Cytochrome is a protein found in blood cytochrome is found in the mitochondrial membrane and helps our cells produce energy during cellular respiration based on the information in the table below, which organisms is most closely related to humans?
-Rhesus Monkey
-Fruit Fly
-Horse
-Chimpanzee
Answers
Based on the number of differences of the COI protein among organisms we can conclude that chimpanzees are most closely related to humans.
What is the meaning of protein sequence homology in evolution?The meaning of protein sequence homology in evolution is based on the fact that organisms that share more similarity levels are likely closer due to the evolution of these types of sequences million years ago.
Therefore, with this data, we can see that meaning of protein sequence homology in evolution is based on a minor number of differences.
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The two strands of DNA: Group of answer choices run in the same direction. are antiparallel. are held together by ionic bonds. are covalently linked to each other. are none of the other answers are true.
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The two strands of DNA are antiparallel, meaning that they run in opposite directions. One strand runs in the 5' to 3' direction, while the other runs in the 3' to 5' direction. This antiparallel orientation is essential for DNA replication and protein synthesis.
The two strands are held together by hydrogen bonds between complementary base pairs, with adenine (A) bonding with thymine (T) and guanine (G) bonding with cytosine (C). Additionally, the sugar-phosphate backbone of each strand is covalently linked through phosphodiester bonds.
The combination of these bonds creates the double helix structure of DNA. The antiparallel nature of the strands allows for the complementary base pairing and covalent bonding that make up the stable structure of DNA.
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1. Living at high altitude is beneficial because hypoxia . . . a. causes a beneficial left shift of the HbO2 curve b. induces increased production of RBCs c. increases muscle ability to obtain and use oxygen d. causes an chronical increase sympathetic output, increasing respiratory muscle contraction
Answers
Living at high altitude is beneficial because hypoxia option b induces increased production of RBCs, a condition known as erythropoiesis.
Additionally, hypoxia, or low oxygen levels, can also cause a beneficial left shift of the HbO₂ curve, which allows hemoglobin to more readily release oxygen to tissues. This can help to counteract the effects of hypoxia. While hypoxia can increase sympathetic output and respiratory muscle contraction, this is not necessarily beneficial in the long term and can lead to respiratory distress.
Similarly, while hypoxia may increase muscle ability to obtain and use oxygen through mechanisms such as increased angiogenesis, this effect is likely outweighed by the negative effects of hypoxia on muscle function.
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A point mutation occurs that leads to a stop codon in the 500th amino acid of a polypeptide containing 10,000 amino acids. This mutation is known as _____.
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A point mutation occurs that leads to a stop codon in the 500th amino acid of a polypeptide containing 10,000 amino acids. This mutation is known as as a nonsense mutation.
A point mutation is a change in a single nucleotide within a DNA sequence.
When this mutation leads to the formation of a stop codon, it results in premature termination of protein synthesis.
In your case, the stop codon appears at the 500th amino acid in a polypeptide containing 10,000 amino acids, causing the protein to be truncated and potentially non-functional.
This type of mutation is called a nonsense mutation because it leads to the production of a non-functional or shorter protein due to the early appearance of a stop codon.
The point mutation in question, which causes a stop codon at the 500th amino acid of a 10,000 amino acid polypeptide, is referred to as a nonsense mutation.
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In their test of the theory of island biogeography, Simberloff and Wilson found that species richness increases with _____ and decreases with _____.
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In their test of the theory of island biogeography, Simberloff and Wilson found that species richness increases with island size and decreases with distance from the mainland.
Simberloff and Wilson conducted a pioneering study on the theory of island biogeography, which suggests that species richness on an island is determined by the balance between immigration and extinction rates. In their study, they found that species richness increases with island size and decreases with isolation.
Island size is an important determinant of species richness because larger islands have a larger area of habitat available for colonization by species, and hence can support a larger number of species.
In contrast, smaller islands have less area of suitable habitat, which limits the number of species that can be supported.
Isolation, or the distance of an island from a source of colonizing species, is also an important determinant of species richness. Islands that are more isolated have a lower immigration rate, which limits the number of species that can colonize the island.
In contrast, islands that are closer to a source of colonizing species have a higher immigration rate, which increases the number of species that can colonize the island.
Overall, the study by Simberloff and Wilson provided important empirical support for the theory of island biogeography and highlighted the importance of island size and isolation in determining species richness.
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ENZYMES that undergo many rounds of catalysis before dissociating from the substrate are described as
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Enzymes that undergo many rounds of catalysis before dissociating from the substrate are described as processive enzymes.
