Use LEFT and RIGHT arrow keys to navigate between flashcards;
Use UP and DOWN arrow keys to flip the card;
H to show hint;
A reads text to speech;
145 Cards in this Set
- Front
- Back
Metabolism
|
all reactions in body that involve energy transformations
|
|
Metabolism divided into
|
-catabolism
-anabolism |
|
Catabolism
|
breaks down molecules and releases energy
-is the primary source of energy for making ATP |
|
Anabolism
|
makes larger molecules and requires energy
-source of body's large energy-storage compunds |
|
Aerobic cellular respiration
|
series of chemical reactions whereby glucose (or other moelecues) and oxygen are converted into carbon dioxide and water in the process of making adenosine triphosphate (ATP)
|
|
1 glucose molecule can be made into
|
30-38 ATP molecules
|
|
Anaerobic cellular respiration
|
series of chemical reactions whereby glucose (no oxygen) is converted into carbon dioxide and water in the process of making ATP
|
|
1 glucose molecule can be made into
|
2 ATP molecules
|
|
Both aerobic and anaerobic respirations begin with
|
glycolysis
|
|
Glycolysis
|
metabolic pathway by which glucose (C6H12O6) is converted to 2 pyruvates
|
|
Pyruvates
|
-pyruvic acid
(C3H4O3) -occurs in cytoplasm -does not require oxygen |
|
Glycolysis net equation
|
glucose+2NAD+2ADP+2Pi> 2pyruvates+2NADH+2ATP
|
|
NAD
|
Nicotinamide adenine dinucleotide
|
|
NAD carries
|
electrons
|
|
Glycolysis prodouces net gain of
|
2ATPs and 2NADHs
|
|
Glycolysis involves _ indivual steps
|
9
|
|
Step 1 glycolysis
|
-Glucose must be activated with ATP (phosphorylation) before energy can be ontained
-phosphorylation traps glucose inside cell by forming glucose 6-phosphate |
|
Step 2 glycolysis
|
glucose 6-phosphate is converted to its isomer fructose 6-phosphate
|
|
Step 3 glycolysis
|
another ATP is used to form fructose 1, 6-biphosphate
|
|
Step 4 glycolysis
|
fructose 1, 6 -biphosphate is converted into two 3C molecules, 3-phosphoglyceraldehyde
|
|
Step 5 glycolysis
|
2 pairs of hydrogens are removed and added to NAD forming NADH and 1,3-biphosphoglyceric acid
|
|
Step 6 glycolysis
|
a phosphate is removed from each 1, 3-biphosphoglyceric acid forming 2 ATP and 3-phosphoglyceric acid
|
|
Step 7 Glycolysis
|
3-phosphoglyceric acid is changed to the isomer 2-phosphoglyceric acid
|
|
Step 8 Glycolysis
|
2-phosphoglyceric acid is changed to the isomer phosphoenolpyruvic acid
|
|
Step 9 glycolysis
|
last phosphate is removed from phosphoenolpyruvic acid forming 2 more ATP and pyruvic acid
-Net gain of 2ATP |
|
To avoid end-product inhibition,
|
there must be sufficient NAD
-NADHs produced in glycolysis need to give Hs away |
|
Anaerobic respiration aka
|
lactic acid fermentation
|
|
Lactic acid is formed when
|
NADH gives its Hs to pyruvate (in absense of O2)
|
|
Lactic acid is the cause for
|
-muscle fatigue
-cell death in excessive high concentrations |
|
RBCs dont' have _ so they use _
|
mitochondria, lactic acid pathway
|
|
Step 5 glycolysis
|
2 pairs of hydrogens are removed and added to NAD forming NADH and 1,3-biphosphoglyceric acid
|
|
Step 6 glycolysis
|
a phosphate is removed from each 1, 3-biphosphoglyceric acid forming 2 ATP and 3-phosphoglyceric acid
|
|
Step 7 Glycolysis
|
3-phosphoglyceric acid is changed to the isomer 2-phosphoglyceric acid
|
|
Step 8 Glycolysis
|
2-phosphoglyceric acid is changed to the isomer phosphoenolpyruvic acid
|
|
Step 9 glycolysis
|
last phosphate is removed from phosphoenolpyruvic acid forming 2 more ATP and pyruvic acid
-Net gain of 2ATP |
|
To avoid end-product inhibition,
|
there must be sufficient NAD
-NADHs produced in glycolysis need to give Hs away |
|
Anaerobic respiration aka
|
lactic acid fermentation
|
|
Lactic acid is formed when
|
NADH gives its Hs to pyruvate (in absense of O2)
|
|
Lactic acid is the cause for
|
-muscle fatigue
-cell death in excessive high concentrations |
|
RBCs dont' have _ so they use _
|
mitochondria, lactic acid pathway
|
|
Why can't cells store a lot of seperate glucose molecules?
