Exam 4- Chapter 6 Part 2 Flashcards

1
Q

What is the difference between anaerobic and aerobic respiration

A

anaerobic uses terminal electron acceptors other than oxygen and produces less ATP

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2
Q

Why does anaerobic respiration yield less ATP

A

Redox potential of electron acceptors are less positive than that of oxygen
The differential is not as large

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3
Q

Fermentation

A

like glycolysis but with extra steprs to recycle NAD+ by getting rid of electrons carried by NADH

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4
Q

Why do organisms ferment?

A

Do not encode genes to use ETC
Can use ETC sometimes but live in environments where terminal acceptor is not available

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5
Q

importance of fermentation

A

allows organisms to adjust to changes in their environment

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6
Q

Why does fermentation generate less energy than aerobic and anaerobic respiration?

A

does not use ETC
relies solely on glycolysis (substrate-level phosphorylation)
substrate is only partially oxidized

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7
Q

What is used as the electron acceptor in fermentation

A

endogenous acceptor
pyruvate or derivative

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8
Q

Respiration VS Non-Respiration

A

respiration invovles ETC and exogenous acceptor
non-respiration uses endogenous acceptor and no ETC

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9
Q

Homo-lactic acid fermentation

A

uses lactic acid dehydrogenase
generates 2 lactic acid and nets 2 ATP

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10
Q

What organisms carry our homo-lactic acid fermentation

A

Lactic acid bacteria (gram-positive microbes)

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11
Q

Hetero-lactic acid fermentation

A

Uses pentose phosphate pathway
generates both lactic acid and ethanol
nets 1 ATP

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12
Q

Penetose phosphate pathway

A

Energy investment phase yields a 5-carbon sugar which is then broken into a 3-carbon and a 2-carbon

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13
Q

What does 3-carbon lead to

A

broken down into lactic acid using pathway similar to Embden-meyerhof
1 ATP

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14
Q

What does 2-carbon lead to

A

Ethanol
purpose is to recycle carriers
no ATP generated

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15
Q

What organisms carry out hetero-lactic acid fermentation?

A

LAB Leuconostoc

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16
Q

Alcohol fermentation

A

Produces ethanol and CO2
Eventually comes to an end when the concentration of end products gets too high and kills organisms
Nets 2 ATP

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17
Q

What organisms carry out alcohol fermentation?

A

yeasts
some bacteria

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18
Q

Mixed acid fermentation

A

Different end products dependent on the acid

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19
Q

Why have mixed acid fermentation

A

many acids dont let the concentration of end products get too high and kill organisms

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20
Q

What organisms carry out mixed acid fermentation

A

several bacteria
fungi

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21
Q

What mixed acid fermentation processes have been adapted for commercial use?

A

acetone production
butanol production

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22
Q

Metabolism of polysaccharides

A

Partially broken down into smaller subunits by secreted enzymes outside the cell
Smaller subunits are broken down by the usual pathways in the cell

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23
Q

metabolism of Proteins/Amino acids

A

Protease breaks polypeptides into individual amino acids
Amino group is detached from individual amino acids leaving an organic acid
Organic acid is used in TCA

24
Q

metabolism of Lipids

A

Lipases separate fatty acid tails off of glycerol
Beta-oxidation pathway cleaves fatty acids into smaller chunks at the beta carbon
Chunks are sent to TCA

25
Why is metabolism of lipids tightly regulated
Don't want to catabolize the cells' lipids, as they are only found in the plasma membrane If these lipids are catalyzed the cell wont be a cell anymore
26
Chemolithotrophy
Electrons are released from an inorganic molecule energy source, then transferred to the terminal electron acceptor in ETC
27
Why does chemolithotrophy generate less ATP
no substrate phosphorylation electron carriers are more positive than organic molecules- smaller differential
28
T/F chemolithotrophy makes less ATP than fermentation
FALSE
29
Photophosphorylation
ATP synthesis and the light reaction used in conjunction with ATP Light reaction captures light and uses it to create PMF
30
Site of light capture in eukarya
photosystem in specialized thylakoid cells Light is harvested by pigments
31
What pigments to plants use
Chlorophyll A and B
32
What pigments do cyanobacteria use?
chlorophyll a only
33
what are photosystems composed of
numerous antennae that absorb light energy
34
How do photosystems work?
light energy is passed to eelctron in reaction center An electron is sent onto the electron transport system
35
Anoxygenic photosynthesis
H2O is used as an electron source and O2 is not produced Only 1 photosystem used
36
Why is O2 not produced in anoxygenic photosynthesis
wavelength does not have enough energy
37
What is used to generate reducing power for anoxygenic photosynthesis
bacteriochlorophylls
38
What organisms carry out anoxygenic photosynthesis
green bacteria phototrophic puple bacteria heliobacteria
39
oxygenic photosynthesis
oxygen is generated and released into environment as a byproduct because H2O is split to donate electrons uses both photosystems
40
What organisms carry out oxygenic photosynthesis
photosynthetic eukaryotes cyanobacteria
41
chlorophylls
major light absorbing pigments different chlorophylls have different absorption peaks
42
Accessory pigments
transfer light energy to chlorophylls absorb different wavelengths of light than chlorophylls
43
Examples of accessory pigments
carotenoids Phycobiliproteins
44
Bacteriorhodopsin-based phototrophy
invovles bacteriorhodopsin to generate a proton motor force still uses ATP synthase Does not include ETC
45
What is an example of a bacteriorhodopsin-based phototroph
Halobacterium
46
WHy does bacteriorhodopsin-based phototrophy still exist
archaea live in extreme environments and ont have substrates to use anything else
47
Anabolism
energy from catabolism is used for biosynthetic pathways using carbon source and inorganic molecules to synthesize new organelles and cells
48
How do cells form macromolecules
generate precursors from major metabolic pathways utilize precursors to build common building blocks uses building blocks to form polymers and macromolecules
49
Turnover
continual degradation and resynthesis of cellular constituents by nongrowning cells
50
Why is metabolism carefully regulated
for the rate of turnover to be balanced by the rate of synthesis
51
Biosynthesis efficiency
1. large molecules are made from small molecules 2. many enzymes do double duty (amphibolic) 3. some enzymes function in one direction only 4. anabolic pathways are irreversible (biosynthesis is coupled with ATP) 5. catabolism and anabolism are physically separated 6. catabolism and anabolism use different cofactors 7. Large assemblies form spontaneously from macromolecules by self-assembly
52
Precursor metabolites
anything used to build precursors critical step in anabolism
53
How are carbon skeletons used
precursor metabolites starting substrates for biosynthetic pathways
54
Two pathways for biosynthesis
Salvage pathway De novo synthesis
55
Salvage pathway
take things they find in environment and build onto it
56
De novo synthesis
build any molecules they need from scratch