1. Chapter at a Glance
When you look around, you see both living and non-living things. What is it that an organism has that an inanimate thing does not? The answer is the presence of the basic unit of life — the cell — in all living organisms. All organisms are composed of cells. Some are composed of a single cell and are called unicellular organisms, while others, like us, composed of many cells, are called multicellular organisms. Unicellular organisms are capable of independent existence and performing the essential functions of life. Anything less than a complete structure of a cell does not ensure independent living. Hence, the cell is the fundamental structural and functional unit of all living organisms. This chapter covers the cell theory, prokaryotic and eukaryotic cells, and each cell organelle in detail. NEET asks two to three questions every year from this chapter, often on membrane structure, the endomembrane system, ribosome types, mitochondria and chloroplast, centrioles and cilia, and chromosome types.
- Cell theory (Schleiden, Schwann, Virchow); sizes of cells.
- Prokaryotic cell: cell envelope, mesosome, plasmids, 70S ribosomes, inclusion bodies, Gram staining.
- Fluid mosaic model (Singer and Nicolson); lipid and protein ratio of RBC membrane; active and passive transport.
- Endomembrane system: ER, Golgi (cis/trans faces), lysosomes, vacuoles; mitochondria and plastids are not part of it.
- Ribosome types (70S, 80S); cytoskeleton; 9 + 2 cilia, 9 + 0 basal body and centriole (cartwheel).
- Nucleus: nuclear pores, nucleolus (rRNA synthesis), chromatin; metacentric to telocentric chromosomes; satellite.
2. Discovery of the Cell and Cell Theory
- Anton Von Leeuwenhoek first saw and described a live cell. Robert Brown later discovered the nucleus. The invention of the microscope and its improvement leading to the electron microscope revealed all the structural details of the cell.
- In 1838, Matthias Schleiden, a German botanist, examined a large number of plants and observed that all plants are composed of different kinds of cells which form the tissues of the plant.
- At about the same time, Theodore Schwann (1839), a British zoologist, studied different types of animal cells and reported that cells had a thin outer layer, which is today known as the "plasma membrane". He also concluded, based on his studies on plant tissues, that the presence of a cell wall is a unique character of plant cells. On the basis of this, Schwann proposed the hypothesis that the bodies of animals and plants are composed of cells and products of cells.
- Schleiden and Schwann together formulated the cell theory. This theory, however, did not explain how new cells were formed.
- Rudolf Virchow (1855) first explained that cells divided and new cells are formed from pre-existing cells (Omnis cellula-e cellula). He modified the hypothesis of Schleiden and Schwann to give the cell theory a final shape.
- All living organisms are composed of cells and products of cells.
- All cells arise from pre-existing cells.

3. An Overview of the Cell
Onion cells, which are typical plant cells, have a distinct cell wall as their outer boundary, and just within it is the cell membrane. The cells of the human cheek have an outer membrane as the delimiting structure of the cell. Inside each cell is a dense membrane-bound structure called the nucleus. This nucleus contains the chromosomes, which in turn contain the genetic material, DNA. Cells that have membrane-bound nuclei are called eukaryotic, whereas cells that lack a membrane-bound nucleus are prokaryotic. In both prokaryotic and eukaryotic cells, a semi-fluid matrix called cytoplasm occupies the volume of the cell. The cytoplasm is the main arena of cellular activities in both plant and animal cells.
- Besides the nucleus, the eukaryotic cells have other membrane-bound distinct structures called organelles, like the endoplasmic reticulum (ER), the Golgi complex, lysosomes, mitochondria, microbodies and vacuoles. The prokaryotic cells lack such membrane-bound organelles.
- Ribosomes are non-membrane-bound organelles found in all cells — both eukaryotic and prokaryotic. Within the cell, ribosomes are found not only in the cytoplasm but also within the two organelles — chloroplasts (in plants) and mitochondria — and on rough ER.
- Animal cells contain another non-membrane-bound organelle called the centrosome, which helps in cell division.
- Cells differ greatly in size, shape and activities. Mycoplasmas, the smallest cells, are only 0.3 µm in length, while bacteria could be 3 to 5 µm. The largest isolated single cell is the egg of an ostrich. Among multicellular organisms, human red blood cells are about 7.0 µm in diameter. Nerve cells are some of the longest cells.
