Download Microbial Nutrition

Survey
yes no Was this document useful for you?
   Thank you for your participation!

* Your assessment is very important for improving the workof artificial intelligence, which forms the content of this project

Document related concepts
no text concepts found
Transcript
Chapter 5
Microbial Nutrition
1
Nutrient Requirements
• Macroelements (macronutrients)
– C, O, H, N, S, P, K, Ca, Mg, and Fe
– required in relatively large amounts
• Micronutrients (trace elements)
– Mn, Zn, Co, Mo, Ni, and Cu
– required in trace amounts
– often supplied in water or in media
components
2
All Organisms Require Carbon,
Hydrogen, Oxygen and Electron
Source
3
• Heterotrophs
– use organic molecules as carbon sources which often
also serve as energy sourc
• Autotrophs
– use carbon dioxide as their sole or principal carbon
source
– must obtain energy from other sources
4
Sources of Carbon, Energy and
Electrons
Table 5.1
5
Nutritional Types of Organisms
• based on energy source
– phototrophs use light
– chemotrophs obtain energy from oxidation
of chemical compounds
• based on electron source
– lithotrophs use reduced inorganic substances
– organotrophs obtain electrons from organic
compounds
6
Nutritional Types of
Microorganisms
Table 5.2
7
Nitrogen, Phosphorus, and Sulfur
• Needed for synthesis of important
molecules (e.g., amino acids, nucleic acids)
• Nitrogen usually supplied as organic and
inorganic N-source (NH3 , NO3-)
• Phosphorus usually supplied as inorganic
phosphate (H3PO4)
• Sulfur usually supplied as sulfate (SO42-)
8
Growth Factors
• Organic compounds
• Essential cell components (or their
precursors) that the cell cannot
synthesize
• Must be supplied by environment if
cell is to survive and reproduce
9
Classes of growth factors
• Amino acids
– needed for protein synthesis
• Purines and pyrimidines
– needed for nucleic acid synthesis
• Vitamins
– function as enzyme cofactors
10
11
Uptake of Nutrients
• Some nutrients enter by passive
diffusion
• Most nutrients enter by:
– facilitated diffusion
– active transport
– group translocation
12
Passive Diffusion
• Molecules move from region of
higher concentration to one of lower
concentration
• H2O, O2 and CO2 often move across
membranes this way
13
•rate of facilitated
diffusion increases
more rapidly and
at a lower
concentration
•diffusion rate
reaches a plateau
when carrier
becomes
saturated
Figure 5.3
14
Facilitated Diffusion
• Similar to passive diffusion
– movement of molecules is not energy
dependent
– direction of movement is from high
concentration to low concentration
– size of concentration gradient impacts
rate of uptake
15
Facilitated diffusion…
• Differs from passive diffusion
– uses carrier molecules (permeases)
– smaller concentration gradient is required
for significant uptake of molecules
– effectively transports glycerol, sugars, and
amino acids
• more prominent in eucaryotic cells than
in procaryotic cells
16
Copyright © McGraw-Hill companies, Inc. Permission required for reproduction or display.
note conformational change of carrier
Figure 5.4
17
Active Transport
• Energy-dependent process
– ATP or PMF
• Carrier proteins needed (permeases)
– carrier saturation effect is observed at
high solute concentrations
18
ABC transporters
• ATP-binding
cassette
transporters
• observed in
bacteria,
archaea, and
eucaryotes
Figure 5.5
19
Copyright © McGraw-Hill companies, Inc. Permission required for reproduction or display.
Figure 5.6
20
Group Translocation
• Chemically modifies molecule as it is
brought into cell
• Best known system: transports a variety of
sugars while phosphorylating them using
phosphoenolpyruvate: sugar
phosphotransferase system (PTS)
• Phosphoenolpyruvate (PEP) as the
phosphate donor
21
Copyright © McGraw-Hill companies, Inc. Permission required for reproduction or display.
Group Translocation
• energydependent
process
Figure 5.7
22
Iron Uptake
• ferric iron is very
insoluble so uptake is
difficult
• microorganisms use
siderophores to aid
uptake
• siderophore complexes
with ferric ion
• complex is then
transported into cell
Figure 5.8
23
Copyright © McGraw-Hill companies, Inc. Permission required for reproduction or display.
Types of Media
Table 5.4
24
Defined or Synthetic Media
• all components
and their
concentrations
are known
Table 5.5
25
Complex Media
• contain some
ingredients of
unknown
composition
and/or
concentration
Table 5.6
26
Some media components
• peptones
– protein hydrolysates prepared by partial
digestion of various protein sources
• extracts
– aqueous extracts, usually of beef or yeast
• agar
– sulfated polysaccharide used to solidify
liquid media
27
Types of Media
• General purpose media
– support the growth of many microorganisms
– e.g., tryptic soy agar
• Enriched media
– general purpose media supplemented by
blood or other special nutrients
– e.g., blood agar
28
Copyright © McGraw-Hill companies, Inc. Permission required for reproduction or display.
Figure 5.9
29
Types of media…
• Selective media
– favor the growth of some
microorganisms and inhibit growth of
others
– e.g., MacConkey agar
30
Copyright © McGraw-Hill companies, Inc. Permission required for reproduction or display.
Table 5.7
31
Types of media…
• Differential media
– distinguish between different groups of
microorganisms based on their
biological characteristics
– e.g., blood agar
• hemolytic versus nonhemolytic bacteria
– e.g., MacConkey agar
• lactose fermenters versus nonfermenters
32
Copyright © McGraw-Hill companies, Inc. Permission required for reproduction or display.
Table 5.7
33
Isolation of Pure Cultures
• Spread plate, streak plate, and pour
plate are techniques used to isolate
pure cultures
34
Spread-plate technique
1. dispense cells onto
medium in petri dish
Figure 5.10 (a)
35
4. spread cells
across surface
2. - 3. sterilize spreader
Copyright © McGraw-Hill companies, Inc. Permission required for reproduction or display.
Appearance of a Spread Plate
Figure 5.10 (b)
36
Copyright © McGraw-Hill companies, Inc. Permission required for reproduction or display.
Streak plate technique
Figure 5.11
37
The Pour Plate
• Sample is diluted several times
• Diluted samples are mixed with
liquid agar
• Mixture of cells and agar are poured
into sterile culture dishes
38
Copyright © McGraw-Hill companies, Inc. Permission required for reproduction or display.
Figure 5.12
39
Copyright © McGraw-Hill companies, Inc. Permission required for reproduction or display.
Bacterial Colony Morphology
Figure 5.13 (a)
40
Copyright © McGraw-Hill companies, Inc. Permission required for reproduction or display.
Bacterial Colony Morphology
Figure 5.13 (b) and (c)
41