Processive enzymes are able to remain bound to the substrate even after catalyzing a reaction, allowing them to catalyze multiple reactions in a row. This is different from distributive enzymes, which dissociate from the substrate after each catalytic event. Examples of processive enzymes include DNA polymerase, which adds nucleotides to a growing DNA strand, and cellulase, which breaks down cellulose into glucose molecules.
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It is more useful for biochemists to know the specific activity of an enzyme than the activity of the enzyme because:
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The specific activity of an enzyme is a measure of the activity of an enzyme per unit of protein, while the activity of an enzyme is a measure of the total activity of an enzyme sample. Biochemists prefer to know the specific activity of an enzyme because it allows them to compare different enzyme preparations and determine their purity.
A higher specific activity indicates a purer enzyme preparation because it means that more of the enzyme's activity is coming from the actual enzyme protein rather than contaminating proteins or other molecules. Additionally, knowing the specific activity allows biochemists to calculate the amount of enzyme needed for a particular reaction and to monitor the progress of purification steps. Therefore, the specific activity of an enzyme is a more accurate measure of enzyme activity and is more useful for biochemists in their research.
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If you were to think of the cell as a car, and mitosis as a process that drives that car to go, what would be a good analogy for a cell that has a mutation in a proto-oncogene resulting in an overactive kinase
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A good analogy for a cell with an overactive kinase due to a mutation in a proto-oncogene would be a car with a stuck accelerator pedal that causes the car to go faster than intended.
If we think of the cell as a car and mitosis as the process that drives the car, then a cell with a mutation in a proto-oncogene resulting in an overactive kinase would be like a car with a stuck accelerator pedal.
Just as a stuck pedal causes the car to accelerate uncontrollably, an overactive kinase causes the cell to divide uncontrollably, leading to the development of a tumor.
In normal cells, proto-oncogenes are responsible for promoting cell growth and division.
However, when mutations occur in these genes, they can become oncogenes, which promote uncontrolled cell growth and division. One way that oncogenes can become overactive is through the activation of kinases, which are enzymes that regulate cell signaling pathways.
When an oncogene becomes overactive, it can cause the kinase to become stuck in the "on" position, leading to continuous activation of cell signaling pathways and uncontrolled cell growth. This is similar to a stuck accelerator pedal, which causes continuous acceleration of the car.
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Anti-activation can sometimes occur by an ADP-ribosylation-dependent mechanism. What is the mechanism regarding Class I and II CAP-dependent promoters
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The mechanism of anti-activation involving ADP-ribosylation in Class I and II CAP-dependent promoters is the inhibition of RNA polymerase binding and transcription initiation.
In both Class I and II CAP-dependent promoters, the catabolite activator protein (CAP) binds to specific DNA sites, enhancing the binding of RNA polymerase to the promoter region and promoting transcription initiation.
Anti-activation by an ADP-ribosylation-dependent mechanism involves the transfer of an ADP-ribose group from NAD+ to a specific amino acid residue in the RNA polymerase, which inhibits its activity.
This modification reduces the affinity of RNA polymerase for the promoter region, preventing its binding and subsequent transcription initiation.
Anti-activation via ADP-ribosylation-dependent mechanisms in Class I and II CAP-dependent promoters occurs through the inhibition of RNA polymerase binding and transcription initiation, which is achieved by modifying the RNA polymerase with an ADP-ribose group.
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The pituitary stimulates another endocrine gland to secrete its hormone. Then, this second hormone signals the pituitary to inhibit further secretion of the initial pituitary hormone. This is an example of what type of inhibition
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The pituitary stimulates another endocrine gland to secrete its hormone. Then, this second hormone signals the pituitary to inhibit further secretion of the initial pituitary hormone. This is an example of negative feedback inhibition.
Negative feedback inhibition is an important mechanism by which the pituitary gland regulates hormone production. It occurs when the level of a hormone in the body increases, and this increase signals the hypothalamus and pituitary gland to decrease the production and release of that hormone. In this process, the hormone released by the second endocrine gland signals the pituitary gland to stop secreting its initial hormone, thus maintaining hormonal balance within the body. Negative feedback inhibition is also important in the regulation of other hormones produced by the pituitary gland, such as growth hormone, thyroid-stimulating hormone, and adrenocorticotropic hormone. Negative feedback inhibition is a critical mechanism by which the pituitary gland regulates hormone production, and helps to maintain a balance of hormones in the body.
