Class 11 Biology NCERT Solutions
~5 min readThe complete NCERT exercise solutions for Chapter 8, Cell: The Unit of Life — 14 questions from Ex, each worked through step by step in the CBSE marking pattern. Cell theory, prokaryotic and eukaryotic cells, the cell envelope, organelles, the nucleus and ribosomes.
Chapter 8 carries 1 exercise question, numbered Ex. All of them are solved step by step on this page, along with the chapter's key formulas and exam pointers.
This chapter is the largest of the first block and the fourteen questions below are the complete rationalised NCERT exercise set for Chapter 8, worked in the board pattern. The chapter is really three movements, and the questions follow the same order: the cell theory, the prokaryotic cell, and the eukaryotic cell with its organelles and the membrane transport. Two of the fourteen are objective and matching questions, and the rest need short paragraphs, so the answer length here is shorter than in the earlier chapters, and the discipline required is precision rather than detail.
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14Exercise questions
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The incorrect statement is (a), since Robert Brown did not discover the cell. The cell was first described by Robert Hooke in 1665, when he saw the empty rectangular compartments in the cork of the Calotropis and named them cells. Robert Brown's contribution was different, for in 1831 he discovered the nucleus in the cells of the orchid, Orchis, and he also described the cell in unstained material. The other three statements are correct. Schleiden and Schwann, the botanist and the zoologist, formulated the cell theory in 1838-1839, having independently concluded that all plants and animals are composed of cells and that the cell is the basic structural and functional unit of the body. Virchow in 1855 gave the further proposition that cells arise only from pre-existing cells, omnis cellula-e cellula, rejecting spontaneous generation. And a unicellular organism does carry out all its life activities, metabolic and reproductive, within the single cell that constitutes its entire body, which is precisely why the cell is both the structural and the functional unit of life.
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(c) Pre-existing cells. This is the third proposition of the cell theory, given by Rudolf Virchow in 1855, that every cell arises only from a pre-existing cell, omnis cellula-e cellula, and it completes the two propositions of Schleiden and Schwann, that all living organisms are composed of cells and their products and that the cell is the basic structural and functional unit of the body. The alternatives are wrong: the view that living cells could arise from non-living matter was the theory of spontaneous generation, which Virchow rejected, and it is not a route by which new cells are generated; bacterial fermentation is merely a metabolic process of certain bacteria and has no bearing on cell origin; and regeneration of old cell substance is not what happens, since a cell does not rebuild itself but divides, and by that division each cell gives two daughter cells, so that the increase in cell number is always the result of the division of cells already present.
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(a) Cristae — (ii) Infoldings in mitochondria, since the cristae are the inward folds of the inner membrane of the mitochondrion that project into the matrix and carry the electron transport system and ATP synthesis, the infoldings increasing the surface for these reactions. (b) Cisternae — (iii) Disc-shaped sacs in Golgi apparatus, since the cisternae are the stacks of flattened disc-like sacs that constitute the Golgi body and that modify, package and transport the proteins and lipids arriving from the endoplasmic reticulum. (c) Thylakoids — (i) Flat membranous sacs in stroma, since the thylakoids are the flat membranous sacs lying within the stroma of the chloroplast, arranged in stacks called grana and joined by stroma lamellae, and they bear the chlorophyll and carry out the light reaction of photosynthesis. The three are best kept apart by remembering that the crista is a fold of the mitochondrion, the cisterna a sac of the Golgi and the thylakoid a sac of the chloroplast, and that the mitochondrion is the only one of the three in which the named part is an infolding rather than a sac.
