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Size
 Very small (0.5-1m)
 Surface Area (SA)/ Volume ratio very high
 Large SA helps to enter nutrients and leave waste
 Small Volume impart high growth rate
 (SA / VOLUME) ratio
Disadvantage: SA/VOLUME ratio limits bacterial size
Shape & Arrangement
 Shape due to its rigid cell wall
 Cells are:
Mass of cell subs to be
nourished close to cell surface
No circulatory m/c needed to
distribute nutrients
Spherical (Cocci)
Straight rods (Bacilli)
Helically curved (Spirilla)
Fig.1 Different shapes of bacteria
 Some cells are Pleomorphic (variety in shapes)
 Arrangement Cocci appear in various characteristic
arrangements depending on Cell
division and daughter cell
 Diplobacilli Most occur in pairs or single i.e. Bacilli
 Streptobacilli Form chains i.e. Bacillis subtilis
 Trichomes Similar to chain but ↑ SA to contact with
adjacent cells i.e. Saprospira grandis
 Palisade arrangement Cells lined side by side
i.e. Corynebacterium diphthetiae
 Hyphae Long, branched, multinucleate filaments that
collectively form Mycelium i.e. Streptomyces
viridochromogenes
Fig.2 Characteristics arrangements of cocci
Fig.3 Characteristics shapes of different bacteria
Fig.4 Pleomorphic form of Arthrobacter
Vibrioid and helical shape
Bacteria < one twist or turn i.e. Genus Vibrio
Bacteria > one twist or turn
e.g. Spirochetes Flexible, can twist to change shape
Spirilla Rigid
 BACTERIAL STRUCTURE
 A. Structure external to cell wall
Flagella
Description Hair-like helical structure that protrude through cell wall
Much thinner than eucaryotes flagella or celia(0.01m)
Simple structure
Helps in motility/swimming
Location Polar at one or both end of bacterium
Lateral along sides
Fig.5 Types of Flagella
Fig.5 Different parts of Flagella
Parts 3 parts:
 Protein of filament is called Flagelin
 Flagellum grows at its tip
Mortility
1. Hydrodyamics of flagella
 Small size of bacteria BLOCK inertia of H2O for propulsive force and
viscosity of H2O (x 1000)
 Bacteria propel by rotating helical flagella (e.g. like corkscrew)
 Polar flagella can swim back and forth and can reverse direction by
reversing Flagella rotation
 Basal body (with cytoplasmic membrane)
 Hook (with cell wall) composed of protein
 Filament (long/helical structure) composed of subunit
2. Swimming and tumbling e.g. Petrichous flagella
Swimming Rotate counter clockwise to form a bundle
Tumbling Flagella reverse their rotation
Portion acquire short wavelength and right
handed configuration; Bundle flies apart
exhibit a chaotic motion (crossed arrows)
3. Swimming mortality without flagella
 Some helical bacteria exhibit swimming
 They have gel like structure in cell Peri-plasmic flagella (axial
fibrils)
e.g. Spirochetes & Spiroplasm spp
4. Gliding mortality
 Mortal with solid surface
 Exhibits flexing motion (very slow)
e.g. cytopbaga spp
Mortality (in viscous
medium) without
Flagella
Fig.6 Hydrodyamics of flagella (Swimming and tumbling )
5. Bacterial Chemotaxis Mortal bacteria capable of swimming towards
or away from various chemical compound a
phenomenon called Chemotaxis
 Swimming towards chemical is +ve Chemotaxis
 Swimming away is - ve Chemotaxis
 Chemical may act as Attractant or
Repellants
 Stimulus is change Temporal gradient
(concentration with time)
