metabolic processes review Flashcards
The energy of life
The living cell generates thousands of different reactions
- Metabolism is the totality of an organism’s chemical reactions, which arises from interactions between molecules
- An organism’s metabolism transforms matter and energy, subject to the laws of thermodynamics
Metabolic Pathways
- Biochemical pathways are organized units of metabolism 🡪 chemical reactions of an organism
- A metabolic pathway has many steps that begin with a specific molecule and end with a product, catalyzed by a specific enzyme
- The function of many metabolic pathways is to break down energy-rich compounds such
as glucose and convert the energy into a form that the cell can use. - Reactions that join small molecules together to form larger, more complex molecules are anabolic
- Reactions that break large molecules down into smaller subunits are catabolic
- A sequence of chemical reactions, where the product of one reaction serves as a substrate for the next; also called a biochemical pathway
- Most metabolic pathways take place in specific regions of the cell
Bioenergetics and energy
- The study of how organisms manage their energy resources via metabolic pathways
- Catabolic pathways: release energy by breaking down complex molecules into simpler compounds
- Anabolic pathways: consume energy to build complex molecules from simpler ones
(where are we allocating this energy and resources → we need good proportions of stuff → we need to balance the ctabaolic and anabolic pathways → what are we building and breaking )
Energy is the capacity to do work that is to cause change or move matter against an opposing force like gravity or friction. Any change in the universe requires energy.
2 forms:
- Potential energy is stored energy, including chemical energy stored in molecular structure. No change is currently taking place. (energy that available but not released)
- Kinetic energy is currently causing change. This always involves some type of motion. (energy of motion)
Energy can be converted from one form to another.
Kinetic energy and potential energy may themselves be classified as different types. For
example, the kinetic energy of particles moving in random directions is thermal energy.
An increase in the kinetic energy of particles of an object increases the temperature of the
object. Heat is the transfer of thermal energy from one object to another due to a temperature
difference between the objects. Chemical energy is potential energy stored in the arrangement
of the bonds in a compound.
Whenever a chemical bond forms between two atoms, energy is released. The amount of
energy needed to break a bond is the same as the amount of energy released when the bond
is formed. This amount of energy is called bond energy. Because energy is always released
when a bond forms, free (unbonded) atoms can be considered to have more chemical energy than any compound.
The energy released from chemical reactions in a laboratory is
usually in the form of thermal energy (heat). The energy released from chemical reactions in living cells can include thermal energy, but it can also be in the form of the movement of compounds across cell membranes, contraction of a muscle, or even the emission of light from compounds within specialized cells in certain organisms. In many cases, energy released from one reaction is used to make another reaction occur as part of a metabolic pathway.
Laws of energy transform/Thermodynamics
All activities—those that are necessary to enable and sustain life processes as well as
those that occur in the non-living world and anywhere else in the universe—involve
changes in energy.
Thermodynamics is the study of energy changes
A system can be a whole
organism, a group of cells, or a set of substrates and products—whatever object or objects
are being studied. Surroundings are defined as everything in the universe outside of the system. In terms of thermodynamics, biological systems are considered to be open systems, meaning that the system and its surroundings can exchange matter and energy with each other. The laws of thermodynamics describe how a system can interact with its
surroundings and what can, and cannot, occur within a system.
The First Law of Thermodynamics:
Energy cannot be created or destroyed; it can only be transferred or transformed from one form to another and from one object to another. Thus, when a chemical reaction occurs and energy is released, some of the energy can be transformed into mechanical energy, such as the motion of a contracting muscle, and the rest can be transformed into heat or other forms of energy.
The Second Law of Thermodynamics:
Disorder (entropy) in the universe is continuously increasing; transformations proceed spontaneously to convert matter from a more ordered, but less stable form, to a less ordered, more stable form. (disorder is easy and is not done on purpose → organizing is done purposely
when organized it’s less stable since it’s not going to stay like that for long or requires lots of energy to stay like that whereas with disorder it can stay like that without doing anything so it’s stable) (According to the first thermodynamics law, the total amount of energy in the universe
remains constant. Despite this, however, the energy available to do work decreases as more
of it is progressively transformed into unusable heat. The second law of thermodynamics
concerns the transformation of potential energy into heat, or random molecular motion.
It states that the disorder in the universe—more formally called entropy—is continuously
increasing. Put more simply, disorder is more likely than order.) (When the universe
formed, it held all the potential energy it will ever have. It has become increasingly more
disordered ever since, with every energy exchange increasing the amount of entropy.)
Because organisms are highly ordered, it might seem that life is an exception to the laws
of thermodynamics. However, the second law applies only to closed systems. While they
are alive, organisms remain organized because they are not closed systems. They use inputs
of matter and energy to reduce randomness (decrease entropy) and thus stay alive. The
energy that keeps organisms alive comes ultimately from the Sun. That is, plants transform
light energy into the chemical bonds of carbohydrates, which humans and other organisms
temporarily store and later use as an energy source.
Second law of thermodynmaics: During each conversion, some energy dissipates into the environment as heat, and becomes unusable. Living cells unavoidably convert organized forms of energy to heat. Every energy transfer or transformation increases the entropy (disorder) of the universe.
Biological Order and Disorder
Living systems:
-Increase the entropy of the universe
-Use energy to maintain order; free energy can do work under cellular conditions.
Free energy: portion of a system’s energy able to do work when temperature and pressure is uniform, as in a living cell; also refers to energy available to break and subsequently form other chemical bonds.
Gibbs’ free energy (G): in a cell; the energy contained in a molecule’s chemical bonds (constant T & P)
Change in free energy = ΔG
It takes energy to break the chemical bonds that hold atoms together. Heat, because it
increases the kinetic energy of atoms, makes it easier for the atoms to pull apart. Both
chemical bonding and heat have a significant influence on a molecule. Chemical bonding
reduces disorder; heat increases it. The net effect—the amount of energy actually available
to break and subsequently form other chemical bonds—is referred to as the free energy of
that molecule. In a more general sense, free energy is defined as the energy available to do
work in any system.
