A mutation to the enzyme kyneuranine aminotransferase (EC# 2.6.1.7; PDB ID 2qlr) to allow it to accept and catalyze a chemical reaction with a unique substrate.
The unique substrate must have the ability to bind with the kyneuranine aminotransferase enzyme. The effects of the mutation on the native km, kcat, and kcat/km should also be taken into consideration. The substrate must bind to the enzyme’s active site in order for the enzyme to catalyze a reaction. The active site is where the substrate binds to the enzyme and where the reaction takes place. The mutation of the enzyme can affect the structure of the active site, thus altering the substrate’s binding affinity and the reaction kinetics of the enzyme.
The mutation can also alter the native km, kcat, and kcat/km of the enzyme, as the mutation affects the structure of the active site and thus the catalytic rate of the enzyme. The km and kcat values can be determined by the kinetic analysis of the enzyme-substrate complex, which can be done in vitro or in silico. Additionally, the kcat/km ratio is the efficiency of the enzyme-substrate complex. All of these values can be used to determine the effects of the mutation on the enzyme.
References:
1. Michel, N. B., & McKee, T. C. (2004). Enzyme Kinetics: A Modern Approach. Elsevier Science.
2. Huang, Y., & Reynolds, S. E. (2007). Protein–Ligand Interaction: Principles, Methods, and Applications. The Journal of Physical Chemistry B, 111(25), 7122–7138. doi:10.1021/jp070006f
Learn more about enzyme kyneuranine : https://brainly.com/question/14577353
#SPJ11
please someone fill this picture out according to the following. i want a PICTURE NOT AN EXPLANATION OF WHAT A DICHOTOMOUS KEY IS!!!!!
- Can it produce its own food?
Yes: Go to 2
No: Go to 3
- Is the organism unicellular?
Yes: It is a yeast
No: It is a hydra
- Does the organism have hair?
Yes: It is a cat
No: Go to 4
- Is the organism unicellular?
Yes: It is a bacteria
No: The organism cannot be identified using this key.
The Dichotomous Key is a tool that scientists use to determine the classification of living things in the natural world.
What is the Dichotomous Key?Scientists use the Dichotomous Key to categorize all living things in the natural world, including fungi, animals, and trees. Typically, a flowchart is used to show it, with two possibilities on each branch to make the identification process simpler.
The nested, connected, and branched dichotomous keys are the three common varieties of dichotomous keys.
For instance, a dichotomous key in tree identification would inquire as to whether the tree has leaves or needles. After that, if the tree has leaves, the key sends the user down one list of questions; if it has needles, an other list of questions is presented.
Learn more about dichotomous key on:
https://brainly.com/question/1726339
#SPJ1
are
the proportions of each type of zygote, consistent with Mendels law
of segregation, true or false?
The given statement "The proportions of each type of zygote, consistent with Mendels law" True. Each gamete caries only one allele.
The proportions of each type of zygote are consistent with Mendel's law of segregation. This law states that during gamete formation, the alleles for each gene segregate from each other so that each gamete carries only one allele for each gene, each allele has an equal chance of being expressed
This results in a 1:2:1 ratio of homozygous dominant: heterozygous: homozygous recessive zygotes in a cross between two heterozygous individuals. This ratio is consistent with the proportions of each type of zygote observed in Mendel's experiments and has been confirmed through countless genetic studies.
Learn more about Mendel's law of segregation at:
https://brainly.com/question/23067535
#SPJ11
Researchers have discovered that cockroaches collected from the Upper East Side and Upper West Side are in fact genetically distinct populations (populations that are genetically very different from one another but are the still the same species). Assuming both populations came from a single cockroach population that landed in NYC 300 years ago, explain, in a few sentences, how these 2 different populations may have developed. Use terminology and mechanisms we discussed in Lectures 1+2. Propose 1 experiment that researchers could perform to test that these populations are still the same species?
It is likely that the two cockroach populations from the Upper East Side and Upper West Side developed into genetically distinct populations through a process called genetic drift. Genetic drift occurs when a small population experiences random changes in allele frequencies due to chance events.
