unknown organisms provided by the instructor in a nutrient broth. It is only known that the two organisms are from vomit; one is gram-positive and the other is gram-negative. It is necessary to first separate the two organisms by inoculating a nutrient agar plate using the streak-plate method. The initial streak-plate procedure was performed and placed in the incubator at 37◦C for 24-48 hours. Upon observing the growth on this plate‚ it is fairly obvious that one of the organisms is Serratia marcescens
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Biology Assessment: Influenza Structure: Viruses are non-cellular obligate intracellular parasites‚ requiring a living host cell in order to reproduce. A developed viral particle (virion) lacks the metabolic machinery of cells‚ containing just a single type of nucleic acid (DNA or RNA) encased in a protein coat or capsid. Viruses can be distinguished by their structure and by the nature of their genetic material (single or double stranded DNA or RNA). Viruses that affect humans are more difficult
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Question: How does the size of the cell affect its efficiency in exchanging substances through several ways‚ like diffusion? Aim: To plan and carry out an investigation to show the relationship between volume/Cm3‚ surface area‚ and diffusion using agar cubes measured in time/s; and to demonstrate‚ using diffusion‚ why the size of cells is limited‚ keeping the room temperature and pressure constant. Hypothesis: I expect to find that when the surface area to volume of a cell reaches a certain level
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17th‚ October 2010 Margarita SA: VOL RATIO AND AGAR BLOCKS Conclusion: For this experiment the agar jelly had to be cut in to five different block sizes‚ after that has been done we had to add all five blocks in to the test tube with the acid and time to see how long it would take for the colour to change from a pinky purple to clear. From this experiment I learnt that the bigger the size of the jelly is the
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Agar.io is a addictive multiplayer action packed game developed by Matheus Valadares. In the game you are a cell and your goal is to gain as much mass as you can by consuming both pellets and smaller cells without being swallowed by bigger enemy cells. You can either play a deathmatch where everyone is the enemy‚ in a party with your friends or as a colored team that must consume other colors accept for your own. While playing the game‚ there is no set score‚ players have to respawn when all of
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incomes? Interviewing sellers of a consumption shop‚ cloth shop‚ CDs shop‚ food shop and their customers. ____________________________________________________________ As a part of the course trans-border studies‚ we went to Wat Kutao in Chiang Mai where Shan’s New Year festival was taken place and celebrated by Shan Literature and Cultural Committee to practice participant observation method. Shan‚ a sub-group of Tai ehnic group of Southeast Asia‚ primarily live in the Shan State of Burma (Myanmar)
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4017B Decade counter (5-stage Johnson counter) Navigation The Beastie Zone contains detailed information about lots of useful integrated circuits‚ including test circuits with easy to follow prototype board layouts... | | | 1. Pin connections | More updated pages... | 2. What is a decade counter? | DDE2 : Logic Gates | 3. Basic operation | DDE3 : Astables | 4. RESET and ENABLE inputs | DDE4 : Monostables | 5. Sequencing | | 6. Inside the 4017 | Safety Lights
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The Role of Agarase in Agar-Degrading Bacteria Abstract Agar-Degrading (agarolytic) Bacteria is physiological class of bacteria capable of utilising agar as a sole carbon source. This ability is made available by the use of agarases - enzymes which break down agarose into oligosaccharides. This physiological class branches through genii‚ regardless of Gram Stain status or morphology. Through a review of scientific literature we can find identification methods‚ optimum conditions and the
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_____________________________________________________________________________ Agarose is a polymeric cross-linked polysaccharide extracted from the seaweed agar. Agarose is used widely in gel electrophoresis because it gels at a lower temperature‚ does not contain the inhibitors of virus growth frequently present in agar‚ and has more uniform pore size than that of agar. It is also easily poured and does not denature the samples. In agarose gel electrophoresis‚ DNA or RNA fragments are separated or isolated according
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Making Agar Cushions 1. Start with wearing gloves and swabbing them with 70% ethanol to keep the materials that will be used in the experiment sterile. 2. Wipe the work station with Wescodyne and paper towels. It is important to keep the sterile materials such as slides in petri dish‚ Pasteur pipette in container and forceps covered as much as possible. 3. Place four to five filter papers in the petri dish and drip few drops of water on the strips‚ this will maintain moisture in the agar cushions
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