Lipids and Carbohydrates 4 Flashcards

1
Q

What are reducing sugars?

A

Glucose and other sugars that can reduce cupric ion Some oxidants such as cupric ion (Cu 2+) can oxidize the carbonyl carbon of sugars to the corresponding acids

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2
Q

What are non reducing sugars?

A

Sugars that don’t react with oxidants

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3
Q

What is an anomeric carbon?

A

The only carbon attached to 2 oxygen atoms that is reactive

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4
Q

Name the properties of the anomeric carbon

A

electrophilic most reactions involving ring forms of sugars take place at this position

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5
Q

What are glycosides?

A
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6
Q

What is glycosidic bond?

A

C-O

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7
Q

What is a glycosylic bond?

A

C-N

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8
Q

What kind of sugar does glycosidic bonds make?

A

Non Reducing sugars but only the open chain forms of the sugar can undergo oxidation by cupric ions

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9
Q

Why do glycosidic bonds of sugars become non reducing sugars?

A

If the anomeric carbon is associated in a glycosidic bond, the sugar can’t open from its ring form to become a linear form

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10
Q

What is disaccharide?

A

2 monosaccharides formed through a glycosidic bond

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11
Q

How does a dissacharide formed?

A

When the anomeric carbon of one sugar (electrophile) reacts with hydroxyl group (nucleophile) of the other

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12
Q

What does ß mean in terms of OH orientation?

A

The OH group on the anomeric carbon is facing “up”

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13
Q

What does alpha mean in terms of OH group on the anomeric carbon?

A

It means that the OH group on the anomeric carbon is facing down

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14
Q

How can you make a reducing sugar out of a disaccharide?

A

If the anomeric C atom of the one sugar and the anomeric OH group of glucose form a glycosidic bond.

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15
Q

What is mutarotation?

A

The converting of the alpha and beta OH groups on the anonomer C atom

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16
Q

What is the reducing end?

A

In disaccharides and polysaccharides, the end of a chain with a free anomeric carbon (not involved in a glycosdic bond)

17
Q

Why are polysaccharides often branched?

A

Sugars have several OH groups which can act as the nucleophile in forming a glycosidic bond

18
Q

How does polysaccharides differ from each other?

A

linked to different sugars, length of chains, type of bonds linking units and degree of branching

19
Q

What are the two types of polysccharides?

A

Homopolysccharides and heteropolysaccharides

20
Q

What are homopolysccharides?

A

Made from a single type of sugar monomer

21
Q

What are heteropolysaccharides?

A

Made from two or more kinds of sugar subunits

22
Q

Who first isolated DNA?

A

Friedrich Miescher called it “Nuclein”

23
Q

What is a nucleotide consist of?

A

A sugar, a base and a phosphate group

24
Q

What is the sugar phosphate backbone?

A

The sugars linked together by phosphates form the backbone of nucleic acids

25
What kind of pentoses do nucleic acids have?
2 kinds of pentoses - D-aldoses
26
What are pyrimidines?
1 ring bases of nucleic acids
27
What are purines?
2 ring bases of nucleic acids
28
What is a heterocycle?
Aromatic rings containing non carbon atoms such as N, O and S
29
What are tautomeric forms?
Isomers that differe by the shift of a H atom and a double bond
30
Which are Purine bases?
Adenine and Guanine
31
Which are pyrimidine bases?
Thymine and Cytosine
32
What is a nucleoside?
A sugar and a base WITHOUT the phosphate
33
How is a phosphodiester linkage formed?
A phosphate group bridges between the 5' OH of one nucleotide unit and the 3' OH of anohter
34
What is the charge of phosphate groups in the sugar phosphate backbone?
It is completely ionized (in ion form) and negatively charged at pH 7.
35
What is different about RNA?
RNA can be rapidly hyrolyzed under alkaline conditions because of the 2' hydroxyl of RNA which is absent from DNA
36
What is Chargaff's rule?
A=T and G=C
37
What is Rosalind Franklin's contribution to DNA?
She used X-ray diffraction to show that DNA molecules are helical and that they had priodocities along the long axis, a primry one of 3.4 A and a secondary one of 34 A.
38