Test 2 Flashcards

1
Q

What did Joseph Priestley call oxygen (1771)?

A

Dephlogisticated air

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2
Q

Photosynthesis is the process by which…

A

Some cells can harvest energy from sunlight o produce energy rich organic compounds

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3
Q

What are the 2 types of photosynthesis?

A

1) Oxygenic (produces oxygen)
2) Anoxygenic (No oxygen is produced)

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4
Q

Oxygenic photosynthesis takes place in… (3)

A

1)algae
2)bacteria
3)plants

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5
Q

Anoxygenic photosynthesis is found in four different bacterial groups… (name them)

A

1) Purple Sulphur Bacteria

2) Green Sulphur Bacteria

3) Green non-Sulphur bacteria

4) Heliobacteria

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6
Q

Oxygenic photosynthesis is found in _____, _ groups of algae and essentially all ____ plants.

A

1) Cyanobacteria

2) 7

3) land

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7
Q

Describe some characteristics of chloroplast (3)

A

1) Uses the energy from sunlight to create ATP and organic molecules (ex: sugar)

2) Contains their own circular DNA and ribosomes

3) Double plasma membrane

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8
Q

What is the first step to Oxygenic photosynthesis?

A

Light-Dependent Step

Using light energy to split water and generate an H+ gradient for chemiosmosis (like ETC in aerobic respiration) to make NADPH and ATP.(occurs in thylakoid).

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9
Q

What is step 2 for Oxygenic photosynthesis?

A

Light-Independent Step

Use that ATP to add H+’s to CO2 to make glucose in the Calvin Cycle (occurs in the stroma).

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10
Q

What are pigments?

A

Molecules that absorb light energy in the visible range

-These are required for the successful completion of photosynthesis in the chloroplast.

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11
Q

What are photons?

A

Particles of light that can act as discrete bundles of energy

-The energy of light is directly related to its wavelength (shorter wavelength photon have more energy)

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12
Q

What is the absorption spectrum
(Of a molecule)?

A

The range and efficiency the photons absorb (which colour light is the pigment able to absorb)

-The absorption spectrums determine the colour of light that is absorbed. The colour we see is the colour that is reflected by the object (not absorbed)

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13
Q

True or false?

Each pigment has its own absorption spectrum

A

True

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14
Q

What does chlorophyll a do?

A

Converts light energy to chemical energy

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15
Q

What does chlorophyll b do?

A

Carotenoids, etc. supplement chlorophyll a, and also protect plants from harmful radiation

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16
Q

Why do indoor LED lights for plant production usually don’t have green lights?

A

This saves on electricity, since plants don’t need green lights to make photosynthesis

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17
Q

What is the most important pigment found in the chloroplast and why?

A

Chlorophyll-a

-the only one that can directly convert light to chemical energy (b is an accessory pigment)

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18
Q

How is chlorophyll structured?

A

-Contains a complex ring structure, called a porphyrin ring, with alternating single and double bonds with a magnesium atom at the center of the ring.

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19
Q

How does chlorophyll carry out photosynthesis? (Transfer of energy)

A

The system of double bonds (resonant structures) is able to channel the energy absorbed by light for a few moments

The energy is then passed to a suitable molecule to carry out photosynthesis

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20
Q

_________ and _______are pigments that help carry out photosynthesis

A

1) Carotenoids

2) Flavonoids

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21
Q

How do carotenoids and flavonoids assist photosynthesis?

A

By capturing energy from wavelengths that are not efficiently absorbed by chlorophyll

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22
Q

Are carotenoids and flavonoids always efficient in transferring energy?

A

No

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23
Q

Carotenoids and flavonoids also act as antioxidants to…

A

Counter the production of free radicals generated during photosynthesis

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24
Q

What is a free radical?

A

A molecule that contains an unpaired electron in an atomic orbital

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25
Q

Part of photosynthesis occurs in _______ present in the _______ membrane.

A

1) photosystems

2) thylakoid

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26
Q

What do photosystems contain?

A

Chlorophyll-a, associated pigments, and the accessory proteins required to carry out photosynthesis

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27
Q

What is a photosystems?

A

1) Antenna complex: pigments capture light energy and channels it to the reaction centre

2) Reaction centre: a chlorophyll molecule loses an electron (oxidized)

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28
Q

What do antenna complexes do?

A

Capture and transfer the energy from light to the reaction centre

-Proteins in the complex orient the pigments in an optimal direction for the absorption of light energy

-When light energy is captured, the pigments transfer the energy directly to other pigments until the energy (only energy) is transferred to the reaction centre

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29
Q

What happens after the transfer of energy in antenna complexes?

A

The excited electron in each molecule returns to the low energy level it had before the photon was absorbed

-Thus, it is energy, not the excited electrons themselves, that pass from one pigment molecule to the next

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30
Q

True or false? The antenna complex funnels the energy from one electron to the reaction centre?

A

False, the antenna complex funnels the energy from many electrons to the reaction centre

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31
Q

What does the reaction centre do (photosynthesis)?

A

A special pair of chlorophyll-a acts as a trap for photon energy, passing an excited electrons to an acceptor precisely positioned as its neighbour.

-Note that here in the rxn centre, the excited electron itself is transferred and not just the energy

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32
Q

Where does the transfer of excited electrons from the reaction centre go to?

A

The primary electron acceptor (plastoquinone)

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33
Q

How does chlorophyll get stored to its original condition (after rxn centre)?

A

A nearby weak electron donor (water in plants) passes a low-energy electron to the chlorophyll restoring it to its original condition

-Water splits to create O2 and H+

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34
Q

Summarize the light dependent step of photosynthesis

A

-The antenna complex of the photosystems captures the energy from sunlight and transfers it to the reaction centre

-Magnesium ions, present in the special pair of chlorophyll-a of the reaction centre will donate an electron the the acceptor, a plastoquinone (Pq).

-The magnesium with the help of the reaction centre proteins will then oxidize water (H2O) to regain the lost electron, producing O2.

-It requires the energy from four photons to complete the oxidation of two water molecules to produce molecular oxygen (O2).

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35
Q

Plants use _ photosystems to carry out light dependent reactions

A

2

-photosystems 2: 680nm and is called P680
-photosystems 1: 700nm and is called P700

Both systems are linked by the cytochrome complex (electron transport chain)

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36
Q

The plastoquinone (PQ) carries the electron in the first part of the electron transport chain of the ______ complex.

A

Cytochrome b6-f complex

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37
Q

The cytochrome b6-f complex acts as a _____ pump and will use the energy from the electrons to pump ____ into the ____ ______.

A

1) proton

2) protons

3) thylakoid lumen

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38
Q

The protein plastocyanin (PC) will transport the electrons to ….

A

Photosystems 1

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39
Q

What happens at photosystems 1 (PS1)?

A

-The antenna complex absorbs a photon’s energy which is transferred to the reaction centre.

-in the reaction centre, electrons are excited and donated to an electron accepting protein called ferredoxin.

-The incoming electrons from photosystems 2 replace the donated electrons (no water needed)

-Ferredoxin donates the electrons to NADP+, creating NADPH via the enzyme NADP reductase.

-NADP reductase is located on the stroma side of the thylakoid membrane

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40
Q

What is NADPH?

