MICROBIAL METABOLISM Chapter 6, pp 129-166
I. Metabolism = sum of anabolic and catabolic pathways (Fig 6-1,
p130)
A) anabolism = to build up, generally requires energy
B) catabolism = to break down, may release energy
Cells generally use energy from catabolic pathways to drive
anabolic pathways, and the high energy intermediate here is
usually ATP. Therefore, in catabolism well discuss how ATP
is produced.
C) enzymes - catalyze the steps in metabolism (review what was
covered with Ch 2)
1) components
a) enzyme = protein in nature
b) cofactor = non protein component required for activity such as
metal ions
(Zn, Fe, Mg, Ca, etc) or organic molecules (coenzymes). Many
coenzymes are derived from vitamins (Table 6-5,p 139).
2) inhibitors = competitive vs. noncompetitive (Fig 6-14, p142
for
competitive)
D) control of metabolism - metabolic pathways may be regulated by
regulation of the
enzymes involved
1) control at gene level
2) control of enzyme activity
a) feedback inhibition = product inhibits earlier enzyme
b) allosteric enzymes = a subset of enzymes that can exist in
more favorable (for catalysis) or less favorable confirmations
depending on what effectors are present. Effectors bind to
allosteric site and enhance or decrease enzyme activity depending
on if they are activators or inhibitors (noncompetitive). Fig
6-13, p141
II. ENERGY METABOLISM
Two forms of energy are available to life:
1) chemicals = chemotrophs
2) light = phototrophs
A) Modes of ATP production (all involve oxidation-reduction
reactions)
1) Substrate level phosphorylation
2) Electron transport phosphorylation (oxidative phosphorylation)
3) Photophosphorylation
B) Oxidation-reduction reactions Fig 6-8, p134
Oxidation involves loss or removal of electrons (e-) and is
coupled to reduction where an electron acceptor takes up the
electron. Also, as e- are transferred, many times protons
are as well (1 e- plus 1 proton = H atom). Common
electron carriers = Table 6-2, p135
1) redox reactions with organic molecules:
lactic acid ¤pyruvate
2) redox reactions with metal ions:
Fe+2 ---> Fe+3 + e- oxidation
Fe+3 + e- ---> Fe+2 reduction
Fe+3/Fe+2 together form a redox pair
Note: - energy is required to remove an e-
- energy is gained by adding an e-
* - the amount of energy in each case depends on the chemical
nature of molecules involved
C) Chemiosmotic mechanism of ATP production involving redox
reactions
Fig 6-19, p149; Accounts for how e- flow generates ATP
III. Energy producing pathways (generally catabolic) = generate
ATP
(fermentation; respiration (includes aerobic and anaerobic);
photosynthesis
A) Fermentation = an anaerobic process (oxygen not needed)
- incomplete oxidation where organic compounds serve both as e-
donor and acceptor
Fermentation generally begins with glycolysis, the splitting of
sugar. Glycolysis is generally divided into 2 parts: breakdown of
glucose to pyruvate, then utilization of pyruvate
1) Glycolysis = glucose to pyruvate Fig 6-15, p143
1 glucose + 2Pi + 2ADP + 2NAD+ ---> 2
pyruvate + 2ATP + 2NADH + 2H+ + 2H2O
2) pyruvate utilization (a means by which NAD+ may be regenerated
= NADH must be oxidized to produce NAD+; some bacteria accomplish
this by reduction of pyruvate or reduction of the metabolic
products of pyruvate)
a) lactic acid fermentation - Fig 6-22, p152 (Streptococcus,
Lactobacillus)
pyruvate to lactic acid (if only lactate produced = homolactic)
pyruvate to lactic acid and other products = heterolactic
b) alcoholic fermentation
pyruvate to ethanol and carbon dioxide
c) other products from pyruvate Fig 6-23, p 152
B) Respiration = metabolic degradation of a substrate in which
inorganic molecules function as terminal electron acceptors
1) aerobic = oxygen is terminal electron acceptor (reguires
oxygen)
ATP produced here = substrate level phosphorylation and oxidative
phosphorylation,
involves glycolysis and Krebs cycle (Fig 6-16 p145), generates NADH, FADH2
Electron transport chain takes e- from NADH and FADH2, passes the
electron along different electron carriers to O2 producing water
and ATP is produced via chemiosmotic mechanism
2) anaerobic = inorganic ions are terminal e- acceptors (NO3,
SO4)
(ATP yield varies) Fig 6-20, p150
electron acceptors such as: NO3-1 SO4-2 CO3-2 (generating
nitrite, hydrogen sulfide, methane respectively)
Pseudomonas and Bacillus reduce nitrate ion to
nitrite ion to nitrous oxide or nitrogen gas
Desulfovibrio reduces sulfate to hydrogen sulfide
Methanogens generate methane
C) ATP yield from aerobic respiration Table 6-4, p137
per glucose oxidized = 38 ATP (36 in eucaryotes)
D) Photosynthesis (microbial) as done by photoautotrophs
(Cyanobacteria, green and
purple sulfur bacteria)
1) Phase 1 = light phase = energy from light is captured
a) oxygenic = water is broken down into protons, electrons, and
oxygen (water split as a source of electrons).
(Table 6-9, p157)
b) anoxygenic = water is not electron donor but rather sulfur,
hydrogen or organic compounds = oxygen not generated
- produces NADPH2 and ATP Fig 6-27, p158
2) Phase 2 = dark phase = NADPH2 and ATP are used to reduce CO2
(fix) into
organic compounds (Calvin Cycle Fig 6-28, p160)
IV. Classification of organisms according to where they derive
energy and carbon
A) energy source
1) sunlight = phototrophs
2) molecules = chemotrophs
B) carbon source
a) inorganic (CO2) = autotrophs (lithotrophs = rock
eating)
b) organic = heterotrophs SEE TABLE 4-4, p91
| Nutritional type | Energy Source | Carbon source | Occurrence |
| photoautotroph | light | CO2 | plants, algae, some bacteria |
| photoheterotroph | light | organic compounds | some bacteria |
| chemoautotroph | chemicals | CO2 | some bacteria |
| chemoheterotroph | chemicals | organic compounds | animals, fungi, protozoans, most bacteria |
photoautotrophs = classical photosynthesis (oxygenic)
vs. anoxygenic
Cyanobacteria are oxygenic (=produce oxygen)
Green sulfur and purple sulfur bacteria are anoxygenic
photoheterotrophs = green nonsulfur and purple nonsulfur
bacteria.
chemoautotrophs = inorganic compounds (e.g. hydrogen sulfide, sulfur, ammonia,
nitrites, hydrogen gas, iron) serve as energy source, obtain energy by oxidation
of inorganic substrates coupled to electron transport chains . Examples: (Table
6-8, p155)
a) sulfur oxidizing bacteria (Thiobacillus)
b) nitrifying bacteria oxidize ammonia to nitrate
NH3 to NO2 to NO3 (Nitrosomonas - Nitrobacter)
chemoheterotrophs = most bacteria et al
saprophytes = live on dead organic matter (decay)
parasites = obtain nutrients from a live host
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ATP generated is used to drive anabolic pathways, active
transport, motility, etc.