For a molecule within a cell, where pressure and volume usually do not change, the
free energy is denoted by the symbol G. G is equal to the energy contained in a molecule’s
chemical bonds, called enthalpy and designated H, together with the energy term related
to the degree of disorder in the system. This energy term is designated TS, where S is the
symbol for entropy and T is temperature. Thus:
G = H 2 TS
Chemical reactions break some bonds in the reactants and form new ones in the
products. As a result, reactions can produce changes in free energy. When a chemical
reaction occurs under conditions of constant temperature, pressure, and volume—as do
most biological reactions—the change in free energy (ΔG) is
ΔG = ΔH 2 TΔS
- Endergonic: any reaction requiring an input of energy
-Exergonic: any reaction that releases free energy
Exergonic reactions:
- Reactants have more free energy than products
- Involve a net release of energy and/or an increase in entropy
- Occur spontaneously (without a net input of energy)
- (For other reactions, the ΔG is negative. In this case, the products of the reaction contain less free energy than the reactants. Thus, either the bond energy is lower, or the disorder is higher, or both. Such reactions tend to proceed spontaneously. These reactions release the excess free energy as heat and are said to be exergonic, which literally means “outward
energy.” Any chemical reaction tends to proceed spontaneously if the difference in disorder (TΔS) is greater than the difference in bond energies between reactants and products (ΔH).)
Endergonic reactions:
- Reactants have less free energy than products
- Involve a net input of energy and/or a decrease in entropy (so decrease in stability)
- Do not occur spontaneously
- (For some reactions, the ΔG is positive, which means that the products of the reaction contain more free energy than the reactants. Thus, the bond energy
(H) is higher, or the disorder (S) in the system is lower. Such reactions do not proceed spontaneously, because they require an input of energy. Any reaction that requires an input of energy is said to be endergonic, which literally means “inward energy.”)
Energy Coupling:
- Living organisms have the ability to couple exergonic and endergonic reactions
- Energy released by exergonic reactions is captured and used to make ATP from ADP and Pi
- ATP can be broken back down to ADP and Pi, releasing energy to power the cell’s endergonic reactions
- Energy is released from ATP when the terminal phosphate bond is broken (through hydrolysis)
A cell does three main kinds of work: Mechanical, transport and chemical
- Energy coupling is a key feature in the way cells manage their energy resources to do this work
- ATP powers cellular work by coupling exergonic reactions to endergonic reactions
- Releasing the third phosphate from ATP to make ADP generates energy (exergonic)
- Linking the phosphates together requires energy
- Catabolic pathways drive the regeneration of ATP from ADP and phosphate
thermodynamic and metabolism
(similar to previous card)
In fact, most reactions require an input of energy to get started. This energy destabilizes existing chemical bonds and initiates the reaction. this input energy is called activation energy. An exergonic reaction may proceed very slowly if
the activation energy is quite large. One way that the activation energy of a reaction can be reduced is by using a catalyst. In metabolic pathways, biological catalysts—enzymes— decrease the activation energy of each reaction.
- In cells, energy from catabolic reactions is used to power anabolic reactions. The source of energy that links these sets of reactions is the molecule ATP, adenosine triphosphate. ATP is often called the energy currency of the cell, because so many cellular activities
depend on ATP. It is the major product of most catabolic pathways, and it is the major
source of energy for anabolic pathways.
Figure 3.6 shows the structure of ATP and the hydrolysis of the terminal (last)
phosphate group. The red tilde symbols (wavy lines) represent high-energy bonds that, when hydrolyzed, release energy. Each of the phosphate groups in an ATP molecule is negatively charged. The negative charges of the phosphate groups repel each other in
such a way that the phosphate groups strain away from each other like opposing teams in a tug-of-war contest. When one of the bonds between the phosphate groups is broken, ATP becomes ADP (adenosine diphosphate) plus an inorganic phosphate (Pi), and a large quantity of energy is released.
Cells use ATP to drive endergonic reactions. These reactions do not proceed spontaneously, because their products possess more free energy than their reactants. However, if the cleaving of ATP’s terminal high-energy bond releases more energy than the other reaction consumes, the two reactions can be coupled so that the energy released by the hydrolysis of ATP can be used to supply the endergonic reaction with energy. Coupled together, these reactions result in a net release of energy (−ΔG) and are therefore exergonic and proceed
spontaneously.
The use of ATP can be thought of as a cycle. Cells use exergonic reactions to provide the energy needed to synthesize ATP from ADP 1 Pi; they then use the hydrolysis of ATP to provide energy for endergonic reactions. Most cells typically have only a few seconds’ supply of ATP at any given time and continually produce more
from ADP and Pi.
Redox reactions are coupled reactions that play a key role in the flow of energy through
biological systems. Electrons that pass from one atom to another carry energy with them, so the reduced form of a molecule is always at a higher energy level than the oxidized form. Thus, electrons are said to carry reducing power. The amount of energy
they carry depends on the energy level they occupy in the atom donating the electrons. Electron carriers are compounds that pick up electrons from energy-rich compounds and then donate them to low-energy compounds. An electron carrier is recycled.
Two important electron carriers in metabolic reactions are NAD+ (nicotinamide
adenine dinucleotide) and FAD (flavin adenine dinucleotide). these electron carrier are used when creating atp in the ets
how cells harvest chemical energy
glucose + oxygen –> carbon dioxide + water + ATP (energy)
cell matabolism involves glycolysis, aerobic cellular respiration (optimal o2 condition) and anaerobic cell repriation (low o2 condition)
Cellular metabolism how we harvest chemical energy
It consists of glycolysis, aerobic and anaerobic cellular respiration (depends on conditions → going from glucose to monosachardie reacts with o2 that is converted to energy where co2 and h2o is a byproduct and co2 is exhaled)
Breathing and cellular respiration
sugar + o2 –> atp + co2 + H2o
Repriartion has to take place at the cellular level → u start by breathing bring o2 into ur lungs, then it goes under other processes to get the cell ?
muscle cells carry out cellular respiration
How our breathjing has to take place at a cellular level and the oxygen has ti do this because we need oxygen to go to our muscles because then the oxygen will help with our mobility
efficency of cellular respiration
ellular Respiration uses oxygen and glucose to produce Carbon dioxide, water, and ATP.
Not that efficient → when u burn glucose it’s 100% efficient as the glucose is converted into light and heat energy → if we were to burn glucose in cellular respiration to lift weight, energy is released from the glucose banked in ATP, it’s inefficient as 40% is only directed to completing the task the other 60 is lost as heat, water loss production but mostly heat which is why we sweat, we produce energy in the form of sweat and heat → combustion of gasoline to move the car forward only 25 % relates to moving it, rest goes to the engine heating up and the sound coming fromthe car
redox reaction in cellular respiration
gain or loss of e is often in the form of hydrogen
glucose losses hydrogen atoms to become co2 while o2 gains hydrogen atoms becoming h2o while energy/atp is also being produced
glucose gives off energy as it is oxidized –> Hydrogen is then passed to a coenzyme such as NAD+ (nicotinamide adenine dinucleotide). –> NAD+ and FAD (flavin adenine dinucleotide) are two important coenzymes. –> both receive hydrogen and become nadh + h and FADH2 –> NAD+ and FAD transfer high-energy electrons to the electron transport systems (ETS) during cell respiration. –> As the electrons move from carrier to carrier, energy is released in small quantities.
