2. Life Processes in Living Organisms Part – 1​

Chapter 2: Life Processes in Living Organisms — Part 1

Chapter Flow

Living Organisms & Life Processes Energy Production in Cells Nutrients & Energy Efficiency Cell Division (Mitosis & Meiosis)

Can you recall?

  • Why is a balanced diet essential?
  • Role of digestive juices & enzymes?
  • How do muscles help in daily work & sports?
  • Which system removes body wastes?
  • How does the circulatory system aid energy supply?
  • How are body processes controlled (nervous & endocrine)?
  • What is cellular respiration?

Living Organisms & Life Processes

In all organisms (including humans), organ systems like digestive, respiratory, circulatory, excretory, nervous and endocrine work in coordination. Cells need a continuous supply of energy; this is derived mainly from carbohydrates, lipids (fats) and sometimes proteins, using oxygen in the mitochondria. The circulatory system delivers nutrients and oxygen to every cell; control systems keep everything in sync.

Plants are autotrophs. They synthesize food and store it in roots, stems, leaves, fruits, etc. Animals (including us) eat these parts to obtain carbohydrates, fats, proteins, vitamins, minerals.

Energy from diet (quick view)

NutrientExamplesEnergy YieldSpecial Notes
CarbohydratesMilk, fruits, jaggery, sugar, cereals, potatoes~ 4 kcal/gMain fuel; stored as glycogen in liver & muscles
ProteinsPulses, milk, eggs, fish, meat, soy~ 4 kcal/gBuilds tissues; excess not stored (deaminated)
Lipids (Fats)Oils, ghee, nuts, butter, seeds~ 9 kcal/gStored in adipose; membrane & hormone synthesis

Living Organisms & Energy Production

Cellular respiration oxidizes food (mostly glucose) to produce ATP, the cell’s energy currency. It occurs in two broad ways:

Aerobic Respiration (with O2) Anaerobic Respiration (without O2)

Overall aerobic equation

\( \displaystyle \text{C}_6\text{H}_{12}\text{O}_6 + 6\,\text{O}_2 \;\longrightarrow\; 6\,\text{CO}_2 + 6\,\text{H}_2\text{O} + \text{Energy (ATP)} \)

The three stages (Aerobic)

1) Glycolysis (Cytoplasm)

  • Glucose → 2 Pyruvic acid
  • Net gain: 2 ATP, 2 NADH2
  • No O2 needed

2) Link & TCA (Krebs) Cycle (Mitochondria)

  • Pyruvate → Acetyl-CoA (+ CO2, NADH2)
  • Acetyl-CoA fully oxidized → CO2, NADH2, FADH2, small ATP (as GTP)

3) Electron Transport Chain (Mitochondria)

  • NADH2/FADH2 donate electrons
  • Drives ATP synthesis
  • Water formed at the end
Classic textbook yield (older convention): each NADH2 ≈ 3 ATP; each FADH2 ≈ 2 ATP.
Total from complete aerobic oxidation of one glucose: up to \(\; \approx 38\;\) ATP (organism & conditions dependent).
ATP (Adenosine Triphosphate) stores energy in its phosphate bonds. Hydrolysis: \( \text{ATP} \rightarrow \text{ADP} + \text{P}_{\text{i}} + \text{Energy} \). That’s why ATP is called the energy currency of the cell.

Anaerobic Respiration (Fermentation)

When oxygen is absent/low (some microbes, germinating seeds in water-logged soil, vigorously working muscles), cells switch to fermentation:

  • Alcoholic fermentation (e.g., yeast): Pyruvate → Ethanol + CO2
  • Lactic acid fermentation (e.g., muscle cells, some bacteria): Pyruvate → Lactic acid

Less energy is produced because glucose is incompletely oxidized.

Heavy exercise → temporary oxygen debt → muscle cells perform anaerobic respiration → lactic acid accumulates → fatigue and soreness.

When carbs run low…

If dietary carbohydrates are insufficient (fasting, prolonged exercise):

  • Lipids → Fatty acids → Acetyl-CoA → enter Krebs cycle
  • Proteins → Amino acids → (deaminated) some → intermediates → Krebs cycle

Some Nutrients & Energy Efficiency

Proteins

Proteins are polymers of amino acids. After digestion and absorption, cells assemble the amino acids into specific proteins needed by the body:

  • Blood: Haemoglobin, antibodies
  • Muscles: Actin, myosin
  • Skin/Hair: Keratin, melanin
  • Hormones/Enzymes: Insulin, trypsin, pituitary hormones
  • Bones: Ossein (matrix protein)
  • Cell membranes: various transport & receptor proteins

Excess amino acids are not stored; they are deaminated and the nitrogen is excreted (e.g., as urea). Carbon skeletons can be used for energy or converted (e.g., to glucose via gluconeogenesis).