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The correct statement is (c), that in prokaryotes there are no membrane-bound organelles. The prokaryotic cell is bounded by a plasma membrane of a single unit membrane and has no cell envelope of the multilayered, compartmentalised kind; it has no endoplasmic reticulum, no Golgi apparatus, no mitochondria, no lysosomes, no chloroplasts and no nucleus, and it therefore lacks the internal compartmentalisation that characterises a eukaryotic cell. The other three are incorrect. Statement (a) is wrong because the prokaryotic cell has no true nucleus, its genetic material being a naked circular double-stranded DNA molecule that lies loosely in the cytoplasm in a region called the nucleoid without being enclosed by a nuclear membrane, so a membrane-bound nucleus belongs only to the eukaryotic cell. Statement (b) is wrong because only the plant cell of the two has a well defined cell wall, made of cellulose, hemicellulose, pectin and proteins, whereas the animal cell has no cell wall at all and is bounded only by a plasma membrane, although cell walls are also present in fungi and bacteria. Statement (d) is wrong because cells are never formed from abiotic materials, since every cell arises only from a pre-existing cell, which is Virchow's third proposition of the cell theory.
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A mesosome is a membranous infolding or invagination of the plasma membrane of a prokaryotic cell that projects inwards into the cytoplasm, appearing as a vesicle, tubule or lamellar structure, and a group of them is called a mesosome, or mesosomata. It is a characteristic feature of the prokaryotic cell, arises by the infolding of the plasma membrane, and performs four functions. First, respiration: it acts as an analogue of the mitochondrion, carrying out the electron transport and oxidative phosphorylation as a respiratory apparatus, since the prokaryotic cell has no mitochondria. Second, formation of the new cell wall: it helps in cell wall formation, the new wall material appearing in the septa that form during cell division. Third, replication of the DNA: it assists in the replication of the chromosomal DNA and in the formation of the daughter cells, being the site to which the circular DNA is attached, so that the DNA can be distributed to the daughter cells. Fourth, secretions: it helps in secretory processes and by its infoldings increases the surface area of the plasma membrane available for transport. Thus the four functions are respiration, cell wall formation, replication and distribution of the DNA, and help in secretion.
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Neutral solutes, that is small, non-polar, lipid-soluble molecules such as oxygen, carbon dioxide, nitrogen, water and glycerol, cross the plasma membrane by simple diffusion. The plasma membrane is a lipid bilayer whose hydrophilic polar heads face outward and whose hydrophobic non-polar tails face inward, so the interior of the bilayer is a hydrophobic region in which a small non-polar molecule dissolves; the solute therefore moves from higher to lower concentration, down the concentration gradient, at a rate that depends on the size of the molecule and on the gradient, with no carrier and no expenditure of energy, so the process is passive. Polar molecules cannot cross in the same way, for the hydrophobic interior of the bilayer is not soluble in a polar or charged molecule, and the lipid phase is impervious to them however steep the gradient may be. Polar molecules are accordingly transported with the help of protein, in two ways. Small and medium polar molecules such as glucose, sucrose and amino acids pass by carrier-mediated facilitated diffusion, in which the solute binds to a specific site on a carrier protein, the carrier changes conformation and releases it on the far side, the movement still being down the gradient and still requiring no energy. Large macromolecules such as proteins and polysaccharides, and polar material generally, pass by endocytosis, in which the membrane invaginates, bulges and pinches off to enclose the material in a small membrane-bound vesicle, called phagocytosis when the material is solid and pinocytosis when it is liquid, with exocytosis as the reverse process by which the vesicle fuses with the membrane and releases its contents. Thus the neutral solutes use the lipid phase directly by simple diffusion, whereas the polar molecules must use a carrier protein or the vesicle mechanism, and both processes are passive, the difference being structural rather than energetic.
