Origin of life, cell metabolism, cellular processes, thermodynamics, organelle structure and function, mitosis/meiosis, cell structure Flashcards

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1
Q

What is the Primordial soup?

A

Origin of life theory.

  1. Early Earth had a chemically reducing atmosphere.
  2. This atmosphere, exposed to energy in various forms, produced simple organic compounds (“monomers”).
  3. These compounds accumulated in a “soup”, which may have been concentrated at various locations (shorelines, oceanic vents etc.).
  4. By further transformation, more complex organic polymers – and ultimately life – developed in the soup.
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2
Q

What is the Primordial soup?

A

Origin of life theory.

  1. Early Earth had a chemically reducing atmosphere.
  2. This atmosphere, exposed to energy in various forms, produced simple organic compounds (“monomers”).
  3. These compounds accumulated in a “soup”, which may have been concentrated at various locations (shorelines, oceanic vents etc.).
  4. By further transformation, more complex organic polymers – and ultimately life – developed in the soup.
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3
Q

What type of monomers were produced in the Miller-Urey experiment?

A

Formation of organic molecules spontaneously from inorganic precursors: methane, amonia, and hydrogen gasses were used to form amino acid monomers.

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4
Q

What is the most crucial challenge unanswered by the primordial soup theory?

A

how the relatively simple organic building blocks polymerise and form more complex structures, interacting in consistent ways to form a protocell.

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5
Q

What is the Electric Spark Theory?

A

Origin of Life Theory.
Miller demonstrated how an electric spark (simulating lightening) passed through simple inorganic gasses said to resemble the conditions of the early earth, resulted in the formation of amino acids, the basic building blocks of most living tissues

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6
Q

Community Clay

A

The first molecules of life might have met on clay, an idea by Cairns-Smith. These surfaces might not only have concentrated these organic compounds together, but also helped organize them into patterns much like our genes do now. Cairns-Smith suggests that mineral crystals in clay could have arranged organic molecules into organized patterns. After a while, organic molecules took over this job and organized themselves.

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7
Q

Community Clay

A

The first molecules of life might have met on clay, an idea by Cairns-Smith. These surfaces might not only have concentrated these organic compounds together, but also helped organize them into patterns much like our genes do now. Cairns-Smith suggests that mineral crystals in clay could have arranged organic molecules into organized patterns. After a while, organic molecules took over this job and organized themselves.

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8
Q

Chilly Start

A

Ice might have covered the oceans 3 billion years ago, as the sun was about a third less luminous than it is now. This layer of ice, possibly hundreds of feet thick, might have protected fragile organic compounds in the water below from ultraviolet light and destruction from cosmic impacts. The cold might have also helped these molecules to survive longer, allowing key reactions to happen.

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9
Q

RNA World

A

Origin of life Theory.
The self-replicating ribonucleic acid (RNA) molecules were precursors to all current life on Earth. Later DNA and proteins succeeded this “RNA world,” because they are more efficient. It is generally accepted that current life on Earth descends from an RNA world, although RNA-based life may not have been the first life to exist.The question still remains how RNA got here in the first place. And while some scientists think the molecule could have spontaneously arisen on Earth, others say that was very unlikely to have happened.

Other nucleic acids other than RNA have been suggested as well, such as the more esoteric PNA or TNA.

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10
Q

Panspermia

A

Origin of life Theory.
Perhaps life did not begin on Earth at all, but was brought here from elsewhere in space, a notion known as panspermia. For instance, rocks regularly get blasted off Mars by cosmic impacts, and a number of Martian meteorites have been found on Earth that some researchers have controversially suggested brought microbes over here, potentially making us all Martians originally. Other scientists have even suggested that life might have hitchhiked on comets from other star systems. However, even if this concept were true, the question of how life began on Earth would then only change to how life began elsewhere in space

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11
Q

Community Clay

A

Origin of life Theory.
The first molecules of life might have met on clay, an idea by Cairns-Smith. These surfaces might not only have concentrated these organic compounds together, but also helped organize them into patterns much like our genes do now. Cairns-Smith suggests that mineral crystals in clay could have arranged organic molecules into organized patterns. After a while, organic molecules took over this job and organized themselves.

