gen bio 2 exam 2 Flashcards

(123 cards)

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
If a cation channel is open, where does Na+ flow?
Generally out to in, but highest concentration to lowest concentration
26
If a cation channel is open, where does Cl- flow?
it doesn't, cl- is an anion
27
What is metabolism?
All chemical reactions in the human body
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anabolic metabolism
- Synthetic metabolism - Small molecules combined to larger ones, energy stored in chemical bonds - required energy input
29
catabolic metabolism
- breaks down large molecules to small molecules - energy in the bonds is released
30
How does delta G effect the reversibility of reactions?
The higher the delta G the more difficult it is to reverse the reaction
31
What is the function of enzymes?
Make it easier for reactions to occur, lowers activation energy Often end with -ase
32
How do enzymes work?
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
33
how do temp/pH effect enzyme effectiveness?
There is an optimal pH and temperature, and the further you get from each optimum the effectiveness of the enzyme decreases
34
How does aspirin cyclooxygenase
Aspirin inhibits the enzyme to stop leukotrienes and protoglastins
35
Irreversible enzyme inhibition
when the inhibitor permanantly binds to an enzyme
36
Types of reversable inhibitors
A) competitive : inhibitor binds to the active site of the enzyme B) Non-competitive: the inhibitor binds to a different spot of the enzyme
37
Types of cofactors
Inorganic: Cu Fe Mg Zn Organic: porphyry in hemoglobin holding the iron
38
ATP structure
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
39
What is oxidation?
The loss of electrons
40
What is reduction?
The gain of electronsT
41
Two main electron shuttles
NAH+ and FADH+
42
NAD+ redox reaction
NAD+ (oxidized) -> NADH (reduction)
43
FADH redox reaction
FADH+ (oxidized) -> FADH2 (reduced)
44
What is the primary fuel source of the body to make ATP
Glucose is the primary fuel source of ATP production
45
What is glycolysis?
Breaking down of 1 glucose to 2 pyruvate molecules in the cytosol
46
Anaerobic respiration
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
47
Aerobic respiration
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
48
krebs cycle
acetate breaks down to 2 co2 and releases one high energy electron to the etc
49
Electron transport chain
etc leads to oxidative phosphorylization, ADP + P -> ATP, making 26-28 ATP with one glucsose. oxyen
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Glycolysis general
- Splitting of sugar in cytosol - 10 Steps - 1 Glucose -> 2 pyruvate
51
Glycolysis Steps
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
Fermentation
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
Pyruvate formula
C3H3O3
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Lactate formula
C3H5O3
55
Aerobic Respiration
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
Acetate formula
C2H3O2
57
Citric Acid Cycle
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
General Results from Citric Acid Cycle
+2 ATP +2 GTP +10 NADH +2 FADH2
59
Electron Transport Train
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
How are other monosaccharides incorporated into the krebs cycle?
converted to glucose/fructose, polysaccharides broken down into monomers
61
how are triglycerides catalyzed?
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
how are ptorines catalyzed
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
Cyanide
Prevents 4th cytochrome from give its electron to oxygen, backs up metabolism and causes cell to starve
64
Carbon Monoxide
Displaces oxygen in iron of hemoglobin Also does same thing as cyanide
65
What is photosynthesis
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
Absorption of light energy
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
Anatomy of a chloroplast
Outer membrane intermembrane space inner membrane stroma (cytosol) Grana (stack of thylakoids)
68
Photosystem 2
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
Photosystem 1
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
Where do chemical bond energy originate?
Glucose/food
71
Where is the carbon after... (carbon book-keeping) glycolysis fermentation aerobic respiration
pyruvate co2+ ethanol/lactate co2
72
Chemiosmotic mechanism n chloroplasts
Protons concentrated in thylakoids, chl680 ECT pumps protons into thylakoid,
73
Cell cycle is important for...
