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PROPERTIES OF CELLS AND
CELL MEMBRANE
Dr. Pulipati Sowjanya
Professor & Head
Vignan Pharmacy College
Vadlamudi, Guntur (Dt)
The Discovery of Cells
All living things are made up of one or more cells.
• A cell is the smallest unit that can carry on all of the
processes of life.
Hooke
– In 1665, Robert Hooke discovered cells in slices of cork.
• Leeuwenhoek
– In 1673, Anton van Leeuwenhoek was the first to observe living cells in
microorganisms;
Leeuwenhoek called these organism animalcules~ we now call them
protists.
Cell Diversity
Cell Shape
– A cell’s shape reflects its function.
Cell Diversity
Cell Size
– Cell size is limited by a cell’s surface area–to volume ratio.
Cell Diversity
Cell Size
• Unicellular organisms are made up of one cell
• Multicellular organisms are made up of many cells that often
specialize according to function - differentiation
OVERVIEW OF CELL STRUCTURE
https://www.youtube.com/watch?v=URUJD5NEXC8&t=278s
Prokaryotic Cells
Cells lack a nucleus and
membrane bound organelles
-Includes bacteria
-Single, circular chromosome in
nucleoid region
-Surrounded by cell membrane
and a cell
wall made up of peptidoglycan
PROKARYOTE STRUCTURES
1. Appendages- flagella, pili, fimbrae
2. Cell envelope- glycocalyx, cell wall ,
cell membrane
3. Cytoplasm- ribosomes,
granules,
nucleoid/chromosome.
BACTERIAL APPENDAGES:
• Pili (pl), pilus (s)
–
–
only found in gram negative bacteria
tubulare, hairlike structures of protein larger
and more rare than fimbriae.
•
-
-
2 types of pili
attachment pilus - allow bacteria to attach to
other cells
sex pilus, - transfer from one bacterial cell to
another- conjugation.
FIMBRIAE
• fimbriae (pl) fimbria (s)
– Adhesion to cells and surfaces
– Responsible for biofilms.
– Pathogenesis of gonococcus and E.coli
Escherichia
coli.
FLAGELLA
• Flagella (pl), flagellum(s)
– long appendages which rotate by means of a "motor"
located just under the cytoplasmic membrane.
– bacteria may have one, a few, or many flagella in
different positions on the cell.
• Advantages
- chemotaxis - positive and negative.
- motility
• All spirilla, half of bacilli, rare cocci.
FLAGELLA
FLAGELLA
Three morphological
regions
•
–
–
Helical filament
long outermost region; composes up to 90% of its length
contains the globular (roughly spherical) protein flagellin
arranged in several chains and form a helix around a hollow
core
–
• Hooked or curved area
filament is attached; consists of a different protein
•
–
–
–
Basal body
terminal portion of the flagellum
fix the flagellum to the cell wall and plasma membrane
composed of a central rod inserted into a series of rings
Gram negative - 2 pairs of rings
•
•
Outer pair - fixed to the outer membrane and
peptidoglycan layer
Inner pair - fixed to the plasma membrane (SM ring)
Gram positive - only inner pair is present
MOTILITY
•
–
–
–
Types of bacterial motility
run or swim - when a bacterium moves in one direction
for a length of time
tumbles - periodic, abrupt random changes in direction
swarming - rapid wavelike growth across a solid culture
medium
•
Mechanism of flagellar movement - relative rotation
of the rings in the basal body of the flagellum
Antigenicity
–
flagellar or H antigen - useful in the serological
identification of serotypes of Salmonella organisms
ARRANGEMENTS
• Flagella vary in number and arrangement.
• Polar arrangment
– Monotrichious - 1 flagellum at one end
• Fastest; Pseudomonas -example
– Lophotrichious - tuft at one end
– Amphitrichious- bipolar
– Peritrichious - multiple flagella; randomly
dispersed around the bacterial cell
• E. coli - example
FLAGELLAR ARRANGEMENTS
A. Monotrichous
B. Lophotrichous
C. Amphitrichous
D. Peritrichous
E. Atrichous
AXIAL FILAMENTS
AXIAL FILAMENTS
•
tuft of fibrils that arise at the ends of
the cell under the outer membrane
and spiral around the cell
•
rotation an opposing of the outer
membrane movement that propels
the spirochetes by causing them to
move like corkscrews
Found in Spirochetes and are similar
to flagella, but are located between
the cell wall and an outer membrane,
and are attached to one end of the
organism.
