Answer:
The correct answer will be option- Phagocytosis
Explanation:
Phagocytosis or cell eating is a process performed by the living cell in which the cell engulfs or ingests the foreign material.
The engulfed material is usually a macromolecule or large substance which could be either another living cell or the organic compounds or some debris. The engulfed material through phagocytosis process is transported inside the cell through vesicles formed.
Thus, Phagocytosis is the correct answer.
Answer:
Endocytosis
Explanation:
Endocytosis: is a type of active transport that moves or transports particles, such as large molecules, parts of cells, and even whole cells, into a cell.
6. Before direct proof of DNA being the genetic material, several lines of indirect evidence had suggested DNA as the appropriate macromolecule. Which ONE of the following statements supports the hypothesis that DNA is the genetic material?
a. RNA is more stable than DNA or protein.
b. Molecular composition of DNA is variable in different cells of an organism, whereas the molecular composition of RNA and protein does not change in different cells of an organism.
c. DNA consists of only four bases while proteins are comprised of twenty different amino acids.
d. protein content is most abundant in cells just prior to division.
e. Gametes have 1/2 the amount of DNA as somatic cells.
Answer:
e. Gametes have 1/2 the amount of DNA as somatic cells.
Explanation:
a. RNA is more stable than DNA or protein
-the reverese is the case, DNA has double helix structure as a result of phosphodiester bonds in the sugar-phosphate backbone plus 2 or 3 Hydrogen bonds between the nitrogenous bases.
DNA is more stable
b. Molecular composition of DNA is variable in different cells of an organism, whereas the molecular composition of RNA and protein does not change in different cells of an organism.
with the exception of gametes which contain half the amount of DNA necessary, each Cells have equal amount of DNA when compared to variable amount in cells RNA and proteins due to the different degree of expression and cell differentiation
c. DNA consists of only four bases while proteins are comprised of twenty different aminoacids.
This evidence lacks basis of why DNA is the genetic material.
d. Protein content is most abundant in cells just prior to division.
This evidence lacks basis of why DNA stands as the genetic material in individual organisms
e. Gametes have 1/2 the amount of DNA as somatic cells.
-this Argument is firmly supported since half of parent DNA is donated to its offspring forming the total genome of a somatic cell
Saccharomyces cerevisiae is a diploid yeast species that can reproduce either sexually or asexually. An experiment was performed to induce mitotically dividing S. cerevisiae cells in G2 to undergo meiosis. Which of the following best describes the steps these cells will follow to form gametes?
A. The first division will result in crossing over between homologous chromosomes, and the second division will reduce the original number of chromosomes by half in the daughter cells.
B. The first division will reduce the number of chromosomes by half for each daughter cell, and the second division will result in each daughter cell having one-fourth of the original number of chromosomes.
C. The first division will move single chromatids to each daughter cell, and the second division will double the number of chromosomes in each daughter cell.
D. The first division will reduce the number of chromosomes by half for each daughter cell, and the second division will move single chromatids to each daughter cell.
The statement that best describes the steps these cells will follow to form gametes is "the first division will reduce the number of chromosomes by half for each daughter cell, and the second division will move single chromatids to each daughter cell"
MEIOSIS:
Meiosis is the process by which a single cell produces four daughter cells with a reduced number of chromosomes (by half). Meiosis occurs in two step division process namely: meiosis I and meiosis II. In meiosis I, homologous chromosomes are separated while in meiosis II, sister chromatids are separated. Meiosis I reduces the chromosome number by half i.e. from diploid (2n) to haploid (n). Therefore, in the experiment that was performed to induce mitotically dividing S. cerevisiae cells in G2 to undergo meiosis, the first division will reduce the number of chromosomes by half for each daughter cell, and the second division will move single chromatids to each daughter cell.Learn more at: https://brainly.com/question/12327654?referrer=searchResults
Meiosis is a reduction division in which number of chromosomes in the daughter cells are halved. In mitosis, the number of chromosomes in the daughter and parent cell are similar after cell division. The statement which describes the correct sequence is:
The first division will reduce the number of chromosomes by half for each daughter cell, and the second division will move single chromatids to each daughter cell.The yeasts are the unicellular microorganisms that can reproduce sexually or asexually. During the sexual reproduction, the number of chromosomes in the in the daughter cells are halved. Some of the features of meiosis are:
Meiosis in yeasts produces four haploid daughter cells, known as gametes. Meiosis takes place in two steps, meiosis I and meiosis II. In meiosis I, the homologous chromosomes are separated, whereas, in the meiosis II separation of sister chromatids occur. Meiosis I is the reduction division in which diploid cell produces haploid cells. Thus, the experiment performed on yeast to induce mitosis will result in the cells undergoing meiosis during G1 phase. The first division will lead to reduction in the chromosome numbers by half and the second division will move single chromatids to each daughter cell.Therefore, option D is correct.