|
because the osmotic pressure would draw large amounts of water into cells, instead some organs store glucose as glycogen
|
|
Glycongenesis
|
process of polymerizing glucose into glycogen
|
|
Step 1 glycongenesis
|
glucose is converted to glucose 6-phosphate
|
|
Step 2 glycongenesis
|
glucose 6-phosphate is then converted to its isomer, glucose 1-phosphate
|
|
Step 3 glycongenesis
|
enzyme glycogen synthase removes phosphates as it polymerizes glucose to form glycogen
|
|
Glycongenolysis
|
conversion of glycogen to glucose 6-phosphate
|
|
what enzyme removes phosphate to free glucose?
|
glucose 6-phosphatase from liver to blood
|
|
Step 1 glycogenolysis
|
glycogen is catalyzed by glycogen phophorylase
|
|
Step 2 glycogenolysis
|
glucose 1-phosphate is formed
|
|
Step 3 glycogenolysis
|
glucose 6-phosphate is converted
-can be used for glycolysis by skeletal muscle |
|
Cori cycle
|
2-way traffic between skeletal muscle and the liver
|
|
Most of _ produced in _ respiration is eliminated by _respiration where is made into _ and _.
|
lactic acid, anaerobic, aerobic, CO2 and H2O
|
|
Lactic acid dehydrogenase converts
|
lactic acid to pyruvic acid to glucose 6-phosphate
|
|
Some of the _ produced in _ goes to _ where it is converted back to _
|
lactic acid, anaerobic, liver pyruvate
|
|
In cori cycle, _ can then be converted to _ or _
|
glucose 6-phosphate, free glucose, glycogen
|
|
Aerobic respiration is preceded by
|
glycolysis (2 pyruvates, 2
ATP, 2 NADH) |
|
what is the end product of aerobic respiration?
|
CO2, H2O and ATP
|
|
Step 1 Aerobic Respiration
|
pyruvic acid leaves the cytoplasm and enters the mitochondria
|
|
Step 2 Aerobic respiration
|
CO2 is enzymatically removed from each 3-carbon long pyruvic acid to form a 2-carbon long acetic acid
|
|
Step 3 Aerobic respiration
|
the acetic acid is combined with a coenzyme, Coenzyme A= Acetyl conenzyme A
|
|
acetyl CoA=_ C molecule
|
2 carbon molecule
|
|
1 pyruvic acid converted into _ molecules of _ and _ of _
|
one, acetylCoA, one, CO2
|
|
1 glucose converted into _ molecules of _ and _ of _
|
two, acetylCoA, two, CO2
|
|
Oxygen derive in CO2 is derived from _ not from _ gas
|
pyruvic acid, oxygen
|
|
Energy in _is extracted during aerobic respiration in _
|
acetylCoA, mitochondria
|
|
CO2 is goes to
|
the lungs
|
|
During glycolysis, 1 glucose>
|
2 pyruvate
|
|
1 pyruvate (3 carbon)> _
|
1 acetylCoA + 1 CO2
|
|
1 glucose>
|
2 acetyl CoA + 2CO2
|
|
Oxygen in CO2 is not from breathed O2 gas, it's from
|
glucose
|
|
Kreb cycle aka _ aka _
|
citric acid cyle, tricarboxylic acid (TCA) cycle
|
|
1 acetyl CofA (2 carbons) combines with _ to form _
|
oxaloacetic acid (4 carbons), citric acid (6C carbon)
|
|
In kreb cycle, 1 guanosine triphosphate (GTP) which donates a _ to _ to produce _.
