Respiration in Plants

Complete Notes

Contents Respiration — Introduction and Types Respiratory Substrate Do Plants Breathe? Glycolysis Fermentation (Anaerobic Respiration) Aerobic Respiration — Link Reaction and Krebs Cycle Electron Transport System and Chemiosmosis Total ATP Yield Amphibolic Pathway and Respiratory Quotient Practice Questions Download Notes

Respiration — Introduction

Cellular Respiration is the process which involves oxidation of food (glucose) to release energy, with the breaking of carbon-carbon (C-C) bonds of complex compounds through a series of enzyme-catalysed reactions, resulting in the release of CO₂, water, and energy.

Important Glucose Formula: C₆H₁₂O₆ + 6O₂ → 6CO₂ + 6H₂O + Energy

Types of Respiration (Based on Oxidation of Carbon)

Complete Oxidation: All C-C bonds are broken — the substrate is completely oxidised, yielding CO₂, H₂O, and maximum energy. Occurs in Aerobic Respiration.
Incomplete Oxidation: Carbon-carbon bonds are not completely broken — yields different molecules (e.g. ethanol, lactic acid) and less energy compared to complete oxidation. Occurs in Anaerobic Respiration / Fermentation.

Energy carriers like NADH + H⁺ and FADH₂ are formed during oxidation. These carry electrons to the Electron Transport System (ETS), where they are used to generate ATP.

Respiratory Substrate

The molecule which is oxidised during respiration is called the Respiratory Substrate. On the basis of the substrate used, respiration is of types:

Floating Respiration: Carbohydrates and Fats are the most favoured/commonly used respiratory substrates.
Protoplasmic Respiration: Uses Protein as the substrate. Organic acids can also be used as respiratory substrates.

Important Features of Respiration

Link Between Photosynthesis and Respiration

Green plant parts convert light energy into chemical energy through photosynthesis. Organisms that make their own food are called Producers, e.g. green plants, BGA (Blue-Green Algae). Other organisms (e.g. Goat, Tiger — Herbivores/Carnivores) depend directly or indirectly on plants for food — these are called Consumers.

Do Plants Breathe?

Plants need O₂ to oxidise food and make ATP. However, plants do not have a specialised respiratory system like animals — gas exchange occurs by simple diffusion through stomata in leaves, and through the general surface of stem and root.

Why Plants Don't Need a Respiratory System

Early Organisms and Anaerobic Respiration

The early atmosphere on earth lacked free oxygen. Early organisms were anaerobic (living without oxygen). Anaerobes are of two types:

TypeDescriptionExample
Facultative AnaerobesCan live with or without free oxygen.—
Obligate AnaerobesCannot survive in the presence of oxygen.e.g. Clostridium, Mycoplasma

Early organisms developed a process called Glycolysis to generate ATP without O₂ — it is considered a universal process, since it is the first step common to both aerobic and anaerobic respiration.

Glycolysis

Glycolysis means "breakdown of sugar" (Glycos = sugar, Lysis = breakdown). It is an incomplete oxidation pathway, occurring in the cytoplasm, consisting of 10 steps, also called the EMP pathway (named after Embden, Meyerhoff, and Parnas). It can occur without O₂ (anaerobic) and is also found in eukaryotes.

Glycolysis — Overview

One molecule of Glucose (6C) [or Sucrose, broken into Glucose + Fructose, both 6C] is converted into 2 molecules of Pyruvate (3C) through 10 sequential steps.

Step-by-Step Outline of Glycolysis

StepConversionEnzyme/NoteATP/NADH Change
Step 1Glucose → Glucose-6-PhosphateHexokinase−1 ATP (ATP used)
Step 2Glucose-6-Phosphate → Fructose-6-Phosphate——
Step 3Fructose-6-Phosphate → Fructose-1,6-bisphosphatePFK-1 (Phosphofructokinase-1) — Pacemaker enzyme−1 ATP (ATP used)
(Split)Fructose-1,6-bisphosphate (6C) splits into 2 molecules of 3C — Glyceraldehyde-3-phosphate (G3P) and Dihydroxyacetone phosphate (DHAP); DHAP converts to G3P——
Step (oxidation)G3P → 1,3-bisphosphoglycerate (BPG)Oxidation; +2 NAD⁺ → 2 NADH+H⁺+2 NADH+H⁺ (for both 3C molecules)
(Phosphorylation)1,3-BPG → 3-phosphoglycerateADP + Pi → ATP (substrate level phosphorylation)+2 ATP
Step 10Phosphoenolpyruvate (PEP) → PyruvatePyruvate kinase; H₂O removed+2 ATP
Key points about glycolysis:

Fermentation (Anaerobic Respiration)

In the absence of O₂, pyruvate produced in glycolysis is further processed by fermentation, regenerating NAD⁺ from NADH+H⁺ (needed to keep glycolysis running).