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2.What feature of the adaptive immune system decreases the amount of time it takes for the body to respond to a particular antigen
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Memory cells are the features of the adaptive immune system which happen to decrease the amount of time which is taken by the body in order to respond to a particular antigen.
The correct option is option B.
Memory cells are a crucial component of the adaptive immune system, and they play an important role in causing a rapid as well as effective response to a previously encountered antigen.
When the body is first exposed to an antigen, such as a virus or bacteria, the adaptive immune system mounts a response to eliminate the invader. During this initial response, some of the immune cells differentiate into memory cells, which can recognize and respond to the same antigen more quickly and efficiently in the future.
Hence, the correct option is option B.
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--The given question is incomplete, the complete question is
"What feature of the adaptive immune system decreased the amount of time it takes for the body to respond to a particular antigen?
A. Unbroken skin
B. Memory cells
C. Cytotoxic T-cells
D. Inflammation"--
____________are proteins that bind to the core promoter near the start point for transcription and are involved in the recruitment of RNA polymerase II.
Answers
Transcription factors are proteins that bind to the core promoter near the start point for transcription and are involved in the recruitment of RNA polymerase II.
What are Transcription factors?The promotion of gene expression is reliant on the presence of specific proteins called transcription factors that bind to certain DNA molecules located in a target gene's promoter region.
These regulators are vital for governing various biological processes like embryonic development, tissue differentiation, and response mechanisms towards molecular signals from their surroundings.
Through their interactions with RNA polymerases or recruitment of co-regulating agents to the relevant machinery, transcription factors modify expression rates based on their activation-repression tendencies.
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An example of a GMO animal used in farming is a pig. Making transgenic animals is a controversial process because the animals are used in food production. However, these pigs produce an extra enzyme in their manure that is better for the environment. What are the advantages of creating a transgenic animal instead of synthesizing the enzymes and treating the manure directly?
Answers
1. Cost-effectiveness: Creating a transgenic animal to produce the enzyme can be more cost-effective than synthesizing large quantities of the enzyme in a lab and then adding it to the manure.
2. Efficiency: A transgenic animal can produce the enzyme continuously and in large amounts, whereas adding the enzyme directly to the manure would require repeated treatments to achieve the same effect.
3. Sustainability: By producing the enzyme naturally in the animal's body, there may be less waste generated in the process of treating the manure, which can be more sustainable and environmentally friendly.
4. Animal welfare: If the enzyme is produced naturally in the animal's body, there may be fewer concerns about the welfare of the animal than if it were given large doses of the enzyme directly.
That being said, the creation of transgenic animals is a controversial process, and there are also potential drawbacks and ethical considerations to take into account.
True or False: All extant species have been described by taxonomists:
True
False
Answers
False. There are estimated to be millions of species on Earth, and taxonomists are still discovering and describing new species all the time. In fact, it is believed that only a fraction of the total number of species on Earth has been described so far.
Taxonomists use various methods to identify and classify new species, such as DNA analysis, morphological characteristics, and geographical distribution. Additionally, some species may be difficult to describe and may require specialized knowledge and equipment. Therefore, while taxonomists have described a large number of extant species, there are still many more waiting to be discovered and documented.
All extant species have not been described by taxonomists. Taxonomists are scientists who classify and describe organisms based on their characteristics and relationships. While taxonomists have made significant progress in cataloging known species, there are still many organisms that have not been discovered or properly classified. The vast biodiversity of our planet makes it difficult to document every species, and new species are continually being discovered. Furthermore, some habitats, such as deep-sea environments or remote regions, are challenging to explore, which contributes to the incomplete documentation of all extant species.
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Vertebrates are distinguished from other chordates by (select all that apply): Group of answer choices
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Hi! Vertebrates are a subgroup of chordates that possess distinct characteristics, setting them apart from other chordates. In 120 words, I will outline the key features that distinguish vertebrates from other chordates:
1. Vertebral column: Vertebrates have a segmented backbone made of individual vertebrae, which surrounds and protects the spinal cord.
2. Endoskeleton: Vertebrates possess an internal skeleton made of bone or cartilage, providing structural support and allowing for movement.
3. Cranium: Vertebrates have a well-developed, bony or cartilaginous skull that encloses and protects the brain.
4. Complex organ systems: Vertebrates have more advanced organ systems, including a closed circulatory system with a multi-chambered heart, specialized respiratory organs (e.g., lungs or gills), and a centralized nervous system.
These key features differentiate vertebrates from other chordates, such as tunicates and lancelets, which lack these complex structures.