EVIDENCE OF MOTILITY
Two ways by which motility can be demonstrated:
• direct or microscopic
– hanging drop preparation or wet mount preparation by dark field
mycroscope
– Distinguishes:
• Brownian movement - when the bacteria show molecular
movement
• true motility - if a bacterium describes a rotatory,
undulatory or sinuous movement
• indirect or macroscopic
– Stab inoculation of the semisolid media
• nonmotile - growth is limited at the point of inoculation
• motile - growth is diffuse or moves away from the line of
inoculation; turbidity of the medium
DETECTION OF MOTILITY
• Direct • Indirect
Presence mobile
bacteria
2. BACTERIAL SURFACE STRUCTURE
- cell envelope
A. Glycocalyx - some extracellular material
secreted by many bacterial cells in the form of:
a. capsule - attached tightly to the bacterium and has
definite boundaries.
b. slime layer - loosely associated with the bacterium
and can be easily washed off
Compositions:
-
-
layer of polysaccharide
proteins - sometimes
FUNCTIONS OF THE CAPSULE
• Protection
• Identification
• Vaccine preparation
• Tissue attachment
• Antibiotic barrier
MEDICAL IMPORTANCE -
rapid serological identification of:
• Several groups of streptococci
• Meningococcus
• Hemophilus influenzae
• Klebsiella pneumoniae
• Some of the coliforms
• Yersinia and Bacillus specie
CELL WALL
peptidoglycan (polysaccharides + protein)
Components of the peptidoglycan layer:
–
–
– Repeating glycan chains (N acetyl
glucosamine and N acetyl muramic acid)
a set of identical tetrapeptide side chains
attached to N- acetylmuramic acid
a set of identical peptide cross bridges
PEPTIDOGLYCAN
DIFFERENCES IN CELL WALL STRUCTURE
• Basis of Gram Stain Reaction
– Hans Christian Gram- 1884
• Differential Stain
– Gram Positive vs Gram Negative Cells
• Gram Positive Cells-
– Thick peptidoglycan layer with embedded teichoic
acids
• Gram Negative Cells-
– Thin peptidoglycan layer, outer membrane of
lipopolysaccharide.
GRAM STAIN REACTION
• Hans Christian Gram- 1880s
• Divides bacteria into 2 main groups-
– Gram positive
– Gram negative
• Also- gram variable
• Gram nonreactive
• Gram positive bacteria
– many layers of peptidoglycan and teichoic acids.
– form a crystal violet-iodine-teichoic acid complex
• Large complex, difficult to decolorize
GRAM POSITIVE BACTERIA
• Gram negative bacteria
– Very thin peptidoglycan
– No teichoic acids
– Alcohol readily removes the crystal violet.
– Alcohol also dissolves the lipopolysaccharide of the cell wall.
• Gram variable cells
– Some cells retain crystal violet; some decolorize and take up the
safranin
– 4 factors-
• Genetics- variable amount of teichoic acid.
• Age of culture- older cultures have variable
amount of teichoic acid
• Growth medium- necessary nutrients not available
• Technique-
– smear not thin or evenly made.
– Staining procedure not done correctly- decolorizer left on too long.
GRAM STAIN REACTION
GRAM NEGATIVE BACTERIA
GRAM STAIN TECHNIQUE
 Maintenance of the shape (due to rigidity of
peptidoglycan).
 Protects the cytoplasmic membrane cell
contents
 Rigidity
 Cell wall is osmotically insensitive
 Hypotonic solution – cell burst.
 Hypertonic solution – cell shrank.
 Isotonic solution – bacteria is life.
Function of Cell Wall
Cell membrane
Peripheral
Membrane
Protein
Integral
Membrane
Protein
Peripheral
Membrane
Protein
Phospholipid
 Selective permeability to different
molecules.
 Active transport aided by permease.
