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Chapter 5b Respiration and cellular activities

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Title: Chapter 5b Respiration and cellular activities


1
Chapter 5b Respiration and cellular activities
  • I- The Krebs Cycle in LIPID (Fats) and PROTEIN
    metabolism (So far we have discussed only
    carbohydrates)
  • II- Respiration and Heat production (Through
    regulation, some plants and animals can release
    larger quantities of heat, and produce less ATP)
  • III- Control of respiration (Cell respiration and
    energy production are closely regulated)

2
FAT and PROTEIN metabolism
  • Carbohydrates (sugars) are the main source of
    energy for cell respiration, and account for the
    largest of cell respiration. When most
    organisms need energy, glucose is broken down
    thru cell respiration. Thus, glucose is the
    central energy-liberating pathway in all
    organims.
  • Lipids (fats) are important energy storage
    molecules and are used upon certain
    circumstances. The energy yield of fats is higher
    than the energy yield of carbohydrates.
  • Under some special conditions, proteins can also
    be used as substrates for cell respiration and
    ATP generation, but they are not the choice
    molecules to break down, as usually they are
    important structurally (skeletal system), or as
    functional molecules in other vital process
    (enzymes, hormones, etc.)
  • The energy yield of carbohydrates and lipids (and
    proteins if needed) is liberated gradually thru a
    series of reactions, each catalyzed by specific
    enzymes.
  • Fats and proteins are metabolized by being
    converted into molecules found into some step of
    the regular aerobic respiration process that we
    have already learned.

3
Fat cells their number doesnt change much thru
time
4
Breaking down fats and proteins
  • Hydrolysis (breaking with water) is the process
    used in the initial breaking down of
    carbohydrates, fats and proteins. H2O is
    required.
  • Macromolecules must be broken down initially
  • Lipids (Fats and oils) ? to Glycerol and Fatty
    Acids.
  • Proteins ? to individual Aminoacids, then
    remove amino groups
  • Carbohydrates ? to glucose

Proteins to aminoacids
Carbohydrates to glucose
Lipids to Glycerol fatty acids
5
(Remember how they are formed ?)
6
Fats, Proteins Carbohydrates in cell respiration
  • Cells can extract E from all 3 macromolecules.
  • Fats and proteins are broken down into products
    that can enter the Krebs Cycle. They can enter at
    various places.
  • Once these raw products enter the Krebs Cycle,
    the processes continue just as we have learned.
  • Under normal conditions most energy requirements
    are met with carbohydrate and some fat
    metabolism. Structural proteins (muscles, etc)
    will be used as substrate for cell respiration
    only under very special circumstances
    (starvation).

7
Metabolism of Fats (Fatty acids and glycerol)
  • Fat metabolism requires O2 Most of it bypasses
    glycolysis enters the Krebs cycle. Without O2,
    most of the energy from fats cannot be
    transferred into ATP.
  • From a fat only the glycerol portion (the
    smallest part) can be metabolized in the absence
    of O2.
  • Glycerol (3-C molecule) is brought as PGAL into
    glycolysis, and will then continue to pyruvate
    and enter the Krebs Cycle, or to fermentation.
  • Fatty acids are first broken down to acetate by
    enzymes from mitochondria then Coenzyme A (CoA)
    brings the acetate into the regular Krebs Cycle.
  • Fatty acids can not go the anaerobic way
    (fermentation).
  • Since fats are more completely reduced compounds
    than Carbohydrates (higher of H), they yield
    more E per unit weight 1 gram of fat yields over
    twice the amount of E than a carbohydrate.

8
Metabolism of Proteins - aminoacids
  • Proteins are first broken to aminoacids in
    digestion (Note that this is not part of cell
    respiration). Only in special conditions
    (starvation), structural proteins (muscle, etc)
    would be used in cell respiration.
  • Other enzymes remove the amino groups and
    convert them first to ammonia (NH3) and then to
    urea or uric acid for excretion (waste removal,
    involving kidneys).
  • Carbon skeletons are then brought into Krebs
    cycle as oxalacetate or ketoglutarate.
  • Thus, protein metabolism bypasses completely both
    glycolysis and the possibility of fermentation
    after pyruvate.

9
Using building blocks in synthesis
  • In autotrophs, the Calvin Cycle (from
    photosynthesis) and the Krebs Cycle (from
    respiration) lead to the synthesis of every
    organic compound needed.
  • In heterotrophs this is partly true, except for
    vitamins, some aminoacids and certain fatty acids
    we cannot synthesize.
  • By investing energy (ATP), the cells can reverse
    the direction that some of these molecules move
    along the metabolic partways, and use the system
    in biosynthesis reactions to make fats or
    proteins, or carbohydrates. But additional ATP is
    needed (from food).
  • Not all the pathways are 2-ways (double arrows),
    and even those that are, reversing implies
    different enzymes.

10
Respiration and HEAT PRODUCTION
  • Mammals have a tissue called brown fat.
  • Rich in mitochondria, brown fat cells produce a
    lot of heat very fast, but produce little ATP.
  • Brown fat cells are not the same as the lipocytes
    that we discussed above, where excess E from food
    is stored. Instead, brown fat cells have a
    specific function.
  • Brown fat cells are useful in winter for
    hibernating animals, and in infants of all
    mammals, because they tend to loose heat very
    fast.
  • Some plants are also able to divert E from cell
    respiration towards heat production, with less
    ATP generation. In an extreme case (skunk
    cabbage), the heat from the plant melts the snow
    allowing the emerging flowers to come out.

11
Control of Respiration
  • The organisms must decide whether glucose is
    going to be used in cell respiration, or whether
    it will be stored as starch, glycogen or fat.
  • The controls operate in a supply-and demand
    principle.
  • Under conditions of low E demand, cells use
    excess glucose to synthetize glycogen, and then
    fat (protein building has already been met).
  • Under high E demand, glucose from blood (or plant
    tissues) is catabolized rapidly, and replenished
    with new glucose from glycogen (liver), or starch
    (plants).
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