DNA polymerase III is the enzyme responsible for adding new nucleotides to the growing DNA strand during replication.
If the template base is C and the enzyme inserts an A instead of a G into the new chain, the 3' → 5' exonuclease activity removes the misplaced nucleotide hydrolytically.
The 5' → 3' polymerase adds activity to the template, then replaces it with the correct nucleotide.
The 3' → 5' exonuclease and 5' → 3' polymerase are located on different subunits of DNA pol I.
The 3'-hydroxyrye group of the RNA primer is the acceptor of the first deoxyribose nucleotide, DNA polymerase I begins to add nucleotides along the single-stranded template that specifies the sequence of bases in the new synthesis.
DNA polymerase I is a highly processive enzyme that remains bound to the template as it moves along and does not diffuse away and then rebinds before adding each new nucleotide.
The processivity of DNA polymerase I is the result of the β subunits of the holozyme forming a ring that encircles the template and moves along with it, thus serving as a siding DNA chain.
DNA replication is initiated by binding to specific nucleotide sequences (DNA boxes) within oriC.
Binding causes a change in the DNA unwinding element (AT-rich region) in the origin of melting, resulting in a short, localized region of single-stranded DNA.
DNA helices require energy provided by ATP hydrolysis (see Figure 3010).
Unwinding at the replication fork causes supercoiling in other regions of the DNA molecule.
There are three major structural forms of DNA: the B form, the A form, and the Z form.
The B form is a right-handed helix with 10 base pairs per 360° turn (or opposite), and with the planes of the bases perpendicular to the helical axis.
Chromosomal DNA is primarily composed of B-DNA, as shown in Figure 307.
The A form is produced by moderately dehydrating the B form.
The A form is also a right-handed helix, but there are 11 base pairs per turn, and the planes of the bases are tilted 20° away from the helical axis.
The Z form is a left-handed helix that contains 12 base pairs per turn.
Lagging strand: The strand that is being copied in the direction away from the replication fork for continuously, with small fragments of DNA being copied near the replication fork.
These short stretches of discontinuous DNA, termed Okazaki fragments, are eventually joined (lagged) by lagging strand.
The new strand of DNA produced by this mechanism is termed the lagging strand.
RNA primer is a short piece of RNA base-paired to the DNA template, forming a double-stranded DNA-RNA hybrid.
The free hydroxyl group on the 3' end of the RNA primer serves as the first acceptor of a deoxy nucleotide by action of a DNA polymerase.
Each chromosome is associated with no histone proteins that help compact the DNA to form an nucleoid.
Most species of bacteria contain small, circular, extrachromosomal DNA molecules called plasmids.
Plasmids carry genetic information and undergo replication independently of the chromosomes.
Plasmids are used in genetic engineering to introduce new genetic information into the host bacterium and facilitate the transfer of genetic information from one bacterium to another.
When the two strands of ds DNA are separated, each can serve as a template for the replication of a new complementary stand.
The production of two daughter molecules, each containing two DNA strands, results in the formation of two double-stranded DNA molecules.
DNA is written in a more styled form, emphasizing the deoxyribosome-phosphate backbone.
The simplest representation of the nucleotide sequence is a double-helix, where the two chains are coiled around a common axis, called the helical axis.
In the DNA helix, the hydrophilic deoxyribose-phosphate backbone is on the outside of the molecule, while the hydrophobic bases are stacked inside.
The DNA helix structure resembles a ladder, with the two strands separated by a major groove and a minor groove.
The major groove in the DNA helix is a wide groove, while the minor groove is a narrower groove.
Stretches of Z- DNA can occur naturally in regions of DNA that have a sequence of altering purines and pyrimidines (for example, polG C).
Transitions between the B- form and Z- form of DNA may play a role in regulating gene expression.
B- DNA and Z- DNA have different structures, with B- DNA being linear and Z- DNA being circular.
Each chromosome in the nucleus of a eukaryotic cell consists of one long, linear molecule of DNA, which is bound by a complex of proteins.
Eukaryotic cells have closed, circular, Z- DNA molecules in their mitochondria.
A typical prokaryotic organism contains a single, circular, Z- DNA molecule.
Circulair DNA is "supercoiled," meaning it has double helix crosses over itself one or more times.