SlideShare a Scribd company logo
1 of 79
Download to read offline
BY:
MRS. MALI DHANASHRI R.
ASSISTANT PROFESSOR,
GES’S SIR DR. M. S. GOSAVI COLLEGE OF PHARMACEUTICAL
EDUCATION AND RESEACH
 Bacteria represent a large and diverse group of microorganisms
that can exist as single cells or as cell clusters.
 Bacteria prokaryotic microorganisms a single-celled microscopic
organisms that lack nuclei and other organized cell structures.
 "Bacteria" is the plural form of “bacterium”.
 The small size, simple design, and broad metabolic capabilities of
bacteria allow them to grow and divide very rapidly and to inhabit
and flourish in almost any environment.
 Both deoxyribonucleic acid (DNA) and Ribonucleic acid (RNA).
 Prokaryotic microorganisms
 Do not contain chlorophyll: need a host to supply food and also a
supportive environment
 Present in water, soil, air, food, and all natural environment.
 They can grow in a multiplicitynof environments ranging from
 hot sulphur springs (65 ° C) to deep freezers ( − 20 ° C),
 from high (pH 1) to low (pH 13) acidity and
 high (0.7 m) to low osmolarity (water).
 In addition, in both nutritionally rich (compost) and nutritionally
poor (distilled water) situations.
Terms Used To Describe Bacteria
MORPHOLOGY
 Bacteria display a wide diversity of shapes and sizes called morphologies
 Cannot be seen with human eyes (microscopic)
 Their presence was only first recognized in 1677, when the Dutch naturalist Antonie van
Leeuwenhoek saw microscopic organisms in a variety of substances with the aid of primitive
microscopes.
 Now bacteria are usually examined under light microscopes capable of more than 1,000-fold
magnification
 Details of their internal structure can be observed only with the aid of much more powerful
transmission electron microscopes.
 Unless special phase-contrast microscopes are used, bacteria have to be stained with a
coloured dye so that they will stand out from their background.
Cell size
The smallest free - living organisms
Their size being measured in micrometres (microns)
The size & shape vary between the dimensions of 0.75 to 4.0 μm.
The cocci diameter near about 1 μm
An average rod-shaped bacterium measures approximately 1 μm in
diameter and 4 Îźm in length.
They usually vary in size considerably from < 0.5 to 1.0 μm in
diameter to 10–20 μm in length in some of the longer spiral forms.
smallest bacteria- Mycoplasma, which measure about 0.1 to
0.25 Îźm in diameter, as small as the largest viruses.
E. coli, a normal inhabitant of the intestinal tract of humans
and animals, is about 2 Îźm long and 0.5 Îźm in diameter
Spherical cells of Staphylococcus aureus - up to 1 μm in
diameter.
Some bacteria are relatively large, such as Azotobacter,
which has diameters of 2 to 5 Îźm or more
Cell Shape
• On basis of shape, bacteria are
classified as follows….
Cocci
Bacilli
Vibrios
Spirilla
Spirochetes
Actinomycetes
Mycoplasams
Cocci
Cocci are small, spherical or oval in shape
In greek ‘kokkos’ means berry
E.g. Micrococcus
Bacilli
 They are rod in shapes.
 It is derived from greek word ‘Bacillum’ meaning
stick.
 Some of the bacilli the length of the cell may be
equal to width those are called coccobacilli
 E.g. Bracella
Vibrios
 Vibrios are comma in shaped,
curved rods
 E.g. Vibrio comma
Spirilla
Those are longer rigid rods
with several curves or coils.
Those are helical in shape &
rapid bodies.
E.g. Spirillum ruprem.
Spirochetes
 They are slender
& flexuous spiral
forms.
Acetinomycetes
 These are branching
filamentous bacteria.
 The characteristics shape due
to the presence of rigid cell
wall.
 E.g. Streptomyces species.
Mycoplasma
Those are cell wall deficient bacteria
So that, they do not have stable
morphology.
They occur as round or oval bodies
with interlacing fillaments.
Arrangement of Bacteria
• Cocci appears as several characteristics arrangement or
grouping.
1.Diplococci
2.Streptococci
3.Tetracocci
4.Staphylococci
5.Sarcinae
Cocci- Arrangement
Diplococci
They split in one plane and remains in pair.
Eg: diplococcus pneumoniae.
Streptococci
 These cells divide in one planes and remain
attached, to form chains.
 Eg: streptococcus lactis.
Tetracocci
They divide in two planes and live in
groups of four.
Eg: Gaffyka tetragena.
Staphylococci
Cocci cells divide in three planes in an
irregular pattern.
These cells produce bunches of cocci as
in grapes.
Eg: staphylococcus aureus,
staphylococcus albus.
Sarcinae
 Sarcinae cells divide in three
planes in a regular pattern.
 These cells produces a cuboidal
arrangement of group of a eight
cells.
 Eg: Micrococcus tetragena.
Bacilli- Arrangement
Arrangement of grouping formed by bacilli species
1. Diplobacilli
2. Streptobacilli
3. Trichomes
DIPLOBACILLI
Arrangement of groupings formed by
bacilli species are limited & those split
across their short axis.
They may appear as pair those called
Diplobacilli e.g.
klebisella pneumoniae
STREPTOBACILLI
Some bacilli species are
found in chain like structure
those called streptobacilli
e.g Bacillus subtilis.
TRICHOMES
Some bacilli species are found in chain like structure
but have much large area of contact between the
adjacent cells those are called trichomes
e.g.Saprospira species
Bacterial Structures
Flagella
Pili
Capsule
Plasma
Membrane
Cytoplasm
Cell Wall
Ribosomes
mesosomes
Inclusions
Spores
1. FLAGELLA
Flagella are long, slender, thin hair-like cytoplasmic
appendages,
which are responsible for the motility of bacteria.
These are the organs of locomotion.
They are 0.01 to 0.02 μm in diameter, 3 to 20 μm in
length.
Flagella are made up of a protein- flagellin.
 Flagella found in both Gram-positive &
negative bacteria.
 Few coccal forms, most bacilli & almost
all of the spirilla & vibrios are motile by
flagella.
 They can be seen by compound
microscope with special staining
technique & can be seen easily under
electron microscope & dark filled
microscope.
Flagellum
The flagellum has three basic parts ,
1. Filament
2. Hook
3. Basal body
• Filament is the thin, cylindrical, long outermost region with a
constant diameter.
• The protein in filament is flagellin similar to keratin, Mol. Wt 20,000-
40,000.
• The filament is attached to a slightly wider hook. It consist of diffent
proteins.
• The basal body is composed of a small central rod inserted into a
series of rings.
 Gram negative bacteria contain four rings
as L-ring, P-ring, S-ring, M-ring.
 Gram positive bacteria have only S and M
rings in basal body.
 L- ring is embedded in lipolysaccharide
layer of outer membrane
 P- ring in pepetidoglycan layer
 S- ring- Just above cytoplasmic membrane
( Semi position of membrane)
 M- ring- within cytoplasmic membrane
 Flagella may be seen on bacterial body in following manner.
1. Monotrichous: These bacteria have single polar flagellum.
 Eg: vibrio cholera
2. Lophotrichous: These bacteria have two or more flagella
 only at one end of the cell. Eg: pseudomonas fluorescence.
3. Amphitrichous: These bacteria have single polar flagella or
 tuft of flagella at both poles. Eg :Aquaspirillum serpens.
4. Peritrichous: Several flagella present all over
the surface of
 bacteria. Eg: Escherichia coli, Salmonella typhi.
Fimbriae
 Fimbriae are similar structure like flagella but not involved in
motility.
 shorter than flagella (3 μm).
 distributed over the entire surface of the cell.
 act primarily as adhesions & allow to microorganism to attach
to surface.
 Responsible for haemagglutination & cell clumping in
bacteria.
 Each bacteria possess 100 to 200 fimbriae
Pili
 Pili are hair-like microfibrils, 0.5 to 2 μm in length and 5 to 7
nm in diameter.
 thinner, shorter and more numerous than flagella.
 present only on gram negative cells.
 composed of protein known as pillin.
 unrelated to motility and are found on motile and non-motile
cells.
 Pili are usually longer than fimbriae and number only one or
two per cell.
 Pili play an important role in attachment to surfaces. Hence
pili is also called organ of adhesion.
 Specialized pili, the sex pili, allows the transfer of genetic
material from one bacteria to another in a process called
conjugation where they are called conjugation pili or "sex
pili"
Capsule
 Glycocalyx : sticky coating produced by many bacteria
covering the surface of cell.
 The glycocalyx is composed of polysaccharidesn(sugars) and
proteins.
 Bacteria synthesize loose amorphous organic exopolymer
which is deposited outside and tightly to cell wall
 The EPS(extracelluar polysaccharides) contains 2%
carbohydrate & 98% water so, they produce gummy exterior to
the cell.
 Morphologically two extreme forms exist…
i. Capsules and ii. Slime
 Capsules: which forms rigid, tightly & closely associated
with cell
 Slimes: which are loosely associated with cell.
 Capsulated bacteria produces smooth colonies and non
capsulated bacteria produces rough colonies on the
surface of agar media.
Function of capsule & slime
 They protect from desiccation.
 They provide a protection barrier against the penetration of
biocides.
 They protect against engulfment by phagocytes & protozoa.
 They may promote the stability of bacterial suspension by
preventing the cells from aggregation & settling.
 They may promote attachments of bacteria to surface.
Cell wall
 Cell wall is rigid structure which gives definite shape to cell (spherical, rod and
spiral).
 situated between the capsule and cytoplasmic membrane.
 It is about 10 – 20 nm in thickness and constitutes 20-30 % of dry weight of
cell.
 The cell wall cannot be seen by direct light microscopy and does not stain
easily by different staining reagents.
 Composed of peptidoglycan (polysaccharides + protein)
 Mycoplasma are bacteria that have no cell wall and therefore have no definite
shape.
 The cell wall of bacteria contains
diaminopimelic acid (DAP), muramic
acid and teichoic acid.
 These substances are joined together to
give rise to a complex polymeric
structure known as peptidoglycan or
murein or mucopeptide.
 Peptidoglycan is the major constituent
of the cell wall of gram positive bacteria
(50 to 90 %) where as in gram negative
bacterial cell wall its presence is only 5 -
10 %.
Peptidoglycan = (polysaccharides +
protein),
Peptidoglycan (murein) is a large macromolecules containing glycan (polysaccharide)
chains that are cross-linked by short peptide bridge.
peptidoglycan is made from polysaccharide chains
cross-linked by peptides containing D-amino acids
The glycan chain act as a backbone to peptidoglycan
Those short peptide bridge composed of alternating residues of
N-acetyl muramic acid (NAM) &
 N-acetyl glucosamine (NAG).
 Each molecule of NAM attached a tetrapeptide.
 Tetrapeptide consisting of the amino acids L-alanine, Dalanine, D-glutamic
acid & lycine or diaminopimelic acid (DAP).
 This glycan tetrapeptide repeat unit is cross -linked to adjacent glycan chain.
 This adjacent glycan chain occurs through a direct peptide linkage or a
peptide interbridge.
 The type & number of cross linking amino acids vary from organism to
organism.
Functions of cell wall
 Cell wall is involved in growth and cell division of bacteria.
 It gives shape to the cell.
 It gives protection to internal structure and acts as supporting layer.
 To prevent rupture of bacteria caused by osmotic pressure differences
between intra cellular and extra cellular environment.
 To provide support for flagella.
 To regulate a certain degree of passage of molecules into and out of the
cell.
 It serve as the sites of attachment for most bacterial viruses.
• On the basis of structure of cell wall, bacteria can be classified as
1. Gram-positive
2. Gram- negative
• The staining technique used to distinguish this bacteria is called as Gram staining
technique.
Gram Staining
 Developed in 1884 by Danish scientist Christian Gram.
 It is a differential stain.
 In this, bacteria are first stained with crystal violet, then
treated with a mordant - a solution that fixes the stain
inside the cell.
 Bacteria are then washed with a decolorizing agent, such
as alcohol, and counterstained with safranin, a light red
dye.
 Gram-positive bacteria are those that are stained dark blue or
violet by Gram staining.
 Gram-negative bacteria cannot retain the crystal violet stain,
instead take up the counterstain and appearred or pink.
 The walls of gram-positive bacteria have more peptidoglycans than
do gram-negative bacteria.
 Thus, gram-positive bacteria retain the original violet dye and
cannot be counterstained.
Gram-positive Cells
 Gram positive bacterial cell wall
consist of a single type of molecules.
 Cell wall thick near about 20 to 80 nm.
 In that present of 60 to 80 %
peptidoglycan.
 Gram positive walls frequently
contains acidic polysachrides are
called teichoic acids.
 Teichoic acid are either ribitol phosphate or glycerol
phosphate molecules that are connected by phosphodiester
bridge.
 In some gram positive bacteria glycerol-teichoic acids are
bound to lipids membrane and termed as lipoteichoic acid.
 Those lipoteichoic acid create infection by killing bacteria &
shows inflammation.
Gram-negative
• Gram negative cell wall are multilayered & complex type
structure.
• Gram negative cell wall consist 10 to 20 % peptidoglycan.
• In that second layer found outside the peptidoglycan
layer.
• This layer is asymmetrical & contains proteins,
lipoproteins, phospholipids & lipopolysaccharide (LPS).
• This outer layer is attached to
peptidoglycan & the other end is fixed in
the outer membrane.
• In the inner leaf of the outer layer conatins
phospholipids & it’s outer layer composed
with LPS (lipopoysaccharide), a
polysaccharide-lipid molecule.
• In gram negative cell, the LPS is an
important molecule because it determine
the antigenicity & it is extremely toxic to
animal cell.
• In the LPS molecules contains three
regions
• Lipid A linked to core polysaccharide by the molecule KDO
(ketodeoxyoctonate) & other end of core polysaccharide is the O-
