Skip to topic
    ← Back to course topics

    Microbiology — Eduqas A-Level Biology

    Test yourself on Microbiology with EDUQAS A-Level practice questions.

    Start free

    7 days Premium · Then the free plan continues · No card, no charge

    Microbiology explained

    This topic focuses on the classification, culture, and growth monitoring of bacteria.

    Read the full explanation

    It emphasizes the importance of aseptic techniques in laboratory settings and the use of Gram staining to categorize bacteria based on their cell wall structure.

    What to demonstrate

    1. Classification of bacteria by shape and Gram stain reaction
    2. Understanding the relationship between Gram stain reaction and cell wall structure
    3. Principles and application of aseptic techniques
    Show all 5 objectives
    1. Methods for culturing microorganisms in the laboratory
    2. Techniques for monitoring population growth including viable counts, serial dilutions, plating, and colony counting

    Microbiology exam tips

    Topic Overview

    Microbiology is the study of microorganisms, including bacteria, viruses, fungi, and protozoa. In WJEC A-Level Biology, this topic focuses on the structure, classification, growth, and control of microbes, with an emphasis on their roles in disease, biotechnology, and the environment. You'll explore how bacteria divide by binary fission, how viruses replicate inside host cells, and how we can control microbial growth using antibiotics, antiseptics, and sterilisation techniques. Understanding microbiology is crucial for grasping concepts in immunology, genetics, and ecology, and it has direct applications in medicine, food production, and industry.

    This topic is particularly important because it links to real-world issues like antibiotic resistance, vaccine development, and the use of microorganisms in genetic engineering. You'll learn about the aseptic techniques used in labs to prevent contamination, the different phases of bacterial growth (lag, log, stationary, death), and how to calculate generation time. You'll also study the structure of viruses, including the lytic and lysogenic cycles of bacteriophages, and the differences between prokaryotic and eukaryotic cells. By the end, you should appreciate how microbes can be both harmful pathogens and beneficial tools in biotechnology.

    Microbiology builds on your knowledge of cell structure and biochemistry. It also connects to topics like respiration (e.g., using yeast in anaerobic respiration), photosynthesis (e.g., cyanobacteria), and genetics (e.g., bacterial transformation). Mastering this topic will help you answer synoptic questions in the exam and prepare you for further study in biomedical sciences, pharmacy, or environmental biology.

