1 / 103

Microscopy and Cell Structure

Microscopy and Cell Structure. Chapter 3. Microscope Techniques Microscopes. Microscopes Most important tool for studying microorganisms Use viable light to observe objects Magnify images approximately 1,000x Electron microscope, introduced in 1931, can magnify images in excess of 100,000x

tassos
Télécharger la présentation

Microscopy and Cell Structure

An Image/Link below is provided (as is) to download presentation Download Policy: Content on the Website is provided to you AS IS for your information and personal use and may not be sold / licensed / shared on other websites without getting consent from its author. Content is provided to you AS IS for your information and personal use only. Download presentation by click this link. While downloading, if for some reason you are not able to download a presentation, the publisher may have deleted the file from their server. During download, if you can't get a presentation, the file might be deleted by the publisher.

E N D

Presentation Transcript

  1. Microscopy and Cell Structure Chapter 3

  2. Microscope TechniquesMicroscopes • Microscopes • Most important tool for studying microorganisms • Use viable light to observe objects • Magnify images approximately 1,000x • Electron microscope, introduced in 1931, can magnify images in excess of 100,000x • Scanning probe microscope, introduced in 1981, can view individual atoms

  3. Principles of Light Microscopy • Light Microscopy • Light passes through specimen, then through series of magnifying lenses • Most common and easiest to use is the bright-field microscope • Important factors in light microscopy include • Magnification • Resolution • Contrast

  4. Principles of Light Microscopy • Magnification • Microscope has two magnifying lenses • Called compound microscope • Lens include • Ocular lens and objective lens • Most bright field scopes have four magnifications of objective lenses, 4x, 10x, 40x and 100x • Lenses combine to enlarge objects • Magnification is equal to the factor of the ocular x the objective • 10x X 100x = 1,000x

  5. Principles of Light Microscopy • Magnification • Bright field scopes have condenser lens • Has no affect on magnification • Used to focus illumination on specimen

  6. Principles of Light Microscopy • Resolution • Usefulness of microscope depends on its ability to resolve two objects that are very close together • Resolving power is defined as the minimum distance existing between two objects where those objects still appear as separate objects • Resolving power determines how much detail can be seen

  7. Principles of Light Microscopy • Resolution • Resolution depends on the quality of lenses and wavelength of illuminating light • How much light is released from the lens • Maximum resolving power of most brightfield microscopes is 0.2 μm (1x10-6) • This is sufficient to see most bacterial structures • Too low to see viruses

  8. Principles of Light Microscopy • Resolution • Resolution is enhanced with lenses of higher magnification (100x) by the use of immersion oil • Oil reduces light refraction • Light bends as it moves from glass to air • Oil bridges the gap between the specimen slide and lens and reduces refraction • Immersion oil has nearly same refractive index as glass

  9. Principles of Light Microscopy • Contrast • Reflects the number of visible shades in a specimen • Higher contrast achieved for microscopy through specimen staining

  10. Principles of Light Microscopy • Examples of light microscopes that increase contrast • Phase-Contrast Microscope • Interference Microscope • Dark-Field Microscope • Fluorescence Microscope • Confocal Scanning Laser Microscope

  11. Principles of Light Microscopy • Phase-Contrast • Amplifies differences between refractive indexes of cells and surrounding medium • Uses set of rings and diaphragms to achieve resolution

  12. Principles of Light Microscopy • Interference Scope • This microscope causes specimen to appear three dimensional • Depends on differences in refractive index • Most frequently used interference scope is Nomarski differential interference contrast

  13. Principles of Light Microscopy • Dark-Field Microscope • Reverse image • Specimen appears bright on a dark background • Like a photographic negative • Achieves image through a modified condenser

  14. Bright field vs. Dark field

  15. Bright field vs. Dark field

  16. Principles of Light Microscopy • Fluorescence Microscope • Used to observe organisms that are naturally fluorescent or are flagged with fluorescent dye • Fluorescent molecule absorbs ultraviolet light and emits visible light • Image fluoresces on dark background