polysaccharide.
• In the O-polysaccharide or O-antigen usually contains six-carbon sugars as
well as one or more usually deoxy sugars such as abequose
• In the lipid A components are gives toxic & pathogenic properties to the
gram-negative bacteria.
• Gram negative bacterial outer membrane is relatively permeable to small
molecules but not for enzymes or large molecules.
• The region between the outer surface of the cytoplasmic membrane & the
inner surface of the outer membrane is called the periplasm.
• outer membrane
• • Similar to the plasma membrane, but is less permeable .
• This membrane has tiny holes or openings called porins.
• Porins block the entrance of harmful chemicals and antibiotics, making G-ve
bacteria much more difficult to treat than G+ve cells.
• Composed of lipopolysaccharides (LPS).
• LPS is a harmful substance classified as an endotoxin.
• Lipopolysaccharides, which acts as an endotoxin, are composed of
polysaccharides and lipid A (responsible for much of the toxicity of G-ve
bacteria).
• These differences in structure can produce differences in antibiotic susceptibility
• Ex: vancomycin can kill only Gram +ve bacteria and is ineffective against Gram -
ve pathogens, such as Haemophilus influenzae or Pseudomonas aeruginosa.
• Cell wall
• If the bacterial cell wall is entirely removed, it is called a
protoplast while if it's partially removed, it is called a
spheroplast.
• Antibiotics such as penicillin inhibit the formation of
peptidoglycan cross-links in the bacterial cell wall.
• The enzyme lysozyme, found in human tears, also digests the
cell wall of bacteria and is the body‘s main defense against
eye infections.
CYTOPLASMICMEMBRANE
• The cytoplasmic (plasma) membrane is a thin ( 5 to 10
nm).
• It separates the cell wall and cytoplasm.
• It composed of phospholipids (20 to 30 %) and proteins (
60 to 70 %).
• Prokaryotic plasma membranes are less rigid than
eukaryotic membrane due to lack of sterols.
• The phospholipids molecules are arranged in two parallel rows, called a
phospholipid bilayer.
• Each phospholipid molecule contains a polar head & tail.
• Polar head composed of a phosphate group & glycerol.
• The non-polar tails are interior of the bilayer.
• numerous proteins moving within or upon this layer are primarily responsible for
transport of ions, nutrients and waste across the membrane.
Functions of cytoplasmic
membrane
• They including in transportation of
nutrients.
• It provides mechanical strength to the
bacterial cell.
• It helps in DNA replication.
• It contains the enzymes involved in
the biosynthesis ofmembrane lipids &
various macromolecules of the
bacterial cell wall.
Periplasmic space
• Gram-negative bacteria : space between the cytoplasmic
membrane and the cell wall and space found between cell wall and
the outer membrane
• Periplasm may constitute up to 40% of the total cell volume in G-ve
species.
• Gram-positive bacteria : space between the cytoplasmic
membrane and the cell wall.
• The periplasm is filled with water and proteins and is reminiscent of
the cytoplasm.
• However periplasm contains proteins
and other molecules distinct from those
in the cytoplasm because the membrane
prevents the free exchange between
these two compartments.
• Periplasmic proteins have various
functions in cellular processes including:
transport, degradation, and motility.
• Periplasm controls molecular traffic
entering and leaving the cell.
Cytoplasm
• Portion of the cell that lies within the PM
• substances within the plasma membrane, excluding the genetic material.
• Gel-like matrix composed of mostly water(4/5 th ), enzymes, nutrients,
wastes, and gases
• The bacterial cytoplasm is a suspension of organic, inorganic solutes in a
viscous water solution.
• The cytoplasm of bacteria differs from that of higher eukaryotic
microorganisms in not containing endoplasmic reticulum, Golgi apparatus,
mitochondria and lysosomes.
• • It contains the ribosomes, proteins and other water soluble components and
reserve material.
• • In most bacterial, extrachromosal DNA ( plasmid DNA ) is also present.
• It is relatively featureless by electron microscope - although small granules can
be seen.
• • carries out very important functions for the cell - growth, metabolism, and
replication .
Constituents
• Proteins including enzymes
• Vitamins
• Ions
• Nucleic acids and their precursors
• Amino acids and their precursors
• Sugars, carbohydrates and their derivatives
• Fatty acids and their derivatives
Mesosomes
• Mesosomes are respiratory sites of bacteria.
• The mesosomes are attached to the bacterial chromosomes and is involved in DNA segregation
during cell division.
• They are predominant in Gram positive bacteria.
• In most of the bacteria, particularly in Gram-positive bacteria the growth condition depending
upon the membrane appears to be infolded at more than one point.
• Such infoldings are called mesosomes.
• Mesosomes presents in two types…
• In central (septal) mesosomes & peripheral (lateral) mesosomes
• Central mesosomes present deep into the
cytoplasm & locate near the middle of the
cell.
• These are involved in the DNA segregation &
in the formation of cross walls during cell
division.
• The peripheral mesosomes are not present
at central location & are not associated with
nuclear material.
• Mesosomes are also called as chondroids
& are visible only under electron
microscope.
• Larger numbers of mesosomes have a
Nucleoid
• Unlike the eukaryotic (true) cells, bacteria do not have a membrane enclosed
nucleus.
• The nucleoid is a region of cytoplasm where the chromosomal DNA is located.
• It is not a membrane bound nucleus, but simply an area of the cytoplasm where
the strands of DNA are found.
• The genome consists of a single molecule of double stranded DNA arrangement
in a circle.
• The bacterial chromosome is haploid & replicated by simple fission instead of
mitosis as in an eukaryotic cell.
Plasmids
• small extra-chromosomal DNA
• contain genes for antibiotic resistance or virulence.
• Structure Similar to most bacterial chromosomes, but considerably smaller.
• plasmids are covalently closed circular DNA
• In a few species linear plasmids have been found.
• Size : Chromosomal DNA is typically about 4000 kb,
• plasmid DNA ranges from 1-200 kb.
• • Number of plasmids: 1-700 copies of plasmid in a cell.
Plasmid Function
• The function of plasmids is not always known, but they are not normally
essential for survival of host, although their presence generally gives the host
some advantage.
• Antibiotic resistance - Some plasmids code for proteins that degrade
antibiotics-a big advantage for pathogens.
• Some encode for proteins which confer virulence factors on the host. For
example- E. coli plasmid Ent P307 codes for an enterotoxin which makes E.
coli pathogenic.
• Conjugative plasmids - These allow exchange of DNA between bacterial
cells.
• Plasmids and the associated traits can be transferred between bacteria, even
from one bacterial species to another.
• Plasmids are not involved in reproduction.
• Plasmids replicate independently of the chromosome.
• Plasmids are passed to other bacteria by two means.
• For most plasmid types, copies in the cytoplasm are passed on to daughter
cells during binary fission.
• Other types of plasmids ,form tube like structure at the surface called a pilus
that passes copies of the plasmid to other bacteria during conjugation, a
process by which bacteria exchange genetic information.
• Plasmids have been shown to be instrumental in the transmission of
special properties, such as antibiotic drug resistance, resistance to
heavy metals, and virulence factors necessary for infection of
animal or plant hosts.
• The ability to insert specific genes into plasmids have made them
extremely useful tools in the area of genetic engineering/RDNA
Technology
Ribosomes
• Ribosomes are most important structure in bacterial cytoplasm.
• They involved in protein synthesis.
• Ribosomes numbers varies with the rate of protein synthesis.
• If greater the number of ribosomes then the greater the protein synthesis.
• They have 200 Ao in diameter.
• They are characterised by their sedimentation properties.
• These bacterial ribosomes are called as 70 S ribosomes.
• S= svedberg unit..unit of sedimentation.
• After sedimentation carried in ultra-centrifuge & then placed
• in low concentration of magnesium that time 70 S ribosomes
• dissociated into 50 S & 30 S particles.
• Each 50 S particles contain…one molecule of 23 S RNA, one
• molecule of 5 S RNA & 32 different proteins.
• And, each 30 S particles contains…one molecule of 16 S RNA &
• 21 different proteins.
• During protein synthesis these ribosomes are associated with
• the m-RNA & such association are called polysomes
• This 70s ribosomes are made up of two subunits namely a large subunits 50s and a small subunit 30s.
• During active protein synthesis the ribosomes are associated with mRNA and such associations are called polysomes.
• They translate the genetic code from the molecular language of nucleic
• acid to that of amino acids—the building blocks of proteins.
• • Bacterial ribosomes are similar to those of eukaryotes, but are smaller and
• have a slightly different composition and molecular structure.
• • Bacterial ribosomes are never bound to other organelles as they
• sometimes are bound to the endoplasmic reticulum in eukaryotes, but are
• free-standing structures distributed throughout the cytoplasm.
• • There are sufficient differences between bacterial ribosomes and eukaryotic ribosomes that some antibiotics will
inhibit the functioning of bacterial ribosomes, but not a eukaryote's, thus killing bacteria but not the eukaryotic
organisms they are infecting.
• • Streptomycin binds 70S ribosome and stops protein synthesis but it can not bind 80S ribosome of eukaryotes and
thereby eukaryotic cell remains unaffected.
Bacterial Chromosome - Genophore
• • The bacterial chromosome consists of a single,
• circle of deoxyribonucleic acid.
• • DNA is double stranded- two strands line up
• antiparrallel to each other and the bases are
• linked together with hydrogen bonds.
• • It includes most of the genetic material of the
• organism .
Inclusion bodies
• Inclusion bodies: Bacteria can have within their cytoplasm a variety of small
bodies collectively referred to as inclusion bodies.
• Some are called granules and other are called vesicles.
• Inclusions are considered to be nonliving components of the cell that do not
possess metabolic activity and are not bounded by membranes.
• The most common inclusions are glycogen, lipid droplets, crystals, and
pigments.
Inclusion bodies - Granules
• Granules: Densely compacted substances without a membrane covering.
• Nutrients and reserves may be stored in the cytoplasm in the form of glycogen,
lipids, polyphosphate, or in some cases, sulfur or nitrogen for later use.
• Each granule contains specific substances, such as glycogen (glucose
polymer) and polyphosphate (phosphate polymer, supplies energy to metabolic
processes).
• Sulfur bacteria contains reserve granules of sulfur.
• These granules are depleted in starvation
Inclusion bodies-vesicles
• Some aquatic photosynthetic bacteria and cyano bacteria have rigid gas-filled
vacuoles and it helps in floating at a certain level - allowing them to move up or
down into water layers with different light intensities and nutrient levels.
• Some magnetotactic bacterium, eg Aquaspirillium magnetotacticum , stores
Magnetitite (Ferric oxide).
• The presence of such magnetic inclusions enables these bacteria to responds to
magnetic fields.
Spores
• Many bacterial species produce spores inside the cell & outside the
cell.
• endospores Inside the spores are called & outside the spores are
called exospores. E.g Bacillus anthracis, Bacillus subtilis etc.
• Spores are extremely resistant to desiccation, staining, radiation,
disinfecting chemicals & heat.
• Each bacterial spore on germination forms a single vegetative cell.
• The process of endospore formation is known as sporulation and it
may take 4 to 8 hours in a vegetative cell.
• Endospores are thick-walled, highly refractile bodies that are
produced one per cell.
• They remain viable for long time & help bacteria to survive for long
period under unfavourable condition.
• Endospore can remain dormant for thousand of years.
• Spores of all medically important bacteria are destroyed by moist
heat sterilization ( autoclave ) at 121 °C for 20 minutes.
• All the endospores contain large
amount of DPA (dipicolinic acid).
• It occurs in combination with large
amount of calcium, which is present in
central part of the spore (core).
• Calcium & DPA complex play
important role in the heat resistant of
endospores.
• Endospores consists of a core or envelope or protoplast.
• In the core or protoplast consist of DNA & ribosomes, t-RNA &
enzymes.
• The spore envelop consist of the inner membrane, outer membrane,
cortex & spore coat.
• In some species have the outer layer called exosporium which bears
ridges & fold.
SPORULATION
• The process of endospore formation is known as
sporulation
• It may take 4 to 8 hrs in a vegetative cell.
• Sporulation process
• Firstly the bacterial chromosomes replicate
• A newly replicated bacterial chromosomes & small portion
of cytoplasm are isolated by an in growth of the plasma
membrane called a spore septum.
• The septum derived from the cytoplasmic membrane
• It is then formed by a process of invagination which divides
into a forespore & sporangium.
• The forespore is subsequently encircled by a dividing septum
as a double layered membrane.
• Between the two layers is laid a spore cortex & outer layer is
transformed into spore coat which consists of several layer.
• After formation of spore mother cell is lyses to release it
bacteria-200824080643.pdf