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which of these is not a basic function of a cell
obtaining energy
storing energy
destroying energy
releasing energy
Answer: destroying energy
Explanation:
The cell is the basic unit of life. It consists of several components such as
Nucleus,
Mitochondria: it helps in obtaining energy through lipid oxidation within its layer
Cytosol: It helps in releasing energy from glucose breakdown (glycolysis)
Vacuoles, endoplasmic reticulum also help in storing energy in cells of adipose tissues.
But, NONE of the cell components helps in destroying energy, since energy is needed and usually well-regulated.
All of the following can reduce crop water use, except for which one? Group of answer choices Applying irrigation water at times of day when evaporation is low. Leaving the soil surface bare to improve infiltration. Selecting crop varieties that are well-suited to the local climate. Using drip irrigation techniques to apply water only where plants can use it.
Answer:
Leaving the soil surface bare to improve infiltration.
Explanation:
All of the following can reduce crop water use, except Leaving the soil surface bare to improve infiltration.
Leaving the soil bare will do no good to soil's water retention capacity rather it would decrease significantly. This happen because of water runoffs as there would no crops to hold water and the top fertile layer of the soil will runoff along with water.
Answer:
Explanation:
Leaving the soil surface bare for infiltration. When the soil surface is bare it exposes the it's layers to direct sunlight which absorbs all the water content present in the soil and thus is harmful for the soil and crop
In the datura plant, purple flower color is controlled by a dominant allele P. White flowers are found in plants homozygous for the recessive allele p. Suppose that a purple-flowered datura plant with an unknown genotype is self-fertilized and that its progeny are 28 purple-flowered plants and 10 white-flowered plants.
Part A
Use the results of the self-fertilization to determine the genotype of the original purple-flowered plant.
a. Pp
b. PP
c. pp
Part B
If one of the purple-flowered progeny plants is selected at random and self-fertilized, what is the probability it will breed true?
a. 1/3
b. 1/4
c. 3/4
d. 2/3
Answer:
Part A: Pp
Part B: 1/3
Explanation:
A: The purple flower color is regulated by dominant allele "P". Since self-fertilization of the purple-flowered plant with unknown genotype gives both purple and white-flowered progeny in almost 3:1 ratio, the parent plant was heterozygous dominant for the trait. Its genotype is "Pp".
Segregation of recessive and dominant alleles during gamete formation leads to the production of two types of gametes with either "P" or "p" alleles. The random fusion of these gametes produces progeny in following phenotype ratio= 3 purple: 1 white.
B. Out of the 3 purple-flowered progeny, 1 is homozygous dominant (PP). Therefore, the probability of the purple-flowered progeny to breed true is 1/3.
Final answer:
The genotype of the original purple-flowered datura plant is determined to be heterozygous (Pp) based on the ratios of purple to white flowered progeny. The probability that a randomly selected purple-flowered progeny will breed true for the purple color is 1/4, meaning there is a 25% chance it is homozygous dominant (PP).
Explanation:
Part A: Genotype Determination
To determine the genotype of the original purple-flowered datura plant, we can look at the progeny from its self-fertilization. Given that the purple flower color is dominant and represented as allele P and the white color is recessive and represented as allele p, we can infer the genotype of the parent plant based on the ratio of purple to white flowered plants among its progeny. The progeny consists of 28 purple-flowered plants and 10 white-flowered plants. This suggests that the parent plant is not a homozygous dominant (PP) because we expect all progeny to have purple flowers in that scenario. Since white flowers (pp) are a recessive trait, they can only appear in the offspring if the parent carries the recessive allele. Therefore, the parent plant must be heterozygous Pp.
Part B: Probability of True Breeding
The probability that a randomly selected purple-flowered progeny plant will breed true (be homozygous dominant PP) can be inferred from the parent's genotype. Since the parent plant is heterozygous Pp, its possible gametes are P or p. With self-fertilization, there is a 1 in 4 chance (or 25%) of getting PP, a 1 in 4 chance of pp, and a 2 in 4 chance of Pp. The probability that the purple progeny plant selected is a homozygote (PP) is the same as finding a homozygous dominant offspring in the self-fertilization, which is 1/4 or option 'b'. The other two-thirds will be heterozygous purple (Pp).
Toemas’s syndrome is a autosomal dominant disease, homozygous lethal, seen at a frequency of 1 in 10,000 cats. Felines with this disease have a very strong desire to have their backs scratched. Assume the locus is in Hardy Weinberg Equilibrium.
A male cat with Toemas's syndrome and an unaffected female cat have a newborn kitten. What is the probability that the kitten is male AND he has Toemas’s syndrome? Assume mating is at random.
(Hint: recall your work on matings for two independent loci!)
Answer: 50% or 25% according to the genotype of the male cat.
Explanation:
The female cat is unaffected, and since this is an autosomal dominant diease, it means this cat does not have any affected alleles. Thereby, its genotype is aa. This is because dominant alleles show their effect even if the organisms only has one copy of the allele. The male cat is affected with this syndrome so its genotype is either AA or Aa. For this disease to manifest itself, only one affected allele is needed. Although both alleles can be affected so the individual can be homozygous dominant or heterozygous.
