Biochemistry
Biochemistry
9th Edition
ISBN: 9781319114671
Author: Lubert Stryer, Jeremy M. Berg, John L. Tymoczko, Gregory J. Gatto Jr.
Publisher: W. H. Freeman
bartleby

Concept explainers

bartleby

Videos

Question
Book Icon
Chapter 22, Problem 37P
Interpretation Introduction

(a)

Interpretation:

The precursor of the given unsaturated fatty acid must be determined.

Concept introduction:

Double bond/bonds can be introduced in the newly synthesized fatty acid by both eukaryotes and prokaryotes. In eukaryotes, Cyt b5, oxygen-dependent desaturase, and NADH-cytochrome b5 reductase are responsible for the unsaturation of fatty acids. The desaturase enzyme used here contains a non-heme iron atom and this enzyme is an integral membrane protein.

Interpretation Introduction

(b)

Interpretation:

The precursor of the given unsaturated fatty acid must be determined.

Concept introduction:

Double bond/bonds can be introduced in the newly synthesized fatty acid by both eukaryotes and prokaryotes. In eukaryotes, Cyt b5, oxygen-dependent desaturase, and NADH-cytochrome b5 reductase are responsible for the unsaturation of fatty acids. The desaturase enzyme used here contains a non-heme iron atom and this enzyme is an integral membrane protein.

Interpretation Introduction

(c)

Interpretation:

The precursor of the given unsaturated fatty acid must be determined.

Concept introduction:

Double bond/bonds can be introduced in the newly synthesized fatty acid by both eukaryotes and prokaryotes. In eukaryotes, Cyt b5, oxygen-dependent desaturase, and NADH-cytochrome b5 reductase are responsible for the unsaturation of fatty acids. The desaturase enzyme used here contains a non-heme iron atom and this enzyme is an integral membrane protein.

Interpretation Introduction

(d)

Interpretation:

The precursor of the given unsaturated fatty acid must be determined.

Concept introduction:

Double bond/bonds can be introduced in the newly synthesized fatty acid by both eukaryotes and prokaryotes. In eukaryotes, Cyt b5, oxygen-dependent desaturase, and NADH-cytochrome b5 reductase are responsible for the unsaturation of fatty acids. The desaturase enzyme used here contains a non-heme iron atom and this enzyme is an integral membrane protein.

Interpretation Introduction

(e)

Interpretation:

The precursor of the given unsaturated fatty acid must be determined.

Concept introduction:

Double bond/bonds can be introduced in the newly synthesized fatty acid by both eukaryotes and prokaryotes. In eukaryotes, Cyt b5, oxygen-dependent desaturase, and NADH-cytochrome b5 reductase are responsible for the unsaturation of fatty acids. The desaturase enzyme used here contains a non-heme iron atom and this enzyme is an integral membrane protein.

Interpretation Introduction

(f)

Interpretation:

The precursor of the given unsaturated fatty acid must be determined.

Concept introduction:

Double bond/bonds can be introduced in the newly synthesized fatty acid by both eukaryotes and prokaryotes. In eukaryotes, Cyt b5, oxygen-dependent desaturase, and NADH-cytochrome b5 reductase are responsible for the unsaturation of fatty acids. The desaturase enzyme used here contains a non-heme iron atom and this enzyme is an integral membrane protein.

Blurred answer
Students have asked these similar questions
29. Labels. Suppose that you had an in vitro fatty acid- synthesizing system that had all of the enzymes and cofactors required for fatty acid synthesis except for acetyl CoA. To this system, you added acetyl CoA that contained radioactive hydrogen (³H, tritium) and carbon 14 (¹4C) as shown here. 3H O 14 3H-C-C SCOA 3H The ratio of ³H/¹4C is 3. What would the ³H/14C ratio be after the synthesis of palmitic acid (C₁6) with the use of the radioactive acetyl CoA?
Consider the complete oxidation of a mixed TAG containing the following fatty acid residues:At carbon 1: cerotic acidAt carbon 2: heptadecanoic acidAt carbon 3: palmitoleic acid Draw the structure of the mixed TAG.
IX. Insulin, a hormone vital in blood sugar regulation and having a polypeptide chain with disulfide linkages, loses its regulatory activity when heated at nearly 100°C for 5-10 minutes. Explain the molecular basis of this observed thermal property of insulin relative to its native structure and function. I--
Knowledge Booster
Background pattern image
Biochemistry
Learn more about
Need a deep-dive on the concept behind this application? Look no further. Learn more about this topic, biochemistry and related others by exploring similar questions and additional content below.
Similar questions
SEE MORE QUESTIONS
Recommended textbooks for you
Text book image
Biochemistry
Biochemistry
ISBN:9781319114671
Author:Lubert Stryer, Jeremy M. Berg, John L. Tymoczko, Gregory J. Gatto Jr.
Publisher:W. H. Freeman
Text book image
Lehninger Principles of Biochemistry
Biochemistry
ISBN:9781464126116
Author:David L. Nelson, Michael M. Cox
Publisher:W. H. Freeman
Text book image
Fundamentals of Biochemistry: Life at the Molecul...
Biochemistry
ISBN:9781118918401
Author:Donald Voet, Judith G. Voet, Charlotte W. Pratt
Publisher:WILEY
Text book image
Biochemistry
Biochemistry
ISBN:9781305961135
Author:Mary K. Campbell, Shawn O. Farrell, Owen M. McDougal
Publisher:Cengage Learning
Text book image
Biochemistry
Biochemistry
ISBN:9781305577206
Author:Reginald H. Garrett, Charles M. Grisham
Publisher:Cengage Learning
Text book image
Fundamentals of General, Organic, and Biological ...
Biochemistry
ISBN:9780134015187
Author:John E. McMurry, David S. Ballantine, Carl A. Hoeger, Virginia E. Peterson
Publisher:PEARSON
Macromolecules | Classes and Functions; Author: 2 Minute Classroom;https://www.youtube.com/watch?v=V5hhrDFo8Vk;License: Standard youtube license