Principles of Micro 2 Flashcards
describe the experiment by Louis Pasteur
he did the experiment with the swan neck flask where he boiled broth to get rid of all the microorganism and it stayed sterile because microorganism were trapped in the neck of the flask
what happened to the broth when the neck of the flask was broken
it became contaminated once exposed to the air
describe the work of Robert Koch
he wanted to figure out how disease occurred using pure culture from a diseased mice and infecting a healthy mice
what are Koch’s postulates
- the suspected causative organisms should always be present with the specific disease and absent in healthy animals
- the suspected organism can be grown in pure culture
- organisms taken from pure culture should cause disease in healthy animal
- the suspected organism can be re-isolated and shown to be the same as the original
what were problems with Koch’s postualtes
- not all microorganisms are culturable
- some microorganisms are opportunistic - so they can be present in a healthy individual and not cause disease unless under the right conditions
- re-isolated microorganisms might not be the same as original
who is John Snow
- father of epidemiology
- showed contaminated pump handles were contaminating water causing cholera
who is Edward Jenner
- he inoculated a young boy with cowpox to create immunity against smallpox
- brought about the concept of vaccination
what is Ignaz Semmelweiss known for
washing hands between patients can reduce incidence of infections (though his idiot companions paid him no mind)
describe the work of Anthon von Leeuwenhoek
he came up with the early microscope
what is magnification, resolution, and resolving power
magnification - enlarging of object
resolution - degree to which detail is maintained in object
resolving power - minimum spacing between two points where can be clearly as separate entities
factors the limit microscopic magnification of microorganisms
resolution, resolving power, wavelength
light source and max magnification for brightfield
visible
1500x
light source and max magnification for fluorescence
UV
1500x
light source and max magnification for TEM
electrons
500,000 - 1,000,000 x
light source and max magnification for SEM
electrons
10,000 - 1,000,000x
what are two different ways to prep specimen for microscopic viewing
- placing live specimen on surface then putting a coverslip
- kill specimen then put coverslip
for both preparation one can put dye or stain