(The coenzyme is helpful as it work with fad → we need them because tehy work to transfer high energy e to the ets (improtant part of cellular respiration cause this is where u get more atp being produced, ex. U gotta spend money to make money, so u make atp to make even more atp (investing energy to get it started then it produces much more units of energy that we need but this all starts with the oxidation of glucose) in one step during cell respiration)
Generation of atp
Two ways to generate ATP:
- Chemiosmosis: In chemiosmosis, cells use the energy released by “falling” electrons in the ETS to pump H+ ions across a membrane using an enzyme, ATP synthase.
- Substrate-Level Phosphorylation: ATP can also be made by transferring phosphate(that may come from food) groups from organic molecules to ADP
general overview of cr
glucose undergoes glycolysis (the breaking of glucose) to form pyruvic acid
- with oxygen = aerobic –> goes under transition reaction, krebs cycle and gets and has a net production of 36 atp
- without oxygen = anaerobic –> goes under fermentation and has a net production of 2 atp
(Aerobic is ideal as it produces an efficient amount of atp
Fermentation isnt efficient and is slightly toxic
Human muscle cells also use fermentation. This occurs when muscle cells cannot get oxygen fast enough to meet their energy needs through aerobic respiration.
Humans undergo lactic acid fermentation when the body needs a lot of energy in a hurry. When you are sprinting full speed, your cells will only have enough ATP stored in them to last a few seconds. Once the stored ATP is used, your muscles will start producing ATP through lactic acid fermentation.)
Glycolysis 1
first reaction in the metabolic pathway of cellular respiration
it takes places in the cytosol and it breaks down glucose into pyruvic acid or pyruvate acid
the glucose whihc is asymetrcial uses two atp, gets phosphorylates twice to become fructose with 2 phaspahets (symetrical) (2 phsopahte groups are tranferred to glucose via phosphorlation where atp is conevrted to adp and the product is fructose 1,6 bisphosphate). This fructose will get split/break/cleaves into DHAP and G3P which are isomers of eachother where DHAP will use an enzyme to convert into G3P. The G3P now gets phosphorylated into BPG with NAD which becomes NADH(x2)(attatches phosphate). The BPG converts into 3PG whihc produces 2 units of ATP (the phosphate transfered to adp creating atp) –> 3PG now undergoes a condensation reaction to become PEP and h2o is realesed. The PEP turns into pyruvate producing 2 atp (phosphtae transfered to adp making atp). The final products of glycolysis is 2 NADH and 2 ATP (net).
Glycolysis 2 and Pyruvate oxidation
the glucose (6C) is split into 2 molecules of pyruvate (2 x 3C)
*Net production of ATP during glycolysis is 2 ATP
*Glycolysis is only around 2% efficient as there is still a lot of energy stored in pyruvate
pyruvic acid will now follow aerobic respiration metabolic pathway which includes transition reaction, krebs cycle and ets making 36atp if there enough oxygen. if there isnt enough or no oxygen then it undergoes fermentation, the anaerobic pathway which causes lactic acid, a toxic byproduct and only produces 2 atp.
in aerboic repriation after glyclysis, the pyruvic acid undergoes a transition reaction called pyruvate oxidation before it goes into the krebs cycle.
Pyruvate oxidation: Each pyruvic acid molecule is broken down to form 2 NADH, CO2 and a two-carbon acetyl group, acetyl CoA, a coenzyme which then enters the Krebs cycle.
Basically we take in nutrients, we break it down into glucose monomers, it undergoes glycolysis which creates 2 atp, it becomes pyruvate and nadh. pyruvate will undergo fermentation or it goes into the mitochondria undergoing pyruvate oxidation/transition reaction and becomes acetyl CoA which then will undergo the creb cycle producing 2atp and then the etc/s producing 26 atp as well as o2 and h2o.
General overview of glycolysis
Step 1: ATP is used up and a
phosphate is added to glucose,
increasing the molecule’s energy.
In the first few steps of glycolysis, the
sugar molecule is energized, giving it
energy to start the glycolysis process.
The first 5 steps are called the
prepatory phase. Enzymes that use up or build ATP are often called kinases.
Step 2: Atoms are rearranged in the
glucose-6-phosphate molecule by the
enzyme to create a substrate
(fructose-6-phosphate) that the next
enzyme can use.
Step 3: ATP is used up and a
phosophate is added to
fructose-6-phosphate, creating a highly energized molecule called
fructose-1,6-bisphosphate. This
molecule is not stable and is easy to
“pull apart” in step 4. This step is the most important step in glycolysis because it is the rate limiting
step, the decision point. If the cell
decides to perform step 3 on a sugar
molecule, the rest of aerobic
respiration must happen afterwards.
Step 4: Fructose-1,6-bisphosphate is
broken apart into two smaller 3
carbon molecules, glyceraldehyde
3-phosphate and dihydroxyacetone
phosphate.
Step 5: The dihydroxyacetone
phosphate molecule’s atoms are
rearranged to create another
glyceraldehyde 3-phosphate, which is
the ideal substrate for the 6th enzyme. After step 5, because there are 2 three carbon sugars, each step happens twice, as shown with 2 arrows and 2 enzymes. Steps 6-10 are called the pay-off phase,
because the cell starts to harvest the
energy from the sugar. It stores the
energy in ATP.
Step 6: In this step, inorganic phosphate ions (phosphate groups not already attached to ATP) are added to the glyceraldehyde 3-phosphate molecules to create 1,3-bisphosphoglycerate. Also, some energy is released and stored
in an energy carrier molecule called
Nicotinamide Adenine Dinucleotide
(NAD). The energized form is called
NADH and the low energy form is
NAD+. These NADH molecules are
important later in aerobic respiration,
during the oxidative phosphorylation
process.
Step 7: In this step, high energy
phosphate groups are transferred to
ADP, creating the first 2 ATP
molecules to form during glycolysis.
1,3-bisphosphoglycerate becomes
glycerate 3-phosphate.
