Exam 1 Flashcards

(53 cards)

1
Q

How were microbes first discovered?

A

In 1684, Antoni van Leeuwnhoek saw them through the first-ever microscope and called them “animalcules”.

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2
Q

What are the types of microscopy?

A
Light Microscopy
Electron Microscopy (Scanning and Transmission)
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3
Q

What is the difference between SEM and TEM?

A

SEM: Scanning, shows surface by collecting back-scattered electrons, less magnification possible, but is in 3D
TEM: Transmission, electron beam passes through sample to show outside and inside structures, higher magnification possible, but only 2D

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4
Q

What are the three domains of life?

A

Bacteria - Prokaryotes
Archaea - Prokaryotes
Eukarya - Eukaryotes

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5
Q

Saprophyte

A

An organism that is important in the decomposition of dead plant matter. Typically fungal.

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6
Q

How much of Earth’s biomass is microbial?

A

~60%

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7
Q

What is the Germ Theory of Disease?

A

Louis Pasteur and Robert Koch demonstrated that specific microbial pathogens cause diseases.

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8
Q

What were initial classifications of organisms based upon?

A

Morphology and feeding (1860s Ernest Haeckel)

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9
Q

What was the first classification scheme of organisms?

A

Animalia: move and consume food
Planta: dont move, produce food (incl some bact and fungi)
Protista: Everything else (incl some bact and sponges)

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10
Q

What classification scheme supplanted the Animalia/Protista/Plantae scheme?

A

5 Kingdoms: Plantae, Fungi, Animalia, Protista, Monera. Did not work well for protista or monera because they were the “precursors” to the others.

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11
Q

How do we pick genes for phylogenetic trees?

A

Must be universally present
No horizontal transfer
Highly Conserved
Sufficiently large to have differences and be useful for statistical analysis

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12
Q

What genes do we typically sequence to compare organisms?

A

Ribosomal rRNA. Large Subunit: 23S in Bact and Arch, 28S in Euk
Small Subunit rRNA: 16S in Bact and Arch, 18S in Euk.

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13
Q

To what extent are modern phylogenetic trees useful?

A

Modern trees are MULTIgene trees and are therefore not useful at the species level.

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14
Q

What class of enzymes is required for supercoiling of DNA?

A

Topoisomerases

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15
Q

How can microbes regulate the shapes of the fatty acids in their membrane lipids to affect physiology?

A

More saturated/straight chains = more rigid/dense, higher melting point.

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16
Q

Symport

A

One molecule with conc gradient, other against it, both in same direction

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17
Q

Antiport

A

One with gradient, one against, but in OPPOSITE directions

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18
Q

Gram-positive Cell Wall

A

THICK

Has lots of PG

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19
Q

Gram-negative Cell Wall

A

Thinner
Some, but little PG
Has LPS

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20
Q

How do BACTOPRENOL and AUTOLYSIN function in PG synthesis?

A

Bactoprenol exports sugars out of cell so that Autolysin can cleave a space for them in the PG molecule

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21
Q

What does PENICILLIN do?

A

Inhibits synthesis of new PG, therefore stopping bact growth, but not killing existing amount.

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22
Q

How many pores are in each porin?

A

FOUR. Three in a triangle and one in the center

23
Q

What are capsules and how do they differ from LPS?

A

They are thick coats of “slime” (exact composition varies) that are meant to protect the bacterium from hostile environments. LPS can still exist within an encapsulated bacterium, but is not by definition part of a capsule.

24
Q

How do archaeal cell membranes differ from those of bacteria and Eukarya?

A

The bonds between glycerol and the hydrophobic side chains on the lipids are ETHER bonds, not Ester. The Ether bond allows them to resist hydrolysis in extreme environments.

25
How does binary fission occur?
Min CD is synth'd starting at pole, MinE bounces back and forth, breaking CD off in bits. FtsZ forms where MinCD conc is lowesst.
26
What are exoenzymes?
Enzymes that are secreted into the periplasmic space to degrade large molecules (e.g. cellulose, proteins)
27
What % of a bacterium's dry weight do C, N, S, and P comprise?
``` C = 50% N = 15% S = 1% P = 3% ```
28
Psychrophile, Mesophile, Thermophile, Extreme Thermophile
Psychro = COLD Meso = Mild Thermo = Hot Extreme Thermo = Very Hot
29
What adaptations do THERMOphiles have?
Heat-stable Proteins Saturated Fatty acids in lipids Ether linked lipids
30
What adaptations do PSYCHROphiles have?
Cold-stable enzymes | Unsaturated (Mono + Poly) FA's in lipids
31
What three enzymes are essential for an organism to deal with reactive oxygen species?
CATALASE, PEROXIDASE, and SUPER OXIDE DISMUTASE
32
Copiotrophs
Adapted to high levels of nutrients
33
Oligotrophs
Adapted to low levels of nutrients
34
Capnophiles
Need high CO2 levels
35
What are some ways to measure cell number?
Directly by countint (Petroff-Hauser counter, Coulter Counter) Indirectly by plating (CFU's), Indirectly by turbidity (Light transmitted vs absorbed)
36
Strict Aerobe
REQUIRES oxygen for growth
37
Strict Anaerobe
Requires ABSENCE of oxygen
38
Facultative anaerobes
AKA Facultative aerobes, can do either pending availability
39
Aerotolerant anaerobes
Can survive with O2, but do NOT use it
40
Microaerophiles
Require Oxygen for metabolism, but cannot survive at normal atmospheric concentrations
41
What do Chaperones do?
Repair misshaped proteins as part of heat shock response
42
What do proteases do?
Degrade denatured proteins during heat shock response
43
What sigma factor is used to upregulate the heat shock response?
Sigma H
44
Sterilization
Kills all viable organisms, including endospores and viruses
45
Disinfection
Removal of pathogens from inanimate SURFACES, may not eliminate all microbes
46
Antisepsis
removal of pathogens from LIVING TISSUE, may not eliminate all microbes
47
Sanitation
removal of PATHOGENS to SAFE LEVEL
48
Decimal Reduction Time
AKA D-value. Amt of time to reduce viability of cells tenfold
49
Bacteriostatic
Stops growth, does not kill bacteria
50
Bacteriocidal
Kills the cells, but does not destroy them
51
Bacteriolytic
Kills bacteria by destroying cells completely
52
Sulfa Drugs
Discovered by Gerhard Domagk in 1930s, inhibit growth of bacteria.
53
How can DNA inspire antimicrobial drugs?
Compounds are made to mimic nucleotide bases and cause fatal errors in transcription