6. Phototaxis
 Exhibit +ve phototaxis with: light intensities
 Repelled by: light intensities
e.g. Phototropic bacteria
 Pili (fimbriae)
 Hollow, non-helical filaments that are thinner, shorter and more
numerous
 Not helps in mortality (found in mortal and non mortal species)
 F Pilus (special type) acts as port of entry of genetic material in mating
 Attach to epithelial cell lining of Respiratory / Intestinal tract human
infection
 Capsules
Description
 A viscous substance forming a covering layer/envelop around cell
(visible under Light microscope) “Capsule”
 Too thin layer microcapsule
 When too many cells embedded in common matrix the material is
SLIME
 Appear as amorphous gelatinous area
 Highly H2O soluble (dissolves readily) in medium viscosity of
broth
Fig.7 Different parts & structure of bacterial cell
Functions
 Protect against temporary drying by binding H2O molecule
 Bacteriophage attachment blocking
 Anti-phagocytic i.e. inhibit engulfment of pathogenic bacteria WBC
 Helps in attachment to surface e.g. Streptococcus mutans (dental caries)
attach to teeth surface by secreting H2O insoluble glucan
Composition
 Polysaccharide (sugar)
 Made of single sugar called Homopolysaccharide
e.g. S mutans synthesize Glucan ( a polymer of glucose) from
sucrose
When capsule carry
charge (Sugar- uronic
acid)
Bacterial suspension by
preventing aggregating &
setting out
provide stability of
Heteropolysaccharide
synthesized from
sugar precursors
Attach to
Lipid carrier molecule and
transported across
Cytoplasmic membrane &
Polymerized outside cell
 Sheaths
 A group of chains/trichomes that are enclosed by hollow tube
 Found in species from fresh H2O and marine environment
 Can be readily seen when some cells migrated
 Prosthecae and Stalks
 Semi-rigid extensions of cell wall & cytoplasmic membrane
 Diameter less than cell
 Found in aerobic bacteria of fresh H2O e.g. Caulobacter
 SA of cells for nutrient absorption
 Stalk Ribbon like/tubular structure excreted by cell that helps
cell attachment to surface
 CELL WALL
 A rigid structure that gives shape to cell
 Remains beneath capsule/sheaths and flagella
Function
 Main function to prevent bacteria from expanding or bursting because of
uptake of H2O
 Due to cell wall
 Cell wall of G- bacteria (10-15 nm) thinner than G+ bacteria (20-25nm)
 Cell wall very important for bacterial growth and division
i.e. Protoplasts
Structure and chemical composition (Cell Wall)
Peptidologlycan
 Mostly Peptidolycan
 Insoluble , porous, cross-linked polymer
 Rigid structure and found in prokaryotes only
Retain original shape
when subject to high
pressure
To get isolated Cell wall for
analysis
Mechanical disintegration by
sonic/ultrasound treatment.
where walls
completely removed
incapable of Normal growth
and Division
 A “bag-shaped” molecule around cytoplasmic membrane
 Must be continuously degraded by hydrolytic enzyme to add polymer
Basic constituents A polymer of: N-acetylglucosamine
N-acetylmuramic acid
L- alanine
D-glutamine
Di-amino acid
Wall of Archaeobacteria
 No peptidoglycan
 Cell-wall and chemical composition different from Eubacteria
 Cell wall consists of: Proteins/glycoproteins/polysaccharide
Pseudomurein A polymer whose structure resembles eubacteria
peptidoglycon but differ in chemical composition. e.g.