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The two double membrane organelles are the mitochondrion and the plastid, and these are the organelles whose presence in a cell means the cell is said to have a double membrane, since the whole cell is bounded by one; the two are thought to have arisen by endosymbiosis. The mitochondrion is a small rod-shaped or oval organelle with an outer and an inner membrane, the inner membrane being thrown into folds called cristae that project into the matrix, and the cristae bear the electron transport system and the ATP synthase; the matrix contains circular double-stranded DNA, 70S ribosomes, the components of protein synthesis and the enzymes of the Krebs cycle, so the mitochondrion is semi-autonomous and can make some of its own proteins. Its functions are to be the principal site of aerobic respiration and of oxidative phosphorylation, so that it is called the powerhouse of the cell and is the main site of ATP synthesis, to be the site of the Krebs cycle and of the oxidation of pyruvate and therefore of carbohydrate and fat metabolism, to store and release calcium ions, to be the site of the enzymes of apoptosis, for which it is called the suicide bag, and to help in the synthesis of certain amino acids. Its labelled diagram must show the outer membrane, the inner membrane with the cristae, the matrix, the circular DNA and the 70S ribosomes. The plastid occurs in three types: the chloroplast, with chlorophyll, the site of photosynthesis; the chromoplast, with the carotenes and xanthophylls, which gives the red, orange and yellow colour to flowers, to fruits and to autumn leaves; and the leucoplast, which is colourless and stores reserve food, the amyloplast storing starch as in the potato, the elaioplast storing oils as in the groundnut and the allanioplast storing protein. The chloroplast is bounded by two membranes, the inner one being infolded, and it contains flat membranous sacs called thylakoids which are stacked into grana, singular granum, and the grana are joined by the stroma lamellae or intergranal lamellae; it also contains 70S ribosomes, circular DNA and the enzymes of the dark reaction, so it is semi-autonomous. Its functions are that it is the site of photosynthesis, converting light energy to chemical energy stored as sugars, and the site of both the light and the dark reactions, that the chromoplast gives colour to attract pollinators and seed dispersers, that the leucoplasts store starch, oil and protein for later use, and that all three types are interconvertible since a chloroplast in a leaf may become a chromoplast in a flower or a fruit. Its labelled diagram must show the outer and the inner membrane, the stroma, the thylakoid, a granum, and the stroma lamella.
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A prokaryotic cell is the primitive, simplest and earliest form of cell, and the term means a nucleus before the true nucleus, so its defining feature is the absence of a membrane-bound nucleus. It is smaller than a eukaryotic cell, usually about 0.5 to 5 micrometres, with the smallest, the Mycoplasma, at about 0.1 micrometre, and its shapes are diverse, the commonest being the coccus and then the bacillus or rod, with also the vibrio or comma, the spirillum and the spirulina. The cell is surrounded by a cell envelope of glycocalyx, cell wall and plasma membrane; the glycocalyx is a viscous mucous capsule or slime layer in the bacteria and a mucilaginous sheath in the cyanobacteria; the plasma membrane is a single unit membrane of the fluid mosaic type that performs the transport and secretory functions and, with the mesosomes, the respiration; and the cell wall is present in most prokaryotes and is made of peptidoglycan or murein, a polymer of N-acetyl glucosamine and N-acetyl muramic acid joined by peptide bonds, while the archaebacteria differ in having pseudopeptidoglycan and a branched-chain lipid membrane and in lacking peptidoglycan, and the Gram-positive bacteria have a thick peptidoglycan wall with teichoic acids and stain purple while the Gram-negative have a thin wall and an outer lipopolysaccharide membrane and stain pink. The genetic material is a single naked circular double-stranded DNA molecule lying loosely in the cytoplasm in a region called the nucleoid, with no nuclear membrane, no nucleolus and no spindle, and no histone of the eukaryotic type. Ribosomes are present, being the one organelle-like body a prokaryote has, and they are made of 30S and 50S subunits giving 70S, in contrast to the 60S and 40S giving 80S in the eukaryote, which is the basis of the differential sensitivity to antibiotics. All the membrane-bound organelles are absent, with no endoplasmic reticulum, Golgi apparatus, lysosomes, mitochondria, chloroplasts or vacuoles, and the photosynthetic bacteria photosynthesise without chloroplasts by means of special lamellar membranes. The cytoplasm also carries the reserve granules, the glycogen and the polyphosphate, the latter being the volutin or metachromatic bodies, and in the cyanobacteria the gas vacuoles. Where the cell is motile it moves by flagellation, gliding or twitching, and the flagella are of three types, the bacterial flagellum being a naked proteinaceous structure of flagellin several times the length of the body with no 9 plus 2 arrangement, the eukaryotic flagellum having the 9 plus 2 microtubular arrangement, and the archaebacterial flagellum being a thick hollow cylinder, this last type distinguishing the archaebacteria. Shorter and simpler appendages, the fimbriae and the sex pili, serve for attachment and for conjugation. Finally the cell divides amitotically by binary fission and never by mitosis or meiosis, since it has no spindle and no true nucleus.