- Cells also vary greatly in their shape. They may be disc-like, polygonal, columnar, cuboid, thread-like or even irregular. The shape of the cell may vary with the function they perform.
4. Prokaryotic Cells
The prokaryotic cells are represented by bacteria, blue-green algae, mycoplasma and PPLO (pleuro-pneumonia-like organisms). They are generally smaller and multiply more rapidly than eukaryotic cells. They may vary greatly in shape and size. The four basic shapes of bacteria are bacillus (rod-like), coccus (spherical), vibrio (comma-shaped) and spirillum (spiral).

- All prokaryotes have a cell wall surrounding the cell membrane, except in mycoplasma.
- The fluid matrix filling the cell is the cytoplasm. There is no well-defined nucleus. The genetic material is basically naked, not enveloped by a nuclear membrane. In addition to the genomic DNA (the single chromosome / circular DNA), many bacteria have small circular DNA outside the genomic DNA. These smaller DNA are called plasmids. The plasmid DNA confers certain unique phenotypic characters to such bacteria. One such character is resistance to antibiotics. In higher classes you will learn that this plasmid DNA is used to monitor bacterial transformation with foreign DNA.
- Nuclear membrane is found in eukaryotes. No organelles, like the ones in eukaryotes, are found in prokaryotic cells except for ribosomes. Prokaryotes have something unique in the form of inclusions. A specialised differentiated form of cell membrane called mesosome is the characteristic of prokaryotes. They are essentially infoldings of the cell membrane.

Cell envelope and its modifications
- Most prokaryotic cells, particularly the bacterial cells, have a chemically complex cell envelope. The cell envelope consists of a tightly bound three-layered structure, i.e. the outermost glycocalyx, followed by the cell wall and then the plasma membrane. Although each layer of the envelope performs a distinct function, they act together as a single protective unit.
- Bacteria can be classified into two groups on the basis of the differences in the cell envelopes and the manner in which they respond to the staining procedure developed by Gram, viz. those that take up the Gram stain are Gram positive and the others that do not are called Gram negative bacteria.
- Glycocalyx differs in composition and thickness among different bacteria. It could be a loose sheath called the slime layer in some, while in others it may be thick and tough, called the capsule.
- The cell wall determines the shape of the cell and provides a strong structural support to prevent the bacterium from bursting or collapsing.
- The plasma membrane is semi-permeable in nature and interacts with the outside world. This membrane is similar structurally to that of the eukaryotes.
- The mesosome is formed by the extensions of the plasma membrane into the cell. These extensions are in the form of vesicles, tubules and lamellae. They help in cell wall formation, DNA replication and distribution to daughter cells. They also help in respiration, secretion processes, to increase the surface area of the plasma membrane and enzymatic content.
- In some prokaryotes like cyanobacteria, there are other membranous extensions into the cytoplasm called chromatophores, which contain pigments.
- Bacterial cells may be motile or non-motile. If motile, they have thin filamentous extensions from their cell wall called flagella. A bacterial flagellum is composed of three parts — filament, hook and basal body. The filament is the longest portion and extends from the cell surface to the outside.
- Besides flagella, pili and fimbriae are also surface structures of the bacteria but do not play a role in motility. The pili are elongated tubular structures made of a special protein. The fimbriae are small bristle-like fibres sprouting out of the cell. In some bacteria, they are known to help attach the bacteria to rocks in streams and also to the host tissues.
Ribosomes and inclusion bodies
- In prokaryotes, ribosomes are associated with the plasma membrane of the cell. They are about 15 nm by 20 nm in size and are made of two subunits — 50S and 30S — which, when present together, form the 70S prokaryotic ribosome. Ribosomes are the site of protein synthesis. Several ribosomes may attach to a single mRNA and form a chain called polyribosomes or polysome. The ribosomes of a polysome translate the mRNA into proteins.
- Reserve material in prokaryotic cells is stored in the cytoplasm in the form of inclusion bodies. These are not bounded by any membrane system and lie free in the cytoplasm, e.g. phosphate granules, cyanophycean granules and glycogen granules. Gas vacuoles are found in blue-green and purple and green photosynthetic bacteria.
