Answer:
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Explanation:
The lagging strand runs in a 5’ to 3’ direction and is replicated discontinuously.
<h3>Why a discontinuous or delayed tape?</h3>
The other strand, called delayed, is replicated discontinuously. In this case, the presence of Okazaki fragments is necessary, small pieces of DNA that will bind to form a new strand. - DNA is degraded by two types of enzymes.
The ends of a DNA strand are classified as 5' and 3', as they correspond to the carbon number of the pentose where the phosphate and hydroxyl (OH) group are located, which join in a phosphodiester bond.
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<span>Apart from their habitats, Bacteria and Archaea differ in cell wall structure and membrane lipid composition. All bacteria have peptidoglycans in the cell wall whereas the archaea do not. Both also are different in RNA polymerases and thus in their protein synthesis. </span>
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Pyruvate carboxylase and phosphoenolpyruvate carboxykinase catalyze reactions of gluconeogenesis that bypass the reaction of glycolysis that is catalyzed by pyruvate kinase.
<h3>Gluconeogenesis:</h3>
The tissues of some organs, including the brain, the eye, and the kidney, use glucose as their primary or only source of metabolic fuel. Glycogen stores become exhausted during a protracted fast or intense exercise, and glucose must be created from scratch to keep blood glucose levels stable. The process through which glucose is created from non-hexose precursors such glycerol, lactate, pyruvate, and glucogenic amino acids is known as gluconeogenesis.
Glycolysis is effectively reversed during glucose synthesis. However, gluconeogenesis makes use of four distinct enzymes to skip the three highly exergonic (and essentially irreversible) phases of glycolysis. The pyruvate carboxylase, PEP carboxykinase, fructose 1,6-bisphosphatase, and glucose 6-phosphatase enzymes are specific to gluconeogenesis. Gluconeogenesis can only take place in particular tissues because these enzymes are not found in all cell types. In humans, the liver and, to a lesser extent, the renal cortex are the primary locations for gluconeogenesis.
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