CHAPTER 3 CELLS:
2.
Robert Hooke
first used the term cell for the small cubicles he observed in a thin section of
cork in 1665. Robert Brown
was the first to observe name the nucleus in 1835. Matthias Schleiden and
Theodor Schwann proposed the cell theory in 1838-39. Louis Pasteur
had many great accomplishments, but in this unit we will recognize his
experiments with microorganisms, which conclusively disproved the spontaneous
generation of life. Rudolf
Virchow observed the process of cell division and mitosis in the late
1860’s.
3.
The cell
theory states that all living things
are composed of cells and cell products and that cells are produced by
preexisting cells.
4.
Magnification is the apparent increase in size of an object, while
resolution is the ability to see the object or the ability to distinguish
the distinctness of two distinct points.
Contrast is the ability to distinguish various shades of light and
dark or color.
5.
Cell size is determined
by the ratio of cell surface area to cell volume. The volume of the cell
increases at a faster rate than the surface area of the cell. Volume increases
by a power of 3 while surface area increases by a power of 2. Other factors such
as cell shape, surface folding or metabolic rate are also involved in size
determination.
6.
Cell wall - A
rigid non-living wall located outside the cell membrane. In land plants the cell
wall is composed of cellulose and hardening materials such as
lignin. Suberin,
another material found in the cell wall is a waxy compound that is involved in
water proofing some tissues. The
cell wall provides protection and support for the cell.
7.
The primary cell
wall is the first wall produced by the plant cell. It is composed of loosely arranged
fibers of cellulose, which allow the cell to grow and stretch. Young tissues and soft tissues are
composed of cells that only have a primary cell wall. Many mature and hard tissues contain
cells with one or more layers of secondary wall are deposited inside the
primary wall. The secondary
wall is composed of tightly arranged fibers of cellulose, which are often
hardened by lignin. Secondary walls
can be very thick in wood and other supporting tissues. The living cell produces cell wall
material. In multicellular
plants the middle lamella is located between plant cells. It is often filled with a gel-like
material, pectin, which helps cells adhere to each other.
8.
Plasmodesmata are
cytoplasmic connections that pass through the cell walls of adjacent cells. They allow the movement of ions and
small molecules from cell to cell.
9.
Membrane
function:
a.
PLASMA MEMBRANE
·
Separate the living
cell from the nonliving environment.
·
Control or play an
active role in the movement of substances into and out of the
cell.
·
Sense and interact with
the external environment.
·
Involved with cell
identity and interactions with other cells.
b. INTRACELLULAR
MEMBRANES
·
Responsible for the
structural integrity of most cellular organelles and
ultrastructures.
·
Compartmentalizes the
cytoplasm, forming unique chemical regions or
environments.
·
Provides surface area
for the attachment of enzymes and cellular structures such as
ribosomes.
·
Involved with numerous
biochemical processes.
·
Facilitates transport
and secretion through the action of transport vesicles.
10.
The current model for
membrane structure is the fluid mosaic model. This model includes the following
structural concepts.
· The primary structural component of
cellular membranes are phospholipids which form bilayers when
mixed with water. Other membrane lipids include glycolipids and
sterols.
· Embedded within this lipid bilayer
are numerous proteins involved with transport, cell identity, recognition and
reception.
LIPID BILAYER
PROPERTIES:
·
PHOSPHOLIPIDS
include two hydrophobic fatty acid tails which are repelled by water, and a
phosphate/choline region which is hydrophilic (attracted to water).
Phospholipids are amphipathic, meaning they are composed of both non-polar
(hydrophobic) and polar (hydrophilic) regions.
·
GLYCOLIPIDS are
likewise made up of a non-polar lipid region and a polar region composed of one
or more sugars.
·
STEROLS such as
cholesterol (animals) and phytosterols (plants) are non-polar except for polar
functional groups such as the hydroxyl group.
·
PHOSPHOLIPIDS
are organized into bilayers due to the fatty acid regions being repelled by
water thus being turned toward each other. The phosphate "heads" are attracted
by water thus forming both exposed surfaces. Phospholipids exhibit considerable
lateral movement within the membrane, but do not cross from one layer of the
bilayer to the other. Movement helps maintain fluidity.
