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An introduction An introduction into into
MicroMicrobiobiologylogy
Dr. Majid Zare Bidaki(PhD in Medical Microbiology, Assistant professor)
Birjand University of Medical Science
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ReferencesReferences
1. Jawetz, Melnick, & Adelberg; Medical Microbiology, 24th ed.
2. Zinsser, Hans, And Joklik, Wolfgang K.; Medical Microbiology, 17th ed.
3. Baron, Samuel; Medical Microbiology, 4th ed.
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Antonie van LeeuwenhoekAntonie van Leeuwenhoek
First to observe living microbes
his single-lens magnified up to 300X
(1632-1723)
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Louis Pasteur (1822-1895) Louis Pasteur (1822-1895)
Showed microbes caused fermentation & spoilage
Disproved spontaneous generation of microbes
Developed aseptic techniques.
Developed a rabies vaccine.
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Robert Koch Robert Koch
Proposed: Germ theory of disease
Developed: pure culture methods.
Identified: cause of anthrax, TB, & Cholera.
(1843-1910)
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Acellular and cellular Microorganisms
Acellular: VirusesViruses ViroidsViroids PrionsPrions
Cellular:BacteriaBacteriafungifungiProtista: Protozoa & algaeProtista: Protozoa & algaehelminths (worms) helminths (worms)
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Prokaryotic or EukaryoticProkaryotic or Eukaryotic
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Prokaryotes vs EukaryotesProkaryotes vs Eukaryotes
Size smaller Larger
Nucleus - +
Organelles - +
Chromosomes 1 circular Multiple, linear
Ribosomes smaller 70s Larger 80sr
In prokaryotes against Eukaryotes, cell membranes lack In prokaryotes against Eukaryotes, cell membranes lack sterols (e.g. cholesterol)sterols (e.g. cholesterol)
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Living OrganismsLiving OrganismsClassificationClassification
• Domain
• Kingdom
• Phylum
• Class
• Order
• Genus
• Species
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Scientific nomenclatureScientific nomenclature
Binomial (scientific) nomenclature Gives each microbe 2 namesGenusGenus - noun, always capitalizedspeciesspecies - adjective, lowercase
Both italicized or underlined– Staphylococcus aureus (S. aureus)– Escherichia coli (E. coli)
Bergey's Manual of Systematic Bacteriology
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Shapes of BacteriaShapes of Bacteria
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Shapes of BacteriaShapes of Bacteria
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Bacterial shapesBacterial shapes
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Size of Bacteria
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Gram positiveGram positive Gram negativeGram negative
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LipopolysaccharideLipopolysaccharide
Lipid A• Glucosamine disaccharide• Beta hydroxy fatty acids
Core • Heptoses• Ketodeoxyoctonic acid
O-antigenHighly variable
(Hydroxy myritic Acid)
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LPS functionLPS functionEndotoxinsEndotoxinsExotoxinsExotoxins
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PeptidoglycanPeptidoglycan
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Cytoplasmic membrane Cytoplasmic membrane ProtoplastProtoplast
SpheroplastSpheroplast L formsL forms
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Gram positiveGram positive
Gram negativeGram negative
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4 groups based on cell wall 4 groups based on cell wall compositioncomposition
1. Gram positive cells
2. Gram negative cells
3. Bacteria without cell walls
4. Bacteria with chemically unique cell walls
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Gram positive wall
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Gram negative cell wallGram negative cell wall
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CytoplasmCytoplasm
CytoplasmCytoplasm
Lipoteichoic acidPeptidoglycan-teichoic acid
Cytoplasmic membrane
Inner (cytoplasmic) membrane
Outer Membrane
LipopolysaccharidePorin
lipoprotein
Peri
plas
mic
spa
ce
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r r rrr
r
Gram Positive Cell EnvelopeGram Positive Cell Envelope
rrrr
Lipoteichoic acidPeptidoglycan-teichoic acid
Cytoplasmic membrane
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Bacteria classification based on Bacteria classification based on cell wall structurecell wall structure
Grasilicutes (Gram Negative)Grasilicutes (Gram Negative)Firmicutes (Gram Positive)Firmicutes (Gram Positive)Tenricutes (with no Cell wall)Tenricutes (with no Cell wall)Mendosicutes (with no Peptidoglycan in Mendosicutes (with no Peptidoglycan in