Some bacteria (e.g. Bacillus, Clostridium) survive harsh conditions by forming an endospore inside the cell. A septum forms near one end, the smaller part becomes a forespore, a thick spore coat develops around it, and the mature endospore is released when the mother cell breaks down. Endospores resist heat, drying and chemicals, which is why autoclaving at high temperature and pressure is used to sterilise medical equipment.

5. Eukaryotic Cells
The eukaryotes include all the protists, plants, animals and fungi. In eukaryotic cells there is an extensive compartmentalisation of cytoplasm through the presence of membrane-bound organelles. Eukaryotic cells possess an organised nucleus with a nuclear envelope. In addition, eukaryotic cells have a variety of complex locomotory and cytoskeletal structures. Their genetic material is organised into chromosomes.
All eukaryotic cells are not identical. Plant and animal cells are different, as the former possess cell walls, plastids and a large central vacuole, which are absent in animal cells. On the other hand, animal cells have centrioles, which are absent in almost all plant cells.


| Feature | Plant cell | Animal cell | NEET Note |
|---|---|---|---|
| Cell wall | Present (cellulose) | Absent | — |
| Plastids | Present | Absent | — |
| Vacuole | Large central vacuole (up to 90% of volume) | Small or absent | — |
| Centrioles | Absent in almost all | Present | — |
| Storage | Starch | Glycogen | — |
Cell membrane
- The detailed structure of the membrane was studied only after the advent of the electron microscope in the 1950s. Chemical studies on the cell membrane, especially in human red blood cells (RBCs), enabled scientists to deduce the possible structure of the plasma membrane.
- These studies showed that the cell membrane is mainly composed of lipids and proteins. The major lipids are phospholipids arranged in a bilayer. The lipids are arranged within the membrane with the polar head towards the outer sides and the hydrophobic tails towards the inner part. This ensures that the non-polar tail of saturated hydrocarbons is protected from the aqueous environment. In addition to phospholipids, the membrane also contains cholesterol.
- Later, biochemical investigation clearly revealed that the cell membranes also possess protein and carbohydrate. The ratio of protein and lipid varies considerably in different cell types. In human beings, the membrane of the erythrocyte has approximately 52 per cent protein and 40 per cent lipids.
- Depending on the ease of extraction, membrane proteins can be classified as integral or peripheral. Peripheral proteins lie on the surface of the membrane, while the integral proteins are partially or totally buried in the membrane.
- An improved model of the structure of the cell membrane was proposed by Singer and Nicolson (1972), widely accepted as the fluid mosaic model. According to this, the quasi-fluid nature of lipid enables lateral movement of proteins within the overall bilayer. This ability to move within the membrane is measured as its fluidity.
- The fluid nature of the membrane is also important from the point of view of functions like cell growth, formation of intercellular junctions, secretion, endocytosis, cell division etc.
- One of the most important functions of the plasma membrane is the transport of the molecules across it. The membrane is selectively permeable to some molecules present on either side of it. Many molecules can move briefly across the membrane without any requirement of energy, and this is called passive transport. Neutral solutes may move across the membrane by the process of simple diffusion along the concentration gradient, i.e. from higher concentration to the lower. Water may also move across this membrane from higher to lower concentration. Movement of water by diffusion is called osmosis. As the polar molecules cannot pass through the non-polar lipid bilayer, they require a carrier protein of the membrane to facilitate their transport across the membrane. A few ions or molecules are transported across the membrane against their concentration gradient, i.e. from lower to the higher concentration. Such a transport is an energy-dependent process, in which ATP is utilised, and is called active transport, e.g. the Na⁺/K⁺ pump.

RBC membrane ≈ 52% protein, 40% lipid. The fluid mosaic model was given by Singer and Nicolson in 1972. Fluidity comes from the quasi-fluid lipids, which allow lateral movement of proteins. Active transport (e.g. Na⁺/K⁺ pump) uses ATP and moves substances against the gradient.