To find this we have to do a punnett square. Here, we use the gametes produced by each individual. Gametes are sex cells, egg or sperm, which only have one allele of each gene.
Assuming that the cross is between aa and AA, the gametes produced by "aa" are "a", and the gametes produced by "AA" are "A" So we are having a cross between an "a" gamete and a "A" gamete. 100% of the offspring will be Aa so it is a heterozygous, which will develope this syndrome. And, males have one Y chromosome and one X chromosomes, thereby the chances of having a male kitten is 50%. Then, to conclude, there is a 50% chances of having a male kitten with this syndrome.
And, assuming that the cross is between aa and Aa, the gametes produced by "Aa" are "A" but also "a" So we are habing a cross between an "a" gamete and "A" or "a" gamete (See picture) In this example, there is a 50% chances of having a kitten with the syndrome, because only one genotype produced (Aa) has the affected allele. And, as we said before, since there is a 50% chances of having a male kitten, we can said that there is a 25% chances of having an affected male. Because to calculate both probabilities so that they occur simultaneously, it is necessary to multiply them. That is, 0.5 x 0.5 = 0.25 x 100 = 25%.
Which of the following best describes the change in kdr genotype frequencies over time in A. gambiae?a)From pre-2006 to post-2006, the frequency of the r/r genotype increased slightly while the frequencies of +/+ and +/r genotypes decreased dramatically.b)From pre-2006 to post-2006, the frequency of the r/r genotype increased dramatically while the frequencies of +/+ and +/r genotypes decreased dramatically.c)From pre-2006 to post-2006, the frequency of the r/r genotype increased dramatically while the frequencies of +/+ and +/r genotypes remained relatively constant.d)From pre-2006 to post-2006, there was little change to the r/r, +/+, and +/r genotype frequencies.
Answer:
b)From pre-2006 to post-2006, the frequency of the r/r genotype increased dramatically while the frequencies of +/+ and +/r genotypes decreased dramatically.
Final answer:
The frequency of the resistant r/r genotype in Anopheles gambiae mosquitoes increased dramatically post-2006, while the susceptible +/+ and +/r genotypes decreased dramatically, indicating evolution due to insecticide selection pressure.
Explanation:
Population genetics examines the changes in allele frequencies and genotype frequencies in a population over time. According to the provided reference, the change in kdr genotype frequencies in Anopheles gambiae mosquitoes indicates that the frequency of the resistant allele (denoted as 'r') and the corresponding homozygous genotype (r/r) increased dramatically post-2006, which suggests that the use of anti-vector interventions may have selected for this resistance allele at a higher rate. On the contrary, the frequencies of the susceptible homozygous genotype (+/+) and heterozygous genotype (+/r) decreased dramatically over this time period.
The correct description of these changes would most likely be that from pre-2006 to post-2006, the frequency of the r/r genotype increased dramatically while the frequencies of +/+ and +/r genotypes decreased dramatically. This reflects a population undergoing evolution due to selection pressure from the use of insecticides, as alleles that confer resistance to these chemicals are favored and become more common within the population.
Most consumers have a wide variety of choices in terms of the food products they choose to buy. These decisions can be influenced by factors like food advertising or the labels on the products themselves.Choose the correct statements about marketing and labeling.Select all that apply.__Organic foods are free of all pesticides.__All free-range animals have unlimited access to the outdoors.__Most food advertising is for processed foods and packaged foods.__Organic foods have higher levels of nutrients than their conventional counterparts.__The term "natural" on food labels has no standardized definition.
Not all organic foods are free from pesticides and 'free-range' does not necessarily mean unlimited outdoor access. Most food advertising is for processed and packaged foods, organic foods do not always have more nutrients and the term 'natural' has no standardized definition in food labeling.
Explanation:It's true that many consumer decisions related to food purchases are influenced by marketing and labeling. However, not all the statements listed are accurate. Organic foods are not necessarily free of all pesticides. Sometimes, organic farmers use naturally-derived pesticides over synthetic ones but this doesn't mean they are pesticide-free. Similarly, while free-range animals should have access to the outdoors, it doesn't necessarily mean that they have unlimited access.
Furthermore, it's a fact that most food advertising is indeed aimed at processed and packaged foods. This could be because they have a longer shelf-life compared to fresh produce, making them more appealing to grocery stores. As for nutrient levels, organic foods do not always have higher levels of nutrients than their conventional counterparts. The nutrient content can vary greatly depending on a variety of factors, including how the food is grown and harvested.
Finally, the term 'natural' on food labels indeed has no standardized definition. Therefore, it can be used loosely by companies to market their products.
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Which statement describes double fertilization in an angiosperm?
a. Two egg cells are fertilized within each ovule.
b. A sperm nucleus fuses with an egg cell and a sperm nucleus fuses with polar nuclei.
c. Two sperm are required for fertilization of one egg cell.
d. A flower can engage in both self-pollination and cross pollination.
e. One sperm fertilizes the egg while two polar nuclei fuse with a second egg.
