Answer:
Simplified diagram of pyruvate oxidation. Pyruvate—three carbons—is converted to acetyl CoA, a two-carbon molecule attached to coenzyme A. A molecule of coenzyme A is a necessary reactant for this reaction, which releases a molecule of carbon dioxide and reduces a NAD+ to NADH.
Simplified diagram of pyruvate oxidation. Pyruvate—three carbons—is converted to acetyl CoA, a two-carbon molecule attached to coenzyme A. A molecule of coenzyme A is a necessary reactant for this reaction, which releases a molecule of carbon dioxide and reduces a NAD+ to NADH.
In eukaryotes, this step takes place in the matrix, the innermost compartment of mitochondria. In prokaryotes, it happens in the cytoplasm. Overall, pyruvate oxidation converts pyruvate—a three-carbon molecule—into acetyl two-carbon molecule attached to Coenzyme A—producing an t, N, A, D, H, end text and releasing one carbon dioxide molecule in the process. Acetyl C, o, A, end text acts as fuel for the citric acid cycle in the next stage of cellular respiration.
Pyruvate oxidation steps
Pyruvate is produced by glycolysis in the cytoplasm, but pyruvate oxidation takes place in the mitochondrial matrix (in eukaryotes). So, before the chemical reactions can begin, pyruvate must enter the mitochondrion, crossing its inner membrane and arriving at the matrix.
In the matrix, pyruvate is modified in a series of steps:
More detailed diagram of the mechanism of pyruvate oxidation.
1. A carboxyl group is removed from pyruvate and released as carbon dioxide.
2. The two-carbon molecule from the first step is oxidized, and NAD+ accepts the electrons to form NADH.
3. The oxidized two-carbon molecule, an acetyl group, is attached to Coenzyme A to form acetyl CoA.
More detailed diagram of the mechanism of pyruvate oxidation.
A carboxyl group is removed from pyruvate and released as carbon dioxide.
The two-carbon molecule from the first step is oxidized, and NAD+ accepts the electrons to form NADH.
The oxidized two-carbon molecule, an acetyl group, is attached to Coenzyme A to form acetyl CoA.
Image credit: "Oxidation of pyruvate and the citric acid cycle: Figure 1" by OpenStax College, Biology, CC BY 3.0
Step 1. A carboxyl group is snipped off of pyruvate and released as a molecule of carbon dioxide, leaving behind a two-carbon molecule.
Step 2. The two-carbon molecule from step 1 is oxidized, and the electrons lost in the oxidation are picked up 2 \text{NADH}NADHstart text, N, A, D, H, end text are generated from \text{NAD}^+NAD
Step 3. The oxidized two-carbon molecule—an acetyl group, highlighted in green—is attached to Coenzyme A (\text{CoA}CoAstart text, C, o, A, end text), an organic molecule derived from vitamin B5, to form acetyl \text{CoA}CoAstart text, C, o, A, end text. Acetyl \text{CoA}CoAstart text, C, o, A, end text is sometimes called a carrier molecule, and its job here is to carry the acetyl group to the citric acid cycle.
The steps above are carried out by a large enzyme complex called the pyruvate dehydrogenase complex, which consists of three interconnected enzymes and includes over 60 subunits. At a couple of stages, the reaction intermediates actually form covalent bonds to the enzyme complex—or, more specifically, to its cofactors. The pyruvate dehydrogenase complex is an important target for regulation, as it controls the amount of acetyl \text{CoA}CoAstart text, C, o, A, end text fed into the citric acid cycle^{1,2,3}
1,2,3
start superscript, 1, comma, 2, comma, 3, end superscript.
If we consider the two pyruvates that enter from glycolysis (for each glucose molecule), we can summarize pyruvate oxidation as follows:
Two molecules of pyruvate are converted into two molecules of acetyl \text{CoA}CoAstart text, C, o, A, end text.
Two carbons are released as carbon dioxide—out of the six originally present in glucose.
2 \text{NADH}NADHstart text, N, A, D, H, end text are generated from \text{NAD}^+NAD
+
start text, N, A, D, end text, start superscript, plus, end superscript.
Why make acetyl \text{CoA}CoAstart text, C, o, A, end text? Acetyl \text{CoA}CoAstart text, C, o, A, end text serves as fuel for the citric acid cycle in the next stage of cellular respiration. The addition of \text{CoA}CoAstart text, C, o, A, end text helps activate the acetyl group, preparing it to undergo the necessary reactions to enter the citric acid cycle.