1) growth in multicellular organisms 2) repair lost/damaged cells 3) reproduction, sexual/asexual
74
Four events for cell division
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
How do prokaryotes divide?
binary fission
76
Chromatin
DNA and associated proteins
77
Chromatid
two chromatids make up a chromosome
78
Chromosome
condensed chromatin, histones condense it
79
Naked DNA
has no proteins
80
Nucleosome
histones and DNA around it, 4x2
81
linken DNA
DNA inbetween nucleosomes
82
Gene
DNA that codes for a protein
83
Differentiation
what genes a cell expresses
84
Interphase
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
G0
not in the cell cycle
86
M phase
mitotic phase Prophase Prometaphase metaphase Anaphase telophase
87
Anatomy of chromosome
2 sister chromatids connected by centromere, and has kinetochore proteins
88
Prophase
Chromatin to chromosome and centrosome migrates
89
Centrosome
2 centrioles connected forming a right angle, have microtubule fibers connecting to center
90
Prometaphase
nuclear envelope breaks down, chromosomes move to the mitotic spindles
91
Metaphase
Chromosomes aligned at the center of the cell, pulled on by mitotic spindles
92
Telophase
Chromatids pulled apart to opposite poles Chromosomes to chromatin Spindle apparatus dismanteld Cytokinesis
93
MTOC
Microtubule organizing center (centrosome)
94
Meiosis general
gonads 2 nuclear divisions 4 n cells creates genetic diversity
95
Meiosis 1
Synapse Cross Over Independant Assortment Segregation
96
Prophase 1
Chromatin -> chromosome centrosomes -> opposite poles Chromosomes pair up nuclear envelope dissapates chromosomes attatch to spindles Synapses -> tetrad formation -> crossing over
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Metaphase 1
homologous pairs align at equator of the cell independant assortment
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Anaphase 1
homologous pairs pulled away to poles (still 2 chromatids, segregation)
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Telophase 1
nuclear envelope rforms MTOC dissasembles chromsome -> chromatin cytokinesis follows
100
Interkinesis
stage between meiosis 1 +2
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Prophase 2
chromatin -> chromosome MTOC assembly Nuclear envelope dissipation chromosomes to MTOC
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Metaphase 2
Chromosomes align at equator of cell
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Anaphase 2
Homologous pairs puled apart, sister chromatids migrate to edge of cell
104
Telophase 2
MTOC disassembly nuclear envelope reforms chromosome -> chromatin 4 haploid cells (chromatids)
105
Cystic Fibrosis
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
LDL
Brings cholesterol to tissues
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HDL
Brings cholesterol to liver, then bile, then feces
108
Familia Hypercholesteremia
LL severe, causes nonfunctioning LDLR receptors Ll is mild ll is normal
109
Polygenic Inheritence
Inheritance based on two or more traits/loci
110
plerotrophy
single locus that affects multiple traits
111
Merton Syndrome
One locus mutations causes: - Thinness - Limb elongation - hyper mobility - lens discoloration - increase risk to heart disease
112
Penetrance
proportion of people with a genotype that express the expected phenotype example, 5% of people with huntingtons don't express the diease
113
Length of the human sex chromosomes
y - 25-40 loci x - 800 loci
114
Hemizygous
one pair of chromosomes, each is different
115
Why are autosomal recessive disorders more common than autosomal dominant?
Dominant less likely to pass on the gene
116
PKU
phenylketonuria - can't metabolize phenylalanine - build up this AA is toxic to neurons - not lethal, manageable
117
Sickle cell genotypes
AA - no SC Aa SC trait (mild) aa SC anemia (severe)
118
Tay Sachs
Loss of an enzyme that metabolizes glycolipids, build up in the brain and is lethal by 5 years old - not manageable
119
Non-disjunction
chromosomes fail to separate, and an aneuploidy is caused
120
3 examples of aneuploidy defects
Trisomy 21 (down syndrome) trisomy 18 (Edwards syndrome) trisomy 13 (Patau syndrome)
121
Klinefelter's Syndrome
XXY - Taller, low test - Some breast tissue - Low fertility Small testes some have no symptoms
122
Amniocentesis
Take up amitotic fluid through a needle, use it to make a culture of fetal cells and then do a karyotype
123
Chorionic Villus Sampling
A suction tube shoved up uterus, sucks up placental tissue and grows a culture of fetal cells to then karyotype