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Division of labour is the phenomenon in which the cells of a multicellular organism are grouped into specialised units, and each group performs one particular function, so that the work of the organism is divided among the groups and the whole organism carries out its life activities more efficiently than a single cell could, whereas in a unicellular organism all the metabolic, excretory and reproductive activities are performed within the one cell. It is achieved in a particular way. A multicellular organism arises by the repeated mitotic division of a single cell, the zygote, and the cells so produced do not all remain alike, for while a part of them keeps dividing and retains the capacity to divide, forming the meristematic tissue, a part stops dividing, changes its shape and takes on a particular function, forming the permanent differentiated tissue. The differentiated cells of one kind form a tissue, tissues combine to form an organ, and the organs work together as an organ system, so the division of the cells is differential and the cells end up specialised, and this is possible because all the cells descend from the one original zygote and share the same genetic constitution. The consequences are several. Each specialised group performs its own work far more efficiently, as in the human body where the muscle cells contract, the nerve cells conduct, the lung tissue respires and the kidney tissue excretes. Division of labour is responsible for the differentiation and specialisation that produce the complex organisation of the body and its organ systems. It raises the efficiency of the organism, since a specialised cell does one thing better than a general cell, which allows a larger body and a higher rate of activity. It also integrates the organism, since the specialised groups do not act independently but are co-ordinated so that the whole is a co-ordinated whole and not a collection of parts. Thus division of labour is the process by which the single cell becomes a functional unit of a larger integrated organism.
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The cell is called the basic unit of life for several reasons, and they are the reasons the cell theory was formulated to express. First, the cell is the basic structural unit, for all living organisms are composed of cells and their products, which was the first proposition of Schleiden and Schwann, and in a multicellular organism the cells are not a loose collection but are arranged into tissues, organs and organ systems, so the whole structure of the body is built on the cell. Second, the cell is the basic functional unit, since all the life activities of the organism, the metabolic and physiological processes by which it lives, are performed within the cell, and the cell is the smallest unit that can carry out all of them, including ingestion, digestion, respiration, excretion, synthesis, growth and reproduction; this is why the cell is called both the structural and the functional unit of life. Third, the cell is the basic unit of reproduction, since every cell reproduces and the division of a cell is the basis of all reproduction, in a unicellular organism the one cell dividing to give two new organisms and in a multicellular organism the cells dividing to build the body and to produce the gametes, so that no new organism arises except by the division and growth of cells. Fourth, the cell is the basic unit of metabolism and of heredity, being the site of all the chemical reactions of the organism and the place where the DNA, the chromosomes and the machinery of protein synthesis lie, so the cell carries both the information and the means of expressing it, and the hereditary characters pass from cell to cell and from parent to offspring through the cell. Fifth, the cell is the basic unit of growth and development, since an organism grows by an increase in the number of its cells and not by an increase in the size of its material, and every organism begins as one cell, the zygote, which divides to form the whole. Finally, the cell is the smallest unit that can exhibit all the characters of life, because structures smaller than a cell, such as the organelles, cannot live independently, while a cell can, as it does in a unicellular organism. These facts are summed up in the two sentences of the cell theory: that the cell is the basic structural and functional unit of life, and that every new cell arises only from a pre-existing cell.
