Title: Microbiology - Chapter 7
1Microbiology - Chapter 7 8
- Microbial Growth Bacteria reproduce by binary
fission, a cell divides into two, two to four,
four to eight, etc. - Cell division can occur quite rapidly depending
on nutrient levels, temperature, etc. E. coli
can divide every 20 minutes (time to double
generation time) in nutrient media at 37 degrees
C. The numbers get so large we express them as
the log of the number of cells.
2Microbiology - Chapter 7 8
- Microbial Growth is affected by two major
factors - Environmental temperature, pH, Osmotic
conditions - Chemical Proper concentrations of C, H, O, N,
P, S, some trace elements, and some organic
cofactors
3Microbiology - Chapter 7 8
- Bacterial Growth Curve
- A Lag phase C Stationary phase
- B Log phase D Death Phase
- Know this and be able to explain what is
occurring during each phase. - Bacteria that produce endospores may not have a
death phase. Why?
4Microbiology - Chapter 7 8
- Why study such a growth curve?
- Helps us understand how microbes grow under
different conditions - Helps us understand how pathogen grow in our body
- Helps us study the effect of different chemicals,
osmotic conditions, even the effect of
temperature on bacterial growth. - Ex. What would the growth curve for E.coli look
like if we incubated at 4 degrees Celsius? At 65?
5Microbiology - Chapter 7 8
- How do we measure growth of bacteria in a growth
curve? - Direct cell count using stained slides that have
a grid for counting. (Tedious, a real pain) - Indirect Serial dilution, plates are
innocculated - incubated and colonies counted.
Number of colonies X dilution factor gives the
number of bacteria.
6Microbiology. Chapter 7 -8 How do we measure
growth of bacteria in a growth curve? Direct
cell count. Tedious and time consuming
7Microbiology - Chapter 7 8
- How do we measure growth of bacteria in a growth
curve?
8Microbiology - Chapter 7 8
- How do we measure growth of bacteria in a growth
curve? Measure cloudiness in a test tube as the
number of cells increase (turbidity) using a
spectrophotometer. Correlate this data with a
standard plate count and now just use the
turbidity measurement look up number from a
chart from then on. Saves time and money.
9Microbiology - Chapter 7 8
- How do we measure growth of bacteria in a growth
curve? - Coulter counter. Electronically counts number of
bacteria as bacteria pass through a tiny tube.
Expensive.
10Microbiology - Chapter 7 8
- Physical factors that affect bacterial growth
- Mesophiles grow best moderate temp. 25 40
degrees - most of our lab microbes
- Psychrophiles adapted to survive and grow at
cooler temp., even in the frig (below 25
degrees) - Listeria (in cheeses and meat)
- Thermophiles adapted to and grow at much higher
temp. - Thermus aquaticus, from oceanic vents, survives
at 60 degrees C - Leprosy bacilli prefer 30 degrees, most pathogens
prefer 37 degrees.
11Microbiology - Chapter 7 8
- Physical/Chemical factors that affect bacterial
growth pH measure acidity and alkalinity of
media - Bacteria grow best at pH range of 6.5 to 7.5
- Fungi grow better at slightly acid condition (5.0
to 5.5) - Sabaraud dextrose and Potato dextrose agars
- One pathogen, Helicobacter pylori, is adapted to
and survives in stomach acid (cause of ulcers) - Hydrostatic pressure some bacteria grow really
well deep in the ocean at pressures that crush
submarines like and egg
12Microbiology - Chapter 7 8
- Physical/Chemical factors that affect bacterial
growth pH measure acidity and alkalinity of
media - Osmotic pressure relative salt concentrations in
water solutions - Hypertonic higher salt concentrations, slows or
stops bacterial growth salt preservative in meat - some prefer higher salt Halophiles
- some survive and thrive, Vibrio bacteria, V.
cholera - Hypotonic lower salt, fresh water, net flow
water into cells, bacteria have rigid cell wall
resist rupture - Isotonic equal solute (salt) no net flow,
preferable
13Microbiology - Chapter 7 8
- Chemical factors that affect bacterial growth
Nutrition - How microbe acquire nutrients. C, H, O, N, S, P,
Ca, Mg, etc - Carbon
- Autotroph producers, photosynthetic, use CO2
and H2O, sunlight as energy, make their own
food - Heterotroph require preformed food, digestive
and absorptive, most microbes - Chemoautotroph unique metabolism, use chemical
energy from inorganic molecules, Sulfur and
Iron
14Microbiology - Chapter 7 8
- Chemical factors that affect bacterial growth
Nutrition - How microbe acquire nutrients. C, H, O, N, S, P,
Ca, Mg, etc - Oxygen
- Obligate aerobes require molecular oxygen (as
final electron acceptor in catabolism) - Pseudomonas spp.