A

Coenzyme (high energy electron carrier)

Nicotinamine adenine dinucleotide phosphate (NADP+)

-It carries the electrons (2x) and proton (1x H)

-Carries the energy captured from light to the stroma where it will be used to generate high energy organic molecules (sugars).

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41
Q

How does ATP get created from the H+ gradient?

A

-The electron transport chain permits the pumping of H+ into the thylakoid lumen.

-Chemiosmosis carried out during photosynthesis is carried out in a similar manner than in the mitochondrion

-ATP is generated with the help of ATP synthase

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42
Q

What is produced during the light dependent step of photosynthesis?

A

NADPH (electrons and proton)
ATP (with the help ofATP synthase)

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43
Q

Where does the light-dependent and light-independent step of photosynthesis occur?

A

Light-dependent: thylakoid

Light-independent: stroma

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44
Q

What does the Calvin Cycle do?

A

Converts inorganic carbon into organic carbon in the form of carbohydrates

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45
Q

What are the 3 phases of the Calvin cycle?

A

1) Carbon fixation

2) Reduction

3) Regeneration of RuBP

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46
Q

What happens in Phase 1 of the Calvin Cycle?

A

CARBON FIXATION

-A carbon atom from CO2 is added to a five-carbon molecule (RuBP).

-This is done by Rubisco, a large multienzyme compex that catalyzes the fixation of CO2 and RuBP to PGA

The resulting 6 carbon molecule is unstable and immediately splits into 2x3 carbon molecules (PGA)

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47
Q

What happens in phase 2 of the Calvin cycle?

A

REDUCTION

-Energy from ATP add a phosphate to the 3-carbon molecule

-This phosphate is afterwards replaced by a hydrogen atom from NADPH (and electron)

-2 molecules of G3P will combine to make glucose (this process is NOT part of the Calvin cycle)

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48
Q

What is phase 3 of the Calvin cycle?

A

REGENERATION OF RuBP

-You need 6 CO2 to make one glucose (6C).

-So, 10 molecules of G3P will be used to regenerate RuBP.

-This is a multi step process that requires 6 ATP to transform 10 molecules of G3P (3C) into 6 molecules of RuBP (5C).

10 G3P X 3C= 6 RuBP x 5C
10 x 3 = 6 x 5
30C

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49
Q

How do cells build carbohydrates like glucose?

(Hint: light-independent process of photosynthesis)

A

-Use carbon from the CO2

-Energy from ATP produced by the light dependent step

-Reduction potential of the NADPH, produced by the light dependent step of photosystem I, provides a source of H+ and electrons needed to bind them to carbon atoms.

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50
Q

What is the net equation of the Calvin cycle?:

_CO2+__ATP + __NADPH + Water —> _ G3P + __ Pi + __ADP + __ NADP+

A

1) 6
2) 18
3) 12

4) 2
5) 16
7) 18
8) 12

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51
Q

What’s the problem with ATP and NADPH ratio for the light dependent step of photosynthesis?

A

Ratio ATP/NADPH: ~1
We need a ratio of 1.5 for Calvin cycle

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52
Q

What is the solution for the ATP and NADPH ratio issue for the Calvin Cycle?

A

Light-dependent step: cyclic phosphorylation

-The chloroplast needs to make extra ATP

-It does this by ‘’short-circuiting’’ the non-cyclic phosphorylation, and reverting to cyclic phosphorylation to make up the missing ATP

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53
Q

True or false? Some bacteria use only cyclic photo phosphorylation

(Hint: solution for ATP and NADPH ratio section)

A

True

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54
Q

What is the light-dependent step (cyclic phosphorylation)?

hint: solution for ATP and NADPH ratio issue

A

-Light energy absorbed at PS I is used for ATP synthesis rather than NADPH synthesis

-High-energy electrons generated by photon absorption are transferred by the ferrodoxin (Fd) and plastoquinone (Pq) to the cytochrome bf complex rather than to NADP+.

-The cytochrome bf complex uses the electrons to pump H+ from the stoma to the thylakoid lumen

-The electrons are then returned to photosystem I by plastocyanin (PC)

-The H+ gradient between the lumen and stoma is used to create ATP by the ATP synthase

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55
Q

What is the problem with photorespiration?

A

-Rubisco that catalyzes the fixation of CO2 to RuBP (carboxylation) creating PGA.

-The carboxylation and oxidation of RuBP are catalyzed at the same active site on Rubisco, thus, CO2 and O2 compete with each other at this site.

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56
Q

Oxidation of RuBP occurs when….

A

Oxygen levels are relatively high, because O2 and CO2 compete for the same active site on RUBISCO

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57
Q

Fix carbon lost to photorespiration at 25 degrees is…

At 28 degrees is…

(For Rubisco photorespiration)

A

25 degrees: 20%
28 degrees: 50%

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58
Q

How do plants regulate water and gases?

A

Plants have little doors, called stomata, that can open and close to let water and gases go in or out of their leaves.

In hot temperature, plants will close their stomata to prevent water loss, limiting at the same time the entrance of CO2 inside the leaf and the exit of O2.

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59
Q

Under normal temperate conditions, stomata…

A

-Are open so CO2 can enter the leaf and O2 can exit it

-Water loss is not excessive, since temperature is not too high

-Therefore, photorespiration is not a major problem

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60
Q

Under high temperate conditions, stomata…

A

-Leaves lose water by evaporation

-Therefore, they close their stomata

-This will lead to an accumulation of O2 in the plant, and a decrease in CO2.

-Both these conditions will increase photorespiration

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61
Q

What are C3 plants?

A

Temperate plants are called C3 plants because the first fixed carbon molecule (PGA) is a 3-carbon molecule

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62
Q

How do C3 plants regulate photorespiration?

A

They do not possess any mechanism to regulate photorespiration

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63
Q

How do C4 plants avoid the problem of photorespiration?

A

Fixation of CO2 and the Calvin cycle occur in two different cells

(C4 plants include corn, sugar cane and grasses)

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64
Q

1) PEP carboxylase fix the carbon from CO2 to the ____ creating oxaloactetate

2) This is done in the ______ cell in the presence of 02.

3) PEP carboxylase has a higher ___ affinity and no affinity for __.

4) The C4 process requires ___ to function.

5) Oxaloactetate will transform to _____ and be transportated to the ________ cell.

6) Malate will be decarboxylated directly at the site of _____ allowing for a high concentration of ___ without the presence of __.

A

1) Phosphoenol pyruvate (PEP)

2) mesophyll

3) CO2, O2

4) ATP

5) malate, bundle-sheath

6) rubisco, CO2, O2

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65
Q

Each CO2 transported in the bundle-sheath cells cost the equivalent of __ ATP.

(FOR C4 PLANTS)

A

2

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66
Q

The production of 1 glucose requires 12 additional ___ compared to the Calvin cycle alone.

(FOR C4 PLANTS)

A

ATP

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67
Q

Why is maize not grown farther north than the saint-Lawrence?

A

Photorespiration is less of a problem in cooler temperatures

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68
Q

What are CAM plants and how do they avoid the problem of photorespiration?