 Play a role in DNA replication.
 Cell wall biosynthesis.
 Mesosomes ----- cell division.
Function of Cytoplasmic Membrane
Eukaryotic Cell
CELL MEMBRANE
FUNCTIONS OF CELL MEMBRANE
 The prime functions of the cell surface membrane are:
 To control what substances can enter and leave the cell -
like passport / border control the cell surface membrane is
a selectively permeable barrier.
 To sense the environment.
 Chemicals can pass through the cell membrane by one of
the following processes:
 Passive diffusion - passive since it requires no energy
expenditure by the cell, two main types:
 Active transport / pumping - uses energy supplied by the
cell, e.g. in the form of ATP.
CELL TRANSPORT
https://www.youtube.com/watch?v=ufCiGz75DAk
Endoplasmic Reticulum
It is originated from outer membrane of nuclear
membrane . It is of two types - the rough endoplasmic
reticulum (RER), the smooth endoplasmic reticulum
(SER).
The RER consists of interconnected membranous sacs
(cisternae) - unit membrane enclosing a fluid-filled
lumen. The function of the RER is the synthesis,
storage and transport of proteins around the cell. The
proteins are manufactured by the ribosomes, that
stud the outside the RER cisternae.
The RER is continuous with the smooth endoplasmic
reticulum (SER) - a network of branching
membranous tubes that may fill much of the
cytoplasm. The SER is responsible for the synthesis,
storage and transport of lipids and carbohydrates and
also the storage of calcium ions.
Golgi Complex/ Apparatus
Golgi Complex/ Apparatus
The Golgi apparatus (Golgi body or Golgi complex) is the cell's 'post office'. It consists of
stacks of 4-8 fluid-filled membranous disc-like sacs (cisternae, singular cisterna).
The Golgi apparatus above has been sectioned down the middle. One face (the cis) face
points towards the nucleus and RER (the top face in this diagram).
Fluid-filled spherical membranous globules, called vesicles, bud-off from the RER,
carrying synthesised proteins as cargo.
These vesicles travel to the cis-face of the Golgi complex and fuse with it, delivering their
protein cargo (along with the lipids from the membrane of the vesicle).
Inside the Golgi cisternae the proteins (and lipids) are sorted and labeled by attaching
carbohydrate chains (chains of sugar molecules bonded together) to the proteins (a
process called glycosylayion).
The proteins and their attached carbohydrate chains may also be sulphated - sulphur
may be added to them, giving them a negative charge. They may also
be phosphorylated (by addition of phosphate).
These carbohydrates may be required for the final function of the protein (now a
glycoprotein, protein + carbohydrate chain = glycoprotein) or they may serve as address
labels.
Nucleus
It is enclosed in a double unit membrane -
the nuclear envelope (NE). The nuclear
envelope is continuous with the endoplasmic
reticulum (ER). The nuclear envelope
encloses the nuceloplasm. The nucleoplasm is
mostly occupied by chromatin.
Each chromosome consists of a single DNA
molecule coiled around proteins
called histones. The nuclear
envelope is perforated by pores
called nuclear pores. The nuclear pores
allow materials to enter and exit the nucleus
Ribosomes
Ribosomes are factories that manufacture
proteins for cells. They are small (diameter
about 10 nm or 10 millionths of a
millimetre) ribonucleoprotein enzymes. A
ribonucleoprotein is a structure consisting of
protein and RNA (ribonucleic acid).
In eukaryotes the ribosome is 80S and made of
a 60S large subunit + a 40S small subunit.
Eukaryotic chloroplasts and mitochondria
contain prokaryote-like 70S ribosomes.
