Chapter 2.2.7: Peroxisomes
It used to be thought that peroxisomes are formed by the budding of smooth Endoplasmic Reticulum (ER). However, now it is thought that they form through self-assembly. (reference)The peroxisome is another major source of Oxygen utilization (along with the mitochondrion). There are specific proteins associated with the peroxisomes membrane, also there are 3 oxidation enzymes associated with peroxisomes:
- D-amino acid oxidase
- Urate Oxidase
- Catalase
The enzyme contents vary with various types of cells. One of the main functions of peroxisomes in liver cells is detoxification. This is done by the oxidation of substances like:
- Alcohol - About 1/2 of the ethanol one drinks is converted to
acetaldehyde by oxidation.
- Phenols
- Formic acid
- Formaldehyde
Why peroxisomes are not like lysosomes. Peroxisomes are organelles that contain oxidative enzymes, such as D-amino acid oxidase, urate oxidase, and catalase. They may resemble a lysosome, however, they are not formed in the Golgi complex. Peroxisomes are distinguished by a crystalline structure inside a sac which also contains amorphous gray material. They are self replicating, like the mitochondria. Components accumulate at a given site and they can be assembled into a peroxisome. They may look like storage granules, however, they are not formed in the same way as storage granules.
Peroxisomes function to rid the body of toxic substances like hydrogen peroxide, or other metabolites. They are a major site of oxygen utilization and are numerous in the liver where toxic byproducts are going to accumulate.
The peroxisome is made as a phospholipid bilayer, encapsulating oxidative materials. They would be 'sphere-ish' in shape, not necessarily a perfect sphere, and sometimes, they may take other shapes. But most electron micrographs I have seen (2 dimensions) show them as circles. (As you may be aware, the Cell membrane is also a phospholipid bilayer.) Peroxisomes have membrane proteins that are critical for peroxisomal function, to import proteins into their interiors, proliferate or segregate to daughter cells (reference)The main differences would be: 1. Types of phospholipids used. 2. Size of the membrane (i.e. peroxisomes are MUCH smaller than the cell).
Please send questions/comments/suggestions to: Mark Dalton at markwdalton@gmail.com.
Chapter 2.1.5: Na _ K ATPase (Sodium-Potassium ATPase pump)
 This is both an example of how Active anti-port and co-transport works and an example showing part of how nerves and other cells generate a electrical potential on their membrane surfaces.
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Chapter 2.2.5: Golgi Apparatus/complex
 The Golgi apparatus is involved in intracellular membrane maintainance. It modifies products via glycosylation, packages them and vesicles which transport the product to the proper destination.
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Chapter 2.2.1: The Endoplasmic Reticulum
The Endoplasmic Reticulum (ER) is a very amazing part of the cell! (Well I guess every part of the cell is amazing if you see all of what it does). It is responsible for a wide range of tasks! Including the biosynthesis of: lipids for constructing new membranes, proteins (via ribosomes) and complex carbohydrates. The ER membrane typically makes up more than half of the total membrane in the cell and is located between the nucleus and the cytosol and specifically the golgi apparatus. This means that there is 2 membranes between the nucleus and the Golgi Apparatus, the outside ER membrane and the nuclear membrane (This is because the ER is continuous with the outer nuclear membrane). However, there are 2 membranes between the golgi and the ER and there is a LARGE amount of transfer between the two organelles, which suggests there is probably transport occurring through transport vesicles (shown below).
The ER is a made up of two phospholipid bilayer membranes. The enclosed 'sac' is called the ER lumen, the internal space of the ER. The ER is thought to be a single continuous membrane (Reference). Also there are two types of ER:
- Rough ER: Is associated with ribosomes (the dots on its boundaries)
and the membranes tend to be in 'sheets' or flatten sacs called cisternae. - Smooth ER: Which lacks ribosomes, and is also more of a mesh of
smaller interconnecting tubes.
The Endoplasmic Reticulum:  
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Chapter 2.2.2: The Mitochondria
 Mitochondrion is the singular form of mitochondria. The mitochondria major role is ATP production in the eukaryotic cell. These are mobile and flexible organelles, although in some cells they tend to stay in a fixed position. The fixed position is especially true of cells or locations in cells where there will be a need for a high amount of ATP production, such as, near flagella or between myofibrils of muscle. Note this organelle has a double membrane the folded inner membrane is called the Cristae, while the outter membrane is smooth. Mitochondria are also self-reproducing, they have their own circular DNA, with a slightly modified version of the codons. This differs with the eukaryote codon table.
Please send questions/comments/suggestions to: Mark Dalton at markwdalton@gmail.com.