A

-Tropical plants have found ways to avoid the problem of photorespiration

-Fixation of CO2 and the Calvin cycle occur in the same cells, but at different times (Night/day).

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69
Q

Fixation of CO2 into oxaloactetate (C4) (PEP carboxylase) happens at ____, while the stomata are ____, when the temperature is cooler.

Those oxaloactetate are transformed in other _____ molecules (organic acids) and accumulates at ____.

(FOR CAM PLANTS)

A

Night
Open

Organic
Night

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70
Q

Stomata are closed during the ___, the organic molecules are decarboxylated to ___ that enter the Calvin cycle.

(FOR CAM PLANTS)

A

1) day

2) CO2

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71
Q

True or false? CAM photosynthesis needs to invest ATP in the same way than C4 plants.

A

True

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72
Q

True or false? For CAM plants, light-independent steps produce the electrons and protons (NADPH) necessary to the Calvin cycle

A

False, light dependent

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73
Q

What are some nucleic acids’ functions?

A

-Storing genetic information (DNA)

-structural/catalytic function (r-RNA)

-directing the synthesis of proteins (m-RNA, t-RNA).

-Energy reaction molecules (ATP, NAD, FAD).

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74
Q

What are the 3 types of nucleic acids?

A

1) Deoxyribonucleic acid (DNA)

2) Ribonucleic acid (RNA)

3) Energy reaction

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75
Q

What are the types of RNA?

A

-Messenger ribonucleic acid (m-RNA)

-Transfer ribonucleic acid (t-RNA)

-Ribosomal ribonucleic acid (r-RNA)

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76
Q

What are the types of energy reactions? (Nucleic acids)

A

-Adenosite triphosphate (ATP)

-Nicotinamide adenine dinucleotide (NAD)

-Flavin adenine dinucleotide (FAD)

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77
Q

What are monomers and polymers of nucleic acids called?

A

1) Monomers: nucleotide

2) Polymer: nucleic acids

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78
Q

What is the structure of nucleic acids?

A

Phoshpte group

Pentose sugar:
-Ribose: OH in C-2 (RNA)
-Deoxyribose: H in C-2 (DNA)

Nitrogenous base

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79
Q

What is the back-bone in nucleic acids?

A

-Phosphate group + sugar

-Link together by phosphodiester bonds

-Links are made on C-5 and C-3 of the sugar giving the direction of the DNA 5’ to 3’.

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80
Q

Synthesis of DNA polymer (polynucleotide) is done by polymerase enzyme which adds nucleotide, one by one, only to the free _____ end of a growing DNA strand (5’ —> 3’)?

A

Hydroxyl (OH)

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81
Q

What are the purines and pyrimidines in nucleic acids?

A

Purines: Adenine (A) and Guanine (G)

Pyrimidines: Cytosine (C), Thymine (T) and Uracil (U) (only in RNA)

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82
Q

What is the double helix of DNA?

A

Two polynucleotide strands connected by hydrogen bonds

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83
Q

What are complementary base-pairing rules for DNA?

A

-Adenine (A) with Thymine (T) (2x H bonds)

-Guanine (G) with Cytosine (C) (3x H bonds)

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84
Q

How is the double helix formed for DNA?

A

The complementary strands of DNA are ‘’antiparallel’’

-The 5’ end of one strand is the 3’ end of the other

-In DNA, the paired chains of nucleotides twist together into a double helix

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85
Q

The double helix is considered DNA’s ____ structure

A

Secondary

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86
Q

What are characteristics of RNA?

A

1) Contain Ribose sugar instead of Deoxyribose

2) Includes the base uracil instead of thymine

3) Single polynucleotide strand

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87
Q

What are the several functions of RNA within the cell?

A

1) m-RNA:
Transfer information from DNA to the ribosome

2) r-RNA:
Structural part of the ribosome and has catalytic functions

3) t-RNA:
Carries amino acids to the ribosome

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88
Q

The subunits of the ribosome are composed of…

A

Proteins and rRNA

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89
Q

What do NAD and FAD do (nucleic acids)?

A

They are electron carriers for many cellular reactions

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90
Q

Who showed the heredity of traits (DNA)?

A

Gregor Mendel

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91
Q

Who discovered DNA?

A

Friedrich Miescher (german scientist)

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92
Q

In 1920, the study of DNA revealed that it is made up of….

A

A phosphate group, a pentose sugar and a nitrogenous base (A,T,G,C).

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93
Q

What did Frederick Griffith discover?

A

Transformation

-Traits (such as virulence) can be passed from the dead bacteria to the live non pathogenic strains

-It must be due to passing of molecules between dead and live cells

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94
Q

Who discovered the hereditary molecule? (3 ppl)

A

Colin Macleod
Oswald Avery
Maclyn McCarthy

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95
Q

What was the experiment to find the hereditary molecule?

(I.e: what did they do to find the molecule)

A

To determine which macromolecule is responsible for transmitting the information of virulence, they added specific enzymes that degrade proteins, RNA, and DNA

After the enzymes degraded their specific macromolecule, the researchers did the Frederick Griffith experiment and added a non virulent R strain to each tube.

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96
Q

What is the hereditary molecule?

A

DNA

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97
Q

What did Hershey and Chase do?

A

Used bacteriophages to prove that DNA is the hereditary molecule

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98
Q

What are phages?

A

-Viruses that infect bacteria

-Made up of proteins and DNA

-Reprogram bacteria to produce other phage viruses

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99
Q

What did Erwin Chargaff find?

A

The matching proportion of nucleotides

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100
Q

What are Chargaff’s rules (DNA)?

A

-The proportion of A = the proportion of T
-The proportion of C = the proportion of G

(This led to the AT and CG base pairing rules of today)

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101
Q

True or false? Erwin Chargaff figured out the structure of DNA

A

False, he discovered the nitrogenous base pairing

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102
Q

What did Rosalind Franklin do?

A

She was a researched in the Wilkins Lab and produced the first good DNA x-ray crystallography

-To work, X-Ray diffraction technique needs solids with regular, repeating units of atoms (crystal)

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103
Q

What is the diameter of…
Purine + Purine
Pyrimidine + Pyrimidine
Purine + Pyrimidine

A

Pur+Pur >2nm
Pyr+Pyr <2nm
Pur+Pyr = 2nm

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104
Q

What did Watson and Crick do?

A

Developed the first molecular model oDNA

-Solved the structure based on Franklin’s patterns and Chargaff’s rules.

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105
Q

What experiment did Watson and Crick do?

A

They never actually did any experiments

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106
Q

What did Watson and Crick propose?

(Hint: bonding)

A

The two strands (of DNA) were held together by formation of hydrogen bonds between bases on opposite strands

-Guanine (G) can form three hydrogen bonds with Cytosine (C)

-Adenine (A) can form two hydrogen bonds with Thymine (T)

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107
Q

What are the three models of possible DNA replication?

(Just the names)

A

1) Semiconservative model

2) Conservative model

3) Dispersive model

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108
Q

What is the semiconservative model?

(DNA replication)

A

-One strand of the parental duplex remains intact in daughter strands (Semiconserved)

-In the first replication, a new complementary strand is built from each parental strand, thus creating a DNA with new and old strands

-In the second replication, you will have an entire new DNA molecule and one DNA molecule with new and old strands

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109
Q

What is the conservative model?