·
STEROLS such as
cholesterol are located between the phospholipid tails of the interior of the
membrane. This helps keep the lipids from packing together thus becoming less
fluid. Sterols help maintain membrane fluidity.
·
GLYCOLIPIDS have
their carbohydrate regions exposed at the cell surface, thus they are involved
with cell recognition and identity.
MEMBRANE PROTEINS - LOCATION AND
FUNCTION:
·
PROTEINS BY
LOCATION:
q
INTEGRAL
PROTEINS - These proteins are
suspended within one layer of the bilayer or they may span the entire bilayer.
Integral proteins are exposed on one or both surfaces of the
membrane.
q
PERIPHERAL
PROTEINS - These are located on the membrane surface, usually loosely
associated with an integral protein.
·
PROTEIN
FUNCTION:
q
TRANSPORT
PROTEINS - Involved with the
movement of substances across the membrane.
q
CARRIERS - Bind
to specific molecules then change shape moving the molecule across the
membrane.
q
CHANNEL
PROTEINS - Serve as pores for the
movement of ions or small polar molecules across the
membrane.
o
REGULATED - Open
or close by the action of molecular gate.
o
NON-REGULATED -
Continually open.
q
RECOGNITION
PROTEINS - Have oligosaccharides attached to the outer surface. Unique for
particular cell types. Function as a cellular finger
print.
q
RECEPTOR
PROTEINS - Serve as binding sites
for hormones or other substances that may need to move across the membrane or
substances that by binding to the membrane may stimulate or inhibit cellular
metabolism.
q
ADHESION
PROTEINS - Proteins involved with
attachment of the cell surface adjacent cells, tissues,
etc.
q
CYTOSKELETAL
PROTEINS - Proteins of the cytoskeleton that are associated with or attached
to the cell membrane.
11.
The endoplasmic
reticulum is a complex network of membrane sheets and vesicles that are found
throughout the cytoplasm. and is the most extensive portion of the endomembrane
system.. The ER is continuous from the outer layer of the nuclear envelope to
the cell membrane.
· Rough
ER
q
Studded with
ribosomes on its outer surface.
q
Involved in the
synthesis of secretory proteins and membrane
· Smooth
ER
q
Involved in lipid
metabolism, the synthesis of lipids, phospholipids and
steroids.
q
Involved in cellular
detoxification.
q
Active in carbohydrate
metabolism..
q
Stores calcium ions
necessary for muscle metabolism.
12.
11. Golgi complex or dictyosome -
Stacks of membrane vesicles derived from the ER which are involved in the
modification, packaging and secretion of cellular
products.
13.
Mitochondria -
Double membrane bound organelles that serve as the site of aerobic cellular
respiration. The inner membrane is
deeply and contains the pigments of the electron transport system. Between the inner and outer membranes is
the intermembrane space and the compartment enclosed by the inner membrane is
the matrix. The roles of these
structures will be discussed in the unit on respiration.
14.
Plastids -
Double membrane bound organelles unique to plants involved with photosynthesis
and storage.
15.
Microfilaments
- Protein filaments, 7 to 9 nm in
diameter, which are involved in cellular movement such as cytoplasmic division,
movement of organelles, cytoplasmic streaming, muscle contractions and
facilitates cellular shape.
Intermediate filaments - Protein filaments, 8 to 12 nm in
diameters, not involved with movement, but provide strength in regions of
stress. Microtubules -
Protein tubule composed of spiral chain of protein globules (tubulin) which are
involved with cellular movements such as flagella, cellular organelles and
chromosomes. Also contribute to the maintenance of cell
shape.
16.
The eukaryotic nucleus
is surrounded by a two layered nuclear membrane (envelope) which
separates the interior of the nucleus from the cytoplasm. The genetic material
is dispersed in the nucleus as a complex network of DNA and protein called
chromatin. A granular region in the nucleus composed of granules of rRNA
is the nucleolus. This is the location of genes that code for the
production of rRNA. The fluid portion of the nucleus is the nucleoplasm.
Chromosomes are only found in dividing cells. They are composed of DNA
organized into short compact structures prior to cell
division.
17.
