BioInformatics Reviewed Links:

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Contacts:

 

Email your links to Dr. Karron: karron@casi.net

Class Site Administrator is Peter Cline: peterc@nytimes.com

This page is maintained by Osman Kabir: Osman_Kabir@yahoo.com

 

UPDATED: December 29, 2001

 


Link Ladder:

 

Name

Published Links

Christopher Conway

8

Changyou Yu

8

Christoforos Christoforou

6

Mohammed Kuddus

6

Tawhidul Chowdhury

5

Zheng Li

5

Xiadong (Sheldon) ÝZou

5

Xiao Lin

3

Lu Tang

3

Qi Chen

2

Peter Cline

2

Yang Li

2

Gang Pang

2

Kit-yu Cheng

1

Ma Da

1

Osman Kabir

1

Ercan Kocabasoglu

1

Rajiv Kumar

1

Ying Li

1

 

Note: As new links are submitted the ladder will be updated. The ladder just displays the top two contributors.


 

Link: http://www.spectrum.ieee.org/WEBONLY/publicfeature/oct01/bio.htm
l
 

Reviewed by: Peter Cline

 

Surveying the Current State of affairs in the detection of Biological 
Agents Christopher Aston has surveyed the current state of affairs in 
Biological warfare. He examines the pros and cons of a number of 
approaches to
biological agent detection. He also briefly touches on 
diplomatic measures
for staving off biological attacks and the 
problems inherent therein.
 
The bulk of the 
article focuses on the state of the art in biological
detection 
methods. The methods reviewed are detecting DNA of disease
pathogens, 
the use of antibodies to detect the presence of pathogens,
tissue-
based sensor, and mass spectrometry.ð All of these methods have
there 
advantages and disadvantages but it seems overall that tissue-
based
electrical impedance and mass spectrometry prove mot 
effective.
&n!
bsp;
Tissue-based electrical impedance uses the 
fact that many toxins will
trigger measurable and differentiated 
responses in living cells.
Researchers at Stanford University have 
successfully constructed a 
Handheld sensor that uses this principal. 
Mammalian cells are cultured in a
laboratory and put in a cartridge 
that contains a microelectrode array.ð 
The introduction of a biotoxin 
causes ion channels on the cells' membranes 
To open or close, causing 
detectable mill volt changes in the membrane.
Researchers can choose 
certain immune system cells that produce fluorescent
proteins upon 
contact with the biological agent to create a visual cue 
in the 
presence of biotoxins. Prototype systems were able to produce 
this
visual cue within 15 seconds of coming in contact with the 
biotoxin.
Drawbacks to this approach include trying to keep the!
 fragile cell 
Samples alive in the field.
 
Mass Spectrometry 
eliminates this drawback by foregoing living 
Bioreagents altogether. 
It works by heating a liquid sample until it vaporizes and 
then 
Ïbombarding" it with "electron beam to give a charge to the 
fragments".
Positively charged particles are sorted by mass and 
charge in a mass
spectrometer, and the ratios of these two measures is 
used to calculate
molecular weights. A second mass spectrometer breaks 
these down 
further into component amino acids. Each fragment will 
have a unique amino 
acid ratio which can be used to identify it. The 
system is said to be able 
to detect as few as 100 bacteria in a 
sample. The drawback here is 
reducing the device footprint to a size 
that is useable in the field.
&n!
bsp;
In conclusion, Aston admits that these 
technologies are in their 
infancy, but will ultimately be important 
components in the changing 
battlefields of tomorrow's wars. Naturally 
one may hope that such systems will find a 
place monitoring civilian 
airspaces as well.

 
 
 
Link : http://gaia.fc.peachnet.edu/bio1010/chapter6.htm
<
![if !supportEmptyParas]> 
Reviewed by: 
Mohammed A. Kuddus
 
This site describes 
energy and enzymes, which are related with any
physiological tests 
that are commonly used in biomedical sciences, and 
to know how to 
select and apply the appropriate tests by means of a
computer-based 
statistical package. The enzyme database can be useful 
to anybody 
working with enzymes and that it can be help in the development 
of 
computer programs involved with the manipulation of metabolic pathways. 
The application, movement, and transformation of energy ultimately 
underlie 
All physical and chemical processes. Thermodynamics deals 
with energy 
Relations in general,!
 but bioenergetics is concerned only with energy in living
systems. 
The first and second laws of thermodynamics define the 
principle of 
energy conservation in the universe and the direction of a process in 
which energy is exchanged between a system and its 
surroundings.
 
