The monomers of nucleic acids are Nucleotides which consist of three components: Pentose sugar, Organic base, and Phosphate group.
The two types of organic bases are Purine and pyrimidine.
Purines are a class of organic bases with a double ring structure and include adenine (A) and guanine (G).
The polypeptide is further modified by adding carbohydrates, lipids or phosphates.
DNA can be purified by precipitation, which involves adding ethanol and a salt to an aqueous solution, centrifuging to obtain a pellet of nucleic acid, washing the pellet with ethanol and centrifuging again.
Different polypeptides may be combined.
Pyrimidines are a class of organic bases with a single ring structure and include cytosine (C), thymine (T), and uracil (U).
The structure of a DNA nucleotide consists of Deoxyribose, Organic base (A, T, C or G), and Phosphate group.
The structure of an RNA nucleotide consists of Ribose, Organic base (A, U, C or G), and Phosphate group.
The structure of an ATP nucleotide consists of Ribose, Adenine, and three phosphate groups.
An endergonic reaction is a non-spontaneous reaction that requires an input of energy, for example, ATP formation.
An intron is a non-coding sequence of DNA that is found between exons.
Each base in a sequence is read once and is only part of one triplet.
The genetic code is universal as the same codons code for the same amino acids in almost all organisms.
Eukaryotic genes are discontinuous with non-coding introns and coding exons.
A specific sequence of three nucleotides (known as a codon) on a molecule of DNA or RNA codes for a particular amino acid in protein synthesis.
The genetic code is degenerate, universal and non-overlapping.
An exon is a region of DNA that codes for an amino acid sequence.
Protein synthesis is the formation of proteins from amino acids, with two stages: transcription and translation.
More than one triplet can code for a particular amino acid.
Prokaryotic genes are continuous with coding sequences only.
The genetic code is the rules by which triplets in a DNA base sequence code for the sequence of amino acids in a polypeptide chain.
Free RNA nucleotides align next to their complementary bases during transcription.
Amino acids carried on adjacent tRNA molecules are joined to form a polypeptide chain during translation.
RNA polymerase binds to promoter region on a gene during transcription.
Translation is the second stage of protein synthesis and takes place in the ribosomes.
mRNA is used as a template for the attachment of tRNA molecules with complementary anticodons during translation.
Transcription is the first stage of protein synthesis and involves the formation of pre-mRNA in eukaryotes and mRNA in prokaryotes from a section of the template strand of DNA.
Post-transcriptional modification, such as splicing, removes introns from pre-mRNA in eukaryotic cells.
The 'one gene - one polypeptide' hypothesis states that each gene encodes a single protein.
Antisense strand acts as a template during transcription.
DNA helicase unwinds section of DNA, breaking hydrogen bonds between the DNA strands.
RNA polymerase reaches stop codon and detaches, resulting in mRNA.
Semi-conservative replication is the replication of DNA to produce two new DNA molecules which both contain one new strand and one old strand from the original DNA molecule.
The structure of rRNA consists of 1800 to 5000 nucleotides, two subunits: one large, one small.
The function of rRNA is to associate with proteins in the cytoplasm to form ribosomes.
Ribosomal RNA (rRNA) associates with proteins in the cytoplasm to form ribosomes.
Transfer RNA (tRNA) carries specific amino acids to the ribosomes.
DNA helicase catalyses the unzipping of double-stranded DNA into two single strands, each of which acts as a template during semi-conservative replication.