Answer:b. A sperm nucleus fuses with an egg cell and a sperm nucleus fuses with polar nuclei.
Explanation:
This mode of fertlization occurs only in angioseprms .One of the sperms forms 2n as zygote.
The second sperm fuses with the two polar nuclei to form 3n as endosperm.
The importance of these are:
1. Restoration of diploid condition with the fusion of haploid male and female gametes.
2.it makes plants to recieve stimulus based on which ovary develops into a fruit and shows thst it is ovules that develops into seeds.
Answer:
B: A sperm nucleus fuses with an egg cell and a sperm nucleus fuses with polar nuclei.
Explanation:
In double fertilization in angiosperms, one sperm fertilizes the egg to form the 2n zygote, while the other sperm fuses with two polar nuclei to form the 3n endosperm. After fertilization, embryonic development begins
In German cockroaches, the curved wing allele (cv) is recessive to the normal allele wing (cv ). Bill, who is raising cockroaches in his dorm room, finds that the frequency of the allele for curved wings in his cockroach population is 0.6. In the apartment of his friend Joe, the frequency of the allele for curved wings is 0.2. One day Joe visits Bill in his dorm room and several cockroaches jump out of Joes' hair and join the population in Bill's room. Bill estimates that 10% of the cockroaches in his dorm room now consist of individual roaches that jumped out of Joe's hair. What will be the frequency of roaches with curved wings among cockroaches in Bill's room?
The new frequency of curved-wing allele in Bill's cockroach population after incorporating cockroaches from Joe's population would be 0.56, assuming no other changes or selective pressures.
Explanation:To determine the frequency of the curved wing allele after Joe's roaches joined the population in Bill's room, we must first determine the combined frequency of the curved wing allele from both populations. Considering that the allele frequency in Joe's roaches was 0.2 and it made up 10% of the new combined population, and Bill's roaches had a frequency of 0.6 and composed 90% of the population, we can calculate a new overall frequency as follows: (0.6 * 0.9) + (0.2 * 0.1) = 0.54 + 0.02 = 0.56.
So, assuming no other changes or selective pressures, this would be the new frequency of the curved wing allele in Bill's roach population after Joe's roaches joined.
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Final answer:
The new frequency of the curved wing allele in Bill's cockroach population after incorporating roaches from Joe's population is 0.56.
Explanation:
To calculate the new frequency of the curved wing allele (cv) in Bill’s cockroach population after the introduction of cockroaches from Joe’s population, we need to account for the change due to the roaches from Joe’s hair.
Initially, Bill’s population had a frequency of 0.6 for the curved wing allele. Joe’s had a frequency of 0.2. After 10% of Bill's population is replaced by Joe's cockroaches, the new frequency (pnew) of the curved wing allele in Bill’s population can be calculated as:
pnew = (0.9 × Bill’s original frequency) + (0.1 × Joe’s frequency)
pnew = (0.9 × 0.6) + (0.1 × 0.2)
pnew = 0.54 + 0.02
pnew = 0.56
Therefore, the new frequency of cockroaches with curved wings among cockroaches in Bill's room will be 0.56.
What is hepcidin?
(A) A substance produced in the spleen that stores iron
(B) An intestinal mucosa protein that assists in iron turnover
(C) A factor in meats that enhances iron absorption
(D) A substance in legumes that interferes with iron absorption
(E) A liver-derived hormone that helps regulate iron absorption and transport
Answer:
The answer is E
Explanation:
A liver-derived hormone that helps regulate iron absorption and transport.
The data from a replicated experiment are very different from the data obtained during the initial experiment. Which statements identify possible reasons for the difference in the data? Check all that apply
The initial experiment was not a valid experiment.
The replicated experiment was performed incorrectly.
The replicated experiment used a different laboratory.
The initial experiment involved more trials and data.
The replicated experiment changed the variables being tested.
The initial experiment was not a valid experiment is the statement which identifies possible reasons for the difference in the data.
Explanation:
The replicated experiment however is crucial but doesn't satisfy the condition of justifying the validity of a scientific theory or hypothesis. However, the initial or repeated experiment are more satisfying in producing logical result from the experiment. It involves repeated methods of a particular experiment with more and more trials and observations of more data.
However, the replicate experiments are individual experiments of a specific hypothesis which fails to experiment are individual experiments of a specific hypothesis which fails to produce a logical result.
Answer:
The initial experiment was not a valid experiment.
The replicated experiment was performed incorrectly.
The initial experiment involved more trials and data.
The replicated experiment changed the variables being tested.
Explanation:
A scientific experiment is performed to test if the predicated hypothesis can be proved or not.
The scientific experiment involves the repetition of the experiment by the same experimenter and the replication of the experiment which could be performed by the same experimenter or another experimenter to test if the results of the initial experiment are valid or not.