Energy-requiring and 
energy-releasing reactions of metabolism are 
coupled in living 
systems, which increases efficiency and allows greater 
orderliness. 
Useful free energy is stored as chemical energy in living cells, 
most
commonly as ATP. The ADP-ATP cycle links reactions, acting as 
common
intermediates in sequences in which energy from breakdown 
reactions 
becomes available for biosynthesis reactions. Energy 
transfers in metabolism 
may proceed by phosphoryl group transfer via 
the ADP-ATP system, by 
electron transfer via redox couples!
 in oxidation-reduction reaction, and by 
other means. Redox couples 
are the oxidized and reduced forms of a compound, 
such as the 
NAD+/NADH couple, and they act as common intermediates in 
coupled 
energy-requiring and energy-releasing reactions involving electron 
transfer.
 
Reaction rates in 
living systems are modulated by unique protein 
catalysts called 
enzymes, which function primarily by lowering the barrier 
of
activation energy of a reaction and thereby increase the otherwise 
sluggish organic chemical rates. Enzymes are highly efficient 
catalysts, since 
they are highly specific for certain substrate 
molecules. Specificity of an
enzymeÌs affinity for its substrate 
depends on the region of the enzyme
called the active site, where 
enzyme and substrate fit together like a 
lock and key. Two !
systems of self-regulation of enzyme actively are feedback
inhibition 
and co-operativity.
 
Regulation of the kind 
of enzyme and the amount of enzyme synthesized 
In cells is controlled 
by the genes. The kind of enzyme made depends on 
genetic information 
encoded in DNA, while the amount of enzyme made is 
regulated at the 
levels of transcription and translation of the informational DNA. 
The 
substrate, or inducer, combines with the repressor product of 
regulator
gene action and releases the repressor from its association 
with DNA. Upon
removal of the repressor, transcription proceeds, and 
enzyme synthesis 
can occur in subsequent translation of the messenger 
RNA copies of DNA
information.

 
 
http://genomeathome.stanford.edu/
 
Reviewed by: Zheng 
Li
 
This is the web page 
of genome@home, a protein
sequence-structure simulation project with a 
goal of
understanding genomes.
 
Genes are the 
functional units of a genome. Each gene
encodes the information for 
how to make a specific
protein. How a gene specifies the amino acid 
sequence
in a protein is known. But it is still unclear how 
and
why many different protein sequences, each encoded by
a 
different gene, can form the same three-dimensional
protein 
structure.
 
Scientists have been 
workin!
g for decades to unravel
the protein "sequence structure 
relationship. Now
that the human genome and many others are 
being
sequenced, there is a unique opportunity to 
compare
natural genomes and their proteins to sets 
of
laboratory-designed proteins to understand and 
answer
questions, such as, why does nature choose 
specific
genes? Can we design better proteins? Why do 
some
genetic mutations that change the protein 
sequences
cause diseases and others do not?
 
Genome@home project 
uses a computer algorithm, based
on the physical and biochemical rules 
by which genes
and proteins behave, to design new proteins hence 
new
genes that have not been found in nature. By 
comparing
these "virtual genomes" to those found in nature, 
a
much better understanding of how!
 natural genomes have
evolved and how natural genes and proteins work 
can be
obtained. The study is also of practical 
significance.
All the new protein sequences obtained from 
the
simulation runs are added into virtual genome 
protein
design database which could has potential 
important
applications, such as engineering new proteins 
for
medical therapy, designing new 
pharmaceuticals,
assigning functions to the dozens of new genes 
being
sequenced every day, understanding protein 
evolution
etc.
 
Genome@home is a very 
exciting basic science project
with its study results of potential 
practical
application significance.

 
 
http://www.di.com/AppNotes/ForceVol/FVMain.html
 
Reviewed by: 
Osman Kabir
 
ÝÝÝÝÝÝÝ Applications of Volume 
Imaging
 
The web space belongs 
to Digital Instruments and Veeco
Metrology group. Digital Instruments 
was co founded by
Dr. Virgil Elings and Dr. John (Gus) Gurley in 
1987.
The article explains the physics and application of 
a
technique called, "Force Volume Imaging." It is 
based
on the phenomenon that any small particle 
that
approaches a surface experiences as a reaction a 
force
before and after that particle makes 
contact.
Measurements are carried out using an Atomic 
Force
Microscope (AFM).The data is essentially stored as 
an
array of force curves over an entire area since most
are 
not homogeneous surfaces. Measurements of these
forces reveals 
electrostatic, chemical and magnetic
properties !
of these surfaces. This technique also
allows one to record a 
topographic image with minimal
damage to the surface. It is believed 
that this
technique will become the standard for 
studying
nanoscale forces and interactions. 
 
