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Chapter2 Bacterial Physiology

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Title: Chapter2 Bacterial Physiology


1
Chapter2 Bacterial Physiology
  • Xin Gang
  • Department of microbiology and immunology Shantou
    University medical college

2
outline
  1. Physical and Chemical Properties
  2. Growth and Proliferation
  3. Metabolism
  4. Cultivation Method
  5. Classification and Nomenclature

3
I Physical and Chemical Properties
  • Chemical composition
  • Water, inorganic salts, proteins, carbohydrates,
    lipids, nucleic acids
  • Macronutrients(macroelements)
  • Carbon, oxygen, hydrogen, nitrogen, sulfur,
    phosphorus and other metal ions (potassium,
    calcium, magnesium and iron)
  • The first six(C, O, H, N, S, and P) are
    components of carbohydrates, lipids, proteins,
    and nucleic acids.
  • Micronutrients(trace elements)

4
  • Physical properties
  • Optical property
  • Surface area
  • Charged phenomena
  • Semi-permeability
  • Osmotic pressure

5
II Growth and Proliferation
  • Bacterial requirements for growth
  • Nutrients
  • pH
  • Temperature
  • Oxygen
  • Osmotic pressure
  • (Optimal environmental condition)

6
Nutrients
  • Nutrient Requirements
  • Carbon sources
  • Nitrogen sources
  • Inorganic salts and trace elements
  • Growth factors
  • Water

7
  • Nutritional types of bacteria
  • Autotroph
  • reduced inorganic molecules
  • Heterotroph
  • organic molecules
  • saprophyte
  • parasite

8
  • Uptake of nutrients by bacteria
  • Passive diffusion
  • simple diffusion
  • Facilitated diffusion
  • Active transport

9
pH
  • Many bacteria grow best at neutral pH. (pH
    7.2-7.6)
  • Some specialized bacteria can survive and even
    grow in acid or alkaline conditions.
  • T.B. pH 6.5-6.8
  • V. cholerae pH 8.4-9.2

10
Temperature
Temperature and Growth
11
Optimal T
Psychrophiles 10-20 ?C
Mesophiles 20-40 ?C
Thermophiles 56-60 ?C
Heat-shock proteins, Hsp
12
Temperature ranges for microbial growth
13
Oxygen Requirements
  • Obligate aerobes
  • Must grow in the presence of air
  • They can not carry out fermentation
  • Microaerophilic bacterium
  • Grow well in low concentrations of oxygen
  • Killed by higher concentrations of oxygen
  • Facultative anaerobe
  • Perform both fermentation and aerobic respiration
  • Can survive in the presence of oxygen
  • Obligate anaerobe

14
  • Obligate anaerobes
  • Do not carry out oxidative phosphorylation
  • Killed by air
  • Lack certain enzymes
  • cytochrome and cytochrome oxidace
  • superoxide dismutase (SOD)
  • O2- 2H to H2O2
  • catalase
  • 2H2O2 to 2H2O O2
  • peroxidase
  • H2O2 to H2O using NAD to NADH

15
  1. Growth and multiplication

mode Binary fission
Generation time the time required for bacterial
mass to double. 20-30min, T.B. 18-20h
16
The growth curve
17
Phases of Microbial Death Curve
Section of curve Phase Growth rate
A Lag Zero
B Log Constant
C stationary Decreasing
D Death Negative(death)
18
  • CO2
  • Osmotic pressure

19
III Metabolism
  • Energy metabolism of bacteria
  • Catabolism
  • anabolism
  • Respiration
  • Fermentation

20
  • Metabolic products of bacteria
  • Catabolism and biochemical reaction
  • Sugar fermentation
  • IMViC
  • Indole
  • Methyl red
  • VP
  • Citrate utilization
  • H2S
  • Urease

21
  • Anabolic products of bacteria
  • Pyrogen
  • Toxin and invasive enzyme
  • (endotoxin, exotoxin)
  • Pigment
  • Antibiotics
  • Bacteriocin
  • Vitamins

22
IV Cultivation Method
  • Environmental factors affecting growth
  • Nutrients pH Temperature Aeration Ionic
    strength Osmotic pressure
  • Basic medium
  • 0.3 ???
  • 1 ???
  • 0.5 NaCl