In the given question, the results of the initial experiment and the replicated experiment are different which could be due to various reasons:
The initial experiment was not valid - if the initial experiment performed is not valid. The replicated experiment was performed incorrectly- the replication procedure differs from the initial experiment or there could be some error while experimenting. The initial experiment involved more trials and data- the initial experiments could have involved more replicas, trials, and data. The replicated experiment changed the variables being tested - the variables of this two experiment could differ.In humans, hemophilia is caused by an X-linked recessive gene. A woman who is a nonbleeder - that is, she does not display the blood-clotting irregularities associated with hemophilia - had a father who was a hemophiliac.
She marries a nonbleeder, and they plan to have children.
Calculate the probability of hemophilia in the female and male offspring.
Answer:
one normal girl
One normal boy
One carrier girl
One colour blind boy
Explanation:
Haemophilia is a sex linked feature as it is transmitted with the chromosomes determining sex.
In humans,the male has XY and the female has XX.the Y chromosome is usually genetically empty.so as mall received his Y chromosomes from his father,he cannot inherit his father's sex linked traits .but women can as they receive and X chromosomes from their fathers.so a cross between a carrier woman Cc and a normal man C result in;
XX--CC
XX--Cc
XY--C
XY--c
The visible colored portion of the eye is the:
a. cornea.b. pupil.c. sclera.d. iris.
Answer:
D. IRIS
Explanation:
Generally in humans and also in most mammals and birds, the iris is a very small circular structure in the eye, responsible for controlling the diameter and size of the pupil and also with the amount of light reaching the retina.
finallly eye color is also known to be defined by that of the iris
How does latitude affect radiation?
Answer:
When the sun's rays strike Earth's surface near the equator, the incoming solar radiation is more direct (nearly perpendicular or closer to a 90˚ angle). ... At higher latitudes, the angle of solar radiation is smaller, causing energy to be spread over a larger area of the surface and cooler temperatures.
Explanation:
Answer:
At higher latitudes, the angle of solar radiation is smaller
Explanation:
Which statements describe telomeres and the actions of telomerase?
a) Telomerase activity is turned off in most human cells, causing the telomeres to gradually shorten as the individual ages.
b) Telomerase contains a G‑rich template sequence that adds a C‑rich DNA sequence to the lagging strand of the chromosome.
c) Telomerase consists of an RNA template and a protein component that adds complementary nucleotides to the 3′ end of DNA.
d) Inappropriate activation of telomerase can result in cellular immortality, one of the cellular changes implicated in the development of cancer.
e)A telomere forms a loop with a section of the complementary DNA strand, protecting the chromosome from degradation by endonucleases.
Final answer:
Correct statements about telomeres and telomerase include telomerase activity being generally off in most human cells (a), telomerase containing an RNA template and a protein component adding to the 3' DNA end (c), and inappropriate activation of telomerase contributing to cellular immortality and cancer (d).
Explanation:
Which statements describe telomeres and the actions of telomerase? The statements that accurately describe telomeres and the actions of telomerase are as follows:
a) Telomerase activity is turned off in most human cells, causing the telomeres to gradually shorten as the individual ages.
c) Telomerase consists of an RNA template and a protein component that adds complementary nucleotides to the 3′ end of DNA.
d) Inappropriate activation of telomerase can result in cellular immortality, one of the cellular changes implicated in the development of cancer.
Statement b) is incorrect because telomerase adds a G-rich sequence to the telomere, not a C-rich sequence. Statement e) describes the formation of a T-loop by the telomere but does not pertain directly to how telomerase functions.
What are the conditions that lead to a "beer gut" due to the excess consumption of alcohol? NADH produced from the metabolism of ethanol stimulates the citric acid cycle for glucose-derived acetyl CoA. Excess ethanol metabolism leads to an accumulation of NADH that inhibits fatty acid metabolism. The processing of acetate in the liver becomes inefficient leading to a pH imbalance in liver cells, reducing enzyme efficiency in general. NADH inhibits ketone body formation, stimulating glucose rather than fatty acid metabolism. NADH stimulates citric acid cycle enzymes that stimulates glucose-derived acetyl CoA metabolism.
Answer: Excess ethanol metabolism leads to an accumulation of NADH that inhibits fatty acid metabolism.
Explanation:
Fatty acid metabolism is often activated by limited or absence of NADH, however ethanol (the main constituent of most alcoholic drinks) on metabolism yields several molecules of NADH which rather stimulates belly/abdominal fat production often referred to as "beer gut".
A person has entered a hunger strike. After 60 days of starvation, this person is on the edge of dying. What is likely to be the cause of death?a. too many ketone bodies in the blood, which causes ketoacidosisb. lack of oxygen in the body for oxidative metabolismc. shut down of gluconeogenesis in the liverd. the breakdown of essential proteins of the brain and hearte. exhaustion of fat from adipose tissue
Answer: option D - the breakdown of essential proteins of the brain and heart
Explanation:
During starvation (food deprivation), the body cells begins to utilize the glycogen reserves in the liver and muscle. Then, it switches to the fats (stored in the adipose tissues).
If starvation persists, the body turns to the proteins for energy derivation. At this stage, the person's DYING STATE is usually visible because the muscles of the body shrinks greatly.