Explanation:
The correct answer is genes.
A trait refers to the feature like size or color, which is passed from the parents and is inherited by the offspring. The genes control traits and come in pairs, that is, one gene from each parent.
The transmission of hereditary traits possesses its molecular framework in the accurate DNA replication. This generates gene copies, which can be transmitted to the offspring from the parents. In plants and animals, the reproductive cells known as gametes are the mediators, which transfer genes from one generation to the next.
According to the data from the experiments of Gregor Mendel, the information about the traits is passed from parents to offspring is through the genes.
In the deep layers of the ocean, various distinct kinds of species are found like fangtooth fish and vampire squid, to sea urchins and coffinfish.
One of the probable adaptation, which is not fully understood in the deep sea is gigantism. This refers to the ability of animals to become highly enormous in size. A well-known illustration is a giant squid, and others, like giant isopod, the kings of herrings selfish, and the colossal squid.
One of the possible reason of gigantism is the tendency of the species in the deep sea to live for long years, that is, for decades or for even centuries. As food is not abundant in the deep zones, thus deep sea creatures have evolved some interesting mechanisms of feeding.
In the non-existence of photosynthesis, the majority of food comprises of detritus, that is, the decaying leftovers of algae, microbes, animals, and plants from the upper layers of the ocean. Apart from that, the corpses of large animals, like whales that sink to the bottom give irregular but huge feasts for deep-sea animals.
Deafness is an autosomal recessive disorder as the first generation is unaffected and the genotype of the fifth generation is AaBb.
Pedigree is a chart representation of the phenotype of specific genes of the organism and its inheritance from the ancestral family. The pedigree can be used for the analysis of the heritable disease and illness in the family root.
The deafness illness in the pedigree is recessive as the first generation of the pedigree remains unaffected but the later generation is affected and is diseased.
From the chart, deafness can be said to be an autosomalrecessive disorder as some generations are unaffected and in some the disease is present. More than one gene is controlling the disease as the fifth and sixth generations are affected but not their offspring.
The parent of the fifth generation are affected but their progenies are normal to know the genotype let's assume the genes A and B to be responsible for the disease and the mutation in any one of the alleles will result in deafness.
Hence, the genotype of the parents 5 and 6 in the fourth generation will be AAbb and aaBB as both of them diseased or deaf, the offsprings produced from their cross will be AaBb that is all the offspring of the fifth generation will be normal and unaffected.
Therefore, the genotype of the fifth generation in the pedigree is AaBb.
Learn more about pedigree and autosomal recessive disorder here:
Answer:
According to the pedigree, It is clear that the F1 generation is not affected but their offspring are affected in F2, which explains that the deafness presented with the pedigree is recessive. It should be an Autosomal recessive inheritance as it is found in both male and female offsprings.
As it is found that the parents are affected in 5th gen and 6th generation but their offspring are not affected which means there must be more than one genes controlled this disorder
B. In 5th generations mentioned above offspring is unaffected but parents are affected, to find the genotype of the individual let assume there are two genes responsible for it A and B, and mutation in any one of them can result in deafness.
So in IV generation Individuals 5 and 6 have genotypeAAbb and aaBB; both are deaf.
gametes:- Ab & aB.
So, the genotype of all offsprings will be AaBb means all are normal.
The Hawaiian Islands were formed by a hot spot occurring in the middle of the Pacific Plate. While the hot spot itself is fixed, the plate is moving. So, as the plate moved over the hot spot, the string of islands that make up the Hawaiian Island chain were formed.
What is hotspot?
"In geology, hotspots (or hot spots) are volcanic locales thought to be fed by underlying mantle that is anomalously hot compared with the surrounding mantle".
What is Pacific plate ?
"The Pacific Plate is an oceanic tectonic plate that lies beneath the Pacific Ocean. At 103 million km2 (40 million sq mi), it is the largest tectonic plate".
To learn more about hotspot here
#SPJ2
Answer:
Explanation:
The Hawaiian Emperor seamount chain is a well-known example of a large seamount and island chain created by hot-spot volcanism. ... The Hawaiian Islands were formed by such a hot spot occurring in the middle of the Pacific Plate.
Answer:photosynthesis
Explanation:
if work,mark brainilest-_-
Answer:Producers make food for the rest of the ecosystem through the process of photosynthesis, where the energy of the sun is used to convert carbon dioxide and water into glucose