cell wall)cell wall)
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Major Taxonomic Groups of BacteriaMajor Taxonomic Groups of Bacteria
Gracilicutes – gram-negative cell walls, thin-skinned
Firmicutes – gram-positive cell walls, thick skinned
Tenericutes – lack a cell wall & are softMendosicutes – archaea, primitive procaryotes
with unusual cell walls & nutritional habits
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CapsuleCapsule
2 types1. Macro capsule - highly organized, tightly
attached2. Micro capsule, Slime layer or Glycocalyx -
loosely organized and attached
Functions attachment inhibits killing by white blood cells Receptor (K antigen)
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2 Types of Capsule2 Types of Capsule
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BiofilmsBiofilms
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FlagellaFlagella
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Fimbrea (Pili)Fimbrea (Pili)
Adhesion to other cells and surfaces
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StructureStructure
Pili & Sex pili
Rigid tubular structure made of pielin protein
Found mostly in Gram negative cells
FunctionsFunctions Adhesionjoins bacterial cells for DNA transfer (Conjugation)
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ConjugationConjugation
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CytoplasmCytoplasmDense gelatinous solution of sugars, amino
acids, & salts70-80% waterServes as solvent for materials used in all
cell functions
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ChromosomeChromosome
single, circular, double-stranded DNA molecule that contains all the genetic information required by a cell
DNA is tightly coiled around a protein, aggregated in a dense area called the nucleoid
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plasmidsplasmids
small circular, double-stranded DNA
free or integrated into the chromosome
duplicated and passed on to offspring
not essential to bacterial growth & metabolism
may encode antibiotic resistance, tolerance to toxic metals, enzymes
& toxins
used in genetic engineering- readily manipulated & transferred
from cell to cell
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RibosomesRibosomes
made of 60% ribosomal RNA & 40% protein
consist of 2 subunits: large (50 S) & small (30 S)
procaryotic differ from eucaryotic ribosomes in
size & number of proteins
site of protein synthesis
All bacterial cells have ribosomes.
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Inclusions, granulesInclusions, granules
intracellular storage bodies
vary in size, number & content
bacterial cell can use them when
environmental sources are depleted
Examples: glycogen, sulfur and polyphosphate granules,
poly-b-hydroxybutyrate, gas vesicles for floating.
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EndosporesEndospores
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Important components in endospore: Important components in endospore:
CalciumCalciumDipicolinic AcidDipicolinic Acid
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Endospore structureEndospore structure
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Spore structureSpore structure
Spherical or Oval
Terminal, subterminal or central
Bulging or nobulging
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Growth in BacteriaGrowth in Bacteria
Temperature
Nutrients
pH
Osmotic pressure
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Minimum temperature – lowest temperature that
permits a microbe’s growth and metabolism
Maximum temperature – highest temperature
that permits a microbe’s growth and metabolism
Optimum temperature – promotes the fastest
rate of growth and metabolism
Temperature Temperature
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3 temperature adaptation groups
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Bacterial MetabolismBacterial Metabolism
• DefinitionDefinition
• RequirmentsRequirments: ? & ?? & ?
Phototroph
Chemotroph
Autotroph
Heterotroph
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Bacterial MetabolismBacterial Metabolism
PhototrophPhotoautotroph (Photolitotroph) Photoheterotroph (Photoorganotroph)
ChemotrophChemoautotroph (ChemolitotrophChemoheterotroph (Chemoorganotroph)
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Stages of metabolism in Stages of metabolism in chemoheterotrophic bacteriachemoheterotrophic bacteria
Digestion
Absorption (Passive and active transportation)
Preparation for oxidation
Oxidation
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Oxidation & ReductionOxidation & Reduction
X Ye- & H+ Cytochromes, …. Cytochromes, ….
