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Microbial Energy Sources and Metabolism

The document discusses microbial energy sources and metabolism. It begins with an introduction to energy sources for living cells and the importance of understanding metabolism. It then covers the basic concepts of metabolism, including the two main pathways of catabolism and anabolism. Catabolism involves breaking down molecules to release energy, while anabolism uses this energy to build larger molecules. The document discusses several key metabolic processes like glycolysis, the Krebs cycle, and the electron transport chain that release energy to produce ATP through cellular respiration. It also briefly discusses anaerobic respiration and fermentation. The summary provides a high-level overview of the key topics and processes covered in the document in 3 sentences.

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Naufal Qaweim
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0% found this document useful (0 votes)
121 views51 pages

Microbial Energy Sources and Metabolism

The document discusses microbial energy sources and metabolism. It begins with an introduction to energy sources for living cells and the importance of understanding metabolism. It then covers the basic concepts of metabolism, including the two main pathways of catabolism and anabolism. Catabolism involves breaking down molecules to release energy, while anabolism uses this energy to build larger molecules. The document discusses several key metabolic processes like glycolysis, the Krebs cycle, and the electron transport chain that release energy to produce ATP through cellular respiration. It also briefly discusses anaerobic respiration and fermentation. The summary provides a high-level overview of the key topics and processes covered in the document in 3 sentences.

Uploaded by

Naufal Qaweim
Copyright
© © All Rights Reserved
We take content rights seriously. If you suspect this is your content, claim it here.
Available Formats
Download as PPTX, PDF, TXT or read online on Scribd

CHAPTER 6

MICROBIAL ENERGY SOURCES


OUTLINE
1) Introduction to energy sources
2) Basic bacterial metabolism
Catabolism
Anabolism
3) Production of ATP
4) Biosynthesis of carbohydrates, protein, fats, and
nucleic acids
Introduction to energy sources
Living cells require energy from outside sources
Some animals, such as the chimpanzee, obtain energy
by eating plants, and some animals feed on other
organisms that eat plants
WHY IS THIS IMPORTANT?
It is important to have a basic understanding of
metabolism because it governs the survival and growth of
microorganisms.
The growth of microorganisms can have a direct effect on
infectious disease.
Good metabolic function makes pathogens more
successful at causing disease.
BASIC CONCEPTS OF METABOLISM

Metabolism is:
A series of chemical processes that go on in living
organisms / The sum of all chemical processes carried out
by living organisms.
Used to obtain energy.
Linked to growth.
Require the use of enzymes and coenzymes
Basic concepts of metabolism
2 major pathways in metabolic activity

Catabolism
Anabolism
 Reactions that release
 Reactions that require
energy by breaking
energy to synthesize
complex molecules
complex molecules
into simpler ones that
from simpler ones.
 Needed for growth, can be reused as
building blocks.
reproduction and
 Provides an organism
repair of cellular
with energy for its life
structures.
processes, including
movement, transport.
OXIDATION & REDUCTION REACTIONS

Metabolism is broken down


into two parts:
Catabolism – molecules are
broken down through metabolic
processes to release the energy
stored in their chemical bonds.

Anabolism – metabolic
processes in which the energy
derived from catabolism is used
to build large organic molecules
from smaller ones.
BASIC CONCEPTS OF METABOLISM
Carbon and energy are required for growth.
There are two processes by which carbon can be
obtained:
Autotrophy – carbon is obtained from inorganic
substances (e.g. plants using CO2 to make sugar)
Heterotrophy – carbon is obtained from other organic
molecules
 Nearly all infectious organisms are chemoheterotrophs.
Chemoheterotrophs obtain energy by breaking
down other organic molecules and compounds.
OXIDATION & REDUCTION
REACTIONS

Both anabolism and catabolism involve electron transfer and


oxidation and reduction reactions – redox reaction.
An oxidation reaction is a chemical reaction in which an atom,
ion or molecule loses one or more electrons.
A reduction reaction is a chemical reaction in which an atom, ion
or molecule gains one or more electrons.
RESPIRATION
In metabolism, respiration occurs at the cellular
level and is not the same as breathing (respiration
at the macroscopic level).
Cellular respiration describes catabolic processes
and is divided into:
Aerobic respiration – metabolism that uses oxygen
Anaerobic respiration– metabolism that does not use
oxygen
Facultatively anaerobic respiration – metabolism that
can use oxygen but can also occur without it
METABOLIC PATHWAYS
Metabolic reactions occur in series of chemical reactions
called pathways.
The following is an example of a pathway. A is the initial
substrate and E is the final product of the pathway, with B,
C, and D being intermediates.
A B C D E
Each step in the pathway is mediated or facilitated by a
specific enzyme.
ENZYMES
Enzymes are proteins that act as catalysts for metabolic
reactions, making the reaction go faster.
Enzymes work by lowering the energy of activation.
Each enzyme is specific for a reaction.

•Enzymes are found in all


living organisms and
most cells contain
hundreds of types which
are constantly being
manufactured and
replaced.
Overview of cell metabolism
CATABOLIC PROCESSES IN
METABOLISM
Catabolic processes in metabolism
cause the breakdown of large
organic molecules into smaller
ones.