In this case, the original cockroach population likely split into two smaller populations, each experiencing different chance events that led to different allele frequencies and thus, genetic differences between the two populations.
Another possible mechanism for the development of genetically distinct populations is natural selection. It is possible that the two populations experienced different environmental pressures, leading to the selection of different traits and thus, genetic differences between the two populations.
To test whether these populations are still the same species, researchers could perform a crossbreeding experiment. If the two populations are still the same species, they should be able to produce viable offspring. If they are unable to produce viable offspring, it is likely that they have developed into two separate species.
Learn more about test the populations: https://brainly.com/question/29885712
#SPJ11
Eye color in fruit flies is a sex-linked trait. Red eye color is dominant over
white eye color. A heterozygous, red-eyed female is crossed with a red-eyed
male.
In their offspring, what is the expected phenotypic ratio of red-eyed females
to white-eyed females to red-eyed males to white-eyed males?
• A. 1:2:1:0
• B. 0:2:1:1
• C. 2:0:1:1
• D. 2:1:0:1
Answer: C
Explanation: I did a punnent square.
Blonde hair (bb) is a recessive trait, and brown hair (Bb) or (BB) is dominant. If both parents have brown hair, what must be true if one of their children has blonde hair?
A. Both parents must be hybrid, with regard to hair color (Bb)
B. Both parents have two brown hair genes (BB)
C. One parent must have two blonde hair genes (bb), while the other has two brown hair genes (BB)
D. One parent must have two genes for blonde hair (bb), and the other must be hybrid for hair color (Bb)
The given statement A. Both parents must be hybrid, with regard to hair color (Bb) is true.
If both parents have brown hair, and one of their children has blonde hair, this means that both parents must carry the recessive gene for blonde hair (b). If one parent had two brown hair genes (BB), then all of their children would have brown hair. Similarly, if one parent had two blonde hair genes (bb) and the other had two brown hair genes (BB), all of their children would have brown hair, because the dominant gene would always be expressed.
Therefore, the only way for one of their children to have blonde hair is if both parents are hybrid for hair color (Bb), meaning they each carry one dominant gene for brown hair and one recessive gene for blonde hair. In this case, there is a 25% chance that their child will inherit two recessive genes for blonde hair (bb) and have blonde hair.
Here is a Punnett square to illustrate this:
| | B | b |
|---|---|---|
| B | BB | Bb |
| b | Bb | bb |
As you can see, there is a 25% chance that their child will inherit two recessive genes for blonde hair (bb) and have blonde hair.
Option B is incorrect because both parents having two dominant brown hair genes (BB) would mean that all of their children would also have brown hair, as the dominant allele would mask the recessive blonde hair gene. Therefore, it would not be possible for one of their children to have blonde hair.
Option C is incorrect because if one parent had two recessive blonde hair genes (bb) and the other parent had two dominant brown hair genes (BB), then all of their children would inherit one copy of each gene and be heterozygous for hair color (Bb). None of their children would have blonde hair unless both parents were heterozygous carriers of the blonde hair gene (Bb).
Option D is incorrect because if one parent had two recessive blonde hair genes (bb), then all of their children would inherit one copy of the recessive blonde hair gene. Therefore, if the other parent was a hybrid (Bb), half of their children would inherit the recessive blonde hair gene, but the other half would inherit the dominant brown hair gene. So, it would not be guaranteed that one of their children would have blonde hair.
To know more about recessive genes click here:
https://brainly.com/question/15481938
#SPJ11
Why can’t we go directly from DNA extraction to analysis?
10. Age, Cholesterol, and Sodium A medical researcher found a significant relationship among a person's age
x 1
, cholesterol level
x 2
, sodium level of the blood
x 3
, and systolic blood pressure
y
. The regression equation is
y ′
=97.7+0.691x 1
+219x 2
−299x 3
. Predict the systolic blood pressure of a person who is 35 years old and has a cholesterol level of 194 milligrams per deciliter
(mg/dl)
and a sodium blood level of 142 milliequivalents per liter
(mEq/l)
.