The article is well 
organized and does a fair job in
explaining the physicsð behind the 
procedure and its
application albeit it does use technical lingo, 
hence
some background knowledge will be required.

 
 
http://doegenomestolife.org/
 
Reviewed by: Zheng 
Li
 
This is the web page 
of U.S. Department of Energy
Genome to Life (GTL) program. 
 
GTL 
is a program proposed by Department of Energy to
achieve the far-
reaching of all the biological goals:
a fundamental, comprehensive, 
and systematic
understanding of life. In order to achieve 
this
ambitious goal, the DOE offices of Biological 
and
Environmental Research and Advanced Scientific
Computing 
Research have formed a strategic alliance to
meet this grand 
challenge.
 
The GTL is a ten-year 
program.!
 The plan is to use DNA
sequences from microbes and higher 
organisms,
including humans, as starting points 
for
systematically tackling questions about the 
essential
processes of living systems. Eventually, the 
program
will move beyond the DNA sequences. It will 
use
advanced technologies and computational tools 
and
resources to identify and understand the 
underlying
mechanisms that enable organisms to develop, 
survive,
carry out their normal functions, and reproduce 
under
various environmental conditions. 
 
Microbial Cell Project 
(MCP), a GLT-related program,
has also been proposed by DOE. MCP takes 
a
whole-genome approach to understand the function 
and
regulation of all genes for a single living system 
and
the pathways in which the protein products interact.
It will provide the ultimate test of GTL findings.
 
With both GTL and the 
MCP programs involved in the
collection, integration, and 
dissemination of diverse
data and the development of appropriate 
tools, the
researches will eventually contribute to the 
shifting
of biology from current level of a 
basically
qualitative science to a more quantitative 
science.
DOE hopes that the ultimate applications of 
the
results obtained from these programs will help 
to
fulfill its broad missions in energy, 
environmental
remediation, and protection of human health. 
 
Although this web page 
is for the introduction of
DOE's program, Genome to Life, I enjoyed 
browsing it
and its related links very much. It has helped me 
to
better unde!
rstand what computational biology and
computer science can do in 
advancing our knowledge and
understanding of life.

 
 
http://www.the-
scientist.com/yr2001/oct/prof_011015.html
 
Reviewed by: Kit-yu 
Cheng
 
ÝÝÝÝÝÝÝ Training for the Bioinformatics 
Boon
 
Because of the 
explosion in genomic and proteomics
research, those who have expertise 
in bioinformatics
are really in high demand.ð Researchers spend more 
and
more time using computer as their tools.ð A $10
million 
program has been created to help institutions
and scientists build 
their bioinformatics.ð Millions
have poured in computer-assisted 
research as well.
Many universities start to offer short courses to 
help
scientists who want to deepen their expertise.
 
Three years ago, the 
concept of creating a central
online warehouse of genetic maps and 
data stored on
supercomputers and made freely available on the 
World
Wide Web was broug!
ht forward by Eric Lander, a
genetics scientist and Vincent Cerf, the 
pioneer of
Worldwide Web.ð In the past three years, 
the
replication of data on the Web has exceeded 
anyone's
ability to centralize and streamline it.ð 
Institutions
are looking for computer specialists who can 
build
links between databases and find new ways to 
compare
data.ð To help with these issues, a special 
interest
group of the American Society for Information 
Science
and Technology is under development.ð Scientists 
with
expertise in both biology and computation are 
sought
after.ð Universities such as University of 
Pittsburgh
and Duke University are offering classes to people 
who
are interested in seeking a career in bioinformatics.
It 
appears universities are very responsive to what
the world is in need 
of.

 
http://www.the-
scientist.com/yr2001/nov/research2_011126.html
 
Reviewed by: Ma 
Da
 
ÝÝÝÝÝÝÝ Saving Lives Past the Emergency 
Room
 
This article 
introduces some recent studies on inflammatory molecules
attempting to 
reduce trauma deaths by using knowledge and techniques of
human genome 
research.
 
