REVIEW OF LITERATURE
Beijerinck(1901) firstly reported, isolate and describe the species of Azotobacter such as A.chroococcum and A.beijerinckii. The former species was described as a soil inhabiting species and the later as a water borne organism. Sengupta, R.K. (1990) reported that the isolated Azotobacter species had ability to fix atmospheric nitrogen in pure culture.Mulder and brontonegoro (1974) described several other species of Azotobacter i.e. A.chroococcum and A.paspaii. Subramoney and Abraham(1962) isolates Azotobacter chroococcum strains from red loamy soils of India. Line and Loult (1973) reported that the Azotobacters are the most intensively investigated heterotrophic group. They are the aerobic bacteria possessing highest respiratory
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Nitrogen fixation requires molybdenum ions, but they can be partially or completely replaced by vanadium ions. If atmospheric nitrogen is not fixed, the source of nitrogen can alternatively be nitrates, ammonium ions, or amino acids. The optimal pH for the growth and nitrogen fixation is 7.0–7.5, but growth is sustained in the pH range from 4.8 to 8.5.[30] Azotobacter can also grow mixotrophically, in a molecular-nitrogen-free medium containing mannose; this growth mode is hydrogen-dependent. Hydrogen is available in the soil, thus this growth mode may occur in …show more content…
The process of nitrogen fixation requires an influx of energy in the form of adenosine triphosphate. Nitrogen fixation is highly sensitive to the presence of oxygen, so Azotobacter developed a special defensive mechanism against oxygen, namely a significant intensification of metabolism that reduces the concentration of oxygen in the cells. Also,a special nitrogenase-protective protein protects nitrogenase and is involved in protecting the cells from oxygen. Mutants not producing this protein are killed by oxygen during nitrogen fixation in the absence of a nitrogen source in the medium. Homocitrate ions play a certain role in the processes of nitrogen fixation by
Methods Unknown microbial #398 went through several of tests in order to identify its characteristics when isolated from a urine sample of Doris, a 64- year old patient with a kidney infection. To identify unknown #398, must prepare a working and a reserve stock by the inoculation from a broth culture and by quadrant streaking method on a PEM and EMP plates. The following test procedures were incubated at 37°C for 48 hours for observation and identification for unknown #398. The identification of unknown #398 followed test procedures from Brown1.
The purpose of this lab report is to employ a myriad of skills, tools and, methods learned throughout this semester to perform the appropriate tests for the identification of the assigned unknown bacteria. Add more background information here!!! The most important tools and techniques used during this identification include aseptic technique, microscopic examination and, the use of selective and differential media. Aseptic technique is an important tool for microbiologists. It is imperative that aseptic technique is maintained throughout the length of any test to avoid any cross-contamination that may lead to inaccurate results.
In this experiment, we cultivated an unknown specimen containing two microorganisms. The purpose of this experiment was to use a variety of biochemical test previously learned in the lab to identify the unknown bacteria. The identification of unknown bacteria is a major part of microbiology. Microbiologist observe samples such as blood and sputum in the laboratory for the presence of microorganisms. Identifying unknown bacteria is extremely important in clinical settings because it helps physicians find treatment for infections.
Figure 3. Testing of transformed and mutant bacteria on minimal medium Growth was observed on the Transformed (Trsf) section and not on the Mutant (Mut)
Most Cyanobacteria, like the ones in the model, are capable of nitrogen fixation. In order to fuel their growth cyanobacteria, rely on fixed forms of nitrogen such as ammonia and nitrate. Cyanobacteria tends to become very abundant in warm, shallow, undisturbed surface water. These conditions allow for them to form blooms that produce surface scum. They can also produce a toxin called microcystins that makes the water unsafe for consumption.
Introduction Our world is composed of many bacteria’s’ that can either help or destroy us. Therefore, its’s imperative to learn and study them. The purpose of the lab was to put into action the methods that have been learned in the laboratory to determine our unknown bacteria. Bacteria’s can have different features, shapes, and or arrangements that help microbiologist determined their role in our life (whether they are good or bad for humans).