(DNA replication)

A

-Both strands of the parental duplex would remain intact (conserved), and a new DNA copy would consist of all-new DNA strands

-In the first replication, both parental strands are being replicated, thus creating a new pair of DNA strands.

-In the second replication, you will have two new DNA duplexes and one new DNA duplex molecule and one old duplex.

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110
Q

What is the dispersive model?

(DNA replication)

A

-Copies of DNA would consist of mixtures of parental and newly synthesized strands.

-That is, the new DNA would be dispersed throughout each strand of both daughter molecules after replication

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111
Q

Which of the 3 models represents the reality of DNA replication?

A

Semiconservative model

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112
Q

What was the Meselson and Stahl experiment?

A

-First, the bacteria are grown in a medium containing a heavy isotope of nitrogen (15N)

-The bacteria will grow and divide, replicating their DNA and incorporating the heavy nitrogen (15N) into the DNA nitrogenous bases.

-They then extracted and purified some of the DNA and measured the density of the DNA using density gradient centrifugation

-This method uses centrifugation which separates molecules into bands according to their density

-DNA with heavy nitrogen (15N) will centrifuge lower in the tube due to its high density

-The bacteria will be transferred to a media containing light nitrogen isotope (14N)

-After one generation (one DNA replication) in light nitrogen isotope (14N), the nitrogen will be incorporated in the DNA

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113
Q

What are chromosomes?

A

Condensed DNA

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114
Q

What do identical twins result from?

A

The accidental split of the embryo during the first stage of cell division

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115
Q

What is the general concept of DNA replication?

A

-The parent molecule has two complementary strands of DNA linked with its specific partner (A-T and G-C)

-The first step in replication is separation of the two DNA strands

-Each parental strand now serves as a template that determines the order of nucleotides along a new, complementary strand.

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116
Q

Where does DNA replication start for prokaryotes?

A

They have a singular circular molecule of DNA, so it starts at the origin of replication (only 1)

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117
Q

Which nitrogenous bases make up the origin of replication and why?

A

Adenine and Thymine because it is easier to separate (melt) because A-T have only 2 hydrogen bonds.

118
Q

Which protein activates initiation of DNA replication at the origin of replication by separating the two DNA strands?

(For prokaryote)

119
Q

What does the DNAa protein permit (after the splitting of the two DNA strands)?

A

This permits the replisome (complex molecular machine which does the replication of DNA) to access the single DNA strand

120
Q

DNA replication occurs in a … manner

(Prokaryote)

A

Bidirectional

121
Q

DNA polymerase enzyme of the replisome adds nucleotides, one by one, only to the free _ end (OH) of a growing DNA strand (_ -> _), never to the _ end.

A

1) 3’
2) 5’->3’
3) 5’

122
Q

What are the 3 things needed for DNA replication?

A

1) Template strand

2) Nucleoside triphosphate (nucleotide)

3) Replisome/DNA polymerase

123
Q

What does helicase do (in DNA replication)?

And what does it require to work?

A

-It is an enzyme that untwists the double helix at the replication forks, separating the two parental strands and making them available as template strands

-This requires ATP

124
Q

What does the single-strand binding protein (SSB) do?

(DNA replication)

A

Binds to the unpaired bases of the DNA strands, stabilizing them until they serve as templates for the synthesis of new complementary strands.

125
Q

What does DNA gyrase do?

(DNA replication)

A

Is a topoisomerase enzyme that cuts and untwists ahead of the replication fork to relieve the strain caused by the helicase

126
Q

What is a replisome?

(DNA replication)

A

The complex molecular machine that carries out replication of DNA (helicase, gyrase, SSB, primase DNA polymerase III, ligase, etc.)

127
Q

What are primers and what are they synthesized by?

(DNA replication)

A

Small pieces of RNA (10-20bp) that is complementary to the DNA template strand

-They are synthesized by an RNA polymerase called primase

128
Q

Primers have a free _’ end.

129
Q

What doesDNA polymerase III have (DNA replication)

A

A beta-subunit that forms a clamp around the template stand

130
Q

What direction is the strand getting replicated? (New strand, not template strand)

A

5’ -> 3’

131
Q

Why are primers essential?

A

DNA polymerases cannot initiate the synthesis of a polynucleotide. They can only add nucleotides to the 3’ end of an already existing chain.

132
Q

What does DNA polymerase I do? (DNA replication)

A

Replaces the RNA nucleotides of the primers with DNA versions (uracil to thymine), adding them one by one onto the 3’ end of the adjacent Okazaki fragment

133
Q

What does DNA ligase do? (DNA replication)

A

Forms a phosphodiester bond between the two Okazaki fragments.

134
Q

DNA Pol I and Pol III have 3’-5’ exonuclease activity which serves as….

A

A proofreading function because it allows the enzyme to ‘’back up’’ and remove a mis-paired base

135
Q

True or false? Synthesis of DNA is done at different times on the leading and lagging strands?

A

False, they are done at the same time

136
Q

True or false? The replisome contains all the enzymes necessary for DNA replication (multi enzyme complex)

137
Q

1) DNA polymerase epsilon:

2) DNA polymerase delta:

3) PCNA SLIDING Clamp:

(Differences between prokaryotes and eukaryotes)

A

1) leading strand

2) lagging strand

3) clamp that attaches enzyme complex to the DNA

138
Q

Why is eukaryotic replication complicated? (2 main factors)

A

1) Large amount of DNA organized into multiple chromosomes

2) Linear structure of the chromosomes

(This process requires new enzymatic activities only for dealing with the end of chromosomes; otherwise, the basic enzymology is the same)

139
Q

Where does DNA replication start (eukaryotes)?

A

-Origin of replication is a stretch of DNA having a specific sequence and chromatin properties

-proteins that initiate DNA replication can recognize this sequence and teach to the DNA, separating the two strands and opening a replication bubble.

-Replication of DNA then proceeds in both directions until the entire molecule is copied

-Eukaryotic chromosomes may have hundreds or even thousands of replication origins, while prokaryotes have only one.

140
Q

What is the problem with eukaryotes in terms of DNA replication?

A

The directionality of polymerase and their requirement for a primer creates a problem.

When the last primer is removed, there is no 3’ end to replicate the DNA using polymerase I.

141
Q

True or false? Chromosomes get shorter at each DNA replication (eukaryote)

142
Q

What is the solution to the problem eukaryotes have for DNA replication?

A

They use telomeres and telomerase

143
Q

What is a telomere?

A

A Region of repetitive non coding nucleotide sequences at each end of a chromosome, which protects the coding portion of the new chromosome.

(Telomeres consist of hundreds or thousands of repeats)

144
Q

What has telomere shortening been connected to?

A

The aging of cells

145
Q

The progressive loss of telomeres may explain why cells can only…

A

Divide a certain number of times

146
Q

What is telomerase?

A

Telomerase is an RNA-dependent DNA polymerase, meaning an enzyme that can make DNA using RNA as a template

147
Q

How can telomere shortening be reversed?

A

Some cells can reverse telomere shortening using the telomerase enzyme that extends the telomeres of chromosomes.

148
Q

What does telomerase do?