Step 8: In this step, the phosphate
group is rearranged to make the next
few reactions easier for the enzymes to perform. Glycerate 3-phosphate
becomes 2-phosphoglycerate.
Step 9: In this step, oxygen and
hydrogen (not shown) are rearranged
in the molecules to make the last step easier for the enzyme to perform. 2-phosphoglycerate becomes phosphoenolpyruvic acid (PEP).
Step 10: In this last step, high energy
phosphate groups are transferred to
ADP, creating the last 2 ATP
molecules to form during glycolysis.
Phosphoenolpyruvic acid becomes
pyruvate, the final sugar product of
glycolysis. Pyruvate is further processed and broken down in the Krebs Cycle (also called the Citric Acid Cycle).
Theres 10 steps in glycolysis. 6 c-c bonds are present in glucose. The two phases of glycolysis is prepatory phase (1-5) and payoff phase (6-10). 2 ATP is used up in the first phase while 4 ATP is built in the second phase. NADH is another molecule that stores energy harvested from the glucose and is involved in the payoff phase. Kinase eznymes are enxzymes that use up or build atp. In pyruvate molecule 3 c-c bonds exist. Glycolysis is an example of an enzymatic pathway as in each product t is a reactant for the next step in the pathway like a cellular assembly line.
Step 3 (phosphofructokinase’s reaction) is the decision point where the cell decides if it will carry out aerobic respiration to collect energy from that sugar molecule or not. Cells decide based on whether they already have enough ATP or not. If there is a lot of ATP around, the cell will not want to break down more sugar and will want to store the sugar
instead. ATP is an inhibitor of phosphofructokinase. ATP molecules can “stick” to the enzyme in allosteric sites (parts of the enzyme that are not directly involved in the chemical reaction) and cause the enzyme to stop “doing its job”, or catalyzing the reaction.
Other two possible “regulators” for phosphofructokinase: AMP and PEP. AMP is produced when the cell breaks down a lot of its ATP. The cell then breaks down a lot of ADP into AMP. AMP is often referred to as the cell’s “starvation signal”. High AMP would activate the phosphofructokinase as there is more energy/sugar needed since all of it has been broken down. PEP is produced at the end of step 9 in glycolysis. Since PEP is turned into pyruvate and creates 2 atp while doing this it means that if there is a high level of it lots of atp and sugar can be produced so it cause phosphofructokinase to slow down its reactions since there already is enough energy to be collected.
Glycolysis review
Stages that occur in glycolysis:
It happens in the cytosol, anaerobic doesnt require oxygen, glucose (6c) broken down into 2 pyruvate molecules (3c), produces atp and nadh and the 10 reactions are divided into 2 phases glycolysis I and glycolysis II.
outline the key steps in glycolysis:
Glycolysis I is an energy investment. Involves 5 reactions. ATP helps power reactions in the cell by transferring its phosphate onto another substrate. Before any atp can be made, glucose needs to be activated by being phosphorylated by 2 atp molecules. Uses 2 atp: energy investment.
Glycolysis I:
- Glucose (phosphorylation - activation) glucose 6 phosphate (isomeraztion rearrangment) fructose 6 phosphate (phosphorylation activation) fructose 1,6 biphospahte (lysis cleavage) G3P and DHAP (isomerization rearrangement) 2 molecules of G3P
phosphorylation: glucose receives a phosphate from ATP to form glucose-6-phosphate
1 ATP used, 1 ADP produced
isomerization: glucose-6-phosphate rearranged to form fructose-6-phosphate
phosphorylation: fructose-6-phosphate receives a phosphate from another ATP to form fructose-1,6-bisphosphate
1 ATP used, 1 ADP produced
lysis: fructose-1,6-bisphosphate cleaved to form G3P and DHAP
isomerization: DHAP rearranged to form G3P
overall glycolysis I: glucose + 2 ATP 🡪 2 G3P + 2 ADP
Glycolysis II: energy payoff, 5 reactions, G3P are ready to release energy, ATP is made through substrate level phosphorylation: phosphate transferred directly form a molecule to aDP to form ATP, produces 4 atp and 2 NADH.
G3P (oxidation) 1,3 BPG (substrate level phosphorylation) 3PG (isomerzation) 2PG (oxidation) PEP (substrate level phosphorylation) pyruvate
oxidation: each G3P is oxidized by NAD+ and an inorganic phosphate is added (Pi) to form 1,3BPG
2 Pi and 2 NAD+ used, 2 NADH and 2 H+ produced
substrate-level phosphorylation: each 1,3BPG gives a phosphate to ADP to form 3PG and ATP
2 ADP used, 2 ATP produced
isomerization: each 3PG is rearranged to 2PG
oxidation: each 2PG is oxidized to form PEP
2 H2O produced (not counted overall)
substrate-level phosphorylation: each PEP gives a phosphate to ADP to form pyruvate and ATP
2 ADP used, 2 ATP produced
overall glycolysis II:
2 G3P + 4 ADP + 2 Pi + 2 NAD+ 🡪 2 pyruvate + 4 ATP + 2 NADH + 2 H+
overall glycolysis:
glucose + 2 ADP + 2 Pi + 2 NAD+ 🡪 2 pyruvate + 2 ATP + 2NADH + 2 H+
2 ATPs are used to prime glucose for splitting (glucose molecules are ‘phosphorylated’).
2 NADH are formed when G3P reduces NAD+ by adding an H.
4 ATP are formed by substrate-level phosphorylation:
Removing 2Pi from each 3 carbon intermediate
2 pyruvates are produced at the end of glycolysis.
identify the names of compounds formed in glycolysis:
G3P = glyceraldehyde 3-phosphate (G3P) molecules
DHAP = dihydroxide acidone phosphate
1,3 BPG = 1, 3 bi
3 PG - 3 phosphoglycerate
2 PG - 2 phosphoglycerate
PEP - phosphoenolpyruvate
identify the types of reactions that occur during glycolysis:
Phosphorylation, isomerization, lysis, oxidation, substrate level phosphorylation.
state the number of ATP/NADH used and produced in glycolysis:
2 ATP is used up, 4 ATP is produce and 2 NADH is produced in glycolysis.
state what steps are involved with ATP/NADH:
ATP is used in steps 1 and 3, NADH is produced in step 6 and ATP is produced in step 7 and 10.
Krebs Cycle simple overview
recall: glycolysis occurs in the cytosol and it metabolzies glucose to yield 2 NADH, 2 ATP and 2 pyruvate. Pyruvate oxidation occurs in the mitochondrial matrix and it metabolizes the 2 pyruvate to yield 2 NADH, 2 CO2 and 2 Acetyl CoA.