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12
Q

Deep-Sea Vents/Hot Thermal Vents

A

Origin of life Theory.
The deep-sea vent theory suggests that life may have begun at submarine hydrothermal vents, spewing key hydrogen-rich molecules.

The deep-sea vent theory suggests that life may have begun at submarine hydrothermal vents, spewing key hydrogen-rich molecules. Their rocky nooks could then have concentrated these molecules together and provided mineral catalysts for critical reactions. Even now, these vents, rich in chemical and thermal energy, sustain vibrant ecosystems.

The mineral Pyrite, (Fe-Sulfide) which occurs in great abundance around deep-sea hydrothermal vents, have crystal surfaces that could attract phosphate complexes contained in many organic molecules, particularly nucleic acids. These organo-phosphate compounds could line up in close order on the pyrite surface. The crowding together of these molecules may eventually cause polymerization via organic bonds. Once polymerized, these new organic complexes could detach from their pyrite template and become free organic molecules. In this way, nucleic acids and even cell membranes may have evolved.

Deep-sea hydrothermal vents are known to be the home of primitive Archaebacteria which live on H2S, on CH4 or in hot salty springs. The primitive Archaebacteria may represent the earliest life forms on earth.

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13
Q

The origin of life time line

A
  1. Life on earth probably didn’t begin until 3.8 - 3.5 billion years ago when the planet had cooled enough such that water was able to condense from the primitive atmosphere.
  2. The oldest known life forms were cyanobacteria (blue-green algae) whose fossils are preserved as tiny filaments in rocks about 3.5 b.y. old. Thus, the earth was already 1 billion years old before the first signs of life appeared.
  3. Once established, the early life forms continued as simple, unicellular bacteria and cyanobacteria over the next 1.5 b.y.
  4. The first multicellular animals did not appear in the fossil record until 600-700 m.y. ago, almost 3 b.y. after the first evidence of life.
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14
Q

What was the early life’s atmosphere like?

A

The earth’s present atmosphere is too oxidizing and corrosive to allow simple organic compounds to combine into more complex molecules. A reducing, oxygen poor environment is required.

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15
Q

What was the early life’s earth atmosphere like?

A

The earth’s present atmosphere is too oxidizing and corrosive to allow simple organic compounds to combine into more complex molecules. A reducing, oxygen poor environment is required.

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16
Q

When did the earth’s atmosphere become oxidizing?

A

The earth’s atmosphere 3.5 b.y. ago was rich in CO2, methane, ammonia and N2, but not free O2. There also was no ozone layer back then, so the earth was constantly bombarded by ultraviolet radiation that helped catalize the breaking of bonds in simple organic compounds to form more complex molecules.

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17
Q

What did Darwin suggest about early life’s atmosphere?

A

He suggested that organic compounds that were the precursors of life must have formed in a warm pond containing ammonia and phosphoric salts that were exposed to light, heat and electricity.

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18
Q

What is required to form C-H compounds? (Origin of life)

A

A reducing (anarobic) environment is required to form C-H compounds. Any free O2 would prevent this by immediately oxidizing carbon to CO2 or CO32+

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19
Q

What organic compounds were formed in the Urey-Miller experiment?

A

The organic compounds produced included cyanide (HCN), formaldehyde (H2CO) and small quantities of four amino acids. Later experiments produced the 12 most common amino acids of the 20 known to occur in life.

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20
Q

From fossil evidence, what are the two groups of early life on earth?

A

The oldest fossils show that life had already split into two groups by 3.5 b.y. ago. One group, the Eubacteria, include true bacteria plus cyanobacteria. The other group comprised the Archaebacteria which can live in extremely hot, anoxic water and include microbes that feed off sulfur compounds or methane.

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21
Q

When did Eukaryotes appear on earth? And what might have caused their appearance?

A

By 1.8 b.y. ago, atmospheric oxygen released from photosynthesis of cyanobacteria reached 1% of the present level.

Aeraobic bacteria developed while anaerobic bacteria sought niches within reduced environments. This was cyst stage of early eukaryotic algae.Eukaryotes may have evolved from earlier colonies of prokaryotes formed through symbiosis of both archae- and eubacteria beginning around 1.75 billion years ago.

