Chemical mutagens are agents that cause changes in the chemical structure of DNA, leading to mutations. These agents can act in two main ways, by chemically modifying bases or stimulating base tautomerization.
Chemical modification of bases, such as thymine pairs with guanine, can lead to changes in base pairing and mispairing of bases. This can lead to changes in the genetic code, resulting in mutations. Stimulation of base tautomerization is the process whereby the chemical structure of a base can be changed by the addition or removal of certain chemical groups.
For example, Cytosine can lose an amino (NH2) group by the action of 5-Brdu, leading to a change in base pairing. Also, chemical mutagens can act as base analogs, such as 5-BrdU, which can be incorporated opposite an adenine during replication, or EMS which can convert guanine to O^6-ethylguanine, or RecBCD which can convert thymine to O^6 -thymine. All of these changes can lead to mutations in the DNA.
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organisms belonging to the domains archaea and eubacteria are composed of single cells. what criterion is used to classify each type of organism into a separate domain?
The criterion used to classify the organisms of Archaea and Eubacteria is their habitat. The organisms of Archaea live in extreme habitats like salty lakes, hot spring or acidic environments.
Archaea is the domain consisting of single celled organisms. They are not eukaryotic in nature but are completely similar to bacterial species. Their special character is their ability to live in extreme habitats. The examples are halophiles, methanogens, etc.
Eubacteria is the domain comprising of the prokaryotic organisms. They are the true bacterial cells which were the first ones to appear on the earth. The examples of eubacteria are E. coli, Salmonella, etc.
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a difference between a g and an a at a particular nucleotide is an example of a(n) snp. str. microarray. dna transposon. microsatellite.
An illustration of snp is a difference between a g and an a at a specific nucleotide. The correct answer is SNP.
The substitution of a C for a G in the nucleotide sequence AACGAT, which results in the sequence AACCAT, is an illustration of an SNP. The DNA of people might contain numerous SNPs since these varieties happen at a pace of one in each 100-300 nucleotides in the human genome.
A single nucleotide change in a genome is known as an SNP. Likewise, it is a sort of change. Base pair substitution, insertion, deletion, duplication, or variation in DNA is known as a mutation.
The primary distinction between an SNP and a mutation is that a mutation is any change in DNA, from a single to many nucleotide difference, whereas an SNP is a single nucleotide difference in DNA.
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The 5' end of the DNA molecule is considered the ______, while the 3' end of the DNA molecule is considered the ______.
a. End, middle
b. Beginning, end
c. End, beginning
d. Middle, end
The 5' end of the DNA molecule is considered the End, while the 3' end of the DNA molecule is considered the beginning.Hence, the correct option is C.
In the context of DNA molecules, the 5' end refers to the end of the DNA strand that has a phosphate group attached to the 5' carbon of the sugar molecule in the DNA backbone. The phosphate group is located at the "end" of the DNA molecule, and hence the 5' end is often referred to as the "end" of the DNA molecule.
On the other hand, the 3' end refers to the end of the DNA strand that has a hydroxyl group (-OH) attached to the 3' carbon of the sugar molecule in the DNA backbone. The hydroxyl group is located at the "end" of the DNA molecule, and hence the 3' end is often referred to as the "beginning" of the DNA molecule.
Hence, the correct option is C.
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variation within species was important to the development of darwin's theory of evolution. which statement does individual variation help explain?
Individual variation within a species helps explain how natural selection can occur, which is a key component of Darwin's theory of evolution.
Variations in traits can arise through genetic mutations, gene flow, and environmental factors, and these variations can be advantageous or disadvantageous to an individual's survival and reproduction. Natural selection favors those individuals with traits that provide a survival advantage in their specific environment, allowing them to pass on their advantageous traits to their offspring.
Over time, these advantageous traits become more prevalent in the population, leading to the evolution of new species. Thus, individual variation is crucial to the process of natural selection and the development of Darwin's theory of evolution.
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population. It also shows the running speed of a new group of
predators that recently moved into the area due to habitat loss.
You have been asked to identify the portion of the rabibit population
that will likely survive to pass on its traits to future generations.
Which portion of the graph will you highlight?
Select one:
O the bottom portion
O
O the far right portion
the far left portion
O the middle portion
The bottom portion of the graph, where the rabbit population reaches its lowest point, is the portion that is most likely to survive and pass on its traits to future generations.
