Here's the chart. Hope this helps! :)
Answer:
The reactions of glycolysis that are shared with those in gluconeogenesis (ie use the same enzymes) are those that Are regulated steps.
Explanation:
Glycolisis and gluconeogenesis are two mechanisms related to the carbohydrates metabolism. Sometimes they are considered reverse processes. However, they are different because of the control points they have where reactions are irreversible.
Glycolisis and gluconeogenesis share 7 common reactions, that are reversible. Thses reactions are coordinated and regulated by F-2 and 6-BP as the answer to the hormonal action.
Glycolisis happens in the muscle, while Gluconeogenesis happens in the liver. Together they form the "Cori Cycle".
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Answer:
More branching or folds.
Explanation:
Adaptation may be defined as the ability of the organism to adapt and survive according to its environment. Physical, physiological and chemical changes occur in the body of organism for the adaptation process.
The evolution of the increase in the size of the animals might also changes their internal physiology. The lungs and digestive tract also evolved as the size of the organism get bigger. The lungs has the alveoli to increase the surface area and inhalation of more oxygen in the body. Digestive system has villi or folds that increases the surface area for digestion and absorption.
Thus, the answer is more branching or folds.
Answer:
Each mutant would be mated to wild type and to every other mutant to create diploid strains. The diploids would be assayed for growth at permissive and restrictive temperature. Diploids formed by mating a mutant to a wild type that can grow at restrictive temperatures identify the mutation as recessive. Only recessive mutations can be studied using complementation analysis. Diploids formed by mating two recessive mutants identify mutations in the same gene if the diploid cannot grow at restrictive temperature (non-complementation), and they identify mutations in different genes if the diploids can grow at restrictive temperature (complementation).
Explanation:
Recessive mutations are those whose phenotypic effects are only visible in homo-zygous individuals. Moreover, a complementation test is a genetic technique used to determine if two different mutations associated with a phenotype colocalize in the same <em>locus</em> (i.e., they are alleles of the same gene) or affect two different <em>loci</em>. In diploid (2n) organisms, this test is performed by crossing two homo-zygous recessive mutants and then observing whether offspring have the wild-type phenotype. When two different recessive mutations localize in different <em>loci</em>, they can be considered as 'complementary' since the heterozygote condition may rescue the function lost in homo-zygous recessive mutants. In consequence, when two recessive mutations are combined in the same genetic background (i.e., in the same individual) and they produce the same phenotype, it is possible to determine that both mutations are alleles of the same gene/<em>locus</em>.
