Bacterial $DNA$ is modified by adding methyl groups. Why is this done?

  • A
    To replicate its own $DNA$
  • B
    To replicate multiple genes simultaneously
  • C
    To activate its genes
  • D
    To protect its own $DNA$ from its own restriction enzymes

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Similar Questions

$pBR322$ contains the recognition sites for which of the following endonucleases at the $amp^R$ site?

Which of the following $DNA$ sequences can be cut by a restriction endonuclease?

Which organism is most commonly used as a host in $r-DNA$ technology?

In bacteria,genes for antibiotic resistance are usually located in:

Restriction enzymes that are used in the construction of recombinant $DNA$ are endonucleases which cut the $DNA$ at 'specific-recognition sequence'. What would be the disadvantage if they do not cut the $DNA$ at specific-recognition sequence?

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