Describe The Relationship Between Bacteria And Phage

Viruses are microscopic particles that invade and take over both eukaryotic and prokaryotic cells. They consist of two structures, which are the nucleic acid and capsid. The nucleic acid contains all genetic material in the form of DNA or RNA, and is enclosed in the capsid, which is the protein coating that helps the virus attach to and penetrate the host cell. In some cases, certain viruses have a membrane surrounding the capsid, called an envelope. This structure allows viruses to become more stealthy and protected. There are two cycles in which a virus can go into: lytic and lysogenic. The lytic cycle consists of the virus attaching to a cell, injecting its DNA, and creating more viruses, which proceed to destroy the host. On the other hand, the lysogenic cycle includes the virus attaching to the cell, injecting its DNA, which combines with the cell’s DNA in order for it to become provirus. Then, the provirus DNA may eventually switch to the lytic cycle and destroy the host.

Some phages infect bacteria to destroy them, which is called lysic lifestyle, while other phages infect bacteria and stay dormant inside them for a while, which is referred to as a lysogenic lifestyle. A phage infects the bacteria cell by injecting its genetic material into the bacteria’s cytoplasm. This allows the bacteria synthesis process to start making the phage’s genetic code instead of its own. Once the bacteria have made enough phages to handle, the walls will break and release all of the phage that was created. The phages that were made are now resetting the process and beginning again by infecting the other near bacteria by injecting their genetic material once again. Those phages that stay within the bacteria and not burst the bacteria will continue to reproduce the phages own genetic code. (Griffiths,

The purpose of this experiment was to determine the reversion rate and recombination rate of two mutant T4 bacteriophages, rII 29 and rII 31. Through recombination rate, the map unit between the two mutants was calculated.

Titer of the Bacterial virus, the Measurement of the Recombination and the Reversion Rate, and the Gene Map Distance (Phage Recombination)

The virus fuses with the cell’s plasma membrane. The capsid proteins are removed, releasing the viral proteins and RNA. Reverse transcriptase catalyzes the synthesis of a DNA strand complementary to the viral RNA. Reverse transcriptase catalyzes the synthesis of a second DNA strand complementary to the first. The double-stranded DNA is incorporated as a provirus into the cell’s DNA. Proviral genes are transcribed into RNA molecules, which serve as genomes for the next viral generation and as mRNAs for translation into viral proteins. The viral proteins include capsid proteins and reverse transcriptase (made in the cytosol) and envelope glycoproteins (made in the ER). Vesicles transport the glycoproteins from the ER to the cell’s plasma membrane. Capsids are assembled around viral genomes and reverse transcriptase molecules. New viruses bud off from the host cell.

The main objectives of this experiment included making dilutions of solutions, plating phage or bacteria, and determining the number of bacterial viruses or phage in a suspension. It was also conducted to demonstrate that two different mutants of phage T4 can exchange genetic material to give rise to wild-type phage. The experiment was used to distinguish mutants from wild-type by their host specificity. The recombination in bacteriophage was performed to determine the concentration of unadsorbed phage from the U series plates, total concentration from B series, and concentration of

Transformation is the transfers of virulence from one cell to another, through the transferring of genetic material. It was originally postulated in 1928 through the works of Federick Griffith, a British microbiologist. Griffith observed that the mutant form, non-virulent form, of the bacteria Streptococcus Pnumoniae could be transformed into the normal, virulent form, when injected into mice along with heat killed normal forms. He concluded that somehow the information the dead virulent form had transformed the mutant form into a virulent form.

Genetic transformation occurs when genes are inserted into another gene to change the organism’s trait (Weedman2016). In this experiment, we proceeded to transform the E. coli bacteria with a gene that contained green fluorescent protein. The green fluorescent protein is used in experiments because it beams a green color under a UV light (Chalfie2008). Typically, it is used to mark the expression of genes, which is why it serves as the symbol for all gene expressions (Tsien1998). In the experiment, we will be using pGLO as the organisms that will transmit the disease, otherwise known as a vector. The pGLO in the experiment

The transposon in this experiment is contains kanR in between the inverted repeats on either end, which will be transposed from the plasmid pVJT128 to the chromosome of the recipient bacteria.

In this last situation, resistant genes become embedded in small units of DNA, called transpons, which can easily move into other DNA molecules. Making matters worse, many bacteria have specialized transpons called integrons, which act like flypaper when catching new genes (3).

We all know that bacteria moves around the body and multiplies to the point where it gets us sick but how does this process work. The process of transduction is our answer to the how this all works. Transduction is a process that introduces non native DNA into a cell by a virus. An example of Transduction is the process having to do with DNA, the viral transfer of DNA from one bacterium to another bacterium.

One reason why I agree and disagree with specialized transduction because the people who are doing genetic engineering know what they are dealing with and know what to do with specialized transduction. Another reason why I agree and disagree with specialized transduction because they are creating antibiotic for specific bacteria but also making the bacteria more resistant. The last reason why I agree and disagree with specialized transduction because it can spot mutated genes and create genes.

The protective capsid helps the virus escape detection and destruction during the invasion of the host. When the virus reaches the target cell, biochemical reactions between the capsid and cell wall allow the virus to latch on and inject its genome into the cell’s interior. Once inside, the viral genetic material insinuates itself into the host’s DNA or RNA. In an efficient feat of natural bioengineering, the host cell’s genetic machinery now does the rest of the work for the virus. The cell, which had already been making copies of its own genome, now also replicates that of the virus. Coded within the viral material is the blueprint for making more copies of the viral genome. Further instructions command the production of capsids and directions for assembly of new viruses. After the host cell becomes engorged with viruses, it explodes, sending the new

Microbiologists believe that Mycobacterium tuberculosis becomes antibiotic resistant when it exchanges genes with other already resistant bacteria because bacteria mutate and spread rapidly within hours. There are three forms of gene mutations categorized as conjugation, transformation, and transduction. Conjugation permits the transfer of DNA from one cell to another whereas transformation occurs when a cell decays. While its cell wall falls apart, the inner genetic makeup becomes available to other

Bacterial transformation is the process of moving genes from a living thing to another with the help of a plasmid.The plasmid is able to help replicate the chromosomes by themselves; laboratories use these to aid in gene multiplication. Bacterial transformation is relevant in everyday lives due to the fact that almost all plasmids carry a bacterial origin of replication and an antibiotic resistance gene(“Addgene: Protocol - How to Do a Bacterial