Lipids (Fats & Oils)

Lipids are made by bonding fatty acids with alcohol (e.g., glycerol). After digestion into fatty acids, cells use them to build:

  • Phospholipids (key components of plasma membranes)
  • Myelin sheaths around axons
  • Steroid hormones: progesterone, estrogen, testosterone, aldosterone

Excess lipids are stored in adipose tissue.

Vitamins & Water

VitaminTypeNotes
A, D, E, KFat-solubleStored in body; excess can be harmful
B-complex, CWater-solubleNot stored; need regular intake

Coenzymes like FAD (from Vit B2 riboflavin) and NAD (from Vit B3 niacin) are essential in glycolysis & TCA.

Water (~65–70% of body mass; ~90% of plasma): vital for transport, temperature control, reactions. Even small deficits impair function.
ORS (salt–sugar solution) helps restore fluids & electrolytes.

Dietary fibre (from fruits, vegetables, cereals) aids digestion and regular bowel movement though it is not digested itself.

Scientists’ Corner
Glycolysis elucidated by Embden, Meyerhof & Parnas (EMP pathway). TCA Cycle discovered by Sir Hans Krebs (Nobel 1953).

Cell Division — A Life Process

Cell division is fundamental for growth, repair (healing wounds), replacement and reproduction. Two types:

Mitosis (equational) — Somatic & stem cells Meiosis (reductional) — Germ cells (gametes/spores)

Chromosome Basics

  • Diploid (2n): pairs of each chromosome type.
  • Haploid (n): one set (e.g., gametes).
  • Before any division, DNA replicates so that chromosomes (2n) effectively become 4n in content (sister chromatids joined at centromere).

Mitosis (Karyokinesis → Cytokinesis)

Prophase

  • Chromosomes condense (short & thick; visible as sister chromatids)
  • Centrioles duplicate; move to poles
  • Nuclear membrane & nucleolus begin to disappear

Metaphase

  • Nuclear envelope gone; chromosomes fully condensed
  • Align on equatorial plane
  • Spindle fibres attach centromeres ↔ centrioles

Anaphase

  • Centromeres split; sister chromatids separate
  • Daughter chromosomes move to opposite poles (banana-like appearance)

Telophase & Cytokinesis

  • Chromosomes decondense; nuclear envelopes reform (two nuclei)
  • Cytokinesis: cleavage furrow in animals / cell plate in plants
Mitosis yields two identical 2n daughter cells. Uses: growth, tissue repair, blood cell formation, replacement.

Meiosis (I & II)

Meiosis I: homologous chromosomes pair, crossing over (recombination) occurs; homologues separate → two haploid (n) cells.

Meiosis II (like mitosis): sister chromatids separate → four haploid (n) daughter cells, all genetically different.

Importance: produces gametes/spores, halves chromosome number, and creates genetic variation via recombination & independent assortment.

Try this (Microscopy Activity)

Observe mitosis in onion root tip — grow roots in water 4–5 days, stain tips with iodine, squash on slide, and view under compound microscope. Identify phases like prophase, metaphase, anaphase, telophase.

Quick Checks & Key Ideas

  • Complete oxidation of glucose occurs only in aerobic respiration in mitochondria.
  • Fermentation is anaerobic and yields less ATP; products differ (ethanol/CO2 vs lactic acid).
  • Proteins are not stored; excess → deamination → excretion; carbon skeletons used for energy or conversion.
  • Vitamins act as coenzymes; water & fibre are essential for homeostasis and digestive health.
  • Mitosis = growth & repair; Meiosis = gametes & variation.

Chapter 2 — Exercise: Perfect Solutions

1) Fill in the blanks (with reasoning)

a) After complete oxidation of a glucose molecule, 38 ATP molecules are formed.

Reason: In classical school-level accounting: Glycolysis (2 ATP) + TCA (2 ATP as GTP) + ETC (10 \(\mathrm{NADH_2}\) × 3 = 30 ATP; 2 \(\mathrm{FADH_2}\) × 2 = 4 ATP) → total ≈ 38 ATP.

b) At the end of glycolysis, two molecules of pyruvic acid are obtained.
(+ Net 2 ATP and 2 \(\mathrm{NADH_2}\))

Reason: One glucose (6C) is split and oxidized in cytoplasm to 2 × 3C pyruvate.

c) Genetic recombination occurs in pachytene phase of prophase-I of meiosis.

Reason: Crossing over via chiasmata formation happens during pachytene, after synapsis (zygotene).

d) All chromosomes are arranged parallel to the equatorial plane in metaphase of mitosis.

Reason: Maximum condensation + spindle attachment aligns chromosomes at the metaphase plate.

e) For formation of plasma membrane, phospholipid molecules are necessary.

