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Class 11 Biology — New Syllabus 2025-26

Unit 2: Bacteria and Viruses — Interactive Notes

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Long Questions — Descriptive

Q1. Comment about latest taxonomic status of bacteria.

Over the years many schemes have been proposed for classifying organisms into kingdoms. The five-kingdom classification system, proposed by Robert H. Whittaker in 1969, is recommended in biology. This system classified the organisms in a comprehensive way that reflects evolutionary history of organisms. According to this classification system, all prokaryotes are included in a separate kingdom i.e., the kingdom Monera.

Reason for Creating Separate Classification for Prokaryote

In the last decade, molecular studies have highlighted serious flaws in the five-kingdom classification system. In 1990, American microbiologist Carl Woese suggested that there are two separate groups of prokaryotes i.e., Archaea and Bacteria. He classified living organisms into three domains i.e., domain Archaea, domain Bacteria and domain Eukarya. According to three-domain system, domain Archaea and domain Bacteria contain prokaryotes but they differ in a number of features e.g. cell membrane lipids, cell wall composition, metabolic differences. Molecular evidence suggests that archaea are more closely related to eukaryotes than to bacteria.

★ Robert H. Whittaker proposed the five kingdoms system of classification i.e. Monera, Protista, Fungi, Plantae and Animalia. The first one includes prokaryotes and other four include eukaryotes.

Most biologists favour replacing it with a new system, called three-domain system. It is more aligned with the data gained from molecular studies. Bacteria are the prokaryotes classified in the domain of their own, i.e., the domain Bacteria.

STRUCTURE OF BACTERIA
Q2. Write composition of bacterial cell wall. Compare and contrast the cell wall of Gram-positive and Gram-negative bacteria.

Cell wall composition: It is a rigid wall around the plasma membrane of bacterial cell. The major component of bacterial cell wall is a unique macromolecule, called peptidoglycan or murein. It is composed of long glycan (polysaccharide) chain, cross-linked with short peptide fragments. Its amount differs in different bacteria. Cell wall also contains lipids, which are linked to peptidoglycan.

Gram's Staining

★ Sir Hans Christian Gram devised the technique of Gram's staining. Gram-positive bacteria stain purple because they retain violet dye (CV-I complex) in their cell walls. Gram-negative bacteria do not retain violet dye (they retain safranin) and so they appear in original (pink) colour.

Gram-Positive Bacteria: The cell wall contains thick layer of peptidoglycan and has less lipid content.

Gram-Negative Bacteria: The cell wall has a thin layer of peptidoglycan and more lipid content. They have an outer membrane made of lipopolysaccharides and lipoproteins (makes them resistant to many antibiotics), containing a protein called porin (pore for specific molecules). Has more periplasmic space than Gram-positive.

Gram-Positive Cell membrane (Protein) Peptidoglycan (thick) Gram-Negative Lipopolysaccharide + Porin Outer membrane / Lipoprotein Peptidoglycan (thin) + periplasmic space Cell membrane
Fig: Cell wall composition of Gram-positive and Gram-negative bacteria
CharacteristicsGram-PositiveGram-Negative
Number of major layersOneTwo
Chemical make upPeptidoglycan (50% of dry weight), Teichoic & lipoteichoic acid, Lipids (1-4%)Peptidoglycan (10%), Lipopolysaccharides & Lipoproteins, Lipids (11-12%)
Overall thickness20-80nm8-11nm
Outer membraneNoYes
Periplasmic spacePresent in somePresent in all
PermeabilityMore permeableLess permeable

Q3. Briefly describe the following bacterial cell structure: (i) Cell membrane (ii) Cytoplasm and Genetic material

(i) Cell Membrane

Location: Present just beneath cell wall. It lies at the outermost in bacteria that lack cell wall (e.g., Mycoplasmas and Spiroplasmas).

Lack Sterols: The cell membrane of bacteria does not have sterols (e.g., cholesterol) in its chemical makeup.

Mesosomes: At some points, cell membrane invaginates and forms vesicles, tubules or lamellae in cytoplasm. These structures are involved in DNA replication, cell division and also serve as respiratory centres.

(ii) Cytoplasm and Genetic Material

Composition: Contains dissolved substances and large structures such as nucleoid, ribosomes, and mesosomes.

Organelles: Lacks cytoskeleton and membrane-bounded organelles. Ribosomes are smaller than eukaryotic (80S); bacterial ribosomes sediment at 70S (larger subunit 50S, smaller 30S).