Krebs cycle was named after hans adolf krebs (nobel winner) and it also sometimes called the citric acid cycle (CAC), it takes placed after pyruvate oxidation in the presence of oxygen so aerobic repiration/conditions
It occurs in mito matrix and it uses the 2 acetyl coa to make 2 atp, 6 NADH, 2 FADH2 and 4CO2
what happens in that the acetylcoa (2c) combines with (4c) oxalacetate to form (6c) citrate and becomes isomer isocitrate which decarboylzes into 2CO2 and oxidizes creating NADH twice becoming (4c) succinyl coA this becomes succinate (4c) as the GDP gets Pi added to become GTP which isomers or phospyls to ADP to become ATP and the succinate now dehydrate into fumarate (4c) while producing FADH2 and fumarate becomes (4c) oxaloacetate and produces NADH while doing that
so the final products were 2 FADH2, 2ATP and 6 NADH when u considered that it happened twice since there’s 2 acetyl coas
Detailed steps of kreb cycle
in mitochondrial matrix
aerobic: requires oxygen
acetyl-CoA completely oxidized to produce CO2
also produces ATP, NADH and FADH2
8 steps
(Note, Two acetyl-Co A molecules enter, so the Krebs Cycle must happen twice for every one molecule of glucose that begins glycolysis.)
acetyl transfer, isomerization, oxidation + decarboxylation, oxidation + decarboxylation, CoA release + substrate-level, phosphorylation, oxidation, hydration, and last oxidation
(Oxidation is the loss of electrons during a reaction by a molecule, atom or ion
Decarboxylation is a chemical reaction that removes a carboxyl group and releases carbon dioxide (CO2)
H+ = Proton When the Hydrogen atom loses an electron all that is left is a proton. It becomes the positively charged hydrogen ion known as H+.)
- acetyl transfer: each acetyl-CoA breaks: the CoA is recycled and the acetyl group (2C) joins with oxaloacetate (4C) to produce citrate (6C)
- 1 water used (not counted in overall equation) - isomerization: each citrate is rearranged to form isocitrate
- oxidation + decarboxylation: each isocitrate (6C) is oxidized by NAD+ and a carbon is released as CO2 to form α-ketoglutarate (5C)
- 1 NAD+ used, 1 NADH, 1 H+ and 1 CO2 produced - oxidation + decarboxylation: each α-ketoglutarate (5C) is oxidized by NAD+, a carbon is released as CO2, and a CoA bonds to the compound to form succinyl-CoA (4C)
- 1 NAD+ and 1 CoA used, 1 NADH, 1 H+ and 1 CO2 produced - substrate-level phosphorylation: each succinyl-CoA breaks: the CoA is recycled and succinate is left behind. The energy released is used to convert GDP and an inorganic phosphate (Pi) into GTP. GTP then phosphorylates ADP to create ATP.
- 1 ADP and 1 Pi used, 1 ATP and 1 CoA produced - oxidation: each succinate is oxidized by FAD to form fumarate
- 1 FAD used, 1 FADH2 produced - hydration: each fumarate has water added to form malate
- 1 water used (not included in overall reaction) - oxidation: each malate is oxidized by NAD+ to form oxaloacetate
- 1 NAD+ used, 1 NADH and 1 H+ produced
overall citric acid cycle for 1 acetyl-CoA:
1 acetyl-CoA + 3 NAD+ + FAD + ADP + Pi –> 2 CO2 + 3 NADH + 3 H+ + FADH2 + ATP + CoA
overall citric acid cycle for 2 acetyl-CoA (1 glucose):
2 acetyl-CoA + 6 NAD+ + 2 FAD + 2 ADP + 2 Pi –> 4 CO2 + 6 NADH + 6 H+ + 2 FADH2 + 2 ATP + 2 CoA
In step 1, acetyl-CoA combines with oxaloacetate to form citrate. NAD+ is reduced to NADH in steps 3, 4 and 8. FAD is reduced to FADH2 in step 6. ATP is formed in step 5 by substrate-level phosphorylation. In step 8, oxaloacetate is formed, which is used as a reactant in step 1. CO2 is released in steps 3 and 4
By the end of the Citric Acid Cycle, the original glucose molecule has been completely dismantled. Original carbon and oxygen atoms are in the form of CO2 and released as waste. All that remains is the hydrogen which are now carried by NADH and FDH2 - these electrons still hold large amount of chemical potential energy.
General Ideas of Pyruvate oxidation and Krebs cycle
The goal of these two processes are to break down pyruvate and collect the energy released from the carbon-carbon bonds. This energy is stored in energy-carrier molecules called nicotinamide adenine dinucleotide (NAD) and flavin adenine dinucleotide (FAD). The low energy forms of these are called NAD+ and FAD and the high energy forms are called NADH and FADH2.
Both the pyruvate oxidation step and the citric acid cycle take place in the mitochondrial matrix. Pyruvate is a product of glycolysis. Because glycolysis happens in the cytosol of the cell, pyruvate has to be transported inside the mitochondria through active transport.
In pyruvate oxidation, pyruvate is
transformed into acetyl-CoA. CoA is an abbreviation for coenzyme A. Coenzymes are large non-protein molecules that attach to enzymes and help them function. Carbon dioxide is released and one NADH is also produced. (for the 2 pyruvates that are produced from one glucose, 2 acetyl coa, 2 nadh and 2 co2 are technically produced)
In the first step of the citric acid cycle (see your diagram), acetyl-CoA reacts with oxaloacetate to form citrate. (coa is removed)
In steps 2-3, citrate is transformed into aconitate and then into isocitrate. Citrate and isocitrate are actually isomers; they look almost exactly alike except some of their oxygen atoms are rearranged.
In step 4, isocitrate is broken down into alpha-ketoglutarate and carbon dioxide. Energy from this reaction is released and collected by NAD+ to form NADH, an energy carrier molecule.
In step 5, a coenzyme A attaches to alpha-ketoglutarate and it is broken down into carbon dioxide and succinyl-CoA. In this step, energy again is released and collected by NAD+ to form another NADH. (sometimes step 4 and 5 are combined so it seems like isocitrate becomes succinyl-coA in one step and 2 NADH are produced)
In step 6, succinyl-CoA’s oxygen atoms are rearranged and coenzyme A is released to form succinate. This process releases energy and the energy is stored in a GTP (Guanosine triphosphate). This GTP (Guanosine triphosphate) is converted to ATP, the main energy-storage molecule or “battery” in the cell.(technically GDP to GTP and then GTP to ADP to ATP)
In step 7, succinate releases two hydrogens, forms a double bond between two of its carbons, and releases more energy to form fumarate. This energy is stored in FADH2, another energy carrier molecule.