A polarized neuron is characterized by the presence of more ________ ions along the plasma membrane outside the cell and less ________ ions along the plasma membrane inside the cell.
Answers
A polarized neuron is characterized by the presence of more positive ions (such as sodium) along the plasma membrane outside the cell and less positive ions and more negative ions (such as potassium and chloride) along the plasma membrane inside the cell.
A polarized neuron has a higher concentration of negatively charged ions, such as chloride (Cl-) and large organic anions, inside the cell compared to outside the cell. This negative charge is balanced by positive ions present on the outside of the cell membrane. This creates a negative charge inside the cell relative to the outside, giving rise to the resting membrane potential.
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A mutation in E. coli makes the lac operator unable to bind the active repressor. How would this mutation affect the cell
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The mutation will affect the cell by preventing the lac repressor from binding to the lac operator, resulting in constitutive expression of the lac operon and the production of lactose-metabolizing enzymes.
The lac operon in E. coli is responsible for the regulation of lactose metabolism. The lac operator is a DNA sequence located upstream of the lac genes that is bound by the lac repressor protein.
When lactose is absent, the lac repressor binds to the operator and prevents the expression of the lac genes.
However, when lactose is present, it binds to the repressor and causes a conformational change, releasing the repressor from the operator and allowing for the expression of the lac genes.
If a mutation occurs in E. coli that makes the lac operator unable to bind the active repressor, this would result in the continuous expression of the lac genes, regardless of the presence or absence of lactose.
This is because the repressor protein is unable to bind to the operator and prevent transcription of the lac genes.
As a result, the E. coli cell would produce enzymes for lactose metabolism continuously, even in the absence of lactose.
This could result in a waste of cellular resources and energy, as well as potentially harmful effects if the metabolites of lactose are toxic to the cell.
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Use what you know about natural selection to fill in
the blanks in the hypothesis. It should answer the
lab question, "What is the effect of the type of food
available on the frequency of different types of bird
beaks?"
Hypothesis: If the type of food available changes,
then...
...because...
Answers
The lambda phage genome is 48.5 kb in size and has 50% GC content. Approximately how many times would you expect HincII to cut lambda phage DNA
Answers
We can expect HincII to cut lambda phage DNA approximately 95 times.
The lambda phage genome is 48.5 kb in size and has 50% GC content.
HincII is a type II restriction enzyme that recognizes and cuts DNA sequences containing "GTYRAC" (where Y stands for pyrimidine and R stands for purine). The probability of a given base being G or C in the lambda phage genome can be calculated as 0.5 * 0.5 = 0.25, since the GC content is 50%. The probability of a four-base sequence being recognized by HincII can be calculated as [tex]0.25^2 * 0.5^2 =[/tex] 0.0078125, or approximately 1/128.
Therefore, the expected number of HincII restriction sites in the lambda phage genome can be estimated by dividing the length of the genome by the length of the recognition sequence:
48.5 kb / 4 bp = 12,125
Multiplying this by the probability of any given site being recognized, we can estimate the expected number of HincII cuts as:
12,125 * 0.0078125 = 94.7
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The amino acids which are not responsible for net glucose resynthesis are somehow labeled with 14C, the label will appear in resynthesized glucose. Explain this observation.
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This observation can be explained by the fact that even though some amino acids are not directly responsible for net glucose resynthesis, they can still contribute to the process indirectly.
During the amino pathway, these 14C-labeled amino acids may be converted into intermediates, which can then be utilized by other pathways that contribute to glucose resynthesis. As a result, the 14C label from these amino acids can eventually be incorporated into the resynthesized glucose molecule.
The process of glucose resynthesis involves the conversion of certain amino acids into glucose. However, not all amino acids contribute to this process. Some amino acids are metabolized through other pathways and do not contribute to the net production of glucose.
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A DNA strand undergoing replication contains the bases TACGTT. Which complementary strand does it produce
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A DNA strand undergoing replication contains the bases TACGTT . The complementary strand produced for TACGTT is ATGCAA.
When a DNA strand undergoes replication, it produces a complementary strand by following the base pairing rules. In this case, the original DNA strand has the bases TACGTT.
To find the complementary strand, we use these pairing rules: Adenine (A) pairs with Thymine (T), and Guanine (G) pairs with Cytosine (C).
