Chapter 24: Problem 16
Draw the structural formula for the tetradeoxynucleotide CGTA.
Short Answer
Expert verified
The structure of CGTA is a linear sequence of four nucleotides: Cytosine, Guanine, Thymine, and Adenine, connected in a 5' to 3' orientation with a sugar-phosphate backbone.
Step by step solution
01
Identify Nucleotides
The tetradeoxynucleotide CGTA is made up of four deoxyribonucleotides: Cytosine (C), Guanine (G), Thymine (T), and Adenine (A). Each of these nucleotides consists of three components: a phosphate group, a deoxyribose sugar, and a nitrogenous base (either C, G, T, or A).
02
Understand Bonding Orientation
DNA nucleotides always connect in a 5' to 3' direction. The phosphate group of one nucleotide connects to the 3' carbon of the deoxyribose sugar of the next nucleotide. This forms the backbone of the DNA strand.
03
Start Drawing from the 5' End
Begin with the 5' phosphate group connected to the deoxyribose sugar of the first nucleotide, Cytosine (C). Draw the nitrogenous base (a single ring for C) attached to the 1' carbon of deoxyribose.
04
Add Second Nucleotide
Link the 3' carbon of Cytosine's deoxyribose to the 5' phosphate of Guanine. Draw Guanine (a double-ring structure) attached to its deoxyribose sugar.
05
Add Remaining Nucleotides
Continue adding Thymine and then Adenine. Link each 3' carbon to the next 5' phosphate group, ensuring each nitrogenous base (a single ring for Thymine and a double ring for Adenine) is attached to the 1' carbon of its deoxyribose.
06
Complete and Check Structure
Finish by ensuring the tetradeoxynucleotide chain runs 5'-C-G-T-A-3'. Check that each deoxyribose, phosphate, and nitrogenous base is correctly linked in the 5' to 3' direction.
Unlock Step-by-Step Solutions & Ace Your Exams!
-
Full Textbook Solutions
Get detailed explanations and key concepts
-
Unlimited Al creation
Al flashcards, explanations, exams and more...
-
Ads-free access
To over 500 millions flashcards
-
Money-back guarantee
We refund you if you fail your exam.
Over 30 million students worldwide already upgrade their learning with Vaia!
Key Concepts
These are the key concepts you need to understand to accurately answer the question.
Nucleotide Structure
Nucleotide structure is fundamental to understanding DNA. A nucleotide consists of three main components:
The deoxyribose sugar is a five-carbon sugar, differing from ribose by the absence of one oxygen atom, hence the "deoxy" prefix. The nitrogenous base can be a purine, such as Adenine (A) and Guanine (G), or a pyrimidine, like Cytosine (C) and Thymine (T). In the tetradeoxynucleotide CGTA, C, G, T, and A represent these bases. The specific sequence of the nitrogenous bases encodes genetic information.
- A phosphate group
- A deoxyribose sugar
- A nitrogenous base
The deoxyribose sugar is a five-carbon sugar, differing from ribose by the absence of one oxygen atom, hence the "deoxy" prefix. The nitrogenous base can be a purine, such as Adenine (A) and Guanine (G), or a pyrimidine, like Cytosine (C) and Thymine (T). In the tetradeoxynucleotide CGTA, C, G, T, and A represent these bases. The specific sequence of the nitrogenous bases encodes genetic information.
Phosphate Backbone
The phosphate backbone is the supporting structure of DNA, providing a stable framework that supports its function and structure. It consists of alternating phosphate groups and deoxyribose sugars linked together. Each nucleotide connects through its phosphate group to the 3' carbon of the neighboring sugar, forming a continuous "chain."
Two key things to remember:
1. The sequence runs from the 5' end to the 3' end of the DNA strand. This directionality is crucial for many biological processes, such as DNA replication and transcription. 2. The phosphate bonds between the 3' carbon and the phosphate group are strong and resist cleavage, which helps protect the integrity of the DNA strand.
This structure not only aids in the proper linkage of nucleotides but also allows the flexibility and twist of the DNA double helix.
Two key things to remember:
1. The sequence runs from the 5' end to the 3' end of the DNA strand. This directionality is crucial for many biological processes, such as DNA replication and transcription. 2. The phosphate bonds between the 3' carbon and the phosphate group are strong and resist cleavage, which helps protect the integrity of the DNA strand.
This structure not only aids in the proper linkage of nucleotides but also allows the flexibility and twist of the DNA double helix.
Nucleotide Pairing
Nucleotide pairing is the mechanism by which the two strands of DNA are held together, ensuring accurate genetic replication. In the context of CGTA, each base pairs with a complementary partner on the opposite DNA strand. This occurs via hydrogen bonding, which stabilizes the structure of DNA.
- Cytosine (C) pairs with Guanine (G) through three hydrogen bonds. - Thymine (T) pairs with Adenine (A) through two hydrogen bonds.
This specific pairing is known as complementary base pairing, and it's essential for DNA's double helix structure. The precise pairing ensures that the genetic code is preserved during DNA replication, as each half of the DNA double helix can serve as a template for reconstructing its pair.
- Cytosine (C) pairs with Guanine (G) through three hydrogen bonds. - Thymine (T) pairs with Adenine (A) through two hydrogen bonds.
This specific pairing is known as complementary base pairing, and it's essential for DNA's double helix structure. The precise pairing ensures that the genetic code is preserved during DNA replication, as each half of the DNA double helix can serve as a template for reconstructing its pair.
Deoxyribose Sugar
Deoxyribose sugar is an essential component of the nucleotide structure in DNA. This sugar is a five-carbon molecule, distinguished from ribose by the absence of one oxygen atom at the 2' position, hence the "deoxy" in deoxyribose. This sugar plays a pivotal role in linking the phosphate group and the nitrogenous base.
The carbons of deoxyribose are numbered 1' through 5':
The carbons of deoxyribose are numbered 1' through 5':
- The 1' carbon attaches to the nitrogenous base.
- The 3' carbon is where the next nucleotide's phosphate group binds.
- The 5' carbon is bonded to the current nucleotide's phosphate group.