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 The outermost component of bacterial cell that provides
structural support &maintains its characteristic shape.
 Multilayered structure. The inner layer is peptidoglycan
and there is an outer membrane.
 In the Gram+ve bacteria peptidoglycan layer is thicker with
fibers of teichoic acid penetrating it.
 Gm-ve have a complex outer layer consisting of
(lipopolysacchride,lipoprotein &phospholipid) a
periplasmic space and porine proteins.
 Mycobacteria have high concentration of lipids (mycolic
acid)result in inaility to be Gram stained.
 Peptidoglycan:
A complex interwoven network , surrounding the
cell ,compose of peptides and suger(glycan).
The carbohydrate backbone is alternating NAG
&NAM molecules connected with tetrapeptide bond.
Present only in bacterial cell but not human cell
(good target for antibiotics).
Lysozyme enzyme in human tears , mucus &saliva
can cleave it (natural protection).
 Lipopolysacchride(LPS):
Part of the outer membrane of Gm-ve bacteria. It is
an endotoxin responsible for fever , hypotension
&shock .
It comopose of a phospholipid (lipid A) responcible
for the toxic effect and polysacchride units used for
identification.
 Teichoic acid:
Fiibers of glycerol &ribitol phosphate in the outer
layer of Gm+ve bacteria only.
It can induce septic shock by the same
mechechanism of Gm-ve bacteria .
 A phospholipid bilayer similer to that of eukaryotic cell but
did not contain sterols
 Function:
a)active transport of molecules inside the cell.
b)Energy generation.
c)synthesis of precursor of cell wall.
d)secretion of enzymes and toxins.
Mesosome:
Invagination in the cytoplasm important during cell
division.
 The cytoplasm has two distinct areas:
a)an amorphus matrix contains
ribosomes, nutrient granules, metabolites
&plasmids.
b)an inner, nucleoid reigon contains the
DNA.
 The site of protein synthesis, it differs from
eukaryotes in size&chemical composition
 They are 70S in size with 50S&30S subunits,
while in human ribosomes are 80Sin size
with 60S & 40S subunits.
 This differerences is the base of selective
action of some antibiotics.
 Different types of granules , some for
storage , some have certain staining
characteristics others are high energy stores
.
 The area where DNA is located
 Prokaryotic DNA is single , circular contain
about 2000 genes.
 Tnucleiod contain no nuclear membrane , no
nucleolus , no mitotic spindles and no
histones.
 Bacterial DNA has no intrones where
eukaryotic DNA does.
 Extachromosomal double-stranded , circular DNA
molecules. Capable of replicating independently.
 Found in both Gm+ve &Gm-ve bacteria.
 Types: a)Transmissible can transfer from cell to cell by
conjugation.
b)Non transmissible, small present in many copies
per cell.
Plasmids carry genes for: Resistance to Antibiotic, heavy
metals , UV light. Genes for production of pili and
exotoxins ,bacteriocins e.g colicns of E.coli & pyocin of
Pseudomonas sp . Also nitrogen fixation enzyme ,
antibiotic production e.g Streptomyces.
 Pieces of DNA that moves readily between
DNS s of bacteria , plasmids and
bacteriophages. (jumping genes)
 Types: a)replicative transposons.
b)direct transposons.
Functions: can code for drug resistant
enzymes and toxins.
They are not capable for self-replication.
 A gelatinous layer covering the entire
bacterium. It compose of polysacchride,
variation in suger type from one species to
other.
 Importance:a)virulance factor
(antiphagocytic)
b)identification
c)vaccination
e)adherence
 Long whip-like appendages move bacteria
toward nutrients.
 It compose of a protien(flagellin),the energy
provided from ATP.
 Flagellated bacteria have different no. and
locations
 Medical importance:
a)flagella play role in pathogenesis
b) used in identification.
 Hair like filaments , shorter & straighter than
flagella , compose of subunits of pilin.
 Found mainly in Gm-ve bacteria.
 Importance:
a)attachment to specific recepters b)sex
pili for conjogation
 Slime layer of polysacchride coat secreated
by many bacteria.
 Allow firm adherance of bacteria to various
structures
 Glycocalyx producing bacteria are more
virulant.
 Highly resistant structures ,formed in adverse conditions by two
genera of medically imp. Gm+ve bacteria ,the genus Bacillus
and the genus Clostrridium.
 The spores formed inside the cell, contain DNA, small amount of
cytoplasm , cell membrane,peptidoglycan & v.little water
surrounded by a thick keratinized coat.
 It resistant to heat, dehydration, radiation and chemicals.
 It had no metabolic activity ,can remain dormant for years.
 Sterlization can not be achieved by heat.
 Autoclaving (steam heating under pressure at 121c for 30
minutes)is required.
