B.Sc. 2nd year zoology syllabus with question&answer2025

 


Unit 1: Biomolecules

 

Biomolecules are the essential organic compounds found in all living organisms. These include amino acids, peptides, and proteins, which are crucial for structure and function. Amino acids are the basic building blocks of proteins and are connected by peptide bonds. Proteins have complex structures: primary (sequence of amino acids), secondary (alpha-helix and beta-sheets), tertiary (3D folding), and quaternary (multiple chains together). Another major class is carbohydrates, which serve as energy sources and structural components. Carbohydrates are classified into monosaccharides like glucose (hexose) and ribose (pentose), disaccharides such as sucrose, lactose, and maltose, and polysaccharides like glycogen, starch, and cellulose, which are important for energy storage and structural support.

Lipids are another important group, playing key roles in cellular membranes, energy storage, and signaling. They include fatty acids, triacylglycerols, phospholipids, and sterols like cholesterol. Lipids are classified based on structure and function. Nucleic acids—DNA and RNA—store and transmit genetic information. They are composed of purine (adenine, guanine) and pyrimidine (cytosine, thymine, uracil) bases. Nucleic acids are vital in all life forms as they control heredity and cell function.

 

Unit 1: Biomolecules:-

1.     Amino Acids, Peptides, and Proteins:

o   Amino acids: Building blocks of proteins.

o   Peptide bond: Link between amino acids.

o   Protein structure:

§  Primary: Amino acid sequence.

§  Secondary: Alpha-helix, beta-sheets.

§  Tertiary: 3D folding.

§  Quaternary: Multiple polypeptides.

2.     Carbohydrates:

o   Biological role: Energy source.

o   Monosaccharides: Hexoses (glucose) and pentoses (ribose).

o   Disaccharides: Sucrose, lactose, maltose.

o   Polysaccharides: Glycogen, starch, cellulose (for storage and structure).

3.     Lipids:

o   Role: Cell membrane structure, energy storage.

o   Types: Fatty acids, triacylglycerols, phospholipids, sterols.

o   Functions: Structural and metabolic.

4.     Nucleic Acids:

o   Role: Genetic information storage (DNA, RNA).

o   Composition: Purine and pyrimidine bases.

 

 

Unit 2: Enzymes and Metabolic Pathways:-

Enzymes are biological catalysts that speed up biochemical reactions in the body. They are named and classified based on the reactions they catalyze. Enzymes have specificity for their substrates and often require cofactors or coenzymes for activity. Some enzymes exist in multiple forms known as isoenzymes. The mechanism of enzyme action involves lowering the activation energy to accelerate reactions.

Protein metabolism involves processes like transamination (transfer of amino groups), deamination (removal of amino groups), and the urea cycle, which removes toxic ammonia from the body. In carbohydrate metabolism, glucose undergoes glycolysis to produce energy, while gluconeogenesis forms glucose from non-carbohydrate sources. The Cori cycle helps recycle lactic acid, and the TCA cycle (Krebs cycle) generates energy from acetyl-CoA. The HMP shunt provides NADPH and ribose sugars, while glycogenolysis breaks down glycogen, and glycogenesis synthesizes glycogen.

In lipid metabolism, stored fats (triglycerides) are mobilized, and glycerol is used for energy. Beta-oxidation breaks down fatty acids for ATP, and ketogenesis forms ketone bodies during fasting or starvation, which are alternative energy sources.

 

Unit 2: Enzymes and Metabolic Pathways:-

1.     Enzymes:

o   Definition: Biological catalysts.

o   Classification: Based on reaction type.

o   Properties: Specificity, use of cofactors, isoenzymes.

o   Mechanism: Lower activation energy.

2.     Protein Metabolism:

o   Transamination: Amino group transfer.

o   Deamination: Removal of amino group.

o   Urea cycle: Ammonia → Urea (waste removal).

3.     Carbohydrate Metabolism:

o   Glycolysis: Glucose → Pyruvate (energy production).

o   Gluconeogenesis: Formation of glucose from non-carb sources.

o   Cori cycle: Lactic acid recycling.

o   TCA cycle: Energy from acetyl-CoA.

o   HMP shunt: NADPH and ribose production.

o   Glycogenolysis: Breakdown of glycogen.

o   Glycogenesis: Formation of glycogen.

4.     Lipid Metabolism:

o   Mobilization of triglycerides.

o   Glycerol metabolism.

o   Beta-oxidation: Fatty acid breakdown.

o   Ketogenesis: Ketone body formation (in fasting/starvation).

 

 

Unit 3: Structure of Chromosomes, Nucleic Acids, and DNA Replication:-

The structure of nucleic acids is fundamental in genetics. DNA is a double-helix composed of nucleotide units and exists in forms like A, B, and Z-DNA. DNA is often supercoiled to fit inside the cell nucleus. Nucleosomes are units where DNA wraps around histone proteins, forming chromatin, which further folds to form chromosomes. These are the carriers of genetic material.

There are different types of RNA: rRNA (forms ribosomes), tRNA (transfers amino acids during protein synthesis), mRNA (carries genetic code from DNA), and non-coding RNA which regulates gene expression.

DNA replication is the process by which DNA makes a copy of itself before cell division. It is semi-conservative, meaning each new DNA has one old strand and one new. Several enzymes like DNA polymerase (adds nucleotides), helicase (unwinds DNA), and ligase (joins DNA fragments) are involved in this process. The chemistry of replication ensures accurate duplication of genetic material, essential for inheritance and cell function.

