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55 Terms

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who founded microbiology

Leeuwenhoek (1674)

pasteur

koch

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leeuwenhoek

founder of microbiology, not a scientist but a lensemaker, first observed small swimming things in water (animalcule)

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pasteur

worked on microbial metabolism, immunity, and identification of causative agents of disease.

Discovery or identification of many medically important pathogenic bacteria and viruses took place between 1875 and early 1900’s

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koch

proposed rigorous criteria to identify pathogens. Focused on the identification of disease-causing microbes.

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what are some typical shapes of bacterial cells

rods

cocci (spheres)

spirochetes

<p>rods</p><p>cocci (spheres)</p><p>spirochetes</p><p></p>
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spirochete shape bacteria

highly motile

can evade immune system + penetrate deep into periodontal pockets

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What distinguishes a prokaryotic cell from a eukaryotic cell?

Prokaryotes

  • No membrane bound nucleus (DNA still supercoiled)

  • No mitochondria or chloroplasts

eukaryotes

Contain a true, membrane bound nucleus

Contain organelles (Mitochondria + Chloroplasts)

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eubacteria (“true” bacteria)

Many different groups

Many different shapes

Some are medically important

Multiply by binary fission

No nuclear membrane

Walls contain peptidoglycan, unique to eubacteria

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Archaea (primitive bacterial-sized organisms, not bacteria)

  Not medically important

  Chemically different from Eubacteria, no peptidoglycan

  More similar to eukaryotes

  Often found in extreme environments (extremophiles)

many believe Archaea are the progenitors to eukaryotic cells

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viruses

Composed of DNA or RNA with a protein coat

Must grow on living cells

Not free-living forms of life

Are obligate, intracellular, parasites

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viroids

Composed of RNA without a protein coat

Can cause disease in plants (potato spindle tuber disease)

1/80 the size of a virus (200-400 bases long)

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prions

Infectious agent is a protein (smallest infectious agent)

Bovine spongiform encephalopathy (Mad Cow Disease)

only problematic if protein misfolds

Creutzfeld-Jacob Disease in humans

About 1/2 to 1/4 the size of viroids

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size of microbes

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resolution

ability of microscope to separate two objects

   

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light microscope

   Resolution of light microscope is ~0.2 mm (microns)

  - one-fifth of a bacterial cell width

  - Can be used for observing living microorganisms

can see larger structures like nucelus, cell walls, chloroplasts

gram stain can help better visualize

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electron microscope

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scanning electron microscope (SEM)

allows viewing of three-dimensional view of surfaces

only can see outside surface (cell membrance, cilla, microvilli)

<p><span style="font-family: &quot;Times New Roman&quot;;">allows viewing of three-dimensional view of surfaces</span></p><p><span style="font-family: &quot;Times New Roman&quot;;">only can see outside surface (cell membrance, cilla, microvilli) </span></p><p></p>
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transmission electron microscope (TEM)

looks through the cells or sections of cells

2D

the best approach for looking at cell structure ( all organelles)

<p><span style="font-family: &quot;Times New Roman&quot;;">looks through the cells or sections of cells</span></p><p><span style="font-family: &quot;Times New Roman&quot;;">2D</span></p><p><span style="font-family: &quot;Times New Roman&quot;;">the best approach for looking at cell structure ( all organelles)</span></p><p></p>
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cryogenic electron microscope (cryo-em)

can see molecules and large protein complexes like RNA polymerase

<p><span style="font-family: &quot;Times New Roman&quot;;">can see molecules and large protein complexes like RNA polymerase</span></p>
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simple stains

Stains all protein and cytoplasm

ex: crystal violet

  1. fix heat to slide by heat before staining

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Differential stains

Stains different bacteria differently

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gram stain

most widely used as diagnostic stain

stains differently due to thickness of peptidoglycan layer

**know these steps

IF YOU DONT COUNTERSTAIN GRAN NEG WILL BE COLORLESS

IF YOU DONT DECOLORIZE ALL WILL BE PURPLE

at end colors

gram positive = purple

gran negative = red

<p>most widely used as diagnostic stain</p><p>stains differently due to thickness of peptidoglycan layer</p><p>**know these steps</p><p>IF YOU DONT COUNTERSTAIN GRAN NEG WILL BE COLORLESS</p><p>IF YOU DONT DECOLORIZE ALL WILL BE PURPLE</p><p></p><p>at end colors</p><p>gram positive = purple</p><p>gran negative = red</p>
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arrangements of cells

chains

packets

clusters

<p>chains</p><p>packets</p><p>clusters </p><p></p>
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chain

cell divides in 1 plane

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packets

cell divides in 2+ planes perpendicular to each other

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clusters

cell divides in planes at random

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cellular organizations

major structural groupings

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cellular organizations: genome

arranged in condensed nucleoid structure

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cellular organizations: cytosol/ cytoplasm

Around genome is the cytosol or cytoplasm containing the proteins and ribosomes and other smaller molecules of cell

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cellular organizations: cell surface

around all of the above

contains membranes, peptidoglycan and all appendages

Medically important: first part to touch infected host cells

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cellular organizations: cellular options

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bacterial cell wall

Peptidoglycan is unique to bacteria

Peptidoglycan

  -Found in all eubacteria (almost all)

  -A network mesh holding cell together

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 lysozyme

(in tears) dissolves peptidoglycan

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antibiotics

inhibit peptidoglycan cross-linking

ex: penicillin

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gram negative cell wall

•Gram negative cells have thin peptidoglycan layer

•Thin wall allows removal of "gram-stain material"

•Gram negative cells have two membranes, an outer and an inner membrane

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gram positive cell wall

Gram positive cells have thick peptidoglycan

Thick wall does not allow removal of "gram-stain material"

Cell wall is stronger than gram-negative cell wall

Gram positive cells have a single cytoplasmic membrane

sensitive to penicillin G or V ( early gen penicillins)

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outer membrane (gram negative)

Outer membrane

  Contains lipopolysaccharide (LPS, endotoxin)

  composed of:

  - lipid A core

Outer membrane prevents access of some antibiotics, like early generation penicillins (PenG or PenV), to their target

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porins

proteins that allow material to

  enter periplasmic space of cell

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periplasm

Material between the two membranes (GRAM NEG ONLYYY)

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