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22
Q

Anabolism

A

These reactions occur by dehydration synthesis, removing a molecule of water to join two smaller molecules. e.g. polysaccharides, lipids, and proteins are constructed via dehydration synthesis. The bond between two amino acids is a peptide bond; two bound amino acids form a dipeptide, while many joined form a polypeptide.

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23
Q

Catabolism

A

Catabolism breaks apart larger molecules into their building blocks. These reactions occur by hydrolysis, wherein a molecule of water is inserted into
a polymer and split into two smaller molecules. The reactions of metabolism are often reversible.

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24
Q

Enzyme Action

A
  1. Enzymes are complex proteins that function to lower the activation energy of a reaction so it may proceed more rapidly.
  2. Enzymes work in small quantities and are recycled by the cell.
  3. Each enzyme is specific, acting on only one kind of substrate.
  4. Active sites on the enzyme combine with the substrate and a reaction occurs.
  5. The speed of enzymatic reactions depends on the number of enzyme and substrate molecules available.
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25
Q

Factors That Alter Enzymes

A

Enzymes (proteins) can be denatured by heat, pH extremes, chemicals, electricity, radiation, and by other causes.

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26
Q

Release of Chemical Energy

A
  1. Release of chemical energy in the cell often occurs through the oxidation of glucose.
  2. Burning glucose requires energy to begin the process.
  3. The end-products of these reactions are heat as well as stored energy.
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27
Q

Anaerobic Respiration

A
  1. The first part of cellular respiration is the splitting of 6-C glucose that occurs through a series enzyme-catalyzed steps.
  2. The result is two 3-C molecules of pyruvate.
  3. Glycolysis occurs in the cytosol and does not require oxygen (is anaerobic).
  4. Energy from ATP is used to start the process but there is a net gain of energy as result.
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28
Q

Aerobic Respiration

A
  1. Oxygen is needed for aerobic respiration, which occurs within the mitochondria.
  2. There is a much greater gain of ATP molecules from aerobic respiration.
  3. The final products of glucose oxidation are carbon dioxide, water, and energy.
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29
Q

ATP Molecules from cellular repiration

A
  1. Up to 38 molecules of ATP are produced for each molecule of glucose oxidized.
  2. ATP molecules contain three phosphates in a chain.
  3. Energy is stored in the last phosphate bond.
  4. Energy is stored while converting ADP to ATP; when energy is released, ATP becomes ADP, ready to be regenerated into ATP.
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30
Q

What is a a metabolic pathway?

A

A sequence of enzyme-controlled reactions.

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31
Q

Where does the first phase of cellular respiration occur?

A

In the cytosol and is anaerobic. Glucose is split into two molecules of pyruvic acid.

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32
Q

What is the second phase of carbohydrate breakdown?

A

pyruvic acid is oxidized to an acetyl group, combines with coenzyme A, and is carried into the mitochondrion.

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33
Q

What are the general steps in lipid metabolism?

A
  1. Lipolysis is carried out by lipases.
  2. Once freed from glycerol, free fatty acids can enter blood and muscle fiber by diffusion.
  3. Beta oxidation splits long carbon chains of the fatty acid into acetyl CoA, which can eventually enter the TCA cycle.
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34
Q

Briefly, what are the steps in β-oxidation (lipolysis of free fatty acids)? Hint: 4 steps.

A
  1. Dehydrogenation by acyl-CoA dehydrogenase in the mitochondria of a cell, yielding 1 FADH2.
  2. Hydration by enoyl-CoA hydratase
  3. Dehydrogenation by 3-hydroxyacyl-CoA dehydrogenase, yielding 1 NADH
  4. Cleavage by thiolase, yielding 1 acetyl-CoA and a fatty acid that has now been shortened by 2 carbons (acyl-CoA)
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35
Q

Where do micro tubules originate from?

A

They originate from basal bodies or centrioles (MYOC)

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36
Q

What the features of a plasma membrane?