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A nuclear pore is a small, protein-lined aperture or opening in the nuclear envelope, the nuclear membrane, through which the movement of substances between the nucleus and the cytoplasm takes place, and it is not an empty hole, since each is occupied by a large complex of about thirty different proteins called the nuclear pore complex, which is seen as a globular plug filling the pore of about 100 nanometres diameter, and many such pores occur all along the envelope, traversing both its membranes so that the perinuclear space is continuous with the cytoplasm through them. The nuclear pores perform four functions. First, they are the main channel of communication between the nucleus and the cytoplasm, permitting the passage of the RNA and the ribosomal subunits made in the nucleus and of the proteins and enzymes made in the cytoplasm, so that the two compartments are in constant exchange. Second, they regulate this two-way traffic, allowing substances to move out of the nucleus and into it and thereby controlling what crosses the envelope in either direction. Third, they permit the exchange of RNA and proteins in both directions, so that the RNA synthesised in the nucleus can pass out to the cytoplasm and the proteins made there can pass in, and they allow the ribosomal proteins, which are made in the cytoplasm, to reach the nucleolus for assembly into the ribosomal subunits. Fourth, they mediate the import of proteins carrying a nuclear localisation signal, so the nuclear pore is the gate through which all traffic between the two compartments must pass. Thus the pore provides the only route of communication between the nucleus and the cytoplasm and keeps the two functionally integrated.
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The two are alike in being parts of the same endomembrane system, since the endomembrane system comprises the endoplasmic reticulum, the Golgi apparatus, the lysosomes and the vacuoles, and both the lysosome and the vacuole arise within it, the lysosome being formed from the Golgi apparatus and the vacuole from the endoplasmic reticulum, and both are bounded by a single unit membrane. They differ in structure and in function. A lysosome is small, spherical and about 0.5 to 1 micrometre across, has an acidic interior of pH about 5, and contains some thirty to forty different hydrolytic or acid hydrolase enzymes, and its function is intracellular digestion and scavenging: it breaks down the complex carbohydrates, lipids and proteins into their simple monomers, and it degrades the worn-out and damaged organelles, the old proteins and any foreign particles that enter the cell, returning the raw materials to the cytoplasm for reuse, which is why it is called the suicide bag and the garbage disposer, and it is present in greatest number in secretory and phagocytic cells. A vacuole is much larger, especially in the plant cell, where it occupies most of the cell and displaces the cytoplasm to the periphery, and it is filled with cell sap and bounded by a tonoplast, and its functions are storage and regulation rather than digestion: in the plant it stores sugars, salts, pigments, proteins and organic acids, it maintains the osmotic pressure and the turgidity that keeps the plant rigid, it maintains the pH, and it stores food as protein in aleurone grains in seeds and as carbohydrate in the potato tuber, while it is permanent and non-contractile there. In the animal cell and in the lower animals the vacuole is small and few and may be a contractile vacuole, as in Amoeba and Paramecium, in which it collects the excess water and expels it and so serves for osmoregulation and the maintenance of water balance. Thus the lysosome digests and recycles, being an intracellular digestive and scavenging organelle, while the vacuole stores and regulates, and this is the functional difference between two structures of the same endomembrane system.