What is the cause of habitual loss?Habitat loss is caused by various human activities such as deforestation, urbanization, industrialization, mining, and agriculture. These activities lead to the destruction, fragmentation, and degradation of natural habitats, making them less suitable for the survival of certain species.
Climate change can also contribute to habitat loss by altering temperature and rainfall patterns, causing some habitats to become unsuitable for certain species.
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Single trait crosses problem set worksheet
The genotype of the heterozygous tall pea plant is Tt, where T represents the dominant allele for tallness and t represents the recessive allele for shortness. The genotype of the homozygous short pea plant is tt, where both alleles are the recessive allele for shortness.
The dominant allele T represents the tall phenotype, and the recessive allele t represents the short phenotype. A heterozygous tall pea plant has one dominant T allele and one recessive t allele. A homozygous short pea plant has two recessive t alleles.
When these two plants are crossed, the offspring can inherit either a dominant T allele or a recessive t allele from the heterozygous parent, resulting in a 50% chance of the offspring being tall and a 50% chance of being short. The Punnett square can be used to illustrate the possible genotypes and phenotypes of the offspring.
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--The complete question is, In pea plants, the allele for tall (T) is dominant over the allele for short (t). A heterozygous tall pea plant is crossed with a homozygous short pea plant.
What is the genotype of the heterozygous tall pea plant?
What is the genotype of the homozygous short pea plant?--
the division between the central nervous system and the peripheral nervous system is based on the anatomical differences between cells in the two locations. true or false
The physical distinctions between the cells in the two regions serve as the foundation for the separation of the central nervous system from the peripheral nervous system. Hence the given statement is true.
The two main components of the nervous system are: Spinal cord and brain together make up the central nervous system. The nerves that emanate from the spinal cord and connect to every area of the body make up the peripheral nervous system. Somatic and autonomic nervous systems are further split under the umbrella term of peripheral nervous system. The several divisions of the peripheral nervous system. Both somatic and visceral divisions can be made within it.
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which statement best describes the role of microorganisms such as rotavirus and attenuated salmonella enterica in the production of recombinant-vector vaccines? multiple choice question. they serve as vectors. they serve as adjuvants. they act as antigens, so these vaccines can protect against rotavirus or salmonella enterica.
The assertion best depicts the job of microorganisms, for model, rotavirus, and lessened salmonella enterica in the plot of recombinant-vector antibodies that act as vectors.
The MMR vaccine is an attenuated (weakened) live virus. This indicates that, prior to being eliminated from the body, the viruses only cause a mild, if any, infection following injection into the person who was vaccinated.
Vaccines that contain organisms that have been killed or inactivated by heat or chemicals are known as inactivated vaccines. In contrast to attenuated vaccines, inactivated vaccines elicit an immune response that is frequently less comprehensive.
The immune system responds to the antigen that is produced by the gene in the body.
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What kind of code is generally used for sending digital information
The most used character encoded scheme for written communication in computers as well as websites is the ISO format (which stands for Information Communication).
How is data conveyed digitally?electronic signals. Electromagnetic waves are used to transport both digital and analogue signals. The music you hear and the graphics you see on screens are made possible by variations in frequency and amplitude. Continuous waves that may possess any frequency and amplitude make up analogue signals.
What is the purpose of digital transmission?In systems for communication, radio waves are usually utilized for sending data across point-to-point or point-to-multipoint pathways, such as copper wiring, optical fibers, mobile communication the media, storage media, or computers buses.
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which of the following mutations would have the greatest affect (deleterious or favorable) on an organism group of answer choices single nucleotide substitution single nucleotide insertion premature stop codon at position 42 of 44. duplication of 12 nucleotides single codon deletion
An organism's single nucleotide insertion would be most affected, either deleteriously or positively, by the following mutations.
In a frameshift transformation, the perusing outline changes because of additions or cancellations of nucleotides. Consequently, the amino acid sequence following the insertion or deletion differs from the sequence of the wild-type polypeptide. Hence, various amino acids in a protein change.
B. nonsense mutations are the kind of mutation that is most likely to have a significant impact on a protein. This is due to the fact that a nonsense mutation causes a premature stop codon, resulting in the protein's incomplete formation and severe effects on its structure and function.
A single nucleotide frameshift mutation is likely to have a significant impact on an organism's phenotype.
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The chromatin remodeling complexes play an important role in chromatin regulation in the nucleus. They ...A. can slide nucleosomes on DNA.B. have ATPase activity.C. interact with histone chaperones.D. can remove or exchange core histone subunits.E. All of the above.