 

 

Unit 3: Structure of Chromosomes, Nucleic Acids, and DNA Replication:-

 

1.     Structure of Nucleic Acids:

o   DNA structure: Double helix, base pairing.

o   Form of DNA: A, B, Z-DNA types.

o   Supercoiling: DNA compaction.

2.     Nucleosome and Histone:

o   DNA wraps around histones → nucleosome → forms chromatin.

3.     Chromosomes:

o   Packaged DNA in nucleus.

4.     RNA Types:

o   rRNA: Part of ribosome.

o   tRNA: Brings amino acids.

o   mRNA: Carries genetic code.

o   Non-coding RNA: Regulatory functions.

5.     DNA Replication:

o   Process: Copying DNA before cell division.

o   Enzymes: DNA polymerase, helicase, ligase.

o   Chemistry: Semi-conservative replication.

 

Unit 4: Central Dogma, RNA Transcription, and RNA Processing:-

 

The central dogma of molecular biology explains the flow of genetic information from DNA to RNA to Protein. It starts with transcription, where DNA-dependent RNA polymerase synthesizes RNA using DNA as a template. In bacteria, sigma factors help RNA polymerase bind to promoters, specific DNA sequences that initiate transcription. Transcription occurs in three stages: initiation (RNA polymerase binds and starts RNA synthesis), elongation (RNA chain grows), and termination (RNA synthesis stops). Termination can be rho-dependent (needs rho protein) or rho-independent (uses hairpin loop structure in RNA).

In eukaryotes, transcription is more complex and involves processing of hnRNA (heterogeneous nuclear RNA) to form mature mRNA. This processing includes 5’-capping (adding a cap at the start), splicing (removing introns and joining exons), and 3’-polyadenylation (adding a poly-A tail at the end). Other RNAs like rRNA and tRNA also undergo modifications and processing to function correctly. This entire process ensures that the correct RNA is produced for translation into protein, maintaining the proper flow of genetic information.

 

Unit 4: Central Dogma, RNA Transcription, RNA Processing:-

 

1.     Central Dogma – Flow of genetic info: DNA → RNA → Protein.

2.     Transcription – RNA made from DNA by RNA polymerase.

o   Stages: Initiation, Elongation, Termination.

o   In bacteria: Sigma factor helps in promoter recognition.

o   Rho-dependent/independent termination types.

3.     Transcription in Eukaryotes – Complex process; RNA is first made as hnRNA.

4.     RNA Processing:

o   Splicing: Remove introns, join exons.

o   5’ Capping: Add cap at 5’ end.

o   3’ Polyadenylation: Add poly-A tail at 3’ end.

o   rRNA & tRNA Modifications: For proper function.

o   Differential RNA Processing: Different proteins from same gene.

 

 

Unit 5: Ribosomes and Translation (Protein Synthesis):-

 

Ribosomes are the cellular machines responsible for protein synthesis (translation). They exist in two types: prokaryotic (70S) and eukaryotic (80S) ribosomes, both made of rRNA and proteins. The genetic code is a set of triplet codons, where three nucleotides specify one amino acid. Due to wobble base pairing, some codons can code for the same amino acid (called synonymous codons), leading to degeneracy of the code. Mutations like missense (changes amino acid), nonsense (forms stop codon), and frameshift (due to insertion/deletion) can affect protein function.

Translation involves three main steps: Initiation (ribosome assembles on mRNA with tRNA), Elongation (amino acids are added one by one), and Termination (synthesis stops at stop codon). After translation, post-translational modifications occur, such as folding or adding functional groups. Protein synthesis in prokaryotes differs slightly from eukaryotes in ribosome size, initiation factors, and timing (transcription and translation occur simultaneously in prokaryotes).

Key steps include aminoacylation of tRNA (attaching amino acid to tRNA), peptide bond formation, translocation (movement of ribosome), and recycling of ribosomes for reuse. Regulation of translation and codon bias (preference for certain codons) also play roles in efficient protein production.]

 

Unit 5: Ribosomes and Translation (Protein Synthesis):-

 

1.     Ribosomes – Sites of protein synthesis; types: Prokaryotic (70S), Eukaryotic (80S).

2.     Genetic Code – Triplet codons; wobble base allows flexibility; degeneracy means multiple codons for same amino acid.

3.     Mutations:

o   Missense: Change in amino acid.

o   Nonsense: Stop codon formed.

o   Frameshift: Shift in reading frame.

4.     Translation Process:

o   Initiation: Ribosome assembles on mRNA.

o   Elongation: Amino acids joined via peptide bonds.

o   Translocation: Ribosome moves along mRNA.

o   Termination: Protein synthesis ends.

o   Recycling: Ribosome used again.

5.     tRNA Aminoacylation – Attachment of amino acid to tRNA.

6.     Post-Translation Modifications – Protein folding, functional group addition.

7.     Regulation of Translation – Control over protein production, codon bias affects efficiency.

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B.Sc. Zoology (2nd Year) - Unit-wise Topics


Unit 1: Biomolecules

Unit 2: Enzymes and Metabolic Pathways

Unit 3: Structure of Chromosomes, Nucleic Acids and DNA Replication

Unit 4: Central Dogma, RNA Transcription, RNA Processing

Unit 5: Ribosomes and Translation (Protein Synthesis)


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