Cell wall
A non-living rigid structure called the cell wall forms an outer covering for the plasma membrane of fungi and plants. The cell wall not only gives shape to the cell and protects the cell from mechanical damage and infection, it also helps in cell-to-cell interaction and provides a barrier to undesirable macromolecules. Algae have a cell wall made of cellulose, galactans, mannans and minerals like calcium carbonate, while in other plants it consists of cellulose, hemicellulose, pectins and proteins. The cell wall of a young plant cell, the primary wall, is capable of growth, which gradually diminishes as the cell matures, and the secondary wall is formed on the inner (towards membrane) side of the cell. The middle lamella is a layer mainly of calcium pectate which holds or glues the different neighbouring cells together. The cell wall and middle lamellae may be traversed by plasmodesmata, which connect the cytoplasm of neighbouring cells.
6. Endomembrane System
While each of the membranous organelles is distinct in terms of its structure and function, many of these are considered together as an endomembrane system because their functions are coordinated. The endomembrane system includes the endoplasmic reticulum (ER), Golgi complex, lysosomes and vacuoles. Since the functions of the mitochondria, chloroplast and peroxisomes are not coordinated with the above components, these are not considered as part of the endomembrane system.
Endoplasmic reticulum
Electron microscopic studies of eukaryotic cells reveal the presence of a network or reticulum of tiny tubular structures scattered in the cytoplasm, called the endoplasmic reticulum. Hence, ER divides the intracellular space into two distinct compartments, i.e. luminal (inside ER) and extra-luminal (cytoplasm). The ER often shows ribosomes attached to its outer surface. The endoplasmic reticulum bearing ribosomes on its surface is called rough endoplasmic reticulum (RER). In the absence of ribosomes, they appear smooth and are called smooth endoplasmic reticulum (SER). RER is frequently observed in cells actively involved in protein synthesis and secretion. They are extensive and continuous with the outer membrane of the nucleus. The SER is the major site for synthesis of lipid. In animal cells, lipid-like steroidal hormones are synthesised in SER.
Golgi apparatus
Camillo Golgi (1898) first observed densely stained reticular structures near the nucleus. These were later named Golgi bodies after him. They consist of many flat, disc-shaped sacs or cisternae of 0.5 µm to 1.0 µm diameter. These are stacked parallel to each other. A varied number of cisternae are present in a Golgi complex. The Golgi cisternae are concentrically arranged near the nucleus with distinct convex cis or the forming face and concave trans or the maturing face. The cis and the trans faces of the organelle are entirely different, but interconnected.
The Golgi apparatus principally performs the function of packaging materials, to be delivered either to the intra-cellular targets or secreted outside the cell. Materials to be packaged in the form of vesicles from the ER fuse with the cis face of the Golgi apparatus and move towards the maturing face. This explains why the Golgi apparatus remains in close association with the endoplasmic reticulum. A number of proteins synthesised by ribosomes on the endoplasmic reticulum are modified in the cisternae of the Golgi apparatus before they are released from its trans face. The Golgi apparatus is the important site of formation of glycoproteins and glycolipids.
Lysosomes
These are membrane-bound vesicular structures formed by the process of packaging in the Golgi apparatus. The isolated lysosomal vesicles have been found to be very rich in almost all types of hydrolytic enzymes (hydrolases — lipases, proteases, carbohydrases) optimally active at the acidic pH. These enzymes are capable of digesting carbohydrates, proteins, lipids and nucleic acids.
Vacuoles
The vacuole is the membrane-bound space found in the cytoplasm. It contains water, sap, excretory products and other materials not useful for the cell. The vacuole is bound by a single membrane called the tonoplast. In plant cells the vacuoles can occupy up to 90 per cent of the volume of the cell. In plants, the tonoplast facilitates the transport of a number of ions and other materials against concentration gradients into the vacuole; hence their concentration is significantly higher in the vacuole than in the cytoplasm. In Amoeba the contractile vacuole is important for osmoregulation and excretion. In many cells, as in protists, food vacuoles are formed by engulfing the food particles.

7. Mitochondria and Plastids
Mitochondria
- Mitochondria (sing. mitochondrion), unless specifically stained, are not easily visible under the microscope. The number of mitochondria per cell is variable depending on the physiological activity of the cells. In terms of shape and size also, considerable degree of variability is observed. Typically it is sausage-shaped or cylindrical, having a diameter of 0.2–1.0 µm (average 0.5 µm) and length 1.0–4.1 µm.
