59.0k views
2 votes
Cells that experience a devastating mutation in the gene that encodes g6p dehydrogenase are most likely to experience problems specifically connected to choose one:

a. the krebs cycle.
b. lipid transport.
c. nucleotide biosynthesis.
d. protein catabolism

User Simulacre
by
8.9k points

1 Answer

7 votes

The right answer is nucleotide biosynthesis.

Favism or deficiency of glucose-6-phosphate dehydrogenase, or deficiency of G6PD, is the most widespread enzymatic deficiency in the world. Of genetic origin, it is characterized by a destruction of the red blood cells (hemolysis) during the ingestion of beans or the taking of certain drugs (especially synthesized antimalarials).

The enzyme Glucose-6-phosphate dehydrogenase is involved in the pentose phosphate pathway that produces riboses that are part of the nucleotide composition.

User Bhavin Chauhan
by
7.8k points
Welcome to QAmmunity.org, where you can ask questions and receive answers from other members of our community.

9.4m questions

12.2m answers

Categories