DNA Flashcards
Nucleotide
Composed of deoxyribose sugar, phosphate and base
Sugar-Phosphate backbone
Connect the sugar (deoxyribose) with the phosphate of two nucleotides together foriming the sugar-phosphate backbone of dna strand
Hydrogen Bond
Weak bond that joins complimentary bases on opposite sides of dna
3’/5’ end of dna
Marks the end of a dna strand. Has either a deoxyribose sugar (3’) or phosphate (5’) at the end forming a double helix
Dna structure summary
Structure of DNA — nucleotides (deoxyribose sugar, phosphate and base), sugar–phosphate backbone, base pairing (adenine–thymine and guanine–cytosine), by hydrogen bonds and double stranded antiparallel structure, with deoxyribose and phosphate at 3’ and 5’ ends of each strand respectively, forming a double helix.
Base sequence of dna forms…
The base sequence of DNA forms the genetic code.
What happens before cell division and what is needed for DNA replication
Prior to cell division, DNA is replicated by a DNA polymerase. DNA polymerase needs primers to start replication. A primer is a short strand of nucleotides which binds to the 3’ end of the template DNA strand allowing polymerase to add DNA nucleotides.
DNA Polymerase
DNA polymerase adds DNA nucleotides, using complementary base pairing, to the deoxyribose (3’) end of the new DNA strand which is forming, ie in the 5’ to 3’ direction
DNA Replication
DNA is unwound and hydrogen bonds between bases are broken to form two template strands.
DNA polymerase can only add DNA nucleotides in one direction resulting in the leading strand being replicated continuously and the lagging strand replicated in fragments.
Ligase
Fragments of DNA are joined together by ligase.
Leading Strand (summary)
Strand of dna which is replicated continuously from 3’ to 5’ end
Lagging Strand
Strand of dna which is replicated in fragments from 3’ to 5’ end
Pcr summary
Polymerase chain reaction (PCR) amplifies DNA using complementary primers for specific target sequences.
PCR Stages
- DNA is heated to between 92 and 98°C to separate the strands.
- It is then cooled to between 50 and 65°C to allow primers to bind to target sequences.
- It is then heated to between 70 and 80°C for heat-tolerant DNA polymerase to replicate the region of DNA.
Repeated cycles of heating and cooling amplify the target region of DNA.
Practical applications of pcr
PCR can amplify DNA to help solve crimes, settle paternity suits and diagnose genetic disorders.