Download Plant cell biology

Survey
yes no Was this document useful for you?
   Thank you for your participation!

* Your assessment is very important for improving the workof artificial intelligence, which forms the content of this project

Document related concepts
no text concepts found
Transcript
Chapter 17
Plant cell biology
By
Clive Lloyd
17.1 Introduction
• Plant and animal cells grow in fundamentally
different ways.
• The tough cell wall prevents:
– cell movement
– uptake of large molecules as food
• Plant development depends upon how
immobile cells manipulate the cell wall.
17.2 How plants grow
• Plants extend into the environment
using apical growing points.
• Plant development continues beyond
the embryonic stage.
• Plant growth is sensitive to the
environment.
17.3 The meristem provides new growth
modules in a repetitive manner
• Apical meristems divide to produce new
cells at the growing points.
• Growth occurs by repeated addition of
new growth modules.
17.3 The meristem provides new growth modules in a repetitive
manner
• Cells divide, expand, then differentiate.
• Massive expansion of cells behind the
tips drives the growing points onward.
17.4 The plane in which a cell divides is
important for tissue organization
• In the absence of cell movement,
orientation of the division plane helps
determine shape.
• Formative divisions generate new cell
types:
– proliferative divisions add more cells.
17.5 Cytoplasmic structures predict the
plane of cell division before mitosis
begins
• The plane of cell division is predicted
before mitosis by a ring of microtubules
and actin filaments around the cortex.
• A sheet of cytoplasm also predicts the
plane of division in vacuolated cells.
17.6 Plant mitosis occurs without
centrosomes
• The poles of plant mitotic spindles:
– do not contain centrioles
– can be much more diffuse than the poles of
animal spindles
17.7 The cytokinetic apparatus builds a
new wall in the plane anticipated by the
preprophase band
• The cytokinetic apparatus—the
phragmoplast—is a ring of cytoskeletal
filaments that expands outward.
17.7 The cytokinetic apparatus builds a new wall in the plane anticipated by the
preprophase band
• Vesicles directed to the midline of this
double ring fuse to form the new crosswall.
• The plane in which the cell plate grows
conforms:
– to the preprophase band
– not to the spindle midzone
17.8 Secretion during cytokinesis forms
the cell plate
• The Golgi apparatus continues to make
secretory vesicles throughout
cytokinesis.
• These vesicles fuse to make a cell plate
lined with new plasma membrane.
17.9 Plasmodesmata are intercellular
channels that connect plant cells
• Primary plasmodesmata are pores in the cell
wall formed at cytokinesis.
• Plasmodesmata interconnect cells into
multicellular units called symplasts, within
which signaling occurs.
• Plasmodesmata can open and close
– Their pore size can be increased by viruses.
17.10 Cell expansion is driven by swelling
of the vacuole
• Uptake of water into the vacuole
provides a unique, pressure-driven
mechanism of cell expansion.
• There is more than one type of vacuole.
17.11 The large forces of turgor pressure
are resisted by the strength of cellulose
microfibrils in the cell wall
• The plant cell wall is based largely on
carbohydrate.
– unlike the protein-rich extracellular matrix
of animal cells
17.11 The large forces of turgor pressure are resisted by the strength of cellulose microfibrils in the
cell wall
• The nonrandom arrangement of stiff
cellulose microfibrils controls the
swelling force of turgor pressure.
• Proteins loosen the cell wall to allow cell
expansion.
• The orientation of cellulose microfibrils
can change from layer to layer.
17.12 The cell wall must be loosened and
reorganized to allow growth
• Proteins loosen the cell wall to allow cell
expansion.
• The orientation of cellulose microfibrils
can change from layer to layer.
17.13 Cellulose is synthesized at the
plasma membrane, not preassembled
and secreted like other wall components
• Cellulose is polymerized by complexes
embedded in the plasma membrane.
• The synthesizing complexes move
along the face of the plasma
membrane.
17.14 Cortical microtubules are thought to
organize components in the cell wall
• During interphase the microtubules in
plant cells are primarily located
immediately beneath the plasma
membrane.
17.14 Cortical microtubules are thought to organize components in the
cell wall
• Cortical microtubules are often
coaligned with the newest cellulose
microfibrils.
• Cortical microtubules may organize the
cell wall by providing tracks for the
synthesis and assembly of cellulose
microfibrils.
17.15 Cortical microtubules are highly
dynamic and can change their orientation
• Plant microtubules polymerize from
multiple sites.
• Microtubules can move along the cortex
after they have been nucleated.
17.15 Cortical microtubules are highly dynamic and can change their
orientation
• Microtubule-associated proteins
organize microtubules into parallel
groups.
• The microtubule array can reorient in
response to:
– hormones
– gravity
– light
17.16 A dispersed Golgi system delivers
vesicles to the cell surface for growth
• The plasma membrane and cell wall
materials needed for growth are
provided by the ER/Golgi system.
• The Golgi apparatus is dispersed in
plants.
• The actin system propels the dynamic
Golgi apparatus over the ER network.
17.17 Actin filaments form a network for
delivering materials around the cell
• Organelles and vesicles move around
the cell by cytoplasmic streaming,
powered by actin-myosin interaction.
• Plants have two unique classes of
myosin.
17.18 Differentiation of xylem cells
requires extensive specialization
• Files of xylem cells undergo
programmed cell death to form waterconducting tubes.
17.18 Differentiation of xylem cells requires extensive
specialization
• The tubes are prevented from inward
collapse by transverse patterns of
secondary wall thickening.
• Cortical microtubules bunch-up to form
patterns that anticipate the pattern of
secondary thickening.
17.19 Tip growth allows plant cells to
extend processes
• Highly localized secretion of cell wall
materials allows plant cells to extend
long processes.
• In tip-growing cells, actin filaments and
microtubules generally run parallel to
the direction of outgrowth.
17.19 Tip growth allows plant cells to extend
processes
• Bundles of actin filaments direct the
movement of vesicles to the tip.
– There, they fuse with the plasma
membrane, driving extension.
• Microtubules seem to control the
number and location of cell tips.
• Symbiotic bacteria turn tip growth in on
itself to gain access into the plant.
17.20 Plants contain unique organelles
called plastids
• Plastids are membrane-bounded
organelles that are unique to plants.
• Several types of plastid exist, each with
a different function.
17.20 Plants contain unique organelles called
plastids
• All plastids differentiate from
proplastids.
• Plastids arose during evolution by an
endosymbiotic event.
17.21 Chloroplasts manufacture food
from atmospheric CO2
• Photosynthesis occurs in specialized
plastids called chloroplasts.
• Leaves maximize the amount of light for
photosynthesis.
• Mesophyll cells are shaped for maximal
gas exchange.