The body's system 
failure, also known as the multi-organ dysfunction
Syndrome is the 
main reason that causes trauma patients death in the emergency 
room. 
For scientists, the reason for organ failure is unknown, but the order of 
the failure always follows in the same way. The blood supply goes 
through 
the lung and blood-borne bacteria from infection or any 
inflammatory substances 
the body releases against infection also pass 
through here. Inflammatory 
reaction in the lung makes gas exchange 
very di!
fficult, and then a series failure will
follow. Therefore, to 
understand the inflammation is the key of all. A study on 
this puzzle 
based human genome research was launched through a cooperation 
of a 
large number of institutions and scientists from last October.
 
Many attempts for 
solving the problem have been made in the past but 
The progress was 
very limited. One reason is that the research only focused 
on each 
individual inflammatory molecule, but the body's complex interplay 
was
ignored by the single-factor approach. Today, the human genome 
project can help
researchers study and compare the complex 
interactions among genes. 
There are promoters and switches in the 
genome that turn the genes on and off. 
Those promoters are often over 
1,000 base pairs long. There are a large 
number of DNA-binding pr!
oteins that read signals, which bind or detach from the
promoter. 
Therefore we have a lot of switches that interact each other. The 
patterns for distinguishing good or bad response can be developed 
through the 
Genomics way.
 
Though progresses have 
been made in this study, technology and 
Techniques such as complex 
mathematical models and computers are still needed for
complex systems 
research. In a positive view, this may be a good news for 
those
computer majors sitting in Bioinformatics 
classroom.
 


Link: http://www.ai.mit.edu/projects/medical-
vision/surgery/surgical_navigation.html
 
Reviewed by: Qi 
Chen
 
ÝÝÝÝÝÝÝ Image Guided Surgery

 

This web page belongs to the Computer Vision Group of the MIT 
Artificial Intelligence Lab. It describes a project on Image Guided 
Surgery that
is collaboration between this group and Brigham and 
Women's Surgical 
planning Laboratory. Parts of the project are 
developing tools, which will 
enable surgeons to visualize internal 
structures through an automated overlay 
of 3D reconstructions of 
internal anatomy on top of live video views of a 
patient.
 
These tools developed 
by this group have been successfully used in
neurosurgery.ð The first 
step of applying of these tools in surgery is
construction of 3D 
Models of a patient's brain.ð Using automated 
techniques and semi-
automated techniques, the segmentation of the anatomical 
structures 
that appear in an internal scan such as MR and CT is performed.ð A!
fter
segmentation, these MR or CT images can be directly used for 
surface
registration or for 3D visualization.ð Then, this group uses 
surface
rendering techniques to display the segmented MRI structures.ð 
This
rendering process removes hidden portions of the surface, and 
allows
glimpses into internal structures.ð In the following step, the 
coordinates of points on the patient's skin are obtained in order to 
register the
patient to the segmented MR skin.ð The following 
automatic registration
process performs a two-step optimization to 
correlate the MRI 
coordinate frame to the operating room frame.ð 
Using the image tools, the MRI skin 
can be removed, which will allow 
the surgeon have x-ray vision to see where 
the internal structures 
are located.ð These tools also allow the tracking 
of medical 
instruments in the frame of reference of the medical imagery.
 
This 
group reported that their navigation system has been successfully 
used for over 200 neurosurgical cases.ð The system achieves high 
positional
accuracy and initial estimates indicate that the use this 
system 
reduces the cost of neurosurgical procedures.
 

Link: http://www.cs.wisc.edu/~johnh/EigenFaces/
 
Reviewed by: 
Christoforos Christoforou 
 
ÝÝÝÝÝÝÝ Eigenfaces and face 
recognition
 
This report discusses 
the procedure for extracting
Eigenfaces and the use of them for the 
purpose of face
recognition.
 
Eigenfaces is a set of 
images that can be considered
as the building blocks of all human-face 
images. Any
image of human-face can be described by the 
quantity
of each eigenface that exist that image. 
Eigenfaces
can be considered as a particular feature that 
is
common to all human-faces. How common that feature is,
is 
described by a value that is calculated at the time
their calculation. 
This value is called eigenvalue.
 
This way of describing 
images is especially helpful!
 in
the area of face identification and face recognition.
It 
reduces the dimensionality of images from the set
of all images to the 
set of all faces. Further
eliminates unnecessary details from the 
image keeping
only the most important information that can be 
used
for identification purposes. For face recognition 
each
image to be recognized is described with its
eigenfaces 
components and then its is tested for
similarity with other images in 
an image database by
the Euclidean distance between 
them.
 