Clinical microbiology structure of bacteria.pptx

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Clinical microbiology structure of bacteria.pptx

  • 1.
  • 2.  The outermost component of bacterial cell that provides structural support &maintains its characteristic shape.  Multilayered structure. The inner layer is peptidoglycan and there is an outer membrane.  In the Gram+ve bacteria peptidoglycan layer is thicker with fibers of teichoic acid penetrating it.  Gm-ve have a complex outer layer consisting of (lipopolysacchride,lipoprotein &phospholipid) a periplasmic space and porine proteins.  Mycobacteria have high concentration of lipids (mycolic acid)result in inaility to be Gram stained.
  • 3.  Peptidoglycan: A complex interwoven network , surrounding the cell ,compose of peptides and suger(glycan). The carbohydrate backbone is alternating NAG &NAM molecules connected with tetrapeptide bond. Present only in bacterial cell but not human cell (good target for antibiotics). Lysozyme enzyme in human tears , mucus &saliva can cleave it (natural protection).
  • 4.  Lipopolysacchride(LPS): Part of the outer membrane of Gm-ve bacteria. It is an endotoxin responsible for fever , hypotension &shock . It comopose of a phospholipid (lipid A) responcible for the toxic effect and polysacchride units used for identification.  Teichoic acid: Fiibers of glycerol &ribitol phosphate in the outer layer of Gm+ve bacteria only. It can induce septic shock by the same mechechanism of Gm-ve bacteria .
  • 5.
  • 6.
  • 7.  A phospholipid bilayer similer to that of eukaryotic cell but did not contain sterols  Function: a)active transport of molecules inside the cell. b)Energy generation. c)synthesis of precursor of cell wall. d)secretion of enzymes and toxins. Mesosome: Invagination in the cytoplasm important during cell division.
  • 8.  The cytoplasm has two distinct areas: a)an amorphus matrix contains ribosomes, nutrient granules, metabolites &plasmids. b)an inner, nucleoid reigon contains the DNA.
  • 9.  The site of protein synthesis, it differs from eukaryotes in size&chemical composition  They are 70S in size with 50S&30S subunits, while in human ribosomes are 80Sin size with 60S & 40S subunits.  This differerences is the base of selective action of some antibiotics.
  • 10.  Different types of granules , some for storage , some have certain staining characteristics others are high energy stores .
  • 11.  The area where DNA is located  Prokaryotic DNA is single , circular contain about 2000 genes.  Tnucleiod contain no nuclear membrane , no nucleolus , no mitotic spindles and no histones.  Bacterial DNA has no intrones where eukaryotic DNA does.
  • 12.  Extachromosomal double-stranded , circular DNA molecules. Capable of replicating independently.  Found in both Gm+ve &Gm-ve bacteria.  Types: a)Transmissible can transfer from cell to cell by conjugation. b)Non transmissible, small present in many copies per cell. Plasmids carry genes for: Resistance to Antibiotic, heavy metals , UV light. Genes for production of pili and exotoxins ,bacteriocins e.g colicns of E.coli & pyocin of Pseudomonas sp . Also nitrogen fixation enzyme , antibiotic production e.g Streptomyces.
  • 13.  Pieces of DNA that moves readily between DNS s of bacteria , plasmids and bacteriophages. (jumping genes)  Types: a)replicative transposons. b)direct transposons. Functions: can code for drug resistant enzymes and toxins. They are not capable for self-replication.
  • 14.
  • 15.  A gelatinous layer covering the entire bacterium. It compose of polysacchride, variation in suger type from one species to other.  Importance:a)virulance factor (antiphagocytic) b)identification c)vaccination e)adherence
  • 16.  Long whip-like appendages move bacteria toward nutrients.  It compose of a protien(flagellin),the energy provided from ATP.  Flagellated bacteria have different no. and locations  Medical importance: a)flagella play role in pathogenesis b) used in identification.
  • 17.  Hair like filaments , shorter & straighter than flagella , compose of subunits of pilin.  Found mainly in Gm-ve bacteria.  Importance: a)attachment to specific recepters b)sex pili for conjogation
  • 18.  Slime layer of polysacchride coat secreated by many bacteria.  Allow firm adherance of bacteria to various structures  Glycocalyx producing bacteria are more virulant.
  • 19.  Highly resistant structures ,formed in adverse conditions by two genera of medically imp. Gm+ve bacteria ,the genus Bacillus and the genus Clostrridium.  The spores formed inside the cell, contain DNA, small amount of cytoplasm , cell membrane,peptidoglycan & v.little water surrounded by a thick keratinized coat.  It resistant to heat, dehydration, radiation and chemicals.  It had no metabolic activity ,can remain dormant for years.  Sterlization can not be achieved by heat.  Autoclaving (steam heating under pressure at 121c for 30 minutes)is required.