
Plant Physiology is a conceptual unit covering fundamental processes in plants. We will explore photosynthesis, respiration, and plant growth and development, crucial topics for competitive exams. The goal is to understand how plants convert light energy into chemical energy, derive energy for their functions, and manage their growth throughout their life cycle.
Photosynthesis combines 'Photo' (light) and 'Synthesis' (to build). Plants use light energy from the Sun to synthesize food, primarily carbohydrates like glucose and sucrose. The Sun is the ultimate source of energy on Earth. Plants convert light energy into chemical energy (glucose), adhering to the Law of Conservation of Energy.
Organisms that produce their own food, such as plants, are called Producers. Only the green parts of the plant, containing pigments like chlorophyll, can trap light energy. Food synthesized in green parts is transported to other non-photosynthesizing parts (stems, roots) via phloem. Xylem transports water, while phloem transports food.
Plants (producers) form the base of the food chain. When a herbivore (Primary Consumer) eats a plant, energy is transferred. Carnivores then consume herbivores, making them Secondary Consumers who indirectly depend on producers.
This illustrates energy flow from plants through the ecosystem. (An analogy from a song describes the food chain: "Leaves consume rays (sunlight), leaves are eaten by goats, goats are devoured by lions." This represents the flow of energy from producers to primary and secondary consumers, illustrating the ecosystem's dynamics.)
Key features derived from the photosynthetic equation include:
Conversion of Energy: Light energy to chemical energy.
Physicochemical Process: Involves both physical (light interaction) and chemical (CO₂ to glucose) phenomena.
Redox Reaction: Reduction of CO₂ to glucose and Oxidation of H₂O to O₂.
Anabolic Process: Synthesizes larger molecules from smaller ones.
Endergonic/Endothermic Reaction: Consumes energy.
Inorganic to Organic Conversion: Converts inorganic (CO₂, H₂O) into organic (glucose) molecules.
Early experiments elucidated the requirements for photosynthesis:
Variegated Leaf Experiment: Demonstrated light is essential for photosynthesis (positive iodine test for starch in exposed parts).
Moll's Half-Leaf Experiment: Proved carbon dioxide (CO₂) is essential (negative iodine test in KOH-treated half).
Joseph Priestley's Bell Jar Experiment (1770): Showed plants restore air quality (produce oxygen) that animals and burning candles deplete, leading to the discovery of oxygen in 1774.
Julius von Sachs (1854): Identified glucose storage as starch and chlorophyll location in chloroplasts. (To remember Julius von Sachs' contributions, associate his name with "sacks" (बोरा), which are used to store things. This reminds you that he identified the storage of glucose as starch and chlorophyll within chloroplasts.)
Jan Ingenhousz Experiment (1779): Using Hydrilla, confirmed light is crucial for oxygen production during photosynthesis. (To remember Ingenhousz's contribution, associate his name with "engine," and remember that "light drives the engine" (of photosynthesis).)
Englemann's experiment (1882) provided the first action spectrum of photosynthesis. He split white light with a prism onto a filamentous green alga, Cladophora. By observing the accumulation of aerobic bacteria, he found highest photosynthetic activity (oxygen release) in blue light and red light.
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Action Spectrum vs. Absorption Spectrum |
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|---|---|---|
|
Feature |
Absorption Spectrum |
Action Spectrum |
|
What it shows |
Light absorbed by pigments at different wavelengths. |
Rate of physiological process (e.g., photosynthesis) at different wavelengths. |
|
Peaks for Chl a |
Blue and red regions. |
Blue and red regions. |
|
Significance |
Indicates which wavelengths are captured. |
|
Plants use diverse pigments (Chlorophyll a, Chlorophyll b, Carotenoids, Xanthophylls) to absorb a wide range of light. Chlorophyll a is the chief pigment because its absorption spectrum closely matches the action spectrum of photosynthesis, directly driving the main reactions. Other pigments are accessory pigments (Analogy: Just as a phone (main item) comes with accessories (charger, headphones) that complement its function, other pigments like chlorophyll b, carotenoids, and xanthophylls are accessory pigments.) Their functions are:
Absorb a wider range of light wavelengths and transfer energy to Chlorophyll a.