Methanobacterium
Fig.8 Structure and chemical composition (Cell Wall)
Walls of G+ Eubacteria
 More peptidoglycan (than G- )
 50% of dry weight of wall (while 10% in G- )
Composition
Polysaccharide Covalently linked with Peptidoglycan that can be
extracted with hot HCl. e.g. Streptococcus pyogenes
Teichoic acid - Acidic polymer of ribitol or glycerol phosphate and
covalently bonded with Peptidoglycan (with
cold HCl)
- Bind Mg+ to protect bacteria from thermal injury (a
pool of cation and stabilize cytoplasmic
membrane)
Walls of G- Eubacteria
 More complex
 Contain an outer membrane that surround layer of peptidoglycan & high
lipid contents (11-22%)
 Outer membrane acts as impermeable barrier prevent
escape of Enzyme from space between Cytoplasmic membrane and
outer membrane
 serve as Barrier to external chemical and Enzyme that damage cell
 Protection against Lysozyme Destroy walls of G+ (by
dissolving Peptidoglycan)
Composition
 In G- cell wall is attached to peptidoglycan by Braun’s Lipoprotein
 The membrane bi layered structure that contains phospholipid,
Protein,
Lipo -Polysaccharide (LPS)
LPS
 Has toxic property (Endotoxin)
 Found in outer layer only
Fig.9 Structure and chemical composition (Cell Wall) of G
_
 Composed of 3 covalently linked parts:
Lipid A firmly embedded in membrane
Core polysaccharide located in membrane surface
Polysaccharide O antigens extend like whiskers from
membrane surface
Porins
 A channel in special proteins that helps passing of:
Nucleosides
Oligosaccharides
Monosaccharide
Peptide and Amino acid
 To penetrate large molecule i.e. vit B12
 As receptor for bacteriophage attachment
Structure internal to Cell Wall
Cytoplasmic membrane
 Membrane beneath cell wall
 Thickness 7.5nm (0.0075 m)
Composition
 Phospholipids (20-30%)
 Phospholipids form a bilayer in which most proteins are held called
Integral protein
 Integral proteins of membrane by detergents
Peripheral proteins mild treatments i.e. osmotic shock
 Lipid matrix of membrane has fluidity (helps components movement)
 Phospholipids difference in Eubacteria & Archaeobacteria
removed by destruction
removed
by
Phospholipids are Phosphoglyceride Polyisoprenoid branched chain lipid
 A hydrophobic barrier (inhibits penetration by H2O soluble molecule)
 Allow Passage of small molecules i.e. nutrients and waste products
 Contain ENZYME (respiratory metabolism and synthesis of capsular
cell wall components)
 Site for proton-motive (Impermeable to H+) force that drive ATP
synthesis
Protoplast
 Consists of cytoplasmic membrane and cell material bounded by it
Preparation
G+ bacteria
Bacteria in antibiotic
e.g. Penicillin
Lysozyme
Dissolve cell wall & gives
Protoplast
Prevention of cell wall formation
& gives Protoplast
Culturing
Bacteria normally occur in
hypotonic environment
Take up H2O by osmosis
& Expand
Bacteria Press
cytoplasm
membrane against
cell wall
Spheroplast
 Cell wall of G- differ from G+ by possessing a Outer membrane ;
because treated cell has 2 membranes (cytoplasmic membrane + outer
membrane) the cell is called Spheroplast
 Some bacteria i.e. mycoplasmae have no cell wall and bounded by
cytoplasmic membrane (these are parasite to animal/plants so live in
isotonic environment)
Membranous intrusions and intracellular membrane system
 Bacterial cell do not contain Membrane bound organelles i.e.
