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The document discusses respiration in plants, detailing cellular respiration, glycolysis, fermentation, and the tricarboxylic acid cycle. It explains the breakdown of glucose for energy production, the role of ATP, and the differences between aerobic respiration and fermentation. Additionally, it covers the respiratory quotient and the amphibolic pathway, highlighting how various substrates can enter the respiratory process.

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0% found this document useful (0 votes)
12 views12 pages

Selfstudys Com File

The document discusses respiration in plants, detailing cellular respiration, glycolysis, fermentation, and the tricarboxylic acid cycle. It explains the breakdown of glucose for energy production, the role of ATP, and the differences between aerobic respiration and fermentation. Additionally, it covers the respiratory quotient and the amphibolic pathway, highlighting how various substrates can enter the respiratory process.

Uploaded by

mryashshah09
Copyright
© © All Rights Reserved
We take content rights seriously. If you suspect this is your content, claim it here.
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Respiration in Plants

Cellular Respiration & Glycolysis

Cellular Respiration

• Mechanism of breakdown of food materials within the cell to release energy, and the
trapping of this energy for ATP synthesis.

• Respiratory substrates: Compounds oxidised during respiration; usually carbohydrates;


these can also be proteins, fats or organic acids

• ATP: Energy currency of a cell; broken down whenever energy is needed

• Plants do not need specialised organs for respiration because:

• Gaseous exchange occurs in each part of a plant.

• Gaseous exchange is not a much-needed factor. During photosynthesis, the need for
gaseous exchange is met.

• Each living cell is located close to the surface of a plant. So the distances that the gases
must diffuse are not great.

• Equation for respiration:

C6H12O6 + 6O2 → 6CO2 + 6H2O + Energy

Glycolysis (Glycos − Sugar, Lysis − Splitting)

• Breakdown of glucose to pyruvic acid by partial oxidation

• Scheme given by Embden, Meyerhof and Parnas

• Common pathway for aerobic and anaerobic cellular respiration

• Occurs in the cytoplasm of a cell

• Present in all living organisms

• In plants, sucrose is converted into glucose.


• A chain of 10 reactions converts glucose into pyruvate.

• Hexokinase: Enzyme that phosphorylates glucose to produce glucose − 6 − phosphate

• 2 ATPs are utilised in two steps:

• Glucose → Glucose − 6 − phosphate (1 ATP)

• Fructose − 6 − phosphate → fructose 1, 6 − bisphosphate (1 ATP)

• Fructose 1, 6 bisphosphate splits into glyceraldehyde − 3 − phosphate and dihydroxy


acetone phosphate.

• Glyceraldehyde − 3 − phosphate converts into two molecules of 1, 3


bisphosphoglycerate (BPGA), with subsequent conversion of NAD+ to NADH + H+.

• 4 ATPs are yielded in two steps:

• BPGA → PGA (1 × 2 = 2 ATPs)

• Phosphoenol pyruvate → Pyruvic acid (1 × 2 =2 ATPs)

• ATPs produced directly = 4 (produced) − 2 (consumed) = 2 ATPs

• Net ATPs Produced = 2 (NADH+ H+) = 6 ATPs + 2 (Directly synthesised) = 8 ATPs


• The pyruvate, so produced, may undergo:

• Lactic acid fermentation


• Alcoholic fermentation

• Aerobic respiration (Krebs cycle)

Fermentation

• Fermentation: Incomplete oxidation of glucose under anaerobic conditions

• In yeast fermentation:

• Pyruvic acid → Ethanol + CO2

• Enzymes involved − Pyruvic acid decarboxylase, Alcohol dehydrogenase

• In bacterial fermentation:

• Pyruvic acid → Lactic acid

• Enzyme involved − Lactate dehydrogenase

• Similar reaction occurs in animal muscles in anaerobic conditions, say during exercise.

• Reducing agent in both reactions is NADH.

NADH + H+ → NAD+

• Only 7% of energy of glucose is released during fermentation.

• Process can be hazardous as alcohol or acid is produced. Yeasts poison themselves to


death when alcohol concentration reaches about 13%.
Tricarboxylic Acid Cycle

Aerobic Respiration

• Site: Mitochondria

• Events:

• TCA cycle (in the mitochondrial matrix) − complete oxidation of pyruvate by stepwise
removal of all hydrogen atoms, which leaves three molecules of CO2

• Electron Transport Chain and Oxidative phosphorylation (in the inner membrane of
the mitochondria) − electrons removed as a part of hydrogen atoms are passed on to
molecular oxygen, with the simultaneous synthesis of ATP

Formation of Acetyl Coenzyme A

• The product of glycolysis, i.e., pyruvate, on entering the mitochondrial matrix,


undergoes Oxidative Decarboxylation, thereby producing acetyl CoA which enters
Krebs cycle.

Krebs cycle (Tricarboxylic acid cycle; TCA)


• Acetyl group condenses with oxaloacetic acid and water to yield citric acid (catalysed by
the enzyme citrate synthase)

• Citrate isomerises into isocitrate

• Two successive decarboxylation steps follow, leading to the formation of α ketoglutaric


acid, followed by succinyl CoA

• This is followed by the conversion of succinyl CoA into succinic acid. During this
process, GDP is converted into GTP (substrate level phosphorylation).