However, eigenfaces do 
not come without fault. Using
eigenfaces have problems recognizing 
faces with
modified facial features, images with different 
light
amounts, and taken from different camera angles. 
These
problems can be partially solved by pre-processing and
normalizing the images.ð
ðð
Eigenfeature, Eigennose, 
Eigenmouth, Eigeneyes are
some variations of Eigenfaces that are being 
tested
for improving performance of face recognition 
systems.
These methods introduce the idea of 
localizing
recognition to specific important areas of the 
face
instead of the face as a whole. 
 

Link: http://www.sciam.com/news/110901/2.html
 
Reviewed by: Yang 
Li
 
ÏAssembling 
Building Blocks of Nanocomputers
 
This report gives a 
brief review on some recent
research activities attempting to assemble 
some novel
tiny molecular electronic elements into simple 
logic
circuits.
 
Chemist Charles Lieber 
and co-workers at Harvard
University created simple logic circuits 
by
crisscrossing nanowires of silicon and gallium-
nitride
grown from their solutions with assistance of a 
laser.
They believed that nanowires could!
 pave the way for
molecular electronics because they are 
more
predictable and can be built without 
conventional
lithography, and can be easily scaled up to next 
level
of complexity.
 
Physicist Adrian 
Bachtold and colleagues at Delft
University of Technology in the 
Netherlands took a
more conventional approach by carving aluminum 
strips
from a layer of the metal and deposited 
carbon
nanotubes on top then attaching gold to both ends 
of
nanotube to create a transistor. And they even
connected 
such nanotubes in different ways to make
circuit such that they can 
perform simple logical
functions.
 
Physicist Jan Hendrik 
Schvn et al at Bell Laboratories
have refined a technique for making 
transistors out
!
of a layer of small carbon molecules, and they found
that just one was 
enough to turn a signal on or off,
making a rudimentary circuit 
element.
 
Nanotechnologists Greg 
Tseng and James Ellenbogen of
the MITRE Corporation remarked that 
there is still a
long way to go to assemble a useful chip out 
of
molecular electronic device, but the future 
is
promising.
 

 
http://www.ccdc.cam.ac.uk/prods/csd/csd.html
 
Reviewed by: Zheng 
Li
 
ÝÝÝÝÝÝÝ The Cambridge Structure 
Database
 
This is the web page 
of the Cambridge Structure
Database (CSD), a database for protein 
structure.
 
The CSD contains 
crystal structure information for
over 245,000 organic and metal 
organic compounds. All
of these crystal structures have been analyzed 
using
X-ray or neutron diffraction techniques. For 
each
crystallographic entry in the CSD, three 
distinct
information types are stored. They are 
conveniently
categorized as 1D, 2D and 3D in terms of 
their
"dimensionality".
 
1D provides all the 
bibliographic information of a
molecule. It includes the crystal 
structural and
experimental information. It also contains the authors
names, 
compound name, the full journal references, and
the crystallographic 
cell dimensions and space group.
Polymorphic form, absolute 
configuration, drug or
biological activity etc. are also included 
where
applicable.
 
2D is the chemical 
structure of a molecule. It
includes the molecule atom and bond 
properties. Atom
property consists of element symbol, number 
of
connected non-hydrogen atoms, number of 
connected
hydrogen atoms, and the net charge. Bond 
property
consists of bond types the molecule possesses. 
There
are seven different types in total.
 
3D provides the 
information which can be used to
generate the three dimensional 
structure of a
molecu!
le.ð It includes the atomic coordinates, the
space group symmetry, the 
covalent radii and the
crystallographic connectivity established by 
using
those radii. The 3D information is matched with the 
2D
chemical structure.
 
The CSD is a unique 
and fully comprehensive research
resource in molecular and super-
molecular chemistry.
About 800 published papers have described the 
uses of
the CSD to study chemical bonding, 
molecular
conformations, hydrogen bonding and 
other
intermolecular interactions with particular 
emphasis
on molecular and drug design. The CSD has 
subscribers
at almost 120 industrial sites and nearly 
1000
academic institutions, covering 56 
countries
worldwide.

 
 
Link: http://www.ai.mit.edu/projects/medical-
vision/surgery/surgical_navigation.html
 
Reviewed by: Qi 
Chen
 
ÝÝÝÝÝÝÝ Image Guided 
Surgery
 
This web page belongs 
to the Computer Vision Group of the MIT 
Artificial Intelligence Lab.ð 
It describes a project on Image Guided Surgery that 
Is collaboration 
between this group and Brigham and Women's Surgical 
Planning 
Laboratory.ð Parts of the project are developing tools, which will 
enable surgeons to visualize internal structures through an automated 
overlay 
of 3D reconstructions of internal anatomy on top of live 
video views of a 
patient.
 
