Chapter 6 Flashcards
what is a cell
In the hierarchy of biological organization, the cell is the simplest collection of matter that can be considered a
living entity
who first saw cells? what did anotni van leeuwenhoek do?
Cell walls were first seen by Robert Hooke in 1665 as he looked
through a microscope at dead cells from the bark of an oak
tree. But it took the wonderfully crafted lenses of Antoni van
Leeuwenhoek to visualize living cells. Imagine Hooke’s excitement when he visited van Leeuwenhoek in 1674 and the
world of microorganisms—what his host called “very little
animalcules”—was revealed to him
who first used microscopes? most likely microscope u will use in the lab?
The microscopes first used by Renaissance scientists, as
well as the microscopes you are likely to use in the laboratory,
are all light microscopes
light microscope (LM)
. In a light microscope (LM), visible light is passed through the specimen and then through
glass lenses. The lenses refract (bend) the light in such a way
that the image of the specimen is magnified as it is projected
into the eye or into a camera (see Appendix D
Three important parameters in microscopy are
magnification, resolution, and contrast
Magnification
is the ratio of
an object’s image size to its real size
Resolution d and ex
is a measure of the clarity
of the image; it is the minimum distance two points can be
separated and still be distinguished as separate points. For
example, what appears to the unaided eye as one star in the
sky may be resolved as twin stars with a telescope, which has
a higher resolving ability than the eye
The third
parameter, contrast, is
the difference in brightness between
the light and dark areas of an image. Methods for enhancing contrast include staining or labeling cell components
to stand out visually
organelles,
the membrane-enclosed structures within
eukaryotic cells
em
focuses a beam of electrons through the specimen or onto its surface. there are different types
relationship between resolution and wavelentgh. max resolution of modern EM in nm? what the smallest structure tey can see? improvement compared to standard LM?
Resolution is inversely related to the wavelength of the light (or electrons) a microscope uses for imaging, and electron beams have much shorter wavelengths than
visible light. Modern electron microscopes can theoretically
achieve a resolution of about 0.002 nm, though in practice
they usually cannot resolve structures smaller than about
2 nm across. Still, this is a 100-fold improvement over the
standard light microscope.
The scanning electron microscope (SEM) is
especially useful for? how does it work?
detailed study of the topography of a specimen (see Figure 6.3). The electron beam scans the
surface of the sample, usually coated with a thin film of
gold. The beam excites electrons on the surface, and these
secondary electrons are detected by a device that translates
the pattern of electrons into an electronic signal sent to a
video screen. The result is an image of the specimen’s
surface that appears three-dimensional.
TEM - d and how does it work
The transmission electron microscope (TEM) is used
to study the internal structure of cells (see Figure 6.3). The
TEM aims an electron beam through a very thin section of
the specimen, much as a light microscope aims light through
a sample on a slide. For the TEM, the specimen has been
stained with atoms of heavy metals, which attach to certain
cellular structures, thus enhancing the electron density of
some parts of the cell more than others. The electrons passing through the specimen are scattered more in the denser
regions, so fewer are transmitted. The image displays the
pattern of transmitted electrons.
A disadvantage of electron microscopy
is that the methods used to prepare the specimen kill the cells.
Specimen preparation for any type of microscopy can introduce artifacts, structural features seen in micrographs that
do not exist in the living cell.
In the past several decades, light microscopy has been
revitalized by major technical advances
(see Figure 6.3).
Labeling individual cellular molecules or structures with
fluorescent markers has made it possible to see such structures with increasing detail. In addition, both confocal and
deconvolution microscopy have produced sharper images of
three-dimensional tissues and cells. Finally, a group of new
techniques and labeling molecules developed in recent years
has allowed researchers to distinguish subcellular structures even as small as
10–20 nm across. this super-resolution microscopy becomes
more widespread.
microscopes? cytology, biochem?
Microscopes are the most important tools of cytology, the
study of cell structure. Understanding the function of each
structure, however, required the integration of cytology and
biochemistry, the study of the chemical processes (metabolism)
of cells.
In early experiments,
researchers used microscopy to. what did these idenfitcations establish a baseline for and what did they let researchers do
identify the organelles in each
pellet and biochemical methods
to determine their metabolic
functions. These identifications
established a baseline for this method, enabling today’s researchers to
know which cell fraction they should collect in order to isolate and study
particular organelles
what kinds of lenses do SEM and TEM use
Instead of using glass
lenses, both the SEM and TEM use electromagnets as lenses
to bend the paths of the electrons, ultimately focusing the
image onto a monitor for viewing
what is the equipment used for cell frax? how does it work? what happens to the pellet at lower speeds? higher speeds?
The piece of equipment that
is used for this task is the centrifuge, which spins test tubes
holding mixtures of disrupted cells at a series of increasing
speeds. At each speed, the resulting force causes a subset
of the cell components to settle to the bottom of the tube,
forming a pellet. At lower speeds, the pellet consists of
larger components, and higher speeds result in a pellet
with smaller components
Cell fractionation enables researchers to
prepare specific
cell components in bulk and identify their functions, a task
not usually possible with intact cells.
what are some things all cells have in common? (4x)
s: They are all bounded by a
selective barrier, called the plasma membrane (also referred to as
the cell membrane). Inside all cells is a semifluid, jellylike substance called cytosol, in which subcellular components are
suspended. All cells contain chromosomes, which carry genes in
the form of DNA. And all cells have ribosomes, tiny complexes
that make proteins according to instructions from the genes.
A major difference between prokaryotic and eukaryotic
cells is
the location of their DNA. In a eukaryotic cell,
most of the DNA is in an organelle called the nucleus, which
is bounded by a double membrane (see Figure 6.8). In a
prokaryotic cell, the DNA is concentrated in a region that
is not membrane-enclosed, called the nucleoid
meaning of eukaryotic and prokaryotic
Eukaryotic means “true nucleus” (from the Greek eu, true,
and karyon, kernel, referring to the nucleus), and prokaryotic
means “before nucleus” (from the Greek pro, before), reflecting the earlier evolution of prokaryotic cells
The interior of either type of cell is called the cytoplasm; explain it in the euk cells
in eukaryotic cells, this term refers only to the region between
the nucleus and the plasma membrane. Within the cytoplasm
of a eukaryotic cell, suspended in cytosol, are a variety of
organelles of specialized form and function.