In step 8, fumarate reacts with water to form malate. In step 9, malate’s oxygen atoms are rearranged to form
oxaloacetate. This reaction releases more energy, which is collected and used to form NADH.
Overall reaction of pyruvate oxidation of one pyruvate:
1 pyruvate + 1 NAD+ + CoA –> 1 Co2 + 1 NADH + 1 acetyl CoA
Overall reaction of pyruvate oxidation for one glucose:
2 pyruvate + 2NAD+ + 2 CoA –> 2Co2 + 2NADH + 2 acetyl CoA
Overall reaction of citric acid cycle for one acetylcoa:
1 acetyl CoA + 3NAD+ + 1GDP + Pi + FAD –> 1CoA + 2Co2 + 3NADH + 1FADH + 1 GTP
Overall reaction of cyrtic acid cycle for one glucose:
2 Acetyl CoA + 6NAD+ + 2GDP + 2Pi + 2FAD –> 2 CoA + 6 NADH + 2 GTP + 2 FADH
Overall reaction of glycolysis:
1 glucose + 2ADP + 2Pi + 2 NAD+ –> 2 Pyruvate + 2 ATP + 2 NADH ( + 2H+?)
When C is removed its called decarboxylation and the byproduct is usually CO2 (known as released as waste)
Hydrogen is removed by NAD+ or FAD
PRODUCTS OF KREB CYCLE:
CO2 is relased as waste
NADH and FADH2 move to the next stage of cellular respiration
Energy is released in form of ATP. A glucose molecule produces 2 molecules of ATP (from GDP/GTP) because two molecules of pyruvate are created from each molecule of glucose.
ETS 1
The Electron Transport Chain, Oxidative Phosphorylation, and Chemiosmosis. –> end of aerobic stage. ets and oxidtative phorphyrlation and chemiosism are last steps of formation of atp → we start with glucose, krebs had side products, which all comes down to here → weve spent a couple of atp and gotten a few, our net is small but in this process we will get lots of a atp
Glycolysis: 2 NADH + 2 ATP
Pyruvate Oxidation: 2 NADH
Krebs Cycle: 6 NADH, 2 FADH2, 2 ATP
The NADHs and FADH2s are what we are interested in for the Electron Transport Chain. Electrons donated by them are transported through the chain, which provides energy for oxidative phosphorylation
The ets is a chain of protein complexes embedded in the inner mitochondrial membrane; site of oxidative phosphorylation –> produces many ATP. It transports e- by oxidizing NADH and FADH2; pumps H+ ions (protons) into intermembrane space –> creates a gradient
Key components are NADH dehydrogenase, Ubiquinone (Q), Cytochrome b-c1, Cytochrome c, Cytochrome oxidase
NADH produced in the cytoplasm by glycolysis: diffuses from the outer mitochondrial membrane to the intermembrane space, and then into the matrix. NADH produced from Krebs cycle: Already in the matrix
ETS 2
(I) NADH dehydrogenase:
- NADH dehydrogenase oxidizes NADH back to NAD+
(NADH + H+ 🡪 NAD+ + 2H+ + 2e-)
- 2e- from NADH are passed to electron acceptors in ETS one at a time; then passed to ubiquinone (Q)
- H+ ions do not go with the 2e-; remain in solution in the matrix until after 2e- have completed passage through EACH complex of ETC; then they are actively pumped out of matrix and into the intermembrane space –> creates H+ gradient
(II) Ubiquinone (Q)
- A mobile electron carrier (carries e-)
- RECALL: FADH2 from Krebs is already in the matrix
- FADH2 embeds itself into the inner mitochondrial membrane and becomes oxidized:
(FADH2 🡪 FAD + 2e- )
- 2e- attach to Q (skips NADH hydrogenase) and move through remaining complexes in ETC
(III) cytochrome bc1
- Contains cytochrome b, cytochrome c1, and FeS (iron sulfide) proteins
- Q passes 2e- to cytochrome bc1; the energy generated from this passage actively pumps another H+ ion from the matrix into the intermembrane space
Cytochrome C (C)
- Another mobile electron carrier like Q that transports electrons from cytochrome bc1 to cytochrome oxidase complex
(IV) Cytochrome Oxidase Complex
- This is the end of the line for electrons from NADH and FADH2
- Oxygen breathed in is reduced and combines with these electrons to form WATER
For each glucose molecule that enters cellular respiration, chemiosmosis produces up to 38 ATP. (usually between 34-36 tho)
CHEMIOSMOSIS:
- Energy from reduced NADH and FADH2 produces an electrochemical H+ ion gradient in the intermembrane space
- Build up of positive charges in the intermembrane space relative to the matrix
- Electrical potential energy of the positive charges is converted to chemical potential energy of ATP by ATP synthase when H+ ions pass through the inner mitochondrial membrane via ATP synthase
- As H+ moves through the ATP synthase complex, the energy phosphorylates ADP to ATP
YIELD OF ATP = 36 or 38
- For each pair of e- from NADH or FADH2 that pass through one H+ pump, one ATP molecule can be formed. Therefore: 2e- from NADH go through 3 H+ pumps = 3 ATP. 2e- from FADH2 go through 2 H+ pumps(skipped dehydrogenase) = 2 ATP
Recall: Products from Processes
- Glycolysis: 2 NADH –> 4 or 6 ATP** (23)
- Pyruvate Oxidation: 2 NADH –> 6 ATP (23)
Krebs Cycle: 6 NADH, 2 FADH2 –> 18 ATP, 4 ATP(63 & 22)
Glycolysis and Krebs both produce 2 ATP each
* *Mitochondrial membrane is impermeable to NADH made in cytoplasm; 2e- need to be shuttled to either FAD or NAD+ molecule –> result is either 4 or 6 ATP
Aerobic Respiration Overview
Cellular respiration includes the catabolic pathways that break down energy-rich compounds to produce ATP. Aerobic respiration refers to those pathways that require oxygen in order to proceed. The following summary reaction for this process represents more than two dozen reactions that take place in different parts of the cell.
C6H12O6(s) + 6O2(g) –> 6CO2(g) _ 6H2O(l) + energy
Although part of aerobic respiration, the first pathway, glycolysis, is not truly aerobic.