Nucleoid and Genetic Material: Near the centre of cytoplasm, an irregular-shaped dense area i.e., nucleoid contains DNA. A bacterium possesses a single, circular, double stranded DNA without attached histones — sometimes called the chromosome of bacterium.

Plasmids: Circular, double-stranded extra chromosomal DNA molecules, self-replicating, containing genes for resistance against unfavourable conditions (e.g., antibiotics).

Capsule / Cell wall / Cell membrane Nucleoid (DNA) Plasmid Flagellum
Fig: Structure of generalized bacterium
★ Plasmids as Vectors: Plasmids also serve as important vectors in genetic engineering — used to carry selected genes to bacteria for cloning or for the synthesis of specific proteins.

ENDOSPORE FORMATION IN BACTERIA
Q4. State the formation of endospore in bacteria. Explain the mechanism of sporulation.

Definition: Endospores are thick-walled, metabolically inactive (dormant) specialized "resting" cells, which enable bacteria to survive extended periods of harsh conditions.

Sporulation: The process by which bacteria make endospores.

Mechanism of Sporulation

  1. DNA Replication and Septum Formation: Under unfavourable conditions, bacterium replicates its DNA. Cell membrane makes a septum to isolate the new DNA and a small portion of cytoplasm, then the cell membrane surrounds DNA, cytoplasm and isolated membrane.
  2. Double Membrane Formation: Cell membrane again grows around the new DNA, cytoplasm, and septum — new DNA surrounded by two membranes.
  3. Formation of New Peptidoglycan: DNA of vegetative cell disintegrates, whole cell begins to dehydrate. New peptidoglycan layer forms between the membranes around separated DNA and cytoplasm.
  4. Spore Coat Formation and Endospore Release: A spore coat forms around it; structure matures into endospore; vegetative cell breaks and endospore is released — remains dormant unless favourable conditions return.
  5. Endospore Germination: Under favourable conditions, endospore germinates to give rise to a new vegetative cell.
1. Septum forms 2. Double membrane 3-4. Cell wall forms 5-6. Endospore released
Fig: Process of endospore formation (Sporulation) in bacteria

Examples: Endospore formation is common in Gram-positive bacteria like Bacillus and Clostridium.

MOTILITY IN BACTERIA
Q5. Explain different methods of movement/locomotion in bacteria.

Bacteria use different motility patterns to navigate and explore natural habitats.

a. Flagellar movements: Locomotion powered by flagella — swimming (individual bacteria in liquid, most bacilli/spirilla) or swarming (coordinated movement of a group/population in liquid media). Counter clockwise rotation of flagellum pushes the cell forward with flagellum trailing behind.

b. Twitching or crawling: Used to move over surfaces; mediated by pili, which bind to surrounding solid surface and retract, pulling the cell forward.

c. Gliding: Bacteria secrete slimy substance for smooth gliding over solid surfaces — similar to twitching.

d. Sliding: Movement due to expansion created by the pushing force of dividing cells.

e. Brownian movement: Some bacteria (e.g., Streptococcus) without flagella or pili move due to random, uncontrolled movements of particles in fluid.

f. Movement by axial filament: Some bacteria (e.g., spirochaetes) have a modified flagellum called axial filament — anchored at one end, running length-wise in periplasmic space (between cell membrane and outer membrane); two sets of flagella-like fibrils anchored at the two poles; helps flexing, swimming, creeping and spinning movements.

Swimming Swarming Twitching (pili) Gliding Sliding
Fig: Different types of bacterial motility

FLAGELLA
Q6. Explain the structure of bacterial flagellum. Classify bacteria on basis of flagella.

Bacterial flagella are entirely different from eukaryotic flagella. They are not built on the 9+2 pattern of microtubules, but are composed of flagellin protein.

The bacterial flagellum consists of a basal body, a hook and a filament.

i. Basal Body: Present just beneath cell membrane; consists of rotating rings (one pair in Gram-positive, two pairs in Gram-negative bacteria); anchors flagellum in cell membrane and cell wall.

ii. Hook: A curved structure connecting basal body with filament.

iii. Filament: Elongated thread-like structure composed of flagellin protein subunits in helical fashion.

