Chapter 6. Cellular
Respiration
BI 101 Davison
Fall 2008
Respiration
is about breathing, yes, but physiologically why do you need to breathe?
The answer lies in an understanding of the role of the respiratory
gases CO2 and O2.
Each organism “breathes” that is exchanges those respiratory
gases with its environment. For
terrestrial animals the exchange occurs between some body organ
(lungs-humans; skin-earthworms) and the atmosphere. For some aquatic animals the exchange occurs between an
aquatic environment and the body surface. For example, all parts of a
jellyfish’s exposed body takes in O2 and releases CO2
. For other aquatic animals
(e.g. bony fish such as bass) specialized body surfaces called gills are
the sites of gas exchange. Gills
with their greater efficiency in exchanging respiratory gases are required
in order to meet the metabolic needs of the fish whereas in jellyfish no
specialized respiratory organ is needed to meet the needs of the lowly
jellyfish.
As you learn the chemistry of cellular respiration, keep in mind these
questions: “Why do we need O2 or what happens to the O2
once it enters your body?” and “Where in our body’s physiology does
the CO2 we exhale come from?”
The purpose of cellular respiration is however not to intake O2
and release CO2. Those
events are necessary sideline events supporting the main goal of ATP
production. You will learn
that glucose is the fuel broken down producing 38 molecules of ATP for
every single glucose molecule processed.
Cellular Respiration - has 3 series of reactions, each consisting of many
reactions, or each is an example of a specific metabolic pathway mediated
by a series of enzymes.
1.
Glycolysis – occurs in
cytoplasm; splits glucose into two molecules of the three-carbon molecule pyruvate;
transfers energy to produce two molecules of ATP and loads high energy
electrons onto electron carriers (NADH).
2.
Krebs Cycle – occurs in the mitochondria; [as a
simplification we will ignore the transition reaction that occurs between
glycolysis and the Krebs cycle] breaks down the organic residue of pyruvate into CO2
and therein transfers energy to produce two molecules of ATP; high-energy electrons taken from pyruvate
are transferred to electron
carriers (NAD+ & FAD - special molecules that act as transports, much like a
wheelbarrow acts as a transport when carrying electrons these molecules
occur as NADH & FADH2). Electron
carriers shuttle electrons taken from pyruvate to the final series of
respiratory reactions, the electron transfer chain--see below.
The Krebs Cycle is intimately linked to the electron transfer chain
and is dependent, albeit indirectly, on
the presence of O2. [note:
the CO2 produced by the Krebs Cycle makes its way out of the
cell and into the blood
stream via diffusion; once in the lungs, CO2 is eliminated with
exhalation. The meager amount of ATP produced by the Krebs cycle
moves out of the mitochondrion and is available as an energy source needed
to drive energy-requiring metabolism.]
3.
Electron Transfer Chain = Electron Transfer Phorsphorylation – occurs in mitochondria; takes the
electrons delivered by electron carriers (NADH & FADH2) and converts the potential energy of those
high-energy electrons into many ATP molecules.
For each glucose molecule that begins cellular respiration, 34
molecules of ATP are produced from the high-energy electrons removed
during the preceding glycolysis and the Krebs Cycle events.
Of course at the end of the electron transport system there are
electrons whose useable potential energy has been spent in ATP production.
These little negative "waste" particles must be removed. Enter O2! Good
ole O2 will serve as the final electron acceptor and will take
the electrons out of "harms way."
Oxygen,
O2, molecules accept the electrons and combine with H+
's and become water molecules (H2O), a stable and safe
combination for sequestering "spent" electrons.
The above
constitutes what is called aerobic
cellular respiration. (aerobic
is in reference to the presence of O2).
But what if O2 is not present?
Our bodies can deal with that, at least temporarily.
If O2 is not available as during brief periods of
intense exercise in which the blood supply simply can’t meet the O2
demands of the activity, our cells switch to an anaerobic
(w/out O2) method of respiration.