These are called fueling reactions


because they cause a release of
energy.
CATABOLIC PROCESSES IN METABOLISM
There are three important pathways by which most
organisms release energy from nutrient molecules:

Glycolysis
Krebs cycle
Electron transport chain
GLYCOLYSIS
The catabolic pathway used by most organisms.
The best example of this pathway is glucose breakdown.
The process itself is a series of chemical reactions.

Glucose
• Glycolysis occurs in
the cytoplasm and does
not require oxygen.

• Four ATP molecules


are produced in
glycolysis
– The first steps of
the pathway
consume two ATP
molecules.
– The net gain is two
ATP molecules.

4 – 2 = 2 ATP produced
Per glucose molecule (Net)
After a series of steps, the 6-carbon glucose molecule is
broken into two 3-carbon pyruvate molecules -> Krebs cycle.
NAD+ carries electrons to the electron transport chain.

1 molecule of glucose
Produces:

2 ATP (net)
2 reduced NAD+
2 molecules of Pyruvate
Glycolysis can lead to further
energy producing pathways.
Krebs cycle and cellular
respiration (aerobic)
Fermentation (anaerobic)
THE KREBS CYCLE
The Krebs cycle or the citric acid cycle or Tri-
Carboxylic Acid cycle (TCA).
It is an aerobic catabolic pathway seen in aerobic
cellular respiration.
Pyruvate is further metabolized in this process.
Pyruvate is oxidized to reduce NAD+ and modified
with coenzyme A to produce Acetyl-CoA complex.
THE KREBS CYCLE
The Krebs cycle is a series of reactions in which
chemical changes occur.
Within these reactions, hydrogen atoms are
removed and their electrons are transferred to
coenzyme carrier molecules.
The hydrogen atoms are carried by NAD+ and FAD
to the electron transport system.
Three important things happen in the
Krebs cycle:
Carbon is oxidized as CO2.
Energy is captured and stored
when ADP is converted to ATP.
Electrons are transferred to
coenzyme carrier molecules that
take the electrons to the electron
transport chain.
ELECTRON TRANSPORT CHAIN

The electron transport chain is a sequence of molecules.


In eukaryotes, they are found in the inner mitochondrial
membrane.
In prokaryotes, they are organized in the plasma membrane.
ELECTRON TRANSPORT CHAIN
Electrons are transferred to a final electron acceptor.
In aerobic respiration, the final acceptor is oxygen.
In anaerobic respiration, the final acceptor is an inorganic oxygen-
containing molecule.
CHEMIOSMOSIS
As electrons move from one molecule to another in the chain, energy
is released via a process called chemiosmosis.
As electrons are transferred along the electron transport chain, protons
are pumped out of the cell.
This causes the proton concentration outside the cell to be higher than
inside the cell, causing a concentration gradient to form.
CHEMIOSMOSIS
Specialized membrane proteins allow protons to re-enter the cell.
Energy is released as protons re-enter the cell.
This energy is used to bind phosphate to ADP, making the high-
energy molecule ATP.
The difference in proton concentration in this process is called the
proton motive force.
CHEMIOSMOSIS
Cells using anaerobic respiration generate two molecules of
ATP from one glucose molecule.
Cell using aerobic respiration generate thirty eight total
molecules of ATP from one glucose molecule.

Aerobic respiration: 38 ATP / glucose molecule


Anaerobic respiration: 2 ATP / glucose molecule
ANABOLISM
Anabolic reactions are classified as biosynthetic reactions
because they are used to synthesize all the biological
molecules needed by the cells of living organisms.

Biosynthetic reactions form the network of pathways that


produce the components required by the cell for growth
and survival.

These reactions are fueled by the energy stored in high-


energy bonds in ATP.
ANABOLISM
Production of ATP
3 major process of cell metabolism/cellular respiration
that can produce ATP including :
Aerobic respiration
Anaerobic respiration
Fermentation
Cellular Respiration: Aerobic
Harvesting of energy from glucose has three stages
Glycolysis
(breaks down glucose into two molecules of pyruvate)
The citric acid cycle
(completes the breakdown of glucose)
Oxidative phosphorylation
(accounts for most of the ATP synthesis)
Electrons
carried
via NADH

Glycolysis

Glucose Pyruvate

CYTOSOL MITOCHONDRION

ATP

Substrate-level
phosphorylation
Electrons Electrons carried
carried via NADH and
via NADH FADH2

Pyruvate
Glycolysis Citric
oxidation
acid
Glucose Pyruvate Acetyl CoA cycle

CYTOSOL MITOCHONDRION

ATP ATP

Substrate-level Substrate-level
phosphorylation phosphorylation
Electrons Electrons carried
carried via NADH and
via NADH FADH2

Oxidative
Pyruvate
Glycolysis Citric phosphorylation:
oxidation
acid electron transport
Glucose Pyruvate Acetyl CoA cycle and
chemiosmosis

CYTOSOL MITOCHONDRION

ATP ATP ATP

Substrate-level Substrate-level Oxidative


phosphorylation phosphorylation phosphorylation
The process that generates most of the ATP is called oxidative
phosphorylation because it is powered by redox reactions