The systolic blood pressure of a person who is 35 years old and has a cholesterol level of 194 milligrams per deciliter (mg/dl) and a sodium blood level of 142 milliequivalents per liter (mEq/l) is 159.8 mmHg.
To predict the systolic blood pressure of a person who is 35 years old and has a cholesterol level of 194 milligrams per deciliter (mg/dl) and a sodium blood level of 142 milliequivalents per liter (mEq/l), we need to substitute the given values into the regression equation.The regression equation is y′=97.7+0.691x1+219x2−299x3y′=97.7+0.691x1+219x2−299x3
Substituting the values for x1, x2, and x3, we get:y′=97.7+0.691(35)+219(194)−299(142)y′=159.8 mmHg
Therefore, the systolic blood pressure of a person who is 35 years old and has a cholesterol level of 194 milligrams per deciliter (mg/dl) and a sodium blood level of 142 milliequivalents per liter (mEq/l) is 159.8 mmHg.
More on systolic blood pressure is here: https://brainly.com/question/28492028
#SPJ11
If a strand of DNA has a sequence TAGGATC, what would be the complementary sequence? a. CGAAGAT b. TACCGGA c. CGAAGTC d. ATCCTAG.
In DNA, the complementary base pairs are A and T, and C and G. The correct answer would be option d. ATCCTAG.
This means that when a strand of DNA has the sequence TAGGATC, the complementary sequence will have the bases A, T, C, and G in the positions opposite to where they are in the original sequence.
So, the complementary sequence would be:
T --> A
A --> T
G --> C
G --> C
A --> T
T --> A
C --> G
Therefore, the complementary sequence would be ATCCTAG, which is option d.
Here you can learn more about complementary base pairs
https://brainly.com/question/21591871#
#SPJ11
The ______ ________ ________ is when
excited electrons lose
their energy in a series of reactions that capture that energy
necessary to "keep life living."
The electron transport chain is when excited electrons lose their energy in a series of reactions that capture that energy necessary to "keep life living."
This process occurs in the mitochondria of cells and is a crucial part of cellular respiration, as it generates ATP (adenosine triphosphate), which is the energy currency of the cell. The electron transport chain is the final step in the process of converting the energy stored in food molecules into usable energy for the cell.
The electron transport chain is a series of protein complexes that transfer electrons through a membrane within the mitochondria of cells. The net result of this process is the production of energy in the form of ATP, which can then be used to power various cellular activities. The electron transport chain begins with the oxidation of NADH and FADH2 molecules, which then donate electrons to a series of electron carriers.
Learn more about electron transport chain
https://brainly.com/question/18686654
#SPJ11
Why did scientists suspect that DNA does not code for proteins directly? a) DNA cannot bind to proteins directly. b) Viruses have RNA genomes. c) In prokaryotic cells, DNA and proteins are not found together. d) In eukaryotic cells, transcription and translation occur in different compartments. e) The four bases in DNA could not code for the 20 amino acids.
Since "the four bases in DNA could not code for the 20 amino acids," scientists assume that DNA does not directly code for proteins. Thus, Option E is correct.
In the early days of molecular biology, scientists were puzzled by how the genetic information encoded in DNA could be used to produce the vast array of proteins found in living organisms. The discovery of the genetic code, which showed how groups of three bases in DNA (codons) correspond to specific amino acids, provided a key insight into this process.
However, it also raised a new question: with only four different bases (A, C, G, and T), how could DNA possibly code for the 20 different amino acids that make up proteins? Scientists soon realized that the genetic code must be more complex than a simple one-to-one correspondence between bases and amino acids, and that additional factors, such as RNA intermediaries and post-translational modifications, are necessary to account for the diversity of proteins in living organisms.
Learn more about DNA https://brainly.com/question/16099437
#SPJ11
sickle cell disease is a blood cell disorder. It causes an abnormality in the blood cells shape. The cell assumes the shape of a crescent. This also inhibits the cells, ability to carry oxygen leading to painful symptoms, and even death the person inherits the alleles for SED from their parent a person who is heterozygous for the sickle cell allele often shows no symptoms of the disease and is considered a carrier. A person who is homozygous recessive for the sickle cell allele will exhibit signs and symptoms of sickle cell anemia if 9% of the population exhibit signs and symptoms of the disease what percent of the population is a carrier.