Note that DEATH set in when essential proteins of the BRAIN and HEART are metabolized to produce energy due to the vital functions both organs do in the overall body processes.
What is the function of the lacZ gene?
a. This gene encodes an enzyme, galactoside permease, which transports lactose into the cell.
b. This gene encodes an enzyme, b-galactosidase, that cleaves lactose into two glucose molecules.
c. This gene encodes an enzyme, b-galactosidase, which cleaves lactose into glucose and galactose.
d. This gene encodes the repressor of the lac operon.
Answer:
the answer is c
Explanation:
The lacZ gene encodes an enzyme called β-galactosidase, which is responsible for splitting lactose (a disaccharide) into readily usable glucose and galactose (monosaccharides). The lacY gene encodes a membrane protein called lactose permease, which is a transmembrane "pump" that allows the cell to import lactose.
The lacZ gene encodes the enzyme β-galactosidase, which breaks down lactose into glucose and galactose, playing a crucial role in lactose metabolism in bacteria such as E. coli.
Explanation:The function of the lacZ gene is to encode an enzyme called β-galactosidase, which is responsible for cleaving the disaccharide lactose into its monosaccharide components, glucose and galactose. This process is an essential step in the metabolism of lactose by bacteria such as E. coli. When lactose is present in the environment, E. coli can use the lac operon system to express the lacZ gene, along with other genes necessary for the utilization of lactose as a carbon source, such as the lacY gene for lactose permease and the lacA gene for transacetylase.
When a sudden change in the environment, such as a flood or fire, reduces the size of a population, the survivors' collective gene pool will be only a limited representation of what was present before the disaster. This phenomenon is called: a. The bottleneck effect. b. Founder effect. c. Hardy-Weinberg effect. d. Culling effect. e. Genetic load.
Answer: option A - bottleneck effect
Explanation:
Whenever sudden change caused by human or natural disasters occurs in the environment leading to the reduction of organisms or biodiversity present to a lower size, such condition is referred to as BOTTLENECK EFFECT.
What are the functions of the three major forms of RNA (ribosomal RNA, messenger RNA, and transfer RNA)?
Answer:
Ribosomal RNA: Structural part of ribosomes
Messenger RNA: Carry genetic information from DNA to proteins
Transfer RNA (tRNA): Transport amino acids to protein synthesizing complex.
Explanation:
Ribosomes are made up of ribosomal RNA (rRNA) and proteins. The catalytic activity for the formation of peptide bonds between amino acids during protein synthesis resides the RNA of ribosomes.
Messenger RNA (mRNA) is formed by the process of transcription during which the nucleotide sequence of the template DNA strand is copied into that of the RNA. The mRNA serves as a template for protein synthesis. The nucleotide sequence of mRNA is read in the form of genetic codes to specify the amino acid sequence of a protein. In this way, the genetic information stored in DNA is carried to the proteins.
During the process of protein synthesis, tRNAs carry amino acids to the mRNA-ribosome complex so that the amino acids are incorporated into the polypeptide. For the purpose, there is a tRNA with a specific anticodon sequence for a particular amino acid.
Your friend is a pioneer in ES cell research. In her research, she uses an ES cell line that originated from an inbred strain of laboratory mice called FG426. She has just figured out methods that allow her to grow an entire liver from an ES cell and has successfully grown 10 livers. She demonstrates that the newly grown livers are functional by successfully transplanting one of the new livers into a FG426 laboratory mouse. You are particularly excited about this, because you have a sick pet mouse, Squeaky. You are very attached to Squeaky, as you found him when you were out camping in New Hampshire. Unfortunately, Squeaky has developed liver disease and will not live much longer without a liver transplant. After you see your friend on TV talking about her new method for growing mouse livers, you immediately grab your cell phone to ask her whether Squeaky could have one of the newly grown livers. Just as you are about to dial your friend, you remember something you learned in cell biology and realize that instead, you should ask your friend about possibly using therapeutic cloning for Squeaky’s benefit.
A. Why do you think that one of the newly grown livers may not work in Squeaky?
B.Explain how using iPS cells could solve this problem.
Answer:
Explanation:
a)Organ transplantation requires that the donor organism and recipient be genetically close so that the graft or transplant will not be attacked by the immune system of the recipient leading to rejection and damage. Squeaky is likely to be made up of a different genetic configuration compared to laboratory inbred FG426 mouse
b) ips (induced pluripotent stem cell) on the other hand can benefit squeaky since the cells are somatic cells such as B cells, Keratinocytes, neuronal progenitors cells, kidney and muscles gotten from the donor that are reprogrammed by reactivating silent genes through fusing of another different cell such as ES (embryonic stem cell) and introduction of some transcriptional factors such oct4, sox2,kf4, and k-myc leading to transcriptional activity and DNA methylation. This induced pluripotent stem cells can be grown into organ that can be transplanted to the recipient who was initially the donor of the reprogrammed somatic cells. Because it is from the host, the transplanted organ is not likely to trigger immune response compare to those grown from ES from other bred.
