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Catalase test
Background
• Enzyme name catalase
important enzyme in protecting the cell from oxidative
damage by reactive oxygen species (ROS).
• Substrate name hydrogen peroxide
• Enzyme action breakdown of toxic H2O2
producing oxygen gas and water
catalase
• 2H2O2 2H2O + O2
• Hydrogen peroxide produce due to the aerobic
respiration of the cells and have to be breakdown to
prevent it’s toxic action on DNA and cell membrane
Background
• When hydrogen peroxide is added to a colony of catalase-
producing bacteria, it is broken down and the oxygen that is
produced can be seen as bubbles .
• By catalase test we can distinguish between:
– G (+ve) cocci : Staphylococcus positive where
Streptococcus is catalase negative
– G (+ve) bacilli : Bacillus is catalase positive
whereas Clostridium is catalase negative
– All enterobactrieacae (a gram negative bacilli) are
catalse positive
– Lesteria monocytogenes ( a gram positive bacilli)
are catalase positive
PROCEDURE
a. Place a small amount of growth from culture
onto a clean microscope slide.
If using colonies from a blood agar plate, be very
careful not to scrape up any of the blood agar— blood
cells are catalase positive and any contaminating agar
could give a false positive.
b. Add a few drops of H2O2 onto the smear. If
needed, mix with a toothpick. DO NOT use a
metal loop or needle with H2O2; it will give a
false positive and degrade the metal.
Interpretation
c. +ve result rapid evolution of O2 as
evidenced by bubbling.
d. –ve result no bubbles or only a few
scattered bubbles.
To Know
• Catalase is usually located in a cellular, bipolar
environment organelle called the peroxisome
• Louis Jacques Thénard, who discovered
H2O2 (hydrogen peroxide)
• Oscar Loew was the first to give it the name catalase
• Human catalase works at an optimum temperature
of 45 °C
• pH between 6.8 and 7.5
• one catalase molecule can convert approximately 5
million molecules[2] of hydrogen peroxide to water
and oxygen each second

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Catalase test

  • 2. Background • Enzyme name catalase important enzyme in protecting the cell from oxidative damage by reactive oxygen species (ROS). • Substrate name hydrogen peroxide • Enzyme action breakdown of toxic H2O2 producing oxygen gas and water catalase • 2H2O2 2H2O + O2 • Hydrogen peroxide produce due to the aerobic respiration of the cells and have to be breakdown to prevent it’s toxic action on DNA and cell membrane
  • 3. Background • When hydrogen peroxide is added to a colony of catalase- producing bacteria, it is broken down and the oxygen that is produced can be seen as bubbles . • By catalase test we can distinguish between: – G (+ve) cocci : Staphylococcus positive where Streptococcus is catalase negative – G (+ve) bacilli : Bacillus is catalase positive whereas Clostridium is catalase negative – All enterobactrieacae (a gram negative bacilli) are catalse positive – Lesteria monocytogenes ( a gram positive bacilli) are catalase positive
  • 4. PROCEDURE a. Place a small amount of growth from culture onto a clean microscope slide. If using colonies from a blood agar plate, be very careful not to scrape up any of the blood agar— blood cells are catalase positive and any contaminating agar could give a false positive. b. Add a few drops of H2O2 onto the smear. If needed, mix with a toothpick. DO NOT use a metal loop or needle with H2O2; it will give a false positive and degrade the metal.
  • 5. Interpretation c. +ve result rapid evolution of O2 as evidenced by bubbling. d. –ve result no bubbles or only a few scattered bubbles.
  • 6. To Know • Catalase is usually located in a cellular, bipolar environment organelle called the peroxisome • Louis Jacques Thénard, who discovered H2O2 (hydrogen peroxide) • Oscar Loew was the first to give it the name catalase • Human catalase works at an optimum temperature of 45 °C • pH between 6.8 and 7.5 • one catalase molecule can convert approximately 5 million molecules[2] of hydrogen peroxide to water and oxygen each second