Vol. 4, No. 2
INTRODUCTION
This study was done to determine unknown microorganisms that were retrieved from pond water in Rocklin, California. If the study involves identifying microorganisms from water, various amount of test are done to find what type of bacterias are in water. The most common bacteria in the genera Eschericha, Pseudomonas, Acinteobacter, and Aeromons are amongst the top bacteria found in water. As a result, one or more of these microorganism will be found in the pond water collected. It is important to specify one of these bacteria in the water sample as it is potentially harmful. Some strains of Eschericha Coli are known to cause “serve gastrointestinal infection, dysentry and even death in susceptible individuals”(Wilson, 2015). Most importantly, it is important to find these species that can cause danger to humans. So, they can be treated accordantly with the right antibiotics if they presented any of the side effects.
MATERIALS AND METHODS
Culturing/Streak: Trypticase soy agar (TSA) plate: Since the unknown sample contains Gram (-), it was appropriate to use this type of agar. Using a sterilized loop a sample was streaked on the TSA. The purpose of this producer is to allow growth of the unknown sample. Taking extra to prevent contamination. The inoculated TSA was stored in a plastic bag at room temperature. After two days, The TSA plate was analyzed through visual examination. In addition, the determination of colony and cell morphology were
The first step toward identifying this unknown organism was to perform a Gram Stain to differentiate between gram positive and gram negative bacteria. This is an important step because it directs what the next tests will be. My Gram Stain on sample #12 showed that the bacteria was gram negative, however, after receiving the results of the OF glucose, H2S, Citrate, Urease and Motility tests, it was apparent that my Gram Stain was contaminated. I then performed a catalase test which came back negative, so I ordered a Bacitracin disc, Optochin disc and a CAMP test which had to be incubated overnight. After receipt of those test results,
Bacteria are ubiquitous; they can be found on the skin, in the soil, and inside the body. Because of the very nature of this ubiquity, it is important to be able to determine between different strains of bacteria. An example of this is determining the causative agent for a disease so that the patient will be treated with the appropriate antibiotics. It may be important to determine the bacteria in a certain region, because like with enteric bacteria, it is normal to find them in the digestive tract as they are in a symbiotic relationship with our bodies in this area; however, they also cause opportunistic infections in places outside of the digestive tract to our detriment, such as with a urinary tract infection. Some strains of bacteria are common to nosocomial infections, and identifying these bacteria as such helps create the guidelines for healthcare workers in antiseptic technique. All of the morphology and characteristics of each strain of bacteria help us to better understand the role of bacteria in the body as well as helps us understand how they can cause illness, and what treatment regimen to set in place. In lab this semester, a sample of unknown
The main idea of this experiment was to correctly identify the unknown bacteria, #3. Identification of unknown bacteria yields multiple benefits in many different areas in the research of microorganisms. In this experiment I performed many different test dealing with things such as the presence of enzymes, fermentation abilities and different chemical reactions. Observations made from the tests were then compared to a gram negative unknown chart in order to identify the bacteria. Based off of my results and the chart, I concluded the bacteria #3 was the bacteria Escherichia coli. E. coli is most commonly found in the intestines of warm blooded organisms. Most E. coli strands are non pathogenic however, there are strands
The purpose of the bacterial unknown independent study experiment completed throughout the course of this lab was to determine the identity of an unknown bacterial species. The unknown bacteria sample was chosen from numerous samples provided by the instructor. The starting unknown sample, unknown #15 was a mixed bacterial culture and a broad approach taken to identify the sample. Various biochemical tests were completed to identify the bacterial species along with the use of databases such as Gideon and Bergey’s to compare the test results of known bacteria to the results of the unknown sample. Information was gathered from the other sources and databases and phenotypic testing completed and the results compared to the database results. Aseptic
Introduction: Having a hands-on academic experience of the different techniques for instance aseptic technique and procedures like gram staining is important characteristics for understanding the concept of learning to identify a type of bacteria. During this lab report each student would be using a variety of lab techniques and process/procedures from the lab course taught from the professor and learned from students this semester. To include, by performing the multiple test with three types of medias the students should be able to administer the methods to identify the unknown bacteria. With the information from results and extra notes assist the students to identifying the unknown bacteria. Lastly the benefits from this type of hands-on