A
  1. Has a double phospholipid membrane (phospholipid bilayer)
  2. selective permeability: only small, uncharged, polar molecules (such as H2O) and hydrophobic molecules (non polar like O2, CO2, and hydrocarbons) can pass freely across the membrane. Large polar molecules (e.g. glucose) and ions are impermeable.
  3. contains proteins (peripheral and integral)
  4. contains cholesterol.
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37
Q

What is a Channel protein?

A

Provide open passageways through the membrane for certain hydrophilic e.g. large charged molecules. Aquaporins are channel proteins which increases the passage rate of water.

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38
Q

What is an Ion channel?

A

Allow the passage of ions across the membrane. In nerve and muscle cells, ion channels called “gated channels” open and close in response to specific chemical or electrical stimuli to allow the passage of specific ions, such as Na and K.

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39
Q

What is a Carrier protein?

A

bind to specific molecules, which are then transferred across the membrane after the carrier protein undergoes a change of shape. The passage of glucose in a cell is by a carrier protein.

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40
Q

What is a Transport protein?

A

Use energy (ATP) to transport materials across the membrane. When energy is used for this purpose, the materials are said to be actively transported, and the process is called “active transport”. The “sodium-potassium pump” for e.g. uses ATP to maintain higher concentrations of sodium and potassium on opposite sides of the plasma membrane.

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41
Q

What is active transport?

A

Any transport across the plasma membrane that requires ATP/energy. e.g. sodium-potassium pump.

42
Q

What is a Recognition protein?

A

They are glycoproteins (proteins with short polysaccharide chains that extend away from the surface of the membrane. This is used for recognition between “self” cells and foreign cells. The difference between blood types, for e.g. are the result of recognition proteins on the surface of RBCs.

43
Q

What is a Receptor protein?

A

Provide binding sites for hormones or other trigger molecules. In response to the hormone or trigger molecule, a specific cell response is activated.

44
Q

What is a Adhesion protein?

A

Attach cells to neighboring cells or provide anchors for the internal filaments and tubules that give stability to the cell.

45
Q

What is a nucleosome?

A

Part of the DNA in the nucleus in which the DNA wraps around histones to organize the lengthy DAN and coiling it into bundles called nucleosomes.

46
Q

What are nucleoli?

A

Concentrations of DNA in the process of manufacturing the components of ribosomes.

47
Q

What is the structure of ribosomes?

A

They consist of RNA and protein. They have 2 subunits, labled 60S and 40S which move across the nuclear envelope through nuclear pores and into the cytoplasm where they are assembled into a single 80S ribosome.

48
Q

What is the function of rER?

A

Creating glycoproteins by attaching polysaccharide groups to polypeptides as they are assembled by the ribosomes.

49
Q

What is the function of smooth ER?

A

Synthesis of lipids, and steroid hormones, especially in cells that produce these substances for export from the cell. In liver cells, smooth ER is involved in the breakdown of toxins, drugs, and toxic by-products from cellular reactions.

50
Q

What is the function of Golgi apparatus?

A

Collect and modify proteins and lipids made in other areas of the cell and package them into vesicles. e.g. a glycopotein made and packaged into a vesicle by the ER may be transported to the Golgi apparatus, where it is modified as it passes through its chambers. At the outer side of the Golgi apparatus, the modified protein can be packaged into a secretory vesicle, which migrates to and merges with the plasma membrane, releasing its contents to the outside of the cell.

51
Q

What is the function of lysosomes?

A

Contain hydrolytic enzymes (that break down molecules by hydrolysis). They breakdown food, cellular debris, and foreign invaders (such as bacteria) and generally contribute to a recycling of cellular nutrients. A low pH (favorable to the activity of the the enzymes) is maintained inside the lysosomes. Any enzymes that might escapte from the lysosome remains inactive in the neutral pH of the cytosol.

52
Q

What is the function of peroxysomes?

A

Break down of hydrogen peroxide (forming water and oxygen), fatty acids, and amino acids. Peroxiysomes are common in liver and kidney cells, where they break down toxic substances. In plant cells, peroxisomes modify by-products of phtorespiration.

53
Q

What is the function of mitochondria?

A

Carries out aerobic respiration, in which ATP is obtained from carbs, fats, and occasionally proteins.

