BIOCHEMISTRY (LOOSELEAF)-W/ACCESS
BIOCHEMISTRY (LOOSELEAF)-W/ACCESS
9th Edition
ISBN: 9781319425784
Author: BERG
Publisher: Macmillan Higher Education
Question
Book Icon
Chapter 22, Problem 59P
Interpretation Introduction

(a)

Interpretation:

The effect of soraphen A and its varying concentration on the fatty acid synthesis should be determined.

Concept introduction:

Acetyl-CoA carboxylase (ACC) is a biotin-dependent enzyme, which catalyzes the conversion of acetyl-CoA into malonyl-CoA, in the presence of bicarbonate ion. It has two catalytic activities, carboxyltransferase and biotin carboxylase. This enzyme is found in the chloroplasts of the plants, and endoplasmic reticulum of the animals. The main motive of ACC is to synthesize malonyl CoA for the synthesis of fatty acids.

Interpretation Introduction

(b)

Interpretation:

The effect of soraphen A on fatty acid oxidation must be determined.

Concept introduction:

Acetyl-CoA carboxylase (ACC) is a biotin-dependent enzyme, which catalyzes the conversion of acetyl-CoA into malonyl-CoA, in the presence of bicarbonate ion. It has two catalytic activities, carboxyltransferase and biotin carboxylase. This enzyme is found in the chloroplasts of the plants, and endoplasmic reticulum of the animals. The main motive of ACC is to synthesize malonyl CoA for the synthesis of fatty acids.

Interpretation Introduction

(c)

Interpretation:

The results of graph B should be explained keeping in mind that sorpahen A inhibits acetyl CoA carboxylase.

Concept introduction:

Acetyl-CoA carboxylase (ACC) is a biotin-dependent enzyme, which catalyzes the conversion of acetyl-CoA into malonyl-CoA, in the presence of bicarbonate ion. It has two catalytic activities, carboxyltransferase and biotin carboxylase. This enzyme is found in the chloroplasts of the plants, and endoplasmic reticulum of the animals. The main motive of ACC is to synthesize malonyl CoA for the synthesis of fatty acids.

Interpretation Introduction

(d)

Interpretation:

The effect on phospholipid synthesis by inhibition of carboxylase must be determined.

Concept introduction:

Acetyl-CoA carboxylase (ACC) is a biotin-dependent enzyme, which catalyzes the conversion of acetyl-CoA into malonyl-CoA, in the presence of bicarbonate ion. It has two catalytic activities, carboxyltransferase and biotin carboxylase. This enzyme is found in the chloroplasts of the plants, and endoplasmic reticulum of the animals. The main motive of ACC is to synthesize malonyl CoA for the synthesis of fatty acids.

Interpretation Introduction

(e)

Interpretation:

The effect of phospholipid synthesis on cell’s viability must be determined.

Concept introduction:

Acetyl-CoA carboxylase (ACC) is a biotin-dependent enzyme, which catalyzes the conversion of acetyl-CoA into malonyl-CoA, in the presence of bicarbonate ion. It has two catalytic activities, carboxyltransferase and biotin carboxylase. This enzyme is found in the chloroplasts of the plants, and endoplasmic reticulum of the animals. The main motive of ACC is to synthesize malonyl CoA for the synthesis of fatty acids.

Interpretation Introduction

(f)

Interpretation:

The result of soraphen A on cancer cell viability should be determined.

Concept introduction:

Acetyl-CoA carboxylase (ACC) is a biotin-dependent enzyme, which catalyzes the conversion of acetyl-CoA into malonyl-CoA, in the presence of bicarbonate ion. It has two catalytic activities, carboxyltransferase and biotin carboxylase. This enzyme is found in the chloroplasts of the plants, and endoplasmic reticulum of the animals. The main motive of ACC is to synthesize malonyl CoA for the synthesis of fatty acids.

Blurred answer
Students have asked these similar questions
Here is my literature Beta Carotene HPLC analysis graph. Can you help me explain what each peak is at each retention time?   Thank You :D
I have a literature B-Carotene HPLC graph in which showcases a retention time of roughly 23.6 and 25.1.  Please help me compare my two different Anti-Oxidant Juice graphs. (Attached) The juices provided are: V8 Carrot Ginger Blend and V8 Original Blend Noticing the HPLC graphs I saw no peaks for the Original Blend for B-Carotene. However the Carrot Ginger Blend showed similar peaks --> Why is this reason? Please explain in terms of Retention time and Area (Under Curve).   Thank You!
Calculate pH of a solution prepared by dissolving 1.60g of sodium acetate, in 88.5 mL of 0.10 M acetic acid. Assume the volume change upon dissolving the sodium acetate is negligible. Ka is 1.75 x 10^-5
Knowledge Booster
Background pattern image
Similar questions
SEE MORE QUESTIONS
Recommended textbooks for you
  • Text book image
    Biochemistry
    Biochemistry
    ISBN:9781305577206
    Author:Reginald H. Garrett, Charles M. Grisham
    Publisher:Cengage Learning
    Text book image
    Biology 2e
    Biology
    ISBN:9781947172517
    Author:Matthew Douglas, Jung Choi, Mary Ann Clark
    Publisher:OpenStax
    Text book image
    3-2-1 Code It
    Biology
    ISBN:9781337660549
    Author:GREEN
    Publisher:Cengage
  • Text book image
    Biochemistry
    Biochemistry
    ISBN:9781305961135
    Author:Mary K. Campbell, Shawn O. Farrell, Owen M. McDougal
    Publisher:Cengage Learning
    Text book image
    Human Heredity: Principles and Issues (MindTap Co...
    Biology
    ISBN:9781305251052
    Author:Michael Cummings
    Publisher:Cengage Learning
Text book image
Biochemistry
Biochemistry
ISBN:9781305577206
Author:Reginald H. Garrett, Charles M. Grisham
Publisher:Cengage Learning
Text book image
Biology 2e
Biology
ISBN:9781947172517
Author:Matthew Douglas, Jung Choi, Mary Ann Clark
Publisher:OpenStax
Text book image
3-2-1 Code It
Biology
ISBN:9781337660549
Author:GREEN
Publisher:Cengage
Text book image
Biochemistry
Biochemistry
ISBN:9781305961135
Author:Mary K. Campbell, Shawn O. Farrell, Owen M. McDougal
Publisher:Cengage Learning
Text book image
Human Heredity: Principles and Issues (MindTap Co...
Biology
ISBN:9781305251052
Author:Michael Cummings
Publisher:Cengage Learning