All of the above plays important role in chromatin regulation in the nucleus. (E)
Chromatin remodeling complexes play a crucial role in chromatin regulation in the nucleus. They can slide nucleosomes on DNA, have ATPase activity, interact with histone chaperones, and remove or exchange core histone subunits.
These complexes are essential for various cellular processes, such as gene transcription, DNA replication, and DNA repair, by altering chromatin structure and accessibility to other proteins.
The ATPase activity provides energy for these changes, while interactions with histone chaperones assist in the assembly and disassembly of nucleosomes. Removal or exchange of core histone subunits allows for further chromatin regulation and modulation.
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the esophageal phase begins when the esophageal sphincter to allow ingested materials into the esophagus. listen to the complete question
The esophageal phase begins when the esophageal sphincter relaxes to allow ingested materials into the esophagus. This is an essential part of the swallowing process, facilitating the movement of food and liquid from the mouth to the stomach for further digestion.
The esophageal phase of swallowing begins when the upper esophageal sphincter relaxes to allow ingested materials to enter the esophagus. The upper esophageal sphincter is a ring-like muscle at the top of the esophagus that normally stays closed to prevent food and liquids from entering the airway. When we swallow, the muscles in the tongue and pharynx (throat) contract to move the food or liquid into the esophagus. At the same time, the upper esophageal sphincter relaxes to let the food or liquid pass through into the esophagus. From there, the food or liquid is moved down the esophagus by waves of muscular contractions (peristalsis) towards the stomach.
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The esophageal phase begins when the esophageal sphincter opens to allow ingested materials into the esophagus.
What is the esophageal phase?
The esophageal phase is the stage of swallowing when the ingested materials move through the esophagus toward the stomach. It starts when the esophageal sphincter relaxes to allow the materials to enter the esophagus. The esophagus is a muscular tube that connects the throat to the stomach and uses rhythmic contractions, called peristalsis, to move the food toward the stomach.
What is the esophageal sphincter?
The esophageal sphincter is a circular muscle at the end of the esophagus that opens to let the food pass into the stomach and then closes to prevent the contents of the stomach from coming back up. This phase is an essential part of the swallowing process, as it ensures the smooth passage of food or liquid from the mouth to the stomach through the esophagus.
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If the number of sea lamprey stayed small, how big of an effect would it have on the trout? If the sea lamprey population did not reproduce, could it have a big impact on the trout? thank you
Sea lampreys have significantly harmed the Great Lakes fishery and had a huge detrimental impact on it. Canada before the sea lamprey invasion.
What is the trout and lamprey's symbiotic relationship?Sea lampreys are parasitic, active predators that only eat fish blood for a portion of their life cycle. They affix to their victim, typically a lake trout, and draw blood and tissue fluids from it. Typically, they leave their victim alone after feeding it until it becomes weak.
How did the sea lamprey enter the ecosystem of the Great Lakes to feed on the trout?Through artificial shipping canals, sea lampreys made their way into the Great Lakes from the Atlantic Ocean. They were first discovered in Lake Ontario in the 1830s. Niagara The migration of sea lamprey to Lakes Erie, Huron, Michigan, and Superior was impeded by falls, which served as a natural barrier.
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multiple choice question the rise in blood lactate that occurs during incremental exercise may be the cause of the alinear rise in the ventilatory threshold, because the carotid bodies that increase the threshold can be stimulated by a(n) blank .
The carotid bodies that rise to the end can be elicited by an increase in hydrogen ion levels.
Acute NaCl overload, according to the findings, activates carotid bodies, but not mannitol. We conclude that during acute NaCl overload, the carotid bodies contribute to increased sympathetic activity.
The primary peripheral chemoreceptors are the carotid bodies, which are triggered by hypoperfusion, low oxygen partial pressure, high carbon dioxide partial pressure, blood acidity, and oxygen partial pressure.
In conscious humans, we demonstrated that the injection of adenosine selectively stimulates the carotid body, resulting in a dose-dependent increase in minute ventilation and blood pressure while simultaneously lowering heart rate.
In a nutshell, reflex bradycardia and systemic vasodilatation will result from the stimulation of stretch receptors by an increase in carotid sinus blood pressure. During changes in posture, the baroreceptor reflex is also essential for maintaining heart rate and blood pressure.