Chapter 2.2.10: Proteins
- 1. Membrane Proteins.
- 2. Enzymatic Proteins.
- 3. DNA Binding/regulatory Proteins.
- 4. Non-membrane transport Proteins.
- 5. Structural Proteins.
- 6. Peptides and peptide hormones.
One role of proteins in cells is for transport of molecules/ions into or out of cells. Three methods of doing this are through active, facilitated or passive transport. Other roles of membrane proteins are in cell recognition, receptors, cell to cell communication.
Types of Proteins:
- Transmembrane Protein:
- Globular Protein:
- Glyco-protein:
- Glyco-proteins are processed in the Endoplasmic reticulum, and a carbohydrate chain is added on.
- A Functional look at Membrane Proteins:
- Transport Proteins:
- There are two ways that molecules pass through transmembrane proteins:
uniport - which is where one molecule is transported, and cotransport - where 2 molecules are transferred. Also there are two basic types of cotransport: symport, which is where two molecules are transported in the same direction and antiport, where the molecules are transported opposite directions through the membrane (which will be shown by the Na - K ATPase pump coming up). Here are the types of transport. - 2.1.4.1. Active Transport (these can be either uniport or cotransport):
- This transport, which will require energy, is going against
the electro-chemical gradient. An example of this can be found in the Na/K ATPase The Sodium-Potassium ATPase pump, this is important especially in the nerves of all animals. This is commonly used to generate a membrane potential.
- 2.1.4.2. Facilitated Transport (these can be either uniport or cotransport):
- Facilitated transport is as it sounds, facilitates transport.
This occurs because it moves with the electro-chemical gradient.
- 2.1.4.3. Passive Transport:
- Small molecules that are uncharged can move directly through
the membrane in the direction of high concentration to low concentration. Molecules that have a charge (positive or negative) it will tend to move to the side of the membrane that have the opposite electrical potential. Proteins role in this is through forming channels through the membrane that facilitate transfer of the molecules in accordance to the electrical and chemical gradients.
- Putting these all together in a membrane is done in the following
example of the Sodium-Potassium ATPase pump in conjunction with the Potassium leak, and the glucose symport with Sodium.
- Cell Recognition:
Cell recognition occurs through - Cell-Cell Communication:
- Receptors:
- DNA binding
- Hormone transport -
Please send questions/comments/suggestions to: Mark Dalton at markwdalton@gmail.com.
Chapter 2.2: Organelles and Membranes
Chapter 2.1: Cell Membrane
 2.1.1. Phospholipids
2.1.2. Cholesterol
2.1.3. Semi-permiable/Osmosis
2.1.4. Proteins/channels
2.1.5. Hydrophobic/Hydrophilic
2.1.6. Self-assembly
The phospholipid bilayer which the cell membrane is an example of, is composed of various cholesterol, phospholipids, glycolipids and proteins. Below is an example of a simple phospholipid bilayer.

The smaller molecules between the phospholids is Cholesterol which helps to give rigidity or stability to the membrane. The phospholipids are the hydrophilic circles with hydrophobic tails. And since most of the cell and area surrounding the cell is made up of water, these fatty acid tails always 'push' away from the water. Causing either a bilayer as above or a 'micelle' which is a single layer circle of phospholipids with the tails pointing in.
There are different are 10 main types of lipids in cell membranes. Each type of cell or organelle will have a differing percentage of each lipid, protein, and carbohydrate. The main types of lipids are:
- Cholesterol
- Glycolipids
- Phosphatidylcholine
- Sphingomyelin
- Phosphatidylethnolamine
- Phosphatydilinositol
- Phosphatidylserine
- Phosphatidylglycerol
- Diphosphatidylglycerol (Cardiolipin)
- Phosphatidic acid
Phospholipids are made up of a hydrophilic (likes water)head and a hydrophobic (fears/moves away from water) tail. The head group has a 'special' region that changes between various phospholipids. This head group will differ between cell membranes [types of cells] or different concentrations of specific 'head groups'. The fatty acid tails call also differ, but there is always one saturated and one unsaturated 'leg' of the tail.

Phospholipids are 2 fatty acids one saturated and one unsaturated (shown by the double bond) that are linked to a glycerol. I have symbolized cholesterol as:
 Cholesterol is a major component of cell membranes and serves many other functions as well. Cholesterol helps to 'pack' phospholipids in the membranes, thus giving more rigidity to the membranes. Also cholesterol serves diverse functions such as: it is converted to vitamin D (if irradiated with Ultra Violet light, modified to form steroid hormones, and is modified to bile acids to digest fats.