RED-OX
Reduction Oxidation

Oxidant + e- product Reductant product + e-

Electron gained, Electrons lost,


Oxidation number decreased Oxidation number increased
Oxidative phosphorylation accounts for almost 90% of
the ATP generated by cellular respiration
A smaller amount of ATP is formed in glycolysis and
the citric acid cycle by substrate-level phosphorylation
For each molecule of glucose degraded to CO2 and
water by respiration, the cell makes up to 38 molecules
of ATP
In total, one sugar molecule can produce about 38 ATP
through the process of :
1) Glycolysis – 2 ATP
2) Citric Acid Cycle – 2 ATP
3) Oxidative Phosphorylation – 34 ATP

 Total equation:
C6H12O6 + 6O2 ------> 6CO2 + 6H2O + 38 ATP
Cell Respiration : Anaerobic & Fermentation
Fermentation and anaerobic respiration enable cells to
produce ATP without the use of oxygen.
• Most cellular respiration requires O2 to produce ATP.
• Without O2, the electron transport chain will cease to
operate.
In that case, glycolysis couples with fermentation or
anaerobic respiration to produce ATP.
Anaerobic respiration – A bacterial
alternative
Some bacteria use only parts of the Krebs cycle and the
ETC. They are anaerobes that do not use free O2 as
their final acceptor.
Anaerobic respiration -they use inorganic oxygen-
containing molecules such as nitrate, nitrite and
sulfate.
Produce fewer ATP molecules than aerobic organisms.
Anaerobic respiration - uses an electron transport
chain with a final electron acceptor other than O2, for
example sulfate.
Fermentation - uses substrate-level phosphorylation
instead of an electron transport chain to generate ATP.
FERMENTATION
Fermentation is the enzymatic breakdown of carbohydrates
in which the final electron acceptor is an organic molecule.
•Different microorganisms use different
fermentation pathways.
 Lactic acid fermentation 

A biological process by which glucose and other six-carbon 
sugars  are converted into cellular energy and the 
metabolite lactate. It is an anaerobic fermentation reaction 
that occurs in some bacteria and animal cells, such 
as muscle cells.
In homolactic fermentation, one molecule of glucose is 
ultimately converted to two molecules of lactic acid.
Lactic acid fermentation is used to produce foods such as 
yogurt and kimchi.
The most commercially important genus of lactic acid-
fermenting bacteria is Lactobacillus, though other bacteria 
and even yeast are sometimes used. 
 2,3-Butanediol fermentation 
Anaerobic fermentation of glucose with 2,3-butanediol as 
one of the end products. The overall stoichiometry of the 
reaction is
2 pyruvate + NADH --> 2CO2 + 2,3-butanediol.
Butanediol fermentation is typical forKlebsiella and
Enterobacter.

 Alcoholic fermentation (Ethanol fermentation)
A biological process which converts sugars such 
as glucose, fructose, and sucrose into cellular energy, 
producing ethanol and carbon dioxide as a side-effect. 
Because yeasts perform this conversion in the absence 
of oxygen, alcoholic fermentation is considered 
an anaerobic process.
Ethanol fermentation has many uses, including the 
production of alcoholic beverages, the production of ethanol 
fuel, and bread baking.
 Mixed acid fermentation 
An anaerobic fermentation where the products are a complex 
mixture of acids, 
particularly lactate, acetate, succinate and formate as well 
as ethanol and equal amounts of H2 and CO2. It is 
characteristic for members of the Enterobacteriaceae family

 Propionic acid fermentation 


The end product of this fermentation is propionic acid carried 
out by propionic acid bacteria with lactic acid as a substrate.
It is used in the production of Swiss cheese which makes 
holes in the cheese structure and gives its characteristic 
flavour.
 Butyric acid fermentation 
This fermentation carried out by Clostridium. Different 
species form a variety of end products with pyruvate being 
converted to either acetone and carbon dioxide, isopropanol 
and carbon dioxide, butyrate or butanol.
Many of this fermentation products are good organic solvents 
 used for nail polish remover. 
Biosynthesis of carbohydrates, protein, fats,
and nucleic acids
The body uses small molecules to build other
substances
These small molecules may come directly from food,
from glycolysis, or from the citric acid cycle.
For most organisms, including microorganisms,
glucose is a major source of energy.
Microorganism can degrade (catabolize) any organic
substance for energy – microbes found almost
everywhere on our planet, able to degrade dead and
decaying remains and wastes of all organisms.
Fat metabolism
Most microorganisms, like animals, can obtain energy
from lipids.
Fats are hydrolyzed to glycerol and three fatty acids.
The glycerol is metabolized by glycolysis.
Fatty acids are in turn oxidized by beta oxidation,
which results in the release of acetyl CoA then enters
the Krebs cycle.
Protein metabolism
Proteins also can be metabolized for energy.
They are first hydrolyzed into individual amino acids
by proteolytic (protein-digesting) enzymes. Then the
amino acids are deaminated.
The resulting deaminated molecules enter glycolysis,
fermentation or the Krebs cycle.

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