When the antibiotic valinomycin is added to actively respiring mitochondria, several things happen: the yield of ATP decreases, the rate of O2 consumption increases, heat is released, and the pH gradient across the inner mitochondrial membrane increases. Explain these observations by listing the causal order of events that occur beginning with the addition of valinomycin to the respiring mitochondria and ending with the release of heat. Note: some events listed do not occur and should not be placed Valinomycin added The rate of ATP synthesis decreases The rate of electron transfer and oxygen consumption increases The pH gradient across the The valinomycin-K complex moves K ion out of the mitochondrial matrix. The electrical potential across the The rate of ATP hydrolysis increases The electrical potential across the mitochondrial membrane decreases. Valinomycin binds K" ion. The valinomycin-K' complex moves into the mitochondrial matrix. The pH t across the Heat released
Valinomycin binds to K+ ions, disrupting the potassium gradient and causing a decrease in ATP production. Increased efforts to maintain energy result in enhanced electron transport and oxygen consumption, along with heat generation.
When valinomycin is added to actively respiring mitochondria, it complexes with potassium ions (K+) and facilitates their transfer across the mitochondrial membrane. This disrupts the osmotic pressure and affects the proton gradient. This sequence of events begins with valinomycin binding to K+ ions on the surface of the mitochondria and forming the K+-valinomycin complex. The complex becomes highly soluble in the nonpolar interior of the membrane, allowing it to cross the membrane. Once inside, K+ is released, and the valinomycin is free to return and bind to another K+ ion, continually disrupting the normal potassium gradient. This action increases the permeability of the membrane to K+, leading to the dissipation of the electrical potential across the membrane. This reduction in electrical potential affects the proton gradient, which in turn impairs the ATP synthase activity, leading to a decrease in ATP production. Without the efficient generation of ATP, the rate of electron transport and oxygen consumption increases as the mitochondria try to maintain energy production, while the dysfunctional gradient causes the proton pumps to work harder. The extra work results in the generation of heat. Meanwhile, the pH gradient across the inner mitochondrial membrane increases due to the altered balance between proton influx and efflux.
A RNA differs from DNA in all EXCEPT which of the following ways?
A. the presence of uracil
B. the 5'-3' orientation of the polynucleotide strand
C. the sugar molecule
D. the number of different functions performed
Answer: B. the 5'-3' orientation of the polynucleotide strand .
The complimentary pairing of DNA molecules ensures 5' 3' and 3'[ 5 ' arrangement for correct pairing of purines and pyrimidine (Adenine E with thymine and cytosine with guanine) in opposite direction. .
RNA only contains five prime and three prime only, but DNA contains both 5'3' and 3'5'.
RNA differs from DNA in the presence of uracil, the sugar molecule, and its various functions. However, both RNA and DNA share the 5'-3' orientation of the polynucleotide strand.
Explanation:The RNA differs from DNA in several ways, including the presence of uracil, the type of sugar molecule it contains, and its various functions. However, the 5'-3' orientation of the polynucleotide strand is a feature that RNA shares with DNA. Both RNA and DNA have this orientation, which describes the direction that the molecules are read and synthesized in cellular processes such as DNA replication and transcription.
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People with full blown sickle-cell disease will experience harmful effects such as, red blood cells break down, clump, and clog blood vessels. Broken cells can accumulate in the spleen. This can lead to many symptoms such as physical weakness, heart failure, pain, and brain damage. Having so many symptoms can be explained by __________.
a. the polygenic nature of sickle-cell disease
b. side effects of the drugs used to treat sickle-cell disease
c. a bacterial infection interacting with the sickle-cell allele
d. the sickle-cell allele can impact many different body systems
Answer :a. the polygenic nature of sickle-cell disease
Explanation:
SS is a genetic disorder in which more than two genes control a single character. Contrary to single gene to a trait. It exhibit an abnormal clinical heterogeneous traits for Mendel inheritance with multiple factors exerting influence on an individual disease outcome. Therefore multiple complications arises with symptoms
Answer:d. the sickle-cell allele can impact many different body systems
Explanation:sickle cell anaemia is the shortage of red blood cells.red bloods cells functions to carry oxygen through out the body aided by the haemoglobin.when however a person has sickle cell anaemia,his red blood cells become abnormal.they are no longer flexible and round ,they become stiff and sickle-shaped.when this changes in the red blood cell occurs,it is no longer flexible to pass through the blood vessels,causing the blockage of the vessels and the red blood cells break apart easily ,causing its shortage in the body.as body organs need oxygen to survive, people with sickle cell anaemia tends to have organ failures,pain crises , infections etc.
Under which of the following conditions is a on most likely no evolve abimodaldistribution? o selection favors muniple distinct trait vaues, and similar individuals tend to mate with each other O Traits are strongly corelated and a low carrying capacity keeps the population size small O Environmental conditions change rapidly, and alow muation rate limits the establishment of new variants Selection is weak, and individuals produce large numbers of omspring each generation. the lab, which of the following factors made it more Check al apply: Selectivity in choosing mates The avaiability of smaller seeds Geogaphic barriers separating subpopul Long term weather pattems submit questions D e B a S Web and Windows
Answer:
The correct answer is "selection favors multiple distinct trait values, and similar individuals tend to mate with each other".