Mitochondria
Site of cellular
respiration (Energy from the breakdown of
organic molecules isused to phosphorylate
ADP to produce ATP)
“powerhouse of the cell”
More metabolic activity= more
mitochondria
Chloroplast
Found in plants and eukaryotic algae
Site of photosynthesis
Contain the green pigment chlorophyll
ChloroplastStructure
Thylakoids
• Grana = stacks of thylakoids
• (Light Dependent Phase)
Stroma
• Fluid outside the thylakoids
Cytoskeleton
Maintains shape of cell
Responsible for movement of cell and
movement of organelles within cell
Made of three types of protein fibers:
Microtubules, microfilaments &
intermediate filaments
Components of Cytoskeleton:
Microtubules – 25 nm diameter
Intermediate Filaments – 8 – 12 nm
diameter
Microfilaments – 7 nm diameter
Microtubules: Hollow tubes made up of A-
and B tubulin responsible for cell motility
Properties of cells & cell membrane

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Properties of cells & cell membrane

  • 1. PROPERTIES OF CELLS AND CELL MEMBRANE Dr. Pulipati Sowjanya Professor & Head Vignan Pharmacy College Vadlamudi, Guntur (Dt)
  • 2. The Discovery of Cells All living things are made up of one or more cells. • A cell is the smallest unit that can carry on all of the processes of life. Hooke – In 1665, Robert Hooke discovered cells in slices of cork. • Leeuwenhoek – In 1673, Anton van Leeuwenhoek was the first to observe living cells in microorganisms; Leeuwenhoek called these organism animalcules~ we now call them protists.
  • 3. Cell Diversity Cell Shape – A cell’s shape reflects its function.
  • 4. Cell Diversity Cell Size – Cell size is limited by a cell’s surface area–to volume ratio.
  • 5. Cell Diversity Cell Size • Unicellular organisms are made up of one cell • Multicellular organisms are made up of many cells that often specialize according to function - differentiation
  • 6. OVERVIEW OF CELL STRUCTURE https://www.youtube.com/watch?v=URUJD5NEXC8&t=278s
  • 7. Prokaryotic Cells Cells lack a nucleus and membrane bound organelles -Includes bacteria -Single, circular chromosome in nucleoid region -Surrounded by cell membrane and a cell wall made up of peptidoglycan
  • 8. PROKARYOTE STRUCTURES 1. Appendages- flagella, pili, fimbrae 2. Cell envelope- glycocalyx, cell wall , cell membrane 3. Cytoplasm- ribosomes, granules, nucleoid/chromosome.
  • 9. BACTERIAL APPENDAGES: • Pili (pl), pilus (s) – – only found in gram negative bacteria tubulare, hairlike structures of protein larger and more rare than fimbriae. • - - 2 types of pili attachment pilus - allow bacteria to attach to other cells sex pilus, - transfer from one bacterial cell to another- conjugation.
  • 10. FIMBRIAE • fimbriae (pl) fimbria (s) – Adhesion to cells and surfaces – Responsible for biofilms. – Pathogenesis of gonococcus and E.coli Escherichia coli.
  • 11. FLAGELLA • Flagella (pl), flagellum(s) – long appendages which rotate by means of a "motor" located just under the cytoplasmic membrane. – bacteria may have one, a few, or many flagella in different positions on the cell. • Advantages - chemotaxis - positive and negative. - motility • All spirilla, half of bacilli, rare cocci.
  • 13. FLAGELLA Three morphological regions • – – Helical filament long outermost region; composes up to 90% of its length contains the globular (roughly spherical) protein flagellin arranged in several chains and form a helix around a hollow core – • Hooked or curved area filament is attached; consists of a different protein • – – – Basal body terminal portion of the flagellum fix the flagellum to the cell wall and plasma membrane composed of a central rod inserted into a series of rings Gram negative - 2 pairs of rings • • Outer pair - fixed to the outer membrane and peptidoglycan layer Inner pair - fixed to the plasma membrane (SM ring) Gram positive - only inner pair is present
  • 14. MOTILITY • – – – Types of bacterial motility run or swim - when a bacterium moves in one direction for a length of time tumbles - periodic, abrupt random changes in direction swarming - rapid wavelike growth across a solid culture medium • Mechanism of flagellar movement - relative rotation of the rings in the basal body of the flagellum Antigenicity – flagellar or H antigen - useful in the serological identification of serotypes of Salmonella organisms
  • 15. ARRANGEMENTS • Flagella vary in number and arrangement. • Polar arrangment – Monotrichious - 1 flagellum at one end • Fastest; Pseudomonas -example – Lophotrichious - tuft at one end – Amphitrichious- bipolar – Peritrichious - multiple flagella; randomly dispersed around the bacterial cell • E. coli - example
  • 16. FLAGELLAR ARRANGEMENTS A. Monotrichous B. Lophotrichous C. Amphitrichous D. Peritrichous E. Atrichous
  • 18. AXIAL FILAMENTS • tuft of fibrils that arise at the ends of the cell under the outer membrane and spiral around the cell • rotation an opposing of the outer membrane movement that propels the spirochetes by causing them to move like corkscrews Found in Spirochetes and are similar to flagella, but are located between the cell wall and an outer membrane, and are attached to one end of the organism.