Vacuoles -
Membrane sacs that contain various materials such as food, waste, etc. Plant cell membranes, also called the
central vacuole, play a central role in the life of the plant cell. The central vacuole is involved
with turgor, cell growth, the storage of dangerous metabolites, toxins
and even pigments involved with color in some flower petals or the skin of
certain fruit. Turgor
results from internal water pressure in plant cells due to the diffusion of
water into the cell vacuole which pushes outward against the cell wall causing
the wall to stretch and become rigid. Turgor results from plant roots being in
contact with soil water which is hypotonic to plant cells. As a result water
diffuses into plant cells until the internal physical pressure equals the
osmotic tendency (force) to diffuse into the cell. Turgor is responsible for much of the
support and form of soft plant tissues.
As young cells grow, the central vacuole absorbs water causing the cell
to elongate.
17.
Prokaryotes vs. Eukaryotes
|
PROKARYOTIC |
EUKARYOTIC |
|
No nuclear
membrane |
Have a nuclear
membrane |
|
Chromosome is a single
double stranded loop of DNA |
Have complex membrane
bound organelles |
|
No complex membrane
bound organelles |
Chromosomes are linear
and numerous. |
|
Photosynthetic
lamellae |
No analogous
structure |
|
Chromosome has no
histone protein |
Chromosomes with
histone proteins |
|
Small
ribosomes |
Large
ribosomes |
|
Very small, average 2
m m in diameter
|
Average 10 m m in
diameter. |
|
Kingdom
Monera |
Other four
kingdoms |
18.
Plant vs. animal
cells.
|
PLANT |
ANIMALS |
|
Have a cell wall of
cellulose. |
Do not have a cell
wall. |
|
Have
plastids |
No
plastids. |
|
Have a large central
cell vacuole. |
No large central cell
vacuole. |
|
No
lysosomes. |
Have
lysosomes. |
|
No
centriole. |
Have
centrioles. |
18. Define the following
terms.
a.
Cell Cycle
– The life cycle of a cell from division to division, includes both the
non-dividing and dividing phases of the cell.
b.
Mitosis - The division of the nucleus in which
daughter nuclei are identical in ploidy to the mother
nucleus.
c.
Cytokinesis - Division of the cytoplasm.
d.
Chromosome
- Condensed DNA protein complex, results from the coiling of strands of
chromatin at the beginning of mitosis.
e.
Homologous
Chromosomes – Like chromosomes, have genes for the same characteristics located
at the same locus.
f.
Chromatids
– After a chromosome duplicates it is composed of two identical copies, sister
chromatids.
g.
Centromere
– The point where two chromatids are joined together.
h.
Kinetochore
– A deposit of protein located at the centromere on each
chromatid.
i.
Kinetochore
Microtubules – A spindle fiber or bundle of microtubules that extends from the
mitotic pole to the kinetochore, contract to pull sister chromatids apart during
mitosis.
j.
Nonkinetochore
Microtubules – Microtubules that extend from the mitotic poles past the mitotic
equator of the cell, involved with the elongation of the cell during
mitosis.
k.
Haploid -
condition in which there is only one set
of chromosomes in the nucleus of the cell. This means that the cell has one
chromosome of each kind.
l.
Diploid -
condition in which there are two sets of
chromosomes in the nucleus, that is two chromosomes of each type in the
cell.
19.
The cell cycle is the
period of time required for the cell to complete one life cycle, that is from
one division to the next. The cell cycle includes a nondividing period,
interphase, and a dividing period, either mitosis or meiosis.
Interphase is divided into three phases, G1, S and G2. G1 is a period of
cell growth and a time when the cell is synthesizing necessary nucleotides and
proteins for the duplication of DNA. The S phase is the time during which
DNA is duplicated, and G2 is a final phase of growth and the synthesis of
proteins and materials needed for mitosis. Mitosis is the period or time during
which the chromosomes and nucleus is dividing. It is divided into four phases,
but requires much less time than interphase.
20.
Mitosis is divided into prophase, metaphase, anaphase and
telophase. Listed below
is an outline of the events of each phase.
a.
Prophase
·
Chromosomes coil
becoming visible under the light microscope.
·
Chromosomes continue to
coil, shortening and thickening, until they become short rod-like
structures.
·
Centrosome
duplicates with the two centrosomes moving toward opposite poles of the cell to
establishing the mitotic spindle. Centrosomes of animal cells contain a
pair of rod-like bodies called centrioles.
b. Prometaphase
·
The nuclear envelope
disintegrates.
·
The nucleolus
disappears.
