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Bacterial Metabolism and Energy Generation

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Title: Bacterial Metabolism and Energy Generation


1
  • Bacterial Metabolism and Energy Generation
  •  

2
  • An Overview of Metabolism

3
  • Metabolism the sum of all chemical reactions
    occurring within a cell simultaneously. Involves
    degradation and biosynthesis of complex
    molecules.
  • Catabolism-the breakdown of larger, more complex
    molecules into smaller, simpler ones, during
    which energy is released, trapped, and made
    available for work
  • Anabolism-the synthesis of complex molecules from
    simpler ones during which energy is added as input

4
  • Multi-stage process of catabolism
  • Stage 1-breakdown of large molecules
    (polysaccharides, lipids, proteins) into their
    component constituents with the release of little
    (if any) energy

5
  • Stage 2-degradation of the products of stage 1
    aerobically or anaerobically to even simpler
    molecules with the production of some ATP, NADH,
    and/or FADH2

6
  • Stage 3-complete aerobic oxidation of stage 2
    products with the production of ATP, NADH, and
    FADH2 the latter two molecules are processed by
    electron transport to yield much of the ATP
    produced

7
  • Metabolic efficiency is maintained by the use of
    a few common catabolic pathways, each degrading
    many nutrients
  • Microorganisms are catabolically diverse, but are
    anabolically quite uniform
  • Amphibolic pathways function both catabolically
    and anabolically, and sometimes employ separate
    enzymes to catalyze the forward and reverse
    reactions this separation enables independent
    regulation of the forward and reverse reactions

8
Definitions
  • Oxidation
  • Reduction
  • Redox reactions
  • Standard Reduction potential
  • Oxidative phosphorylation
  • Chemiosmosis
  • Electron transport chain

9
Oxidation
  • The loss of electrons from an atom or chemical
    compound.
  • Results in the generation of energy.

10
Reduction
  • The gain of electrons
  • Requires energy

11
Redox reactions
  • Reactions involving the transfer of electrons
    from a donor to an acceptor
  • Redox couple
  • Reducing agent reductant donor
  • Oxidizing agent oxidant acceptor
  • Oxidant ne- (number of electrons transferred)?
    Reductant

12
Standard Reduction Potential (Equilibrium
Constant Eo at pH 7.0)
  • Measures the tendency of the reductant to lose
    electrons.
  • Redox couples with more negative Eo values will
    donate elecrron to redox couples with more
    positive Eo values, releasing free enegy (G)
  • Energy is required to reverse the process (e.g.
    photosynthesis)

13
  • The larger the difference in Eo values between
    electron donors and electron acceptors, the
    greater the free energy that is generated.
  • Therefore, the more negative the reduction
    potential, the better electron donor it is, and
    the more numerous the potential acceptors.

14
Oxidative phosphorylation
  • A metabolic sequence of reactions occurring
    within a membrane in which an electrons
    transferred from a reduced coenzyme by a series
    of electron carriers, establishing an
    electrochemical gradient across the membrane that
    drives the formation of ATP from ADP and
    inorganic phosphate by chemiosmosis.
  • Powered by redox reactions
  • Aerobic respiration uses O2 as TEA
  • Anaerobic respiration uses SO42-, NO3-, CO2 as
    TEA (not as efficient as using O2 as TEA)

15
Chemiosmosis
  • The generation of ATP by the movement of hydrogen
    ions into pores in the cytoplasmic membrane that
    are associated with the ATPase system.

16
Electron Transport Chain
  • A series of oxidation-reduction reactions in
    which electrons are transported from a substrate
    through a series of intermediate electron
    carriers to a final acceptor, establishing an
    electrochemical gradient across a membrane that
    results in the formation of ATP.
  • Electrochemical gradient proton motive force
  • Examples of donors coenzymes NADH, NADPH, and
    FADH2 --gt often referred to as reducing power

17
  • Electron Transport and Oxidative Phosphorylation

18
  • Mitochondrial Electron Transport (Figure 9.13)

19
Three differences between prokaryotes and
eukaryotes
  • 1 Prokaryotes use different electron carriers
    (cytochromes vary)

20
  • 2 The bacterial electron transport chain may
    be extensively branched with several terminal
    oxidases
  • Electrons may enter at several different points
    and use different TEAs
  • Often dependent on growing conditions of bacteria
  • Different cytochromes used depending on O2 status
    (log vs stationary)