More Related Content

Similar to bacteria-200824080643.pdf

Morphology of bacteria
Morphology of bacteriaMorphology of bacteria
Morphology of bacteriaSnehal Patel
 
structure & classification of microbes
structure & classification of microbesstructure & classification of microbes
structure & classification of microbesKHyati CHaudhari
 
EUBACTERIA :OVERVIEW
EUBACTERIA :OVERVIEWEUBACTERIA :OVERVIEW
EUBACTERIA :OVERVIEWHimanshi Chauhan
 
What is bacteria?(Structures Present in Bacteria And their Functions | Prokar...
What is bacteria?(Structures Present in Bacteria And their Functions | Prokar...What is bacteria?(Structures Present in Bacteria And their Functions | Prokar...
What is bacteria?(Structures Present in Bacteria And their Functions | Prokar...sehriqayyum
 
Lecture 2:- Bacterial morphology , bacterial cell structure
Lecture 2:- Bacterial morphology , bacterial cell structureLecture 2:- Bacterial morphology , bacterial cell structure
Lecture 2:- Bacterial morphology , bacterial cell structureRaghda alomari
 
General Biology - Ultra structure of Prokaryotes - Dr. S. Ganesh
General Biology  - Ultra structure of Prokaryotes - Dr. S. GaneshGeneral Biology  - Ultra structure of Prokaryotes - Dr. S. Ganesh
General Biology - Ultra structure of Prokaryotes - Dr. S. GaneshGanesh Sekaran
 
structure of mo.pptx
structure of mo.pptxstructure of mo.pptx
structure of mo.pptxDiptiPriya6
 
basic introdution on bacteria.pdf
basic introdution on bacteria.pdfbasic introdution on bacteria.pdf
basic introdution on bacteria.pdfShubhamkumarMaurya7
 
MORPHOLOGY OF BACTERIA AND FUNGI.pptx
MORPHOLOGY OF BACTERIA AND FUNGI.pptxMORPHOLOGY OF BACTERIA AND FUNGI.pptx
MORPHOLOGY OF BACTERIA AND FUNGI.pptxMeghaVysakh
 
2. General characteristics of microbes (Microbiology)
2. General characteristics of microbes (Microbiology)2. General characteristics of microbes (Microbiology)
2. General characteristics of microbes (Microbiology)Jay Khaniya
 
Morph and nature of bacteria
Morph and nature of bacteriaMorph and nature of bacteria
Morph and nature of bacteriaBruno Mmassy
 
Unit 1 cell biology
Unit 1 cell biologyUnit 1 cell biology
Unit 1 cell biologyNusrat Gulbarga
 
Unicellular microorganism
Unicellular microorganismUnicellular microorganism
Unicellular microorganismMacVasquez
 
Chapter 4 prokaryotic profiles micro 1
Chapter 4 prokaryotic profiles micro 1Chapter 4 prokaryotic profiles micro 1
Chapter 4 prokaryotic profiles micro 1Erika Brockmann
 
Introduction to microbiology, Bacterial Cell wall, Difference between Gram p...
Introduction to microbiology,  Bacterial Cell wall, Difference between Gram p...Introduction to microbiology,  Bacterial Cell wall, Difference between Gram p...
Introduction to microbiology, Bacterial Cell wall, Difference between Gram p...Zunaira Gillani
 
1) Strategies and structuresIn Protozoans the method of movement .pdf
1) Strategies and structuresIn Protozoans the method of movement .pdf1) Strategies and structuresIn Protozoans the method of movement .pdf
1) Strategies and structuresIn Protozoans the method of movement .pdfaptelecom16999
 
1. Introduction Microbiology.pdf
1. Introduction Microbiology.pdf1. Introduction Microbiology.pdf
1. Introduction Microbiology.pdfGOALLWORLD
 

Similar to bacteria-200824080643.pdf (20)

Morphology of bacteria
Morphology of bacteriaMorphology of bacteria
Morphology of bacteria
 
structure & classification of microbes
structure & classification of microbesstructure & classification of microbes
structure & classification of microbes
 
bacterial cell.pptx
bacterial cell.pptxbacterial cell.pptx
bacterial cell.pptx
 
EUBACTERIA :OVERVIEW
EUBACTERIA :OVERVIEWEUBACTERIA :OVERVIEW
EUBACTERIA :OVERVIEW
 
What is bacteria?(Structures Present in Bacteria And their Functions | Prokar...
What is bacteria?(Structures Present in Bacteria And their Functions | Prokar...What is bacteria?(Structures Present in Bacteria And their Functions | Prokar...
What is bacteria?(Structures Present in Bacteria And their Functions | Prokar...
 