·
Kinetochore
microtubules (spindle fibers) extend from each centrosome and attach to the
kinetochore of the centromere of each duplicated chromosome.
·
Each duplicated
chromosome consist of two complete copies of the original chromosome. Each copy
is a chromatid, with the two sister chromatid being attached at the
centromere.
·
Then microtubules pull
on the chromosomes from each pole causing considerable agitation as the
chromosomes move toward the center of the mitotic spindle.
·
Non-kinetochore
microtubules extend from mitotic pole to pole, ultimately pushing the poles
apart causing the cell to elongate.
c.
Metaphase
·
Centromeres move to the
equatorial plane of the cell (metaphase plate). This is a plane equidistant
between the mitotic poles and perpendicular to the axis of the mitotic
spindle.
·
Non-kinetochore
microtubules push the mitotic poles apart elongating the
cell.
d. Anaphase
·
Anaphase begins as the
chromatids separate at the centromere. Each sister chromatid becomes an
independent chromosome and sister chromatid moves to opposite poles of the cell,
thus sister chromatids ends up as chromosomes in different nuclei at the
conclusion of mitosis.
·
Chromosomes continue to
move to the poles of the cell as kinetochore microtubules
shorten.
e.
Telophase
·
Telophase is more or
less the opposite of prophase.
·
Chromosomes collect in
dense clumps at the poles of the cell.
·
Chromosomes begin to
uncoil, dispersing into the chromatin network.
·
Nuclear envelope
regenerates.
·
Nucleolus
reappears.
·
The cytoplasm usually
divides in a process called cytokinesis.
1.
Meristems are composed
of cells that retain the ability to divide. Simple tissues are composed of only one
cell type while complex tissues contain several different cell
types.
2.
Apical meristems are
located at the tips of the stems and roots. The vascular cambium and cork cambium
are lateral meristems that produce lateral growth. The vascular cambium produces secondary
xylem to the inside and secondary phloem to the inside, while the cork cambium
produces the cork cells of the outer bark of woody roots and stems. Tissues produced by a cambium are
secondary tissues while those produced by meristems are secondary tissues. An intercalary meristem is located at
the base of the stem or at the nodes of plants that do not have an apical
meristem and produces growth in length.
Note that the vascular cambium is only in dicots, and that the cork
cambium only in woody plants.
3.
Recognize that primary
tissues are derived from the cells produced by an apical or intercalary meristem
and that secondary tissues develop from cells produced by a cambium or other
lateral meristem like the cork cambium.
4.
Parenchyma cells
are large, thin walled (primary cell wall only), living cells at maturity. They are involved with photosynthesis
and storage. The photosynthetic
cells of the leaf are parenchyma cells called chlorenchyma. Collenchyma, also living at
maturity have some thickening of the secondary cell wall. Collenchyma cells provide support or
protection in regions of stress, are involved with storage and even
photosynthesis in some cases
Sclerenchyma tissue is composed of cells that are usually
non-living at maturity. They have
very thick cell walls and provide support, strength and protection. Sclerids are small somewhat round
cells with very thick cell walls, while fibers are very long.
5.
The epidermis is a
simple tissue usually only one cell thick. It is an outer protective layer of
cells found on non-woody roots, stems and leaves. Root hairs are extensions of individual
root epidermal cells that greatly increase the absorptive surface area of the
root. The periderm is the corky
bark of woody roots and stems. It
is composed of several layers of cell and includes the cork cambium and cork.
6.
The cutical is a waxy
layer on the outer surface of the epidermis of leaves and stems. Cutin is the waxy material that makes up
the cuticle. Stomata are openings
in the epidermis of leaves and stems that functions in gas exchange. Guard cells are a pair of cells that
form the stomata. Guard cells can
change shape to open and close the stomata. Lenticels are openings in the bark of
woody stems that allow gas exchange.
Cork cells are non-living at maturity and make up the outer portion of
the woody bark. Suberin is a
waxy material in the cell walls of cork cells that makes them waterproof. and root hairs.
7.
Xylem is a complex
vascular tissue involved with structural support and the transport of water and
minerals upward in plants. The
functional elements in xylem are tracheids and/or vessels. Functional xylem cells are non-living at
maturity, have thickened secondary cell walls and provide passage ways for the
transport of water and minerals.
