Problem 59
Question
(a) Draw the chemical structure of a generic amino acid, using \(\mathrm{R}\) for the side chain. (b) When amino acids react to form proteins, do they do so via substitution, addition, or condensation reactions? (c) Draw the bond that links amino acids together in proteins. What is this called?
Step-by-Step Solution
Verified Answer
A generic amino acid has the chemical structure H2N-C-COOH, with R as the side chain:
H
|
H2N-C-COOH
|
R
Amino acids react to form proteins via condensation reactions. The bond that links amino acids in proteins is called a peptide bond, formed between the carboxyl group of one amino acid and the amino group of another:
--O-NH--
This bond connects the amino acids, releasing a water molecule in the process.
1Step 1: Drawing the chemical structure of a generic amino acid
To draw the chemical structure of a generic amino acid, start with a central carbon atom called the alpha-carbon. Attach an amino group (-NH2), a carboxyl group (-COOH), and a hydrogen atom to the alpha-carbon. Finally, attach the side chain (R) to the alpha-carbon. Here is the structure:
H
|
H2N-C-COOH
|
R
2Step 2: Determining the reaction type that forms proteins from amino acids
When amino acids react to form proteins, they do so via condensation reactions. This is because a water molecule is released when the peptide bond is formed between the amino acids.
3Step 3: Drawing the bond that links amino acids in proteins and naming it
The bond that links amino acids together in proteins is called a peptide bond. A peptide bond is formed between the carboxyl group of one amino acid and the amino group of the neighboring amino acid. A water molecule is released in this condensation reaction. Here's the representation of the peptide bond between two amino acids:
H H
| |
H2N-C-COOH + NH2-C-COOH
| |
R1 R2
\ /
\ /
--O-NH--
The peptide bond is the O-N-H bond, which is formed by releasing the water molecule.
Key Concepts
Protein SynthesisPeptide BondCondensation Reaction
Protein Synthesis
Protein synthesis is a vital biological process that allows our cells to build proteins, which are crucial for many bodily functions. In simple terms, protein synthesis involves creating proteins from amino acids. It happens in two main stages: transcription and translation.
- Transcription: During this stage, the DNA in a cell's nucleus is used to create messenger RNA (mRNA). This mRNA serves as a template that guides the building of proteins.
- Translation: In this stage, the mRNA moves to a cell part known as ribosomes. Here, the ribosome reads the sequence of the mRNA and translates it into a specific chain of amino acids. This chain will eventually fold into a fully functioning protein.
Peptide Bond
A peptide bond is a special type of covalent bond that serves as the glue binding amino acids together to form proteins. It's also known as an amide bond.
- Formation: A peptide bond forms between the carboxyl group of one amino acid and the amino group of another amino acid.
- Structure: Chemically, it is represented as a bond between a carbon atom and a nitrogen atom, often shown as C-N or CO-NH.
Condensation Reaction
Condensation reactions are chemical reactions where two molecules combine to form a larger molecule while releasing a small molecule, such as water, as a byproduct. This is the same reaction type used to form peptide bonds.
- In Protein Formation: When amino acids join to form proteins, the condensation reaction involves the release of a water molecule. This occurs as the carboxyl group of one amino acid reacts with the amino group of another, forming the peptide bond.
- Role in Biology: Condensation reactions are crucial not only in protein synthesis but also in the creation of other biological molecules, such as nucleic acids and polysaccharides.
Other exercises in this chapter
Problem 57
How many chiral carbons are in 4 -bromo- 2 -chloro-2butanol? \((\mathbf{a}) 0,(\mathbf{b}) 1,(\mathbf{c}) 2,(\mathbf{d}) 3,(\mathbf{e}) 4\) or more.
View solution Problem 58
Is 2-butanol chiral?
View solution Problem 60
Indicate whether each statement is true or false. (a) Tryptophan is an aromatic amino acid. (b) Lysine is positively charged at pH 7. (c) Asparagine has two ami
View solution Problem 61
Draw the two possible heterodimeric dipeptides formed by condensation reactions between glycine and alanine.
View solution