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Aerobics, Fermentors, Anaerobics
• In Aerobics:
Last e- receptor is Oxigen.
• In Fermentors:
Last e- receptor is an organic material.
• In Anaerobics:
Last e- receptors is a mineral material.
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Oxygen requirementsOxygen requirements
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Bacterial growth in closed & Bacterial growth in closed & continuous culturescontinuous cultures
• Closed culture:
There is no chance for adding or reducing the requirements or wastes.
• Continuous culture:
Fresh requirements come in and wastes goes out continuously.
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The curve of bacterial growth in a closed The curve of bacterial growth in a closed cultureculture
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Growth Curve
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Bacterial growth in a Bacterial growth in a continuous culturecontinuous culture
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FermentersFermenters
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Bacterial growth Bacterial growth
Binary divisionBinary division
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Microbial growth calculationMicrobial growth calculation
b = a.2n
G (Generation time) = T / n (n = The number of generations, T = The total time of growth for the population)
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Measuring the bacterial growthMeasuring the bacterial growth
• Measuring the number of bacteria- Turbidity- Cell counting• Measuring the mass of bacteria
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Measuring the number of bacteriaMeasuring the number of bacteria
• Torbidity (light absorbtion)Torbidity (light absorbtion)
- Measuring with eye
- Measuring with devices
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Measuring with devices
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Cell counting(by device)
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Cell counting(by Microscopy)
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Cell counting(by culture)
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FermentationFermentation
• Defined as an energy yielding process
• Organic molecules serve as both electron donors and electron accepters.
• The molecule being metabolized does not have all its potential energy extracted from it. (not completely oxidized.)
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• NAD+ is almost always reduced to NADH
• Remember that metabolism involves the oxidation of the substrate. These electrons are removed from the organic molecule and most often given to NAD. (This is true both in fermentation and respiration).
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• Fermentation results in a excess of NADH
• Accumulation of NADH causes a problem for anaerobes. They have too much of it and it prevents further oxidation of substrate due to a lack of an NAD+ pool to accept electrons.
• In many fermentation pathways, the steps after energy generation are performed in part to get rid of the NADH:
pyruvate + NADH + H+ → lactate + NAD+
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Glycolysis - Embden-Meyerhoff-Parnas pathway (EMP)
• The most commonly used series of reactions for oxidizing glucose glucose toto pyruvate pyruvate.
• EMP is so ubiquitous. However, it is not the only method for the fermentation of glucose.
• It is an essential part of many organisms catabolism.
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• A complete fermentation pathway begins with a substrate, includes glycolysisglycolysis and results in various end-productsvarious end-products.
• The different fermentation pathways typically are named for the end products that are formed.
• yeast, convert NADH back to NAD+ in a process called ethanol fermentation. In this process, the pyruvate pyruvate is converted first to acetaldehyde acetaldehyde andand carbon dioxide carbon dioxide, then to ethanolethanol.
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PyruvatePyruvate
• Pyruvate is often an important intermediate
• Many of the reactions that we will look at eventually end up making pyruvate.
• Pyruvate is a valuable intermediate because it can be used for cell synthesis.
• Many different enzymes can act on it. It gives the microbe flexibility.
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Fermentation Vs Aerobic oxidation
.C6H12O6------------>2C2H5OH + 2CO2 (2ATP) ∆G = -
33 Kcal تخمیر
C6H12O6 + 6O2------------>6CO2 + 6H2O (36ATP) ∆G =
686 Kcal_تنفس
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FermentationFermentation
Incomplete oxidation of glucose or other carbohydrates in the absence of oxygen
Uses organic compounds as terminal electron acceptors
Yields a small amount of ATP
Production of ethyl alcohol by yeasts acting on glucose
Formation of acid, gas & other products by the action of various bacteria on pyruvic acid
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GlycolysisGlycolysis
Embden-Meyerhof-Parnas Embden-Meyerhof-Parnas (EMP pathway)(EMP pathway)
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Entner–Doudoroff pathwayEntner–Doudoroff pathway
• The Entner–Doudoroff pathway describes an alternate series of reactions that catabolize glucose to pyruvate using a set of enzymes different from those used in either glycolysis or the pentose phosphate pathway
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Homolactic FermentationHomolactic Fermentation ((Lactic acid)Lactic acid)
- It is the sole end product.