Tracheids are long thin cells with tapering end walls. Water moves through pits as it passes
from tracheid to tracheid. While
tracheids are more common in more primitive plants, vessels are common in more
advanced plants. Vessels are
usually larger in diameter, stacked end to end and have reduced or no end cell
walls. Xylem tissue also contains
parenchyma cells and fibers.
8.
Phloem is a
complex, vascular tissue that functions in the transport of foods in
plants. Sieve tube elements are the
functional elements that transport food.
They are living at maturity, have no nucleus, are stacked end have
perforated end cell walls called sieve plates. Companion cells are small cells located
along the side of sieve tube elements.
Companion cells have a nucleus and provide for the nuclear needs of sieve
tube elements. There are numerous
plasmodesmata that connect companion cells and sieve tube elements. Like xylem phloem tissue also contains
parenchyma cells and fibers.
CHAPTER 5 ROOTS:
1.
Root systems are
involved with anchoring the plant into the ground, absorption of water and
minerals from the soil, food storage, water storage and
reproduction.
2.
The radicle of the
plant embryo produces the root.
3.
A fibrous root system
is one that does not have one primary of main root, but is made up of many
branching roots of more or less equal size. In tap root systems there is
usually one primary or main root that usually grows more or less straight down
with smaller lateral or branch roots developing from it.
4.
Adventitious roots are
roots that grow from stems or leaves; they develop from tissues other than
roots. Root hairs are extensions of
individual root epidermal cells that greatly increase the absorptive surface
area of the root.
5.
There is considerable
development of cells and tissue that occurs in the first inch of the root
tip. Starting at the tip of the
root we will explore each tissue and their functions. The root cap is a cap-like layer of
cells that develops over the tip of the root. It provides protection from abrasion by
soil p[articles and secretes a lubrication fluid that allows the root tip to
more easily push through the soil.
Cells of the root cap and of the remainder of the root are produced by
the apical meirstem that is located above the root cap. Cells of the apical meristem retain the
ability to divide, thus they produce the cells of the root cap and all primary
growth in the root. The Region of
Elongation is just above the apical meristem, and is a region where cells
elongate or grow rapidly. It is
this region that produces all growth in length. Above the region of elongation is the
Region of Maturation where cells mature into the mature and functional tissues
of the root.
6.
The root hair zone is
in the region of maturation. Root
hairs are extensions of individual root epidermal cells that greatly increase
the absorptive surface area of the root.
7.Listed below is a comparison of the characteristics
of monocots and dicots
which are the two classes of flowering plants.
|
Monocots |
Dicots |
|
One
Cotyledon |
Two
Cotyledons |
|
Narrow
Leaves |
Broad
Leaves |
|
Parallel
Veins |
Netted
Veins |
|
Floral
Parts in 3’s |
Floral
Parts in 4’s or 5’s |
|
Most
Advanced |
|
7.
Monocot roots have a
central pith where dicot roots have a solid core of xylem. Additionally bundles of xylem are
located in a ring near the outside of the stele. Bundles of phloem are located between
and to the outside of the xylem and there is no vascular cambium
in the roots of monocots. The stele
is the central cylinder of the root that contains the vascular tissue; it
includes the tissues inside the endodermis. Dicots have a solid core of xylem and no
pith. Phloem is found between the
radiating arms of xylem and the vascular cambium is found between the xylem and
phloem of the dicot root. Both the
monocot and dicot have a pericycle located just inside the endodermis. Observe photos or diagrams of cross
sections of monocot and dicot roots for a good comparison.
8.
The epidermis is an
outer protective covering of cells on the outside of the root. Near the root tip root hairs develop as
extinctions of epidermal cells. The
cortex made up of the epidermis cortex parenchyma and the endodermis. The cortex parenchyma is a region of
large parenchyma cells located between the epidermis and endodermis. The cortex parenchyma is involved with
the transport of water across the root, food storage and water storage. The endodermis is the inner most layer
of the cortex. The lateral surfaces
of endodermal cells contain a waxy region the Casparian strip that prevents the
movement of water through the cell walls of the endodermis. As a result water must pass through the
cytoplasm of the endodermal cells allowing control on the movement of ions and
water into and out of the stele.
Some endodermal cells do not have a Casparian strip and sereve as passage
cells that allow a rapid flow of water and minerals into the stele. Ceel of the pericycle are meristematic
and produce branch or lateral roots.
