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9 November, 07:34

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

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  1. 9 November, 09:28
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    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.
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