|
phosphate group, ADP, ATP
|
|
3 molecules of NAD are reduced to
|
NADH
|
|
1 molecule of FAD is reduced to
|
FADH2
|
|
_ and _ carry electrons to _
|
NADH, FADH2, electron transport chain (ETC)
|
|
Byproducts of kreb cycle
|
2 more CO2 (waste)
|
|
ETC is a _ on _
|
linked series of proteins, foldings of mitochondria
|
|
Foldinds of mitochondria
|
cristae
|
|
Proteins in michondria include
|
flavin mononucelotide FMN
conenzyme Q iron containing pigments (cytochromes) |
|
cytochromes are
|
iron pigments found in cristae
|
|
_ and _ are regenerated to shuttle more _ from _ to _
|
NAD, FAD, electrons, krebs cycle, ETC
|
|
_ and _ are _ when by transferring their electrons to _
|
NADH, FADH2, oxidized, ETC
|
|
Exergonic process is
|
ETC reduces electrons and oxydizes at the same time
|
|
Energy gained from exergonic process is used to _ _ to _.
|
phosphorylation of ADP, ATP
|
|
Oxydative phosphorylation is
|
the production of ATP though the coupling of the ET system with phosphorylation of ADP
|
|
Chemiosmotic theory states
|
energy gathered by ETC by the passage of e- is used to pump H+ into mitochondria outer chamber
-creates high H+ concentration |
|
ATP synthasis
|
ADP+Pi=ATP
|
|
_ added to the beginning of _ by _ and _ are passed along until they reach the last member of ETC (_)
|
e-, ETC, NADH and FADH2, cytochrome a3
|
|
_ is reduced and serves as the final e- acceptor by combining with _ to form _
|
O2, 4H+, H2O
|
|
O2+4e-+4H >
|
2 H2O
|
|
_ is deadly because it blocks transfer of _ to _
|
cyanide, e-, cytochrome a3
|
|
ATP can be made in 2 ways
|
-Direct (substrate level)phosphorylation
-oxidative phosphorylation |
|
Direct phosphorylation is where
|
ATP is generated when bonds break (i.g.glycolysis and 2 ATPs/glucose in krebs)
|
|
Oxidative phosphorylation is where
|
ATP is generated by ETC, 30-32 ATPs made this way
-H+s pass thru ATP synthase to generate ATP |
|
theoretically yields _ ATPs/glucose
|
36-38, however some ATPs are used to pump ATPs out of mitochondria
|
|
_ ATPs/ glucose include
|
30-32
26 ATP produced in ETC 2 from glycolysis 2 from direct phosphorylation in Krebs |
|
For energy, Fats can be _ to _ and _
|
hydrolyzed, glycerol and fatty acids
-can be modified to run thru Krebs to make ATP |
|
For energym Proteins can be broken down to _, which can be _, converted into _ and run through krebs
|
amino acids, deaminated, pyruvate
|
|
When more _ is taken in than consumed _ is inhibited
|
energy (food)
ATP sysnthesis -we do not store ATP |
|
_ converted into _ and _ can be broken down to form _
|
glucose
glycogen fat ATP |
|
When _ is going to be converted to _, _ first occurs forming _, which is converted to _
|
glucose
fat glycolysis pyruvate acetylCoA |
|
_ is a common substrate for energy and synthetic pathways because it can be sent to _ or made into
|
acytolCoA
krebs cholesterol bile salts steroid hormones ketones fatty acids |
|
_ + _= fat (triglycerides)
|
fatty acids
glycerol |
|
fat production occurs mainly in
|
adipose and liver tisse when blood glucose are high after meal
|
|
1 g fat= _ _kilocalories of energy vs. 1 g carbohydrate= _kilocaries of energy
|
9
4 |
|
Lypolysis is the
|