  17. Principles of Light Microscopy • Confocal Scanning Laser Microscope • Used to construct three dimensional image of thicker structures • Provides detailed sectional views of internal structures of an intact organism • Laser sends beam through sections of organism • Computer constructs 3-D image from sections

  18. Principles of Light Microscopy • Electron Microscope • Uses electromagnetic lenses, electrons and fluorescent screen to produce image • Resolution increased 1,000 fold over brightfield microscope • To about 0.3 nm (1x10-9) • Magnification increased to 100,000x • Two types of electron microscopes • Transmission • Scanning

  19. Principles of Light Microscopy • Transmission Electron Microscope (TEM) • Used to observe fine detail • Directs beam of electrons at specimen • Electrons pass through or scatter at surface • Shows dark and light areas • Darker areas more dense • Specimen preparation through • Thin sectioning • Freeze fracturing or freeze etching

  20. Principles of Light Microscopy • Scanning Electron Microscope (SEM) • Used to observe surface detail • Beam of electrons scan surface of specimen • Specimen coated with metal • Usually gold • Electrons are released and reflected into viewing chamber • Some atomic microscopes capable of seeing single atoms

  21. Microscope TechniquesDyes and Staining • Dyes and Staining • Cells are frequently stained to observe organisms • Satins are made of organic salts • Dyes carry (+) or (-) charge on the molecule • Molecule binds to certain cell structures • Dyes divided into basic or acidic based on charge • Basic dyes carry positive charge and bond to cell structures that carry negative charge • Commonly stain the cell • Acidic dyes carry positive charge and are repelled by cell structures that carry negative charge • Commonly stain the background

  22. Microscope TechniquesDyes and Staining • Basic dyes (+) more commonly used than acidic dyes (-) • Common basic (+) dyes include • Methylene blue • Crystal violet • Safrinin • Malachite green

  23. Microscope TechniquesDyes and Staining • Staining Procedures • Simple stain uses one basic stain to stain the cell • Allows for increased contrast between cell and background • All cells stained the same color • No differentiation between cell types

  24. Microscope TechniquesDyes and Staining • Differential Stains • Used to distinguish one bacterial group from another • Uses a series of reagents • Two most common differential stains • Gram stain • Acid-fast stain

  25. Microscope TechniquesDyes and Staining • Gram Stain • Most widely used procedure for staining bacteria • Developed over century ago • Dr. Hans Christian Gram • Bacteria separated into two major groups • Gram positive • Stained purple • Gram negative • Stained red or pink

  26. Dyes and Staining • The Gram Stain

  27. Gram Positive and Gram Negative Cells

  28. Microscope TechniquesDyes and Staining • Acid-fast Stain • Used to stain organisms that resist conventional staining • Used to stain members of genus Mycobacterium • High lipid concentration in cell wall prevents uptake of dye • Uses heat to facilitate staining • Once stained difficult to decolorize

  29. Microscope TechniquesDyes and Staining • Acid-fast Stain • Can be used for presumptive identification in diagnosis of clinical specimens • Requires multiple steps • Primary dye • Carbol fuchsin • Colors acid-fast bacteria red • Decolorizer • Generally acid alcohol • Removes stains from non acid-fast bacteria • Counter stain • Methylene blue • Colors non acid-fast bacteria blue

  30. The Ziehl-Neesen Acid-Fast Stain

  31. Microscope TechniquesDyes and Staining • Special Stains • Capsule stain • Example of negative stain • Allows capsule to stand out around organism • Endospore stain • Staining enhances endospore • Uses heat to facilitate staining • Flagella stain • Staining increases diameter of flagella • Makes more visible

  32. Morphology of Prokaryotic Cells • Prokaryotes exhibit a variety of shapes • Most common • Coccus • Spherical • Bacillus • Rod or cylinder shaped • Cell shape not to be confused with Bacillus genus