Lactic Acid Fermentation

Occurs in muscle cells during vigorous exercise, and in lactic acid bacteria. Pyruvate is converted into Lactate (Lactic acid) by the enzyme Lactate Dehydrogenase (LDH), with NADH+H⁺ being oxidised to NAD⁺ (regeneration). Accumulation of lactic acid in muscles causes muscle pain/cramps.

Alcoholic Fermentation

Occurs in yeast (e.g. Saccharomyces). Pyruvate is converted to Acetaldehyde (2C) with release of CO₂, and then Acetaldehyde is reduced to Ethanol (C₂H₅OH) by the enzyme Alcohol Dehydrogenase, with NADH+H⁺ converted to NAD⁺.
Note: Yeast can poison themselves at around 13% alcoholic content — beyond this, the yeast dies. Absolute alcohol (100%) is formed by distillation. Fermentation is incomplete oxidation: energy released is <7% of what is released in complete (aerobic) oxidation. NADH+H⁺ formed during glycolysis is NOT sent to ETS in fermentation — it is converted back to NAD⁺ via lactic acid/alcoholic fermentation pathways, without producing additional ATP.

Aerobic Respiration

Aerobic respiration occurs in aerobic conditions, involving complete combustion of glucose:

C₆H₁₂O₆ + 6O₂ → 6CO₂ + 6H₂O + Energy (38 ATP)

Link Reaction (Oxidative Decarboxylation of Pyruvate)

This reaction connects glycolysis and the Krebs cycle — it occurs in the mitochondrial matrix. Pyruvate (3C) is converted into Acetyl CoA (2C), with release of CO₂.

Pyruvate + NAD⁺ + CoA → Acetyl CoA + CO₂ + NADH+H⁺
Key components: Carried out by the Pyruvate Dehydrogenase Complex (PDH complex) — requires cofactors Mg²⁺, NAD⁺, CoA (Coenzyme A — pantothenic acid derivative), and lipoic acid (lipoamide).

Link Reaction — Per Glucose Molecule

1 Glucose → 2 Pyruvate → 2 Acetyl CoA + 2 CO₂ + 2 NADH+H⁺.

Krebs Cycle (Citric Acid Cycle / Tricarboxylic Acid Cycle — TCA)

The Krebs cycle is also called the Citric Acid Cycle or Tricarboxylic Acid (TCA) Cycle, because the first product of this cycle is Citric acid (Citrate), which has 3 carboxylic acid (-COOH) groups.

Krebs Cycle — Steps Overview

StepConversionEnzyme / Product
1Oxaloacetic Acid (OAA, 4C) + Acetyl CoA (2C) → Citrate (6C)Citrate Synthase
2Citrate → cis-Aconitate → Isocitrate (6C)—
3Isocitrate (6C) → Alpha-Ketoglutarate (5C) + CO₂Oxidation — produces NADH+H⁺
4Alpha-Ketoglutarate (5C) → Succinyl CoA (4C) + CO₂Oxidative decarboxylation — produces NADH+H⁺
5Succinyl CoA → Succinate (4C)Substrate level phosphorylation — produces GTP/ATP
6Succinate → Fumarate (4C)Produces FADH₂
7Fumarate → Malate (4C)+ H₂O
8Malate → Oxaloacetic Acid (OAA, 4C) — regeneratedProduces NADH+H⁺
Per turn of Krebs cycle (1 Acetyl CoA): Since 1 glucose gives 2 Acetyl CoA, the Krebs cycle runs twice per glucose molecule.

Electron Transport System (ETS) and Chemiosmosis

ETS is located on the Inner Mitochondrial Membrane (IMM). NADH+H⁺ and FADH₂ produced during glycolysis, link reaction, and Krebs cycle donate electrons to the ETS, which are passed through a series of carriers/complexes to finally combine with O₂, forming water.

ETS Complexes

ComplexName / Components
Complex INADH Dehydrogenase — contains FMN (Flavin Mononucleotide) and Fe-S (Iron-Sulphur) centers
Complex IISuccinate Dehydrogenase — contains FAD (Flavin Adenine Dinucleotide) and Fe-S centers
Complex IIICytochrome bc1 Complex — contains Cytochrome b, Cytochrome c1, and Fe-S centers
Complex IVCytochrome c oxidase — contains Cytochrome a, a3, and Cu centers
Complex VATP Synthase — has F0 and F1 subunits
Mobile electron carriers: Ubiquinone (UQ/CoQ) and Cytochrome c shuttle electrons between the complexes.
NADH+H⁺ donates electrons to Complex I, while FADH₂ (from succinate dehydrogenase, Complex II) donates electrons at a later point — electrons eventually pass via UQ → Complex III → Cytochrome c → Complex IV → reduce O₂ to H₂O.

Cu and Fe Oxidation States

In the electron carriers: Cu centers are stable in +1 and +2 oxidation states; Fe centers (in Fe-S clusters and cytochromes) are stable in +2 and +3 oxidation states — these changes in oxidation state allow them to accept and donate electrons.

Chemiosmosis — ATP Synthesis

As electrons pass through the ETS complexes, protons (H⁺) are pumped from the mitochondrial matrix to the intermembrane space (IMS), creating a proton gradient across the inner mitochondrial membrane. This gradient is dissipated through ATP Synthase (Complex V, with F0 and F1 subunits), which uses the proton flow back into the matrix to synthesise ATP from ADP + Pi. This mechanism is called Chemiosmosis (proposed by Peter Mitchell).

ATP Yield Per NADH+H⁺ and FADH₂ via ETS

Electron DonorATP Produced (via ETS)
1 NADH+H⁺3 ATP
1 FADH₂2 ATP
Note (Important): O₂ is NOT directly used in the link reaction or the Krebs cycle. O₂ is used directly only at the end of the Electron Transport System, as the final/terminal electron acceptor — combining with electrons and H⁺ to form H₂O: 4H⁺ + O₂ + 4e⁻ → 2H₂O

Total ATP Yield — Per Glucose Molecule

StageNADH+H⁺FADH₂ATP (Direct/Substrate level)
Glycolysis202 ATP (net)
Link Reaction (Oxidative decarboxylation, ×2)200
Krebs Cycle (×2 turns)622 ATP (GTP/ATP via substrate level)
Total1024

Energy Calculation

Total = 30 + 4 + 4 = 38 ATP per glucose molecule (theoretical maximum).

Note — 36 vs 38 ATP

The 2 NADH+H⁺ from glycolysis are produced in the cytoplasm, and need to be transported into the mitochondria for ETS. Depending on the shuttle mechanism used:

Amphibolic Pathway

Respiration is not solely a catabolic process — it is called an Amphibolic Pathway, because the respiratory pathway is involved in both Catabolism (breakdown) and Anabolism (synthesis). Intermediates of the respiratory pathway (glycolysis and Krebs cycle) are utilised to synthesise other compounds.

Substrates Other Than Glucose — Entering Respiration

Respiratory Quotient (RQ)

Respiratory Quotient (RQ) = Volume of CO₂ evolved / Volume of O₂ consumed.
Respiratory SubstrateRQ ValueReason
CarbohydratesRQ = 1Equal volumes of CO₂ produced and O₂ consumed (e.g. C₆H₁₂O₆ + 6O₂ → 6CO₂ + 6H₂O)
FatsRQ < 1 (e.g. ~0.7)More O₂ is required relative to CO₂ produced, since fatty acids are more reduced (more H, less O) than carbohydrates
Proteins / Organic acidsRQ > 1 (e.g. ~1.33, for some organic acids)Organic acids are more oxidised — less O₂ is required relative to CO₂ released

Practice Questions

Q1. Which enzyme is considered the "pacemaker" of glycolysis, controlling its rate-limiting step?

(a) Hexokinase   (b) Phosphofructokinase-1 (PFK-1)   (c) Pyruvate kinase   (d) Lactate dehydrogenase

Answer: (b) Phosphofructokinase-1 (PFK-1)

Explanation: PFK-1 catalyses step 3 of glycolysis, converting Fructose-6-phosphate to Fructose-1,6-bisphosphate, using 1 ATP. This step is irreversible and tightly regulated, making PFK-1 the "pacemaker" enzyme that controls the overall rate of glycolysis. Steps 1, 3, and 10 of glycolysis are the only irreversible steps, while all other steps are reversible.

Q2. What is the net ATP gain from glycolysis (per glucose molecule)?

(a) 4 ATP   (b) 2 ATP   (c) 6 ATP   (d) 8 ATP

Answer: (b) 2 ATP

Explanation: During glycolysis, 2 ATP are consumed (in steps 1 and 3, by hexokinase and PFK-1 respectively), while 4 ATP are produced via substrate level phosphorylation (2 ATP for each of the two 3-carbon molecules produced from the splitting of fructose-1,6-bisphosphate). The net ATP gain is therefore 4 − 2 = 2 ATP, along with 2 NADH+H⁺ and 2 pyruvate molecules.

Q3. During alcoholic fermentation in yeast, what happens to the NADH+H⁺ produced during glycolysis?

(a) It is sent to the ETS to produce ATP

(b) It is used to convert acetaldehyde to ethanol, regenerating NAD⁺

(c) It accumulates and is not reused

(d) It is converted to FADH₂

Answer: (b) It is used to convert acetaldehyde to ethanol, regenerating NAD⁺

Explanation: In alcoholic fermentation, pyruvate is first decarboxylated to acetaldehyde (releasing CO₂), and then acetaldehyde is reduced to ethanol by alcohol dehydrogenase. This reduction step uses the NADH+H⁺ produced during glycolysis, converting it back to NAD⁺. This regeneration of NAD⁺ is essential because glycolysis cannot continue without a fresh supply of NAD⁺. Importantly, this NADH+H⁺ is NOT sent to the ETS in fermentation, so no additional ATP is generated from it.

Q4. The Krebs cycle is also called the Citric Acid Cycle because:

(a) It occurs only in citrus fruits

(b) The first stable product of the cycle is citrate, which has three carboxylic acid groups

(c) It produces citric acid as a final waste product

(d) Citrate is the substrate that enters the cycle from glycolysis

Answer: (b) The first stable product of the cycle is citrate, which has three carboxylic acid groups

Explanation: The Krebs cycle begins when Acetyl CoA (2C) combines with Oxaloacetic Acid (OAA, 4C) via the enzyme citrate synthase, forming Citrate (6C) — a tricarboxylic acid (having three -COOH groups). This is why the cycle is also called the Citric Acid Cycle or Tricarboxylic Acid (TCA) Cycle. Through a series of steps, citrate is eventually converted back to OAA, regenerating it for the next turn of the cycle.

Q5. In the Electron Transport System (ETS), at which point is molecular O₂ directly utilised?

(a) During the link reaction (oxidative decarboxylation of pyruvate)

(b) During the Krebs cycle, when succinate is converted to fumarate

(c) As the terminal electron acceptor at the end of the ETS, forming water

(d) During glycolysis, when glucose is phosphorylated

Answer: (c) As the terminal electron acceptor at the end of the ETS, forming water

Explanation: A common misconception is that O₂ is used directly in the link reaction or Krebs cycle — but it is not. O₂ is used only at the very end of the Electron Transport System, as the final/terminal electron acceptor. Electrons that have passed through Complexes I to IV combine with H⁺ ions and O₂ to form water (4H⁺ + O₂ + 4e⁻ → 2H₂O), via Complex IV (cytochrome c oxidase). This step is essential to keep the ETS running, since it regenerates the electron carriers (NAD⁺, FAD) for further oxidation steps.

Q6. A respiratory substrate gives a Respiratory Quotient (RQ) of less than 1. What can be inferred about the substrate?

(a) It is a carbohydrate, since RQ = 1 for carbohydrates

(b) It is likely a fat, since fats require more O₂ relative to the CO₂ produced

(c) It is an organic acid, since organic acids are highly oxidised

(d) RQ less than 1 indicates anaerobic respiration is occurring

Answer: (b) It is likely a fat, since fats require more O₂ relative to the CO₂ produced

Explanation: Respiratory Quotient (RQ) = Volume of CO₂ evolved / Volume of O₂ consumed. For carbohydrates, RQ = 1, since equal volumes of CO₂ are released and O₂ consumed. For fats, RQ is less than 1 (around 0.7), because fatty acid molecules are more reduced (containing more hydrogen relative to oxygen) than carbohydrates, and therefore require relatively more O₂ to be fully oxidised compared to the CO₂ they release. For proteins/organic acids, RQ is often greater than 1, since these substrates are more oxidised to begin with and require relatively less O₂.

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