gen bio 2 exam 2 Flashcards

1
Q

Channel Proteins

A

Pore allowing for diffusion with aqueous interior
Has both open and closed states
Still need/follow the concentration gradient

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2
Q

Gating

A

Is the channel protein open/closed

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3
Q

Selectivity

A

What is let through the channel protein

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4
Q

Ligand Gated

A

A ligand is what opens the channel protein

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5
Q

Voltage gated

A

Opens the channel protein by votage differences, usually -70 mV inside cell, 30 outisde

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6
Q

Mechanically gated

A

Channel proteins open when they are stretched

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7
Q

Aquaporins

A

Channel proteins for water

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8
Q

Carrier Proteins

A

Bind a molecule, and bring it to the other side of a membrane

Random switches between its 3 states

Passive

Need concentration gradient

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9
Q

Transport Maximum

A

Carrier proteins are not infinite, and can not move infinite molecules

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10
Q

Pump

A

Active
Integral membrane protein
No concentration gradient is required

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11
Q

Sodium Potassium Pump

A

3 Sodium out (15 mM inside, 150 mM out)
2 Potassium in (140 mM in, 5 mM out)
1 ATP uses

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12
Q

Exocytosis

A

Stuff in a vesicle is sent to the cell wall where the membranes connect, and lumen contents deposited into extracellular fluid

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13
Q

Endocytosis

A

Phagocytosis
Pinocytosis
Receptor mediated endocytosis

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14
Q

Phagocytosis

A

“Cell Eating”, cell evaginates around an item, and cell membrane extends out towards around it to take it in as a vesicle

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15
Q

Pinocytosis

A

“Cell Drinking”, exocytosis but just extracellular fluid no item

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16
Q

Receptor mediated endocytosis

A

LDL connect to LDLRs, and when enough of them are cluster this triggers coating proteins attached to intracellular parts of LDLRs to cause evagination of the cell membrane

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17
Q

Digestion of vesicles

A

Lysosomes merge with the vesicles, and causes the LDLs to be removed from the LDLRs and then the cholesterol is broken down

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18
Q

Energy

A

Physics - capacity to do work
Biochem - capacity to cause change

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19
Q

Potential Energy vs Kinetic Energy

A

middle school science moment

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20
Q

1st + 2nd law of thermodynamics

A

1: Energy can not be created/destroyed, only change forms
2: Energy becomes more unstable/unusable as it changes forms

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21
Q

Entropy

A

increases over time, can be thought of as disorder/unusable energy in a system

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22
Q

H = G + TS

A

Total energy = Usable Energy + (Time*Unusable Energy/Entropy)

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23
Q

delta G

A

dG = G-products - G-reactants
if dG > 0, energy absorbed
if dG < 0, energy released

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24
Q

Exergonic vs endergonic

A

Exer = release, ender = absorb

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25
Q

If a cation channel is open, where does Na+ flow?

A

Generally out to in, but highest concentration to lowest concentration

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26
Q

If a cation channel is open, where does Cl- flow?

A

it doesn’t, cl- is an anion

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27
Q

What is metabolism?

A

All chemical reactions in the human body

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28
Q

anabolic metabolism

A
  • Synthetic metabolism
  • Small molecules combined to larger ones, energy stored in chemical bonds
  • required energy input
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29
Q

catabolic metabolism

A
  • breaks down large molecules to small molecules
  • energy in the bonds is released
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30
Q

How does delta G effect the reversibility of reactions?

A

The higher the delta G the more difficult it is to reverse the reaction

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31
Q

What is the function of enzymes?

A

Make it easier for reactions to occur, lowers activation energy
Often end with -ase

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32
Q

How do enzymes work?

A

1) Proximity Reorientation
- brings substrates together in better position o make reaction easier
2) Physical strain
- makes substrate more unstable
3) chemical charge changes
- changing chemical properties of the substrate makes more unstable

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33
Q

how do temp/pH effect enzyme effectiveness?