A

Adds nucleotides to the overhanging strand of the telomere

DNA replication machinery (RNA primer and DNA polymerase) produce double-stranded DNA

149
Q

What type of cells is telomerase active in?

A

Germ cells (the cells that make sperm and eggs) and some adult stem cells

Note: telomerase is not usually active in most somatic cells (cells of the body)

150
Q

Many cancer cells have […] active, which permits them to do cell division and DNA replication indefinitely

A

Telomerase

151
Q

What is the basic unit of heredity?

152
Q

What are genes composed of and what do they do?

A

A sequence of nucleotides in DNA that encodes the synthesis of RNA and generally induces the production of a polypeptide (protein).

153
Q

Where is a gene present and what does it include?

A

Over a particular physical region (locus) of a double-stranded DNA molecule.

It includes the transcription unit or RNA-coding region, where transcription occurs from the DNA template strand so as to synthesize an RNA transcript in the 5’ to 3’ direction, running between the initiation and termination sites

154
Q

What was Tatum and Beadle’s experiment?

A

-fungus is grown in minimal medium (minimal elements to support growth)

-Any cells that can grow on minimal medium must be able to synthesize all necessary biological molecules

-The fungus is exposed to x-ray to induce mutation of the DNA

-Then the fungus is grown in rich media

-If transferred to a minimal medium, some of the fungus cannot grow anymore but can grow if it’s supplemented with arginine (lost the genes coding from arginine pathway)

155
Q

What were Tatum and Beadle able to do?

A

Genetically dissect the arginine biosynthetic pathway

156
Q

What does the biosynthesis of arginine consist of?

A

A multi-enzyme pathway

157
Q

How were Tatum and Bradley able to identify the specific enzymes that were mutated (inactive)?

A

By supplementing the minimal medium with intermediates molecules of the biochemical pathway

158
Q

The 1st enzyme (E) transforms glutamate into […]

(Arginine multi enzyme pathway)

159
Q

The 2nd enzyme (F) transforms ornithine into […]

(Arginine multi enzyme pathway)

160
Q

The 3rd enzyme (G) transforms Citruline into […]

(Arginine multi enzyme pathway)

A

Arginosuccinate

161
Q

The 4th enzyme (H) transforms arginosuccinate into […]

(Arginine multi enzyme pathway)

162
Q

What did Tatum and Beadle conclude?

A

That a specific stretch of DNA, the gene, encodes for the structure of one enzyme protein

-They called this relation the one gene/one enzyme hypothesis

163
Q

What is the central dogma?

A

Information passes in one direction, from the gene (DNA) it is transcribed to m-RNA, and translated to amino acids polypeptide (protein).

164
Q

What are retroviruses?

A

RNA based viruses that use reverse transcription to insert their own code into the host genome during infection

165
Q

What is the template strand?

A

The DNA that is transcribed to a single-strand m-RNA molecule

166
Q

What is the coding strand?

A

The strand of DNA not used as a template

(Since it has the same sequence as m-RNA transcript (but T are U))

167
Q

The m-RNA transcript’s sequence is ______ to the template strand

A

Complementary

168
Q

The m-RNA transcript used to direct the synthesis of polypeptides (aka protein) is termed […].

A

Messenger RNA (m-RNA)

169
Q

What does m-RNA do?

A

Carry the DNA message to the ribosome for processing

170
Q

Why is the DNA to m-RNA step called transcription?

A

Because it produces a complementary copy of the DNA in m-RNA (T become U in m-RNA)

171
Q

Why is the m-RNA to protein step called translation?

A

Because it requires translating from the nucleic acid to the amino acid ‘’languages’’

172
Q

How many RNA polymerase do prokaryotes have?

173
Q

What does transcription require? (5)

A

1) RNA polymerase

2) Promoter

3) Start site

4) Termination

5) Stop site

174
Q

What are the steps to transcription?

A

1) Initiation

2) Elongation

3) Termination

175
Q

RNA polymerase of prokaryotes exist in which forms? (2)

(Initiation step to prokaryotic transcription)

A

1) Core polymerase: composed of alpha and beta subunits. Can synthesize m-RNA from DNA, but cannot initiate transcription

2) holoenzyme: combination o the core polymerase with the sigma factor. This combo can accurately initiate synthesis.

176
Q

Does transcription require a primer?

177
Q

What are the steps to initiation?

(Prokaryotic transcription)

A

1) sigma factor joins the core polymerase to form the holoenzyme

2) sigma factor permits the recognition specific sequences of DNA called promoter at -35 and -10 base pairs from the start site.

3) The helix is open at -10 base pair regions and transcription begins at the start sites at +1 base pair from the start site.

4) The sigma factor dissociates from the core polymerase. However recent findings suggest that it’s rather weakly bound to the core during elongation

178
Q

The initiation relies on […]

(Prokaryotic transcription)

A

Two sequences present in DNA called the promoter region

179
Q

What is the promoter and what does it contain?

A

A region located upstream (before) the start signal (therefore it is not transcribed).

The promoter contains 2 binding sites for sigma factors of the RNA polymerase at -35 and -10 base pairs before the start sites.

180
Q

When does the RNA polymerase start to unwind the DNA helix?

(Initiation of prokaryotic transcription)

181
Q

What is promoter clearance (elongation for prokaryotic transcription)?

A

The hydrolysis of ATP or GTP provides the energy required for the polymerase to leave the promoter region and start transcription

182
Q

What are the steps to elongation (prokaryotic transcription)?

A

-Promoter clearance: hydrolysis of ATP or GTP provides energy required for the polymerase to leave the promoter region and start transcription

-A transcription bubble is then formed as RNA is elongated

-The m-RNA grows in the 5’ to 3’ direction as ribonucleotides are added

-For each nucleotide in the template, RNA polymerase adds a matching RNA nucleotide to the 3’ end of the m-RNA strand.

-The RNA transcript is nearly identical to the coding strands of DNA (However, U instead of T and ribose sugar instead of deoxyribose)

-After the transcription bubble passes, the now-transcribed DNA is rewound as it leaves the bubble

183
Q

What does the transcription bubble contain?

A

RNA polymerase, DNA template strand, and growing m-RNA transcript

184
Q

What is termination in prokaryotic transcription (General)?

A

The end of a bacterial transcription unit is marked by terminator sequences that signal ‘’stop’’ to the polymerase

185
Q

What are the 2 types of terminations (prokaryotic transcription)

A

1) Rho-dependent termination

2) Rho-independent termination

186
Q

What is Rho-dependent termination (prokaryotic transcription)?

A

-The m-RNA that is produced contains a binding site for the Rho factor

-Rho factor binds to this sequence and starts ‘’climbing’’ up the transcript towards RNA polymerase

-When it catches up with the polymerase, Rho pulls the RNA transcript and the template DNA strand apart

-Another sequence found later in the DNA, called the transcription stop point, causes RNA polymerase to pause and thus helps Rho catch up.

187
Q

What is Rho-independent termination in prokaryotic transcription?

A

-As the RNA polymerase approaches the end of the gene, it hits a region rich in C and G nucleotides

-The RNA transcribed from this region folds back on itself, and the complementary C and G nucleotides bind together

-The result is a stable hairpin that causes the polymerase to stall

-The hairpin is followed by a stretch of U nucleotides in the RNA, which match up with A nucleotides in the template DNA

188
Q

True or false? The complementary U-A region of the RNA transcript forms a strong interaction with the template DNA?