mitochondria and chloroplast
In absence of cell wall
Continuous expansion
Bursting of
protoplast
Prevented by an Isotonic
medium; These protoplast
are soft, fragile and
spherical
 Have special Invagination of cytoplasmic membrane with special
function
Cytoplasm Cell substance bound to cytoplasmic membrane. Divided
in:
Some G+ bacteria have
membrane invaginations in
convoluted tubes and
vesicles
Mesosomes
Some mesosomes deeply
penetrate into cytoplasm
are located middle of the
cell
Some show only shallow
penetration into
cytoplasm and not
associated with nuclear
material
Central Mesosomes; Involved
in DNA replication and division
Peripheral Mesosomes;
Involved in export of exocellular
Enzyme
Ribosome
 Macromolecular RNA protein and granular in size called Ribosome
 Proteins are synthesized on it
Chromatin Rich in DNA
Fluid portion
 Contain dissolved substance
 No endoplasmic reticulum like plants/animal and free of cytoplasm
70s units
Eucaryotic have 80s with 60s and 40s subunit
Ribosome after sedimentation
in centrifuge show
sedimentation co-efficient of
70 svedberg units (70S) and
2 sub units 50S and 30S

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Size, shape and arrangement of bacterial cell

  • 1. Size  Very small (0.5-1m)  Surface Area (SA)/ Volume ratio very high  Large SA helps to enter nutrients and leave waste  Small Volume impart high growth rate  (SA / VOLUME) ratio Disadvantage: SA/VOLUME ratio limits bacterial size Shape & Arrangement  Shape due to its rigid cell wall  Cells are: Mass of cell subs to be nourished close to cell surface No circulatory m/c needed to distribute nutrients Spherical (Cocci) Straight rods (Bacilli) Helically curved (Spirilla)
  • 3.  Some cells are Pleomorphic (variety in shapes)  Arrangement Cocci appear in various characteristic arrangements depending on Cell division and daughter cell  Diplobacilli Most occur in pairs or single i.e. Bacilli  Streptobacilli Form chains i.e. Bacillis subtilis  Trichomes Similar to chain but ↑ SA to contact with adjacent cells i.e. Saprospira grandis  Palisade arrangement Cells lined side by side i.e. Corynebacterium diphthetiae  Hyphae Long, branched, multinucleate filaments that collectively form Mycelium i.e. Streptomyces viridochromogenes
  • 5. Fig.3 Characteristics shapes of different bacteria
  • 6. Fig.4 Pleomorphic form of Arthrobacter
  • 7. Vibrioid and helical shape Bacteria < one twist or turn i.e. Genus Vibrio Bacteria > one twist or turn e.g. Spirochetes Flexible, can twist to change shape Spirilla Rigid  BACTERIAL STRUCTURE  A. Structure external to cell wall Flagella Description Hair-like helical structure that protrude through cell wall Much thinner than eucaryotes flagella or celia(0.01m) Simple structure Helps in motility/swimming Location Polar at one or both end of bacterium Lateral along sides
  • 8. Fig.5 Types of Flagella
  • 9. Fig.5 Different parts of Flagella
  • 10. Parts 3 parts:  Protein of filament is called Flagelin  Flagellum grows at its tip Mortility 1. Hydrodyamics of flagella  Small size of bacteria BLOCK inertia of H2O for propulsive force and viscosity of H2O (x 1000)  Bacteria propel by rotating helical flagella (e.g. like corkscrew)  Polar flagella can swim back and forth and can reverse direction by reversing Flagella rotation  Basal body (with cytoplasmic membrane)  Hook (with cell wall) composed of protein  Filament (long/helical structure) composed of subunit
  • 11. 2. Swimming and tumbling e.g. Petrichous flagella Swimming Rotate counter clockwise to form a bundle Tumbling Flagella reverse their rotation Portion acquire short wavelength and right handed configuration; Bundle flies apart exhibit a chaotic motion (crossed arrows) 3. Swimming mortality without flagella  Some helical bacteria exhibit swimming  They have gel like structure in cell Peri-plasmic flagella (axial fibrils) e.g. Spirochetes & Spiroplasm spp 4. Gliding mortality  Mortal with solid surface  Exhibits flexing motion (very slow) e.g. cytopbaga spp Mortality (in viscous medium) without Flagella
  • 12. Fig.6 Hydrodyamics of flagella (Swimming and tumbling )