Using these rules, the complementary strand for TACGTT is formed as follows:
- Thymine (T) pairs with Adenine (A): T -> A
- Adenine (A) pairs with Thymine (T): A -> T
- Cytosine (C) pairs with Guanine (G): C -> G
- Guanine (G) pairs with Cytosine (C): G -> C
- Thymine (T) pairs with Adenine (A): T -> A
- Thymine (T) pairs with Adenine (A): T -> A
By following these rules, we can determine that the complementary DNA strand for TACGTT is ATGCAA.
During DNA replication, the double helix is unwound, and each strand serves as a template for the synthesis of a new complementary strand. This process ensures accurate replication of genetic information and its transmission to subsequent generations of cells.
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a tumor is in a young boy's brain. Symptoms include the inability to swallow and inability to detect odors what is the most likely location of the tumor
Answers
The most likely location of the tumor causing the inability to swallow and detect odors in the young boy's brain would be the olfactory bulb and the medulla oblongata.
The olfactory bulb is responsible for detecting odors, while the medulla oblongata controls important functions such as swallowing. An explanation for this could be that the tumor is interfering with the function of these specific regions in the brain, leading to the symptoms the young boy is experiencing.
The brainstem is responsible for several vital functions, including swallowing and the relay of sensory information like odors. Damage to this area can lead to the observed symptoms.
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Bronchoconstriction _____ resistance to air flow and _____ the amount of fresh air the enters the alveoli.
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Bronchoconstriction is a narrowing of the air passages in the lungs, which can occur in response to various triggers such as allergens or irritants.
This constriction can increase resistance to air flow, making it harder for air to move in and out of the lungs. As a result, the amount of fresh air that enters the alveoli, the tiny air sacs where oxygen is exchanged with carbon dioxide, can be significantly reduced. This can lead to a range of symptoms, including shortness of breath, wheezing, and coughing. In severe cases, bronchoconstriction can even cause a life-threatening asthma attack. Treatment for bronchoconstriction typically involves medications such as bronchodilators, which work to relax the airway muscles and increase air flow.
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A cross between a black mouse and a brown mouse produced 4 black offspring and 4 brown offspring. Black coat color is dominant to brown coat color, and therefore you can conclude that ________.
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A cross between a black mouse and a brown mouse produced 4 black offspring and 4 brown offspring. Given that black coat color is dominant over brown coat color.
You can conclude that the black parent mouse has a heterozygous genotype (Bb) for the coat color gene, and the brown parent mouse has a homozygous recessive genotype (bb). The equal ratio of black and brown offspring (1:1) supports the conclusion that the black parent is heterozygous since it's able to pass on both the dominant (B) and recessive (b) alleles. In this case, the offspring would have the following genotypes: 50% Bb (black) and 50% bb (brown), explaining the observed ratio.
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Pollutants that destroy fungi that form mycorrhizal associations with plants would directly impact the plant's ability to do what, primarily
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Pollutants that destroy fungi that form mycorrhizal associations with plants would directly impact the plant's ability to absorb essential nutrients, primarily phosphorus, from the soil.
The ability of plants to absorb vital nutrients from the soil, particularly phosphorus, would be directly impacted by pollutants that kill the fungus that form mycorrhizal connections with plants.
This is because mycorrhizal fungi help plants to absorb nutrients that are not easily accessible to them, thereby improving their nutrient uptake and overall growth and development. Without these fungi, the plant may struggle to survive and may exhibit stunted growth and reduced productivity.
A broad class of creatures known as fungi includes yeasts, moulds, and mushrooms. They can grow on organic materials such as plants and animals, and they can be found in a variety of habitats, including soil, water, and air. Humans can benefit from some fungi, such as those that are utilised to produce food (like yeast for bread) or medicines (like penicillin). Others, however, can be harmful and if consumed, can result in infections, allergies, or even poisoning. In ecosystems, fungi are crucial for the cycling of nutrients and are crucial for decomposition.
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The gene for melanin (skin pigment) is transcribed similarly in humans and apes. Where does the transcription of the melanin gene take place
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The transcription of the melanin gene takes place in the nucleus of the cell. The gene for melanin, also known as the melanocortin 1 receptor (MC1R) gene, is transcribed into messenger RNA (mRNA) by the enzyme RNA polymerase II. This process occurs in both humans and apes in the same way.
The MC1R gene encodes a protein that is involved in the production of melanin, the pigment responsible for skin color.
The gene is expressed in melanocytes, specialized cells found in the skin, hair, and eyes. Transcription of the MC1R gene is regulated by a number of factors, including hormones, cytokines, and UV radiation.
Once transcribed, the mRNA is processed and transported out of the nucleus into the cytoplasm, where it is translated into a protein. The protein product of the MC1R gene then plays a role in the synthesis and distribution of melanin within melanocytes.