A

There is an optimal pH and temperature, and the further you get from each optimum the effectiveness of the enzyme decreases

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34
Q

How does aspirin cyclooxygenase

A

Aspirin inhibits the enzyme to stop leukotrienes and protoglastins

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35
Q

Irreversible enzyme inhibition

A

when the inhibitor permanantly binds to an enzyme

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36
Q

Types of reversable inhibitors

A

A) competitive : inhibitor binds to the active site of the enzyme
B) Non-competitive: the inhibitor binds to a different spot of the enzyme

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37
Q

Types of cofactors

A

Inorganic: Cu Fe Mg Zn
Organic: porphyry in hemoglobin holding the iron

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38
Q

ATP structure

A

An adenine (nitrogenous base purine, 2 rings) attatched to a ribose sugar 95c) at carbon 1’, and the phosphates attatch at carbon 5 w/ high energy bonds

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39
Q

What is oxidation?

A

The loss of electrons

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40
Q

What is reduction?

A

The gain of electronsT

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41
Q

Two main electron shuttles

A

NAH+ and FADH+

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42
Q

NAD+ redox reaction

A

NAD+ (oxidized) -> NADH (reduction)

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43
Q

FADH redox reaction

A

FADH+ (oxidized) -> FADH2 (reduced)

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44
Q

What is the primary fuel source of the body to make ATP

A

Glucose is the primary fuel source of ATP production

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45
Q

What is glycolysis?

A

Breaking down of 1 glucose to 2 pyruvate molecules in the cytosol

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46
Q

Anaerobic respiration

A

occurs when o2 levels or enzyme levels are low

Either produces lactate in rbc, muscles, or bacteria (3c)

Or yeast/bacteria produces ethanol and c02

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47
Q

Aerobic respiration

A

occurs when o2 levels and enzyme levels are high

initially starts with breaking down of pyruvate to acetate (2c) and releasing a co2

krebs cycles

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48
Q

krebs cycle

A

acetate breaks down to 2 co2 and releases one high energy electron to the etc

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49
Q

Electron transport chain

A

etc leads to oxidative phosphorylization, ADP + P -> ATP, making 26-28 ATP with one glucsose. oxyen

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50
Q

Glycolysis general

A
  • Splitting of sugar in cytosol
  • 10 Steps
  • 1 Glucose -> 2 pyruvate
51
Q

Glycolysis Steps

A

1) Glucose (6c) -> Glucose 6-Phosphate (ATP-ADP)

2) Glucose 6-Phosphate -> Fructose 6-Phosphate

3)Fructose 6-Phosphate -> Fructose 1,6-Phosphate (ATP - ADP)

4) Fructose 1,6-Phospate -> Dihydroxyacetate Phosphate + Glyceraldehyde-3 Phosphate (DHAP racemizes to G3P)

5)…. NAD+ gets reduced (twice) and ADP->ATP (twice)

ends with 2 pyruvate made
….H.O.O
H-C-C-C-O -
….H

52
Q

Fermentation

A

Pyruvate turns into
1) Lactate
….H.H.O
H-C-C-C-O-
….H.H
or…
2) Ethanol and CO2

and the NADH formed in glycolysis turned back to NAD+

53
Q

Pyruvate formula

54
Q

Lactate formula

55
Q

Aerobic Respiration

A

1) Pyruvate sent through into the mitochondrial matrix, active transport (NAD+ -> NADH, and CO2 lost)

2) Pyruvate is now acetate, is combined with Acetyl CoA to make Acetyl CoA

3) Acetyl CoA combined with Oxaloacetate (4c) to make Citrate (6c)

56
Q

Acetate formula

57
Q

Citric Acid Cycle

A

1) Citrate to 5c molecule (Co2 lost, NAD+ -> NADH)

2) 5c molecule to 4c molecule (NAD+ ->NADH, and CO2)

3) GDP -> GTP

4) FAD+ -> FADH

5) H2O lost

6) NAD+ -> NADH, results in Oxaloacetate, reused in aerobic respiration

this all happens twice per glucose molecule, 2 pyruvates

58
Q

General Results from Citric Acid Cycle

A

+2 ATP
+2 GTP
+10 NADH
+2 FADH2

59
Q

Electron Transport Train

A

NADH gets oxidized, Cytochrome 1 gets reduced and uses some of a high electrons energy to pump 1 hydrogen into the intermembrane space.

