Question

In: Chemistry

A accidental genetic mutation in the lab mice has occurred and affects the glycogen degradation pathway....

A accidental genetic mutation in the lab mice has occurred and affects the glycogen degradation pathway. Dr. Wilson is studying this unexpected mutation and has taken samples of their livers. What he found was excessive glycogen storage but the glycogen structure was unusual. There was a lot of glycogen but size of each glycogen molecule was smaller and each chain end had 4 glucose units (alpha 1,4 bonds) and then a SINGLE glucose attached as a branch point (alpha 1,6 bond) to the 5th carbon from the end. Which enzyme in the glycogen degradation pathway is not working?

a.

glycogen phosphorylase
b. glycogen transferase
c. alpha-1,6-glucosidase
d. glucose 6-phosphatase
e. phosphoglucomutase

Solutions

Expert Solution

Answer:    a. glycogen phosphorylase

Glycogen phosphorylase breaks up glycogen into glucose subunits. Glycogen is now with lesser number of free glucose molecule is in the form of glucose-1-phosphate. In order to be used for metabolism, it must be converted to glucose-6-phosphate by the enzyme phosphoglucomutase. Glycogen phosphorylase can act only on linear chains of glycogen (α1-4 glycosidic linkage), Its work will immediately come to a halt four residues away from α1-6 branch (which are exceedingly common in glycogen). In these situations, a debranching enzyme is necessary, which will straighten out the chain in that area. α1-6 glucosidase enzyme is required to break the remaining (single glucose) α1-6 residue that remains in the new linear chain. After all this is done, glycogen phosphorylase can continue.

For detailed information please see at

https://www.ncbi.nlm.nih.gov/books/NBK22467/

Thank You So Much! Please Rate this answer as you wish.


Related Solutions

A accidental genetic mutation in the lab mice has occurred and affects the glycogen degradation pathway....
A accidental genetic mutation in the lab mice has occurred and affects the glycogen degradation pathway. Dr. Wilson is studying this unexpected mutation and has taken samples of their livers. What he found was excessive glycogen storage but the glycogen structure was unusual. There was a lot of glycogen but size of each glycogen molecule was smaller and each chain end had 4 glucose units (alpha 1,4 bonds) and then a SINGLE glucose attached as a branch point (alpha 1,6...
Segawa syndrome is a genetic mutation that affects the synthesis of dopamine in the body. People...
Segawa syndrome is a genetic mutation that affects the synthesis of dopamine in the body. People with this disorder walk clumsily and have involuntary muscle contractions. Please draw a diagram representing the pathway of neurons involved in segawa syndrome, label the following feature: CNS- central nervous system, spinal nerve, cell body, axon, dendrites, affected organ, afferent pathway, efferent pathway, interneuron, sensory neuron, motor neuron, and synapse.
In one experiment, you have 2 mice of different strains, the first has no mutation or...
In one experiment, you have 2 mice of different strains, the first has no mutation or wild type (WT) and the second is a conditional knockout (KO) of the insulin receptor specifically in skeletal muscle. After an overnight fast, both are fed a glucose solution. One hour later, in both mice blood glucose levels have peaked suggesting that the glucose has been processed through the portal vein and into general circulation. Two hours later, blood glucose levels in the WT...
A patient has a genetic mutation in the gene for glutaminase that significantly reduces the efficiency...
A patient has a genetic mutation in the gene for glutaminase that significantly reduces the efficiency of this enzyme, leading to a decrease in glutamatergic signaling. Which of the following could potentially compensate for this? a. A downregulation of aspartate aminotransferase b. A downregulation of VGLUT c. An upregulation of neuronal glutamate transporters d. An upregulation of VIAAT
A fly has a genetic mutation that accelerates the breakdown of the period protein. a) How...
A fly has a genetic mutation that accelerates the breakdown of the period protein. a) How and why would this change circadian rhythms? b) What do hypothesize the circadian rhythms would look like under normal lighting conditions (12 hours light, 12 hours dark) Describe why this would be the response. c) What will the circadian rhythms look like under constant dark conditions? Describe why this would be the observation.
QUESTION PART A: About 1% of the population has a particular genetic mutation. 900 people are...
QUESTION PART A: About 1% of the population has a particular genetic mutation. 900 people are randomly selected. Find the mean for the number of people with the genetic mutation in such groups of 900. QUESTION PART B: About 4% of the population has a particular genetic mutation. 400 people are randomly selected. Find the standard deviation for the number of people with the genetic mutation in such groups of 400. Round your answer to three decimal places
About 5% of the population has a particular genetic mutation. 300 people are randomly selected. Find...
About 5% of the population has a particular genetic mutation. 300 people are randomly selected. Find the standard deviation for the number of people with the genetic mutation in such groups of 300. Incorrect
1. About 1% of the population has a particular genetic mutation. 200 people are randomly selected....
1. About 1% of the population has a particular genetic mutation. 200 people are randomly selected. Find the standard deviation for the number of people with the genetic mutation in such groups of 200. 2. A drug test is accurate 97% of the time. If the test is given to 1600 people who have not taken drugs, what is the probability that at least 50 will test positive? Probability = Give your answers to at least 3 decimal places. 3....
Introduction to Mendelian genetic lab report general Biology 8. A woman has to type A blood....
Introduction to Mendelian genetic lab report general Biology 8. A woman has to type A blood. Her daughter has type O blood. What are the possible genotypes and blood types of the child’s father? explain 9. In humans, the gene for color blindness is recessive and is located on the X chromosome with no corresponding gene on the Y. If a man and a woman, both with normal vision, marry and have a color-blind son, draw the Punnett square that...
ADVERTISEMENT
ADVERTISEMENT
ADVERTISEMENT