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GATE General Microbiology: practice questions

GATE — Life Sciences (XL), Section U Food Technology · India · IITs and IISc on rotation (2026: IIT Guwahati)

Original practice questions written to the published syllabus · not past papers
10worked here, free
106written to this exam in this subject
12syllabus units

What this subject covers

The microbial world before it meets food: cell structure, staining, growth, nutrition, genetics and control of bacteria, yeasts, moulds and viruses. Food microbiology (phase 2) builds directly on it.

In the exams: GATE XE-G and XL-U Section 2 (characteristics of microorganisms, growth and death kinetics, serial dilution)

Where the 106 questions fall

How our questions for GATE spread across the units of General Microbiology. Difficulty: 24 easy, 61 medium, 21 hard.

Control of microorganisms: physical and chemical agents and death kinetics13
Measurement of growth: serial dilution, plate count, MPN and turbidity10
Microbial genetics: mutation, plasmids, transformation, transduction and conjugation10
Prokaryotic and eukaryotic cell structure; spores and vegetative cells9
Bacteria, yeasts, moulds and actinomycetes: morphology and classification9
Microbial nutrition and culture media9
Growth curve, generation time and growth kinetics9
Microscopy: light, phase-contrast, fluorescence and electron8
Aseptic technique and laboratory biosafety8
History and scope of microbiology7
Staining: simple, Gram, acid-fast and endospore7
Viruses and bacteriophages7

10 practice questions, worked

Choose an answer, then open the working. Each explanation says why the right answer is right and why the others are not.

1 · History and scope of microbiology · easy

Preservation of food by heating it in sealed containers was first practised, without knowledge of microbes, by:

  1. Louis Pasteur
  2. Nicolas Appert
  3. Alexander Fleming
  4. John Tyndall
Answer and working

B. Nicolas Appert

Appert's bottled foods (about 1810) predate the germ theory; Pasteur later explained why heating prevents spoilage.

Further reading: Jay et al., Modern Food Microbiology

2 · History and scope of microbiology · medium

Viruses were first recognised when tobacco mosaic disease was shown to be caused by an agent that:

  1. Was killed by boiling but not by filtering
  2. Grew on agar but only in the dark
  3. Passed through bacteria-proof filters
  4. Was visible as rods under oil immersion
Answer and working

C. Passed through bacteria-proof filters

Ivanovsky and Beijerinck found that the infectious agent passed bacteria-proof filters; Beijerinck called it a contagium vivum fluidum.

Further reading: Madigan et al., Brock Biology of Microorganisms

3 · Microscopy: light, phase-contrast, fluorescence and electron · medium

Using the relation d = 0.61 λ / NA, what is the resolution limit for green light of 550 nm with an objective of numerical aperture 1.25?

  1. 268 nm
  2. 220 nm
  3. 440 nm
  4. 721 nm
Answer and working

A. 268 nm

d = 0.61 × 550 ÷ 1.25 = 268.4 nm. 220 nm uses the Abbe form λ/(2NA), not the formula stated; 440 nm is λ ÷ NA without the 0.61 factor; 721 nm divides by 0.61 instead of multiplying.

Further reading: Madigan et al., Brock Biology of Microorganisms

4 · Viruses and bacteriophages · medium

In lysogeny, a temperate phage:

  1. Integrates its DNA into the host chromosome as a prophage
  2. Lyses the host cell within minutes of infection every time
  3. Exits the cell by budding through a lipid envelope
  4. Destroys the host chromosome and replaces it with its own
Answer and working

A. Integrates its DNA into the host chromosome as a prophage

The prophage is replicated with the chromosome until induction, for example by UV light.

Further reading: Madigan et al., Brock Biology of Microorganisms

5 · Microbial nutrition and culture media · medium

On MacConkey agar, a lactose-fermenting Gram-negative rod gives pink-red colonies. Which components respectively make the medium selective and differential?

  1. Neutral red selects; peptone with sodium chloride differentiates
  2. Lactose selects; bile salts with crystal violet differentiate by colour
  3. Bile salts/crystal violet select; lactose/neutral red differentiate
  4. Agar selects; bile salts with lactose differentiate by colony size
Answer and working

C. Bile salts/crystal violet select; lactose/neutral red differentiate

Bile salts and crystal violet inhibit Gram-positive bacteria; acid from lactose turns neutral red pink.

Further reading: Willey et al., Prescott's Microbiology

6 · Growth curve, generation time and growth kinetics · medium

A yeast culture makes 5 g/L of cells while consuming 10 g/L of glucose. The cell yield coefficient Y(X/S) is:

  1. 0.05 g/g
  2. 5.0 g/g
  3. 0.5 g/g
  4. 2.0 g/g
Answer and working

C. 0.5 g/g

Y = ΔX ÷ ΔS = 5 ÷ 10 = 0.5 g cells per g glucose. 2.0 inverts the ratio.

Further reading: Madigan et al., Brock Biology of Microorganisms

7 · Control of microorganisms: physical and chemical agents and death kinetics · medium

Viable counts fall from 10⁶ to 10² CFU/mL in 12 minutes at a constant temperature. The D-value is:

  1. 2 min
  2. 4 min
  3. 12 min
  4. 3 min
Answer and working

D. 3 min

Four log reductions in 12 min: D = 12 ÷ 4 = 3 min. 4 is the number of log cycles; 2 divides by 6.

Further reading: Madigan et al., Brock Biology of Microorganisms

8 · Microbial genetics: mutation, plasmids, transformation, transduction and conjugation · medium

A mutation in which a purine is replaced by a pyrimidine is called a:

  1. Deletion
  2. Transition
  3. Transversion
  4. Frameshift
Answer and working

C. Transversion

Transition swaps purine for purine or pyrimidine for pyrimidine; transversion swaps between classes.

Further reading: Madigan et al., Brock Biology of Microorganisms

9 · Aseptic technique and laboratory biosafety · easy

Most food-borne bacterial pathogens such as Salmonella and Listeria monocytogenes are handled in the laboratory as:

  1. Risk group 1 organisms
  2. Risk group 4 organisms
  3. Risk group 2 organisms
  4. Organisms with no risk classification
Answer and working

C. Risk group 2 organisms

They can cause disease but are unlikely to spread widely and treatment exists; classification of individual strains varies between national schemes.

Further reading: WHO Laboratory Biosafety Manual, 4th ed.

10 · Aseptic technique and laboratory biosafety · medium

Cultures and contaminated plates from a food microbiology laboratory should be disposed of by:

  1. Leaving open under UV light overnight
  2. Pouring into the drain with tap water
  3. Autoclaving them before any disposal
  4. Placing in general waste in sealed bags
Answer and working

C. Autoclaving them before any disposal

All cultures and contaminated materials are decontaminated, usually by autoclaving, before leaving the laboratory.

Further reading: WHO Laboratory Biosafety Manual, 4th ed.

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Read the subject

General MicrobiologyThe full study manual, free GATEFormat, sections and how it has changed

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General Microbiology for other exams

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