According to these findings, hypoxic stimulation of the carotid bodies results in a dichotomous sympathetic response, which means that sympathetic discharge to the heart decreases while sympathetic discharge to the peripheral vasculature increases simultaneously.
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the genomes of many organisms have been sequenced. what benefits or uses could result from this information?
The sequencing of genomes of various organisms has opened up numerous opportunities for research and advancements in fields such as medicine, agriculture, and ecology.
One major benefit is the ability to understand the genetic basis of diseases and develop targeted therapies. For example, the Human Genome Project has led to the discovery of genes associated with various diseases such as cancer and Alzheimer's, which has aided in the development of new treatments and drugs.
Genome sequencing has also contributed to advancements in agriculture, as it allows for the development of crops with improved yield, disease resistance, and nutrient content. Similarly, it has aided in the conservation of endangered species by allowing scientists to study their genetic diversity and develop strategies for their preservation.
In addition to these practical applications, genome sequencing has contributed to our understanding of evolutionary history and relationships between species. It has provided insight into the mechanisms of adaptation and speciation, as well as the evolution of complex traits such as intelligence and behavior.
Overall, genome sequencing has had a significant impact on various fields of research and has the potential for even greater advancements in the future.
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which enzyme is not part of the calvin cycle? group of answer choices aldolase glyceraldehyde 3-phosphate dehydrogenase phosphofructokinase-1 ribulose-5-phosphate kinase transketolase
The enzyme not a part of the Calvin cycle is: (3) phosphofructokinase-1.
Calvin cycle is the process involved in the fixation of the atmospheric carbon which the plant absorbs from the environment. It is also called C3 cycle. The process occurs in three following steps: fixation, reduction and regeneration. The Calvin cycle is the first process of the light independent reactions for the formation of sugar.
Phosphofructokinase-1 is the enzyme involved in the catalysis of the phosphorylation of fructose-6-phosphate to form fructose-1,6-bisphosphate. This chemical reaction is a part of the glycolysis process and hence this enzyme takes part in glycolysis and not in Calvin cycle.
Therefore, the correct answer is option 3.
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a patient has microcytic hypochromic anemia. which of the following pathogenic mechanisms may cause anemia in this patient? (select all that apply.) 1. increased basal metabolic rate 2. decreased erythrocyte life span 3. disturbances of the iron cycle 4. swelling in the tissues 5. failure of mechanisms of compensatory erythropoiesis
The pathogenic mechanisms that may cause anemia in a patient with microcytic hypochromic anemia are: 2. decreased erythrocyte life span, 3. disturbances of the iron cycle, and 5. failure of mechanisms of compensatory erythropoiesis.
Increased basal metabolic rate and swelling in the tissues are not typically associated with microcytic hypochromic anemia.
The mechanisms that may cause anemia in this patient include:
1. Decreased erythrocyte life span: A reduced red blood cell lifespan can lead to anemia, as there are fewer red blood cells available to transport oxygen.
3. Disturbances of the iron cycle: Iron is essential for hemoglobin synthesis, and disruptions in the iron cycle can cause microcytic hypochromic anemia, as the body is unable to produce enough hemoglobin.
5. Failure of mechanisms of compensatory erythropoiesis: If the body is unable to produce new red blood cells at a rate that compensates for their loss or destruction, anemia may occur.
Increased basal metabolic rate (option 1) and swelling in the tissues (option 4) are not directly related to the pathogenic mechanisms of microcytic hypochromic anemia.
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children born to the same parents are usually very different from each other. which process is primarily responsible for these differences?
The process primarily responsible for the differences among siblings born to the same parents is genetic recombination during meiosis, which generates new combinations of genetic information in each gamete produced.
This means that each sibling receives a unique combination of genes from their parents, leading to variations in physical and behavioral traits. Additionally, environmental factors and chance events can also contribute to differences among siblings.
This is because during meiosis, the process of genetic recombination shuffles the genetic material between homologous chromosomes, creating new combinations of alleles that were not present in either parent. This results in genetic diversity among the offspring, and explains why siblings can have different physical characteristics, susceptibility to diseases, and other traits.
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The process primarily responsible for the differences between children born to the same parents is genetic variation. Each child inherits a unique combination of genes from their parents, which can lead to differences in physical traits, personality, and other characteristics.
Additionally, environmental factors such as upbringing, experiences, and interactions with others can also contribute to the differences between siblings.