(Prokaryotic transcription)

A

False, it is a weak interaction as there are only 2 H bonds between U-A

189
Q

True or false?

Prokaryotes can do transcription and translation at the same time

(And why)

A

True!

Prokaryotes don’t have a nucleus, so they can directly do the transcription of DNA to m-RNA and translate it t polypeptide chains (aka protein)

190
Q

What are the 3 RNA polymerases for Eukaryotes?

(And name their functions)

A

1) RNA polymerase I: transcribes ribosomal RNA (r-RNA)

2) RNA polymerase II: transcribes messenger RNA (m-RNA)

3) RNA polymerase III: Transcribes transfer RNA (t-RNA)

191
Q

True or false? Each RNA polymerase recognizes its own promoter

192
Q

What are the steps to initiation in eukaryotes?

A

-The initiation at RNA polymerase II promoters is analogous to prokaryotes, but eukaryotes use a host of transcription factors allowing promoter recognition

-These factors first bind to the promoter and then recruit RNA polymerase II

-The transcription factors interact with RNA polymerase II to form an initiation complex at the promoter.

193
Q

What are the steps to elongation in eukaryotic transcription?

A

-When the transcript reaches about 20 nucleotides, it is modified by the addition of GTP to the 5’ PO4- group, forming what is known as the 5’ cap.

-This cap is joined to the transcript by its 5’ end, the only 5’ to 5’ bond found in nucleic acids

-The G in the GTP is also modified by the addition of a methyl group, so it often called a methyl-G cap.

(This structure is important for translation, RNA stability, and further processing)

194
Q

What are the steps to termination in eukaryotic transcription?

A

A distinctive feature of eukaryotic transcription is that the 3’ end of transcription is not the real end of the m-RNA

-The transcript is cleaved downstream of a specific site (AAUAAA) while the polymerase is elongating and a series of 100 to 200 adenosine residues (A), called the 3’ poly-A tail, is added to the m-RNA

(The enzyme responsible for this is poly-A polymerase)

195
Q

The G-cap and poly-A tail is added in which stages of eukaryotic transcription?

A

G-cap: elongation

Poly-A tail: termination

196
Q

What is the function of the addition of a 5’cap and 3’ poly-A tail?

A

5’ cap:
-Protects the m-RNA from degradation; involved in translation initiation

3’ poly-A tail:
-Protection of the m-RNA from degradation

197
Q

True or false?

Eukaryotes have a ‘’core promoter’’ like the prokaryote TATA sequence (-10 bp)

A

True, eukaryotes have a ‘’core promoter’’ that can be composed of a number of distinct elements, including the TATA box

198
Q

What are exons and introns?

A

Exons: sequences that will be translated in protein

Introns: non-coding sequences (not translated into proteins)

199
Q

True or false?

Both exons and introns are transcribed in the Pre m-RNA

200
Q

What is eukaryotic pre-m-RNA splicing?

A

Before pre-mRNA can be translated into protein it must first get ready to leave the nucleus. It undergoes a maturing process

-A cutting complex forms called a spliceosome which snips out introns and links together the exons. This is called pre-mRNA splicing

201
Q

How are spliceosomes formed?

(Eukaryotic pre-mRNA splicing)

A

The intron-exon junctions are recognized by small nuclear ribonucleoprotein particles called snRNPs

These snRNPs then cluster together with other associated proteins to form a larger complex called the spliceosome

202
Q

True or false?

Introns all begin with the same 2-base sequence and end with another 2-base sequence that tags them for removal

(Eukaryotic pre-mRNA splicing)

203
Q

What is eukaryotic pre-m-RNA alternative splicing?

A

The same gene doesn’t always produce the same protein

204
Q

21,000 genes of the human genome can encode more than […] different proteins

205
Q

~20,000 genes of the C. elegans genome can encode about […] different proteins (4% alternative splicing)

206
Q

Exons compose only about […]% of the human genome

207
Q

Introns compose about […]% of the human genome

208
Q

Intergenic DNA represents […]% of the human genome and is composed of [….]

A

75%

Noncoding DNA

209
Q

What does intergenic DNA do?

A

Occasionally acts to control nearby genes but most of it has no current known function

210
Q

Remnants of ancient viruses compose about […]% of the human genome.

A

8%

Note: the viral DNA comes from retrovirus, which can copy their genome to the host genome during infection

211
Q

What are the 4 main components for translating from m-RNA to a polypeptides protein

A

1) Amino acids (monomers of the polypeptide (protein))

2) t-RNA (brings the amino acids to the ribosome to make proteins)

3) Ribosome (the organelle that takes the information of the m-RNA and translate it into protein)

4) m-RNA (transcript of gene in RNA)

212
Q

What are t-RNA characteristics?

A

-Different t-RNA molecules carry each 20 types of amino acids to the ribosome for incorporation into a polypeptide

-Accepter end binds to the amino acids

-Anticodon loop contains 3 nucleotides complementary to m-RNA codons

213
Q

The aminoacyl-tRNA synthetases must be able to […]

A

Recognize specific t-RNA molecules as well as their corresponding amino acids

214
Q

What is charged t-RNA?

A

When an enzymatic reaction joins an amino acid to a t-RNA.

(Note: an ATP molecule provides energy for this endergonic reaction)

215
Q

What are the 2 functions of the ribosome?

A

-Decoding transcribed message (m-RNA)

-Forming peptide bonds

216
Q

The formation of peptide bonds requires the enzyme….

A

Peptidyl transferase (ribozyme), which resides in the large subunit)

217
Q

How to translate from m-RNA to a polypeptide?

A

-using codons or triplets of nucleotides in the m-RNA

-The ribosome reads the codons, producing a polypeptide

-Each codon codes for one amino acid but each amino acid can be coded for by more than one codon

218
Q

Why is genetic code considered degenerate?

A

Each codon codes for one amino acid but each amino acid can be coded for by more than one codon

219
Q

Translation always starts with the codon […] and stops with the codon […],[…], or […].

A

1) AUG (methionine)

2) UGA, UAG or UAA

220
Q

What are the ribosome’s t-RNA binding sites?
(3)

A

1) A site - binds the t-RNA carrying the next amino acid

2) P site - binds the t-RNA attached to the growing peptide chain

3) E site - binds the discharged t-RNA so it can exit

221
Q

What is the steps to initiation of translation for DNA to proteins?

(Hint: ribosome)

A

-The start t-RNA molecule with methionine fixes itself on the small ribosomal subunit

-The m-RNA is recruited by the small ribosomal subunit

-The t-RNA anticodon loop fixes itself to the corresponding m-RNA codon using GTP

-The large ribosomal subunit is positioned, so the P site is on top of the Met t-RNA

-The large ribosomal subunit is fixed to the small ribosomal subunit

222
Q

What are the steps to elongation for DNA to proteins?

(Hint: ribosome)

A

Elongation adds amino acids

-2nd amino acid on the t-RNA in site A can bind and form a peptide bond with the amino acid in site P

223
Q

How does the addition of successive amino acids occur (cycle)?