54
Q

What are microtubules made out of? And where are they found?

A

Made of the protein tubulin.

Found in the “spindle apparatus” which guides the movement of chromosomes during cell division, and flagella and cilia, structures that project from the plasma membrane to provide motility to the cell.

55
Q

What is the function of intermediate filaments?

A

Provide support for maintaining the shape of the cell.

56
Q

What are microfilaments made of? and where are they found?

A

Made of the protein actin (think action).

Are found in muscle cells and in cells that move by changing shape, such as phagocytes (WBCs). In plants, microfilaments promote the movement of cytoplasmic materials around the cell (cytoplasmic streaming).

57
Q

What are flagella and cilia structurally made of?

A

Microtubules arranged in a “9+2” array (nine pairs) of microtubules arranged in a circle surrounding a pair of microtubules.

Flagella (long, few, snake-like motion): propels sperm
Cilia (short, many, and move back and forth): sweeps debris in the repiratory tract

58
Q

What is a centrosome?

A

Its where the pair of centriols are housed. It’s the place where they exist.

59
Q

What do basal bodies do?

A

organize the development of flagella and cilia and anchor them to the cell surface.

60
Q

What are centriols and basal bodies made of?

A

They are made up of 9 triplets of microtubules arranged in a circle. Plant cells lack centriols, except for “lower” plants like mosses and ferns that have motile sperm have flagella and basal bodies.

61
Q

What is the function of the central vacules in plants?

A
  1. Storage of starch, nutrients, pigments, cellular waste, or toxins (like nicotin)
  2. Digestion, done by lysosomes in animal cells.
  3. Provides cell “growth” by absorbing water to allow expansion of the cell. Animal cells require nutrients to build macromolecules to generate growth.
  4. Renders larger area-to-volume ratio. Since the central vacuole occupies so much of the cell that the organelles and cytoplasm are flattened into a narrow area between the central vacuole and the plasma membrane.
62
Q

What is the main component of cell walls in plants?

A

Cellulose, a polysaccharide made from B-glucose.

63
Q

What is the man component of cell walls in fungi?

A

Chitin, a modified polysaccharide, differing from cellulose in that one of the hydroxyl groups is replaced by a group containing nitrogen.

64
Q

What are anchoring junctions, and where are they found? Give an example.

A

They are protein attachments found in animal cells. e.g. desmosomes. These provide structural stability to tissues. Desomosomes are associated with intermediate filaments that extend into the interior of the cell and serve to hold cellular structures together.

65
Q

What are tight junctions and where are they found?

A

They tightly stitch seams between animal cells. They completely encircle a cell to prevent the passage of material between cells. They are found in the intestinal tract, where the materials are required to pass through cells, rather than intracellular spaces, to enter the bloodstream.

66
Q

What are gap junctions and what is their function?

A

Cell junction proteins. They are made of proteins that prevent cytoplasmic proteins and nucleic acids of each cell from mixing, but allow the passage of ions and small molecules. Therefore, gap junctions allow communication between cells through the exchange of materials or through the transmission of electrical impulses.

67
Q

What are plasmodesmata (singular, plasmodesma)?

A

They are communication junctions between plant cells. A narrow tube of endoplasmic reticulum, surrounded by cytoplasm and the plasma membrane passes through the channel.

68
Q

What are the distinguishing features between plant and animal cells?

A
  1. the presence of cells walls, chloroplasts, and central vacuoles in plant cells and their absence in animal cells.
  2. the presence of centrioles and cholesterols in animal cells and their absence in plant cells.
69
Q

How do prokaryotic cells differ than Eukaryotic?

A
  1. Prokaryotes do not have a nucleus.
  2. The hereditary material in prokaryotes exists as a single “naked” DNA molecule without the proteins that are associated with the DNA in eukaryotic chromosomes.
  3. Prokaryotic ribosomes are smaller (70S, with 50S and 30S subunits) than those of eukaryoties (80S, with 60S and 40S subunits).
  4. The cell walls of bacteria, when present, are constructed from peptidoglycans, a polysaccharides, but not peptidoglycans, cellulose (as in plants), or chitin (as in fungi).
  5. Flagella in prokaroytes are not constructed of microtubules and are not enclosed by the plasma membrane.
70
Q

What is selective permeability?