Children born to the same parents can indeed be very different from each other. The process is primarily responsible for these differences is genetic recombination, which occurs during meiosis.
This process shuffles and combines the genetic material from both parents, resulting in unique combinations in each child.
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the following graph presents the concentration of glucose and insulin in the blood of a human subject over time. at 15 minutes into the test, the subject ate a high-carbohydrate (sugar) candy bar: the graph plots the concentration of blood glucose and insulin concentrations of a human subject on the y axis. a line depicting the healthy level of glucose is also plotted against the y axis. the x axis measures time in minutes. the line depicting healthy glucose levels is constant at approximately 6,000 mg across all times. the actual glucose levels of the subject are at approximately 6,000 mg at time 0. at 28 minutes, the subjects glucose concentration begins to rise, peaking at approximately 40 minutes at a concentration of 9,500 mg. the subjects glucose concentrations begin to drop right after the peak, reaching a low of 5,500 mg at 75 minutes. the subjects glucose levels return to 6,000 mg at 100 minutes. the subjects insulin concentration is at 9,500 mg at time 0. at approximately 35 minutes, it starts to rise, reaching a peak of 14,000 mg at approx. 50 minutes. insulin levels then start to lower, reaching a low of 9,000 mg at 90 minutes. it then returns to 9,500 mg by 120 minutes. based on this data, which statement is true? group of answer choices the presence of insulin stimulates production of glucose. an increase in glucose triggers production of insulin. a decrease in insulin triggers production of glucose. the production of glucose and insulin are unrelated to each other.
Based on the data presented, the statement that is true is "an increase in glucose triggers production of insulin." This is because at 15 minutes, the subject ate a high-carbohydrate candy bar which caused their glucose concentration to remain constant at around 6,000 mg for the first 28 minutes.
However, at around 28 minutes, the subject's glucose concentration began to rise, peaking at approximately 9,500 mg at 40 minutes. This rise in glucose concentration triggered the production of insulin, which began to rise at approximately 35 minutes, reaching a peak of 14,000 mg at around 50 minutes.
Insulin is a hormone that is released by the pancreas in response to an increase in glucose concentration in the blood. Its primary function is to lower blood glucose levels by stimulating the uptake of glucose by cells and the conversion of glucose to glycogen for storage in the liver and muscle cells.
The data shows that when glucose levels rise, insulin production is stimulated, and when glucose levels drop, insulin production decreases. Therefore, an increase in glucose triggers production of insulin, and not the other way around.
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the article lists 4 things that can disrupt the 3-d structure of a protein. based on this list, what might you infer are the 4 conditions that are essential to the 3-d structure of a protein? what property of the protein does each of the 4 conditions affect?
The 4 essential conditions for the 3-D structure of a protein are temperature, pH, salt concentration, and solvent polarity.
Temperature affects the kinetic energy of the protein and can denature it. pH affects the ionization state of the amino acid residues, which can disrupt hydrogen bonding and alter electrostatic interactions. Salt concentration affects the electrostatic interactions between charged amino acid residues and can disrupt them.
Solvent polarity can affect the hydrophobic interactions that contribute to protein folding and can disrupt them if the solvent polarity is altered. Therefore, maintaining the optimal temperature, pH, salt concentration, and solvent polarity are crucial for maintaining the 3-D structure and proper function of a protein.
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could someone help me
Answer:1. X^nY
2. X^NX^n
3.X^NX^n
4. X^NY
5. X^NY
6. X^NX^n
7. X^nX^n
8. X^NY
9. X^nY
10,11. X^nY
12,14. X^NX^n
13. X^nY
Explanation: colour blindness is X linked recessive so;-
for a diseased female(shaded circle)-both X have to be diseased
for a diseased male(shaded square)-single diseased X
normal female(unshaded circle)-can be a normal(both X normal) or carrier(one X diseased)
normal male(unshaded square)-single normal X required
One characteristic used to place organisms into kingdoms is
Answer:
Cell structure
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explain the difference between anterior and posterior dentition in terms of:a the teeth that comprise each of them.b the general function of each of them.
a tissue with striations and many flattened nuclei under the plasma membrane in each cell would be called
A tissue with striations and many flattened nuclei under the plasma membrane in each cell would be called skeletal muscle tissue.
Skeletal muscle tissue is composed of long, cylindrical cells called muscle fibers, which are multinucleated and contain many flattened nuclei located just beneath the plasma membrane. These fibers have a highly organized structure, with alternating bands of dark and light striations visible under a microscope, giving them a striated appearance.