Protect Chlorophyll a from photo-oxidative damage by dissipating excessive light energy. (Analogy 1 (Chess King): The game (photosynthesis) continues as long as the king (Chlorophyll A) is alive. If the king falls, the game is over. Accessory pigments protect the king.)
Van Niel studied purple sulfur bacteria, showing that CO₂ is reduced using a hydrogen donor.
|
Van Niel's Experiment and the Origin of Oxygen |
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|---|---|---|
|
Feature |
Green Plants (Oxygenic Photosynthesis) |
Purple Sulfur Bacteria (Anoxygenic Photosynthesis) |
|
Hydrogen Donor |
Water (H₂O) |
Hydrogen sulfide (H₂S) |
|
Equation |
CO₂ + H₂O → Carb. + O₂ |
CO₂ + H₂S → Carb. + S |
|
Oxygen Release |
Yes |
No |
Van Niel proposed that oxygen comes from the hydrogen donor. This was later confirmed by radioisotopic techniques using oxygen-18 (O¹⁸) labeled water (H₂O¹⁸), which resulted in O¹⁸ being released as gaseous oxygen. Thus, oxygen released during photosynthesis originates from water, not CO₂.
Photosynthesis occurs in mesophyll cells within chloroplasts. Chloroplasts align at the periphery of cells for optimum sunlight capture.
They have outer and inner membranes. Inside are thylakoids (coin-like sacs) stacked into grana, connected by stroma lamellae. The fluid-filled space is the stroma, containing DNA, ribosomes, and enzymes, making it a semi-autonomous organelle.
Light-Dependent Reactions (Light Reactions): Occur in the thylakoids. Pigments absorb light, leading to the production of ATP, NADPH, and oxygen (O₂).
Light-Independent Reactions (Dark Reactions): Occur in the stroma. Enzymatic reactions convert CO₂ into glucose using the ATP and NADPH from light reactions. The term "dark reaction" is a misnomer as these reactions do not require darkness; they only depend on the products of the light reaction. (Analogy: Like giving a person a misleading name (e.g., "poor" person with millions), the name "dark reaction" is a misnomer.)
The dark reaction begins as soon as ATP and NADPH are available from the light reaction. It occurs in the stroma and converts CO₂ to glucose. It is dependent on the products of the light reaction, not on darkness. The overall products of photosynthesis are oxygen (from water splitting in light reaction) and glucose (from dark reaction).
Paper Chromatographic Technique is used to separate plant pigments based on their solubility and adsorption on chromatographic paper.
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Characteristics of Photosynthetic Pigments |
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|---|---|---|---|
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Pigment |
Color |
Order of Separation (from bottom) |
Role |
|
Chlorophyll B |
Yellowish-green |
1st (heaviest) |
Accessory |
|
Chlorophyll A |
Bright/Bluish-green |
2nd |
Chief |
|
Xanthophyll |
Yellow |
3rd |
Accessory |
|
Carotene |
Yellow to Orange |
4th (lightest) |
Accessory |
(The order from heaviest (least movement) to lightest (most movement) can be remembered as B.A.X.C.)
Photosystems (PS) are complexes of pigments and proteins involved in light capture.
Photosystem I (PS1): Contains P700 (Chlorophyll A absorbing at 700 nm) as its reaction center. Discovered first.
Photosystem II (PS2): Contains P680 (Chlorophyll A absorbing at 680 nm) as its reaction center. Discovered later, but functions first.
Each photosystem has:
Reaction Center: A specific Chlorophyll A molecule (P700 or P680) that directly participates in photochemical reactions.
Light-Harvesting Complex (LHC) / Antenna Molecules: Accessory pigments and proteins that capture light of various wavelengths and transfer energy to the reaction center. (Analogy: Similar to an antenna dish on a house, which captures signals and directs them to the TV, antenna molecules capture light and direct it to the reaction center.)
Absorb a Wider Range of Light Wavelengths: Accessory pigments broaden the spectrum of light captured for photosynthesis, maximizing light harvesting.
Protect Chlorophyll A from Photo-oxidative Damage: They absorb excess light energy and dissipate it, preventing damage to the chief pigment. (Analogy 2 (Hot Halwa): If very hot halwa (intense light energy) is put directly into the mouth (Chlorophyll A), it will burn. The hands (accessory pigments) pass the halwa around to cool it down, even if one hand gets slightly burned, to protect the mouth.)
The light reaction produces ATP, NADPH, and Oxygen (O₂). Oxygen is produced from the splitting of water molecules (photolysis):
2H₂O → 4H⁺ + 4e⁻ + O₂
Metal ions like Manganese (Mn) and Chlorine (Cl) assist in water splitting.
Photophosphorylation is ATP synthesis using light energy.
Non-Cyclic Photophosphorylation: Electrons do not return to their origin. Involves both PS1 and PS2, producing ATP, NADPH, and O₂.
Cyclic Photophosphorylation: Electrons return to their origin. Involves only PS1, producing only ATP.
This involves both PS2 and PS1, with electrons flowing from PS2 to an electron transport chain (ETC), then to PS1, and finally to NADP+ to form NADPH.
PS2 (P680) absorbs 680 nm light, excites electrons, which are accepted by a primary acceptor.
Electrons move through ETC1, losing energy used to synthesize ATP.
Water splitting (photolysis) at PS2 replaces lost electrons, releasing O₂ and accumulating protons (H⁺) in the thylakoid lumen.
Electrons reach PS1 (P700), which also absorbs 700 nm light and excites electrons.
Electrons from PS1 pass to ETC2 via Ferredoxin (FD), then to Ferredoxin NADP Reductase (FNR), which reduces NADP⁺ to NADPH.
This electron path creates a "Z" shape when plotted on a redox potential scale, hence the Z-Scheme.
Only PS1 is involved.
Electrons from PS1 return to PS1.
No water splitting, thus no O₂ release.
No NADPH formation.
Only ATP is produced.
(Memory Tip: "Lout ke Buddhu ghar ko aaye" (The foolish one came back home) – referring to electrons returning to their origin.)
Thylakoid membrane: Contains both PS1 and PS2; where Non-Cyclic Photophosphorylation occurs.
Stroma lamellae: Contains only PS1 (lacks PS2 and NADP reductase); where Cyclic Photophosphorylation occurs.
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Comparative Analysis: Non-Cyclic vs. Cyclic Photophosphorylation |
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|---|---|---|
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Feature |
Non-Cyclic Photophosphorylation |
Cyclic Photophosphorylation |
|
Photosystems Involved |
Both PS2 and PS1 |
Only PS1 |
|
Electron Flow |
Electrons lost from PS2, do not return |
Electrons from PS1 return to PS1 |
|
Water Splitting |
Occurs at PS2 |
Does not occur |
|
Oxygen Release |
Occurs |
Does not occur |
|
NADPH Formation |
Occurs |
Does not occur |
|
ATP Formation |
Occurs |
Occurs |
|
Products |
ATP, NADPH, and Oxygen |
Only ATP |
The electron flow sequence is: PS2 → Plastoquinone (PQ) → Cytochrome b6f complex → Plastocyanin (PC) → PS1 → Ferredoxin (Fd) → FNR → NADPH.
(The intermediate carriers to remember between PS2 and PS1 are PQ, Cytochrome b6f, and PC.)
ATP is produced in both cyclic and non-cyclic photophosphorylation. NADPH is produced only in non-cyclic. Hence, more ATP is typically produced than NADPH. Both are used in Dark Reactions.
This hypothesis explains ATP synthesis through a proton gradient across the thylakoid membrane.
Proton Pumping: As electrons move through the ETC (after PS2), Plastoquinone (PQ) picks up electrons from PS2 and protons from the stroma, then releases protons into the thylakoid lumen. (Analogy for PQ's proton handling: PQ (like a carrier) takes an electron and a proton from the outside (stroma) and, upon moving, releases the proton into the inside (lumen).)
NADPH Formation: FNR uses electrons and protons from the stroma to reduce NADP⁺, further depleting stroma protons.
Water Splitting: Releases protons directly into the thylakoid lumen.
These actions create a high proton concentration in the lumen and a low concentration in the stroma.
ATP Synthase (CF0-CF1 Complex): Protons flow back from the lumen to the stroma through the CF0 channel, driving the CF1 particle to synthesize ATP from ADP + Pi. (Analogy for ATP synthesis: ADP and Pi are close but need a "magic moment" to combine. The rush of protons through ATP Synthase provides this "magic moment" (like a sudden dramatic event in a movie causing characters to embrace), leading to ATP formation.)
Dark reactions involve two main pathways:
C3 Pathway (Calvin Cycle)
C4 Pathway (Hatch and Slack Cycle)
Named after Melvin Calvin.
Called C3 because the first stable product is a 3-carbon compound.
Discovery: Calvin used C¹⁴ to trace carbon path in algae.
Carbon Acceptor: Ribulose-1,5-bisphosphate (RuBP) (5-carbon).
Initial Product: RuBP combines with CO₂ to form an unstable 6-carbon intermediate, which breaks into two molecules of 3-Phosphoglyceric Acid (3-PGA) (3-carbon).
Universality: The C3 pathway is universal, occurring in all photosynthetic plants.
Carboxylation: RuBP reacts with CO₂, catalyzed by RuBisCO, forming 2 molecules of 3-PGA.
Reduction: PGA is converted to Triose phosphate using 2 ATP and 2 NADPH per CO₂ fixed.
Regeneration: RuBP is regenerated from Triose phosphate, consuming 1 ATP.
For glucose (6 carbons) synthesis: 18 ATP and 12 NADPH are consumed in C3 plants.
Ribulose-1,5-bisphosphate carboxylase/oxygenase (RuBisCO) is the most abundant enzyme on Earth due to its ubiquity in plants and its dual enzymatic activity (carboxylase and oxygenase). It has a higher affinity for CO₂ than O₂ when concentrations are equal, but binds to the more abundant gas.
Also known as Photorespiration.
A loss process occurring when RuBisCO binds with O₂ (oxygenase activity).
Produces a 2-carbon compound (phosphoglycolate).
No ATP or NADPH generated; no carbohydrate synthesized; CO₂ is released.
Occurs in C3 plants, leading to lower productivity. Involves chloroplast, peroxisome, and mitochondria (PCM).
Named after Hatch and Slack.
Called C4 because the first stable product is a 4-carbon compound.
Carbon Acceptor: Phosphoenolpyruvate (PEP) (3-carbon).
Initial Product: PEP combines with CO₂ to form Oxaloacetic Acid (OAA) (4-carbon).
Examples: S**orghum, **M**aize, **S**ugarcane (**SMS).
The C4 pathway spatially separates CO₂ fixation to avoid photorespiration:
In Mesophyll Cells: Atmospheric CO₂ is accepted by PEP, catalyzed by PEP Carboxylase (PEPCase), forming OAA. OAA is converted to other 4-carbon acids (e.g., malic acid), which are transported to bundle sheath cells. Mesophyll cells contain PEPCase but lack RuBisCO.
In Bundle Sheath Cells: C4 acids are decarboxylated, releasing CO₂. Due to the impermeability of bundle sheath cells, CO₂ is trapped, leading to a high CO₂ concentration. This ensures RuBisCO (abundant here) functions as a carboxylase, activating the C3 cycle. Bundle sheath cells contain RuBisCO but lack PEPCase.
This acts as a CO₂-delivery system, concentrating CO₂ and enabling C4 plants to thrive in dry tropical areas with high temperatures, minimizing water loss and photorespiration.
For one CO₂ fixed in C4 plants: 5 ATP and 2 NADPH are consumed. (3 ATP + 2 NADPH for C3 cycle + 2 ATP for PEP regeneration).
For glucose (6 carbons) synthesis: 30 ATP and 12 NADPH are consumed. C4 plants use more ATP but efficiently avoid photorespiration.
An adaptation in desert plants (e.g., Euphorbia) for water conservation.
Stomata open at night (when temperatures are lower, reducing water loss) to take in CO₂, which is stored as organic acids.
Stomata close during the day, and stored CO₂ is released internally for photosynthesis.
Photosynthesis is influenced by:
Internal Factors: Genetic predisposition, leaf characteristics (number, size, age, orientation), mesophyll and chloroplast characteristics, chlorophyll content, internal CO₂ concentration.
External Factors: Light (intensity, quality, duration), temperature, external CO₂ concentration, water.
The rate of a biochemical process is determined by the factor in shortest supply or at its sub-optimal quantity. This is the limiting factor. (Analogy (Pen Factory): If a factory produces different quantities of pen components (e.g., 50 refills, 40 bodies, 30 caps), the total number of complete pens will be limited by the component with the lowest quantity (30 caps).)
Quality: Blue and Red light are most effective (400-700 nm is Photosynthetically Active Radiation (PAR)).
Intensity: At low intensities, rate is proportional to light. At high intensities, rate saturates (another factor becomes limiting). Excessive light can cause photodamage.
Duration: Affects total biomass, not the rate per unit time.
Dark reactions are enzymatic and highly temperature-dependent.
C3 plants: Optimum at 20-25°C.
C4 plants: Optimum at 30-40°C (can tolerate higher temperatures).
Often the major limiting factor (atmospheric 0.03-0.04%).
Increasing CO₂ to 0.05% can enhance rates. Above 0.05% can be toxic.
C3 plants: Require higher CO₂ for saturation (~450 µL L⁻¹).
C4 plants: Saturate at lower CO₂ (~360 µL L⁻¹).
Greenhouse crops (tomato, bell pepper) benefit from CO₂ enrichment.
Breathing is physical gas exchange. Respiration is a biochemical process where oxygen oxidizes food to release energy (ATP). Breaking carbon-carbon bonds in glucose releases stored energy. ATP (Adenosine Triphosphate) is the energy currency of the cell, with high energy in its terminal phosphate bonds. Other energy carriers like NADH and FADH₂ are also produced, which are converted to ATP in the Electron Transport System (ETS) (1 NADH = 3 ATP, 1 FADH₂ = 2 ATP).
Complete Oxidation: All carbon-carbon bonds broken, maximizing ATP (e.g., glucose to 6 CO₂).
Incomplete Oxidation: Not all bonds broken, yielding less energy (e.g., glucose to pyruvate).
Any molecule oxidized to release energy. Glucose is the most favored.
Protoplasmic Respiration: Uses proteins.
Floating Respiration: Uses fats or carbohydrates.
Energy Release in Small Steps: Prevents energy loss as heat, allowing efficient ATP trapping.
Energy is Stored, Not Released Freely: Stored as ATP for on-demand use.
Glycolysis: Cytoplasm.
Link Reaction: Mitochondrial matrix.
Krebs Cycle: Mitochondrial matrix.
Electron Transport System (ETS): Inner mitochondrial membrane.
Plants do require oxygen for respiration but lack a specialized respiratory system due to:
Each Plant Part Manages its Own Gas Exchange: Stomata in leaves, lenticels in stems, root surfaces in soil air.
Low Oxygen Demand: Lower metabolic rate than animals.
Local Diffusion is Sufficient: Loosely packed parenchymatous cells with intercellular spaces.
Plants also produce internal oxygen during photosynthesis.
Early Earth lacked oxygen, so early organisms (anaerobic) developed Glycolysis to generate ATP without oxygen.
Universal Pathway: Occurs in nearly all cells (cytoplasm), without oxygen.
Linear Pathway: 10-step process.
Net Result: Converts one 6-carbon glucose into two 3-carbon pyruvate (incomplete oxidation).
Sucrose Hydrolysis: Sucrose breaks into glucose and fructose.
Glucose Phosphorylation: Glucose is trapped inside the cell by ATP-dependent phosphorylation (via Hexokinase) to Glucose-6-phosphate (cost: 1 ATP).
Conversion to Fructose-6-phosphate: Via isomerase for easier cleavage.
Formation of Fructose-1,6-bisphosphate: Another ATP-dependent phosphorylation (via Phosphofructokinase) at the 1st carbon (cost: 1 ATP). This is the rate-determining step.
Cleavage: Fructose-1,6-bisphosphate (6C) is cleaved by Aldolase into two 3-carbon molecules: Glyceraldehyde-3-phosphate (G3P) and Dihydroxyacetone phosphate (DHAP) (DHAP converts to G3P).
Depends on oxygen availability:
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Fate of Pyruvate |
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|---|---|---|---|
|
Feature |
Lactic Acid Fermentation (Anaerobic) |
Alcoholic Fermentation (Anaerobic) |
Aerobic Respiration (Link Reaction) |
|
Oxygen |
Absent/Scarce |
Absent/Scarce |
Present |
|
Process |
Pyruvate → Lactic Acid |
Pyruvate → Acetaldehyde + CO₂ → Ethanol |
Pyruvate → Acetyl-CoA + CO₂ |
|
Enzyme |
Lactate Dehydrogenase |
Pyruvate Decarboxylase, Alcohol Dehydrogenase |
Pyruvate Dehydrogenase Complex |
|
NADH |
NADH → NAD⁺ (regenerated for glycolysis) |
NADH → NAD⁺ (regenerated for glycolysis) |
NADH produced (sent to ETS) |
|
Products |
Lactic acid |
Ethanol, CO₂ |
Acetyl-CoA, NADH |
|
Location |
Cytoplasm (e.g., muscle cells, lactic acid bacteria) |
Cytoplasm (e.g., yeast) |
Mitochondrial matrix |
|
Energy Yield |
Low (2 ATP net from glycolysis) |
Low (2 ATP net from glycolysis) |
High (Acetyl-CoA enters Krebs for more ATP) |
|
Toxicity |
Muscle fatigue |
Toxic to yeast (>13% ethanol) |
Non-toxic products (CO₂, H₂O) |
Discovered by Hans Krebs.
Occurs in the mitochondrial matrix.
Citrate (6C) is the first stable product (TCA Cycle due to 3 -COOH groups).
Cyclic nature: Oxaloacetic Acid (OAA) (4C) is regenerated.
Initiation: OAA (4C) + Acetyl-CoA (2C) → Citrate (6C), catalyzed by Citrate Synthase.
Energy Release (per Acetyl-CoA): 3 NADH, 1 FADH₂, 1 ATP/GTP (substrate-level phosphorylation).
CO₂ Release (per Acetyl-CoA): 2 CO₂ (from Isocitrate to alpha-Ketoglutarate and alpha-Ketoglutarate to Succinyl CoA).
Substrate-Level Phosphorylation: Direct ATP transfer from a substrate (e.g., in glycolysis, Krebs cycle).
Oxidative Phosphorylation: ATP synthesis driven by NADH/FADH₂ oxidation in ETS.
Oxygen is not directly used in glycolysis, link reaction, or Krebs cycle. It is the terminal hydrogen/electron acceptor in the ETS, forming water (H₂O).
The ETS occurs on the inner mitochondrial membrane (folded into cristae). It consists of five major protein complexes and mobile carriers.
Complex I (NADH Dehydrogenase): Oxidizes NADH.
Complex II (FADH₂ Dehydrogenase / Succinate Dehydrogenase): Oxidizes FADH₂.
Complex III (Cytochrome bc₁ Complex): Transfers electrons.
Complex IV (Cytochrome c Oxidase Complex): Transfers electrons to oxygen, forming water.
