When you shear DNA, the covalent bonds within the sugar-phosphate backbone of the DNA strand are broken. This process results in fragments of DNA with free ends that can be used in various molecular Biology techniques such as PCR or DNA sequencing.
Hydrogen bonds between the nitrogenous bases need to be broken for the DNA strand to separate during replication or transcription.
DHISS DiKC
Hydrogen bonds are broken between the nitrogenous bases when DNA unzips during replication. These bonds are relatively weak, which allows the DNA strands to separate and the process of replication to proceed smoothly.
The backbone of a strand of DNA is held together by covalent bonds, specifically phosphodiester bonds. These bonds form between the sugar and phosphate groups of adjacent nucleotides in the DNA chain.
DNA molecules treated with DNAase would undergo degradation, resulting in the cleavage of the phosphodiester bonds between nucleotides. This enzymatic activity would lead to the fragmentation of the DNA molecules into smaller pieces or nucleotides.
The hydrogen bonds are broken in order to unzip the DNA strand. This all occurs during the DNA replication process.
They are broken by the enzyme DNA helicase.
Hydrogen bonds between the nitrogenous bases need to be broken for the DNA strand to separate during replication or transcription.
Hydrogen Bonds
Hydrogen Bonds
DHISS DiKC
Hydrogen Bonds
Hydrogen bonds are broken between the nitrogenous bases when DNA unzips during replication. These bonds are relatively weak, which allows the DNA strands to separate and the process of replication to proceed smoothly.
hydrogen bonds
Hydrogen Bonds.
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The hydrogen bonds between the base pairs in DNA molecules are disrupted at high temperatures. These bonds are relatively weak and can be easily broken by heat, causing the DNA strands to separate. This process is known as denaturation.