The membranes of cells are a fluid, they are semi-permeable, which means some things can pass through the membrane through osmosis or diffusion. The rate of diffusion will vary depending on the its: size, polarity, charge and concentration on the inside of the membrane versus the concentration on the outside of the membrane. When something is permeable it means that something can spread throughout, like (The perfume is permeating the room.). Here is a list of some molecules and how they relate to passing through the membrane without assistance, in other words, through osmosis:
Hydrophobic Molecules:
O2 - Oxygen
N2 - Nitrogen
benzene
Small uncharged Polar Molecules:
H2O - Water
urea
glycerol
C02 - Carbon Dioxide
Large Uncharged Polar Molecules:
Glucose
Sucrose
Ions:
H+ - Hydrogen ion
Na+ - Sodium ion
K+ - Potassium ion
Ca²+ - Calcium ion
Cl- - Chloride ion
Various substances will pass through the membranes at varying rates through osmosis.
One role of proteins in cells is for transport of molecules/ions into or out of cells. Three methods of doing this are through active, facilitated or passive transport. Other roles are in cell recognition, receptors, cell to cell communication. There is more information on membrane proteins and other proteins in later sections.
A very simplistic idea of what these characteristics are is:
Hydrophilic and hydrophobic are, respectively, the like and dislike. Hydrophilic areas of a phospholipid, or a protein are 'attracted' to water, and hydrophobic regions are repelled by water.
Self-assembly occurs due to the thermodynamics, if the phospholipids are in a water (or other polar solution) the tails will want to be 'away' from the solution. The could all go to the top (like oil on water), or they could have the tails point toward each other. With the tails pointing toward each other, this could form 2 different formations.
First would be a micelle which would like like a ball with the phospholipid heads on the outside and the tails pointing together like this or in the form of a lipid bilayer:

Please send questions/comments/suggestions to: Mark Dalton at markwdalton@gmail.com
Chapter 2.0: Parts of the Cell
Chapter 1.2: Types of Cells
 Chapter 1.2: Types of CellsThe major differences between Prokaryotic and Eukaryotic cells are that prokaryotes don't have a nucleus and rarely have membrane bound organelles, (the only exception I have heard of is bacteria with vacuoles). The both do have DNA for genetic material, have a exterior membrane, have ribosomes, accomplish similar functions, and are very diverse. For instance, there are over 200 types of cells in the human body, that very greatly in size, shape, and function. Prokaryotes:
- Prokaryotes are cells without a nucleus. They have genetic materials but are not enclosed within a membrane. These include bacteria and cyanophytes. The genetic material is a single circular DNA and is contained in the cytoplasm, since there is no nucleus. Recombination happens through transfers of plasmids (short circles of DNA that pass from one bacterium to another). They do not engulf solids nor do they have centrioles or asters. There are pictures of two prokaryotes below. Prokaryotes have a cell wall made up of peptidoglycan.
Eukaryotes:
- These are cells with a nucleus, this is where the genetic material is surrounded by a membrane much like the cells membrane. Eucaryotic cells are found in humans and other multicellular organisms (plants and animals) also algae, protazoa. They have both a cellular membrane and a nuclear membrane, also the genetic material forms multiple chromosomes,
that is linear and complexed with proteins that help it 'pack' and is involved in regulation.
Eukaryotes are composed of both plant and animal cells. Plants vary from animal cells in that they have large vacuoles, cell wall, chloroplasts, and a lack of lysosomes, centrioles, pseudopods, and flagella or cilia. Animal cells do not have the chloroplasts, and may or may not have cilia, pseudopods or flagella, depending on the type of cell.

Please send questions/comments/suggestions to: Mark Dalton at markwdalton@gmail.com.
Chapter 1.1: Introduction to Cell biology
Title page
TEXTBOOK OF CELL BIOLOGY Second Edition
Mark Dalton
Copyright © 2006 Mark Dalton
Published and distributed by MedRounds Publications, Inc.
All rights reserved. No part of this publication may be reproduced or transmitted in any form or by any means, electronic or mechanical, including photocopy, recording, or any information storage and retrieval system, without permission in writing from the publisher.
Published in The United States of America.
This course is meant to help those that are interested in learning about Cell Biology. This course material is not for credit, unless you have made some other arrangements or this is being used as a supplement in a 'for credit' course. This course is to help the beginner to biology to understand cell biology in simple term. This textbook is an informal introduction to biology. Chapters will be added as time allows to view the original course: http://www.ccgb.umn.edu/~mwd/cell.htmlIf you have questions, corrections or comments feel free to email me at: markwdalton@gmail.com
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