breakdown of fat into free fatty acids and glycerol via hydrolysis by lipase
|
|
Lypolysis breaks down triglyceride to
|
glycerol
fatty acid chains |
|
Some organs use glycerol to form _
|
phoshphoglyceraldehyde
|
|
Most fatty acids are used in a process called
|
beta oxidation
|
|
Fatty acid chains are
|
long hydrocarbons with COOH at end
|
|
A _ C fatty acid chain can yield _ C acetyl CoA molecules
|
16C
8C |
|
Each acetylCoA molecule can run through krebs giving _ ATPs
|
10
note:oxidative phosphorylation can make 28 ATP per 16 C fatty acid chain |
|
Each acetylCoA can result in _ and _
|
1 NADH
2 FADH |
|
beta oxidation total
|
108 ATP from 16 carbon chain
|
|
Brown fat is a major site for
|
thermogenesis in the newborn
-amount greatest at time of birth |
|
Brown fat not a major source of energy because it produces _ protein
|
uncoupling
|
|
Uncoupling protein caused _ to leak out of inner mitochondiral membrane thus fewer H+ pass through ATP synthase making less _
|
H+
ATP |
|
Lower ATP causes ETC to be _ which generates _ instead of ATP
|
more active
heat |
|
Triglycerides are continually broken down forming _ and _ and _ to ensure its contained for aerobic respiration by other organs
|
glycerol
fatty acids resynthesized |
|
During fasting and diabetes
|
-rate of lipolysis exceeds fatty acid utilization
-blood fatty acid increases |
|
If liver (ATP) are sufficient so that it is not being made, some _ will enter metabolic pathway forming _
|
acetylCoA
ketone bodies |
|
Ketone bodies include
|
acetoacetic acid
acetone beta hydroxybutric acid |
|
In fasting conditions, fat metabolites
|
ketosis
ketonuria |
|
Ketosis
|
too high in blood
|
|
Ketonuria
|
too high in urine
-gives breath an acetone (sweet) |
|
Nitrogen ingested primarily as _ which is used in body as _
|
protein
amino acids |
|
Excess N is excreted mainly as _
|
urea
|
|
N balance=
|
N ingested-N excreted
|
|
Positive N balance
|
more N ingested than extreted bc used in protein synthesis
|
|
Negative N balance
|
less N ingested than excreted bc proteins are broken down
|
|
Excess amino acids can be _ converted into _ and _
|
deaminated
carbohydrates fat |
|
_ used to build all proteins
|
20 amino acids
|
|
_ can be produced by body
|
12
nonessential amino acids |
|
_ must come from diet
|
8
essential amino acids |
|
Tranamination
|
addition of amine (NH2) to pyruvate or krebs cycle acids called "keto acids" (ketone functional) to make new amino acid
Note- not confuse with ketone bodies that derive from acetylCoA |
|
Transaminase is
|
an enzyme that catalyzes in transamination
|
|
Oxidative deamination is the process by which
|
excess amino acids are eliminated
|
|
Steps Oxidative deamination
|
-NH2 is removed from glutamic acid forming keto acid and ammonia
|
|
Ammonia is converted to
|
urea and excreted
|
|
Keto acid goes to
|
Krebs or to fat or glucose
|
|
Main substrates for gluconeogenesis
|
alanine
lactic acid glycerol |
|
Gluconeogenesis is the formation of
|
glucose from non-carbohydrates
|
|
Brain uses _ as its major source of energy
|
glucose
|
|
Under fasting conditions, blood glucose is supplied mostly from _ via _ and _
|
liver
glycogenolysis gluconeogenesis |