• In a coupled reaction, GTP is converted into GDP, simultaneously synthesising ATP


from ADP.

• Conversion of one molecule of pyruvate into acetyl CoA yields 1 molecule of CO2 and 1
NADH.

• One Kreb's cycle yields 2 CO2 + 3 NADH + 1 FADH2 + 1 ATP

• Overall equation:

• For continued oxidation of acetyl CoA in TCA 2 things are required:

• Continued replenishment of oxaloacetic acid

• Regeneration of NAD+ and FAD+ from NADH and FADH2 respectively.


Electron Transport Chain and Oxidative Phosphorylation

Electron Transport Chain (ETS)

• NADH and FADH2 are oxidised to release the energy stored in them.

• Electrons are passed from one carrier to another, and finally to oxygen, resulting in the
formation of water.
• Electrons produced by NADH in the mitochondrial matrix are oxidised by Complex
I (NADH dehydrogenase).

• Electrons are then transferred to ubiquinone, located in the inner mitochondrial


membrane. Ubiquinone receives reducing equivalents through Complex II (FADH2).

• Reduced ubiquinone (ubiquinol) is then oxidised by the transfer of electrons


from Complex III (cytochrome bc1 complex) to cytochrome c.

• Cytochrome c transfers the electrons between Complex III and Complex


IV (Cytochrome c − oxidase complex consists of cyt a and a3, along with two copper
centres).

• In the course of passing from one carrier to another, electrons couple with Complex
V (ATP synthase) and produce ATP.

• Oxidation of 1 NADH produces 3 ATPs.


Oxidation of 1 FADH2 produces 2 ATPs.
• Role of oxygen in the terminal stage of ETS: It acts as the final hydrogen acceptor;
removes hydrogen from the process and drives the whole process

Oxidative Phosphorylation

• Production of proton gradient needed for the production of ATP is provided by the
energy of oxidation−reduction reaction. Therefore, the process is called oxidative
phosphorylation.

• Complex V (ATP synthase) is involved. It has two major components

• F0 − integral membrane protein; forms a channel through which H+ cross the inner
membrane

• F1 − passage of H+ induces conformational changes in F1, which forms a site for


synthesis of ATP from ADP; for each ATP produced, 2H+ pass through F0, down the
electrochemical proton gradient

Respiratory Balance Sheet and Respiratory Quotient

Respiratory Balance Sheet

• It gives the net gain of ATP for every 1 molecule of glucose oxidised.

• Certain assumptions are made for calculating the net gain of ATP:

• An orderly pathway is followed − Glycolysis, followed by TCA cycle, followed by ETS

• NADH synthesised during glycolysis enters the mitochondria to undergo oxidative


phosphorylation.

• Except glucose, no other substrate enters the pathway at any stage.


• Intermediates do not synthesise any other compound in the pathway.

• There can be a net gain of 36 ATPs during aerobic respiration of 1 molecule of glucose.
Glucose + 6O2 + 36ADP + 36Pi → 6CO2 + 42H2O + 36ATP

Comparison between fermentation and aerobic respiration

Fermentation Aerobic Respiration

1. Partial breakdown of glucose 1. Complete breakdown of glucose into


CO2 and H2O

2. Net gain of only 2 molecules of ATP 2. Net gain of 36 molecules of ATP

3. Here, oxidation of NADH to NAD+ is a 3. Here, oxidation of NADH to NAD+ is a


slow reaction vigorous reaction

Amphibolic Pathway

• Favoured substrate for respiration is glucose. All carbohydrates first convert into
glucose to enter the pathways.

• Other substrates do enter the respiratory pathways, but not during the first stage.

• Fats:

• Fats → Glycerol + Fatty acid

• Fatty acids → Acetyl CoA


Acetyl CoA enters the pathway

• Glycerol → PGAL

• Proteins:

• Proteins Amino acids


• Enter intermediate stages of TCA

• Amphibolic pathway: Involved in both anabolism and catabolism

• Fatty acids break into acetyl CoA to enter the respiratory pathway (Anabolism).

• Acetyl CoA is removed from the respiratory pathway whenever fatty acids need to be
synthesised (catabolism).

• Thus, respiratory intermediates form a link during anabolism and catabolism.

Respiratory Quotient (RQ)

• Ratio of the volume of CO2 evolved to the volume of O2 consumed during respiration is
called the respiratory quotient (RQ).

• RQ =

• Depends upon the type of respiratory substrate

• RQ = 1 (When carbohydrate is used as substrate)


• C6H12O6 + 6O2 → 6CO2 + 6H2O + Energy

RQ =

• RQ < 1 (When fat is used as respiratory substrate)

E.g. When fatty acid, tripalmitin is used, RQ = 0.7

• RQ ≈ 0.9 (When protein is used as substrate)

• RQ is infinity in anaerobic respiration as CO2 is evolved, but O2 is not utilised.

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