Biochemistry
Biochemistry
8th Edition
ISBN: 9781285429106
Author: Campbell, Mary K., FARRELL, Shawn O.
Publisher: Cengage Learning,
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Chapter 24, Problem 1RE

RECALL What are the two primary molecules that link anabolic and catabolic reactions?

Expert Solution & Answer
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Interpretation Introduction

Interpretation:

The two primary molecules that link the anabolic and catabolic pathways are to be named.

Concept introduction:

Anabolic pathway is the process that require energy to synthesize the large molecules from simple molecules.

Catabolic pathway is the process that breaks down large molecules into smaller molecules.

Anabolic and catabolic pathways are both opposite to each other.

Answer to Problem 1RE

Solution: ATP and NADPH are the two primary molecules that link anabolic and catabolic pathways. Light energy is used by plants to make ATP and NADH, which are further used to make carbohydrate compounds. These carbohydrates are the source of energy for other organisms.

Explanation of Solution

All the metabolisms are linked to photosynthesis in one way or another. ATP and NADH are the two very important molecules that link all the metabolism pathways. ATP is the currency of energy, which is able to store and transfer energy within the cells. NADH, nicotinamide adenine dinucleotide, is a form of coenzyme found in all organism.

Conclusion

ATP and NADH both are forms of energy.

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Students have asked these similar questions
The beta-lactamase hydrolyzes the lactam-ring in penicillin. Describe the mechanism  of hydrolysis, insuring to include the involvement of S, D, & K in the reaction sequence. Please help
To map the active site of beta-lactamase, the enzyme was hydrolyzed with trypsin to yield a hexapeptide (P1) with the following amino acids. Glu, Lys, Leu, Phe, Met, and Ser. Treatment of P1 with phenyl isothiocyanate yielded a PTH derivative of phenylalanine and a peptide (P2). Treatment of P1 with cyanogenbromide gave an acidic tetrapeptide (P3) and a dipeptide (P4).Treatment of P2 with 1-fluoro-2,4-dinitrobenzene, followed by complete hydrolysis, yields N-2,4-dinitrophenyl-Glu. P1, P2, and P3 contain the active site serine. Why doesn't D in this hexapeptide not participate in the hydrolysis of the beta-lactam ring even though S, K, and D are involved in the catalyst?
To map the active site of -lactamase, the enzyme was hydrolyzed with trypsin to yield a hexapeptide (P1) with the following amino acids. Glu, Lys, Leu, Phe, Met, and Ser. Treatment of P1 with phenyl isothiocyanate yielded a PTH derivative of phenylalanine and a peptide (P2). Treatment of P1 with cyanogenbromide gave an acidic tetrapeptide (P3) and a dipeptide (P4).Treatment of P2 with 1-fluoro-2,4-dinitrobenzene, followed by complete hydrolysis, yields N-2,4-dinitrophenyl-Glu. P1, P2, and P3 contain the active site serine.  Using the experimental results described above derive the primary sequence of the active site hexapeptide. Please help!

Chapter 24 Solutions

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