Lecture 2:- Bacterial morphology , bacterial cell structure
Lecture 2:- Bacterial morphology , bacterial cell structureLecture 2:- Bacterial morphology , bacterial cell structure
Lecture 2:- Bacterial morphology , bacterial cell structure
 
General Biology - Ultra structure of Prokaryotes - Dr. S. Ganesh
General Biology  - Ultra structure of Prokaryotes - Dr. S. GaneshGeneral Biology  - Ultra structure of Prokaryotes - Dr. S. Ganesh
General Biology - Ultra structure of Prokaryotes - Dr. S. Ganesh
 
structure of mo.pptx
structure of mo.pptxstructure of mo.pptx
structure of mo.pptx
 
Study of bacteria
Study of bacteriaStudy of bacteria
Study of bacteria
 
Topic 2 bacteria
Topic 2 bacteriaTopic 2 bacteria
Topic 2 bacteria
 
basic introdution on bacteria.pdf
basic introdution on bacteria.pdfbasic introdution on bacteria.pdf
basic introdution on bacteria.pdf
 
MORPHOLOGY OF BACTERIA AND FUNGI.pptx
MORPHOLOGY OF BACTERIA AND FUNGI.pptxMORPHOLOGY OF BACTERIA AND FUNGI.pptx
MORPHOLOGY OF BACTERIA AND FUNGI.pptx
 
2. General characteristics of microbes (Microbiology)
2. General characteristics of microbes (Microbiology)2. General characteristics of microbes (Microbiology)
2. General characteristics of microbes (Microbiology)
 
Morph and nature of bacteria
Morph and nature of bacteriaMorph and nature of bacteria
Morph and nature of bacteria
 
Unit 1 cell biology
Unit 1 cell biologyUnit 1 cell biology
Unit 1 cell biology
 
Unicellular microorganism
Unicellular microorganismUnicellular microorganism
Unicellular microorganism
 
Chapter 4 prokaryotic profiles micro 1
Chapter 4 prokaryotic profiles micro 1Chapter 4 prokaryotic profiles micro 1
Chapter 4 prokaryotic profiles micro 1
 
Introduction to microbiology, Bacterial Cell wall, Difference between Gram p...
Introduction to microbiology,  Bacterial Cell wall, Difference between Gram p...Introduction to microbiology,  Bacterial Cell wall, Difference between Gram p...
Introduction to microbiology, Bacterial Cell wall, Difference between Gram p...
 
1) Strategies and structuresIn Protozoans the method of movement .pdf
1) Strategies and structuresIn Protozoans the method of movement .pdf1) Strategies and structuresIn Protozoans the method of movement .pdf
1) Strategies and structuresIn Protozoans the method of movement .pdf
 
1. Introduction Microbiology.pdf
1. Introduction Microbiology.pdf1. Introduction Microbiology.pdf
1. Introduction Microbiology.pdf
 

More from dawitg2

bacterial plant pathogen jeyarajesh-190413122916.pptx
bacterial plant pathogen jeyarajesh-190413122916.pptxbacterial plant pathogen jeyarajesh-190413122916.pptx
bacterial plant pathogen jeyarajesh-190413122916.pptxdawitg2
 
unit1_practical-applications-of-biotechnology.ppt
unit1_practical-applications-of-biotechnology.pptunit1_practical-applications-of-biotechnology.ppt
unit1_practical-applications-of-biotechnology.pptdawitg2
 
Introduction-to-Plant-Cell-Culture-lec1.ppt
Introduction-to-Plant-Cell-Culture-lec1.pptIntroduction-to-Plant-Cell-Culture-lec1.ppt
Introduction-to-Plant-Cell-Culture-lec1.pptdawitg2
 
fertilizers-150111082613-conversion-gate01.pdf
fertilizers-150111082613-conversion-gate01.pdffertilizers-150111082613-conversion-gate01.pdf
fertilizers-150111082613-conversion-gate01.pdfdawitg2
 
sac-301-manuresfertilizersandsoilfertilitymanagement-210105122952.pdf
sac-301-manuresfertilizersandsoilfertilitymanagement-210105122952.pdfsac-301-manuresfertilizersandsoilfertilitymanagement-210105122952.pdf
sac-301-manuresfertilizersandsoilfertilitymanagement-210105122952.pdfdawitg2
 
davindergill 135021014 -170426133338.pdf
davindergill 135021014 -170426133338.pdfdavindergill 135021014 -170426133338.pdf
davindergill 135021014 -170426133338.pdfdawitg2
 
preparationofdifferentagro-chemicaldosesforfield-140203005533-phpapp02.pdf
preparationofdifferentagro-chemicaldosesforfield-140203005533-phpapp02.pdfpreparationofdifferentagro-chemicaldosesforfield-140203005533-phpapp02.pdf
preparationofdifferentagro-chemicaldosesforfield-140203005533-phpapp02.pdfdawitg2
 
pesticide stoeage storage ppwscript.ppt
pesticide stoeage storage  ppwscript.pptpesticide stoeage storage  ppwscript.ppt
pesticide stoeage storage ppwscript.pptdawitg2
 
-pre-cautions--on--seed-storage--1-.pptx
-pre-cautions--on--seed-storage--1-.pptx-pre-cautions--on--seed-storage--1-.pptx
-pre-cautions--on--seed-storage--1-.pptxdawitg2
 
Intgrated pest management 02 _ 06_05.pdf
Intgrated pest management 02 _ 06_05.pdfIntgrated pest management 02 _ 06_05.pdf
Intgrated pest management 02 _ 06_05.pdfdawitg2
 
major potato and tomato disease in ethiopia .pptx
major potato and tomato disease in ethiopia .pptxmajor potato and tomato disease in ethiopia .pptx
major potato and tomato disease in ethiopia .pptxdawitg2
 
pesticide formulation pp602lec1to2-211207073233.pdf
pesticide formulation pp602lec1to2-211207073233.pdfpesticide formulation pp602lec1to2-211207073233.pdf
pesticide formulation pp602lec1to2-211207073233.pdfdawitg2
 
diseasespests-2013-130708184617-phpapp02.pptx
diseasespests-2013-130708184617-phpapp02.pptxdiseasespests-2013-130708184617-phpapp02.pptx
diseasespests-2013-130708184617-phpapp02.pptxdawitg2
 
pesticide pp602lec1to2-211207073233.pptx
pesticide pp602lec1to2-211207073233.pptxpesticide pp602lec1to2-211207073233.pptx
pesticide pp602lec1to2-211207073233.pptxdawitg2
 
agricultaraly important agrochemicals.ppt
agricultaraly important agrochemicals.pptagricultaraly important agrochemicals.ppt
agricultaraly important agrochemicals.pptdawitg2
 
agri pesticide chemistry-180722174627.pdf
agri pesticide chemistry-180722174627.pdfagri pesticide chemistry-180722174627.pdf
agri pesticide chemistry-180722174627.pdfdawitg2
 
372922285 -important Fungal-Nutrition.ppt
372922285 -important Fungal-Nutrition.ppt372922285 -important Fungal-Nutrition.ppt
372922285 -important Fungal-Nutrition.pptdawitg2
 
disease development and pathogenesis-201118142432.pptx
disease development and pathogenesis-201118142432.pptxdisease development and pathogenesis-201118142432.pptx
disease development and pathogenesis-201118142432.pptxdawitg2
 
ppp211lecture8-221211055228-824cf9da.pptx
ppp211lecture8-221211055228-824cf9da.pptxppp211lecture8-221211055228-824cf9da.pptx
ppp211lecture8-221211055228-824cf9da.pptxdawitg2
 
defensemechanismsinplants-180308104711.pptx
defensemechanismsinplants-180308104711.pptxdefensemechanismsinplants-180308104711.pptx
defensemechanismsinplants-180308104711.pptxdawitg2
 

More from dawitg2 (20)

bacterial plant pathogen jeyarajesh-190413122916.pptx
bacterial plant pathogen jeyarajesh-190413122916.pptxbacterial plant pathogen jeyarajesh-190413122916.pptx
bacterial plant pathogen jeyarajesh-190413122916.pptx
 
unit1_practical-applications-of-biotechnology.ppt
unit1_practical-applications-of-biotechnology.pptunit1_practical-applications-of-biotechnology.ppt
unit1_practical-applications-of-biotechnology.ppt
 