21
  • 3 Electron transport in bacteria occurs in the
    cytoplasmic membrane
  • In eukaryotic cells this occurs on the inner
    membranes of mitochondria
  • But the mechanism of Ox-Phos is remarkably
    similar
  • Did mitochondria arise from bacteria?
    Endosymbiont theory

22
  • Electrons from NADH and FADH2 are transported in
    a series of redox reactions to a terminal
    electron acceptor
  • Reduced coenzymes (NADH and FADH2) generated in
    glycolysis and TCA cycles must be reoxidized

23
  • Oxidative Phosphorylation
  • Some of the energy liberated during electron
    transport is used to drive the synthesis of ATP
    in a process called oxidative phosphorylation

24
  • The chemiosmotic hypothesis of oxidative
    phosphorylation (Peter Mitchell)
  • Membrane-bound carriers transfer electrons to
    oxygen across a chain
  • Cytochromes, flavoprotein, quinones, non-heme
    iron containing proteins
  • Coupling of electron transport to oxidative
    phosphorylation

25
  • Postulates that the energy released during
    electron transport is used to establish a proton
    gradient (proton motive force due to different
    charge distributions)
  • As electrochemical potential is formed (PMF)
    protons are attracted back into the cell through
    a proton channel
  • F1F0 adenosine triphosphatase (F1F0 ATPase) in
    proton channel releases energy as protons enter

26
  • Blockers
  • inhibit the flow of electrons through the system
  • Examples Cyanide or Azide (block electron
    transport between cyt a and O2
  • Examples Piericidin (competes with Coenzyme Q)
    and Antimycin A (blocks electron transport
    between cyt b and cyt c)

27
  • This proton-motive force is then used to drive
    ATP synthesis
  • Energy is converted to chemical energy by
    phosphorylation of ADP to ATP
  • High energy phosphate bonds used for biosynthetic
    pathways
  • Net result
  • 1 NADP or NADPH 3 ATP
  • 1 FADH2 2 ATP

28
Inhibition of aerobic synthesis of ATP
  • Inhibitors of ATP synthesis fall into two main
    categories

29
  • Uncouplers
  • allow electron flow, but disconnect it from
    oxidative phosphorylation (inhibit ATP synthesis,
    not electron transport)
  • Uncouple electron transport from Ox-Phos ? The
    energy from electron transport is lost as heat,
    not ATP
  • Examples Valinomycin, Dinitrophenol (DNP)

30
  • The Yield of ATP in Glycolysis and Aerobic
    Respiration
  • The yield of ATP in glycolysis and aerobic
    respiration varies with each organism, but has a
    theoretical maximum of 38 molecules of ATP per
    molecule of glucose catabolized
  • Anaerobic organisms using glycolysis can only
    produce two molecules of ATP per molecule of
    glucose catabolized

31
Pasteur Effect
  • Switch from fermentation (anaerobic) to aerobic
    respiration when oxygen is available
  • Much more efficient
  • More ATP using oxygen as TEA
  • Sugar catabolism dramatically decreases

32
Distinction between Respiration and Fermentation
  • Respiration
  • Electrons from oxidative process enter the
    electron transport system, protons are generated
    and energy is generated through OX-PHOS
  • Electrons are passed to an inorganic acceptor
  • Electron transport is used
  • OX-PHOS is used

33
  • Fermentation
  • Electrons and protons from oxidized substrates
    are transferred directly to another organic
    compound (organic acceptor) in the pathway
  • No electron transport
  • No OX-PHOS
  • Substrate-level phosphorylation used instead
  • The oxidation of a phosphorylated compound
    resuluting in the direct formation of a
    high-energy phosphate bond
  • Transferred to ADP to form ATP

34
  • Example of fermentation
  • Glycolysis
  • Glucose ? Pyruvate ? Lactic Acid or Ethanol
  • The final electron acceptor pyruvate (or a
    product of pyruvate such as acetaldehyde
    intermediate)
  • Summary In fermentation, organic compounds are
    the electron donors AND acceptors with some
    energy generated

35
  • The Breakdown of Glucose to Pyruvate

36
  • The glycolytic (Embden-Meyerhof) pathway is the
    most common pathway and is divided into two
    parts
  • The 6-carbon sugar stage involves the
    phosphorylation of glucose twice to yield
    fructose 1,6-bisphosphate
  • requires the expenditure of two molecules of ATP

37
  • The 3-carbon sugar stage cleaves fructose
    1,6-bisphosphate into two 3-carbon molecules,
    which are each processed to pyruvate
  • two molecules of ATP are produced by
    substrate-level phosphorylation from each of the
    3-carbon molecules for a net yield of two
    molecules of ATP
  • 2 molecules of NADH are also produced per glucose
    molecule

38
  • 1 Glucose ? 2 Pyruvate
  • 2 ATP used
  • 4 ATP generated
  • Net yield 2 ATP
  • 2 NAD used
  • 2 NADH generated
  • Net yield 2 NADH (THIS MUST BE OXIDIZED TO KEEP
    THIS PATHWAY RUNNING.)