Glycolysis can proceed with or without oxygen. However, the products of glycolysis are
the starting materials for the metabolic pathways that follow, and they require oxygen.
Glycolysis occurs within the cytoplasm of cells. The starting material for glycolysis is glucose, a six-carbon sugar. Each glucose molecule is broken down, through a series of reactions, into two three-carbon compounds. Each of these compounds is converted into a three-carbon pyruvate molecule. Thus, the end products of glycolysis include two molecules of pyruvate for each molecule of glucose that enters glycolysis. The glycolytic pathway also converts two molecules of NAD+ into two molecules of NADH. The breakdown of glucose into pyruvate includes two reactions that consume ATP, as well as two reactions that produce ATP. Overall, the process consumes two molecules of ATP and produces four molecules of ATP. Thus, this pathway is responsible for a net production of two ATP molecules.
At various steps in the glycolytic pathway, a phosphate group is removed from a substrate molecule and combined with an ADP molecule to form ATP. This process is called substrate level phosphorylation. (Phosphorylation refers to any process that involves the combining of phosphate to an organic compound.)
When oxygen is available, pyruvate from glycolysis is transported across the outer and inner mitochondrial membranes into the mitochondrial matrix. There, the three-carbon pyruvate molecule undergoes oxidation. This produces a two-carbon molecule called acetyl-coenzyme A, abbreviated as acetyl-CoA, and releases one carbon atom in the form of carbon dioxide. In the process, one NAD+ molecule is reduced to form NADH. Since glycolysis produces two pyruvate molecules, pyruvate oxidation actually releases two molecules of carbon dioxide and reduces two molecules of NAD+ to form two molecules of NADH.
Each acetyl-CoA molecule then enters the Krebs cycle, which is also known as the citric acid cycle or the tricarboxylic acid (TCA) cycle. Tricarboxylic acid is a general name referring to an organic acid with three carboxyl groups. Citric acid is one example of a tricarboxylic acid. At physiological pH, citric acid exists in its ionized form, called citrate. Acetyl CoA combines with a four-carbon molecule in the Krebs cycle to form the six-carbon molecule, citrate. In each round of the Krebs cycle, one ATP molecule is formed, three NAD+ molecules are reduced to form three molecules of NADH, and one FAD molecule is reduced to form one molecule of FADH2. Since two molecules of acetyl CoA are produced for every molecule of glucose that enters glycolysis, the total yield from the Krebs cycle is two ATP molecules, six NADH molecules, and two FADH2 molecules.
The substrates, products, and enzymes of the Krebs cycle are in solution in the mitochondrial matrix.
The reduced NADH and FADH2 molecules diffuse to specific locations on the inner membrane of the mitochondrion and donate their electrons to a series of electron carriers that are embedded in the inner mitochondrial membrane. As each electron carrier passes an electron to the next carrier, some energy is released. This energy is used to pump protons, H+, across the inner mitochondrial membrane into the intermembrane space. This creates a proton gradient across the inner mitochondrial membrane, which provides the energy for the enzyme ATP synthase to phosphorylate (add Pi to) ADP molecules to make ATP.
Because this energy comes from the flow of electrons from NADH and FADH2 to oxygen, this process is called oxidative phosphorylation.
A maximum of 38 molecules of ATP can be generated by the breakdown of one molecule of glucose through the overall process of aerobic respiration. This includes ATP generated directly by glycolysis and the Krebs cycle, ATP generated from the two molecules of NADH produced during glycolysis, and ATP produced through oxidative phosphorylation, from reducing power generated during pyruvate oxidation and the Krebs cycle.
Although 36 or 38 ATP molecules per glucose molecule are theoretically possible,
experimental observations of the actual number of ATP molecules per glucose molecule are
much lower. There are several reasons to account for these lower values.
* Some protons leak through the inner mitochondrial membrane without passing through
an ATP synthase complex.
* Some of the energy from the hydrogen ion gradient in the mitochondria is used to
transport pyruvate molecules generated during glycolysis from the cytoplasm into the
mitochondria.
* Some energy is used to transport ATP out of the mitochondria for use in the cytoplasm.
Experimentally measured values are closer to 30 to 32 molecules of ATP produced per
glucose molecule.
most of a healthy diet is used for energy. Carbohydrates other than glucose, as well as fats and
proteins, are used for energy. Most carbohydrates can be broken down and converted into glucose. After the amino group has been removed from some amino acids, the remainder of the molecule is identical to some intermediate in either glycolysis or the Krebs cycle. Fat molecules are broken down into glycerol
and fatty acids. Glycerol can be converted into G3P, one of the intermediates in glycolysis. Fatty acids are transported into the mitochondria, where carbon atoms are removed two at a time and each two-carbon unit becomes an acetyl-CoA molecule, ready to enter the Krebs cycle.
How does the cell
determine and control the rate at which to generate ATP? The answer is feedback control.
- The enzyme phosphofructokinase is the main control point in glycolysis.
Phosphofructokinase has an allosteric binding site for ATP. Thus, when the cell has
sufficient ATP to supply energy for the endergonic reactions taking place at a given time, any excess ATP binds to the allosteric site of phosphofructokinase and inhibits the enzyme. Citrate, one of the intermediates in the Krebs cycle, can also inhibit phosphofructokinase. Thus, if there is an accumulation of citrate, pyruvate from glycolysis is not broken down into acetyl-CoA until some of the citrate is used up. In contrast, high levels of ADP activate phosphofructokinase.
- A second important control site in aerobic catabolic pathways is the conversion of pyruvate into acetyl-CoA and carbon dioxide. The enzyme that catalyzes this reaction, pyruvate dehydrogenase, is inhibited by excess NADH. Several Krebs cycle enzymes are also inhibited by excess ATP, NADH, and acetyl-CoA. When all of these control mechanisms are working together, the level of ATP remains constant within the cell.
General Review Questions of the processes
In substrate-level phosphorylation, ATP is formed form transferring a phosphate group to ADP. In oxidative phosphorylation, the oxidation of NADH and FADH2 by the electron transport system is coupled with the synthesis of ATP by phosphorylation of ADP. (Substrate level phosphorylation is the conversion of ATP to ADP or vice versa on an enzyme. Oxidative phosphorylation is the use of electron transport chains to generate ATP chemiosmotically.)