    Key Concepts
    • →Bacterial cell structure: prokaryotic cells lack a nucleus and membrane-bound organelles; they have a cell wall (peptidoglycan), plasma membrane, cytoplasm, ribosomes (70S), and sometimes a capsule, flagella, or plasmids.
    • →Binary fission: bacteria reproduce asexually by replicating their DNA, elongating, and dividing into two identical daughter cells. Generation time can be as short as 20 minutes under optimal conditions.
    • →Viral structure and replication: viruses are acellular, consisting of genetic material (DNA or RNA) inside a protein capsid. They replicate inside host cells via the lytic cycle (immediate lysis) or lysogenic cycle (viral DNA integrates into host genome).
    • →Control of microbial growth: methods include physical (heat, radiation, filtration) and chemical (disinfectants, antiseptics, antibiotics). Antibiotics like penicillin inhibit cell wall synthesis; resistance arises via mutation or horizontal gene transfer.
    • →Aseptic techniques: procedures to prevent contamination, such as sterilising equipment, using Bunsen burners to create convection currents, and working in a laminar flow hood.
    Marking Points
    • Classification of bacteria by shape and Gram stain reaction
    • Understanding the relationship between Gram stain reaction and cell wall structure
    • Principles and application of aseptic techniques
    • Methods for culturing microorganisms in the laboratory
    • Techniques for monitoring population growth including viable counts, serial dilutions, plating, and colony counting
    Examiner Tips
    • 💡Ensure you can describe the step-by-step process of the Gram stain technique
    • 💡Practice calculations involving serial dilutions and colony forming units (CFU)
    • 💡Be prepared to explain why specific aseptic techniques are necessary to prevent contamination
    • 💡Understand how to interpret growth curves and the logarithmic nature of bacterial population growth
    • 💡When describing bacterial growth curves, always label the four phases (lag, log, stationary, death) and explain what is happening at each stage. Mention that the log phase shows exponential growth because each bacterium divides by binary fission, and that the stationary phase occurs when nutrients are depleted or waste products accumulate.
    • 💡For questions on antibiotic resistance, use specific examples like MRSA (methicillin-resistant Staphylococcus aureus) and explain how natural selection favours resistant bacteria. Mention that resistance genes can be transferred via plasmids (conjugation) or transduction (by bacteriophages).
    • 💡When comparing prokaryotic and eukaryotic cells, be precise: prokaryotes have 70S ribosomes, no mitochondria, and a single circular chromosome; eukaryotes have 80S ribosomes, mitochondria, and linear chromosomes. This is a common exam question.
    Common Mistakes
    • Failure to maintain aseptic conditions leading to contamination
    • Incorrect calculation of dilution factors in serial dilutions
    • Confusing viable counts with total cell counts
    • Misinterpreting the relationship between Gram stain results and cell wall composition
    • Misconception: All bacteria are harmful. Correction: Many bacteria are beneficial, e.g., gut flora aids digestion, and bacteria are used in fermentation to produce yoghurt, cheese, and antibiotics.
    • Misconception: Viruses are living organisms. Correction: Viruses are not considered living because they cannot reproduce or carry out metabolic processes outside a host cell; they are obligate intracellular parasites.
    • Misconception: Antibiotics kill viruses. Correction: Antibiotics target bacterial structures like cell walls or ribosomes; they are ineffective against viruses. Antiviral drugs work differently, e.g., by inhibiting viral enzymes.
    Frequently Asked Questions
    What is the difference between gram-positive and gram-negative bacteria?
    Gram-positive bacteria have a thick peptidoglycan layer in their cell wall that retains the crystal violet stain, appearing purple under a microscope. Gram-negative bacteria have a thinner peptidoglycan layer and an outer membrane, so they do not retain the stain and appear pink after counterstaining. This difference affects their susceptibility to antibiotics: gram-positive bacteria are more susceptible to penicillin, while gram-negative bacteria are often more resistant due to the outer membrane.
    How do antibiotics like penicillin work?
    Penicillin inhibits the enzyme transpeptidase, which cross-links the peptidoglycan strands in bacterial cell walls. This weakens the cell wall, causing the bacterium to burst (lyse) due to osmotic pressure. Penicillin is effective mainly against gram-positive bacteria because they have a thick peptidoglycan layer. Resistance can occur if bacteria produce beta-lactamase, an enzyme that breaks down penicillin.
    What is the lytic cycle of a bacteriophage?
    In the lytic cycle, a bacteriophage attaches to a bacterial cell, injects its DNA, and hijacks the host's machinery to replicate viral components. New phages are assembled, and the host cell lyses (bursts), releasing many phages to infect other cells. This cycle is rapid and results in the destruction of the host cell.
    Why do bacteria become resistant to antibiotics?
    Bacteria become resistant through mutations in their DNA that alter the target site of the antibiotic, produce enzymes that degrade the antibiotic, or reduce drug uptake. Resistance genes can spread via plasmids (conjugation) or bacteriophages (transduction). Overuse and misuse of antibiotics create selective pressure, allowing resistant bacteria to survive and multiply.
    What are aseptic techniques and why are they important?
    Aseptic techniques are procedures used to prevent contamination of cultures by unwanted microorganisms. Examples include sterilising inoculating loops by heating them red-hot, working near a Bunsen flame to create an updraft, and using sterile pipettes. They are crucial for obtaining pure cultures and accurate experimental results, especially in microbiology labs.
    How do you calculate the generation time of bacteria?
    Generation time (doubling time) is the time it takes for a bacterial population to double in number. It can be calculated using the formula: generation time = (time interval) / (number of generations). The number of generations (n) is found from the equation N = N0 × 2^n, where N is the final number of cells and N0 is the initial number. Rearranging: n = log(N/N0) / log(2). Then divide the time interval by n.