Variations in the MC1R gene can affect the amount and type of melanin produced, leading to differences in skin color and other pigmentation traits among individuals.
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QUANTITATIVE Assuming that each replication fork moves at a rate of 500 base pairs per second, how long would it take to replicate the E. coli chromosome (with 4.6 million base pairs) from a single origin of replication
Answers
The E. coli chromosome is a circular DNA molecule that contains approximately 4.6 million base pairs.
Replication of this chromosome starts at a single origin of replication and proceeds bidirectionally, Resulting in two replication forks moving in opposite directions.
Assuming that each replication fork moves at a rate of 500 base pairs per second, the total time required to replicate the entire E. coli chromosome from a single origin of replication can be calculated as follows:
First, we need to determine the total number of base pairs that need to be replicated. Since the E. coli chromosome is circular, it has two replication forks moving in opposite directions, and
thus, the total number of base pairs that need to be replicated is equal to twice the size of the chromosome. Therefore, the total number of base pairs that need to be replicated is:
4.6 million base pairs x 2 = 9.2 million base pairs, Next, we can calculate the time required to replicate these 9.2 million base pairs at a rate of 500 base pairs per second: Time = Total number of base pairs / Rate of replication, Time = 9.2 million base pairs / 500 base pairs per second,
Time = 18,400 seconds or approximately 5 hours and 7 minutes, Therefore, it would take approximately 5 hours and 7 minutes to replicate the E.
coli chromosome from a single origin of replication, assuming that each replication fork moves at a rate of 500 base pairs per second.
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Mammals are divided into three major groups based on: presence of hair. ability to produce milk. where early development of the young occurs. presence or absence of a pouch.
Answers
Answer:
They are based on where early development of young occurs.
A pituitary tumor that increases secretion of growth hormone releasing hormone above normal will result in ______.
Answers
A pituitary tumor that increases the secretion of growth hormone releasing hormone above normal will result in excessive production of growth hormone.
The pituitary gland is responsible for producing and releasing various hormones that regulate bodily functions, including growth hormones.
When a tumor develops in the pituitary gland and increases the production and release of growth hormone-releasing hormone, it leads to excessive production of growth hormone, a condition known as acromegaly.
Acromegaly causes abnormal growth of bones and tissues, particularly in the face, hands, and feet, as well as other health issues such as joint pain, hypertension, and diabetes mellitus. Treatment for pituitary tumors and acromegaly may involve surgery, radiation therapy, and medications to regulate hormone levels.
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phases of cellular respiration
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The phases of cellular respiration has the following characteristics:
Glycolysis: Anaerobic process, breaks down glucose into pyruvate, occurs in the cytoplasm, yields a net total of 2 ATPCitric acid cycle: Also called kreb cycle, aerobic process, occurs in the mitochondrial matrix, involves electron carriers NAD+ and FAD, yields a net total of 2 ATPElectron transport chain: Aerobic process, involves electrons being passed down a series of proteins, oxygen serves as the final electron acceptor, yields a total of 34 ATPWhat are the phases of cellular respiration?Cellular respiration is the process by which cells obtain chemical energy by the consumption of oxygen and the release of carbon dioxide.
Cellular respiration is made up of the following steps or phases;
GlycolysisGlycolysisKreb cycleGlycolysisKreb cycleElectron transport chainGlycolysis involves the breakdown of glucose molecules into pyruvate that will be used in the kreb cycle.
Kreb cycle is a series of enzymatic reactions that occurs in all aerobic organisms; it involves the oxidative metabolism of acetyl units, and serves as the main source of cellular energy.
Electron transport chain is the movement of electrons through proteins that serve as electron acceptors.
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Generally, a very _______ percent of Na in the tubular fluid is reabsorbed, and the reabsorption takes place _________.
Answers
Generally, a very high percent of Na in the tubular fluid is reabsorbed, and the reabsorption takes place primarily in the proximal tubule of the nephron.
The process of sodium reabsorption is tightly regulated by various hormones, including aldosterone and antidiuretic hormone (ADH), which help to maintain sodium and water balance in the body.
This process is critical for maintaining normal blood volume and blood pressure, as well as for regulating the concentration of other ions like potassium and chloride in the body. The remaining 1% of the filtered sodium is excreted in the urine.
The proximal tubule is the first segment of the renal tubule in the nephron of the kidney. It is responsible for reabsorption of ions, nutrients, and water from the filtrate.
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