Cytochrome (CTC) gives the electron to CTC 2, passes it to CTC 3 and CTC 3 pumps another hydrogen ion into the intermembrane space.

CTC 3 gives the electron to CTC4, pumps another H+ into the intermembrane space, CTC 4 gives 2 electrons to an O to make H2O (metabolic water)

ATP Synthase complex uses the electrochemical gradient to make 26-28 ATP, is about 38% efficient in turning glucose energy to ATP energy

60
Q

How are other monosaccharides incorporated into the krebs cycle?

A

converted to glucose/fructose, polysaccharides broken down into monomers

61
Q

how are triglycerides catalyzed?

A

Broken down to glycerol and fatty acids, glycerol -> GTP and fatty acids sent to krebs cycle in 2 carbon intervals ( linoleic and linolenic are 2 essential fatty acids)

62
Q

how are ptorines catalyzed

A

broken down to amino acids, amine groups are removed and the r-group determines which step of the krebs cycle they are integrated at (we can only synthesize 12/20 amino acids)

63
Q

Cyanide

A

Prevents 4th cytochrome from give its electron to oxygen, backs up metabolism and causes cell to starve

64
Q

Carbon Monoxide

A

Displaces oxygen in iron of hemoglobin
Also does same thing as cyanide

65
Q

What is photosynthesis

A

metabolic process of taking 6co2 and 6h2o + photons -> c6h12o6 and 6o2

two parts, light dependant (making of NADPH and ATP)
and light independant (uses ATP and NADPH to fix carbon)

66
Q

Absorption of light energy

A

A photon excites an electron bringing it up one valence shells, where if will de-excite and fall, releasing energy (in this case releasing another photon)

67
Q

Anatomy of a chloroplast

A

Outer membrane
intermembrane space
inner membrane
stroma (cytosol)
Grana (stack of thylakoids)

68
Q

Photosystem 2

A

Chlorophyll 680 gets an excite electron from a photon, Chl 680 loses an electron to the ETC, and this makes ATP and this electron is given to reduce Chl 700 (water is the oxidized to reduce Chl 680)

69
Q

Photosystem 1

A

Chl 700 is excited by a photon, except its excited electron does to reduce NADP+ -> NADPH, Chl 700 is reduced by electron from ETC. NADPH + ATP from PS-2 go to light independent reactions

70
Q

Where do chemical bond energy originate?

A

Glucose/food

71
Q

Where is the carbon after… (carbon book-keeping)
glycolysis
fermentation
aerobic respiration

A

pyruvate
co2+ ethanol/lactate
co2

72
Q

Chemiosmotic mechanism n chloroplasts

A

Protons concentrated in thylakoids, chl680 ECT pumps protons into thylakoid,

73
Q

Cell cycle is important for…

A

1) growth in multicellular organisms
2) repair lost/damaged cells
3) reproduction, sexual/asexual

74
Q

Four events for cell division

A

1) signal to reproduce, ligand or favorable environment
2) replication of genetic material
3) segregation of genetic material to daughter cells
4) cytokinesis, the division of the cell

75
Q

How do prokaryotes divide?

A

binary fission

76
Q

Chromatin

A

DNA and associated proteins

77
Q

Chromatid

A

two chromatids make up a chromosome

78
Q

Chromosome

A

condensed chromatin, histones condense it

79
Q

Naked DNA

A

has no proteins

80
Q

Nucleosome

A

histones and DNA around it, 4x2

81
Q

linken DNA

A

DNA inbetween nucleosomes

82
Q

Gene

A

DNA that codes for a protein

83
Q

Differentiation

A

what genes a cell expresses

84
Q

Interphase

A

G1: Gap 1, cell lives normally
S: synthesis, duplication of DNA
G2: prep to divide, and enlarges, accumulates nutrients
S + G2 centrosome duplicates and migrates to pole

85
Q

G0

A

not in the cell cycle

86
Q

M phase

A

mitotic phase
Prophase
Prometaphase
metaphase
Anaphase
telophase

87
Q

Anatomy of chromosome

A

2 sister chromatids connected by centromere, and has kinetochore proteins

88
Q

Prophase

A

Chromatin to chromosome and centrosome migrates

89
Q

Centrosome

A

2 centrioles connected forming a right angle, have microtubule fibers connecting to center