The Unknown Identification Lab was an experiment that provided the opportunity to apply all the tests that were learned in the semester of lab, to identify the two bacterias that remain unknown. Gram- staining and two other tests will be used to identify the unknowns. This experiment is crucial to the understanding of each test, and can benefit in the ability to identify the characteristics of specific bacteria. Having a clearer understanding of the bacteria can further the research of bacteria for medicine, such as antibiotics. The understanding can also help the development of research in the environment.
In the laboratory, identification of an unknown bacterium is often necessary. In the lab, a random sample consisting of three different bacteria was selected. The sample contained one gram-positive, one gram-negative paracolon, and one gram-negative coliform. The purpose of the experiment is to identify each of the three species that the mixture contained. After receiving an unknown mixture, the sample was streaked for isolation onto TSA, blood agar, and MacConkey plates.
The yeast menace is known by several different terms, candidosis, yeast infection,monilia and thrush. Symptoms of yeast infections are vast, however there are some that are more obvious, these include chronic tiredness, cystitis and thrush that continues to come back even after you have treated it. Some other symptoms which are not as obvious include, anxiety,mood swings, fluid retention ,allergies,depression,inability to loose weight,constipation, diahorrea, PMS, acne and dermatitis as well as hypoglycaemia. With a list as exhaustive as this, it's easy to see why it's deemed one of the most debilitating immune deficiencies and nutritional disorders of our time, As with any infection, one or many of the symptoms may exist, however, advanced
Being able to identify unknown microbes from systematic testing is what makes the field of microbiology so important, especially in infectious disease control. Using the testing procedure laid out by the microbiology field we are able to identify unknown bacteria present in our everyday lives, and along the way learn a lot about their characteristics that separate them from other types of bacteria. Being able to do this is vital in order for us to understand why microbes are present in certain places, how they are able to grow and what restricts their growth, that way they can be combatted if necessary. These techniques for determining unknowns are also important for isolating and testing infectious disease microbes in order to prevent spreading. Another important aspect of being able to identify unknown microbes is the
No, phototrophs can also be heterotrophs. Ex: purple non-sulfur bacteria. Name three bacterial phyla that include phototrophs. Chloroflexi, Firmicutes, and Proteos.
In addition, the bacteria need arabinose that help activate the protein that allows to glow green in the transformed bacteria cells. To let
Results The data obtained from the experiment had undergone statistical analysis using t-tests and the results were recorded in Figure 1.0 and Figure 1.1 above. According to the data obtained in Figure 1.0, the p-value is less than 0.05 in all 5 treatment solutions. It is also shown intensity Figure 1.0, the calculated t-value of each concentration of NaHCO3 in each treatment is greater than the critical t-value.
According to the series of test that my group ran for our unknown specimen, we had a match with the bacteria known as Alcaligenes Faecalis. This bacterium belongs to one of the major group of gram-negative bacteria (Phylum Proteobacteria). Alcaligenes Faecalis (Genus, species) is a rod shaped (bacillus), 0.5-1.2 x 1.0-3.0 µm, round with scalloped margin (colony configuration growth), motile (with one to nine peritrichous flagella), gram-negative, non-fermentative bacteria, obligate aerobic, having oxygen as the principal terminal electron acceptor in the electron transport chain (ETC). We consider we have a match with the species Alcaligenes Faecalis because of the following reasons: Fermentation tests performed (Durham sugars) were negative, which indicate that our bacteria use a different metabolic means for growth (non-fermentative gram-negative bacteria).
They can also act as a final electron acceptor. Many bacteria can be differentiated and are identified by their capacity to reduce nitrates to nitrites. Most of the bacteria belonging to the family Enterobacteriaceae reduce nitrates [165]. OF test is used to differentiate those organisms that utilize carbohydrates aerobically (Oxidation) such as P. aeruginosa, from those that utilize carbohydrates anaerobically (Fermentation) such as members of the Enterobacteriaaceae. The OF medium contains peptone, test carbohydrate and bromothymol blue as indicator.