- Each mitochondrion is a double membrane-bound structure with the outer membrane and the inner membrane dividing its lumen distinctly into two aqueous compartments, i.e. the outer compartment and the inner compartment. The inner compartment is called the matrix. The outer membrane forms the continuous limiting boundary of the organelle. The inner membrane forms a number of infoldings called the cristae towards the matrix. The cristae increase the surface area. The two membranes have their own specific enzymes associated with the mitochondrial function.
- Mitochondria are the sites of aerobic respiration. They produce cellular energy in the form of ATP, hence they are called "power houses" of the cell.
- The matrix also possesses a single circular DNA molecule, a few RNA molecules, ribosomes (70S) and the components required for the synthesis of proteins. The mitochondria divide by fission.
Plastids
Plastids are found in all plant cells and in euglenoides. These are easily observed under the microscope as they are large. They bear some specific pigments, thus imparting specific colours to the plants. Based on the type of pigments, plastids can be classified into chloroplasts, chromoplasts and leucoplasts.
- The chloroplasts contain chlorophyll and carotenoid pigments, which are responsible for trapping light energy essential for photosynthesis.
- In the chromoplasts, fat-soluble carotenoid pigments like carotene, xanthophylls and others are present. This gives the part of the plant a yellow, orange or red colour.
- The leucoplasts are the colourless plastids of varied shapes and sizes with stored nutrients: amyloplasts store carbohydrates (starch), e.g. potato; elaioplasts store oils and fats; and the aleuroplasts store proteins.
Majority of the chloroplasts of the green plants are found in the mesophyll cells of the leaves. These are lens-shaped, oval, spherical, discoid or even ribbon-like organelles having variable length (5–10 µm) and width (2–4 µm). Their number varies from 1 per cell of Chlamydomonas, a green alga, to 20–40 per cell in the mesophyll. Like mitochondria, chloroplasts are also double membrane-bound. Of the two, the inner chloroplast membrane is relatively less permeable. The space limited by the inner membrane of the chloroplast is called the stroma. A number of organised flattened membranous sacs called the thylakoids are present in the stroma. Thylakoids are arranged in stacks like piles of coins called grana (singular: granum) or the intergranal thylakoids. In addition, there are flat membranous tubules called the stroma lamellae connecting the thylakoids of the different grana. The membrane of the thylakoids encloses a space called a lumen. The stroma of the chloroplast contains enzymes required for the synthesis of carbohydrates and proteins. It also contains small, double-stranded circular DNA molecules and ribosomes. Chlorophyll pigments are present in the thylakoids. The ribosomes of the chloroplasts are smaller (70S) than the cytoplasmic ribosomes (80S).
| Feature | Mitochondrion | Chloroplast | NEET Note |
|---|---|---|---|
| Membranes | Double; inner folded into cristae | Double; inner less permeable | Both semi-autonomous |
| Inner space | Matrix | Stroma with thylakoids (grana) and stroma lamellae | — |
| DNA and ribosomes | Circular DNA, 70S | Circular dsDNA, 70S | Supports endosymbiotic origin |
| Function | Aerobic respiration (ATP) | Photosynthesis | Power house / food factory |
8. Ribosomes, Cytoskeleton, Cilia, Centrosome
Ribosomes
Ribosomes are the granular structures first observed under the electron microscope as dense particles by George Palade (1953). They are composed of ribonucleic acid (RNA) and proteins and are not surrounded by any membrane. The eukaryotic ribosomes are 80S while the prokaryotic ribosomes are 70S. Here "S" (Svedberg's unit) stands for the sedimentation coefficient; it indirectly is a measure of density and size. Both 70S and 80S ribosomes are composed of two subunits.
| Ribosome | Subunits | Found in | NEET Note |
|---|---|---|---|
| 70S | 50S + 30S | Prokaryotes, mitochondria, chloroplasts | S values are not additive |
| 80S | 60S + 40S | Eukaryotic cytoplasm and RER | — |
Cytoskeleton
An elaborate network of filamentous proteinaceous structures consisting of microtubules, microfilaments and intermediate filaments present in the cytoplasm is collectively referred to as the cytoskeleton. The cytoskeleton in a cell is involved in many functions such as mechanical support, motility and maintenance of the shape of the cell.
Cilia and flagella
Cilia (sing.: cilium) and flagella (sing.: flagellum) are hair-like outgrowths of the cell membrane. Cilia are small structures which work like oars, causing the movement of either the cell or the surrounding fluid. Flagella are comparatively longer and responsible for cell movement. The prokaryotic bacteria also possess flagella, but these are structurally different from that of the eukaryotic flagella.