  • 13. 5. Bacterial Chemotaxis Mortal bacteria capable of swimming towards or away from various chemical compound a phenomenon called Chemotaxis  Swimming towards chemical is +ve Chemotaxis  Swimming away is - ve Chemotaxis  Chemical may act as Attractant or Repellants  Stimulus is change Temporal gradient (concentration with time) 6. Phototaxis  Exhibit +ve phototaxis with: light intensities  Repelled by: light intensities e.g. Phototropic bacteria
  • 14.  Pili (fimbriae)  Hollow, non-helical filaments that are thinner, shorter and more numerous  Not helps in mortality (found in mortal and non mortal species)  F Pilus (special type) acts as port of entry of genetic material in mating  Attach to epithelial cell lining of Respiratory / Intestinal tract human infection  Capsules Description  A viscous substance forming a covering layer/envelop around cell (visible under Light microscope) “Capsule”  Too thin layer microcapsule  When too many cells embedded in common matrix the material is SLIME  Appear as amorphous gelatinous area  Highly H2O soluble (dissolves readily) in medium viscosity of broth
  • 15. Fig.7 Different parts & structure of bacterial cell
  • 16. Functions  Protect against temporary drying by binding H2O molecule  Bacteriophage attachment blocking  Anti-phagocytic i.e. inhibit engulfment of pathogenic bacteria WBC  Helps in attachment to surface e.g. Streptococcus mutans (dental caries) attach to teeth surface by secreting H2O insoluble glucan Composition  Polysaccharide (sugar)  Made of single sugar called Homopolysaccharide e.g. S mutans synthesize Glucan ( a polymer of glucose) from sucrose When capsule carry charge (Sugar- uronic acid) Bacterial suspension by preventing aggregating & setting out provide stability of Heteropolysaccharide synthesized from sugar precursors Attach to Lipid carrier molecule and transported across Cytoplasmic membrane & Polymerized outside cell
  • 17.  Sheaths  A group of chains/trichomes that are enclosed by hollow tube  Found in species from fresh H2O and marine environment  Can be readily seen when some cells migrated  Prosthecae and Stalks  Semi-rigid extensions of cell wall & cytoplasmic membrane  Diameter less than cell  Found in aerobic bacteria of fresh H2O e.g. Caulobacter  SA of cells for nutrient absorption  Stalk Ribbon like/tubular structure excreted by cell that helps cell attachment to surface  CELL WALL  A rigid structure that gives shape to cell  Remains beneath capsule/sheaths and flagella
  • 18. Function  Main function to prevent bacteria from expanding or bursting because of uptake of H2O  Due to cell wall  Cell wall of G- bacteria (10-15 nm) thinner than G+ bacteria (20-25nm)  Cell wall very important for bacterial growth and division i.e. Protoplasts Structure and chemical composition (Cell Wall) Peptidologlycan  Mostly Peptidolycan  Insoluble , porous, cross-linked polymer  Rigid structure and found in prokaryotes only Retain original shape when subject to high pressure To get isolated Cell wall for analysis Mechanical disintegration by sonic/ultrasound treatment. where walls completely removed incapable of Normal growth and Division
  • 19.  A “bag-shaped” molecule around cytoplasmic membrane  Must be continuously degraded by hydrolytic enzyme to add polymer Basic constituents A polymer of: N-acetylglucosamine N-acetylmuramic acid L- alanine D-glutamine Di-amino acid Wall of Archaeobacteria  No peptidoglycan  Cell-wall and chemical composition different from Eubacteria  Cell wall consists of: Proteins/glycoproteins/polysaccharide Pseudomurein A polymer whose structure resembles eubacteria peptidoglycon but differ in chemical composition. e.g. Methanobacterium
  • 20. Fig.8 Structure and chemical composition (Cell Wall)
  • 21. Walls of G+ Eubacteria  More peptidoglycan (than G- )  50% of dry weight of wall (while 10% in G- ) Composition Polysaccharide Covalently linked with Peptidoglycan that can be extracted with hot HCl. e.g. Streptococcus pyogenes Teichoic acid - Acidic polymer of ribitol or glycerol phosphate and covalently bonded with Peptidoglycan (with cold HCl) - Bind Mg+ to protect bacteria from thermal injury (a pool of cation and stabilize cytoplasmic membrane) Walls of G- Eubacteria  More complex  Contain an outer membrane that surround layer of peptidoglycan & high lipid contents (11-22%)
