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The recombinant DNA becomes part of the transformed cell's genome.

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12y ago
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4mo ago

When a successful cell transformation occurs, the recombinant DNA is integrated into the host cell's genome. This allows the host cell to produce the desired protein encoded by the recombinant DNA. The transformed cell can now replicate and pass on the recombinant DNA to its daughter cells during cell division.

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14y ago

A cell takes in DNA from the outside cell. This external DNA becomes part of the cell's DNA.

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12y ago

It is integrated into one of the chromosomes of the cell

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15y ago

When transformation is successful, recombinant DNA enters the host cell and remains intact (not fragmented). It is now capable of autonomous replication within the host.

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13y ago

the recombinant DNA is integrated into one of the chromosomes of the cell.

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9y ago

Becomes part of the transformed cell's genome

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Q: What happens to a recombinant DNA when a successful cell transformation?
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A recombinant plasmid gets inside a bacterial cell by?

being introduced through a process like transformation, conjugation, or transduction. Once inside the cell, the bacterial machinery can replicate the plasmid along with its inserted DNA fragment.


Compare the transformation of a bacterium cell with the transformation of a plant cell?

In bacteria, if the plasmid containing the foreign DNA manages to get inside a bacterial cell, this sequence ensures that it will be replicated. In Plant Cells, if transformation is successful the recombinant DNA is integrated into one of the chromosomes of the cell.


How are genetic markers related to transformation?

Genetic markers can be used to track the incorporation of foreign DNA during transformation. By selecting for cells that have taken up the new genetic material, researchers can identify successful transformation events based on the presence of the markers. These markers help distinguish transformed cells from those that have not taken up the desired DNA.


Why are bacterial cells useful in recombinant DNA technology?

Bacterial cells are useful in recombinant DNA technology because they can easily take up foreign DNA through a process called transformation. Once the foreign DNA is inserted into a bacterial cell, it can be replicated and amplified quickly. Bacteria are also easy to culture and manipulate in the laboratory, making them ideal for producing large quantities of recombinant proteins or DNA fragments.


When a biological vector is used which process must take place before recombinant DNA can be placed in the host cell?

The biological vector must first be transformed with the recombinant DNA using a suitable method such as heat shock or electroporation. This process involves introducing the recombinant DNA into the vector so that it can carry and deliver the genetic material into the host cell.

Related questions

How can you tell a transformation experiment has been successful?

if transformation is successful , the recombinant DNA is integrated into one of the chromosomes of the cell. The cell will be fundamentally changed, hence the name "transformation".


A recombinant plasmid gets inside a bacterial cell by?

being introduced through a process like transformation, conjugation, or transduction. Once inside the cell, the bacterial machinery can replicate the plasmid along with its inserted DNA fragment.


What occurs in a successful transformation of cells?

In a successful transformation of cells, foreign DNA is integrated into the host cell's genome, allowing the cell to express new traits or characteristics. This can lead to the production of desired proteins, increased resistance to antibiotics, or other useful applications in biotechnology.


Compare the transformation of a bacterium cell with the transformation of a plant cell?

In bacteria, if the plasmid containing the foreign DNA manages to get inside a bacterial cell, this sequence ensures that it will be replicated. In Plant Cells, if transformation is successful the recombinant DNA is integrated into one of the chromosomes of the cell.


What is the role of calcium chloride in transformation?

Calcium chloride is used in transformation to destabilize the cell membrane, making it more permeable to foreign DNA. This helps in improving the uptake of the DNA by the cells, leading to successful transformation.


How are genetic markers related to transformation?

Genetic markers can be used to track the incorporation of foreign DNA during transformation. By selecting for cells that have taken up the new genetic material, researchers can identify successful transformation events based on the presence of the markers. These markers help distinguish transformed cells from those that have not taken up the desired DNA.


Why are bacterial cells useful in recombinant DNA technology?

Bacterial cells are useful in recombinant DNA technology because they can easily take up foreign DNA through a process called transformation. Once the foreign DNA is inserted into a bacterial cell, it can be replicated and amplified quickly. Bacteria are also easy to culture and manipulate in the laboratory, making them ideal for producing large quantities of recombinant proteins or DNA fragments.


Does recombinant DNA involve placing a normal allele in a cell that has a mutation and hoping that the normal allele begins to function?

Recombinant DNA


What happens during transformation?

A cell takes in DNA from the outside cell. This external DNA becomes part of the cell's DNA.


What does a recombinant DNA have?

Recombinant DNA is a DNA molecule formed by combining DNA from two different sources. It typically contains genetic material from multiple organisms or synthetic origins, allowing for the creation of novel genes or gene combinations with unique characteristics. Recombinant DNA is often used in genetic engineering and biotechnology applications to produce desired traits or proteins.


How does a recombinant plasmid get into a bacterium?

Viruses


How is recombinant DNA transffered?

Recombinant DNA can be transferred into host cells using various methods, including transformation (uptake of DNA by bacterial cells), electroporation (brief electrical pulse to create pores in cell membrane for DNA entry), and viral vectors (viruses used to deliver DNA into cells). The specific method chosen depends on the type of host cell and the desired outcome of the genetic engineering.