39
  • The pentose phosphate (hexose monophosphate)
    pathway uses a different set of reactions to
    produce a variety of 3-, 4-, 5-, 6-, and 7-carbon
    sugar phosphates
  • These phosphates can be used to produce ATP and
    NADPH, as well as to provide the carbon skeletons
    for the synthesis of amino acids, nucleic acids,
    and other macromolecules

40
  • The NADPH can be used to provide electrons for
    biosynthetic processes or can be converted to
    NADH to yield additional ATP through the electron
    transport chain

41
  • The Entner-Doudoroff pathway can also be used to
    produce pyruvate with a lower yield of ATP, but
    is accompanied by the production of NADPH as well
    as NADH.

42
  • Fermentation

43
  • In the absence of oxygen, NADH is not usually
    oxidized by the electron transport chain because
    no external electron acceptor is available
  • However, NADH must still be oxidized to replenish
    the supply of NAD for use in glycolysis

44
  • Fermentations are reactions that regenerate NAD
    from NADH in the absence of oxygen
  • Fermentations involve pyruvate or pyruvate
    derivatives as electron acceptors
  • Fermentations may or may not produce additional
    ATP for the cell

45
Six Common Pathways of Fermentation
  • Homoloactic acid
  • Alcoholoic
  • Propionic acid
  • Butylene glycol (Butanediol)
  • Mixed acid fermentation
  • Butyric acid, butanol, acetone

46
  • 1 Homolactic acid fermentation
  • Pyruvate ? lactic acid
  • 2 Alcoholic fermentation
  • Pyruvate ? acetaldehyde ? ethanol

47
  • 3 Propionic acid fermentation
  • Pyruvate ? acetic acid, OAA, malate, fumarate,
    succinate, propionate
  • 4 Butylene glycol fermentation (butanediol)
  • Pyruvate ? acetolactic acid ? acetoin ? 2,3
    butylene glycol (2,3 butanediol)

48
  • 5 Mixed acid fermentation
  • Pyruvate ? Lactate, formate, acetate, ethanol,
    succinate
  • 6 Butyric acid, butanol, acetone fermentation
  • Pyruvate ? acetyl CoA, adetate, ethanol
  • Pyruvate ? acetyl CoA, acetone, isopropanol
  • Pyruvate ? acetyl CoA, butyryl CoA, butanol,
    butyric acid

49
Mixed Acid versus Butanediol Fermenters 3 Tests
to Divide Groups
  • Voges-Proskauer Test
  • Detection of acetoin (intermediary metabolite)
  • Methyl red test
  • Mixed acid fermenter produces a lot of acid
  • pH is 4.4
  • Red color produced for MAF only
  • CO2/H2 ratios
  • Mixed acid 11
  • Butanediol 51

50
Respiration
  • Use of electron transport chain passing electrons
    to an inorganic terminal electron acceptor (TEA)
  • Energy generated through OX-PHOS
  • More energy efficient than fermentation

51
Aerobic Respiration
  • Oxygen Terminal Electron Acceptor
  • Glucose ? CO2
  • 38 ATP

52
Anaerobic Respiration
  • Uses inorganic molecules other than oxygen as
    terminal electron acceptors this produces
    additional ATP for the cell, but not usually as
    much as is produced by aerobic respiration
  • Used mainly by anaerobes but many facultative
    anaerobes may use anaerobic respiration (electron
    transport and OX-PHOS still used)

53
  • Non-oxygen Terminal Electron Acceptor
  • Three major types
  • NO3- ? nitrate reducers
  • Facultative anaerobes
  • TEA nitrate
  • Results in denitrification (loss of nitrates
    froom the soil agricultural dilamma)
  • Advantageous when removing nitrates from sewage

54
  • 2 NO3- 12e- 12H ? N2 6H2O
  • Examples
  • Escherichia
  • Enterobacter
  • Bacillus
  • Pseudomonas
  • Micrococcus
  • Rhizobium

