The hemoglobin holoenzyme (active enzyme) is a complex of an iron ion and 4 subunits- 2 hemoglobin alpha and two hemoglobin beta. People with sickle cell disease have mutated beta hemoglobins. The mutation is a single nucleotide exchange, that changes the 6th amino acid of protein primary struture - a Glutamic acid into Valine. This one alteration changes the tree dimentional structure of hemoglobin beta so, that it forms lond fibres that disrupt the normal circular form of the red blood cells.
The dialysis bag will remain the same size in a isotonic solution.
Answer:
In glycolysis, the generation of ATP takes place at the time of the transformation of 1,3-bisphosphoglycerate to 3-phosphoglycerate and at the time of the transformation of phosphoenolpyruvate to pyruvate. However, when arsenate is used in place of phosphate it results in the generation of 1-arseno-3-phosphoenolpyruvate to pyruvate that further gets dissociated into 3-phosphoglycerate without generating any ATP.
However, in the process, the transformation of phosphoenolpyruvate to pyruvate does not get hampered, and therefore, the reaction will produce two ATP from one glucose. Although at the time of the preparatory phase of glycolysis, two ATPs are used that signifies that the net gain of ATP will be zero.
<span>Na+, cl-, hco3-, and k+ are electrolytes. Na+ is sodium. Cl- is chloride. Hco3- is bicarbonate and k+ is potassium. Electrolytes are needed for our organs and cells to function like they should. We obtain some of these electrolytes through the food we eat, such as sodium from salt and potassium from bananas.</span>
B. sulfur tetrafluoride + water → hydrogen fluoride + sulfur dioxide