- Obligate anaerobes require atmosphere with no
O2 an organic molecule is final electron
acceptor in catabolism (like a fermentation
pathway) - Clostrida - grow in Brewer Jar
- Facultative anaerobes grow with or without O2,
usually are also fermenters, like E. coli - Microaerophile grow best in lower oxygen and
higher carbon dioxide, Strep., candle jar
15Microbiology - Chapter 7 8
- Problems with oxygen oxygen can be toxic, it
oxidizes and destroys vital cell chemicals
aerobic organisms have enzymes and systems to
handle it - SOD superoxide dismutase, enzyme that
chemically alters toxic oxygen free radicals and
toxic high energy singlet oxygen to less toxic
hydrogen peroxide - Catalase Converts hydrogen peroxide to oxygen
and water
16Microbiology - Chapter 7 8
- Nitrogen Found in all the amino acids,
nitrogenous bases of nucleic acids, etc. - Hydrogen found in all biological molecules,
Carbs, fats, proteins, nucleic acids, etc - Phosphorous found in nucleic acids, ATP, and
phospholipdids of membranes - Sulfur found in 2 or 3 amino acids of microbes
- Trace elements inorganic elements needed in very
tiny concentrations (manganese, cobalt, Zn, Cr)
17Microbiology - Chapter 7 8
- Organic cofactors
- Vitamins
- Required by certain bacteria, fastidious hard
to grow - Coenzymes Many microbes produce their own from
scratch, source of our supplements (one a day,
GNC) - Fastidious organisms may require enriched media
to get them to grow (blood, eggs, etc) - Some organisms are almost impossible to culture
because of their strict parasitic-fastidious
nature (syphilis, leprosy)
18Microbiology chapters 7 - 8 part 2
- Metabolism
- Catabolism
- Anabolism Both occur simultaneously in
cells - Catabolism eventually produces the chemical
energy (ATP) required for all cellular functions
such as anabolism (synthesis), membrane
transport, etc.
19Microbiology chapters 7 - 8 part 2
- ATP Adenosine triphosphate, universal cellular
energy - Cyclically made and energy is stored and then
broken down and the energy is released
20Microbiology chapters 7 - 8 part 2
- Note ATP is a ribonucleotide, it has ribose, a
nitogenous base (adenine), and phosphate. The
high energy bond of the terminal of the three
phosphates is the one cyclically broken and
regenerated. - Sugars like glucose can be broken down in a
catabolic pathway controlled by many cellular
enzymes. Some of the energy released by the
breaking of covalent bonds is harvested and
stored in the energy bonds of ATP. - Most any biomolecule can be used for energy we
will focus on the catabolism of glucose (a
monosaccharide) and later show how the others are
involved (lipids, AA, etc)
21Microbiology chapters 7 - 8 part 2
- Quick review on enzymes
- Organic catalyst (made of carbon, speed up rate
of chemical reactions) - Made of protein chains of Amino acids in a
specific sequence that fold and coil into
specific shapes. Their shape is key to
understanding their function. (remember shape
determines function) Also, shape is easily
affected by changes in temperature. So, heat or
cold can cause enzymes to slow down or even stop.
- An enzyme lowers activation energy energy
required for a reaction to begin
22Microbiology chapters 7 - 8 part 2
- Quick review on enzymes
- Substrates are the material that are acted on by
the enzyme - Enzymes are often named using the name of the
substrate and adding ase. Sucrase breaks down
sucrose to glucose and galactose. Enzyme driven
reactions are often reversible.
23Microbiology chapters 7 - 8 part 2
- Aerobic metabolism specifically glucose
catabolism - This stuff is hard Just do It
- Goal
- 1. List the three stages of glucose catabolism
- 2. Know the basic steps of each stage
- 3. Know how much ATP is made at each stage per
molecule of glucose - 4. Starting products and end products, other
important carriers (NAD) - 5. The difference between substrate level
phosphorylation and oxidative phosphorylation - 6. Theory of chemiosmosis and ATP production at
the membrane of the mitochondria
24Microbiology chapters 7 - 8 part 2
- Glucose is a hexose, monosaccharide, C6H12O6
- It is systematically broken down through three
related pathways to Carbon dioxide (CO2) and
Water (H2O) - Overall FormulaC6H12O6 ___ O2 ? CO2 ___
H2O - The three stages
- Glycolysis (anaerobic) (in cytoplasm)
- Krebs cycle (aerobic)
- (in mitochondria)
- Electron transport (with chemiosmosis) (aerobic)
-
25Microbiology chapters 7 - 8 part 2
- Glycolysis Anaerobic, no oxygen required,
linear NZ pathway - Begins with ______
- End products _________
- How much ATP? _______
- How many carrier molecules? ____
- Name the carrier molecule. ____
- Where in the cell? _______
- What happens after if the organism
- Is an aerobe? _____
- Facultative? ______
- Strict anaerobe? ______
- Aerobe deprived of oxygen? ____
26Microbiology chapters 7 - 8 part 2
- Krebs cycle (TCA, Citric acid cycle) Aerobic
stage, Occurs in the fluid of the Matrix
27Microbiology chapters 7 - 8 part 2
- This is a cyclic pathway
- Pyruvic acid is first acted on by an NZ and a
coenzyme (COA). The end product is Acetyl-Coa
and a CO2 molecule. - Remember this occurs twice for each glucose
molecule. (One glucose is split into two
pyruvic acid molecules.)
