midterm 1 Flashcards
Hooke
published first drawing of microbe in Micrographia
Van Leeuwenhoek
“father of microbiology”, detailed drawings and descriptions, sent to Royal Society of London
members of microbial world
Bacteria
Archaea
Eukarya (protists: algae, protozoa, slime molds, water mold; fungi)
viruses
5 Kingdoms
Monera, Protista, Fungi, Animalia, Plantae
basis for Woese’s classification
16S/18S rRNA sequence –> 3 domains
viruses lack rRNA, not in domain
3 domains
Bacteria, Archaea, Eukarya
taxonomic ranks
Domain, Kingdom, phylum, class, order, family, genus, species, strain
Carolus Linnaeus
binomial system: Genus species
Pasteur
sterile, fermentation, rabies vaccine
Koch
bacteria cause disease from study of anthrax, Koch’s postulates, tuberculosis
Fleming
penicillin
Winogradsky
soil microbiology
Beijerinck
virology, microbial ecology, nitrogen fixing bacteria
resolution depends on
wavelength and lens ability (numerical aperture)
Abbe equation
d = .5(wavelength) / nsin(theta)
immersion oil
increases numerical aperture
bright field
dark image against bright background
gross morphology of stained bacteria, dead cells
dark field
light reflected by specimen
living unstained cells and internal structures, larger euk. microbes (fungi, algae)
phase contrast microscope
out of phase light waves amplify differences in refractive index of cells and water
living unstained cells, internal structures, larger
fluorescent microscope
light emitted by specimen
use fluorescent antibodies to identify 1 organism from many
differential interference contrast (DIC)
out of phase light produce interference and form image
2 beams of polarized light by prisms
live unstained cells, colored and 3D
confocal scanning laser microscope
laser beams to illuminate specimen, scans many sections, detector/computer put together, 3D image
light microscope
uses light, condensers, eye
electron microscope
uses electron beam, electromagnets, photographic plate
disadvantages: no living specimen, altered morphology
transmission electron microscope (TEM)
100,000X, .5nm resolution
view internal structures, viruses, DNA
lenses and specimen under high vacuum, thin slices in plastic
*form image from radiation that has passed through specimen
scanning electron microscope
produces image from electrons released from atoms on object’s surface
sample coated with thin layer of metal
gives realistic 3D image
electron cryotomography
rapid freezing (vitreous ice) and tilt series –> 3D inside and outside
scanning probe microscopes
sharp probe moves over surface, can view atoms
scanning tunneling and atomic force microscopes
scanning tunneling microscope
type of scanning probe microscope
steady current maintained between probe and sample, up/down of probe located atoms on surface
atomic force microscope
type of scanning probe microscope
probe moves over specimen at constant distance, up/down creates image, used with surfaces that don’t conduct electricity
2 basic shapes of bacteria
coccus - round
bacillus - rod
coccus arrangements
diplococcus - pairs
streptococcus - chains
staphylococcus - clusters
tetrads - squares, groups of 4
bacillus arrangements
diplobacillus
some strepto-, never staphylo-
vibrios
comma shaped, single curve
spirilla
rigid spirals
spirochetes
flexible spirals
mycelium
network of hyphae
fruiting body
complex structure, bacteria
cell envelope
plasma membrane and all surrounding layers external
basic roles of bacterial plasma membrane
selectively permeable barrier, performs metabolic processes, communication with environment
ethanolamine
bacterial hydrophilic phosphate of phospholipid
lecithin
eukaryotic hydrophilic phosphate of phospholipid
sterols
eukaryotic part of plasma membrane, gives rigidity
hopanoids
bacterial part of plasma membrane, sterol-like, unique to bacteria
macroelements
carbon, oxygen, hydrogen, nitrogen, sulfur, phosphorus
micronutrients
manganese, zinc, cobalt, molybdenum, nickel, copper
growth factors
must be obtained from environment
amino acids, purines/pyrimidines/ vitamins
transported by passive diffusion
glycerol, H2O, O2, CO2
primary active transport
ABC transporters (ATP binding cassette) membrane binding domain/transporter, solute binding/binds substrate, ATP binding domain
secondary active transport
uses potential energy of ion gradients, co-transporters, include major facilitator superfamily (MFS) proteins
symport and antiport
symport
same direction
ex: lactose uptake, lactose + proton
antiport
opposite directions
ex: sodium leaves, proton enters
group translocation
involves chemical modification of substrate
sugar phosphotransferase system (PTS) - sugar transported while being phosphorylated
phosphoenolpyruvate (PEP) - phosphate donor
siderophores
secreted by cell, bind ferric ion, supply to cell
ferrichrome, enterobactin
murein
peptidoglycan
basic PG structure
N-acetylglucosamine (NAG) and N-acetylmuramic acid (NAM) alternate in chains, link together
tetrapeptide attached to NAM
tetrapeptide in PG
L-alanine
D-glutamine
L-lysine or meso-diaminopimelic acid
D-alanine
tetrapeptide cross links
direct or through peptide interbridge (5 glycines)
gram + cell wall
thick, fluffy, PG 60-100%
peptide interbridge - 5 glycines in crosslink
teichoic acid/lipoteichoic acid
periplasmic space?
gram - cell wall
PG 5-10%
direct linkage - no additional amino acid
not all tetrapeptides linked
outer membrane linked to plasma membrane by Braun’s lipoprotein or contact sites
lipopolysaccharide (LPS)
permeability - porin
periplasmic space
lipopolysaccharide (LPS)
hair like, outermost layer of gram neg. lipid A + core polysaccharide + O antigen attachment O antigen = protection Lipid A = endotoxin
gram stain mechanism
crystal violet (+ charge), iodine (dye retention), ethanol (decolorization), safranin ( - charge)
protoplasts
complete loss of cell wall
spheroplasts
gram neg. cells w/out PG
still have OM and plasma membrane