Explanation:
A population with a bimodal distribution are groups of organisms with two major traits or "modes", with practically equal amounts of individuals with these two modes. This type of distributions indicate that the population is not homogenous and that more than one trait is favored in the given circumstances. A bimodal distribution is most likely to evolve when selection favors multiple distinct trait values, and similar individuals tend to mate with each other. In this case natural selection favors more than one value, and due to the individuals with one value tend to mate to each other, only two major traits are favored in the population.
Final answer:
Disruptive selection and nonrandom mating are the conditions most likely to result in a bimodal distribution of traits within a population. These conditions can lead to distinct, adapted phenotypes and facilitate speciation.
Explanation:
A bimodal distribution in a population's traits is most likely to evolve when two conditions are met: selection favors multiple distinct trait values, and there is nonrandom mating, where similar individuals preferentially mate with each other. This scenario describes disruptive selection. Disruptive selection can lead to the formation of two distinct phenotypes within a population, each adapted to different environmental niches or conditions. Gene flow and random mating are factors that can prevent disruptive selection from leading to divergent populations; thus, when geographical barriers or mate selectivity are present, they facilitate the establishment of a bimodal distribution.
Any object struck at its natural frequency will vibrate violently. This is known as resonance. Applications of this include earthquakes knocking down building and
A) rainbows created in air.
B) microwaves created in ovens.
C) light being created by the sun.
D) sound being created in music instruments.
Answer: option D) sound being created in music instruments
Explanation:
Resonance occurs when an object close in contact to a vibrating body begins to vibrate at the same frequency of the vibrating body.
Usually each object has a THRESHOLD frequency which must be equaled or exceeded before it is set into vibration.
Therefore, this is the PRINCIPLE behind MELODY i.e how sound is being created in music instruments.
What is the chance that the 4th child from the couple indicated by the arrow will have a girl who suffers from the disease?
Explanation:
Tho i can see no arrow but there is probability of 75% that a fourth child suffers the disease of the parent
If the hydrostatic pressure of blood flowing through the glomerular capillaries and forcing fluid through the leaky endothelium was 60mmHg, the pressure caused by the lack of proteins in the fluid inside Bowman's capsule was 32 mmHg, and the pressure caused by the inability of the capsule to expand in volume was 18mm Hg, what would the net filtration pressure (in mmHg) be?
Answer:
The net filtration pressure is 10 mmHg.
Explanation:
for calculating net filtration we will plus the pressure inside boman's capsule with pressure caused by inability of capsule expansion and then subtract them from total pressure in leaky epithelium.
net filtration pressure= total blood pressure in leaky epithelium - total blood pressure in capsule
as we know that total blood pressure in capsule is 32 + 18 = 50 mmHg
therefore
net filtration pressure= 60 - 50
net filtration pressure= 10 mmHg
In Drosophila, an autosomal gene determines the shape of the hair, with B giving straight and b giving bent hairs. On another autosome, there is a gene of which a dominant allele I inhibits hair formation so that the fly is hairless (i has no known phenotypic effect). a. If a straight-haired fly from a pure line is crossed with a fly from a pure-breeding hairless line known to be an inhibited bent genotype, what will the genotypes and phenotypes of the
F1
and the
F2
be? b. What cross would give the ratio 4 hairless : 3 straight : 1 bent?
Answer:
a. F1 genotype : IiBb F1 phenotype : Hairless
F2 genotype and phenotype :
I_B_ (hairless), iiB_ (straight), iibb (bent)
b. IiBb X iiBb
Explanation:
a. Fly 1 : pure breeding straight haired : iiBB
Fly 2 : pure breeding hairless with bent genotype : IIbb
Fly 1 X Fly 2 : iiBB X IIbb = IiBb (F1)
All the offspring will be hairless since there is one dominant I allele which will inhibit hair production regardless of the type of allele of other gene.
Two F1 flies will be crossed to obtain F2 flies. IiBb X IiBb :
I_B_ : hairless = 9
I_bb : hairless = 3
iiB_ : straight hair = 3
iibb : bent hair = 1
Hairless : straight : bent will be in 12 : 3 : 1 ratio.
b. The offspring of this cross :
hairless : I_ _ _
straight : iiB_
bent : iibb
There is a bent offspring which has both the recessive alleles of both the genes. Hence it must have obtained the two alleles from the two parents. So their genotype is _i_b and _i_b.
Half of the offspring are hairless as given by the ratio. This is only possible if the cross is between Ii and ii fly:
I i
i Ii ii
i Ii ii
So the genotype is Ii_b and ii_b.
The remaining hairy flies are in 3:1 ratio of straight to bent. This is only possible if the cross is between Bb and Bb fly:
B b
B BB Bb
b Bb bb
So the final genotype of the flies is IiBb and iiBb.