  • 19. EVIDENCE OF MOTILITY Two ways by which motility can be demonstrated: • direct or microscopic – hanging drop preparation or wet mount preparation by dark field mycroscope – Distinguishes: • Brownian movement - when the bacteria show molecular movement • true motility - if a bacterium describes a rotatory, undulatory or sinuous movement • indirect or macroscopic – Stab inoculation of the semisolid media • nonmotile - growth is limited at the point of inoculation • motile - growth is diffuse or moves away from the line of inoculation; turbidity of the medium
  • 20. DETECTION OF MOTILITY • Direct • Indirect Presence mobile bacteria
  • 21. 2. BACTERIAL SURFACE STRUCTURE - cell envelope A. Glycocalyx - some extracellular material secreted by many bacterial cells in the form of: a. capsule - attached tightly to the bacterium and has definite boundaries. b. slime layer - loosely associated with the bacterium and can be easily washed off Compositions: - - layer of polysaccharide proteins - sometimes
  • 22.
  • 23. FUNCTIONS OF THE CAPSULE • Protection • Identification • Vaccine preparation • Tissue attachment • Antibiotic barrier
  • 24. MEDICAL IMPORTANCE - rapid serological identification of: • Several groups of streptococci • Meningococcus • Hemophilus influenzae • Klebsiella pneumoniae • Some of the coliforms • Yersinia and Bacillus specie
  • 25. CELL WALL peptidoglycan (polysaccharides + protein) Components of the peptidoglycan layer: – – – Repeating glycan chains (N acetyl glucosamine and N acetyl muramic acid) a set of identical tetrapeptide side chains attached to N- acetylmuramic acid a set of identical peptide cross bridges
  • 27. DIFFERENCES IN CELL WALL STRUCTURE • Basis of Gram Stain Reaction – Hans Christian Gram- 1884 • Differential Stain – Gram Positive vs Gram Negative Cells • Gram Positive Cells- – Thick peptidoglycan layer with embedded teichoic acids • Gram Negative Cells- – Thin peptidoglycan layer, outer membrane of lipopolysaccharide.
  • 28. GRAM STAIN REACTION • Hans Christian Gram- 1880s • Divides bacteria into 2 main groups- – Gram positive – Gram negative • Also- gram variable • Gram nonreactive • Gram positive bacteria – many layers of peptidoglycan and teichoic acids. – form a crystal violet-iodine-teichoic acid complex • Large complex, difficult to decolorize
  • 30. • Gram negative bacteria – Very thin peptidoglycan – No teichoic acids – Alcohol readily removes the crystal violet. – Alcohol also dissolves the lipopolysaccharide of the cell wall. • Gram variable cells – Some cells retain crystal violet; some decolorize and take up the safranin – 4 factors- • Genetics- variable amount of teichoic acid. • Age of culture- older cultures have variable amount of teichoic acid • Growth medium- necessary nutrients not available • Technique- – smear not thin or evenly made. – Staining procedure not done correctly- decolorizer left on too long. GRAM STAIN REACTION
  • 32.
  • 34.  Maintenance of the shape (due to rigidity of peptidoglycan).  Protects the cytoplasmic membrane cell contents  Rigidity  Cell wall is osmotically insensitive  Hypotonic solution – cell burst.  Hypertonic solution – cell shrank.  Isotonic solution – bacteria is life. Function of Cell Wall
  • 36.  Selective permeability to different molecules.  Active transport aided by permease.  Play a role in DNA replication.  Cell wall biosynthesis.  Mesosomes ----- cell division. Function of Cytoplasmic Membrane
  • 39.