Reason: The membrane is a phospholipid bilayer with embedded proteins & cholesterol.

f) Our muscle cells perform anaerobic (lactic acid) respiration during heavy exercise.

Reason: Oxygen supply lags behind demand → pyruvate reduced to lactate to regenerate NAD\(^+\).

1c) Prophase-I of Meiosis — Five Sub-stages (with neat labelled sketches)

Names & key events

  1. Leptotene — Chromosomes begin to condense; appear as thin threads.
  2. ZygoteneSynapsis: homologous chromosomes pair via synaptonemal complex.
  3. PachyteneCrossing over: genetic recombination between non-sister chromatids.
  4. Diplotene — Synaptonemal complex dissolves; homologues start separating; chiasmata visible.
  5. Diakinesis — Maximal condensation; terminalization of chiasmata; spindle forms; nuclear envelope breaks down.
Leptotene Zygotene Pachytene Diplotene Diakinesis Progress → Crossing over (recombination) in Pachytene Chiasmata visible in Diplotene

2) Definitions

  • Nutrition: Process by which organisms obtain and utilize food for energy, growth, repair and regulation.
  • Nutrients: Chemical substances in food (carbohydrates, proteins, lipids, vitamins, minerals, water, fibre) that nourish the body.
  • Proteins: Large biomolecules made of amino acids linked by peptide bonds; perform structural, enzymatic, transport, hormonal and defensive roles.
  • Cellular respiration: Enzyme-controlled oxidation of food (mainly glucose) in cells to release energy as ATP.
  • Aerobic respiration: Complete oxidation of substrates using oxygen as final electron acceptor to yield CO\(_2\), H\(_2\)O and large ATP.
  • Glycolysis: Cytoplasmic pathway that converts one glucose into two pyruvate with a net gain of 2 ATP and 2 \(\mathrm{NADH_2}\).

3) Distinguish between

a) Glycolysis vs TCA (Krebs) Cycle

GlycolysisTCA (Krebs) Cycle
Occurs in cytoplasmOccurs in mitochondrial matrix
Glucose → 2 PyruvateAcetyl-CoA → CO\(_2\)
O\(_2\) not directly requiredIndirectly depends on O\(_2\) (via ETC regenerating NAD\(^+\)/FAD)
Net 2 ATP + 2 \(\mathrm{NADH_2}\)Per acetyl-CoA: 3 \(\mathrm{NADH_2}\), 1 \(\mathrm{FADH_2}\), 1 ATP (as GTP)
No CO\(_2\) releasedCO\(_2\) released in multiple steps

b) Mitosis vs Meiosis

MitosisMeiosis
One division → 2 daughter cellsTwo divisions → 4 daughter cells
Chromosome number maintained (2n → 2n)Chromosome number halved (2n → n)
No pairing/crossing overHomologous pairing & crossing over (Prophase-I)
Daughters genetically identicalDaughters genetically different
Somatic & stem cells (growth/repair)Germ cells (gametes/spores)

c) Aerobic vs Anaerobic Respiration

AerobicAnaerobic
Requires O\(_2\)Occurs without O\(_2\)
Complete oxidation (CO\(_2\)+H\(_2\)O)Incomplete (lactate / ethanol + CO\(_2\))
High ATP yield (up to ~38)Low ATP yield (net 2 per glucose)
ETC in mitochondriaNo mitochondrial ETC involvement
Occurs in most cellsYeast, some bacteria, muscle under exertion, water-logged seeds

4) Give scientific reasons

  • a) Oxygen is necessary for complete oxidation of glucose.
    Final electron acceptor in the ETC is O\(_2\). Accepting electrons & protons forms H\(_2\)O, regenerating NAD\(^+\)/FAD that keep TCA & glycolysis running to fully oxidize substrates and maximize ATP.
  • b) Fibres are important nutrients.
    Though indigestible, dietary fibre increases bulk, promotes peristalsis, supports gut microbiota, improves glycaemic control and helps lower LDL cholesterol by bile acid binding.
  • c) Cell division is a key property of cells & organisms.
    Enables growth (mitosis), tissue repair & replacement, asexual reproduction, and formation of gametes (meiosis) ensuring genetic continuity & variation.
  • d) Higher plants & animals sometimes perform anaerobic respiration.
    Under low O\(_2\) (e.g., water-logged germinating seeds; vigorously contracting muscles), fermentation regenerates NAD\(^+\) so glycolysis can continue and supply limited ATP.
  • e) Krebs cycle is also called the citric acid cycle.
    The first stable product is citrate (citric acid), formed by condensation of acetyl-CoA with oxaloacetate.

5) Answer in detail

a) Explain glycolysis in detail.

