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
Q

What kind of pentoses do nucleic acids have?

A

2 kinds of pentoses - D-aldoses

26
Q

What are pyrimidines?

A

1 ring bases of nucleic acids

27
Q

What are purines?

A

2 ring bases of nucleic acids

28
Q

What is a heterocycle?

A

Aromatic rings containing non carbon atoms such as N, O and S

29
Q

What are tautomeric forms?

A

Isomers that differe by the shift of a H atom and a double bond

30
Q

Which are Purine bases?

A

Adenine and Guanine

31
Q

Which are pyrimidine bases?

A

Thymine and Cytosine

32
Q

What is a nucleoside?

A

A sugar and a base WITHOUT the phosphate

33
Q

How is a phosphodiester linkage formed?

A

A phosphate group bridges between the 5’ OH of one nucleotide unit and the 3’ OH of anohter

34
Q

What is the charge of phosphate groups in the sugar phosphate backbone?

A

It is completely ionized (in ion form) and negatively charged at pH 7.

35
Q

What is different about RNA?

A

RNA can be rapidly hyrolyzed under alkaline conditions because of the 2’ hydroxyl of RNA which is absent from DNA

36
Q

What is Chargaff’s rule?

A

A=T and G=C

37
Q

What is Rosalind Franklin’s contribution to DNA?

A

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
Q
A