microbial growth Flashcards

(64 cards)

1
Q

name the essential nutrients from microorganisms

A

C,H,O,N,S,Se,P

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2
Q

out of the essential nutrients which ones have simple metabolism

A

P,N,S

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3
Q

sources of C

A

CO2, org compounds

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4
Q

sources of N

A

NH3,NO3,N2, organic N compounds (AA,etc)

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5
Q

sources of H

A

H2O, organic compounds

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6
Q

sources of O

A

H2O,O2, org compounds

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7
Q

sources of P

A

PO4 (3-)

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8
Q

sources of S

A

H2S, SO4 (2-) ,org S compounds (cysteine), metal sulfide (FeS,CuS,ZnS, etc)

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9
Q

sources of K

A

K+ in solution, K+ salts

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10
Q

sources of Mg

A

Mg in solution, Mg salts

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11
Q

sources of Ca

A

in solution, salts

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12
Q

sources of Na

A

in solution, salts

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13
Q

Sources of Fe

A

Fe2+ , Fe3+

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14
Q

what are growth factors

A

vitamins, AA, purines, pyrimidines or other ORGANIC MOLECULES.
- needed for growth and NOT synthesized by the organism

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15
Q

some growth factors are the. —– or —- of another micro-organism

A

by products, waste

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16
Q

growth of the population = increase —- or —-

A

number of cells, biomass

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17
Q

what is a septum

A

the partition created that constricts the cell into 2 daughter cells

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18
Q

explain the process of septum formation

A

cell elongation –> septum formation –> completion of septum –> formation of walls –> cell separation

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19
Q

each daughter cell receives one copy of the —-, sufficient —, —- and etc

A

chromosome, ribosome, macromolecules

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20
Q

cell division requires —- and cell wall —– by —-

A

cell wall synthesis, destruction, autolysins

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21
Q

destroying and making — is the ket to cell division

A

peptidoglycan

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22
Q
  • —- allows peptidoglycan to be exported across the cytoplasmic membrane.
  • location?
A

bactoprenol, where the septum is being made.

- adds new peptidoglycan to initiate separation

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23
Q

at the division ring (FtsZ), —- create some — in the peptidoglycan. this allows:

A

autolysins, gaps, rearrangement of the peptidoglycan and synthesis of a new cell wall

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24
Q

wall bands

A

scar between old and new peptidoglycan

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25
why do different bacterial cultures smell different
they have different metabolic pathways; produces different wastes. - also depends on the characteristics of the species and the media
26
name different selective mediums mentioned in the class
1) bile salts | 2) mannitol salt
27
bile salts ---- gram + , ----- for gram - and enteric pathogens
inhibit, permissive
28
bile salts is toxic for a lot of microorganisms but not for -----
enteric pathogens. like the ones in the intestine
29
lactose fermenters have a --- color. lactose non fermenters are --- . this color change is indicated by a ---
pink, colourless, pH indicator
30
mannitol salt has a high ---- concentration. ----- most gram negative and many gram positive
NaCl, inhibits
31
mannitol salt is used for isolation and detection of ----. how does this work?
staphylococcus, some are mannitol negative (cannot ferment mannitol) and turn the media pink, but some are mannitol positive and produce acids that turn the media yellow
32
staphylococcus, mannitol + --> | staphylococcus, mannitol negative --->
staphylococcus aureus | staphylococcus epidermis
33
function of staphylococcus aureus
wound infection, has a high antibiotic resistance
34
what is a viable count
- measured to test microbial presence - needs a permissive growth medium - results are reliable when there are between 30 - 300 colonies
35
name the methods of viable count
1) spread plate method | 2) pour plate method
36
to get a viable count of culture with ing populations, ---- are done
serial dilutions
37
serial dilution counts -------
the number of cells that are able to grow | - dead cells cannot be counted
38
with ----- you can also count dead cells
microscopic method ** know how to calculate them
39
----- an be used to differential between living and non living cells
viability staining
40
advantages and disadvantages of microscopic method
adv: fast non need to wait until the bacteria has grown disadvantages: small cells can be missed, motile cells are hard to count
41
flow cytometry is better at counting --- cells. like:
big, protozoan, yeast, mammalian cells, etc
42
how does flow cytometry work
1) aligns all cells behind each other 2) the cells go through a detection device which is a laser 3) they pass the laser 4) the light transmitted is detected by a machine - specifies which ones are dead or alive if you use the culture of microscopic counts that are already stained
43
turbidimetric method
measures the contribution of alive and dad cells to turbidity - high optical density = high turbidity
44
turbidimetric method is affected by:
1) clumping: form large particles --> error --> higher OD | 2) attachment to surfaces --> lower OD
45
how is the turbidimetric method done
measured using a spectrometer, by measuring the amount of light that goes through - technically measures the OD: log I0/I
46
The relationship between the number of cells and OD depends on:
the type of the cell: size, shape, composition, cells inclusion, mutations, etc
47
generation time
the time needed for the population to double | - depends on the growth medium and conditions
48
when the conditions are right, microorganisms can grow -----
exponentially , the population forms at a constant rate equation N = N02^n --> number of cells
49
calculating generation time
g = t/n
50
know the growth cycle
in the notes
51
most natural envs are -----, they have:
open systems 1) constant supply of nutrients and diffusion of waste 2) predations 3) competition with other microorganisms 4) changing env conditions
52
chemostats
notes
53
factors affecting growth
1) temp 2) pH 3) osmolarity 4) oxygen 5) pressure 6) radiation
54
extremophiles
microorganism that grow preferentially under extreme conditions
55
membrane gelling
transport processes so low that growth cannot occur
56
what happens above the optimum growth rate
thermolysis
57
membrane gelling occurs at:
minimum temp *doesn't kill them
58
the temp range for most microorganism is typically ----
25- 40 degrees around the optimal temp
59
psychrotolerant
can grow at zero degrees but have a optimal range of 25-40 degrees
60
psychrophile
notes
61
mesophile
notes
62
thermophile
notes
63
hyperthermophile
notes
64
barophilic
grow best at high pressure