Answer:
Lysosomes.
Explanation:
HEXA (Hexosaminidase A) is the functional enzyme and encoded by the HEXA gene. The main function of this enzyme is the hydroxylation of the gangliosides.
The mutation in this gene leads to the lysosomal storage disease. The GM2 starts accumulating in the lysosomes and causes Tay Sach's disease. This is a genetic disorder that leads to the breakdown of the cells of the spinal cord and the brain.
Thus, the answer is lysosomes.
Microorganisms that are involved in the nitrogen cycle are able to break the triple of elemental nitrogen using special enzymes that they have developed and make ammonium. Other organisms like plants are unable to break the triple bond and therefore rely on these microorganisms so that they can absorb the ammonia
D. Sedimantory, metamorphic
If it was wrong I’m very sorry