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(i) The nucleus is a rounded or spherical, double membrane organelle, bounded by an outer and an inner membrane with a perinuclear space of 20 to 40 nanometres between them, and the two together form the nuclear envelope; the outer membrane is continuous with the endoplasmic reticulum and bears ribosomes, and the envelope is interrupted at intervals by the nuclear pores. Within it the interior is filled with the nucleoplasm or karyolymph and contains the chromatin, a material of DNA with the histone and non-histone proteins, which is in the loosely organised euchromatin state when the cell is not dividing and is condensed into the deeply staining chromosomes or heterochromatin when the cell is dividing. The nucleolus is a dense, rounded, non-membranous body lying in the nucleoplasm, and it is the site of the ribosomal RNA synthesis and the assembly of the ribosomal subunits, so it is the site of ribosome formation, while the nucleus as a whole is the control centre of the cell and controls its metabolism, growth and reproduction because it holds the genetic material. The labelled diagram must show the nuclear envelope as a double line, the perinuclear space, a nuclear pore, the nucleoplasm, the chromatin or chromosomes and the nucleolus. (ii) The centrosome is a non-membranous, microtubular organelle present in the cytoplasm of all animal cells and of the lower plants, the lower algae and the fungi, but absent in the higher plants, and it lies near the nucleus; it has two components, the centrioles and the perinuclear material or centrosphere. Each centrosome has a pair of centrioles lying at right angles to each other, and each centriole is a cylinder about 500 nanometres long and 170 nanometres in diameter whose wall is made of nine sets of microtubule triplets arranged in a ring, giving a cartwheel appearance, with a central hub and no central microtubules, so the arrangement is 9 plus 0 in contrast to the 9 plus 2 of the eukaryotic flagellum, and around the centrioles lies the perinuclear material in which microtubules are arranged irregularly and from which the spindle fibres arise. The labelled diagram should show the two rings of the paired centrioles at right angles, each with nine peripheral triplets in a cartwheel and a central hub, surrounded by the perinuclear material. The centrosome is thus the microtubule organising centre of the cell and the centre of cell division, forming the spindle fibres and also the basal bodies of the cilia and flagella.
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A centromere is a specialised constricted, slightly narrow and lightly staining region of a chromosome, present on both the chromatids, at which the two sister chromatids remain joined, and it bears a disc-shaped structure on its surface called the kinetochore, to which the spindle fibres attach and by means of which the chromatid moves towards the pole during division. The position of the centromere is fixed and constant for a given chromosome, and it divides the chromosome into two arms, the short p arm and the long q arm, so the position of the centromere determines the relative length of the two arms and is therefore the basis on which chromosomes are classified. Four types follow, and the diagram should show all four with the centromere in the correct position in each. Metacentric: the centromere lies in the middle, so the two arms are equal in length, the p and the q being the same, as in the chromosomes of man and of most higher organisms; draw a straight rod with the centromere exactly at the centre. Submetacentric: the centromere lies a little to one side of the middle, so the arms are unequal with the p shorter than the q, as in the small V chromosome of man and in chromosome II of Drosophila; draw the rod with the centromere slightly off-centre. Acrocentric: the centromere lies very close to one end, so that the p arm is very short and the q arm very long, as in the Y chromosome of man, in which the short arm ends in a knob-like satellite; draw the rod with the centromere almost at the tip. Telocentric: the centromere lies at or very near the terminal end, so that the p arm is absent and the chromosome consists of a single q arm, as in the grasshopper and in some insects, and it is rare in the higher plants; draw the rod with the centromere at the very tip and no p arm. Thus, keeping the length of the chromosome the same in each case and moving only the centromere, one obtains the metacentric, submetacentric, acrocentric and telocentric types, and the p and q arms labelled in each, which shows that the position of the centromere is what forms the basis of the classification of chromosomes.
Quick Revision
Memorise these equations — direct application numericals and derivations in CBSE & JEE frequently hinge on these.
Ribosome composition
Sanger and Tomlins
Proton-sucrose ratio
Exam Strategy
High-yield question patterns observed across CBSE boards, JEE Main & Advanced, and NEET.
FAQ
There are 1 exercise question in this chapter, numbered Ex. Every one is solved step by step on this page in the official NCERT numbering.
The formulas this chapter's questions actually turn on are: Ribosome composition, Sanger and Tomlins, Proton-sucrose ratio. They are listed with their expressions in the key formulas section below, and the solved questions show where each one is used.
Very important — organelle function and structure are asked in almost every NEET paper, and the prokaryote-versus-eukaryote table is the single most revisited table in this chapter.
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