Basal body (rings) in cell wall + membrane Filament
Fig: Structure of bacterial flagella (basal body, hook, filament)
★ Pili in Bacteria: Non-helical, filamentous appendages, smaller/thinner than flagella. Used for attachment to surfaces and in the mating process (conjugation) between cells.

Classification of Bacteria on Basis of Flagella

1. Atrichous — no flagella. 2. Monotrichous — single polar flagellum. 3. Lophotrichous — tuft of flagella at one pole. 4. Amphitrichous — tuft of flagella at each of two poles. 5. Peritrichous — flagella surrounding the whole cell.

BACTERIA: ECOLOGY AND DIVERSITY
Q7. Elaborate major groups of domain bacteria.

Margulis and Schwartz proposed a useful classification system for all prokaryotes, classifying bacteria into 16 phyla.

1. Omnibacteria — rigid, rod-shaped, heterotrophic, Gram-negative; many pathogens; most have flagella; do not produce spores; usually aerobic. E.g. Escherichia coli, vibrios.

2. Cyanobacteria — photosynthetic; increased free oxygen in Earth's atmosphere; contain chlorophyll-a + carotenoids + blue/red phycobilins; fix atmospheric N in heterocysts; common as mats in soil/sea sediments; found in lichens on rocks. ★ Bulk of modern petroleum deposits formed by decayed cyanobacteria; colourful algal blooms in polluted water from their photosynthetic pigments.

3. Mycoplasmas and Spiroplasmas — lack cell walls (smallest bacteria), resistant to penicillin; mycoplasmas cause pneumonia; spiroplasmas cause lethal yellowing disease of coconuts.

4. Spirochaetes — long spirilla, Gram-negative, 2 to >100 flagella; Treponema causes syphilis.

5. Pseudomonas — straight/curved Gram-negative rods, one or many flagella at one end; found in soil/water; break down organic compounds; many plant pathogens; role in denitrification; Pseudomonas aeruginosa causes infections in weak immunity.

6. Actinomycetes — filamentous growth, produce resistant spores; some are N-fixers in root nodules; some cause dental plaque; Mycobacterium leprae (leprosy), M. tuberculosis (tuberculosis); source of antibiotics (tetracycline, chloramphenicol, erythromycin, neomycin).

7. Nitrogen-fixing aerobic bacteria — economically important, Gram-negative, mostly flagellated; Azotobacter converts atmospheric N into nitrates.

8. Chemosynthetic bacteria (chemoautotrophs) — derive energy from oxidation of inorganic N, S, Fe compounds; Nitrosomonas and Nitrobacter oxidize NH₃ → nitrite → nitrate, vital in the nitrogen cycle.

IMPORTANCE OF BACTERIA
Q8. Briefly describe the economical and ecological importance of bacteria.

a. Ecologically Important Bacteria

1. Recyclers of Nature: Involved in biogeochemical cycles. Nitrifying bacteria (Nitrosomonas, Nitrobacter, Azotobacter) and denitrifying bacteria (Pseudomonas) complete the nitrogen cycle. Decomposer bacteria play a key role in the carbon-hydrogen-oxygen cycle; photosynthetic bacteria (cyanobacteria) increase free atmospheric oxygen.

2. Environmental Cleaners: Degrade organic compounds (bioremediation) — decompose city sewage, digest petroleum hydrocarbons (oil spill cleanup), bioremediate industrial toxic wastes.

b. Economically Important Bacteria

1. Makers of useful products: Fermented foods (cheese, pickles, soy sauce, vinegar, wine, yogurt via Lactobacillus + yeasts/molds); pharmaceutical/agrochemical production; antibiotics; leather goods processing.

2. As biopesticides: Bacillus thuringiensis (Gram-positive, soil-dwelling) used in biological pest control — environmentally friendly, little effect on humans/wildlife/pollinators.

Q9. Explain the use of bacteria in research and technology.

Determine the Function of Genes and Enzymes: Bacteria grow quickly and are easily manipulated (e.g., E. coli) — used in molecular biology, genetics, biochemistry. Scientists mutate bacterial DNA, examine changes, and determine gene/enzyme function — knowledge then applied to more complex organisms.

Human Genes in Bacteria: Scientists insert human genes in bacterial plasmids to produce therapeutic proteins e.g., insulin, growth hormones, antibodies.

NORMAL FLORA
Q10. Define normal flora. State the benefits which we get from normal bacterial flora.

Definition: The mixture of organisms regularly found at any anatomical site.

