MICROBIOLOGY IN THE ANCIENT TIMES Gone are the days when the scientists used the Liquid media for the study of microorganisms and used to grow them in the laboratories. Above all, when they had to segregate the microorganisms to study and gather information on the individual growth pattern and characteristics, the liquid media was not useful at all. In 1881, Robert Koch used aseptically cut slices of the potato as a solid culture medium which was supplemented with gelatin which was poured and allowed to solidify. This Technique however helped them to identify the discrete colonies of the microorganisms. Gelatin did not solidify during the summer and therefore Dr. Hesse came up with the concept of using agar-agar as the medium and this revolutionised the Microbiological Sciences. These methods however were very time consuming, difficult to study the discrete characteristics of the microorganisms and made it necessary to sub culture in the additional media. NEED OF THE HOUR For these reasons we need to develop approaches to the detection, quantification and identification of the microorganisms. This is especially important in the food manufacturing industries as a quality risk management. We need quick methods which can help in efficient monitoring of the manufacturing processes and also helps to ensure the proper state of control HACCP analysis therefore reducing the process variability and increasing the
An unknown bacterium was handed out by Dr. Honer. The appropriate tests were prepared and applied. The first procedure that was done was the gram stain. Under a microscope, if the gram stain is purple, the bacterium is gram positive, if the stain is red, it is gram negative. The next test was the fermentation tests for glucose, sucrose and
Depending on what a bacteria can and cannot do, will help to correctly identify it. It is always important to start out with a purity check. To achieve that, you can inoculate an agar plate and incubate for 48 hours. Make sure you only see one type of colonies on the plate. Knowing the optimal temperature for the bacteria will also let a scientist know where to place the different types of medias he/she inoculates with the unknown bacteria. Knowing if you are working with a gram positive or gram negative bacterium, a scientist will need to perform a gram stain. This will also help to see the shape and arrangement of the bacteria. The size can be determined by doing a simple stain. The size of most bacteria ranges from .5- 10um. This specific bacteria that I was working with, was smaller than 2um. Most bacteria can grow with the presence of oxygen. A simple test like the gas pack can be performed to figure out if growth is possible without oxygen is doable. My unknown bacteria needs oxygen to grow. Throughout my study, the unknown bacteria was tested to see if it can grow in acidic conditions, however no growth occurred. Before inoculation, the substrate was a clear yellow color and in liquid state. After receiving the negative result, I kept the broth in the 37C incubator for 7 more days to confirm the negative result. Using premade slants with different types of sugars such as Mannitol, Sorbitol, Lactose, Trehalose, Maltose and Sucrose, to determine if the bacteria can metabolize glucose and if the bacteria is oxidative or fermentative. It was determined that my bacteria is strictly oxidative (needs oxygen to grow) and cannot metabolize glucose. Another test was done to confirm if the bacteria was able to utilize different carbohydrates in the presence of oxygen. I used Cellobiose, Arabinose, Adonitol, Fructose and Malonate wee tabs. Out of the 5 different types of carbohydrates, only 3 different
There are many reasons for knowing the identity of microorganisms. The reasons range from knowing the causative agent of a disease in a patient, so as to know how it can be treated, to knowing the correct microorganism to be used for making certain foods or antibiotics. This study was done by applying all of the methods that I have been learned so far in the microbiology laboratory class for the identification of an unknown bacterium.
There are many reasons for knowing the identity of microorganisms. The reasons range from knowing the causative agent of a disease in a patient, so as to know how it can be treated, to knowing the correct microorganism to be used for making certain foods or antibiotics. This study was done by applying all of the methods that have been learned so far in the microbiology laboratory class for the identification of unknown bacteria. The identification process can be completed with a series of deferential stains and biochemical tests. Creating a dichotomous key helps to limit the amount of biochemical tests done on an unknown organism and by observation
There are many reasons for identifying an unknown bacterium. The reasons range from medical purposes, such as determining if the unknown could cause ailments in living things or knowing what microorganisms are needed to make antibiotics to other purposes such as knowing the exact microorganism has to be used to make certain foods. This experiment was done by applying methods in order to identify an unknown bacterium.
In this experiment, an unknown bacterium was given to each individual student. The main purpose of this lab was to identify the given unknown bacteria going through a series of biochemical tests as one of the gram negative bacteria among six different Gram negative bacteria Escherichia coli, Enterobacter aerogenes, Klebsiella pneumoniae, Proteus mirabilis, Pseudomonas aeruginosa and Salmonella typhimurium. At the very beginning, streaking method; T-streak technique was used to isolate the pure colonies. For the morphological identification of unknown bacteria, Gram Stain Method was done. Biochemical tests that were conducted for the experiment
The unknown project was an experiment where the student was given a petri dish of unknown bacteria. Tests were performed on it to identify the specific species. The purpose of the experiment was to learn about the identifying tests, and procedures in the identification of specific microbes. The reason the master plate was used to create a working plate is so that if the working plate becomes contaminated, one can resort back to the master plate for the pure strain of the bacteria and create a new working plate. The purpose of the first procedure, the gram stain, was to be able to dye and then distinguish gram negative and gram-positive cells on a smear. The second procedure, the citrate test is used to see if the bacteria can use citrate as
After many performed test such as the API 20E test strip, motility test, inoculated plates, gram stain, an identification flow chart which began with the results from an indole, MR, VP, and citrate test. This amongst many other test. These results brought the conclusion of my unknown culture to be Escherichia coli, my unknown number was 11.
that the bacteria are capable of growing on the agar and that there was nothing
As loathsome as some people find them, leeches played a relevant and predominate role in the field of medicine in Ancient cultures, starting in 2000 B.C. These blood-sucking annelids were used in the c therapeutic treatment of blood-letting to cure a variety of problematic health issues: diseases, blood circulation disorders, and infections. In fact, So great was the demand for the aquatic worms, that an entire profession was built around the supply of leeches. Thus, the job of leech collector was created, and those who worked in the occupation kept the medical practitioners well supplied with the curative parasites.
Microbes would begin a deadly and massive change in each New world and Old world societies. Diseases would help win battles. It would destroy cultures and many groups of people would be completely be destroyed due to the rapid and uncontrolled loss of people. This would go for both ends of the new world people and the old world people in massive ways.
Though the subject was initially limited to study of microbes and their characteristics or properties, latter it was explored to see all possible applications and benefits to man.
In this laboratory experiment, we was introduce to an introduction to streaking and spreading of bacteria in agar plates such that single cells can be isolated from one another, each cell can reproduces to form a visible colony composed of genetically identical clones. Streaking and spreading bacteria is to obtain individual colonies is usually the first step in genetic manipulation of microorganisms.
Another purpose of this experiment is to stress the importance of knowing the identity of a microorganism. Knowing the species of microorganism present in a sample provides a
The purpose of this experiment is to obtain isolation of individual species of particles from the mixed culture. This is completed through the isolation technique of streak plate. The objective of this experiment is to replicate the technique of streak plate but on a much larger scale. Because it is on a larger scale the particles are able to be visually observed as they are isolated using the streaking technique as the experiment is conducted. The benefits of the streaking technique is when a cultures has multiple species they are able to be more easily identified once they have been isolated. This experiment is much like the experiments completed on an agar plate but on one a much larger scale and where techniques