28Microbiology chapters 7 - 8 part 2
- The acetyl-COA reacts with an enzyme and another
substrate (a 4-C molecule called oxaloacetic
acid) to produce Citric Acid, a 6 carbon
tri-carboxylic acid 3 carboxyl groups - Several enzymes systematically oxidize the citric
acid into a 5-C acid, then a 4-C acid and
eventually back to the original oxaloacetic acid
thus a cycle. Each time the terminal carboxyl
group is removed a CO2 molecule is produced. - Thus, one glucose, causes the cycle to turn
twice, each turn produces 3 CO2 (one at Acetyl
COA step and two in the cycle) - Now for the hard part. Understanding that an
oxidation reduction reaction is going on at each
step. (Here Krebs), at glycolysis, and even
electron transport) - Lets first review oxidation- reduction (aka
redox)
29Microbiology chapters 7 - 8 part 2
- Oxidation Reduction
- Organic molecules like glucose have covalent
bonds between C-C, C-H, C-O, O-H
C6H12O6 - When the molecule is broken down -, the covalent
bonds are broken electrons are removed and
transferred to carrier molecules. - Oxidation is the removal of electrons and/or
adding Oxygen - In Glycolysis the glucose is broken into two
Pyruvates, - The electrons and a H are transferred to a
carrier, NAD. - NAD gains the electron (and Hydrogen too), it is
reduced - to NADH, thus oxidation and reduction go
together.
30Microbiology chapters 7 - 8 part 2
- Oxidation Reduction
- Look again at glycolysis.
- Glucose is oxidized and the carrier NAD is
reduced. - For every glucose, two Carriers are produced
- 2 NADH (what happens to them, they have to
- be regenerated oxidized back to NAD)
- Aerobes eventually produce CO2 and H2O
- Thus oxygen is the final electron acceptor(
producing - Water).
- Anaerobes use a different set of enzymes, a
- Fermentative pathway that generates other acids,
- alcohols or gasses (lactic acid, ethanol, CO2)
- electron acceptor is an organic molecule
- If no regeneration of NAD, the glycolysis pathway
- shuts down and the organism dies no ATP
31Microbiology chapters 7 - 8 part 2
- Glycolysis, no oxygen, fermentation, only 2 ATP
per molecule of glucose - Glycolysis, with oxygen, followed by Krebs and
electron transport, can generate much more ATP
(sometimes as much as 36). Aerobic mechanisms
are much more energy efficient. - In the Krebs cycle many more carrier molecules
like NADH are generated and thus lead to more
ATP. (Other carriers FAD, NADP we just use NAD
as a representative type of carrier). - The constantly turning of the cycle produces a
steady stream of reduced carriers (NADH) which
pass the electrons to a set of carrier-processor
molecules imbedded in the membrane of the
Mitochondria. These carriers are called the
electron transport chain.
32Microbiology chapters 7 - 8 part 2
- Return to Krebs and show how it works with
electron transport chain. Note how glycolysis
and Krebs are working together. Note that each
produces reduced carriers that need to be
processed.
33Microbiology chapters 7 - 8 part 2
- The electrons are passed down the chain and end
up being added to oxygen. The Hydrogen ion (H)
is pumped out (proton pump) and flows back in at
special sites to be added to the Oxygen and
electron to form Water. Energy is conserved
(harvested stored) in the bonds of ATP
34Microbiology chapters 7 - 8 part 2
- Theory of Chemiosmosis Proton pump, increased
H ion concentration, flow through ATP synthase
related channel, energy is harvested in high
energy bonds of ATP. Enough to generate 34 more
ATP.
35Microbiology chapters 7 - 8 part 2
- Fermentation Many microbes ferment sugars and
other substrates to make ATP without oxygen - See pg 234 in text NADH reduces pyruvate and
ethanol and carbon dioxide are produced - Other end products are seen lactic acid,
acetic, acid - We use biochemical tests and the end products of
sugar fermentation to ID bacteria (charts in
Bergeys) later in lab, particularly with
unknown 2 - Some bacteria, like E. coli and Bacillus use
nitrogen electron acceptors to regenerate NAD.
Nitrate and Nitrite reduction are examples. Pg
233 in text. The enzyme system is called Nitrate
reductase
36Microbiology chapters 7 - 8 part 2
- Other fuels
- Proteins digested to amino acids
- Amino acids are
- deaminated amino group removed, the
reulting acid can be further metabolized,
more ATP - decarboxylated carboxyl group removed, the
end products then enter glycolysis or Krebs to
make ATP
37Microbiology chapters 7 - 8 part 2
- Lipids are catabolized to Glyerol and Fatty acids
- Glycerol easily enters glycolysis and Krebs just
like pyruvate - Fatty acids are chopped into 2 or 3 acid
fragments that are broken downt to carbondioxide - Even nucleic acids OH SO MUCH MORE!!! Take
biochem.