated, creating ATP. As a result ATP synthase converts electrochemical energy from the chemical gradient in the form of ions into chemical energy, or ATP.

19
Q

Articulate the quantity of ATP produced from a single glucose molecule through the stages of cellular respiration, detailing the contributions of glycolysis, the citric acid cycle, the electron transport chain, and chemiosmosis to the overall energy yield.

A

Glycolysis: 2 ATP, 2 NADH (3 ATP)

Pyruvate Oxidation: 2 NADH (5 ATP)

Citric Acid Cycle: 6 NADH (15 ATP), 2 FADH2 (3 ATP), 2 GTP (2 ATP)

20
Q

nitrogenous bases

A

molecules that contain nitrogen and have the chemical properties of a base that are the building blocks for RNA and DNA nucleotides

they are categorized into either purines (two ring structures) or pyrimidines (one ring structure

21
Q

pentose sugars

A

five-carbon ringed sugars with either two hydroxyl groups (ribose) or one hydroxyl group (deoxyribose) that forms the sugar background of DNA.

22
Q

phosphate groups

A

act as the building blocks for the backbone of the molecule, connecting the sugar molecules of each nucleotide together (sugar-phosphate backbone)

23
Q

phosphodiester bonds

A

covalent bonds that form the backbone of DNA and RNA (pentose to phosphate)

24
Q

N-glycosidic bond

A

the bond between a nitrogenous base and a sugar molecule

25
Q

Explain the process of DNA packaging in eukaryotic cells, detailing how histones organize DNA into nucleosomes during interphase and condense it further into chromosomes for mitotic division

A

Histones are small, positively charged proteins that attract negatively charged backbones of DNA. Eight histones form an octamer, or nucleosome core, that curl DNA around the octamer. This forms the chromatin chain that appears as if the DNA wraps are beads on a long strand of DNA.

The DNA histones keep folding, creating chromatin fibers that loop around and condense further, eventually forming a mitotic chromosome with a centromere in the middle.

26
Q

Connect your learning to cancer biology

A

In cancer, injured cells do not experience apoptosis but continue through cell division, propagating erroneous cells.

Mutations occur at the DNA level in which a cell may change protein structure or function based on mutations caused.

27
Q

Three types of mutations

A

Silent
Nonsense
Missense

28
Q

Silent mutations

A

DNA mutation effects RNA but the correct amino acid is still formed (typically, 3rd litter is affected)

29
Q

Nonsense mutation

A

The change in DNA structure results in the STOP codon and the sequence is shorter than intended so the protein is not fully made (UAG)

30
Q

Missense mutation

A

An amino acid is still synthesized but it is the incorrect one causing altered structures.

Conserved: amino acid created has similar properties to the original

Non-conserved: amino acid created does not have similar properties to original