  • 22.  Outer membrane acts as impermeable barrier prevent escape of Enzyme from space between Cytoplasmic membrane and outer membrane  serve as Barrier to external chemical and Enzyme that damage cell  Protection against Lysozyme Destroy walls of G+ (by dissolving Peptidoglycan) Composition  In G- cell wall is attached to peptidoglycan by Braun’s Lipoprotein  The membrane bi layered structure that contains phospholipid, Protein, Lipo -Polysaccharide (LPS) LPS  Has toxic property (Endotoxin)  Found in outer layer only
  • 23. Fig.9 Structure and chemical composition (Cell Wall) of G _
  • 24.  Composed of 3 covalently linked parts: Lipid A firmly embedded in membrane Core polysaccharide located in membrane surface Polysaccharide O antigens extend like whiskers from membrane surface Porins  A channel in special proteins that helps passing of: Nucleosides Oligosaccharides Monosaccharide Peptide and Amino acid  To penetrate large molecule i.e. vit B12  As receptor for bacteriophage attachment
  • 25. Structure internal to Cell Wall Cytoplasmic membrane  Membrane beneath cell wall  Thickness 7.5nm (0.0075 m) Composition  Phospholipids (20-30%)  Phospholipids form a bilayer in which most proteins are held called Integral protein  Integral proteins of membrane by detergents Peripheral proteins mild treatments i.e. osmotic shock  Lipid matrix of membrane has fluidity (helps components movement)  Phospholipids difference in Eubacteria & Archaeobacteria removed by destruction removed by Phospholipids are Phosphoglyceride Polyisoprenoid branched chain lipid
  • 26.  A hydrophobic barrier (inhibits penetration by H2O soluble molecule)  Allow Passage of small molecules i.e. nutrients and waste products  Contain ENZYME (respiratory metabolism and synthesis of capsular cell wall components)  Site for proton-motive (Impermeable to H+) force that drive ATP synthesis Protoplast  Consists of cytoplasmic membrane and cell material bounded by it Preparation G+ bacteria Bacteria in antibiotic e.g. Penicillin Lysozyme Dissolve cell wall & gives Protoplast Prevention of cell wall formation & gives Protoplast Culturing Bacteria normally occur in hypotonic environment Take up H2O by osmosis & Expand Bacteria Press cytoplasm membrane against cell wall
  • 27. Spheroplast  Cell wall of G- differ from G+ by possessing a Outer membrane ; because treated cell has 2 membranes (cytoplasmic membrane + outer membrane) the cell is called Spheroplast  Some bacteria i.e. mycoplasmae have no cell wall and bounded by cytoplasmic membrane (these are parasite to animal/plants so live in isotonic environment) Membranous intrusions and intracellular membrane system  Bacterial cell do not contain Membrane bound organelles i.e. mitochondria and chloroplast In absence of cell wall Continuous expansion Bursting of protoplast Prevented by an Isotonic medium; These protoplast are soft, fragile and spherical
  • 28.  Have special Invagination of cytoplasmic membrane with special function Cytoplasm Cell substance bound to cytoplasmic membrane. Divided in: Some G+ bacteria have membrane invaginations in convoluted tubes and vesicles Mesosomes Some mesosomes deeply penetrate into cytoplasm are located middle of the cell Some show only shallow penetration into cytoplasm and not associated with nuclear material Central Mesosomes; Involved in DNA replication and division Peripheral Mesosomes; Involved in export of exocellular Enzyme
  • 29. Ribosome  Macromolecular RNA protein and granular in size called Ribosome  Proteins are synthesized on it Chromatin Rich in DNA Fluid portion  Contain dissolved substance  No endoplasmic reticulum like plants/animal and free of cytoplasm 70s units Eucaryotic have 80s with 60s and 40s subunit Ribosome after sedimentation in centrifuge show sedimentation co-efficient of 70 svedberg units (70S) and 2 sub units 50S and 30S