A

Allowing only specific substances to pass.

71
Q

What is bulk flow?

A

The collective movement of substances (solvents or solutes) in the same direction in response to force or pressure. e.g. blood moving through a vlood vessel is an example of bulk flow.

72
Q

What is passive transport? What affects the rate of passive transport?

A

The movement of substances from a region of higher concentration to lower concentration (down a concentration gradient) and do not require the expenditure of energy.

Higher concentrations gradients, higher temperatures, and smaller particle size increases the rate of passive transport.

73
Q

What is simple diffusion?

A

(Passive transport). The net movement of substances from an area of higher concentration to an ara of lower concentration. This movement occurs as a result of random and constant motion characteristic of all molecules, motion that is independent from the motion of other molecules.

74
Q

What is osmosis?

A

Passive transport of water molecules across a selectively permeable membrane. (osmotic pressure= hydrostatic pressure).

75
Q

What is plasmolysis?

A

Passive transport of water out of a cell (by osmosis) that result in the collapse of the cell. Opposite of cell lysis. (happens in plant cells that has a central vacuole)

76
Q

What is cell lysis?

A

Passive transport of water molecules into the cell. The cell volume increases and extends and the cell bursts. (happens in animal cells that lack a cell wall).

77
Q

What is facilitated diffusion?

A

Passive transport of solutes or water through channel proteins or carrier proteins in the plasma membrane. e.g. aquaporins.

78
Q

What is counter current exchange with regards to diffusion?

A

Passive transport of substances between 2 regions in which substances are moving in bulk flow in opposite directions. e.g. direction of water flow through the gills of a fish is opposite to the flow of blood in the blood vessels. Diffusion of oxygen from water to blood is maximized because the relative motion of the molecules between the 2 regions is increased and because the concentration gradients between the 2 regions remain constant along their area of contact.

79
Q

What is the difference between active transport and passive transport?

A
  1. Active transport does not result from random movement of molecules. Active transport moves “specific” solutes across a membrane from “lower” to “higher” concentrations (opposite direction of diffusion).
  2. In Active transport “energy” is used, usually ATP.
80
Q

What are the different types of vesicular transport?

A
  1. Exocytosis
  2. Endocytosis:
  3. phagocytosis (“cellular eating”) occurs when “undissolved” material enters the cell. e.g. WBC which engulfs bacteria.
  4. Pinocytosis (“cellular drinking”) occurs when dissolved substances enter the cell.
  5. Receptor-mediated endocytosis: a form of pinocytosis, occurs when “specific molecules” in the fluid surrounding the cell bind to specialized receptors that concentrate in coated pits in the plasma membrane. Proteins that transport cholesterol in blood (LDL) and certain hormones target specific cells by receptor-mediated endocytosis.
81
Q

What is an excergonic and endergonic reactions? (with regards to delta G)

A

Exo: release of free energy. Delta G is negative.
Endo: addition/input of free energy. Most metabolic reactions are endergonic.

82
Q

What is substrate-level phosphorylation and when does it occur in the cell?

A

It is the transfer of a phosphate group AND its associated energy to ADP to form ATP. Occurs during glycolysis.

83
Q

What is oxidative phosphorylation?

A

The transfer of a phosphate group to ADP to form ATP, but the energy for the bond does not accompany the phosphate group. Instead, electrons give up energy for generating ATP during each step of a process (during electron transfer through electron carriers).

84
Q

What are the 2 basic steps in photosynthesis? What is used up in each step to generate energy?

A
  1. Noncyclic photophosphorylation and cyclic photophosphorylation: both use H2O and the energy in sunlight to generate ATP, NADPH, and O2.
  2. The Calvin cycle: uses CO2 and the energy in ATP and NADPH to make glucose.
85
Q

What are the 7 steps in noncylic photophosphorylation?

