The objective of our project was to determine if different wavelengths of light would affect the growth of the Rhodococcus genus and whether the two bacteria would handle DNA damage from UV light exposure differently. Our hypothesis is that various wavelengths of light would inhibit the growth of bacterial colonies of both Rhodococcus species differently. Also, we believe that Rhodococcus fascians (yellow) is more resistant to DNA damage from UV light than Rhodococcus corynebacterioides (red). To perform this experiment, we first made the bacterial growth medium was made. Then, the process of the dilution of the bacteria is performed to allow the bacteria to be seen easily. The diluted bacteria is spread upon the medium in the petri dishes
In the case of temperatures the cultures were incubated at each determined temperature. For the UV radiation, cells were exposed to UV light for 10 seconds and then grown in 30oC. For the EtBr treatment, 50ul of EtBr was added to the growth medium and cells were incubated at 30oC. In the case of sunlight exposure, cells were exposed to sunlight directly and grown at room temperature
Ryazantseva, I. N., Saakov, V. S., Andreyeva, I. N., Ogorodnikova, T. I. and Zuev, Y. F. 2012. Response of pigmented Serratia marcescens to the illumination. Journal of Photochemistry and Photobiology B: Biology, 106 p. 18-23
In this lab project, the microbiology students were given 2 unknown bacteria in a mixed broth each broth being numbered. The goal of this project is to determine the species of bacteria in the broth. They had to separate and isolate the bacteria from the mixed broth and ran numerous tests to identify the unknown bacteria. The significance of identifying an unknown bacteria is in a clinical setting. Determining the exact bacteria in order to prescribe the right treatment for the patient. This project is significant for a microbiology students because it gives necessary skills to them for future careers relating to clinical and research work.
The purpose of this laboratory is to learn about cultural, morphological, and biochemical characteristics that are used in identifying bacterial isolates. Besides identifying the unknown culture, students also gain an understanding of the process of identification and the techniques and theory behind the process. Experiments such as gram stain, negative stain, endospore and other important tests in identifying unknown bacteria are performed. Various chemical tests were done and the results were carefully determined to identify the unknown bacteria. First session of lab started of by the selection of an unknown bacterium then inoculations of 2 tryptic soy gar (TSA) slants, 1 nutrient broth (TSB), 1 nutrient gelatin deep, 1 motility
al. (1994) explain that a complementary DNA for GFP produces a fluorescent product when expressed in E. coli cells as the expression of GFP can be used to monitor gene expression and protein localization in living things. In this experiment, the heat shock method will be used to deliver a vector (plasmid) of GFP to transform and grow E. coli bacteria. Four plates containing Luria Bertani (LB) broth and either –pGLO or +pGLO will have E. coli bacteria added to it. The plate containing –pGLO (no pGLO) and LB will show growth as ampicillin will be present killing bacteria but no glowing because no arabinose will be present for glowing to be activated, the same result will be seen in the plate containing +pGLO, LB and ampicillin.
Abstract: Bacterial transformation involves the change of genetic composition of bacteria by altering its genetic identity. The pGLO plasmid was ingrained in the E. coli cell, which allows the modified E. coli cell to begin to code for the GFP protein gene and the beta lactamase gene (ampicillin resistance gene). After modifying the bacteria cell, the changes involved with the plasmid were tested on 4 plates, two plates containing the pGLO plasmid (+) were treated with LB nutrient media. One of the LB plates contained arabinose in it, which should fluoresce green under UV light. The other LB plate contained ampicillin. Two other plates which did not contain the pGLO plasmid (-) both had LB media growth, one plate just to show cell growth,
It can be concluded that chloroplast is responsible for photosynthesis, with blue light forming the highest rate of photosynthetic activity. The widespread use of coloured netting in the future could result in indoor plant growth that is unreliant on weather, and the ease of the production of crops with the desirable phenotypes. However, future research is still required to eradicate any unknown data and determine plant responses in relation to wavelength
The purpose of the study is to identify an unknown microorganism using multiple microbiology lab techniques. Through this process I will gain knowledge on how to perform these techniques as well as the importance of these tests on identifying unknown microorganisms. This is significant as the goal of this course is to familiarize ourselves with the common microbiology tests as well as the microorganisms we encounter in our daily activities.
Theodor’s experiment was created in part to learn which wavelengths (colors) of light were most effective in carrying out photosynthesis and to prove that it occurs in chloroplast. The experiment was inspired by Theodor’s observation of aerobic bacteria. Theodor observed that aerobic bacteria would move towards the chloroplasts of green algae. Theodor hypothesized that the reason why the bacteria moved toward the chloroplasts was because the organelle generated oxygen via photosynthesis. If photosynthesis occurs in chloroplasts, then the bacteria would aggregate on the chloroplasts producing the most oxygen. Theodor’s experiment was essential because it demonstrated that chloroplasts were the site of photosynthesis. Furthermore,
Moreover, a future experiment is to determine the effect that the distance between the lamp and the solution has on the rate of photosynthesis. Several experiments with a similar setup to this experiment that vary the distances between the lamp and solution could be used to test this.
[7] Rothschild, Lynn J. “The Influence of UV Radiation on Protistan Evolution.” Journal of Eukaryotic Microbiology (1999), Issue 46 no. 5 pg. 548-555.
Talaro , K., & Chess, B. (2012). Foundations in microbiology. (8th ed., pp. 563-564). New York, NY:
Bacterial pigment plays role as antioxidant by inhibiting photodynamic lipid peroxidation in liposome and give protection against photodamage (Rajagopal et al. 1997).Xanthomonadin is example of this bacterial pigment.
Photosynthesis is a widely studied topic among the world of science due to its importance for life and its many uses. Photosynthetic pigments reflect and absorb different wavelengths of visible light based off their polarity. In this experiment, we studied photosynthetic pigments, first, by determining polarity and then, by measuring the amount of light of a given wavelength that a pigment absorbs. We used two methods in this experiment, chromatography and spectrophotometry. For the first portion of our experiment we determined the distance each pigment migrated, their R_f values, and their polarity. Our predications based off polarity, lead to our hypothesis
Leboffe, M. J., & Pierce, B. E. (2010). Microbiology: Laboratory Theory and Application, Third Edition 3rd Edition (3rd Ed.). Morton Publishing