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glycolysis stage 1
ENERGY INVESTMENT
uses 2 atp
trap glucose in cell and modify it to make 2 phosphorylated 3-carbon compounds
glycolysis stage 2
ENERGY PAYOFF
makes 4 atp and 2 nadh
oxidizes 3-carbon compounds to pyruvate
hexokinase
traps glucose in cell
adds phosphate to glucose
begins glycolysis
turns glucose → glucose 6 phosphate
stages of cellular respiration
glycolysis (happens in cytoplasm)
pyruvate processing
citric acid cycle
electron transport chain
why is glucose an important molecule
can form under prebiotic conditions
its stable
low tendency to make bad bonds with proteins
PFK
adds another phosphate to trap glucose
irreversible
controls glycolysis
2 binding sites: active site and regulatory site
inhibited by atp
stimulated by amp (signal for low energy state)
start of glycolysis phase 2
fructose 1,6 biphosphate turns into DHAP and GAP
reversible reaction
catalyzed by aldolase
DHAP and GAP
GAP can be turned into pyruvate to make atp but DHAP can’t
triose phosphate isomerase lets DHAP be converted to GAP for further metabolism
what happens when GAP is oxidized
it generates 1,3-BPG which has high phosphoryl transfer potential
what enzymes regulates glycolysis
hexokinase
phosphofructokinase
pyruvate kinase
the allosteric regulation of PFK
when atp is low, more PFK is made at a faster rate. when atp is high, It is able to generate and accumulate less and slower
the activation of PFK by fructose 2,6-biphosphate
F 2,6 BP tells PFK there’s plenty glucose and glycolysis needs to happen to give energy to energy consuming processes instead of wasting energy
PFK kickstarts glycolysis so F 2,6 BP tells PFK its okay.
regulation of glycolysis in muscle
long slow run
co2 and h2o is made from pyruvate
oxygen is more abundant
sprint
lactate is made to regenerate NAD+ to keep glycolysis running
oxygen is not abundant you need more
entry points In glycolysis for galactose and fructose
liver and adipose tissue
glucose 6-P
fructose 6-P
2 types of fermentation
lactic acid fermentation
pyruvate → lactate (happens in muscles)
alcohol fermentation
pyruvate → ethanol
fermentation
regenerate NAD+ so glycolysis can continue
catabolism
makes atp
breaks molecules and releases energy
anabolism
use atp to make biomolecules
common denominator between anabolic and catabolic pathways
the regulated, irreversible reactions are always distinct
2 ways organisms get energy
chemotrophs and phototrophs
basic principles for energy manipulation in cells
molecules are made or broken by metabolic pathways
atp is energy currency
atp can be formed by oxidation of carbon fuels
many reactions repeat similar patterns
metabolic pathways are highly regulated
criteria for constructing a metabolic pathway
individual reactions must be specific
total pathway must be thermodynamically favorable (must release energy)
ATP
high potential energy (stores energy)
allows cells to work
works by transferring phosphate group
ATP hydrolysis
breaking atp releases energy because phosphate groups repel each other with negative charges (EXERGONIC RXN)
the energy released can be transferred to another molecule with phosphorylation
muscle atp
creatine phosphate regenerates ATP from ADP, allowing a short burst of activity (ex: a sprint)
why is phosphate important
they’re thermodynamically unstable but kinetically stable
negative charges resist hydrolysis
they are ideal regulatory molecules
ATP → ADP phosphates in biochemical processes
motion
active transport
biosyntheses
signal amplification
ADP → ATP phosphates in biochemical processes
oxidation of fuel molecules
photosynthesis
carbon oxidation
the more reduced a carbon atom is, more free energy is released with oxidation
more oxygens = less energy
what is a better fuel
fats are better than glucose because fats are more reduced
they have more C-H bonds and less oxygen
activated carriers
universal, reusable currency that can do different reactions (ex: ATP is the active carrier of phosphorylation groups, NAD+ and FAD carry activated electrons)
2 characteristics of activated carriers
kinetically stable without specific enzymes
can do metabolism with less carriers
3 regulatory controls of homeostasis
amount of enzyme (can be regulated at gene transcription or after)
catalytic activity of enzyme
accessibility of substrate
how is catalytic activity regulated
allosterically or covalent modification
hormones coordinate metabolic activity (allosteric)
energy status of cell
how to assess energy status of a cell
energy charge and phosphorylation potential
the accessibility of substrates is regulated
with opposing reactions (fatty acid synthesis and degradation)
and regulating flux of substrates between cellular compartments
energy charge regulates metabolism
atp generating pathway: relative rate decreases because the needs are met and doesn’t want to waste resources
atp utilizing pathway: the relative rate increases because it needs more energy