These tools developed 
by this group have been successfully used in
neurosurgery.ð The first 
step of applying of these tools in surgery is
construction of 3D 
Models of a patient's brain.ð Using automated 
techniques and !
semi-automated techniques, the segmentation of the anatomical 
structures that appear in an internal scan such as MR and CT is 
performed.ð After
segmentation, these MR or CT images can be directly 
used for surface
registration or for 3D visualization.ð Then, this 
group uses surface
rendering techniques to display the segmented MRI 
structures.ð This
rendering process removes hidden portions of the 
surface, and allows
glimpses into internal structures.ð In the 
following step, the 
coordinates of points on the patient's skin are 
obtained in order to register the
patient to the segmented MR skin.ð 
The following automatic 
registration process performs a two-step 
optimization to correlate the MRI 
coordinate frame to the operating 
room frame.ð Using the image tools, the MRI 
skin can be removed, 
which will allow the surgeon have x-ray vision to see 
where the inte!
rnal structures are located.ð These tools also allow the tracking 
of 
medical instruments in the frame of reference of the medical 
imagery.
 
This group reported 
that their navigation system has been successfully 
used for over 200 
neurosurgical cases.ð The system achieves high positional
accuracy and 
initial estimates indicate that the use this system 
reduces the cost 
of neurosurgical procedures.
 


Link: http://www.cdc.gov/ncidod/eid/vol4no3/relman.htm
<
![if !supportEmptyParas]> 
Reviewed by: 
Mohammed A. Kuddus
 
ÝÝÝÝÝÝÝ Infectious 
Diseases
 
This site contains 
information about infectious diseases, which are
significant for 
research work in the field of bioinformatics. Modern
infectious 
diseases research requires access to new technologies 
related to 
genomics (e.g., gene array chips), computers software, imaging 
devices,
animal models, microbial strain depositories/collections as 
well as 
large databases. Microorganisms that colonize mucosal 
surfaces and cause 
disease constitute a small portion of the total 
microbial world. The 
relationships of these bacteria with the host 
are delicately balanced and may be
influenced by both environmental 
and genetic factors. The microbes that
possess mechanisms, enable them 
to produce disease, they are called
pathogens. Some microbe!
s cause diseases indirectly by producing toxins
(poisons). These 
toxins may be produced by bacteria in foods that are 
eaten by the 
host.
 
In order to infect a 
host, most microbes must first attach to a 
specific receptor site on 
a tissue of the host. The specify of receptor sites 
may vary from 
organ to organ within the body of the host and from one host
species 
to another. Thus one infectious disease may involve only 
specific 
tissues or organs of the body whereas another disease may involve 
different tissues. Certain bacteria like Streptococcus pneumonia, a 
major causes 
of bacterial pneumonia, induces an acute inflammatory 
response in the 
lungs that results in a rapid accumulation of fluid 
exudates. These fluids
interfere with the normal function on the 
lungs. Various enzymes 
secreted by ce!
rtain pathogenic bacteria thought to contribute to the disease 
process by destroying tissues. Collagenase and lecithinase are 
enzymes produced by 
the bacteria that cause gas gangrane. Hemolysins 
are enzymes that destroy 
red blood cells. Lipase and nucleases are 
bacterial enzymes that break down 
fats and nucleic 
acids.
 
Some microbes produce 
toxins that are important mechanisms in the
productions of diseases. 
There are two general types of toxins, 
exotoxins and endotoxins. 
Exotoxins are extremely powerful biological poisons. As 
an example 
botulisms and tetanus toxins that specifically interfere with 
the 
transmission of nerve impulses, and diptheria toxin that inhibits 
protein synthesis by preventing the elongation of the polypeptide 
chain during 
the process of translation. The effect of endotoxins a!
re general, producing 
such clinical signs and symptoms as fever, 
diarrhea, and circulatory
disturbances, including shocks. Endotoxins 
are composed of complexes of
proteins, polysaccharides and 
phospholipids.
 
To prevent and control 
infectious diseases require a basic 
understanding of the causative 
agent, the pathogenesis of the disease, and the 
individuals at risk. 
In infectious disease medicine, the most rational approach 
to
prevention and control of the diseases is to eliminate the pathogen 
or
reduce the number of pathogen organisms to the point that the host 
defenses can easily block infection. Although many years of research 
on these
diseases have helped elucidate the pathogens, pathogenesis, 
and host
response, efforts to rationally control these diseases are 
limited and 
often infective.