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The bacteriophage lytic cycle begins when the phage attaches via a slender stalk to the host cell. Linear DNA from the viral head is injected into the host cell. The phage DNA circularizes, remaining separate from the host DNA. The phage DNA replicates, and new phage proteins are made. New phage particles are assembled. The cell lyses, releasing the phage. The bacteriophage lysogenic cycle begins the same way as the lytic cycle, with phage infecting a host cell. However, the phage DNA becomes incorporated into the host genome. The cell divides, and phage DNA is passed on to daughter cells. Under stressful conditions, the phage DNA is excised from the bacterial chromosome and enters the lytic cycle.
This is the retrovirus. They store genetic information as RNA rather than DNA. They were responsible for AIDS and a leukemia source. Cause Of Aids, Rna Virus, Dna Polymerase, Amino Acid Sequence, Dna Synthesis, Behavioral Psychology, Dna Replication, Nucleic Acid, Chemistry
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Coronavirus RNA strand. Medical illustration with deep blue hexagon structure background. 3D rendering
Steps of a viral infection, illustrated generically for a virus with a + sense RNA genome.1. Attachment. Virus binds to receptor on cell surface.2. Entry. Virus enters cell by endocytosis. In the cytoplasm, the capsid comes apart, releasing the RNA genome.3. Replication and gene expression. The RNA genome is copied (this would be done by a viral enzyme, not shown) and translated into viral proteins using a host ribosome. The viral proteins produced include capsid proteins.4. Assembly. Capsid proteins and RNA genomes come together to make new viral particles.5. Release. The cell lyses (bursts), releasing the viral particles, which can then infect other host cells.
Science ArticlesCoronavirus Structure, Vaccine and Therapy Development1 comments on article "Coronavirus Structure, Vaccine and Therapy Development"
Schreiben zeigt Text RNA Virus an. Geschäftsansatz eine virusgenetische Information wird in Form von RNA gespeichert
RNA Interference (RNAi) as a Potential Tool for Control of Mycotoxin Contamination in Crop Plants: Concepts and Considerations