The percentage of the population that is a carrier of sickle cell disease is 91%. This is calculated by subtracting the 9% of the population that exhibit signs and symptoms of the disease from the total population (100%).
What is disease?Disease is an abnormal condition that affects the body of an organism and can cause discomfort, dysfunction or even death. It is often caused by pathogens such as viruses, bacteria, fungi, parasites, or environmental factors such as radiation or chemicals. It can be caused by genetic predisposition or lifestyle choices, such as smoking or poor diet. Symptoms of a disease depend on the type and can range from mild to severe.
This leaves 91% of the population that is a carrier of the disease but does not show any symptoms. This is due to the fact that a person who is heterozygous for the sickle cell allele (has one sickle cell allele and one normal allele) typically does not show any symptoms of the disease.
To learn more about disease
https://brainly.com/question/14083398
#SPJ1
Which one of the following will enhance the solubility of calcium and phosphorus in a parenteral nutrition formulation and decrease the chance for precipitation? a. Increase the concentration of lipid emulsion in the formulation
b. Increase formulation temperature
c. Increase the Amino acid concentration
d. Using Calcium chloride instead of Ca gluconate.
Using Calcium chloride instead of Ca gluconate will enhance the solubility of calcium and phosphorus in a parenteral nutrition formulation and decrease the chance for precipitation. Option d.
Calcium chloride has a higher solubility than calcium gluconate, which means that it will dissolve more easily in the formulation and will be less likely to precipitate out of solution. This is important because precipitation can cause blockages in the IV line and can also lead to other complications.
In contrast, increasing the concentration of lipid emulsion, increasing the formulation temperature, and increasing the amino acid concentration will not have a significant effect on the solubility of calcium and phosphorus.
Therefore, the best option to enhance the solubility of these two minerals and decrease the chance for precipitation is to use calcium chloride instead of calcium gluconate. Option d.
Learn more about Solubility at https://brainly.com/question/28170449
#SPJ11
The strongest determinant of an irreversible reaction is:
the free energy product/substrate
concentration enzyme/substrate
concentration the presence of ATP
The strongest determinant of an irreversible reaction is concentration enzyme/substrate. An irreversible reaction is a chemical reaction that proceeds in one direction and cannot return to the starting materials.
These reactions require a large amount of energy to occur due to their high activation energy.
The concentration of enzyme and substrate is the strongest determinant of an irreversible reaction, as it plays a crucial role in determining the rate of enzyme-catalyzed reactions.
Enzymes can break down substrates irreversibly, resulting in the formation of a product that cannot revert back to the starting materials.
Thus, the concentration of enzymes and substrates is a critical factor that has a significant impact on the outcome of an irreversible reaction.
Learn more about irreversible reaction.
https://brainly.com/question/19085986
#SPJ11
Draw an example of antiport, the concentration of the particles on either side of the plasma membrane, and arrows as to where particles are going to go. Don’t forget to draw how the particle can restore its concentration gradient
Antiport is a type of active transport that involves the movement of two different particles in opposite directions across the plasma membrane.
Outside the Cell Inside the Cell
+------------------+ +------------------+
| Na+ | | K+ |
| (High) | | (Low) |
+------------------+ +------------------+
| |
| |
v v
+------------------+ +------------------+
| K+ | | Na+ |
| (Low) | | (High) |
+------------------+ +------------------+
In the above diagram, we see an example of antiport
In this example, the antiporter protein simultaneously transports one sodium ion (Na+) out of the cell while transporting one potassium ion (K+) into the cell. This process is driven by the concentration gradient of these ions, which is higher for Na+ outside the cell and higher for K+ inside the cell. The arrows show the direction of ion movement.