The electron microscopic study of a cilium or the flagellum shows that they are covered with plasma membrane. Their core, called the axoneme, possesses a number of microtubules running parallel to the long axis. The axoneme usually has nine pairs of doublets of radially arranged peripheral microtubules and a pair of centrally located microtubules. Such an arrangement of axonemal microtubules is referred to as the 9 + 2 array. The central tubules are connected by bridges and are also enclosed by a central sheath, which is connected to one of the tubules of each peripheral doublet by a radial spoke. Thus, there are nine radial spokes. The peripheral doublets are also interconnected by linkers. Both the cilium and flagellum emerge from centriole-like structures called the basal bodies.
Centrosome and centrioles
The centrosome is an organelle usually containing two cylindrical structures called centrioles. They are surrounded by amorphous pericentriolar materials. Both the centrioles in a centrosome lie perpendicular to each other, in which each has an organisation like the cartwheel. They are made up of nine evenly spaced peripheral fibrils of tubulin protein. Each of the peripheral fibrils is a triplet. The adjacent triplets are also linked. The central part of the proximal region of the centriole is also proteinaceous and called the hub, which is connected with tubules of the peripheral triplets by radial spokes made of protein. The centrioles form the basal body of cilia or flagella, and spindle fibres that give rise to the spindle apparatus during cell division in animal cells.

Cilia and eukaryotic flagella: 9 doublets + 2 central singlets (9 + 2), nine radial spokes. Centriole and basal body: 9 triplets, no central tubules (9 + 0), cartwheel with a proteinaceous hub. Bacterial flagella are structurally different (filament, hook, basal body; no microtubules).
9. Nucleus and Microbodies
The nucleus as a cell organelle was first described by Robert Brown as early as 1831. Later, the material of the nucleus stained by the basic dyes was given the name chromatin by Flemming.
- The interphase nucleus (nucleus of a cell when it is not dividing) has highly extended and elaborate nucleoprotein fibres called chromatin, nuclear matrix and one or more spherical bodies called nucleoli (sing.: nucleolus).
- Electron microscopy has revealed that the nuclear envelope, which consists of two parallel membranes with a space between (10 to 50 nm) called the perinuclear space, forms a barrier between the materials present inside the nucleus and that of the cytoplasm. The outer membrane usually remains continuous with the endoplasmic reticulum and also bears ribosomes on it.
- At a number of places the nuclear envelope is interrupted by minute pores, which are formed by the fusion of its two membranes. These nuclear pores are the passages through which movement of RNA and protein molecules takes place in both directions between the nucleus and the cytoplasm.
- Normally, there is only one nucleus per cell; variations in the number of nuclei are also frequently observed. Some mature cells even lack nucleus, e.g. erythrocytes of many mammals and sieve tube cells of vascular plants. Would you consider these cells as "living"?
- The nuclear matrix or the nucleoplasm contains nucleolus and chromatin. The nucleoli are spherical structures present in the nucleoplasm. The content of the nucleolus is continuous with the rest of the nucleoplasm as it is not a membrane-bound structure. It is a site for active ribosomal RNA synthesis. Larger and more numerous nucleoli are present in cells actively carrying out protein synthesis.
- The interphase nucleus has a loose and indistinct network of nucleoprotein fibres called chromatin. But during different stages of cell division, cells show structured chromosomes in place of the nucleus. Chromatin contains DNA and some basic proteins called histones, some non-histone proteins and also RNA. A single human cell has approximately two metre long thread of DNA distributed among its forty-six (twenty-three pairs) chromosomes.
- Every chromosome essentially has a primary constriction or the centromere, on the sides of which disc-shaped structures called kinetochores are present. Based on the position of the centromere, the chromosomes can be classified into four types.
- Sometimes a few chromosomes have non-staining secondary constrictions at a constant location. This gives the appearance of a small fragment called the satellite.

