Clokie 3 Prokaryotic metabolic diversity Flashcards
Medical microbiology:
understanding microbial pathogenesis, toxin production, exploitation of host enzymes
Microbiome:
understanding roles of ‘non-pathogenic’ microbes
Diagnostic microbiology:
designing tests to detect specific metabolic intermediates & products (e.g., amylase test, catalase test, etc)
Pharmaceutical microbiology:
Understanding and determining essential, specific metabolic steps allows targeting them to kill pathogens
Biotechnology:
- understanding conditions to control microbial products and to get the right fermentation pathways (biofuel, bioleaching etc)
- exploiting specific microbial metabolic pathways for production of antibiotics, enzymes, etc…
Foods and drugs microbiology:
of plant origin owe their taste, smell, active constituents to microbial metabolism.
Environmental microbiology:
Fundamental understanding of biogeochemical cycling on earth
Chemoheterotrophy:
– Inorganic compounds
- bacteria and archaea
OILRIG
Oxidation
Is
Loss of e-
Reduction
Is
Gain of e-
CHEMOTROPHY:
• Energy accessed by harnessing and linking oxidation/reduction pairs
Oxidized form always written..
..on the left
REACTION COUPLE 1
H2 ->
Becomes..
Tendency…
-> 2e- + 2H+
..oxidised (i.e. electron donor)
..to release e-
REACTION COUPLE 2
O2 + 2 e- + 2H+ ->
Becomes..
Tendency..
-> H2O
Reduced (i.e. electron acceptor)
..to accept electrons
REDOX POTENTIAL:
• Capacity of a pair to donate or accept electrons is measured by the oxidation/reduction potential (E0′)
• Measured electrically by reference to standard
Donate or accept e-
ELECTRON TOWER
ANIMALS USE ORGANICS (VIA NAD, NADP)AS ELECTRON DONOR& O2 AS ELECTRON ACCEPTOR
Prokaryotic energy source s
amonia, nitrate iron etc
CHEMOHETEROTROPHS
• Have two mechanisms for energy conservation
– Respiration
– Fermentation
synthesis of ATP is driven by
energy released in oxidation-reduction reactions