transfer of DNA from one cell into another through a physical connection between the cells. In the following experiment‚ two strains of Escherichia coli bacterial cells (donor F’lac+strs and recipient F-lac-strr) underwent conjugation to produce a transconjugant strain (F’lac+strr). MAC plates and streptomycin were utilized to determine if conjugation had occurred. When plated‚ the donor colonies appeared red and the recipient colonies appeared white. The transconjugant plates showed red and white colonies
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The disease I’ve chosen to write my research paper on is Bacterial Vaginosis. Bacterial Vaginosis is vaginal condition that can produce vaginal discharge and results from an overgrowth of normal bacteria in the vagina. In the past‚ the condition was called Gardnerella vaginitis‚ after the bacteria that was believed to have caused the condition. However‚ the newer name‚ Bacterial Vaginosis‚ reflects the fact that there are a number of species of bacteria that naturally live in the vaginal area and
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Mallory Charland February 9‚ 2015 Mutations of E. coli Lab Report Advanced Biology Deducing Mutations of the Lac Operon of E. coli Abstract: In this lab we determined a possible mutation in unique bacterial strains of E. coli by observing the proper responses of wild type E. coli Lac Operon as a control group. Mutated strains of E. coli were placed in four test tubes‚ each containing a different substance (lactose‚ glucose‚ water and lactose and glucose)
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Bacterial diseases: Introduction Bacterial diseases include any type of illness or disease caused by bacteria‚ a type of microbe. Microbes are tiny organisms that cannot be seen without a microscope and include viruses‚ fungi‚ and some parasites as well as bacteria. The vast majority of bacteria do not cause disease‚ and many bacteria are actually helpful and even necessary to good health. Millions of bacteria normally live on the skin and in the intestines and can also be found on the genitalia
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Transformation is a process which involves plasmid DNA being bound to the cell surface and the subsequent uptake of DNA by the cell (Panja et al.‚ 2008). For artificial transformation of E. coli cells with plasmids‚ plasmid DNA has to be extracted from bacterial cells using the High-Speed Plasmid Mini Kit‚ which is then mixed with competent E. coli cells followed by heat shock and the streaking of transformed cells on two different types of agar plate (LB and LB+ampicillin). The extracted plasmid DNA is
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Formal lab report: Abstarct: The Purpose of this experiment was to perform Agrobacterium-mediated transformation in Wild type Arabidopsis thaliana Columbia by using somatic plant transformation method. The whole process lasted for over a period of 11 weeks and we were successful in getting transformed plants. Agrobacterium tumefaciens strain containing pMP90 (Ti-helper) plasmid and pCAMBIA1391 (T-DNA) plasmid was used for this plant transformation. pCAMBIA1391 plasmid was constructed by cloning Brassica
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Bacterial growth is the division of one bacterium into two daughter cells in a process called binary fission. Providing no mutational event occurs the resulting daughter cells are genetically identical to the original cell. Hence‚ "local doubling" of the bacterial population occurs. Both daughter cells from the division do not necessarily survive. However‚ if the number surviving exceeds unity on average‚ the bacterial population undergoes exponential growth. The measurement of an exponential bacterial
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STAINING FOR BACTERIAL ISOLATION Submitted by: Cherry Luz L. Rezaga Submitted to: Dr. Tomas J. Fernandez Jr. CRITERIA OF REPORTING 1. Thorough research (20%) 1.1. Number of literature cited more than five (5) 1.2. Completeness of the topic (5) 1.3. Principle discussed (5) 1.4. Literature should be cited in the text (5) 2. Confidence (20%) 2.1. Eye to eye contact (5) 2.2. No reading (5) 2.3. Proper handling of visual aids (5) 2.4. Magnified voice (5) 3. Appropriateness of visual
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the F’lac plasmid. It was concluded that significant changes on the genetic makeup can be achieved through transposition and conjugative plasmids in a short amount of time‚ which can have severe implication on the effectiveness of antibiotics for bacterial diseases. Introduction The purpose of this experiment is to study the transfer of genetic information on plasmid F’lac by using the bacteria Escherichia coli. The genome of the bacteria consists of a single circular DNA molecule
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transduction and conjugation. The first half of this experiment focused on exploring the mechanisms of transduction. This was done by creating a spot titer plate for phage carrying kanamycin resistance and E. coli. E. coli was then proven to have gained kanamycin resistance throughout transduction as demonstrated by its ability to grow on a medium containing kanamycin. The second half of this experiment focused on exploring the concept of conjugation. Our experiment specifically focused on conjugation of resistance
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