(Elongation during DNA to proteins)

A

1) Matching t-RNA anticodon with m-RNA codon

2) Peptide bond formation

3) Translocation of ribosome and ejection of the empty t-RNA (needs GTP)

224
Q

What is termination for DNA to proteins?

(Hint: ribosome)

A

-Elongation continues until the ribosome encounters a stop codon

-Stop codons are recognized by release factors which release the polypeptide from the ribosome

225
Q

What is wobble pairing?

A

-There are fewer t-RNAs than codons

-Pairing between the codon and the anticodon is less stringent than normal

-In some t-RNAs, the presence of modified bases with less accurate pairing of the anticodon enhances this flexibility

(Ex: G-U instead of G-C)

226
Q

In eukaryotes, translation may occur in the […] or the […].

A

1) cytoplasm

2) Rough Endoplasmic reticulum (RER)

227
Q

How does protein synthesis occur in the rough Endoplasmic reticulum (RER)?

A

-Signal at the beginning of the polypeptide sequence binds to the signal recognition particle (SRP).

-The signal sequence and SRP are recognized by RER receptor proteins

-Docking holds ribosome to RER and beginning of the protein-trafficking pathway

228
Q

How does sickle cell anemia occur?

A

It is a mutation of only one base

-This single change from A to T, substitutes the polar charge Glutamic Acid to a non-polar Valine amino acid.

-This changes the 3D structure of the polypeptide and makes their quarternary structure into a sickle shape

229
Q

What is point mutation?

A

Single base pair mutation in the DNA

230
Q

What are types of point mutation (3)?

A

-Silent mutation (unchanged amino acid, ex: GGU or GGC gives gly regardless)

-Miss sense (ex: Gly becomes Ser)

-Nonsense (insertion of a stop codon too soon)

231
Q

What are the types of frame shift mutation? (2)

A

Insertion

Deletion

(In both cases, you will have different codons and thus amino acids in the final protein)

232
Q

What is chromosome mutation (large deletion)?

A

-Deletion of a larger region of a chromosome is usually fatal to the organism

  • A large deletion from the short arm of chronometer 5 causes ‘’cri-du-chat’’ syndrome

-Usually results in early death, although many affected individuals show a normal lifespan

-respiratory problems

233
Q

What happens if a region of a chromosome is duplicated?

(Chromosome mutation)

A

-The duplication of a region of a chromosome may or may not lead to phenotypic consequences

-Effects depend upon the location of the ‘’breakpoints’’ where the duplication occurred

-If the duplicated region does not lie within a gene, there may be no effect

234
Q

What is an inversion (chromosome mutation)?

A

-An inversion results when a segment of a chromosome is broken in two places, reversed, and put back together

-An inversion may not have an effect on phenotype if the sites where the inversion occurs do not break within a gene

-In fact, although humans all have the ‘’same’’ genome, the order of genes in all individuals in a population is not precisely the same due to inversions that occur in different lineages

235
Q

What is one of the most common chromosomal inversion variants?

A

Chromosome 9 inversion (with an estimated incidence of about 3.5%)

(note: not known if the rearrangements have clinical significance)

236
Q

What is translocation (chromosome mutation)

A

-When a piece of one chromosome is broken off and joined to another chromosome

-Translocations can also move genes from one chromosomal region to another in a manner that changes the expression of genes in the region involved

-Two forms of leukemia have been shown to be associated with translocations that move oncogenes into regions of a chromosome where they are expressed inappropriately in blood cells

237
Q

When/why do prokaryotes regulate gene expression?

A

Need to respond to their environment (constantly changing — need to adapt)

238
Q

When/why do eukaryotes need to regulate gene expression?

A

In multicellular organisms, gene expression is critical for directing development and maintaining homeostasis

239
Q

What are the 2 types of feedback mechanisms that metabolism control uses?

(Gene regulation)

A

1) Regulation enzymes:
competitive and non-competitive inhibition to turn on and off production

2) Regulation of gene expression:
Activating/deactivating genes using regulatory proteins that switch transcription on or off

240
Q

Regulation of gene expression can be controlled at which levels? (3)

A

1) Transcription

2) Translation

3) Post-translation

241
Q

Gene expression is often controlled by […] binding to specific DNA sequences

A

Regulatory proteins

242
Q

What are characteristics of regulatory proteins?

(Gene regulation)

A

-Gene expression is often controlled by regulatory proteins binding to specific DNA sequences

-Regulatory proteins gain access to the bases of DNA at the major groove

-Within the major groove, nucleotides’ hydrogen bonds are unique for each base pair combination

243
Q

What are DNA-binding motifs?

(Gene regulation)

A

-Regions of regulatory proteins which bind to DNA

-Helix structures form hydrogen bonds with nucleotides in the major groove, thus allowing each regulatory protein to bind to a specific DNA region

244
Q

What is the helix-turn-helix motif in terms of gene regulation?

A

-Most DNA-regulatory sequences recognized by helix-turn-helix motifs occur in symmetrical pairs

-Such sequences are bound by proteins containing two helix-turn-helix motifs separated by 3.4 nm, the distance required for one turn of the DNA helix

-Having 2 protein-DNA-binding sites doubles the zone of contact between protein and DNA and greatly strengthens the affinity between them

245
Q

What is the zinc finger motif?

A

-Zinc finger motif uses one or more zinc atoms to coordinate its binding to DNA

-Zinc finger motif exists in multiple forms, for example, a zinc atom links an alpha-helical segment to a beta-sheet segment so that the helical segment fits into the major groove of the DNA

-The effect is like a hand wrapped around the DNA with the fingers lying in the major groove

-The more zinc fingers in the cluster, the more the protein associates with DNA

246
Q

What is the leucine zipper motif?

A

-Leucine zipper is created where a region on one subunit containing several hydrophobic amino acids (usually leucines) interact with a similar region on the other subunit

-This interaction holds the subunits together and creates a y-shaped structure where the two arms of the Y are helical regions that fit into the major groove of DNA, but on opposite sides of the helix, holding the DNA like a pair of tongs

247
Q

Why regulate gene expression (bacteria example)?

A

Bacteria are frugal: they only express a gene if the protein is needed for the cell to survive

248
Q

What are operons?

A

-Prokaryotic m-RNA may contain multiple genes and thus produce multiple proteins at once

-Prokaryotic genes are often organized such that genes encoding related functions are clustered together

-This grouping of functionally related genes is referred to as an operon

249
Q

What do operons contain? (3)

A

1) A promoter: RNA polymerase building site

2) Operator: ‘’on-off’’ switch in the promoter region (if blocked, RNA polymerase cannot bind to make m-RNA)

3) Structural genes: code for gene products (ex: enzymes)

250
Q

What are negative controls by repressors? (Prokaryote gene regulation)

A

-Repressors are proteins that bind to the operator to prevent or decrease the initiation of transcription

-They act as a kind of roadblock to prevent the polymerase from initiating effectively

251
Q

What are positive controls by activators ( prokaryote gene regulation)?

A

The activators enhance the binding of RNA polymerase to the promoter to increase the frequency of transcription initiation

252
Q

What is a regulatory gene?