| Type | Centromere position | Arms | NEET Note |
|---|---|---|---|
| Metacentric | Middle | Two equal arms | V-shaped at anaphase |
| Sub-metacentric | Slightly away from the middle | One shorter and one longer arm | L-shaped |
| Acrocentric | Close to one end | One extremely short and one very long arm | J-shaped |
| Telocentric | Terminal | One arm only | Rod (I)-shaped; not found in humans |
Microbodies
Many membrane-bound minute vesicles called microbodies, which contain various enzymes, are present in both plant and animal cells (e.g. peroxisomes, glyoxysomes).
10. Master Summary Table
| Organelle | Membrane | Function | NEET Note |
|---|---|---|---|
| Plasma membrane | Single (bilayer) | Selective transport | Fluid mosaic model |
| RER / SER | Single | Protein synthesis / lipid and steroid synthesis | Endomembrane |
| Golgi apparatus | Single | Packaging; glycoproteins, glycolipids | Cis (forming), trans (maturing) |
| Lysosome | Single | Hydrolytic digestion | Acidic pH enzymes |
| Vacuole | Single (tonoplast) | Storage, osmoregulation | Up to 90% of plant cell |
| Mitochondrion | Double | Aerobic respiration | Circular DNA, 70S |
| Chloroplast | Double | Photosynthesis | Thylakoids, grana, stroma |
| Ribosome | None | Protein synthesis | 70S / 80S; Palade |
| Centriole | None | Basal body, spindle | 9 triplets, cartwheel |
| Nucleolus | None | rRNA synthesis | Larger in protein-synthesising cells |
11. Mind Map
- Schleiden, Schwann
- Virchow
- Cell sizes
- Cell envelope, mesosome
- Plasmids, 70S
- Flagella, pili
- Membrane, wall
- Endomembrane system
- Mitochondria, plastids
- Ribosomes, cytoskeleton
- Cilia, centrioles
- Nucleus, chromosomes
12. Tips and Tricks
- Endomembrane system: "Every Good Lab Vessel" — ER, Golgi, Lysosome, Vacuole. Mitochondria, chloroplast and peroxisome are excluded.
- Leucoplasts: Amylo = starch (amylum), Elaio = oil (elaion), Aleuro = protein (aleurone).
- Chromosome shapes at anaphase: Meta = V, Sub-meta = L, Acro = J, Telo = I.
- Ribosome subunits: "70 = 50 + 30, 80 = 60 + 40" — S values are not simply added.
- Including mitochondria or chloroplasts in the endomembrane system.
- Saying the nucleolus is membrane-bound (it is not).
- Saying centrioles have a 9 + 2 arrangement (they are 9 + 0 triplets; cilia are 9 + 2).
- Saying the inner chloroplast membrane is more permeable (it is less permeable).
- Thinking plasmids are part of the genomic DNA (they are extra-chromosomal).
13. Important One-liners
- Virchow stated Omnis cellula-e cellula.
- Mycoplasma (0.3 µm) are the smallest cells; the ostrich egg is the largest single cell.
- Mesosomes help in cell wall formation, DNA replication and respiration in bacteria.
- A bacterial flagellum has a filament, hook and basal body.
- The fluid mosaic model was proposed by Singer and Nicolson in 1972.
- The middle lamella is made mainly of calcium pectate.
- SER synthesises steroid hormones in animal cells.
- Camillo Golgi discovered the Golgi apparatus in 1898.
- The tonoplast surrounds the vacuole.
- George Palade first observed ribosomes in 1953.
- Flemming named the stainable nuclear material chromatin.
- A human cell has about 2 m of DNA in 46 chromosomes.
14. NEET-pattern Questions with Detailed Answers
These questions are original and based on concepts that NEET UG asks again and again.
Who stated that new cells arise from pre-existing cells?
- Schleiden
- Schwann
- Rudolf Virchow
- Robert Brown
Show solution
Virchow (1855) gave the idea Omnis cellula-e cellula and completed the cell theory. Schleiden and Schwann proposed the original cell theory, and Robert Brown discovered the nucleus.
Answer: (C)
The site of active ribosomal RNA synthesis is the:
- Nucleolus
- Golgi apparatus
- Lysosome
- Smooth ER
Show solution
The nucleolus is the site of rRNA synthesis and is larger in cells actively making proteins. The Golgi packages materials, lysosomes digest, and SER makes lipids.
Answer: (A)
Which of the following is NOT a part of the endomembrane system?