To restore its concentration gradient, the cell may use the sodium-potassium pump, a type of active transport mechanism that moves three Na+ ions out of the cell while moving two K+ ions into the cell, using ATP as an energy source. This process helps to maintain the correct ion concentrations inside and outside the cell.
For more question on plasma membrane click on
https://brainly.com/question/19360972
#SPJ11
Attached earlobes is a recessive trait, free earlobes is dominant. A newlywed couple know they are each heterorgous for the attached earlobe gene (Aa), each displaying beautiful, free flowing earlobes. They are planning on having 4 children and want to know the probability of having 3 children with free earlobes. What is the probability of having 3 children with free ear lobes? a. [4!/3!x1!] . (3/4)^3(1/4)^1
b. [4!/3!x1!] . (3/4)^1(1/4)^3
c. 60%
d. 27/256
e. 3x(3/4)^1(1/4)^3
The probability of having 3 children with free ear lobes is option a. [4!/3!x1!] . (3/4)^3(1/4)^1.
Calculate the probabilityTo find the probability of having 3 children with free earlobes, we can use the binomial probability formula:
P(x) = [n!/(x!(n-x)!)] . (p)^x(q)^(n-x)
Where:
- n is the number of trials (in this case, the number of children)
- x is the number of successes (in this case, the number of children with free earlobes)
- p is the probability of success (in this case, the probability of a child having free earlobes)
- q is the probability of failure (in this case, the probability of a child having attached earlobes)
Plugging in the given values, we get:
P(3) = [4!/(3!(4-3)!)] . (3/4)^3(1/4)^(4-3)
Simplifying the factorials, we get:
P(3) = [4!/3!x1!] . (3/4)^3(1/4)^1
Therefore, the probability of having 3 children with free earlobes is [4!/3!x1!] . (3/4)^3(1/4)^1, which is option a.
Learn more about probability at
https://brainly.com/question/9793303
#SPJ11
In performing the sustained maximal inspiration maneuver (SMI) during incentive spirometry, the patient should be instructed to hold the breath for how long?
During the sustained maximal inspiration (SMI) maneuver, the patient should be instructed to hold their breath for 3-5 seconds. This allows for maximum expansion of the lungs and helps to improve lung function. It is important for the patient to take slow, deep breaths and to avoid rapid, shallow breathing.
The sustained maximal inspiration (SMI) maneuver is often used in conjunction with incentive spirometry to help prevent respiratory complications following surgery or in patients with respiratory illnesses.
Here is a step-by-step explanation of how to perform the SMI maneuver:
1. Sit or stand upright with good posture.
2. Take a slow, deep breath in through your nose.
3. Hold your breath for 3-5 seconds.
4. Exhale slowly through your mouth.
5. Repeat the process several times as instructed by your healthcare provider.
6. Use an incentive spirometer if directed by your healthcare provider to help monitor your breathing and lung function.
Here you can learn more about sustained maximal inspiration (SMI) maneuver
https://brainly.com/question/28139522#
#SPJ11
If a ball is thrown upward at e4 teet per second from a height of 4 feet, the height of the ball can be modeled by S=4 + 64t – 16t^2 feet, where is the number of seconds after the ball is thrown. How long after the ball is thrown is the height 64 feet?
The ball reaches a height of 64 feet either 1.5 seconds or 2.5 seconds after it is thrown.
The height of the ball can be modeled by the equation S=4 + 64t – 16t^2 feet, where t is the number of seconds after the ball is thrown. We want to find the time when the height is 64 feet, so we can plug in S=64 and solve for t.
64=4 + 64t – 16t^2
60=64t – 16t^2
0=16t^2 – 64t + 60
0=4t^2 – 16t + 15
Using the quadratic formula, we can find the values of t that make this equation true:
t=(-b±√(b^2-4ac))/(2a)
t=(-(-16)±√((-16)^2-4(4)(15)))/(2(4))
t=(16±√(256-240))/8
t=(16±√16)/8
t=(16±4)/8
t=20/8 or t=12/8
t=2.5 or t=1.5
So the ball reaches a height of 64 feet either 1.5 seconds or 2.5 seconds after it is thrown.