A
  1. PSII: electrons are energized by light.
  2. Primary electron acceptor: electrons from PSII passes to this center.
  3. Electron Transport Chain (ETC): is a series of proteins in the thylakoid membrane of the chloroplast that pass electrons from one carrier protein to the next.
  4. Phosphorylation: as the electrons move “down” the ETC, they lose energy. This lost energy is used to phosphorylate (oxidative phosphorylation).
  5. PSI: the ETC terminates with PSI (P700). Here the electrons are energized by sunlight and passed to a primary electron acceptor (different than the one associated with PSII).
  6. NADPH: the electrons pass to another electron transport chain and at the end of the chain, electrons combine with NADP+ and H+ to form NADPH.
  7. Splitting of water: the electrons associated with PSII are replaced when H2O is split into two electrons, 2H+ and 1/2O2. One of the H+ provides the H in NADPH, and the 1/2 O2 is released as gas.
86
Q

How many ATP molecules are used to convert 12 PGA to 12 G3P?

A

12 ATP

87
Q

How many ATPs are used to convert 10 G3P to 6 RuBP?

A

6 ATP

88
Q

In the Calvin cycle, 12 G3P is created, but only 10 of them are used up in the cycle. What happens to the other 2?

A

They are used to build glucose

89
Q

What is light-independent reactions, or dark reactions?

A

Calvin cycle reactions. The Calvin cycle does need light because it is dependent on ATP and NADPH which can be created only during photophosphorylation, which can occur only in light.

90
Q

What is the difference between the Calvin Cycle and the Krebs Cycle?

A

Krebs cycle:

  1. Aerobic respiration
  2. Takes place in the matrix of the mitochondria
  3. Leads to ATP synthesis
  4. Takes place in ALL organisms with aerobic repiration
  5. Carbon dioxide is produced
  6. The process does not take place without oxygen (#1)

Calvin Cycle:

  1. Part of the dark reaction of photosynthesis
  2. Takes place in the stroma of the chloroblasts
  3. ATP is consumed
  4. Takes place only in photosynthetic plants
  5. Carbon dioxide is used
  6. Does not demand the [direct] presence of oxygen
91
Q

What is photorespiration?

A

The fixation of oxygen. A process that is done by rubisco (the most common protein on Earth).

92
Q

What causes a ligand-gated ion receptor and voltage-gated-ion receptor responds to?

A

The first responds to a molecular signal, the second responds to voltage differences across the membrane.

93
Q

What type of receptors are vision, taste, airborne signals (odors and pheromones), hormones, neurotransmitters, and immune system activity?

A

G Protein-Coupled Receptor (GPCR).

94
Q

Which signaling pathway does glycogen breakdown use?

A

G Protein-Coupled Receptors in liver cells. Utilizes the cAMP signaling pathway. The signaling molecule is the hormone epinephrine.

95
Q

What type of signaling does insulin transduction use?

A

Insulin signaling is an example of RTK (Receptor Tyrosin Kinase)

96
Q

What are the cell cycle phases?

A
  1. G (0) phase
  2. G1 phase (growth)
  3. S phase (duplication of DNA and growth)
  4. G2 phase (preparation of cell division and growth
97
Q

What are the phases of mitosis?

A
  1. prophase
  2. metaphase
  3. anaphase
  4. telephase
98
Q

What happens during prophase?

A
  1. nucleoli disappear and chromatin condenses into chromosomes
  2. nuclear envelop breaks down
  3. the mitotic spindle is assembled
99
Q

What is the kinetochore?

A

a specialized region in the centromere. Moves microtubles.

100
Q

What happens during telephase?

A
  1. nuclear envelop is restored around each pole, forming two nuclei.
  2. the chromosomes disappear into chromatin and the nucleoli reappears.
101
Q

How does cytokinesis happen in plant cells?

A

Vesicles originating from Golgi bodies migrate to the plane between the 2 newly formed nuclei. The vesicles fuse to form a CELL PLATE which subsequently becomes the plasma membranes for the 2 daughter cells. Cell walls develop between the membranes.

102
Q

How does cytokinesis happen in animal cells?

A

Actin filaments (microfilaments) form a ring inside the plasma membrane between the tow newly forming nuclei. As the actin filaments shorten, they pull the plasma mmbrane into the center, dividing the cell into two daughter cells. The groove that form is called the CLEAVAGE FURROW.