Not all the bacteria that live in well water are bad, but a few strains
Prokaryotes are ubiquitous, successfully adapting to diverse environments as well as developing symbiotic relationships with host organisms (Lengeler, Drews, & Schlegel, 1999). Prokaryotes may have both autotrophic and heterotrophic characteristics. A cyanobacteria is photosynthetic, commonly called blue-green algae, and may produce toxins (Crayton, 1993). Bacteria are most commonly associated in the general
This laboratory experiment’s objective was to take a pure culture and isolate it from a mixed culture. The other part of the objective was to ascertain what species of bacteria that the pure culture was. The hypothesis made stated that so long as lab protocol was followed, the unidentified culture would be positively recognized/identified. An isolated pure colony of the unknown culture was obtained using the quadrant streak plate method. Afterward, the culture was Gram stained, and the results showed that it was Gram positive. Motility tests were done on the unknown using a filter paper bridge on a petri dish that contained TTC with agar. The unknown was revealed to not be motile, which meant that it did not possess flagella. The last test done was to learn the metabolic capabilities of the unknown bacteria. There were tests done for citrate utilization, the mixed fermentation pathway, catalase presence, carbohydrate fermentation in mannitol, lactose and glucose, urease production and the butanediol fermentation pathway in order to better identify the unknown bacteria. The results from each of the metabolic tests in conjunction with the motility and Gram staining tests were ultimately compared to results from database containing many different kinds of results from various bacteria. The unknown from the mixed culture was identified as Staphylococcus
Aeromonas hydroplilia species are ubiquitous bacteria found in a wide range of aquatic environments. They cause infection in vertebrates and invertebrates, including frogs, birds, and various fish species. Although primarily associated with diseases in immunocompromised humans, new evidences infer that Aeromonas hydroplilia species are potential evolving human pathogens regardless of the host’s status. The Environmental Protection Agency (EPA), and U.S. water supplies routinely examine the organisms. Elevated numbers of Aeromonas hydroplilia species, above the EPA code, are continuously recorded in recreational water samples in San Diego
|MSA Agar |For organisms that are |Isolates for mannitol fermentation |Yellow color change in |Staphylococcus aureus |
A mixed culture of two unknown bacteria was provided by the instructor. The methods used for
This microscopic biome is characterized by its bacterial diversity and density. Studies have shown that bacteria cell count to be higher in the microfilm than the average 106 cells per ml of sea water (Cole 1982). Some examples of associated bacterium genera include Pseudomonas and Acnromobacter, both Gram-negative, aerobic, and have been distinguished as human pathogens in patients with conditions that suppress their immune system (Watanabe et. al,
Escherichia coli are commonly found in lower intestine of warm blooded animals. Most E. coli are harmless. The bacteria can be grown easily and its genetics are relatively simple and easy to study, making it the best-studied prokaryotic organism. Certain strains of E. coli can produce toxins that can cause food poisoning when eating unwashed vegetables. (Wikipedia, 2010)
Microorganisms can easily be found in water. In third world countries, this can pose a huge threat, because lots of people can get sick from drinking water. SODIS is a method used by many in undeveloped countries as means of attaining microbe-free water. It involves allowing water to stay exposed to sunlight in order to kill whatever microbes are living in it. For this experiment, microbial diversity was determined by collecting a sample of water of different from shaded water and water directly hit by the sunlight. Microbes were then cultured for 7 days. The abundance of the different colony types was then counted. Results exhibited that the community from the light area was more biodiverse. It was concluded that a possible reason for this is due to the different structures of bacteria, allowing some of them to sustain the light and others to be restricted by it. Since SODIS relies on light to kill microorganisms, it should be accompanied by another method that will also kill the bacteria that may survive in the water after being treated in the sunlight.
Introduction: Through the conduction of numerous experiments, the identity of two bacterial isolates was determined. The tested specimen was an unknown sample of a mixed culture of two different species of bacteria. The first step that was taken was obtaining a pure culture of each species of bacteria by isolating one species from the other. Once isolation was complete, the isolated cultures were tested using procedures that had been performed during previous lab sessions. A gram stain was performed on the two isolates. The isolate which had tested gram negative was then tested for the presence of cytochrome C and lactose fermentation. For the gram positive isolate, cell shape was determined and a catalase test was performed.