55
  • SO42- ? sulfate reducers
  • TEA sulfate
  • which is reduced to sulfide
  • SO42- 8e- 8H ? S2- 4H2O
  • Examples
  • Desulfovibrio
  • Desulfotomaculum

56
  • CO2 ? methane bacteria
  • TEA CO2 which is reduced to methane
  • Habitat rumen of cud-chewing animals, black mud
    of ponds and composts and sewage tanks
  • CO2 8e- 8H ? CH4 2H2O

57
  • Metals can also be reduced
  • Elemental sulfur (So)
  • Ferric iron (Fe3)

58
  • The Tricarboxylic Acid Cycle-a series of reactions

59
  • Acetyl-CoA (produced by decarboxylation of
    pyruvate) reacts with oxaloacetate to produce a
    6-carbon molecule
  • Subsequently, two molecules of carbon dioxide are
    released, regenerating the oxaloacetate
  • ATP is produced by substrate-level phosphorylation

60
  • Three molecules of NADH and one molecule of FADH2
    are produced per acetyl-CoA, and can be further
    processed to produce more ATP
  • Even those organisms that lack the complete TCA
    cycle usually have most of the cycle enzymes
    because one of the TCA cycle's major functions is
    to provide carbon skeletons for use in
    biosynthesis

61
  • Catabolism of Carbohydrates and Intracellular
    Reserve Polymers

62
  • proceeds by either hydrolysis or
  • phosphorolysis to produce molecules that can
    enter the common catabolic pathways already
    discussed

63
  • Lipid Catabolism

64
  • Lipases
  • Degrade lipids to glycerol free fatty acids

65
  • Fatty acid degradation proceeds by the beta
    -oxidation pathway, which produces acetyl-CoA,
    which can enter the TCA cycle

66
  • Glycerol degradation proceeds via the
    Embden-Meyerhof pathway (glycolysis) entering as
    glyceraldehyde 3-phosphate

67
  • Protein and Amino Acid Catabolism

68
  • Proteins are degraded by secreted proteases to
    their component amino acids, which are
    transported into the cell and catabolized
  • The amino group is removed by deamination or
    transamination
  • The resulting organic acids are converted to
    pyruvate, acetyl-CoA, or a TCA-cycle intermediate

69
Anabolism
  • Building up structural and functional components
    of a cell using energy and building blocks (small
    molecular intermediates)
  • Includes synthesis of nucleic acids (DNA RNA),
    cell wall (lipid bilayer PTG) and proteins.

70
  • Two important features
  • Biosynthetic pathways of most cellular components
    is different from degradative pathways at key
    regulatory steps (regulated by endproducts
    ATP NAD
  • Biosynthetic pathways are often induced by
    combining reactants to form activated
    intermediates

71
  • Polysaccharide biosynthesis
  • Some monosaccharides are derived from metabolic
    pathway intermediates
  • React with nucleoside triphosphates to form
    activated intermediates (or adenosine or uridine
    diphosphate)
  • Examples in bacteria
  • Capsular polysaccharides
  • Outer membrane LPS
  • Glycogen
  • PTG (NAGUDP intermediate)
  • Gluconeogenesis also used
  • Synthesis of glucose from a non-carbohydrate
    precursor

72
  • Lipid biosynthesis
  • Two lipids predominate in bacteria in the lipid
    bilayer
  • Phosphatidyl glycerol
  • Phosphatidylethanolamine

73
  • Glycerol phosphate backbone plus two fatty acids
    (12-18 carbons in length)
  • Glycerol derived from dihydroxyacetone phosphate
    (Embden-Meyerhoff)
  • Fatty acids added from fatty acyl-CoA
    intermediates (FAs built up 2 carbons at a time
    using acetyl CoA)

74
  • Amino acid and protein biosynthesis
  • Autotrophs
  • Capable of synthesizing all 20 amino acids
    starting with CO2 (can survive in completely
    inorganic environment)
  • Majority of prototrophs
  • Similarly do not require added amino acids
  • Some bacteria (e.g. Neisseria and Streptococci)
    require preformed amino acids
  • Auxotrophs
  • Mutant strains that DO require growth factors and
    sometimes amino acids

75
  • Amino acids are synthesized by complex pathways
    often involving multiple unique enzymes
  • Histidine synthesis requires 9 enzymes
  • Synthesis begins with metabolic pathway
    intermediates of glycolysis or Krebs cycle
  • Once made ? protein synthesis on ribosomes can
    ensue.
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