The correct answer is: B) "All roads lead to Rome"
Citric acid cycle also called tricarboxylic acid (TCA) cycle and Krebs cycle is a central process in cellular respiration. Citric acid cycle that connects carbohydrate, fat, and protein metabolism so “all the roads” from the different metabolic pathways come to this cycle.
Acetyl-CoA which is produced through the oxidation of pyruvate (pyruvate is a product of glycolysis) enters the cycle which then produces reduced electron carriers NADH, FAD2 and energy molecule ATP. These electron carriers will then pass their electrons into the electron transport chain and, through the process of oxidative phosphorylation, will produce more ATP.
A phospholipid is made of glycerol, two the fatty acid tails, and a phosphate-linked head group. More unsaturated fatty acids it means less tightly packed phospholipids its results to the greater membrane fluidity. Unsaturated fatty acids are naturally occurring, meaning that the remaining hydrogen is on the same side of the molecule and result in a bending of the hydrocarbon chain.
Genotype is your complete heritable genetic energy Phentype is a discription of your actual physical characteristics.
answer - green pea plant is phenotype yellow is genotype
Answer:
B. The father did not contribute a sex chromosome to his daughter due to nondisjunction of the sex chromosomes. The daughter is XO and her only X chromosome came from her mother, who was a carrier.
A.The mother's X chromosomes failed to separate during meiosis, and the daughter inherited two X chromosomes with the Lesch-Nyhan mutation. The father contributed no sex chromosomes.
Explanation:
As seen in the question above, a little girl was diagnosed with Lesch-Nyhan syndrome, which is an X-linked recessive condition caused by a mutation in the HPRT1 gene responsible for purine metabolism.
The little girl's parents do not have the syndrome, and no one in the little girl's paternal family presented this syndrome, however, we know that the maternal grandfather of the little girl's mother had the syndrome, which means that it was the mother's genetic material that contributed to the development of the syndrome in the little girl. This was because the little girl did not receive any X chromosomes from her father, but she inherited the two X chromosomes from her mother that coded for the Lesch-Nyhan mutation. This happened because the mother's X chromosome disjuction did not occur during meiosis I.
As shown above, the father did not contribute any sex chromosomes to his daughter, which means that the daughter is XO and her only X chromosome came from her mother, who was a carrier.