  • 40. FUNCTIONS OF CELL MEMBRANE  The prime functions of the cell surface membrane are:  To control what substances can enter and leave the cell - like passport / border control the cell surface membrane is a selectively permeable barrier.  To sense the environment.  Chemicals can pass through the cell membrane by one of the following processes:  Passive diffusion - passive since it requires no energy expenditure by the cell, two main types:  Active transport / pumping - uses energy supplied by the cell, e.g. in the form of ATP.
  • 41.
  • 42.
  • 43.
  • 44.
  • 46. Endoplasmic Reticulum It is originated from outer membrane of nuclear membrane . It is of two types - the rough endoplasmic reticulum (RER), the smooth endoplasmic reticulum (SER). The RER consists of interconnected membranous sacs (cisternae) - unit membrane enclosing a fluid-filled lumen. The function of the RER is the synthesis, storage and transport of proteins around the cell. The proteins are manufactured by the ribosomes, that stud the outside the RER cisternae. The RER is continuous with the smooth endoplasmic reticulum (SER) - a network of branching membranous tubes that may fill much of the cytoplasm. The SER is responsible for the synthesis, storage and transport of lipids and carbohydrates and also the storage of calcium ions.
  • 48. Golgi Complex/ Apparatus The Golgi apparatus (Golgi body or Golgi complex) is the cell's 'post office'. It consists of stacks of 4-8 fluid-filled membranous disc-like sacs (cisternae, singular cisterna). The Golgi apparatus above has been sectioned down the middle. One face (the cis) face points towards the nucleus and RER (the top face in this diagram). Fluid-filled spherical membranous globules, called vesicles, bud-off from the RER, carrying synthesised proteins as cargo. These vesicles travel to the cis-face of the Golgi complex and fuse with it, delivering their protein cargo (along with the lipids from the membrane of the vesicle). Inside the Golgi cisternae the proteins (and lipids) are sorted and labeled by attaching carbohydrate chains (chains of sugar molecules bonded together) to the proteins (a process called glycosylayion). The proteins and their attached carbohydrate chains may also be sulphated - sulphur may be added to them, giving them a negative charge. They may also be phosphorylated (by addition of phosphate). These carbohydrates may be required for the final function of the protein (now a glycoprotein, protein + carbohydrate chain = glycoprotein) or they may serve as address labels.
  • 49. Nucleus It is enclosed in a double unit membrane - the nuclear envelope (NE). The nuclear envelope is continuous with the endoplasmic reticulum (ER). The nuclear envelope encloses the nuceloplasm. The nucleoplasm is mostly occupied by chromatin. Each chromosome consists of a single DNA molecule coiled around proteins called histones. The nuclear envelope is perforated by pores called nuclear pores. The nuclear pores allow materials to enter and exit the nucleus
  • 50. Ribosomes Ribosomes are factories that manufacture proteins for cells. They are small (diameter about 10 nm or 10 millionths of a millimetre) ribonucleoprotein enzymes. A ribonucleoprotein is a structure consisting of protein and RNA (ribonucleic acid). In eukaryotes the ribosome is 80S and made of a 60S large subunit + a 40S small subunit. Eukaryotic chloroplasts and mitochondria contain prokaryote-like 70S ribosomes.
  • 51. Mitochondria Site of cellular respiration (Energy from the breakdown of organic molecules isused to phosphorylate ADP to produce ATP) “powerhouse of the cell” More metabolic activity= more mitochondria
  • 52. Chloroplast Found in plants and eukaryotic algae Site of photosynthesis Contain the green pigment chlorophyll ChloroplastStructure Thylakoids • Grana = stacks of thylakoids • (Light Dependent Phase) Stroma • Fluid outside the thylakoids
  • 53. Cytoskeleton Maintains shape of cell Responsible for movement of cell and movement of organelles within cell Made of three types of protein fibers: Microtubules, microfilaments & intermediate filaments Components of Cytoskeleton: Microtubules – 25 nm diameter Intermediate Filaments – 8 – 12 nm diameter Microfilaments – 7 nm diameter Microtubules: Hollow tubes made up of A- and B tubulin responsible for cell motility