Bio 1
Bio 1
Eukaryotic Cells
Plant and animal cells are both eukaryotic cells
They have the components listed in the table above (so a cell membrane,
cytoplasm and ribosomes), as well as others
Animal and plant cells are both eukaryotic cells as their genetic material is
packaged in a nucleus
Prokaryotic Cells
The cell membranes of all prokaryotic cells are surrounded by a cell wall
(usually made from a substance called peptidoglycan)
Prokaryotic cells do not have a nucleus, and are much smaller than
eukaryotic cells
Prokaryotic cells table
You need to show an understanding of the size and scale of cells (and the
subcellular structures within them)
You need to be aware that many subcellular structures in eukaryotic cells are
the same size as or bigger than prokaryotic cells!
Very small (or very big) numbers are represented using standard form; this
helps to avoid confusion
Let’s say we want to represent the length of a Vibrio cholerae cell, which is
1.5µm, in mm
The nucleus
Cell membranes
Mitochondria
Ribosomes
Cytoplasm
Some cellular structures can only be seen when viewed with an electron
microscope
A cell wall made of cellulose (algal cells also have this structural
feature)
Plant cells found in the leaf and stem may also contain chloroplasts
The plant cell shown above contains chloroplasts, so it would be found in the
leaves of a plant
Specialised cells
A specialised cell is a cell that has a structure that aids its specific
function
Function:
Nerve cells are long, meaning that they can conduct nerve
impulses between different areas of the body
Muscle cells
Function:
All muscle cells contain protein filaments that can slide over each other
to allow muscle contraction
Sperm cells
Sperm cells are mobile – their tail helps propel them forward in search of an
egg cell
The tail rotates, propelling the sperm cell forward and allowing it
to move
The acrosome in the head contains digestive enzymes that can break
down the outer layer of an egg cell so that the haploid nucleus can
enter to fuse with the egg’s nucleus
The root hair is an extension of the cytoplasm, increasing the surface area of
the cell in contact with the soil to maximise absorption of water and minerals
Function:
Root hairs increase surface area (SA) so the rate of water uptake by
osmosis is greater
Thinner walls than other plant cells so that water can move through
easily due to shorter diffusion distance
Xylem vessels
Xylem cells lose their top and bottom walls to form a continuous tube
through which water moves from the roots to the leaves
Function:
Phloem cells
Phloem cells are adapted for the transport of dissolved sugars and amino
acids
Function:
Cells are joined end-to-end and contain holes in the end cell
walls (sieve plates); this forms tubes which allow sugars and amino
acids to flow easily
Cells have very few subcellular structures to aid the flow of materials
• Aim: To use a light microscope to observe, draw and label a selection of plant
and animal cells, including a magnification scale
• You will:
◦ Use a light microscope to make observations of biological specimens and
produce labelled scientific drawings
Care must be taken to avoid smudging the glass slide or trapping air bubbles
under the coverslip
Using a microscope
Light microscopes have a lens in the eyepiece which is fixed and two or three
objective lenses of different powers
Procedure:
In this practical, prepared Petri dish plates should be provided which are
used to investigate bacterial growth
You will most likely use safe strains of coli or Micrococcus luteus bacterial
cultures in your practical
It is vital that one of the paper discs placed on the bacterial agar plate
is not soaked in antiseptic or antibiotic but sterile water instead
Incubating the plates allows the bacteria in the agar to multiply by binary
fission, this may be visible by the agar darkening or by colonies appearing
The antiseptics present in the discs will diffuse into the agar, with the
concentration decreasing with distance from the disc
Clear zones of inhibition are not always perfectly circular, so the diameter
of each zone should be measured twice (at 90° angles to each other) and
a mean diameter and area calculated for each clear zone