Introduction-to-Plant-Cell-Culture-lec1.ppt
Introduction-to-Plant-Cell-Culture-lec1.pptIntroduction-to-Plant-Cell-Culture-lec1.ppt
Introduction-to-Plant-Cell-Culture-lec1.ppt
 
fertilizers-150111082613-conversion-gate01.pdf
fertilizers-150111082613-conversion-gate01.pdffertilizers-150111082613-conversion-gate01.pdf
fertilizers-150111082613-conversion-gate01.pdf
 
sac-301-manuresfertilizersandsoilfertilitymanagement-210105122952.pdf
sac-301-manuresfertilizersandsoilfertilitymanagement-210105122952.pdfsac-301-manuresfertilizersandsoilfertilitymanagement-210105122952.pdf
sac-301-manuresfertilizersandsoilfertilitymanagement-210105122952.pdf
 
davindergill 135021014 -170426133338.pdf
davindergill 135021014 -170426133338.pdfdavindergill 135021014 -170426133338.pdf
davindergill 135021014 -170426133338.pdf
 
preparationofdifferentagro-chemicaldosesforfield-140203005533-phpapp02.pdf
preparationofdifferentagro-chemicaldosesforfield-140203005533-phpapp02.pdfpreparationofdifferentagro-chemicaldosesforfield-140203005533-phpapp02.pdf
preparationofdifferentagro-chemicaldosesforfield-140203005533-phpapp02.pdf
 
pesticide stoeage storage ppwscript.ppt
pesticide stoeage storage  ppwscript.pptpesticide stoeage storage  ppwscript.ppt
pesticide stoeage storage ppwscript.ppt
 
-pre-cautions--on--seed-storage--1-.pptx
-pre-cautions--on--seed-storage--1-.pptx-pre-cautions--on--seed-storage--1-.pptx
-pre-cautions--on--seed-storage--1-.pptx
 
Intgrated pest management 02 _ 06_05.pdf
Intgrated pest management 02 _ 06_05.pdfIntgrated pest management 02 _ 06_05.pdf
Intgrated pest management 02 _ 06_05.pdf
 
major potato and tomato disease in ethiopia .pptx
major potato and tomato disease in ethiopia .pptxmajor potato and tomato disease in ethiopia .pptx
major potato and tomato disease in ethiopia .pptx
 
pesticide formulation pp602lec1to2-211207073233.pdf
pesticide formulation pp602lec1to2-211207073233.pdfpesticide formulation pp602lec1to2-211207073233.pdf
pesticide formulation pp602lec1to2-211207073233.pdf
 
diseasespests-2013-130708184617-phpapp02.pptx
diseasespests-2013-130708184617-phpapp02.pptxdiseasespests-2013-130708184617-phpapp02.pptx
diseasespests-2013-130708184617-phpapp02.pptx
 
pesticide pp602lec1to2-211207073233.pptx
pesticide pp602lec1to2-211207073233.pptxpesticide pp602lec1to2-211207073233.pptx
pesticide pp602lec1to2-211207073233.pptx
 
agricultaraly important agrochemicals.ppt
agricultaraly important agrochemicals.pptagricultaraly important agrochemicals.ppt
agricultaraly important agrochemicals.ppt
 
agri pesticide chemistry-180722174627.pdf
agri pesticide chemistry-180722174627.pdfagri pesticide chemistry-180722174627.pdf
agri pesticide chemistry-180722174627.pdf
 
372922285 -important Fungal-Nutrition.ppt
372922285 -important Fungal-Nutrition.ppt372922285 -important Fungal-Nutrition.ppt
372922285 -important Fungal-Nutrition.ppt
 
disease development and pathogenesis-201118142432.pptx
disease development and pathogenesis-201118142432.pptxdisease development and pathogenesis-201118142432.pptx
disease development and pathogenesis-201118142432.pptx
 
ppp211lecture8-221211055228-824cf9da.pptx
ppp211lecture8-221211055228-824cf9da.pptxppp211lecture8-221211055228-824cf9da.pptx
ppp211lecture8-221211055228-824cf9da.pptx
 
defensemechanismsinplants-180308104711.pptx
defensemechanismsinplants-180308104711.pptxdefensemechanismsinplants-180308104711.pptx
defensemechanismsinplants-180308104711.pptx
 

Recently uploaded

Software Engineering Methodologies (overview)
Software Engineering Methodologies (overview)Software Engineering Methodologies (overview)
Software Engineering Methodologies (overview)eniolaolutunde
 
Computed Fields and api Depends in the Odoo 17
Computed Fields and api Depends in the Odoo 17Computed Fields and api Depends in the Odoo 17
Computed Fields and api Depends in the Odoo 17Celine George
 
POINT- BIOCHEMISTRY SEM 2 ENZYMES UNIT 5.pptx
POINT- BIOCHEMISTRY SEM 2 ENZYMES UNIT 5.pptxPOINT- BIOCHEMISTRY SEM 2 ENZYMES UNIT 5.pptx
POINT- BIOCHEMISTRY SEM 2 ENZYMES UNIT 5.pptxSayali Powar
 
call girls in Kamla Market (DELHI) 🔝 >༒9953330565🔝 genuine Escort Service 🔝✔️✔️
call girls in Kamla Market (DELHI) 🔝 >༒9953330565🔝 genuine Escort Service 🔝✔️✔️call girls in Kamla Market (DELHI) 🔝 >༒9953330565🔝 genuine Escort Service 🔝✔️✔️
call girls in Kamla Market (DELHI) 🔝 >༒9953330565🔝 genuine Escort Service 🔝✔️✔️9953056974 Low Rate Call Girls In Saket, Delhi NCR
 
Alper Gobel In Media Res Media Component
Alper Gobel In Media Res Media ComponentAlper Gobel In Media Res Media Component
Alper Gobel In Media Res Media ComponentInMediaRes1
 
_Math 4-Q4 Week 5.pptx Steps in Collecting Data
_Math 4-Q4 Week 5.pptx Steps in Collecting Data_Math 4-Q4 Week 5.pptx Steps in Collecting Data
_Math 4-Q4 Week 5.pptx Steps in Collecting DataJhengPantaleon
 
“Oh GOSH! Reflecting on Hackteria's Collaborative Practices in a Global Do-It...
“Oh GOSH! Reflecting on Hackteria's Collaborative Practices in a Global Do-It...“Oh GOSH! Reflecting on Hackteria's Collaborative Practices in a Global Do-It...
“Oh GOSH! Reflecting on Hackteria's Collaborative Practices in a Global Do-It...Marc Dusseiller Dusjagr
 
Biting mechanism of poisonous snakes.pdf
Biting mechanism of poisonous snakes.pdfBiting mechanism of poisonous snakes.pdf
Biting mechanism of poisonous snakes.pdfadityarao40181
 
The Most Excellent Way | 1 Corinthians 13
The Most Excellent Way | 1 Corinthians 13The Most Excellent Way | 1 Corinthians 13
The Most Excellent Way | 1 Corinthians 13Steve Thomason
 
CARE OF CHILD IN INCUBATOR..........pptx
CARE OF CHILD IN INCUBATOR..........pptxCARE OF CHILD IN INCUBATOR..........pptx
CARE OF CHILD IN INCUBATOR..........pptxGaneshChakor2
 
Introduction to ArtificiaI Intelligence in Higher Education
Introduction to ArtificiaI Intelligence in Higher EducationIntroduction to ArtificiaI Intelligence in Higher Education
Introduction to ArtificiaI Intelligence in Higher Educationpboyjonauth
 
Class 11 Legal Studies Ch-1 Concept of State .pdf
Class 11 Legal Studies Ch-1 Concept of State .pdfClass 11 Legal Studies Ch-1 Concept of State .pdf
Class 11 Legal Studies Ch-1 Concept of State .pdfakmcokerachita
 
Pharmacognosy Flower 3. Compositae 2023.pdf
Pharmacognosy Flower 3. Compositae 2023.pdfPharmacognosy Flower 3. Compositae 2023.pdf
Pharmacognosy Flower 3. Compositae 2023.pdfMahmoud M. Sallam
 
Solving Puzzles Benefits Everyone (English).pptx
Solving Puzzles Benefits Everyone (English).pptxSolving Puzzles Benefits Everyone (English).pptx
Solving Puzzles Benefits Everyone (English).pptxOH TEIK BIN
 
Crayon Activity Handout For the Crayon A
Crayon Activity Handout For the Crayon ACrayon Activity Handout For the Crayon A
Crayon Activity Handout For the Crayon AUnboundStockton
 
Final demo Grade 9 for demo Plan dessert.pptx
Final demo Grade 9 for demo Plan dessert.pptxFinal demo Grade 9 for demo Plan dessert.pptx
Final demo Grade 9 for demo Plan dessert.pptxAvyJaneVismanos
 
Sanyam Choudhary Chemistry practical.pdf
Sanyam Choudhary Chemistry practical.pdfSanyam Choudhary Chemistry practical.pdf
Sanyam Choudhary Chemistry practical.pdfsanyamsingh5019
 
A Critique of the Proposed National Education Policy Reform
A Critique of the Proposed National Education Policy ReformA Critique of the Proposed National Education Policy Reform
A Critique of the Proposed National Education Policy ReformChameera Dedduwage
 
EPANDING THE CONTENT OF AN OUTLINE using notes.pptx
EPANDING THE CONTENT OF AN OUTLINE using notes.pptxEPANDING THE CONTENT OF AN OUTLINE using notes.pptx
EPANDING THE CONTENT OF AN OUTLINE using notes.pptxRaymartEstabillo3
 

Recently uploaded (20)

Software Engineering Methodologies (overview)
Software Engineering Methodologies (overview)Software Engineering Methodologies (overview)
Software Engineering Methodologies (overview)
 
Computed Fields and api Depends in the Odoo 17
Computed Fields and api Depends in the Odoo 17Computed Fields and api Depends in the Odoo 17
Computed Fields and api Depends in the Odoo 17
 
Model Call Girl in Tilak Nagar Delhi reach out to us at 🔝9953056974🔝
Model Call Girl in Tilak Nagar Delhi reach out to us at 🔝9953056974🔝Model Call Girl in Tilak Nagar Delhi reach out to us at 🔝9953056974🔝
Model Call Girl in Tilak Nagar Delhi reach out to us at 🔝9953056974🔝
 
POINT- BIOCHEMISTRY SEM 2 ENZYMES UNIT 5.pptx
POINT- BIOCHEMISTRY SEM 2 ENZYMES UNIT 5.pptxPOINT- BIOCHEMISTRY SEM 2 ENZYMES UNIT 5.pptx
POINT- BIOCHEMISTRY SEM 2 ENZYMES UNIT 5.pptx
 
call girls in Kamla Market (DELHI) 🔝 >༒9953330565🔝 genuine Escort Service 🔝✔️✔️
call girls in Kamla Market (DELHI) 🔝 >༒9953330565🔝 genuine Escort Service 🔝✔️✔️call girls in Kamla Market (DELHI) 🔝 >༒9953330565🔝 genuine Escort Service 🔝✔️✔️
call girls in Kamla Market (DELHI) 🔝 >༒9953330565🔝 genuine Escort Service 🔝✔️✔️
 
Alper Gobel In Media Res Media Component
Alper Gobel In Media Res Media ComponentAlper Gobel In Media Res Media Component
Alper Gobel In Media Res Media Component
 
_Math 4-Q4 Week 5.pptx Steps in Collecting Data
_Math 4-Q4 Week 5.pptx Steps in Collecting Data_Math 4-Q4 Week 5.pptx Steps in Collecting Data
_Math 4-Q4 Week 5.pptx Steps in Collecting Data
 
“Oh GOSH! Reflecting on Hackteria's Collaborative Practices in a Global Do-It...
“Oh GOSH! Reflecting on Hackteria's Collaborative Practices in a Global Do-It...“Oh GOSH! Reflecting on Hackteria's Collaborative Practices in a Global Do-It...
“Oh GOSH! Reflecting on Hackteria's Collaborative Practices in a Global Do-It...
 