- Golgi complex
- Lysosome
- Vacuole
- Mitochondrion
Show solution
The functions of mitochondria, chloroplasts and peroxisomes are not coordinated with those of the ER, Golgi, lysosomes and vacuoles. So mitochondria are not counted in the endomembrane system.
Answer: (D)
The approximate protein and lipid composition of the human RBC membrane is:
- 40% protein, 52% lipid
- 52% protein, 40% lipid
- 75% protein, 25% lipid
- 50% protein, 50% lipid
Show solution
The erythrocyte membrane has about 52% protein and 40% lipid; the rest is mainly carbohydrate. Option (A) reverses the values.
Answer: (B)
The arrangement of microtubules in the axoneme of a cilium is:
- 9 + 0
- 9 + 2
- 9 + 3
- 8 + 2
Show solution
A cilium has nine peripheral doublets and two central singlets (9 + 2). Centrioles and basal bodies have nine triplets and no central tubules (9 + 0).
Answer: (B)
Elaioplasts store:
- Starch
- Proteins
- Oils and fats
- Carotenoids
Show solution
Elaioplasts store oils and fats. Amyloplasts store starch, aleuroplasts store proteins, and chromoplasts contain carotenoids.
Answer: (C)
Assertion (A): Proteins can move laterally within the plasma membrane.
Reason (R): The lipid bilayer of the membrane is quasi-fluid.
- Both A and R are true, and R explains A
- Both A and R are true, but R does not explain A
- A is true, R is false
- A is false, R is true
Show solution
According to the fluid mosaic model, the quasi-fluid nature of the lipids allows proteins to move sideways within the bilayer. R explains A.
Answer: (A)
Which statement about the Golgi apparatus is correct?
- The cis face is concave and the trans face is convex
- Materials from the ER fuse with the trans face
- It is an important site of formation of glycoproteins and glycolipids
- It is a double membrane-bound organelle
Show solution
The Golgi apparatus forms glycoproteins and glycolipids. The cis face is convex (forming) and the trans face is concave (maturing). ER vesicles fuse with the cis face, and the cisternae are single-membraned.
Answer: (C)
A chromosome with the centromere close to one end, giving one extremely short and one very long arm, is:
- Metacentric
- Sub-metacentric
- Acrocentric
- Telocentric
Show solution
An acrocentric chromosome has its centromere close to one end. In metacentric it is in the middle, in sub-metacentric slightly away from the middle, and in telocentric it is terminal.
Answer: (C)
Match: (a) Mesosome (b) Tonoplast (c) Cristae (d) Thylakoids — (i) Vacuole membrane (ii) Infoldings of inner mitochondrial membrane (iii) Infoldings of bacterial plasma membrane (iv) Sacs bearing chlorophyll.
- a-iii, b-i, c-ii, d-iv
- a-i, b-iii, c-ii, d-iv
- a-iii, b-ii, c-i, d-iv
- a-iii, b-i, c-iv, d-ii
Show solution
Mesosomes are infoldings of the bacterial plasma membrane. The tonoplast surrounds the vacuole, cristae are infoldings of the inner mitochondrial membrane, and thylakoids carry chlorophyll.
Answer: (A)
15. Quick Revision Summary
- Cell theory: Schleiden (1838), Schwann (1839), Virchow (1855). All organisms are made of cells; cells come from pre-existing cells.
- Prokaryotes: no nuclear membrane; glycocalyx–wall–membrane envelope; mesosome; plasmids; 70S; inclusion bodies; flagellum = filament, hook, basal body.
- Membrane: phospholipid bilayer + proteins (fluid mosaic, Singer & Nicolson 1972); passive (diffusion, osmosis) and active transport (Na⁺/K⁺ pump).
- Endomembrane: ER (RER proteins, SER lipids), Golgi (cis–trans, packaging), lysosome (acid hydrolases), vacuole (tonoplast).
- Mitochondria (cristae, matrix, circular DNA, 70S) and plastids (chloro-, chromo-, leucoplasts; grana, stroma lamellae).
- Ribosomes 70S (50S + 30S) and 80S (60S + 40S); cytoskeleton; cilia 9 + 2; centriole 9 triplets, cartwheel.
- Nucleus: double envelope with pores; nucleolus (rRNA); chromatin with histones; chromosome types by centromere; satellite.