The main function of glycolysis is to break down glucose in to 2 pyruvate molecules and generate side products like ATP and NADH. Water also is formed but not really counted in the equation. The role of the Krebs Cycle is to oxidize acetyl COA to Co2, regenerates a compound that connects to acetyl CoA so that the cycle can continue and create ATP, FADH2 and NADH. The side products of the Krebs Cycle are much more important as they actually move on to the next stage of respiration.
Why is oxidative phosphorylation an important process in aerobic respiration?
It effectively converts the energy stored in NADH and FADH2 to energy in the form of ATP. By oxidizing these two energy-rich compounds, it also forms NAD+ and FAD which are needed by the Krebs cycle, which will reduce them again while oxidizing carbon. Oxidative phosphorylation actually allows for the most ATP/energy to actually be produced.
The ETS is a series of e-carriers and proteins that are embedded in the inner membrane of the mitochondria. E- donated by NADH and FADH2 are transported through this chain which provides the energy needed for oxidative phosphorylation.
Chemiosomis is the process that uses energy in the hydrogen ion/proton gradient that was formed across the inner mitochondrial membrane by the ets/oxidative phosphorylation to drive the phosphorylation of ADP to form ATP. ATP synthase will catalyze the phosphorylation of ADP and most of the energy of cellular respiration is created by this.
The Krebs cycle requires NAD+ and FADH+ to reduce pyruvate. If there is no oxygen, the electron transport chain does not pass electrons to it to produce water. This means that electrons are not taken from the NADH and FADH2, and therefore NAD+ and FADH+ are not available.
If the electron transport chain is inhibited, very little ATP is produced, and human metabolism would not have enough energy to continue.
Cell Respiration Summary
Cell respiration supplies energy for the functions of life. Cell respiration is the controlled release of energy from organic compounds to produce ATP.
The organic compounds used for cellular respiration are mostly glucose and fatty acids… but sometimes proteins.
Net equation for cellular reprition is glucose + 602 –> 6CO2 + 6H2O and energy (glucose is the organic molecule used to make atp, cells make more atp when oxygen is available, co2 is released as waste, water is a final product of preparation and atp is the energy currency of the cells)
In cells, energy is transferred in the form of adenosine triphosphate, ATP, which is immediately available for use. Cells will continuously produce and consume ATP. ATP is produced by the phosphorylation of ADP. Phosphorylation is the addition of a phosphate group to an organic molecule, either from inorganic (Pi) or organic sources.
Phosphorylation refers to the chemical reactions that make ATP. Phosphorylation takes place in two different kinds of reactions in cells:
Substrate-Level Phosphorylation and Oxidative Phosphorylation
Substrate-level phosphorylation: The formation of ATP in the cytoplasm occurs by substrate-level phosphorylation. Energy from a high-energy substrate (food molecule) is used to transfer a phosphate group to ADP to form ATP.
Oxidative phosphorylation: links an electron transport system, which creates a proton gradient, with ATP synthase, an enzyme that is activated by protons flowing through it, down the gradient. Chemiosmosis is a process that generates ATP by the movement of hydrogen ions across a biological membrane down an electrochemical (proton/concentration) gradient. In cell respiration, the gradient forms due to movement of electrons through the electron transport chain. In photosynthesis, the gradient forms due to electron transport and the photolysis of water. Oxidative phosphorylation occurs in mitochondria during the cell respiration. Electrons move by a series of redox reactions from one carrier protein to another along the inner membrane. This provides the energy to pump protons (H+) from the matrix to the intermembrane space, building up a concentration gradient. Protons flow back to the matrix by facilitated diffusion through the enzyme ATP synthase, which catalyzes phosphorylation of ADP. Photophosphorylation occurs in chloroplasts in the first stage of photosynthesis. Sunlight energy is used to pump hydrogen ions into the thylakoids. This creates a concentration gradient between the thylakoid and the stroma. Protons flow back to the stroma by facilitated diffusion through the enzyme ATP synthase, which catalyzes phosphorylation of ADP.
ATP is too unstable to be stored by cells. Instead, organisms store energy in polysaccharides and lipids. ATP is used for many things in the cell like active transport, DNA replication, muscle contraction, protein synthesis and cell signalling.
All of the processes that use ATP also generate heat. This means eventually, all energy becomes heat. This heat energy may be used to raise the organism’s body temperature, but is eventually lost to the environment.
Enzymes are used in metabolic pathways and cycles, which break down the release of energy from glucose and other food molecules into multiple small steps. Enzyme-catalyzed reactions are controlled by end-product inhibition.
Anaerobic cell respiration gives a small yield of ATP from glucose.
All cellular preparation begins with glycolysis. Glycolysis = “splitting glucose”. Glycolysis is an anaerobic process that occurs in the cytoplasm of all cells. . It is a multi-step pathway that produces 2 ATP and 2 molecules of pyruvate. And 2 molecules of NADH and H+
What happens to pyruvate in cells depends on the availability of oxygen: If sufficient oxygen is available, pyruvate is further broken down by Krebs cycle and the electron transport chain. If there is insufficient oxygen, a fermentation pathway allows glycolysis to continue forming ATP.
Aerobic cell respiration requires oxygen and gives a large yield of ATP from glucose. When cells have lots of oxygen available, pyruvate formed by glycolysis enters the mitochondria for aerobic respiration. Aerobic respiration consists of two processes in cells: Krebs cycle (a.k.a. citric acid cycle) produces carbon dioxide (waste) and a small amount of ATP. The electron transport chain (ETC) uses electrons released by glycolysis and Krebs cycle to generate a large amount of ATP.
Oxidation: addition of oxygen, removal of hydrogen, loss of e-, results in c-o bonds, and release of energy (lower potential energy). An oxidizing agent is a substance that oxidizes something else. Oxidizing agents give oxygen to another substance or remove hydrogen from it
Reduction: removal of oxygen, addition of hydrogen, gain of e-, reulst in many c-h bonds and uptake of energy (higher potential energy). A reducing agent is a substance that reduces something else. Reducing agents remove oxygen from another substance or give hydrogen to it.
During cellular respiration, the coenzyme NAD and FAD accepts hydrogen ions (and electrons), becoming reduced.
Thermodynamics:
- 1st Law: Energy cannot be created or destroyed. It can be converted from one form to another. The sum of the energy before the conversion is equal to the sum of the energy after the conversion.
- 2nd Law: During changes from one form of energy to another, some usable energy dissipates, usually as heat. The amount of usable energy therefore decreases.
In cells, energy is transferred in the form of adenosine triphosphate, ATP. Cells continuously produce & consume ATP.