lecture material Flashcards
microscopic
all kinds of shapes
- budding yeasts
- coccus
- rods
macroscopic
mushrooms molds fungi algal blooms biofilms
Francesco Redi (spontaneous generation)
1668
maggots do not arise from rotting meat
no support for spontaneous generation
John Needham (spontaneous generation)
1745
boiled broth, poured it into a flask and covered it; soon it was teeming with growth
supports spontaneous generation
Spallanzani (spontaneous generation)
1765
4 treatments with broth
no support for spontaneous generation
Louis Pasteur (golden age)
1861
Swan-necked flask
spontaneous generation does not occur
Basi (germ theory)
1835
silkworm disease caused by a fungus
Berkeley (germ theory)
1845
potato blight caused by a fungus
irish potato famine
Semmelweis (germ theory)
1840s
child-bed fever was contagious
maternal death rate - 13-18% (1 in 5)
instituted washing hands between patients (rate decreased to 2%)
Robert Koch (germ theory)
one specific microbial agent causes one specific disease
Koch’s postulates
Schwann (microbial effects on matter)
1837
sugar —> alcohol (by yeilding yeast)
Pasteur (microbial effects on matter)
1857-1860
beer
all fermentations are due to the activities of specific yeasts and bacteria
Winogradsky (microbial effects on matter)
1892
microbes are involved in the cycling of nutrients in soil/aquatic environments
columns
what is a species
organisms that do interbreeding naturally
microbial species
lack obvious morphological differences
traditional approaches for microbial species
staining
metabolic differences
biochemical tests
genetic approaches for microbial species
based on DNA similarity
light microscopy
uses visible light
magnification up to 1,000x
resolving power = .2 um
bright field
light goes directly through specimen
dark specimen, bright background
used to view killed/stained microbes
dark field
light does not go through specimen, but is refracted off
light specimen, dark background
used to view living, unstained microbes
phase contrast
light is moved out of phase
slowing light down
enhances small differences
used to view internal structures in living microbes, especially eukaryotes
fluorescence microscopy
- UV light is used, shorter wavelength (100-400 nm)
- invisible light
- bright, fluorescent specimen, dark background
- natural
- used to view a specimen against a complex background
electron microcopy
- uses electrons, even shorter wavelength (0.005)
- need to kill and/or stain the cells that you are viewing
transmission electron microscopy
- transmitting electrons through a specimen
- slice the cells really thin
- view internal structures
- RP = 0.2 nm
scanning electron microscopy
- scan the surface with electrons
- surface view of electrons
- RP = 20 nm
prokaryotic cell: composition
H2O - 70%
macromolecules - 26%
small molecules - 4%
prokaryotic cell: cell sizes “average”
E. coli
1 um x 2-6 um