Biting mechanism of poisonous snakes.pdf
Biting mechanism of poisonous snakes.pdfBiting mechanism of poisonous snakes.pdf
Biting mechanism of poisonous snakes.pdf
 
The Most Excellent Way | 1 Corinthians 13
The Most Excellent Way | 1 Corinthians 13The Most Excellent Way | 1 Corinthians 13
The Most Excellent Way | 1 Corinthians 13
 
CARE OF CHILD IN INCUBATOR..........pptx
CARE OF CHILD IN INCUBATOR..........pptxCARE OF CHILD IN INCUBATOR..........pptx
CARE OF CHILD IN INCUBATOR..........pptx
 
Introduction to ArtificiaI Intelligence in Higher Education
Introduction to ArtificiaI Intelligence in Higher EducationIntroduction to ArtificiaI Intelligence in Higher Education
Introduction to ArtificiaI Intelligence in Higher Education
 
Class 11 Legal Studies Ch-1 Concept of State .pdf
Class 11 Legal Studies Ch-1 Concept of State .pdfClass 11 Legal Studies Ch-1 Concept of State .pdf
Class 11 Legal Studies Ch-1 Concept of State .pdf
 
Pharmacognosy Flower 3. Compositae 2023.pdf
Pharmacognosy Flower 3. Compositae 2023.pdfPharmacognosy Flower 3. Compositae 2023.pdf
Pharmacognosy Flower 3. Compositae 2023.pdf
 
Solving Puzzles Benefits Everyone (English).pptx
Solving Puzzles Benefits Everyone (English).pptxSolving Puzzles Benefits Everyone (English).pptx
Solving Puzzles Benefits Everyone (English).pptx
 
Crayon Activity Handout For the Crayon A
Crayon Activity Handout For the Crayon ACrayon Activity Handout For the Crayon A
Crayon Activity Handout For the Crayon A
 
Final demo Grade 9 for demo Plan dessert.pptx
Final demo Grade 9 for demo Plan dessert.pptxFinal demo Grade 9 for demo Plan dessert.pptx
Final demo Grade 9 for demo Plan dessert.pptx
 
Sanyam Choudhary Chemistry practical.pdf
Sanyam Choudhary Chemistry practical.pdfSanyam Choudhary Chemistry practical.pdf
Sanyam Choudhary Chemistry practical.pdf
 
A Critique of the Proposed National Education Policy Reform
A Critique of the Proposed National Education Policy ReformA Critique of the Proposed National Education Policy Reform
A Critique of the Proposed National Education Policy Reform
 
EPANDING THE CONTENT OF AN OUTLINE using notes.pptx
EPANDING THE CONTENT OF AN OUTLINE using notes.pptxEPANDING THE CONTENT OF AN OUTLINE using notes.pptx
EPANDING THE CONTENT OF AN OUTLINE using notes.pptx
 