Description: Internal tissues (blood, brain, muscle) are normally free of microorganisms; surface tissues (skin, mucous membranes) are constantly colonized. Normal flora of humans consists of bacteria, a few fungi and protists, and some methanogenic archaea — bacteria are the most numerous.

Benefits to normal flora: Mutualistic association — normal flora gets nutrients, stable environment, constant temperature, protection, and transport.

Benefits to Humans:
i. Synthesis of vitamins: enteric bacteria secrete Vitamin K and B₁₂; lactic acid bacteria produce B-vitamins.
ii. Prevent colonization by pathogens: compete for attachment sites and nutrients.
iii. Inhibit or kill pathogens: intestinal bacteria produce inhibitory substances.
iv. Stimulates production of cross-reactive antibodies: normal flora behaves as antigens, low antibody levels cross-react with pathogens preventing infection.

VIRUS
Q11. Explain the structure and shapes of viruses.

Structure of Virus: Extremely small infectious agents, seen only under electron microscope.

Size: Range from 20 nm (parvovirus) to 250 nm (pox viruses) — 10 to 1000 times smaller than most bacteria; can pass through filter paper pores.

Genome: Central core is the genome, made of nucleic acid (DNA or RNA).

Capsid and Capsomeres: Core surrounded by a protein coat (capsid), giving definite shape; made of protein subunits (capsomeres) — number/kind characteristic of a particular virus. Herpes virus: 162 capsomeres; Adenovirus: 252 capsomeres. Central core + capsid = nucleocapsid.

Helical Icosahedral Complex Enveloped Non-enveloped
Fig: Diversity in virus shapes

Envelope: Lipid-rich membrane derived from host cell, covering nucleocapsid in enveloped viruses. Non-enveloped viruses = naked viruses.

General appearance: Animal/plant viruses may be polyhedron or helical. Bacterial viruses (bacteriophages) may be cubical, icosahedral (20 faces), helical, or complex (polyhedral head + rod-shaped tail).

Q12. Explain the structure of a model bacteriophage.

Bacteriophages are a diverse group of viruses that attack bacteria — among the most complex viruses. Best known phages of Escherichia coli are T-phages.

Structure of T4 phage

Consists of a head and a tail.

i. Head: Elongated pyramidal (two triangles with common base), hexagonal, prism-shaped. Capsid made of proteins; core contains long double-stranded DNA. A straight tail is attached with head.

ii. Tail: Made of inner core and outer sheath (different proteins). A neck attaches sheath with head; an end plate is on the other side of sheath. Six tail fibres attached with end plate.

Function: Tail fibres help the phage attach to the bacterial wall.

Capsid+Core=Head Sheath+Tail core=Tail Tail fibers, End plate, Pin
Fig: Structure of a bacteriophage (T4 phage)

Q13. Explain the structure of HIV.

Human Immunodeficiency Virus (HIV) belongs to the group called retroviruses — a special group of animal viruses. Retroviruses contain RNA and capsids.

Envelope: Surrounded by lipid-rich envelope comprising glycoprotein spikes, which help the virus identify and bind to its target. Spherical, about 100 nm in diameter.

Reverse transcriptase: The most distinguishing character of retroviruses — catalyses reverse transcription, where single-stranded RNA is reversely transcribed into a strand of DNA; the enzyme then uses this DNA strand to complete a double helix of DNA.

Glycoprotein spikes / envelope / capsid / RNA / reverse transcriptase
Fig: Structure of HIV

Q14. How possibly did HIV get entry to humans? Relate its discovery with AIDS.

★ Possible Origin of HIV: Experts concluded HIV originated in the jungles of Africa among wild chimps. Evidence suggests a form of this virus entered the human species and became HIV via monkey bites or ingesting monkey meat and brains.

AIDS: HIV is responsible for Acquired Immunodeficiency Syndrome — weakens the immune system; fatal because the body cannot defend against other viral/bacterial (opportunistic) infections without an immune system.

Discovery: First reported in 1981, patients found homosexual. Later discovered in non-homosexual patients who received blood/blood products from AIDS patients. In 1984, the causative agent was found to be a virus. In 1986, it was named Human Immunodeficiency Virus (HIV) — a host-specific virus that can multiply in monkeys but does not cause AIDS in them, because HIV attaches to human cells using the specific binding factor CD4 receptor, which is not present in monkeys.

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