Plants and bacteria can also switch to anaerobic methods.
Some species of bacteria actually require anaerobic environments.
(more on anaerobic respiration below)
Anaerobic Cellular Respiration
ATP
production can continue (briefly) in most organisms without the presence of O2
and without the Krebs Cycle and Electron Transport System.
These anaerobic routes of respiration provide for only limited ATP
production as produced by glycolysis only; O2 is soon required to sustain the tremendous
turnover in ATP production required for most life forms. Thus, look upon these anaerobic routes of respiration as
temporary means of limited ATP production during temporary, brief episodes
of O2 shortages in higher plants and animals. A number
of microbes (e.g. yeast & certain bacteria) are anaerobic to a
greater degree, some are even obligate anaerobes, i.e. they are killed by
the presence of O2.
Anaerobic respiration consists of only 2 reaction series and only the
first of these, glycolysis, produces ATP:
1.
Glycolysis
– occurs exactly the same as in aerobic cellular respiration.
Two molecules of pyruvate result from the breakdown of glucose.
Two ATP are synthesized. As
in aerobic respiration, Glycolysis also delivers high-energy electrons
taken from glucose to electron
carriers. In order for
glycolysis to occur, that is in order to split a molecule of glucose into
2 molecules of pyruvate, some electrons must be removed from glucose.
Removing electrons from glucose results in glucose falling apart
forming two molecules of pyruvate. Electron
carriers (NAD+) must be available to accept these removed electrons.
Electron carriers that have accepted electrons (NADH) must unload those
electrons before accepting additional electrons. When the wheelbarrow is
full it must be emptied before it can accept more load.
Under aerobic conditions the electron carriers deliver the
high-energy electrons to the Electron Transport System in the mitochondria
and the electrons are “milked” of their energy to produce more ATP and
O2 serves as the final electron acceptor and becomes H2O.
The electron carriers, once they have dropped off the electrons to
the electron transport chain are free to return to the cytoplasm and aid
the process of glycolysis. (I
can see that empty wheelbarrow hustling back to that big pile of sand! The sand can’t be moved if there aren’t any empty
wheelbarrows to move it.) Glycolysis
cannot continue without electron carriers available to take away
electrons. So, in the absence of O2, the reactions below occur
for one reason: to make
electron carriers available so that glycolyis and the ATP production
inherent to glycolysis can continue.
2.
Fermentation – pyruvate is chemically altered in one of two
ways. Each of these
alterations requires additional electrons.
The additional electrons are delivered to the fermentation process
by electron carriers (NADH) that have been loaded with electrons during
glycolysis. As electrons are
delivered to the fermentation process NADH is converted back into
NAD+ and these electron carriers are now capable of
accepting electrons as needed to help drive glycolysis and ATP production
therein.
A.
Alcoholic fermentation – occurs in germinating seeds when
they are waterlogged and without O2.
(the seeds will die if they don’t get O2 eventually).
Also, yeast perform this producing the CO2 and ethanol,
both important to the baking and brewing industries. The conversion
of pyruvate into waste ethanol & CO2 requires the addition
of electrons.
Pyruvate is converted to CO2 and ethanol:
pyruvate + electrons from NADH --------> CO2, ethanol,
& NAD+
B. Lactate fermentation
– occurs in our muscle cells during periods of O2 shortage
as when muscle activity surpasses O2 delivery .
Also, certain bacteria perform this. The conversion of
pyruvate into lactate requires the addition of electrons.
pyruvate + electrons from NADH -------->
lactate & NAD+
In both fermentation examples above, the addition of electrons during the
fermentation of pyruvate has the sole benefit of this (i.e. the whole
point of fermentation is this final point!): electron carriers
delivering electrons to the fermentation process are freed of their
electron load and are thus available for use in glycolysis--glycolysis is
the only a process that
produces ATP in anaerobic respiration. Without electron
carriers available to accept electrons glycolysis and all ATP production
would cease.
Click
Here to Return to BI 101 Home Page
|