Complex V (ATP Synthase / F0F1 Particle): Synthesizes ATP using proton gradient.
Mobile Carriers: Ubiquinone (UQ) (hydrogen carrier), Cytochrome c (Cyt c) (electron carrier).
Electrons moving through ETS complexes I, III, and IV pump protons (H⁺) from the matrix to the intermembrane space, creating a proton gradient. Protons then flow back into the matrix through ATP Synthase (F0F1), driving ATP synthesis.
The 38 ATP yield is theoretical, based on assumptions:
Sequential Pathway: Glucose → Glycolysis → Link Reaction → Krebs Cycle → ETS (not always true; fermentation can occur).
NADH Always Enters ETS: Not always true (e.g., NADH used in fermentation).
No Intermediates Utilized for Other Compounds: Intermediates like Acetyl-CoA can be used for biosynthesis (e.g., fatty acids).
Only Glucose is Respired: Other molecules (fats, proteins) can also be substrates.
Respiration is amphibolic (dual nature):
Catabolic: Breaks down glucose, fats, proteins for energy.
Anabolic: Intermediates (e.g., Acetyl-CoA, pyruvate, OAA) serve as precursors for synthesizing other molecules (fatty acids, amino acids).
RQ = Volume of CO₂ evolved / Volume of O₂ consumed
|
Substrate |
RQ Value |
|---|---|
|
Carbohydrates |
1 |
|
Proteins |
~0.9 |
|
Fats |
~0.7 |
|
Organic Acids |
> 1 |
|
Alcoholic Fermentation |
Infinite |
Growth: An irreversible increase in mass and/or cell number, driven by metabolism. It is a defining feature of living organisms.
Development: Sum total of growth and differentiation; all events from seed germination to senescence.
Indeterminate / Unlimited / Open Growth: Plants grow continuously throughout life due to meristems (root and shoot apical meristems).
Limited Growth of Plant Parts: Individual organs (leaves, flowers) have finite growth.
Primary Growth: Increase in length (apical meristems).
Secondary Growth: Increase in girth/thickness (lateral meristems/cambium), mainly in dicots and gymnosperms.
Measured by: increase in cell number (maize root meristem: 17,500 cells/hr), cell size (watermelon cell: 3.5 lakh times), surface area (leaf), length (pollen tube), or volume (fruit).
Region of Meristematic Activity (RMA): Small, thin-walled, dense protoplasm, prominent nucleus, actively dividing cells.
Region of Elongation: Cells rapidly elongate and enlarge, primarily responsible for root length increase.
Region of Maturation: Cells differentiate and mature, forming specialized tissues and root hairs for absorption.
Growth rate is growth per unit time.
Absolute Growth Rate: Total increase in size (Final - Initial size).
Relative Growth Rate: Growth relative to initial size [(Absolute growth / Initial size) x 100%].
One daughter cell remains meristematic, the other differentiates.
Linear increase in cell number (1, 2, 3…).
Produces a linear graph.
Formula: L_t = L_0 + RT.
Both daughter cells remain meristematic.
Exponential increase (1 → 2 → 4 → 8…).
Produces an S-shaped (Sigmoid) curve: Lag phase → Log (Exponential) phase → Stationary phase.
Formula: L_t = L_0 * e^(RT).
Characteristic of most organisms and initial plant development.
Differentiation: Meristematic cell → Permanent cell with specific function.
Dedifferentiation: Permanent cell → Regains ability to divide (becomes meristematic, e.g., medullary ray cells forming cambium).
Redifferentiation: Dedifferentiated meristematic cell → New permanent cell (e.g., cambium forming secondary xylem/phloem).
Ability of a plant to form different structures in response to life phases or environmental conditions.
Heterophylly: Producing different leaf forms.
Phases of life: C**otton, **C**oriander, **L**arkspur (**CLC).
Environmental conditions: Buttercup (aquatic vs. terrestrial leaves). (For Buttercup, remember "cup" for water.)