Catabolic pathways break glucose own into simpler molecules, releasing energy to build ATP. Is the catabolism of glucose exergonic
Fermentation results from the partial catabolism of glucose. Aerobic respiration is the full catabolism of glucose, releasing as much energy as possible for ATP construction
Fermentation results from the partial catabolism of glucose
Aerobic respiration is the full catabolism of glucose, releasing as much energy as possible for ATP construction
Cellular aerobic respiration converts organic molecules and oxygen to carbon dioxide and water, with a large energy release
Redox reactions are chemical reactions where electrons are transferred between reactants
If all the energy is released all at once, it cannot be harvested efficiently
A cell’s first electron transfer in controlled energy harvest moves H (electros + proton) from glucose to NAD+
There is only a small amount of energy loss in the electron transfer from glucose to NAD+. NAD+ and NADH can cycle back and forth easily, so they are convenient molecules to act as electron recipients, and NADH can pass electrons along in the next steps
NADH is now carrying a high potential energy, in the form of the electrons it got from glucose. NADH passes it electrons to a series of several carrier molecules in multiple small redox reactions
O2 ultimately receives the electrons (and partner protons) at the end of this chain
If H2 plus half of an O2 are released too quickly, explosive things happen
Electrons are passed from NADH through several intermediates. This releases small amounts of energy at each transfer
Coupling controlled small exergonic reactions with other reactions result in endergonic ATP synthesis
Energy from glucose, first step is glycolysis and it occurs in all living cells. Three phases are energy investment phase, cleavage phase, and energy payoff phase
In the energy investment phase, each P contributed by an ATP bumps G up a little bit, helping glucose get over the activation energy hump
Kinase is an enzyme that catalyzes the transfer of a phosphate group from high-energy, phosphating donating molecules to other substrates
Isomerase is an enzyme that convert one isomer to another
Dehydrogenase is an enzyme that transfers hydrogen atoms from organic compounds to electron acceptor, thereby oxidizing the organic compounds
Glycolysis starts with 1 glucose, invest 2 ATP, end with 2 pyruvate, 4 ATP, 2 NADH
When a compound donates (loses) electrons, that compound becomes oxidized (OIL)
When a compound accepts (gains) electrons, that compound becomes reduced (RIG)
In glycolysis, the carbon-containing compound that functions as the electron donor is glucose
Once the electron donor in glycolysis gives up its electrons, it is oxidized to a compound called a pyruvate
NAD+ is the compound that functions as the electron acceptor in glycolysis
The reduced form of the electron acceptor in glycolysis is NADH
Among the products of glycolysis, the compound that contain energy that can be used by other biological reactions are pyruvate, ATP, and NADH
A bond must be broken between an organic molecule and phosphate before ATP can form
One of the substrates is a molecule derived from the breakdown of glucose
The citric acid cycle starts with 2 carbons from acetyl CoA, where it then has 6 carbons in citrate to 6 carbons isocitrate, then to 5 carbons for alpha-ketoglutarate (loses CO2 and NAD+ -> NADH), then again to 4 carbons for succinyl CoA (loses CO2 and NAD+ -> NADH), then 4 carbons for succinate (ADP +Pi -> ATP loses CoA), 4 carbons fumarate (FAD -> FADH2), 4 carbons malate (NAD+ -> NADH), then 4 carbons oxaloacetate
Pyruvate is oxidized to CO2 and NAD+ is reduced to NADH and FAD is reduced to FADH2
The citric acid cycle is is a cyclic pathway rather than a linear pathway because it is easier to remove electrons and produce CO2 from compounds with three or more carbon atoms than from a two carbon compound
Although possible to oxidize the two carbon acetyl group of acetyl CoA to two molecules of CO2, it is much more difficult than adding the acetyl group to a four carbon acid to form a six carbon acid (citrate). Citrate can then be oxidized sequentially to release two molecules of CO2
In mitochondrial electron transport, the direct role of O2 is to function as the final electron acceptor in the electron transport chain
O2 only has a place at the end of cellular respiration during electron transport chain as the final electron acceptor. Oxygen has a high affinity for electrons which contributes to the formation of a proton gradient and synthesizing ATP
Oxidative phosphorylation is a cellular process that harnesses the reduction of oxygen to generate high energy phosphate bonds in the form of ATP
Anaerobic conditions would stop the rate of electron transport and ATP synthesis
Fewer protons are pumped across the inner mitochondrial membrane when FADH2 is the electron donor than when NADH is the electron donor (which explains why more ATP is made per molecule of NADH)
Gramicidin causes membranes to become very leaky to protons, so that a proton gradient cannot be maintained and ATP synthesis stops. However, the leakiness of the membrane has no effect on the ability of electrons to move along the electron transport chain. Thus, the rates of electron transport and oxygen uptake remain unchanged