Liquid medium
(1-2 agar) Solid medium (0.3-0.5 agar)
Semi-solid medium
23
  • Growth of bacteria in culture medium
  • Liquid medium or Broth
  • Homogeneous turbidity
  • Surface
  • Bottom
  • Solid agar medium
  • Colony and mossy
  • Smooth colony
  • Rough colony
  • Mucoid colony
  • Semi-solid agar medium

24
  • Types of Culture medium
  • basic medium
  • nutrient medium
  • selective medium
  • differential medium
  • anaerobic medium

25
  • Usage of bacterial culture
  • Diagnosis, prevention and treatment of infection
    diseases
  • Characterization of bacteria
  • Preparation of vaccines, toxoids and other
    biologic prducts
  • Application in industry and agriculture
  • Uses for genetic engineering

26
V Classification and nomenclature
Taxonomic ranks
Formal rank Example
Kingdom Prokaryotae
Division Gracillicutes
Class Scotobacteria
Order Eubacteriales
Family Enterobacteriaceae
Genus Escherichia
Species Coli
27
  • Familya group of related genera.
  • Genusgroup of related species.
  • Species a group of related strains.
  • Type sets of strain within a species
  • serotype
  • Phage-type
  • biotype
  • genotype
  • Strain one line or a single isolate of a
    particular species.

28
  • Bionomial Nomenclature
  • genusspecies

Genus Species ?? ??
S. aureus ??? ????
N. meningitides ??? ???
E. coli ?? ???
29
Chapter3 Disinfection and sterilization
30
outline
  • Definition
  • Physical methods
  • Chemical methods

31
I Definition
  • Disinfection
  • Sterilization
  • Antisepsis
  • Asepsis, asepsis technique

32
  • Disinfection
  • killing, or removal of microorganisms that may
    cause disease.
  • primary goal is to destroy potential pathogens.

33
  • Sterilization
  • all living cells, viable spores, viruses, and
    viroids are either destroyed or removed from an
    object or habitat.
  • totally free of viable microorganisms, spores,
    and other infectious agents.

34
  • Antisepsis
  • prevention of sepsis and is accomplished with
    antiseptics.
  • Asepsis
  • without living microorganisms

35
Methods for control of microorganisms
  • Physical methods
  • Heat Hot-air sterilizer
  • Autoclaving
  • Radiation
  • Filtration
  • Ultrasound
  • Dryness
  • Low temperature
  • Chemical agents

36
II physical methods
  • Heat
  • Dry heat
  • Incineration
  • Direct flames
  • Hot-air sterilizer
  • 160-170?C for 2 hours----spores
  • Glass petri dishes and pipettes
  • Infrared
  • microwave

37
  • Moist heat
  • Pasteuriztion
  • 63?C for 30min
  • Flash pasteuriztion - 72?C for 15s
  • Ultrahigh-temperature(UHT) sterilization-140 to
    150?C for 1 to 3s
  • Boiling
  • Free-flowing steam disinfection
  • Autoclaving
  • 15 pounds(1.05kg/cm2), 121?C for 15-20min

38
  • Radiation
  • Ultraviolet, UV
  • 250-260nm
  • Quite lethal but does not penetrate glass, dirt
    films, water, and other substances very
    effectively.
  • To sterilize the air and any exposed surfaces
  • Can burn the skin and damage eyes
  • Ionizing radiation
  • An excellent sterilizing agent and penetrates
    deep into objects
  • Cobalt 60 source

39
  • Filtration
  • Rather than directly destroying contaminating
    microorganisms, the filter simply removes them.
  • Membrane filter

40
  1. Ultrasound
  2. Dryness
  3. Low temperatures

41
III The Use of Chemical Agents in Control
  • Chemical agents
  • Phenolics ?
  • Alcohols ?
  • Heavy metals ???
  • Halogens ??
  • Detergents ???
  • Aldehydes ?

42
  • Factors affecting the results
  • Nature, concentration and acting time of the
    disinfectant
  • Type and amount of the microbe
  • Temperature
  • pH
  • Organic matter
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