To know more about the height of the ball click here:
https://brainly.com/question/8982997
#SPJ11
1st question pls quick
In a large range herd of black cattle it is observed that 5 out of every 100 cattle are red. Assuming that the black coat color gene (B) is completely dominant to red (b), give answers to the following:
Frequency of the B gene in this population of cattle? Frequency of the b gene?
The rancher prefers the black coat color and selects against red. She eliminates all the red bulls in the herd, leaving only black bulls for breeding. What will be the frequencies of the following in the next generation after this selection pressure is applied? Assume that she does not apply selection based on color among the cows; the only selection against color is among the bulls used for breeding.
Genotypic frequencies? BB______ Bb______ bb______
Phenotypic frequencies? Black______ Red______
Gene frequencies? B______ b______
The frequency of the B gene in this population of cattle is 0.95, while the frequency of the b gene is 0.05. This is because 5 out of every 100 cattle are red, meaning that 95 out of every 100 cattle are black. Since the black coat color gene (B) is completely dominant to red (b), this means that the frequency of the B gene is 0.95 and the frequency of the b gene is 0.05.
After the rancher eliminates all the red bulls in the herd, the frequencies of the genotypes and phenotypes will change. The genotypic frequencies will be BB: 0.9025, Bb: 0.095, and bb: 0.0025. The phenotypic frequencies will be Black: 0.9975 and Red: 0.0025. The gene frequencies will be B: 0.95 and b: 0.05.
These frequencies are calculated using the Hardy-Weinberg equation, which states that p^2 + 2pq + q^2 = 1, where p is the frequency of the dominant allele, q is the frequency of the recessive allele, p^2 is the frequency of the homozygous dominant genotype, 2pq is the frequency of the heterozygous genotype, and q^2 is the frequency of the homozygous recessive genotype. By plugging in the frequencies of the B and b genes (0.95 and 0.05, respectively), we can calculate the frequencies of the genotypes and phenotypes in the next generation.
For such more questions on Genotypic frequencies:
brainly.com/question/19865120
#SPJ11
WILL GIVE BRAINLIST TO BEST ANSWER
A When considering two traits, independent assortment means that you need to consider 4 possible gametes.
Finish filling in the possible gametes of each parent.
Answer:
Gametes of Parent one (not already there):
Gs and gs
Gametes of Parent two:
gS and gS and gs and gs
Hope this helps!
Review your answer to the question on page 1 about where the energy in each of the food groups found in pizza comes from. Revise your answer to this question as necessary, then describe the path of energy, starting with the sun, for each food group.
Food provides us with energy, and that energy comes from the sun! Photosynthesis is the process by which plants turn water and carbon dioxide into useful carbohydrates using energy from the sun. These plants might then be consumed by bugs, which might then be consumed by animals, which might then be consumed by larger creatures.
How does energy travel from the sun to you?Radiation carried by electromagnetic waves travels from the sun to Earth. Visible light and infrared light make up the majority of the energy that travels through the upper atmosphere and reaches Earth's surface. This light is primarily in the visible spectrum.
Where in the food chain is the sun?The sun is the source of all energy for plants, which converts sunlight into energy through photosynthetic processes. Herbivores subsequently consume these plants to obtain energy. The sunlight is transferred from the sun to the plant to the herbivore to the carnivore, which is then consumed by the carnivores.
To know more about the food chain visit:
https://brainly.com/question/30764162
#SPJ1
Select all the mechanisms that help regulate the final amount of
protein produced in a cell
-mRNA degradation
-protein degradation
-multiple ribosomes translating a single mRNA
-multiple RNA polymeras
The mechanisms that help regulate the final amount of protein produced in a cell are mRNA degradation, protein degradation, and multiple ribosomes translating a single mRNA.
mRNA degradation helps regulate the final amount of protein produced in a cell by breaking down mRNA molecules after they have been used to produce proteins. This prevents the mRNA from being used to produce more proteins than are needed.
Protein degradation helps regulate the final amount of protein produced in a cell by breaking down excess proteins. This prevents the cell from having too many proteins, which can be harmful.