The pith, if present, is composed mostly of parenchyma cells involved
with food storage.
9.
Specialized roots are identified and
pictured in your text. Please refer
to the text for this information.
10.
The term mycorrhizae
means “fungus root”, thus this is a mutualistic symbiotic association between
the roots of most vascular plants and certain fungi. The fungus assist the plant by
increasing the absorption of water and minerals, especially phosphorus, from the
soil. In turn the roots provide
food for the fungus. Root nodules
are not-like growth of root tissue causec by an infection of nitrogen fixing
bacteria. This is another
mutualistic symbiotic association.
In this association the bacteria convert atmospheric nitrogen into
nitrogen compounds which plants use in their matabolism and the bacteria receive
food from the association.
CHAPTER 6 STEMS:
1.
Stems function in the
transport of water, minerals and food; support, food and or water storage, leaf
display, reproduction and the development and support of the shoot
system.
2.
The
following structures are common external features of a woody stem. The terminal bud is located at the stem
tip. It is made up of leaf scales,
embryonic leaves and the apical meristem.
Scales protect the delicate tissues of the apical meristem. As one moves down the stem from the
terminal bud we encounter slightly enlarged areas called nodes. Nodes are regions of growth that produce
leaves and lateral stem growth.
Bundles of meristematic tissue are lacated at the nodes. These bundles of meristematic tissue
produce lateral or axillary buds that produce leaves and lateral stems. Leaf scars are also located at the
node. This is the point where last
season’s leaf broke from the stem.
With in the leaf scar are leaf bundle scars where vascular bundles passed
from the stem to the leaf petiole.
The space between two nodes if an internode. The length of the internodes varies and
is designed to separate and display the leaves for phothsynthesis. Lenticels are located along the
stem surface. These are small
raised areas in the bark that allow gas exchange.
3.
A
longitudinal section of a stem tip will show many embryonic and developing
tissues. Observe drawings and
photos in your text and lab handouts for location and appearance. The apical meristem is composed of
mitotic cells that produce the primary tissue of the stem. The protoderm is the embryonic
epidermis. The procambium develops into the vascular cylinder and the ground
meristem matures into the cortex and pith.
Bud primordial and leaf primordial are embryonic buds and leaves that
will mature as the stem grows.
4.
Observe drawings and
photos of herbaceous dicot, woody dicot and monocot stem. Be able to describe the anatomical
differences. Herbaceous dicots do
not have any woody tissue. Vascular
bundles form a ring near the outside of the stem. Herbaceous dicots have a large pith
inside the ring of vascular bundles.
The vascular bundles of herbaceous dicots usually have a protective cap
of fibers on the outside that provides support and protects the bundle from
damage and herbivory. The vascular
bundles of woody dicots grow in contact with each other as the stem develops,
thus forming a solid region of xylem, the wood of the plant. Xylem is a complex tissue with
parenchyma rays (xylem ray) involved in lateral transport and fibers involved
with support. Woody dicots have a
vascular cambium that separates the xylem from the phloem. The phloem is the inner bark while the
cork and cork cambium form the outer bark.
As described earlier phloem is a complex tissue containing alternating
layers of functional phloem and phloem fibers. Regions of functional phloem and phloem
fibers are separated from each other by phloem rays (cortex) made up of
parenchyma cells. Monsocot stems
have vascular bundles scattered through out the stem, but more concentrated near
the outside. The vascular bundles
of the monocot do not have a vascular cambium. Even though there is a considerable
amount os parenchyma tissue in the stem it is not divided into a cortex and pith
but is simply the parenchyma. There
is no woody tissue associated with the monocot stem.
5.
Primary xylem is
derived from the apical meristem, while secondary xylem is produced you activity
of the vascular cambium. Monocots
have no secondary tissue. Annual
ring are rings in the xylem of woody plants produced by alternating bands of
large xylem cells (spring wood) and small xylem cells (summer wood), thus in
temperate regions annual rings correspond to years. In the tropics rings form, but do not
correspond to years, but more likely variations in growing conditions. Identify
the function of each of the specialized stems listed on the slide, “Specialized
Stems”.
6.
Specialized stems are
identified and pictured in your text.
Please refer to the text for this
information.