bacteria-200824080643.pdf

  • 1. BY: MRS. MALI DHANASHRI R. ASSISTANT PROFESSOR, GES’S SIR DR. M. S. GOSAVI COLLEGE OF PHARMACEUTICAL EDUCATION AND RESEACH
  • 2.  Bacteria represent a large and diverse group of microorganisms that can exist as single cells or as cell clusters.  Bacteria prokaryotic microorganisms a single-celled microscopic organisms that lack nuclei and other organized cell structures.  "Bacteria" is the plural form of “bacterium”.  The small size, simple design, and broad metabolic capabilities of bacteria allow them to grow and divide very rapidly and to inhabit and flourish in almost any environment.
  • 3.  Both deoxyribonucleic acid (DNA) and Ribonucleic acid (RNA).  Prokaryotic microorganisms  Do not contain chlorophyll: need a host to supply food and also a supportive environment  Present in water, soil, air, food, and all natural environment.  They can grow in a multiplicitynof environments ranging from  hot sulphur springs (65 ° C) to deep freezers ( − 20 ° C),  from high (pH 1) to low (pH 13) acidity and  high (0.7 m) to low osmolarity (water).  In addition, in both nutritionally rich (compost) and nutritionally poor (distilled water) situations.
  • 4. Terms Used To Describe Bacteria
  • 5. MORPHOLOGY  Bacteria display a wide diversity of shapes and sizes called morphologies  Cannot be seen with human eyes (microscopic)  Their presence was only first recognized in 1677, when the Dutch naturalist Antonie van Leeuwenhoek saw microscopic organisms in a variety of substances with the aid of primitive microscopes.  Now bacteria are usually examined under light microscopes capable of more than 1,000-fold magnification  Details of their internal structure can be observed only with the aid of much more powerful transmission electron microscopes.  Unless special phase-contrast microscopes are used, bacteria have to be stained with a coloured dye so that they will stand out from their background.
  • 6. Cell size The smallest free - living organisms Their size being measured in micrometres (microns) The size & shape vary between the dimensions of 0.75 to 4.0 Îźm. The cocci diameter near about 1 Îźm An average rod-shaped bacterium measures approximately 1 Îźm in diameter and 4 Îźm in length. They usually vary in size considerably from < 0.5 to 1.0 Îźm in diameter to 10–20 Îźm in length in some of the longer spiral forms.
  • 7. smallest bacteria- Mycoplasma, which measure about 0.1 to 0.25 Îźm in diameter, as small as the largest viruses. E. coli, a normal inhabitant of the intestinal tract of humans and animals, is about 2 Îźm long and 0.5 Îźm in diameter Spherical cells of Staphylococcus aureus - up to 1 Îźm in diameter. Some bacteria are relatively large, such as Azotobacter, which has diameters of 2 to 5 Îźm or more
  • 8. Cell Shape • On basis of shape, bacteria are classified as follows…. Cocci Bacilli Vibrios Spirilla Spirochetes Actinomycetes Mycoplasams
  • 9. Cocci Cocci are small, spherical or oval in shape In greek ‘kokkos’ means berry E.g. Micrococcus
  • 10. Bacilli  They are rod in shapes.  It is derived from greek word ‘Bacillum’ meaning stick.  Some of the bacilli the length of the cell may be equal to width those are called coccobacilli  E.g. Bracella
  • 11. Vibrios  Vibrios are comma in shaped, curved rods  E.g. Vibrio comma
  • 12. Spirilla Those are longer rigid rods with several curves or coils. Those are helical in shape & rapid bodies. E.g. Spirillum ruprem.
  • 13. Spirochetes  They are slender & flexuous spiral forms.
  • 14. Acetinomycetes  These are branching filamentous bacteria.  The characteristics shape due to the presence of rigid cell wall.  E.g. Streptomyces species.
  • 15. Mycoplasma Those are cell wall deficient bacteria So that, they do not have stable morphology. They occur as round or oval bodies with interlacing fillaments.
  • 16. Arrangement of Bacteria • Cocci appears as several characteristics arrangement or grouping. 1.Diplococci 2.Streptococci 3.Tetracocci 4.Staphylococci 5.Sarcinae
  • 17. Cocci- Arrangement Diplococci They split in one plane and remains in pair. Eg: diplococcus pneumoniae. Streptococci  These cells divide in one planes and remain attached, to form chains.  Eg: streptococcus lactis.
  • 18. Tetracocci They divide in two planes and live in groups of four. Eg: Gaffyka tetragena. Staphylococci Cocci cells divide in three planes in an irregular pattern. These cells produce bunches of cocci as in grapes. Eg: staphylococcus aureus, staphylococcus albus.
  • 19. Sarcinae  Sarcinae cells divide in three planes in a regular pattern.  These cells produces a cuboidal arrangement of group of a eight cells.  Eg: Micrococcus tetragena.
  • 20. Bacilli- Arrangement Arrangement of grouping formed by bacilli species 1. Diplobacilli 2. Streptobacilli 3. Trichomes
  • 21. DIPLOBACILLI Arrangement of groupings formed by bacilli species are limited & those split across their short axis. They may appear as pair those called Diplobacilli e.g. klebisella pneumoniae
  • 22. STREPTOBACILLI Some bacilli species are found in chain like structure those called streptobacilli e.g Bacillus subtilis.
  • 23. TRICHOMES Some bacilli species are found in chain like structure but have much large area of contact between the adjacent cells those are called trichomes e.g.Saprospira species
  • 25. 1. FLAGELLA Flagella are long, slender, thin hair-like cytoplasmic appendages, which are responsible for the motility of bacteria. These are the organs of locomotion. They are 0.01 to 0.02 Îźm in diameter, 3 to 20 Îźm in length. Flagella are made up of a protein- flagellin.
  • 26.  Flagella found in both Gram-positive & negative bacteria.  Few coccal forms, most bacilli & almost all of the spirilla & vibrios are motile by flagella.  They can be seen by compound microscope with special staining technique & can be seen easily under electron microscope & dark filled microscope.
  • 27. Flagellum The flagellum has three basic parts , 1. Filament 2. Hook 3. Basal body
  • 28. • Filament is the thin, cylindrical, long outermost region with a constant diameter. • The protein in filament is flagellin similar to keratin, Mol. Wt 20,000- 40,000. • The filament is attached to a slightly wider hook. It consist of diffent proteins. • The basal body is composed of a small central rod inserted into a series of rings.
  • 29.  Gram negative bacteria contain four rings as L-ring, P-ring, S-ring, M-ring.  Gram positive bacteria have only S and M rings in basal body.  L- ring is embedded in lipolysaccharide layer of outer membrane  P- ring in pepetidoglycan layer  S- ring- Just above cytoplasmic membrane ( Semi position of membrane)  M- ring- within cytoplasmic membrane
  • 30.  Flagella may be seen on bacterial body in following manner. 1. Monotrichous: These bacteria have single polar flagellum.  Eg: vibrio cholera 2. Lophotrichous: These bacteria have two or more flagella  only at one end of the cell. Eg: pseudomonas fluorescence. 3. Amphitrichous: These bacteria have single polar flagella or  tuft of flagella at both poles. Eg :Aquaspirillum serpens. 4. Peritrichous: Several flagella present all over the surface of  bacteria. Eg: Escherichia coli, Salmonella typhi.
  • 31. Fimbriae  Fimbriae are similar structure like flagella but not involved in motility.  shorter than flagella (3 Îźm).  distributed over the entire surface of the cell.  act primarily as adhesions & allow to microorganism to attach to surface.  Responsible for haemagglutination & cell clumping in bacteria.  Each bacteria possess 100 to 200 fimbriae
  • 32. Pili  Pili are hair-like microfibrils, 0.5 to 2 Îźm in length and 5 to 7 nm in diameter.  thinner, shorter and more numerous than flagella.  present only on gram negative cells.  composed of protein known as pillin.  unrelated to motility and are found on motile and non-motile cells.
  • 33.  Pili are usually longer than fimbriae and number only one or two per cell.  Pili play an important role in attachment to surfaces. Hence pili is also called organ of adhesion.  Specialized pili, the sex pili, allows the transfer of genetic material from one bacteria to another in a process called conjugation where they are called conjugation pili or "sex pili"
  • 34. Capsule  Glycocalyx : sticky coating produced by many bacteria covering the surface of cell.  The glycocalyx is composed of polysaccharidesn(sugars) and proteins.  Bacteria synthesize loose amorphous organic exopolymer which is deposited outside and tightly to cell wall  The EPS(extracelluar polysaccharides) contains 2% carbohydrate & 98% water so, they produce gummy exterior to the cell.
  • 35.  Morphologically two extreme forms exist… i. Capsules and ii. Slime  Capsules: which forms rigid, tightly & closely associated with cell  Slimes: which are loosely associated with cell.  Capsulated bacteria produces smooth colonies and non capsulated bacteria produces rough colonies on the surface of agar media.
  • 36. Function of capsule & slime  They protect from desiccation.  They provide a protection barrier against the penetration of biocides.  They protect against engulfment by phagocytes & protozoa.  They may promote the stability of bacterial suspension by preventing the cells from aggregation & settling.  They may promote attachments of bacteria to surface.
  • 37. Cell wall  Cell wall is rigid structure which gives definite shape to cell (spherical, rod and spiral).  situated between the capsule and cytoplasmic membrane.  It is about 10 – 20 nm in thickness and constitutes 20-30 % of dry weight of cell.  The cell wall cannot be seen by direct light microscopy and does not stain easily by different staining reagents.  Composed of peptidoglycan (polysaccharides + protein)  Mycoplasma are bacteria that have no cell wall and therefore have no definite shape.
  • 38.  The cell wall of bacteria contains diaminopimelic acid (DAP), muramic acid and teichoic acid.  These substances are joined together to give rise to a complex polymeric structure known as peptidoglycan or murein or mucopeptide.  Peptidoglycan is the major constituent of the cell wall of gram positive bacteria (50 to 90 %) where as in gram negative bacterial cell wall its presence is only 5 - 10 %.
  • 39. Peptidoglycan = (polysaccharides + protein), Peptidoglycan (murein) is a large macromolecules containing glycan (polysaccharide) chains that are cross-linked by short peptide bridge. peptidoglycan is made from polysaccharide chains cross-linked by peptides containing D-amino acids The glycan chain act as a backbone to peptidoglycan Those short peptide bridge composed of alternating residues of N-acetyl muramic acid (NAM) &  N-acetyl glucosamine (NAG).
  • 40.  Each molecule of NAM attached a tetrapeptide.  Tetrapeptide consisting of the amino acids L-alanine, Dalanine, D-glutamic acid & lycine or diaminopimelic acid (DAP).  This glycan tetrapeptide repeat unit is cross -linked to adjacent glycan chain.  This adjacent glycan chain occurs through a direct peptide linkage or a peptide interbridge.  The type & number of cross linking amino acids vary from organism to organism.
  • 41. Functions of cell wall  Cell wall is involved in growth and cell division of bacteria.  It gives shape to the cell.  It gives protection to internal structure and acts as supporting layer.  To prevent rupture of bacteria caused by osmotic pressure differences between intra cellular and extra cellular environment.  To provide support for flagella.  To regulate a certain degree of passage of molecules into and out of the cell.  It serve as the sites of attachment for most bacterial viruses.
  • 42. • On the basis of structure of cell wall, bacteria can be classified as 1. Gram-positive 2. Gram- negative • The staining technique used to distinguish this bacteria is called as Gram staining technique.
  • 43. Gram Staining  Developed in 1884 by Danish scientist Christian Gram.  It is a differential stain.  In this, bacteria are first stained with crystal violet, then treated with a mordant - a solution that fixes the stain inside the cell.  Bacteria are then washed with a decolorizing agent, such as alcohol, and counterstained with safranin, a light red dye.
  • 44.  Gram-positive bacteria are those that are stained dark blue or violet by Gram staining.  Gram-negative bacteria cannot retain the crystal violet stain, instead take up the counterstain and appearred or pink.  The walls of gram-positive bacteria have more peptidoglycans than do gram-negative bacteria.  Thus, gram-positive bacteria retain the original violet dye and cannot be counterstained.
  • 45. Gram-positive Cells  Gram positive bacterial cell wall consist of a single type of molecules.  Cell wall thick near about 20 to 80 nm.  In that present of 60 to 80 % peptidoglycan.  Gram positive walls frequently contains acidic polysachrides are called teichoic acids.
  • 46.  Teichoic acid are either ribitol phosphate or glycerol phosphate molecules that are connected by phosphodiester bridge.  In some gram positive bacteria glycerol-teichoic acids are bound to lipids membrane and termed as lipoteichoic acid.  Those lipoteichoic acid create infection by killing bacteria & shows inflammation.
  • 47. Gram-negative • Gram negative cell wall are multilayered & complex type structure. • Gram negative cell wall consist 10 to 20 % peptidoglycan. • In that second layer found outside the peptidoglycan layer. • This layer is asymmetrical & contains proteins, lipoproteins, phospholipids & lipopolysaccharide (LPS).
  • 48. • This outer layer is attached to peptidoglycan & the other end is fixed in the outer membrane. • In the inner leaf of the outer layer conatins phospholipids & it’s outer layer composed with LPS (lipopoysaccharide), a polysaccharide-lipid molecule. • In gram negative cell, the LPS is an important molecule because it determine the antigenicity & it is extremely toxic to animal cell. • In the LPS molecules contains three regions
