chapter 7 section 3 Flashcards

(31 cards)

1
Q

What makes maltose, isomaltose, and cellobiose homodisaccharides?

A

They each contain only one kind of monosaccharide: glucose.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

How is maltose formed?

A

From starch by amylase enzymes during grain germination; hydrolyzed by diastase.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

What glycosidic linkage is found in maltose and cellobiose?

A

1→4 linkage between glucose units

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

How do maltose and cellobiose differ?

A

Maltose: α-1→4 linkage; cellobiose: β-1→4 linkage.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

What is the linkage in isomaltose?

A

α-1→6 linkage between two glucose units

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

What is the formal IUPAC name for maltose?

A

O-α-D-glucopyranosyl-(1→4)-D-glucopyranose

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

What is β-D-lactose composed of?

A

D-galactose and D-glucose via a β-1→4 linkage

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

Why is lactose a reducing sugar?

A

It has a free anomeric carbon capable of mutarotation.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

Why can most adults not digest lactose?

A

Lactase enzyme levels decrease after infancy in most populations

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

What is sucrose composed of?

A

Glucose and fructose.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

How is sucrose hydrolyzed?

A

By invertase enzyme or dilute acid

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

Why is sucrose called “invert sugar” after hydrolysis?

A

Optical rotation changes from positive (+66.5°) to negative due to component monosaccharides.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

re maltose, lactose, and sucrose absorbed directly in humans

A

No; they must first be hydrolyzed by maltase, lactase, or sucrase

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

What is the main “blood sugar” in insects?

A

Trehalose, a nonreducing disaccharide.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

In which organisms is trehalose commonly found?

A

Insects, bacterial spores, fungi, and yeast—organisms exposed to environmental stresses.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
16
Q

Why don’t honeybees use trehalose in their hemolymph?

A

their colonial lifestyle maintains stable temperature, reducing environmental stress.

17
Q

What is a proposed biological function of trehalose?

A

Acts as a natural cryoprotectant, protecting cells from freezing/thawing damage.

18
Q

Why is trehalose especially effective as a cryoprotectant?

A

It protects biological structures at low concentrations better than other polyhydroxy compounds.

19
Q

What evidence supports trehalose’s role in stress protection?

A

Trehalose levels in Saccharomyces cerevisiae rise under high salt and high temperature stress.

20
Q

How is the α or β configuration of a sugar ring determined?

A

By the position of the —OH at the anomeric carbon: α = below the ring, β = above the ring.

21
Q

What does “HOH” mean in disaccharide notation?

A

The configuration at that position can be either α or β.

22
Q

Does sucrose have a free anomeric carbon?

A

No, sucrose has no free anomeric carbon and is a nonreducing sugar.

23
Q

What defines a disaccharide?

A

Two monosaccharide units linked by a glycosidic bond.

24
Q

What is a residue in an oligosaccharide?

A

Each individual monosaccharide unit in the chain.

25
Name the three most common naturally occurring disaccharides
Sucrose, maltose, and lactose.
26
What is a mixed acetal in a disaccharide?
One hydroxyl comes from the monosaccharide itself, one from the other monosaccharide.
27
What is the reducing end of a disaccharide?
The end containing the free anomeric carbon capable of oxidation.
28
Why is sucrose a nonreducing sugar?
Both anomeric carbons are substituted, so it cannot convert to the aldehyde form.
29
What is the nonreducing end of a disaccharide?
The end without a free anomeric carbon.
30
Where are higher oligosaccharides found?
In both prokaryotic and eukaryotic organisms, naturally or as hydrolysis products of larger carbohydrates.
31
how do higher oligosaccharides differ from disaccharides?
They contain more than two monosaccharide residues.