1/21
Looks like no tags are added yet.
Name | Mastery | Learn | Test | Matching | Spaced |
|---|
No study sessions yet.
What Is the role of oxygen in cellular respiration?
acts as the final electron acceptor in the ETC. It combines with hydrogen ions and electrons to make water.
what is oxidized in the cellular respiration reaction
C6H12O6 (glucose) is oxidized into 6CO2 (carbon dioxide)
what is reduced in the cellular respiration reaction
6O2 (oxygen) is reduced to 6H2O (water)
where does glycolysis take place
the cytosol
where does the Krebs cycle take place
the matrix of the mitochondria
where does ETC take place
the intermembrane surface of the mitochondria
how does ATP generation in glycolysis and the Krebs cycle different from ATP generation via the ETC
glycolysis and Krebs cycle are substrate level phosphorylation ATP while ETC is oxidative phosphorylation ATP
how many ATP molecules per molecule of glucose are generated during glycolysis
2
how many ATP molecules per molecule of glucose are generated during Krebs cycle
2
how many ATP molecules per molecule of glucose are generated during ETC
32-34
how many ATP molecules per molecule of glucose are generated during the entire cellular respiration
38
the difference between substrate level phosphorylation and oxidative phosphorylation
Substrate-level phosphorylation directly transfers a phosphate from a substrate to ADP via an enzyme, occurring in cytoplasm (glycolysis) or mitochondria (Krebs cycle) and needing no oxygen, while oxidative phosphorylation indirectly generates lots of ATP using the ETC in mitochondria, driven by NADH/FADH2 and requiring oxygen as the final acceptor, producing a proton gradient for ATP synthase
Electron carriers NAD+ what is considered the oxidized form and reduced form and explain that
NAD+ is the oxidized form as its not storing electrons so it can accept them whereas NADH is the reduced form as its storing electrons that it gained through reduction
FAD is the oxidized form as its not storing electrons so it can accept them whereas FADH2 is the reduced form as its storing electrons that it gained through reduction
why is the krebs cycle important if your only making a small amount of ATP
it produces electron carriers for oxidative phosphorylation it produces 6 NADH and 2 FADH2 and they transport electrons to the ETC feeding them into the ETC allowing for much larger amounts of ATP to be produced it is also important to producing CO2 to be exhaled keeping a proper carbon balance
where you get the most energy in all the areas
oxidative phosphorylation, specifically via the process of chemiosmosis in the ETC. This occurs in the intermembrane surface of the mitochondria in eukaryotes
Why do you think the glycolysis to be thought the first metabolic pathway to be evolved
its anaerobic so it doesn't require oxygen which life on earth first evolved without free oxygen in the atmosphere
its found in nearly all organisms (bacteria, plants, animals)
Occurs in the cytoplasm, not requiring organelles which prokaryotes don't have
Produces ATP and NADH, essential for basic cellular functions
Prokaryotes that evolved glycolysis are ancestors of all modern life All cells still utilize glycolysis
Why do you feel muscle burn after sprinting
your muscles working so hard they use ATP faster than oxygen can be delivered to produce move so cells switch to performing anaerobic respiration to produce ATP this involves lactic acid fermentation in order to recycle NADH back to NAD+ through pyruvate accepting electrons from NADH allowing glycolysis to continue producing ATP this produces lactic acid and a build up of this in muscle cells is what produces muscle burn
describe how Catabolism of glucose in glycolysis and pyruvate oxidation contributes to ATP synthesis
breaks down glucose to generate ATP directly (small amount via substrate-level phosphorylation) and produce electron carriers (NADH, FADH₂) that power oxidative phosphorylation in ETC. Glycolysis produces 2 ATP and NADH, while pyruvate oxidation converts pyruvate to Acetyl-CoA, producing more NADH Acetyl-CoA is produced for entry into Kreb's cycle for further electron carrier production, ultimately leading to massive ATP generation.
describe how Oxidation of intermediates in the Krebs cycle contribute to ATP synthesis
releasing electrons that are transferred to the electron carriers NAD+ and FAD reducing to NADH and FADH2 these reduced carriers shuttle the electrons to the ETC as the electrons move down the chain energy is released and used to pump protons across the intermembrane surface creating a proton gradient it also produces 2 ATP through substrate level phosphorylation of ADP
describe how formation of a proton gradient by the electron transport chain contributes to ATP synthesis
as electrons move through the ETC energy is released and used to pump H+ from the mitochondrial matrix into the intermembrane space forming a proton gradient across the inner mitochondrial membrane creating a electrochemical gradient storing potential energy which drives protons back into the matrix through ATP synthase energy released from this movement drives the oxidative phosphorylation of ADP to ATP
what are the exergonic reations
exergonic releases energy which is when glucose is oxidized to carbon dioxide during glycolysis, Krebs cycle, and the ETC releasing energy that is captured in ATP NADH and FADH2 the movement of electrons down the ETC is exergonic
what are the endergonic reations
endergonic receives energy which is when in glycolysis ATP is used to phosphorylate glucose and the synthesis of ATP from ADP and pi these reactions are driven by energy released from exergonic reactions demonstrating energy coupling