Question

Show how the structure of lactose may be deduced from the following: (1) The sugar is hydrolyzed by \(\beta-D\) -galactosidase to a mixture of equal parts of \(D\) -glucose and \(D\) -galactose. (2) Lactose mutarotates and forms a phenylosazone. (3) Bromine oxidation of lactose followed by hydrolysis gives \(D\) -gluconic acid and \(D\) -galactose. (4) Methylation and hydrolysis of lactose gives a tetra-O-methyl- \(D\) -galactose and \(2,3,6\) -tri-O-methyl- \(D\) -glucose. The same galactose derivative can be obtained from the methylation and hydrolysis of \(D\) -galactopyranose. (5) Bromine oxidation of lactose followed by methylation and hydrolysis yields tetra-O-methyl-1,4-gluconolactone and the same galactose derivative as in (4).

Short answer

Lactose is a β-1,4-linked disaccharide of D-glucose and D-galactose with glucose at the reducing end.

Step-by-step solution

Analyze Hydrolysis by β-D-Galactosidase

The statement that lactose is hydrolyzed by β-D-galactosidase into equal parts of D-glucose and D-galactose suggests that lactose is a disaccharide composed of these two monosaccharides. The hydrolysis reveals that the glycosidic bond in lactose links D-glucose and D-galactose.

Evaluate Mutarotation and Phenylosazone Formation

Lactose's ability to undergo mutarotation indicates it contains a hemiacetal group, which is typical for reducing sugars. This means lactose has a free anomeric carbon. The formation of a phenylosazone is consistent with the presence of both glucose and galactose as sugars capable of forming osazones due to their reducing ends.

Interpret Bromine Oxidation and Hydrolysis

Bromine oxidation of lactose resulting in D-gluconic acid and D-galactose indicates that the glucose component is at the reducing end of lactose. The oxidation converts the aldehyde group of glucose to a carboxylic acid (gluconic acid), confirming glucose as the reducing sugar in lactose.

Understand Methylation and Hydrolysis Outcomes

The methylation of lactose yielding a tetra-O-methyl-D-galactose and a 2,3,6-tri-O-methyl-D-glucose suggests specific linkages. The tetra-methylation of galactose implies all of its hydroxyl groups are free and not linked, while the tri-methylation of glucose indicates that one hydroxyl group was involved in a glycosidic bond, specifically the one at position 4.

Re-examine Bromine Oxidation with Methylation

Upon bromine oxidation and then methylation, the formation of tetra-O-methyl-1,4-gluconolactone supports previous findings. This suggests that in lactose, glucose is linked via its C1 and C4 positions, forming the lactoside linkage to the C1 position of galactose, consistent with beta-1,4 linkage.

Key concepts

Disaccharide Comprehension

Lactose is a fascinating example of a disaccharide, which is a type of sugar formed when two monosaccharides join together. The bond between these two sugar molecules is known as a glycosidic bond. In particular, lactose is composed of one molecule each of \(D\)-glucose and \(D\)-galactose.
\(D\)-glucose and \(D\)-galactose are both hexose sugars, meaning they each have six carbon atoms. The hydrolysis of lactose by \(\beta-D\)-galactosidase highlights this composition, as it splits lactose into its individual glucose and galactose components.
This degredation process confirms that lactose is a disaccharide since it consists of exactly two monosaccharides. Understanding the basic structure of lactose is key in comprehending its biological significance and its role in metabolism.

• Disaccharides like lactose play an essential role in providing energy by breaking down into simpler sugars, which the body can then utilize.
• Knowing how lactose is made up helps in recognizing why certain enzymes, like \(\beta-D\)-galactosidase, are needed for its digestion.

Glycosidic Bond Analysis

The glycosidic bond in lactose is a crucial feature for its structure and function. This bond is the link that connects the glucose and galactose monosaccharides, and is specifically referred to as a \(\beta-1,4\) glycosidic bond. The numbering "1,4" points to the position of carbon atoms in each sugar molecule that participate in the bond. For lactose, the bond occurs between the first carbon (C1) of \(D\)-galactose and the fourth carbon (C4) of \(D\)-glucose.
In analyzing the bond, it is significant to note that the "\(\beta\)" prefix indicates the orientation of the bond, which affects the overall structure and how enzymes recognize and cleave lactose.

• Mutarotation and the ability to form a phenylosazone reveal insights about this bond, showing it connects reducing ends of these sugars, another key feature of the glycosidic link in lactose.
• Methylation studies, which result in tetra-O-methyl-D-galactose and 2,3,6-tri-O-methyl-D-glucose, reinforce the structural insights about the precise carbon connections involved in the glycosidic bond.

Reducing Sugars

Reducing sugars, like lactose, possess the ability to act as reducing agents. This property is due to the presence of a free aldehyde group or a free hemiacetal group. In lactose, the presence of reducing sugars is evidenced through its ability to undergo mutarotation and its reaction in forming a phenylosazone.
The evaluation of lactose using chemical processes, such as bromine oxidation, further supports its characterization as a reducing sugar. This oxidation reveals that the glucose component of lactose, at the reducing end, can be oxidized to \(D\)-gluconic acid. Through these reactions, we understand that \(D\)-glucose acts as the reducing sugar in the lactose disaccharide.
Recognizing lactose as a reducing sugar is important in understanding its nutritional and chemical interactions:

• Reducing sugars like lactose play significant roles in typical metabolic pathways, being precursors to a range of essential biochemical reactions.
• The ability to reduce other substances makes these sugars critical in food chemistry, correlating with browning processes and flavors.