90
Q

Prometaphase

A

nuclear envelope breaks down, chromosomes move to the mitotic spindles

91
Q

Metaphase

A

Chromosomes aligned at the center of the cell, pulled on by mitotic spindles

92
Q

Telophase

A

Chromatids pulled apart to opposite poles
Chromosomes to chromatin
Spindle apparatus dismanteld
Cytokinesis

93
Q

MTOC

A

Microtubule organizing center (centrosome)

94
Q

Meiosis general

A

gonads
2 nuclear divisions
4 n cells
creates genetic diversity

95
Q

Meiosis 1

A

Synapse
Cross Over
Independant Assortment
Segregation

96
Q

Prophase 1

A

Chromatin -> chromosome
centrosomes -> opposite poles
Chromosomes pair up
nuclear envelope dissapates
chromosomes attatch to spindles
Synapses -> tetrad formation -> crossing over

97
Q

Metaphase 1

A

homologous pairs align at equator of the cell
independant assortment

98
Q

Anaphase 1

A

homologous pairs pulled away to poles (still 2 chromatids, segregation)

99
Q

Telophase 1

A

nuclear envelope rforms
MTOC dissasembles
chromsome -> chromatin
cytokinesis follows

100
Q

Interkinesis

A

stage between meiosis 1 +2

101
Q

Prophase 2

A

chromatin -> chromosome
MTOC assembly
Nuclear envelope dissipation
chromosomes to MTOC

102
Q

Metaphase 2

A

Chromosomes align at equator of cell

103
Q

Anaphase 2

A

Homologous pairs puled apart, sister chromatids migrate to edge of cell

104
Q

Telophase 2

A

MTOC disassembly
nuclear envelope reforms
chromosome -> chromatin
4 haploid cells (chromatids)

105
Q

Cystic Fibrosis

A

A mutation that causes the chloride transporter in simple columnar epilthelium of air passageways to not work, preventing osmosis, low water content in mucus, high mucin protien concentration makign the mucous exxtremely thick

106
Q

LDL

A

Brings cholesterol to tissues

107
Q

HDL

A

Brings cholesterol to liver, then bile, then feces

108
Q

Familia Hypercholesteremia

A

LL severe, causes nonfunctioning LDLR receptors
Ll is mild
ll is normal

109
Q

Polygenic Inheritence

A

Inheritance based on two or more traits/loci

110
Q

plerotrophy

A

single locus that affects multiple traits

111
Q

Merton Syndrome

A

One locus mutations causes:
- Thinness
- Limb elongation
- hyper mobility
- lens discoloration
- increase risk to heart disease

112
Q

Penetrance

A

proportion of people with a genotype that express the expected phenotype
example, 5% of people with huntingtons don’t express the diease

113
Q

Length of the human sex chromosomes

A

y - 25-40 loci
x - 800 loci

114
Q

Hemizygous

A

one pair of chromosomes, each is different

115
Q

Why are autosomal recessive disorders more common than autosomal dominant?

A

Dominant less likely to pass on the gene

116
Q

PKU

A

phenylketonuria
- can’t metabolize phenylalanine
- build up this AA is toxic to neurons
- not lethal, manageable

117
Q

Sickle cell genotypes

A

AA - no SC
Aa SC trait (mild)
aa SC anemia (severe)

118
Q

Tay Sachs

A

Loss of an enzyme that metabolizes glycolipids, build up in the brain and is lethal by 5 years old
- not manageable

119
Q

Non-disjunction

A

chromosomes fail to separate, and an aneuploidy is caused

120
Q

3 examples of aneuploidy defects

A

Trisomy 21 (down syndrome)
trisomy 18 (Edwards syndrome)
trisomy 13 (Patau syndrome)

121
Q

Klinefelter’s Syndrome

A

XXY
- Taller, low test
- Some breast tissue
- Low fertility
Small testes
some have no symptoms

122
Q

Amniocentesis

A

Take up amitotic fluid through a needle, use it to make a culture of fetal cells and then do a karyotype

123
Q

Chorionic Villus Sampling

A

A suction tube shoved up uterus, sucks up placental tissue and grows a culture of fetal cells to then karyotype