Multiple ribosomes translating a single mRNA helps regulate the final amount of protein produced in a cell by allowing multiple ribosomes to translate a single mRNA molecule at the same time. This increases the efficiency of protein production and helps ensure that the cell has enough proteins.
Multiple RNA polymerase is not a mechanism that helps regulate the final amount of protein produced in a cell. RNA polymerases are enzymes that create mRNA molecules from DNA templates. While they are important for protein production, they do not directly regulate the final amount of protein produced in a cell.
Learn more about mRNA degradation here: https://brainly.com/question/16012106.
#SPJ11
Please explain and cite references if possible:
1. Explain why stool specimen must not be frozen nor placed in incubators for testing in the lab
Stool specimens should not be frozen nor placed in incubators for testing in the lab because both freezing and incubation can alter the composition of the sample and impact the accuracy of the test results.
Freezing can damage the cells in the stool, making it difficult to identify pathogens, while incubation can promote the growth of bacteria and alter the pH of the sample, leading to false positive or false negative results.
Therefore, it is important to collect and transport the stool sample to the laboratory promptly at the appropriate temperature, following the specific instructions provided by the laboratory.
References:
Forbes, B. A., Sahm, D. F., & Weissfeld, A. S. (2007). Bailey & Scott's diagnostic microbiology. Mosby/Elsevier.
Winn, W. C., Allen, S., Janda, W., Koneman, E. W., Procop, G., Schreckenberger, P., & Woods, G. (2006). Koneman's color atlas and textbook of diagnostic microbiology. Lippincott Williams & Wilkins.
For more questions like Stool specimens click the link below:
https://brainly.com/question/28258725
#SPJ11
True or False: E. coli has pre-mRNA processing such as intron
splicing occurring during transcription? please explain
The given statement E. coli has pre-mRNA processing such as intron splicing occurring during transcription is True because during transcription, introns are removed from the pre-mRNA and the remaining exons are spliced together to form the mature mRNA.
E. coli has pre-mRNA processing such as intron splicing occurring during transcription. This process is known as co-transcriptional splicing and is a common feature of eukaryotic cells.
During transcription, introns are removed from the pre-mRNA and the remaining exons are spliced together to form the mature mRNA.
This process is important for the proper expression of genes and the production of functional proteins. Without intron splicing, the mRNA would contain unnecessary and potentially harmful sequences that could interfere with protein synthesis. Therefore the given statement is true.
For such more question on mRNA:
https://brainly.com/question/24885193
#SPJ11
Genetic geneology sites are becoming very popular. Recently a
geneology site was used by the police to identify a candidate for a
cold case serial killer. Explain how geneology can be a powerful
tool
Genetic genealogy sites are a powerful tool because they can be used to identify genetic relationships between individuals.
This can be helpful in identifying potential suspects or relatives in criminal investigations. Additionally, genetic genealogy can be used to uncover familial connections that may not have been previously known. By comparing the DNA of an individual to the DNA of others in the genealogy database, connections can be made and relationships can be established.
This can help investigators solve cold cases and identify potential suspects. In the case of the cold case serial killer, the police were able to use genetic genealogy to identify a candidate for the crime by comparing the DNA of the suspect to the DNA of others in the database. This allowed them to establish a familial connection and potentially solve the case.
To learn more about genetic, click here:
https://brainly.com/question/12985618
#SPJ11
How can an extinct species be an ancestor to a living species?
An extinct species can be an ancestor to a living species if the living species has evolved from the extinct species through a process of genetic and environmental changes over time.
What is Extinct Species?
An extinct species is a type of organism that no longer exists on Earth. Extinction occurs when a species dies out completely, with no surviving individuals remaining. Extinction can be caused by a variety of factors, including changes in the environment, competition with other species, and human activities such as hunting, habitat destruction, and pollution.
An extinct species can be an ancestor to a living species through the process of evolution. Evolution is the gradual process by which species change over time in response to changes in their environment, genetic mutations, and other factors.
All living species have evolved from earlier, extinct species, as evidenced by the fossil record. Fossils are the remains or traces of organisms that lived in the past, and they provide evidence of how species have changed over time.