A

A regulatory gene is located upstream of the operon and codes for the regulator protein (ex: repressor) which will affect the operator

253
Q

What are the 2 types of operon?

A

1) inducible operon

2) repressible operon

254
Q

What is an inducible operon?

A

Operon is off by default

(Ex: a bacterium will have their operon for lactase off by default and only produce the enzymes when it encounters lactose. It’s an inducible operon, since lactose induces the production of enzyme)

255
Q

What are repressible operons?

A

Operon is on by default

(Ex: a bacterium will synthesize the amino acid tryptophan by default, their operon is on. However, when tryptophan is available in their food, it will stop producing this amino acid. It’s a repressible operon, since tryptophan represses the production of enzymes)

256
Q

How do inducible operons work?

A

Regulator gene makes a functioning form a repressor protein

The repressor protein will bind to the operator and prevent the RNA polymerase from binding to the promoter site

257
Q

How do repressible operons work?

A

Regulator gene makes a non-functioning form a repressor protein

RNA polymerase is able to bind to promoter and genes are transcribed

258
Q

Multicellular organisms must activate or deactivate their genes according to… (3)

A

External stimuli
Internal stimuli
Regulate genes according to the type of cell (liver, skin, etc.)

259
Q

Any human cell probably only expresses about […] of its genes at a time, and this proportion is […] in highly specialized cells (ex muscle cells, neurons, etc.)

A

1) 20%

2) even lower

260
Q

The expression of eukaryotic genes can be regulated in which places? (5)

A

1) Chromatin modification (DNA and protein)

2) Transcription

3) RNA maturation

4) Translation

5) Degradation of proteins

261
Q

What is chromatin?

A

-Chromatin is a complex of DNA and protein found in eukaryotic cells

-The primary function is to pack DNA into more compact structures

-The primary protein components of chromatin are histones, which bind to DNA wrapped around the histone

262
Q

To be readable, DNA needs to be accessible to the […]

A

RNA Polymerase II

263
Q

The […] of histones leads to the […] of the structure of the chromatin.

The […] structure of chromatin, permits access of the RNA polymerase to the […] and the initiation of transcription.

A

1) acetylation

2) loosening

3) loose

4) DNA

264
Q

Histone methylation is the modification of certain amino acids in a histone protein by…

A

The addition of one, two, or three methyl groups

265
Q

What is histone methylation associated with?

A

Transcriptional repression

(However, methylation of some lysine and arginine residues of histones results in transcriptional activation)

266
Q

What is the correlation between histones and ATP?

A

-ATP-dependent chromatin remodelling factors

  • Function as molecular motors that use energy from ATP hydrolysis to alter the relationships between histones and DNA

-Make DNA more accessible to regulatory proteins that in turn affect gene expression

267
Q

What is epigenetic inheritance?

A

-It’s an alteration that must persist in the absence of the initiating stimulus, and be inherited through cell division

-The inheritance of traits transmitted by mechanisms not directly involving the nucleotide sequence

-DNA methylation and histone modification changes the way genes are expressed but not the DNA sequence

(For example, rice plants exposed to drought had offspring that increased tolerance to drought due to induced DNA methylation patterns)

268
Q

What is the role of transcription factors?

A

-To initiate transcription, eukaryotic RNA polymerase II requires the help of proteins called transcription factors

269
Q

What are the 2 types of transcription factors?

A

1) General transcription factors

2) Specific transcription factors

270
Q

What do general transcription factors do?

(Eukaryotic gene regulation)

A

Necessary for the assembly of a transcription apparatus and recruitment of RNA polymerase II to a promoter to initiate transcription

271
Q

What do specific transcription factors do?

A

Increase the level of transcription in certain cell types or in response to signals

272
Q

What are general transcription factors?

A

Proteins that bind to the DNA promoter

-A host of general transcription factors are necessary to recruit RNA polymerase II to a promoter and assemble an initiation complex

-These factors are required for transcription to occur, but they do not increase the rate above this basal rate

273
Q

High levels of transcription of particular genes depends on….

(GENE REGULATION)

A

The control elements interacting with specific transcription factors called an activator

274
Q

What do activators do?

(Gene regulation)

A

Acts in specific tissue or in a time dependent manner to stimulate higher levels of transcription than the basal level

275
Q

What are the 2 protein domains of activators?

(Eukaryotic gene regulation)

A

1) DNA-binding domain: recognizes a specific sequence of DNA of the control elements

2) Activation domain: interacts with the transcription apparatus (by binding to regulatory proteins such as coactivator and mediator proteins)

276
Q

What do linked activators do?

(Eukaryotic gene regulation)

A

Facilitate a sequence of protein-protein interactions leading to the enhanced transcription of a given gene

277
Q

Each enhancer is composed of…

(Gene regulation)

A

Approximately 10 control elements (each can only like 1 or 2 specific coacivators, mediator proteins and transcription factors)

278
Q

A combination of control elements can only activate transcription when the appropriate […] are present.

(Gene regulation)

A

Activator proteins

279
Q

The ultimate level of transcription depends on the presence of…

(Gene regulation)

A

-Activators

-Coactivators

-Mediator proteins

280
Q

The nucleotide sequences that influence the lifespan of m-RNA in eukaryotes reside in the….

A

Untranslated region (UTR) at the 3’ end of the molecule

281
Q

What leads to. The degradation of m-RNA by exonuclease?

(Hint: RNA maturation for eukaryotic gene regulation)

A

An enzyme recognizes a sequence in the UTR (untranslated region) and cuts the poly-A tail (leading to the degradation of m-RNA…)

282
Q

What are microRNAs (mi-RNA)

A

-Small single stranded RNA molecules that are coded in the DNA but do to produce proteins

-Micro RNAs have specific bases that binds to m-RNA (complementary base pairs)

-Mi-RNA forms a complex with the protein that cleaves the m-RNA or blocks its translation by the ribosome

283
Q

What is small interference RNA (si-RNA)

A

-Production of si-RNAs is similar to that of mi-RNAs, except that they arise from a long piece of double-stranded RNA (long loop)

-RNAs are processed by Dicer to yield multiple si-RNAs

-The si-RNA are then associated with proteins that will cleave the m-RNA when they will find a complementary the base pairs

-Most likely to evolve to protect against RNA virus by silencing them

284
Q

How can the initiation of translation of selected m-RNAs be blocked?

A

-By regulatory proteins which bind to m-RNA sequences or structures (usually in the 5’ to 3’ UTR regions) and prevent the ribosome from binding

285
Q

True or false?

The translation of all m-RNAs in a cell can be regulated simultaneously

286
Q

How is the labeling of a protein for destruction carried out?

(Eukaryotic gene regulation)

A

By attaching a small ubiquitin protein to the targeted protein

287
Q

What is a proteasome?

A

An organelle that degrades proteins marked with ubiquitin

288
Q

What does the proteasome contain at its center and what is its function?

A

The protease enzyme (which cuts protein in small polypeptide fragments)

289
Q

Why is proteasome important?

A

It isolates the protease enzyme from the rest of the cell and prevents the arbitrary destruction of other proteins

290
Q

True or false?

The amino acids of the polypeptide fragments cannot be recycled to make new proteins

A

False!

They CAN be