  33. Morphology of Prokaryotic Cells • Prokaryotes exhibit a variety of shapes • Other shapes • Coccobacillus • Short round rod • Vibrio • Curved rod • Spirillum • Spiral shaped • Spirochete • Helical shape • Pleomorphic • Bacteria able to vary shape

  34. Morphology of Prokaryotic Cells • Prokaryotic cells may form groupings after cell division • Cells adhere together after cell division for characteristic arrangements • Arrangement depends on plan of division • Especially in the cocci

  35. Morphology of Prokaryotic Cells • Division along a single plane may result in pairs or chains of cells • Pairs = diplococci • Example: Neisseria gonorrhoeae • Chains = streptococci • Example: species of Streptococcus

  36. Morphology of Prokaryotic Cells • Division along two or three perpendicular planes form cubical packets • Example: Sarcina genus • Division along several random planes form clusters • Example: species of Staphylococcus

  37. Morphology of Prokaryotic Cells • Some bacteria live in groups with other bacterial cells • They form multicellular associations • Example: myxobacteria • These organisms form a swarm of cells • Allows for the release of enzymes which degrade organic material • In the absence of water cells for fruiting bodies • Other organisms for biofilms • Formation allows for changes in cellular activity

  38. Cytoplasmic Membrane • Cytoplasmic membrane • Delicate thin fluid structure • Surrounds cytoplasm of cell • Defines boundary • Serves as a semi permeable barrier • Barrier between cell and external environment

  39. Cytoplasmic Membrane • Structure is a lipid bilayer with embedded proteins • Bilayer consists of two opposing leaflets • Leaflets composed of phospholipids • Each contains a hydrophilic phosphate head and hydrophobic fatty acid tail

  40. The Basic Structural Component of the Membrane: Phospholipid Molecule

  41. Cytoplasmic Membrane • Membrane is embedded with numerous protein • More that 200 different proteins • Proteins function as receptors and transport gates • Provides mechanism to sense surroundings • Proteins are not stationary • Constantly changing position • Called fluid mosaic model

  42. The Fluid-Mosaic Model of the Membrane Structure

  43. Cytoplasmic Membrane • Cytoplasmic membrane is selectively permeable • Determines which molecules pass into or out of cell • Few molecules pass through freely • Molecules pass through membrane via simple diffusion or transport mechanisms that may require carrier proteins and energy

  44. Cytoplasmic Membrane • Simple diffusion • Process by which molecules move freely across the cytoplasmic membrane • Water, certain gases and small hydrophobic molecules pass through via simple diffusion

  45. Cytoplasmic Membrane • Simple diffusion • Osmosis • The ability of water to flow freely across the cytoplasmic membrane • Water flows to equalize solute concentrations inside and outside the cell • Inflow of water exerts osmotic pressure on membrane • Membrane rupture is prevented by rigid cell wall of bacteria

  46. Cytoplasmic Membrane • Membrane also the site of energy production • Energy produced through series of embedded proteins • Electron transport chain • Proteins are used in the formation of proton motive force • Energy produced in proton motive force is used to drive other transport mechanisms

  47. Cytoplasmic Membrane • Directed movement across the membrane • Movement of many molecules directed by transport systems • Transport systems employ highly selective proteins • Transport proteins (a.k.a permeases or carriers) • These proteins span membrane • Single carrier transports specific type molecule • Most transport proteins are produced in response to need • Transport systems include • Facilitated diffusion • Active transport • Group translocation

  48. Cytoplasmic Membrane • Facilitated diffusion • Moves compounds across membrane exploiting a concentration gradient • Flow from area of greater concentration to area of lesser concentration • Molecules are transported until equilibrium is reached • System can only eliminate concentration gradient it cannot create one • No energy is required for facilitated diffusion • Example: movement of glycerol into the cell

  49. Cytoplasmic Membrane • Active transport • Moves compounds against a concentration gradient • Requires an expenditure of energy • Two primary mechanisms • Proton motive force • ATP Binding Cassette system

More Related