CHMI-2227EL Lecture Notes - Lecture 17: Cell Nucleus, Guanine, Polynucleotide
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Biochemistry - Day 17 2018.03.21.
Question
-What distinguishes nucleotides from nucleosides
-a) nucleosides lack the phosphate group TRUE
-b) nucleosides lack the sugar group
-c) nucleosides lack a nitrogenous base
-d) the two words are synonymous
-Which of the following is the most distinguishing difference between a purine and
pyrimidine?
-e) purines are double ring structures while pyrimidines have a single ring
-Which of the following bases is not found in RNA?
-d) Thymine (T)
-Which of the following nucleases is a purine?
-a) Adenine
-The fundamental differences between RNA and DNA are
-d) bases and the ribose units only
-Which of the following groups is not found in nucleosides?
-a) phosphates
Nomenclature of Nucleosides
-Nucleosides are nucleotides minus phosphate group
-Purine nucleosides have the ending OSINE from purine
-Pyrimidine nucleosides have the ending IDINE from
pyrimidine
-Ignore Hypoxanthine in chart, and thymine, he accepts
thymidine
Conformation of Nucleosides
-In nucleosides, the base can exist in 2 distinct orientations
about the N-glycosidic bond
-These conformations are identifies as:
-syn: the base is above the sugar
-anti: the base is moved away from the sugar
-It is the anti confirmation that predominates in naturally
occurring nucleosides
Nucleotides
-Nucleotide: when a phosphoric acid is esterified to one of the hydroxyl groups on the
sugar group of a nucleoside, a nucleotide is then formed
-Ester formation for ribonucleosides can occur at 2’ , 3’ , 5’ position of the sugar
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Document Summary
A) nucleosides lack the phosphate group true. E) purines are double ring structures while pyrimidines have a single ring. The fundamental differences between rna and dna are. D) bases and the ribose units only. Purine nucleosides have the ending osine from purine. Pyrimidine nucleosides have the ending idine from pyrimidine. Ignore hypoxanthine in chart, and thymine, he accepts thymidine. In nucleosides, the base can exist in 2 distinct orientations about the n-glycosidic bond. Syn: the base is above the sugar. Anti: the base is moved away from the sugar. It is the anti con rmation that predominates in naturally occurring nucleosides. Nucleotide: when a phosphoric acid is esteri ed to one of the hydroxyl groups on the sugar group of a nucleoside, a nucleotide is then formed. Ester formation for ribonucleosides can occur at 2" , 3" , 5" position of the sugar. Ester formation for deoxyribonucleosides can occur at 3" , 5" position of the sugar.