- Pathway of the homolactic acid bacteria (Lactobacillus, Lactococcus and most streptococci).
- The bacteria are used to ferment milk and milk products in the manufacture of yogurt, buttermilk, sour cream, cottage cheese, cheddar cheese….
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Mixed Acid FermentationsMixed Acid Fermentations..• Mainly the pathway of the Enterobacteriaceae.
• End products are a mixture of lactic acid, acetic acid, formic acid, succinate and ethanol.
• Possibility of gas formation (CO2 and H2) if the bacterium possesses the enzyme formate formate dehydrogenasedehydrogenase, which cleaves formate to the gases.
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• Mixed acids and gases but in addition, butanediol from the condensation of 2 pyruvate. The use of the pathway decreases acid formation (butanediol is neutral) and causes the formation of a distinctive intermediate, acetoin.
• Specific tests to detect low acid and acetoin in order to distinguish non fecal enteric bacteria (butanediol formers, such as Klebsiella and Enterobacter) from fecal enterics (mixed acid fermenters, such as E. coli, Salmonella and Shigella).
Butanediol FermentationButanediol Fermentation
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Butyric acid fermentationsButyric acid fermentations((Butanol-acetone fermentation)
• Butyric acid Butyric acid fermentations as well as the butanol-butanol-acetoneacetone fermentation, are run by the clostridia, the masters of fermentation.
• In addition to butyric acid, the clostridia form acetic acid, CO2 and H2 from the fermentation of sugars. Small amounts of ethanol and isopropanol may also be formed.
• Butanol and acetone were discovered as the main end products of fermentation by Clostridium acetobutylicum
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• Carried out by the propionic acid bacteria which include corynebacteria, Propionibacterium and Bifidobacterium.
• Propionic acid bacteria ferment lactate to acetic acid, CO2 and propionic acid.
• The formation of propionate is a complex and indirect process involving 5 or 6 reactions.
• The propionic acid bacteria are used in the manufacture of Swiss cheeseSwiss cheese, which is distinguished by the distinct flavor of propionate and acetate, and holes caused by entrapment of CO2.
Propionic acid fermentation.
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FermentationFermentation
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Fermentations in bacteria that proceed through the Embden-Meyerhof pathway. Representive bacteria that utilize these pathways
are in shown in BLUE.
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MediumMedium
DefinitionDefinitionTypes based on solidity:Types based on solidity:
1. Liquid medium
BHI, TSB, SF, NB, …
2. Solid medium
Blood agar, Nutrient agar, chocolate agar, Columbia agar, EMB
3. Semi-solid medium
SIM
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•A Undefined mediumUndefined medium (a basal or complex medium). Contains: - A source of amino acids and nitrogen (e.g., beef, yeast extract)- A carbon source such as glucose for bacterial growth- water- Various salts needed for bacterial growth
•A defined mediumdefined medium (a synthetic medium) is a medium in which- all the chemicals used are known- no yeast, animal or plant tissue is present
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Nutrient media (Broth/Agar)
Nutrient agar medium composition:Nutrient agar medium composition: - Beef Extract-0.3gm (mineral and carbohydrate) - Peptone-0.5gm (protein and nitrogen source) - NaCl-0.5gm (electrolyte) - Agar-1.5gm (solidifying agent) - Distilled water-100ml pH-7
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Minimal media
contain the minimum nutrients possible for colony growth, generally without the presence of amino acids.used to grow "wild type" microorganisms and select for or against recombinants.
Minimal medium typically contains:Minimal medium typically contains:-A carbon source carbon source (such as glucose, or a less energy-rich source like succinate.- various saltssalts (provide essential elements such as magnesium, nitrogen, phosphorus, and sulfur to allow the bacteria to synthesize protein and nucleic acid- WaterWater
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Supplementary minimal media
• A type of minimal media that also contains a single selected agent, usually an amino acid or a sugar.