  • 49. • Lipid A linked to core polysaccharide by the molecule KDO (ketodeoxyoctonate) & other end of core polysaccharide is the O- polysaccharide. • In the O-polysaccharide or O-antigen usually contains six-carbon sugars as well as one or more usually deoxy sugars such as abequose • In the lipid A components are gives toxic & pathogenic properties to the gram-negative bacteria. • Gram negative bacterial outer membrane is relatively permeable to small molecules but not for enzymes or large molecules. • The region between the outer surface of the cytoplasmic membrane & the inner surface of the outer membrane is called the periplasm.
  • 50. • outer membrane • • Similar to the plasma membrane, but is less permeable . • This membrane has tiny holes or openings called porins. • Porins block the entrance of harmful chemicals and antibiotics, making G-ve bacteria much more difficult to treat than G+ve cells. • Composed of lipopolysaccharides (LPS). • LPS is a harmful substance classified as an endotoxin. • Lipopolysaccharides, which acts as an endotoxin, are composed of polysaccharides and lipid A (responsible for much of the toxicity of G-ve bacteria). • These differences in structure can produce differences in antibiotic susceptibility • Ex: vancomycin can kill only Gram +ve bacteria and is ineffective against Gram - ve pathogens, such as Haemophilus influenzae or Pseudomonas aeruginosa.
  • 51. • Cell wall • If the bacterial cell wall is entirely removed, it is called a protoplast while if it's partially removed, it is called a spheroplast. • Antibiotics such as penicillin inhibit the formation of peptidoglycan cross-links in the bacterial cell wall. • The enzyme lysozyme, found in human tears, also digests the cell wall of bacteria and is the body‘s main defense against eye infections.
  • 52. CYTOPLASMICMEMBRANE • The cytoplasmic (plasma) membrane is a thin ( 5 to 10 nm). • It separates the cell wall and cytoplasm. • It composed of phospholipids (20 to 30 %) and proteins ( 60 to 70 %). • Prokaryotic plasma membranes are less rigid than eukaryotic membrane due to lack of sterols.
  • 53. • The phospholipids molecules are arranged in two parallel rows, called a phospholipid bilayer. • Each phospholipid molecule contains a polar head & tail. • Polar head composed of a phosphate group & glycerol. • The non-polar tails are interior of the bilayer. • numerous proteins moving within or upon this layer are primarily responsible for transport of ions, nutrients and waste across the membrane.
  • 54. Functions of cytoplasmic membrane • They including in transportation of nutrients. • It provides mechanical strength to the bacterial cell. • It helps in DNA replication. • It contains the enzymes involved in the biosynthesis ofmembrane lipids & various macromolecules of the bacterial cell wall.
  • 55. Periplasmic space • Gram-negative bacteria : space between the cytoplasmic membrane and the cell wall and space found between cell wall and the outer membrane • Periplasm may constitute up to 40% of the total cell volume in G-ve species. • Gram-positive bacteria : space between the cytoplasmic membrane and the cell wall. • The periplasm is filled with water and proteins and is reminiscent of the cytoplasm.
  • 56. • However periplasm contains proteins and other molecules distinct from those in the cytoplasm because the membrane prevents the free exchange between these two compartments. • Periplasmic proteins have various functions in cellular processes including: transport, degradation, and motility. • Periplasm controls molecular traffic entering and leaving the cell.
  • 57. Cytoplasm • Portion of the cell that lies within the PM • substances within the plasma membrane, excluding the genetic material. • Gel-like matrix composed of mostly water(4/5 th ), enzymes, nutrients, wastes, and gases • The bacterial cytoplasm is a suspension of organic, inorganic solutes in a viscous water solution. • The cytoplasm of bacteria differs from that of higher eukaryotic microorganisms in not containing endoplasmic reticulum, Golgi apparatus, mitochondria and lysosomes.
  • 58. • • It contains the ribosomes, proteins and other water soluble components and reserve material. • • In most bacterial, extrachromosal DNA ( plasmid DNA ) is also present. • It is relatively featureless by electron microscope - although small granules can be seen. • • carries out very important functions for the cell - growth, metabolism, and replication .
  • 59. Constituents • Proteins including enzymes • Vitamins • Ions • Nucleic acids and their precursors • Amino acids and their precursors • Sugars, carbohydrates and their derivatives • Fatty acids and their derivatives
  • 60. Mesosomes • Mesosomes are respiratory sites of bacteria. • The mesosomes are attached to the bacterial chromosomes and is involved in DNA segregation during cell division. • They are predominant in Gram positive bacteria. • In most of the bacteria, particularly in Gram-positive bacteria the growth condition depending upon the membrane appears to be infolded at more than one point. • Such infoldings are called mesosomes. • Mesosomes presents in two types… • In central (septal) mesosomes & peripheral (lateral) mesosomes
  • 61. • Central mesosomes present deep into the cytoplasm & locate near the middle of the cell. • These are involved in the DNA segregation & in the formation of cross walls during cell division. • The peripheral mesosomes are not present at central location & are not associated with nuclear material. • Mesosomes are also called as chondroids & are visible only under electron microscope. • Larger numbers of mesosomes have a
  • 62. Nucleoid • Unlike the eukaryotic (true) cells, bacteria do not have a membrane enclosed nucleus. • The nucleoid is a region of cytoplasm where the chromosomal DNA is located. • It is not a membrane bound nucleus, but simply an area of the cytoplasm where the strands of DNA are found. • The genome consists of a single molecule of double stranded DNA arrangement in a circle. • The bacterial chromosome is haploid & replicated by simple fission instead of mitosis as in an eukaryotic cell.
  • 63. Plasmids • small extra-chromosomal DNA • contain genes for antibiotic resistance or virulence. • Structure Similar to most bacterial chromosomes, but considerably smaller. • plasmids are covalently closed circular DNA • In a few species linear plasmids have been found. • Size : Chromosomal DNA is typically about 4000 kb, • plasmid DNA ranges from 1-200 kb. • • Number of plasmids: 1-700 copies of plasmid in a cell.
  • 64. Plasmid Function • The function of plasmids is not always known, but they are not normally essential for survival of host, although their presence generally gives the host some advantage. • Antibiotic resistance - Some plasmids code for proteins that degrade antibiotics-a big advantage for pathogens. • Some encode for proteins which confer virulence factors on the host. For example- E. coli plasmid Ent P307 codes for an enterotoxin which makes E. coli pathogenic. • Conjugative plasmids - These allow exchange of DNA between bacterial cells.
  • 65. • Plasmids and the associated traits can be transferred between bacteria, even from one bacterial species to another. • Plasmids are not involved in reproduction. • Plasmids replicate independently of the chromosome. • Plasmids are passed to other bacteria by two means. • For most plasmid types, copies in the cytoplasm are passed on to daughter cells during binary fission. • Other types of plasmids ,form tube like structure at the surface called a pilus that passes copies of the plasmid to other bacteria during conjugation, a process by which bacteria exchange genetic information.
  • 66. • Plasmids have been shown to be instrumental in the transmission of special properties, such as antibiotic drug resistance, resistance to heavy metals, and virulence factors necessary for infection of animal or plant hosts. • The ability to insert specific genes into plasmids have made them extremely useful tools in the area of genetic engineering/RDNA Technology
  • 67. Ribosomes • Ribosomes are most important structure in bacterial cytoplasm. • They involved in protein synthesis. • Ribosomes numbers varies with the rate of protein synthesis. • If greater the number of ribosomes then the greater the protein synthesis. • They have 200 Ao in diameter. • They are characterised by their sedimentation properties.
  • 68. • These bacterial ribosomes are called as 70 S ribosomes. • S= svedberg unit..unit of sedimentation. • After sedimentation carried in ultra-centrifuge & then placed • in low concentration of magnesium that time 70 S ribosomes • dissociated into 50 S & 30 S particles. • Each 50 S particles contain…one molecule of 23 S RNA, one • molecule of 5 S RNA & 32 different proteins. • And, each 30 S particles contains…one molecule of 16 S RNA & • 21 different proteins. • During protein synthesis these ribosomes are associated with • the m-RNA & such association are called polysomes • This 70s ribosomes are made up of two subunits namely a large subunits 50s and a small subunit 30s. • During active protein synthesis the ribosomes are associated with mRNA and such associations are called polysomes.
  • 69. • They translate the genetic code from the molecular language of nucleic • acid to that of amino acids—the building blocks of proteins. • • Bacterial ribosomes are similar to those of eukaryotes, but are smaller and • have a slightly different composition and molecular structure. • • Bacterial ribosomes are never bound to other organelles as they • sometimes are bound to the endoplasmic reticulum in eukaryotes, but are • free-standing structures distributed throughout the cytoplasm. • • There are sufficient differences between bacterial ribosomes and eukaryotic ribosomes that some antibiotics will inhibit the functioning of bacterial ribosomes, but not a eukaryote's, thus killing bacteria but not the eukaryotic organisms they are infecting. • • Streptomycin binds 70S ribosome and stops protein synthesis but it can not bind 80S ribosome of eukaryotes and thereby eukaryotic cell remains unaffected.
  • 70. Bacterial Chromosome - Genophore • • The bacterial chromosome consists of a single, • circle of deoxyribonucleic acid. • • DNA is double stranded- two strands line up • antiparrallel to each other and the bases are • linked together with hydrogen bonds. • • It includes most of the genetic material of the • organism .
  • 71. Inclusion bodies • Inclusion bodies: Bacteria can have within their cytoplasm a variety of small bodies collectively referred to as inclusion bodies. • Some are called granules and other are called vesicles. • Inclusions are considered to be nonliving components of the cell that do not possess metabolic activity and are not bounded by membranes. • The most common inclusions are glycogen, lipid droplets, crystals, and pigments.
  • 72. Inclusion bodies - Granules • Granules: Densely compacted substances without a membrane covering. • Nutrients and reserves may be stored in the cytoplasm in the form of glycogen, lipids, polyphosphate, or in some cases, sulfur or nitrogen for later use. • Each granule contains specific substances, such as glycogen (glucose polymer) and polyphosphate (phosphate polymer, supplies energy to metabolic processes). • Sulfur bacteria contains reserve granules of sulfur. • These granules are depleted in starvation
  • 73. Inclusion bodies-vesicles • Some aquatic photosynthetic bacteria and cyano bacteria have rigid gas-filled vacuoles and it helps in floating at a certain level - allowing them to move up or down into water layers with different light intensities and nutrient levels. • Some magnetotactic bacterium, eg Aquaspirillium magnetotacticum , stores Magnetitite (Ferric oxide). • The presence of such magnetic inclusions enables these bacteria to responds to magnetic fields.
  • 74. Spores • Many bacterial species produce spores inside the cell & outside the cell. • endospores Inside the spores are called & outside the spores are called exospores. E.g Bacillus anthracis, Bacillus subtilis etc. • Spores are extremely resistant to desiccation, staining, radiation, disinfecting chemicals & heat. • Each bacterial spore on germination forms a single vegetative cell.
  • 75. • The process of endospore formation is known as sporulation and it may take 4 to 8 hours in a vegetative cell. • Endospores are thick-walled, highly refractile bodies that are produced one per cell. • They remain viable for long time & help bacteria to survive for long period under unfavourable condition. • Endospore can remain dormant for thousand of years. • Spores of all medically important bacteria are destroyed by moist heat sterilization ( autoclave ) at 121 °C for 20 minutes.
  • 76. • All the endospores contain large amount of DPA (dipicolinic acid). • It occurs in combination with large amount of calcium, which is present in central part of the spore (core). • Calcium & DPA complex play important role in the heat resistant of endospores. • Endospores consists of a core or envelope or protoplast. • In the core or protoplast consist of DNA & ribosomes, t-RNA & enzymes. • The spore envelop consist of the inner membrane, outer membrane, cortex & spore coat. • In some species have the outer layer called exosporium which bears ridges & fold.
  • 77. SPORULATION • The process of endospore formation is known as sporulation • It may take 4 to 8 hrs in a vegetative cell. • Sporulation process • Firstly the bacterial chromosomes replicate • A newly replicated bacterial chromosomes & small portion of cytoplasm are isolated by an in growth of the plasma membrane called a spore septum.
  • 78. • The septum derived from the cytoplasmic membrane • It is then formed by a process of invagination which divides into a forespore & sporangium. • The forespore is subsequently encircled by a dividing septum as a double layered membrane. • Between the two layers is laid a spore cortex & outer layer is transformed into spore coat which consists of several layer. • After formation of spore mother cell is lyses to release it