Overall: \( \displaystyle \text{Glucose} + 2\,\mathrm{NAD^+} + 2\,\text{ADP} + 2\,\mathrm{P_i} \rightarrow 2\,\text{Pyruvate} + 2\,\mathrm{NADH_2} + 2\,\text{ATP} + 2\,\text{H}_2\text{O} \)
  • Investment phase: Glucose → glucose-6-P → fructose-6-P → fructose-1,6-bisphosphate (uses 2 ATP).
  • Cleavage: F-1,6-BP → DHAP + GAP; DHAP ↔ GAP.
  • Payoff: Each GAP → 1,3-BPG → 3-PG → 2-PG → PEP → Pyruvate (produces total 4 ATP & 2 \(\mathrm{NADH_2}\); net 2 ATP).
End products: 2 pyruvate, 2 ATP (net), 2 \(\mathrm{NADH_2}\), water. In absence of O\(_2\), pyruvate is reduced to lactate/ethanol (fermentation).

b) With suitable diagrams, explain mitosis.

  1. Prophase: Chromosomes condense; spindle begins; nuclear envelope & nucleolus fade.
  2. Metaphase: Chromosomes align at the equator attached to spindle fibres.
  3. Anaphase: Centromeres split; sister chromatids pulled to opposite poles.
  4. Telophase: Chromosomes decondense; nuclear envelopes re-form (two nuclei).
  5. Cytokinesis: Cleavage furrow (animal) / cell plate (plant) → two identical 2n cells.
Prophase Metaphase Anaphase Telophase Cytokinesis

d) How do all life processes contribute to growth & development?

  • Nutrition & Digestion: Supply building blocks (amino acids, sugars, fatty acids) & energy.
  • Respiration: Converts substrates to ATP powering biosynthesis, transport, division, movement.
  • Circulation: Distributes O\(_2\), nutrients, hormones; removes CO\(_2\), wastes.
  • Excretion: Maintains internal chemical balance by removing nitrogenous & metabolic wastes.
  • Coordination (nervous/endocrine): Regulates rates and timing of processes (e.g., growth hormone).
  • Cell division: Adds cells (growth), repairs damage, and renews tissues (skin, blood, gut lining).

e) Explain the Krebs (TCA) cycle with reaction.

Entry: \( \text{Pyruvate} + \mathrm{CoA} + \mathrm{NAD^+} \rightarrow \text{Acetyl-CoA} + \mathrm{CO_2} + \mathrm{NADH_2} \) (Link step)

Per Acetyl-CoA (TCA):
\( \text{Acetyl-CoA} + 3\,\mathrm{NAD^+} + \mathrm{FAD} + \mathrm{GDP} + \mathrm{P_i} + 2\,\mathrm{H_2O} \rightarrow 2\,\mathrm{CO_2} + 3\,\mathrm{NADH_2} + \mathrm{FADH_2} + \mathrm{GTP} + \mathrm{CoA} \)

Key steps: Citrate synthase (citrate), isomerization (isocitrate), oxidative decarboxylations (α-ketoglutarate), succinyl-CoA → succinate (GTP/ATP), FADH\(_2\) at succinate dehydrogenase, NADH\(_2\) at malate dehydrogenase; oxaloacetate regenerated.

6) How is energy formed from oxidation of carbohydrates, fats & proteins?

  • Carbohydrates: Glucose → Glycolysis (→ pyruvate) → Acetyl-CoATCA → \(\mathrm{NADH_2}\)/\(\mathrm{FADH_2}\) → ETC → ATP.
  • Fats: Lipids → fatty acids + glycerol; glycerol enters glycolysis; fatty acids undergo β-oxidation → multiple Acetyl-CoA + \(\mathrm{NADH_2}\) + \(\mathrm{FADH_2}\) → TCA → ETC → lots of ATP.
  • Proteins: Proteins → amino acids → deamination; carbon skeletons → pyruvate/acetyl-CoA/TCA intermediates → TCA → ETC → ATP (nitrogen excreted as urea, etc.).
Hence, all three converge on Acetyl-CoA / TCA and ultimately feed the electron transport chain to synthesize ATP.

7) Correct the diagram (Energy pathways)

Correct flow from carbohydrates, fats and proteins to ATP via central metabolism:

Carbohydrates Fats (Lipids) Proteins Glycolysis Pyruvic acid Acetyl-CoA Glycerol + Fatty acids β-oxidation → Acetyl-CoA Amino acids Deamination → Keto acids Krebs (TCA) Cycle ETC (Oxidative phosphorylation) ATP (Energy)
Corrections made: Proteins → amino acids → deamination → intermediates (not directly to pyruvate always); Fats → glycerol (to glycolysis) & fatty acids (β-oxidation → Acetyl-CoA); all converge on Acetyl-CoA/TCA then ETC → ATP.

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