• This supplementation allows for the culturing of specific lines of auxotrophic recombinants.
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Culture mediaCulture mediabased on the application in clinical labsbased on the application in clinical labs
General medium (Nutrient agar, Muller hinton agar, Nutrient broth, …)
Selective/Special medium (EMB, MSA, …)
Differential medium (MAC [MacConkey agar], EMB, XLD, …)
Enrichment medium (SF, RV [Rappaport-Vassiliadis Broth], TT, …)
Enriched medium (Blood agar, Chocolate agar, cold enrichment)
Transport medium (Stuart, Cary-Blair, Amies, …)
Cary-Blair: exclusively associated with enteric transport
Stuart & Amies: widely used for the transportation of a diverse range of clinical swab samples from sites including the eye,
ear, nose, throat, skin, genital tract and wounds.
Galleries (TSI, SIM, MRVP, Citrate agar, ….)
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General mediumGeneral medium
• Theoretically it supports cultivation of many bacteria.
• Nutrient agar, Muller hinton agar, Nutrient broth, …
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Selective/Specialized medium• Some examples of selective media include:
• Eosin methylene blue (EMB) that contains methylene blue – toxic to Gram-positive bacteria, allowing only the growth of Gram negative bacteria
• YM (yeast and mold) which has a low pH, deterring bacterial growth
• MacConkey agar for Gram-negative bacteria
• brilliant green agar, a medium that inhibits Gram-positive bacteria while permitting Gram-negative organisms such as Salmonella species to grow.
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Selective/Special medium• Hektoen enteric agar (HE) which is selective for Gram-
negative bacteria
• Mannitol salt agar (MSA) which is selective for Gram-positive bacteria and differential for mannitol
• Terrific Broth (TB) is used with glycerol in cultivating recombinant strains of Escherichia coli.
• xylose lysine desoxyscholate (XLD), which is selective for Gram-negative bacteria
• Buffered charcoal yeast extract agar, which is selective for certain gram-negative bacteria, especially Legionella pneumophila
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Differential media• Blood agar which contains bovine heart blood that
becomes transparent in the presence of hemolytic streptococcus.
• Eosin methylene blue (EMB), which is differential for lactose and sucrose fermentation.
• MacConkey (MCK), which is differential for lactose fermentation.
• Mannitol salt agar (MSA), which is differential for mannitol fermentation.
• violet red bile agar is used to distinguish coliform bacteria from noncoliform organisms.
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Transport Media
• Maintain the viability Maintain the viability of organisms in specimen.• No altering No altering microorganism concentration.• Contain only buffersbuffers and saltsalt. • Lack of carbon, nitrogen, and organic Lack of carbon, nitrogen, and organic growth
factors.• Transport media used in the isolation of anaerobesanaerobes
must be free of molecular oxygenfree of molecular oxygen.
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Transport Media
• ThioglycolateThioglycolate brothbroth for restrict anaerobes.• Stuart transport medium Stuart transport medium - a non-nutrient soft agar
gel containing a reducing agent to prevent oxidation, and charcoal to neutralise.
• Certain bacterial inhibitors- for gonococci, and buffered glycerol saline for enteric bacilli.
• Venkat-Ramakrishnan(VR) medium for v. cholerae.
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• Some organisms, termed fastidious organisms, require specialized environments due to complex nutritional requirements.
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Methods in bacterial identificationMethods in bacterial identification
1. Microscopic morphology
2. Macroscopic morphology – colony appearance
3. Physiological / biochemical characteristics
4. Chemical analysis
5. Serological analysis
6. Genetic & molecular analysis G + C base composition DNA analysis using genetic probes Nucleic acid sequencing & rRNA analysis
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Bacterial ColoniesBacterial Colonies
• Standard Bacterial Count
• Colony-Forming Units
• Plaque-Forming Units
•Spread Plate
• Pour Plate
• Soft-Agar Overlay
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Types of culture methodsTypes of culture methods
Isolation culture
Spread culture
Pour plate culture
Colony count culture
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