Learn more about Extinct Species from given link
https://brainly.com/question/1027555
#SPJ1
Earth is able to maintain relatively stable temperatures even with the large
amount of solar heat energy sent. (8 points)
A. What are four factors that contribute to Earth's stable temperatures? (4
points)
B. How does each factor affect Earth's temperature? (4 points)
A. The four factors that contribute to Earth's stable temperatures are:
The greenhouse effectThe carbon cycleThe water cycleThe albedo effectHow each of these factors affects Earth's temperature:The greenhouse effect: Earth's atmosphere contains gases like carbon dioxide and water vapor, which trap some of the heat energy from the sun and prevent it from escaping into space. This helps to keep Earth's temperatures within a relatively stable range.
The carbon cycle: Carbon is cycled between the atmosphere, oceans, land, and living organisms. This cycle helps to regulate the amount of carbon dioxide in the atmosphere, which is a key factor in the greenhouse effect. When carbon is absorbed by plants and other organisms, it reduces the amount of carbon dioxide in the atmosphere, which can help to regulate temperatures.
The water cycle: Water is constantly cycling between the atmosphere, oceans, and land. This helps to regulate Earth's temperatures by moving heat energy around the planet. For example, when water evaporates from the surface of the oceans, it takes heat energy with it, which helps to cool the oceans and transfer heat energy to the atmosphere.
The albedo effect: The amount of sunlight that is reflected back into space by Earth's surface can have a significant impact on temperatures. Bright surfaces, like snow and ice, reflect more sunlight than dark surfaces, like forests and oceans. When there is more snow and ice on the planet, it reflects more sunlight and helps to cool the planet.
Learn more about Earth at:
https://brainly.com/question/15205710
#SPJ1
Answer the question please
The equation of photosynthesis is; 6CO2 + 6H2O → C6H12O6 + 6O2.
How does photosynthesis affect the presence of oxygen on earth?Photosynthesis plays a critical role in the presence of oxygen on Earth. Photosynthesis is the process by which green plants and some other organisms use sunlight to synthesize foods with the help of carbon dioxide and water.
During this process, oxygen is released as a byproduct, which contributes to the oxygen levels in the Earth's atmosphere.
The oxygen produced by photosynthesis is essential for the survival of many organisms, including humans, who rely on oxygen for respiration.
Learn more about photosynthesis:https://brainly.com/question/29764662
#SPJ1
What is the characteristic type that can be used to classify
Fungi mold into two major group?
Group of answer choices
Nutrition
Hyphae
Cell wall
Mycelium
Hyphae is the characteristic type that can be used to classify fungi mold into two major groups.
What are fungi?Fungi are a diverse group of heterotrophic organisms that include yeasts, molds, and mushrooms. The classification of fungi has been the subject of much debate, with scientists disagreeing on how best to classify them into groups.
The morphology of filamentous fungi is characterized by a branching network of hyphae, which is the characteristic type that can be used to classify fungi mold into two major groups.
In conclusion, the correct answer is ''Hyphae''
See more about fungi at https://brainly.com/question/10878050.
#SPJ11
What molecule is used to present epitope from the pathogen to
mark an infected cell for removal from its tissue?
a.
Class III MHC
b.
Class II MHC
c.
Class I MHC
d.
CD8
e.
CD4
The molecule that is used to present epitope from the pathogen to mark an infected cell for removal from its tissue is Class I MHC.
Thus, the correct option is C.
Class I MHC molecules are found on the surface of all nucleated cells and are used to present endogenous antigens, such as those from viruses or intracellular bacteria, to CD8+ T cells. These T cells can then recognize and eliminate the infected cells.
Class II MHC molecules, on the other hand, are found on antigen-presenting cells and are used to present exogenous antigens to CD4+ T cells. Class III MHC molecules are involved in the complement system and do not present antigens. CD8 and CD4 are types of T cells, not molecules involved in antigen presentation.
For more information about Class I MHC refer to the link: https://brainly.com/question/28326297
#SPJ11