Skeletal muscle tissue is responsible for voluntary movement of the body, such as walking and running, as well as for the maintenance of posture and the generation of heat. It is attached to bones by tendons and is under conscious control, meaning that it can be contracted and relaxed at will.
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in the context of elbow movements, the movement of the forearm to the shoulder by bending the elbow to decrease its angle is known as _____.
In the context of elbow movements, the movement of the forearm to the shoulder by bending the elbow to decrease its angle is known as flexion.
Flexion is a type of movement that occurs in a joint where the angle between two bones decreases. In the case of the elbow joint, flexion is the movement that brings the forearm closer to the shoulder by decreasing the angle between the humerus and the radius/ulna bones of the forearm.
Flexion is an essential movement for everyday activities such as lifting objects and bringing food to one's mouth. It is also a fundamental movement in many sports, including weightlifting, gymnastics, and baseball.
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as the size (area) of the body exposed to cold immersion increases, the temperature of the immersion should:
As the size (area) of the body exposed to cold immersion increases, the temperature of the immersion should decrease.
This is because a larger surface area of the body exposed to the cold water results in more heat being lost from the body, causing the body to feel colder and the immersion to feel warmer in comparison. When the body is exposed to cold, it responds by trying to conserve heat and maintain core body temperature. The body's first response to cold is to constrict blood vessels near the skin's surface, which reduces blood flow to the skin and conserves heat within the body's core. However, when a large area of the body is exposed to cold immersion, this response may not be sufficient to maintain core body temperature, and the body's temperature may drop.
In summary, the temperature of the immersion should decrease as the size (area) of the body exposed to cold immersion increases, leading to a greater loss of heat from the body and a greater drop in body temperature.
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Describe what hydrogen bonds connect in the double helix
Answer:
Hm
Explanation:
In the double helix of DNA, hydrogen bonds connect the nitrogenous bases of the two complementary strands of DNA. Specifically, hydrogen bonds form between the purine and pyrimidine base pairs. Adenine (A) always pairs with thymine (T), and guanine (G) always pairs with cytosine (C). The hydrogen bonds between these complementary base pairs help to stabilize the double helix structure of DNA. Each base pair is connected by two or three hydrogen bonds, which create a weak, yet essential, attraction between the two strands of DNA. These hydrogen bonds play a crucial role in the process of DNA replication and the transfer of genetic information from one generation to the next.
Answer:
Each molecule of DNA is a double helix formed from two complementary strands of nucleotides held together by hydrogen bonds between G-C and A-T base pairs.
Many exoenzymes from pathogens are virulence factors. 1) True 2) False
True. Exoenzymes from pathogens are virulence factors which are molecules or compounds released by a pathogen that enables it to cause disease.
Exoenzymes, also known as extracellular enzymes, are proteins expressed and secreted by a pathogenic organism. These enzymes allow the organism to move, invade, and damage host cells. Exoenzymes also allow bacteria to break down host components to obtain nutrients, degrade host defenses, and protect the organism from host defenses.
Exoenzymes can cause disruption of the cell membrane and damage to cell organelles, leading to cell death. They can also induce inflammation which can lead to tissue damage. In addition, exoenzymes can inhibit the host’s immune response and interfere with the healing process. Thus, exoenzymes are important virulence factors that enable pathogens to cause disease.
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of the following, the most unusual genomic feature of a single-celled eukaryote would be the presence of introns. centromeric sequences. telomeric sequences. roughly 10,000 genes, about twice the number in a typical bacterial genome. a pan genome considerably larger than its core genome.
Of the given option, the most unusual genomic feature of a single-celled eukaryote would be: (4) a pan genome considerably larger than its core genome.
Eukaryotes are the organisms which possess a true nucleus. The eukaryotes also contains several cell organelles like mitochondria, endoplasmic reticulum, Golgi apparatus, lysosomes, centrioles, chloroplast, etc.
Pan genomes are the genetic material which are not present in every strain of an organism. They are unique to a single strain, unlike the core genome which is common in all the strains. The presence of pan genome along with core genome can be seen in the prokaryotic cells but in eukaryotes.
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Mitochondrion definition
Answer:
an organelle found in large numbers in most cells, in which the biochemical processes of respiration and energy production occur. It has a double membrane, the inner layer being folded inward to form layers (cristae).
Explanation: