Cyclization or cytoplasmic streaming is a term that describes the movement of chloroplasts within plant cells.
They push, slide, and dart inside the cell, often catching on the edge of the cell, but sometimes appearing to fill the cell completely with constant movement. This movement is common inside cells and is called cyclonic or cytoplasmic flow.
Chloroplasts migrate in response to varying light intensities. Under low light, chloroplasts cluster in illuminated areas to maximize the rate of light absorption and photosynthesis (storage reaction). In contrast, chloroplasts escape intense light to avoid photodamage (avoidance response).
This idea is motivated by the fact that chloroplasts have their own DNA, separate from plant cells. However, over time, this bacterium becomes dependent on plant cells and vice versa, unable to survive or replicate itself could not proliferate.
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if you buy food in a can that is bulging or spurts liquid, the food is likely to contain toxins produced by a type of bacteria called
if you buy food in a can that is bulging or spurts liquid, the food is likely to contain toxins produced by a type of bacteria called clostridium botulinum.
Under low oxygen levels, the bacterium Clostridium botulinum releases harmful toxins. One of the deadliest poisons ever discovered is a botulinum toxin. In addition to obstructing nerve activity, botulinum toxins can cause respiratory and muscle paralysis. Gram-positive, rod-shaped, anaerobic, spore-forming, motile, and capable of producing the neurotoxin botulinum, Clostridium botulinum is a bacterium.
The majority of bacteria are free-living, omnipresent organisms that frequently just have one biological cell. They make up a sizable group of prokaryotic bacteria. Bacteria, which are among the earliest life forms to exist on Earth and are typically a few micrometres in length, are found in most of its environments. Some bacteria aid in food digestion, eliminate disease-causing cells, and supply the body with vital vitamins.
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which joint is highlighted? which joint is highlighted? sternoclavicular sternal end acromioclavicular acromion
Joint which is highlighted is : acromioclavicular. The acromioclavicular joint is formed by the cap of the shoulder and the collar bone and is held together by strong ligaments.
What is the function of acromioclavicular (AC) joint ?The AC joint is a plane type synovial joint, which allows only gliding movement under normal physiological conditions. It attaches the scapula to the thorax, hence it allows an additional range of motion to the scapula and helps in arm movement such as shoulder abduction and flexion.
AC joint inflammation causes pain on the top of the shoulder and also at the point where the collarbone meets the highest point of the shoulder blade . Pain may spread to the lower part of the side of the neck or ear.
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which cells carry antigen-specific receptors and are stimulated when antigens bind to those receptors?
The surface immunoglobulin that serves as the B cell antigen receptor (BCR) has two functions in B cell activation. First, like the antigen receptor on T cells, it transmits signals directly into the cell when it binds to the antigen receptor. antigen.
B cells have B cell receptors (BCRs) on their surface, which they use to bind to a specific protein. Once B cells bind to this protein, called an antigen, they release antibodies that attach to the antigen and prevent it from harming the body. The antigen receptor on most T cells, the α:β T-cell receptor, is composed of two protein chains, the α T-cell receptor and the β T-cell receptor, and resembles in many respects a single immunoglobulin Fab fragment. T cell receptors are always membrane bound. The membrane-bound immunoglobulin on the surface of B cells serves as the cell's receptor for the antigen and is known as the B cell receptor (BCR). Terminally differentiated B cells, plasma cells, secrete immunoglobulin with the same antigen specificity as antibody.
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check your understanding cyu 12.1 what are the three main areas of investigation (categories of evidence) accompanying a new fossil find?
The three main areas of investigation accompanying a new fossil find are impression fossils, trace fossils, and replacement fossils. Fossils are the remains or traces of ancient life that have been preserved by natural processes.
Impression fossils preserve the prints or impressions of extinct plants or animals. The plant or animal makes an impression when it touches down in mud, silt, or sand. It eventually vanishes, yet the effect endures. The mud, silt, or sand becomes rock and a fossilized impression is left behind. Trace fossils document the behavior of extinct creatures. In the soft mud, silt, or sand, these animals leave their prints or scats, which leave impressions. The soil preserves a sign of the animal when it solidifies into rock, just way impression fossils do. Replacement fossils are exact copies of objects that were once alive, like trees and aquatic life. These living things become imprisoned, perish, and are covered with water that is mineral-rich. The organic components decompose and are replaced by silica, a hard mineral. The minerals fill in the gaps and produce a substitute or duplicate fossil of the live object.
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Imagine a population evolving by genetic drift in which the frequency of the k allele is 0. 2. What is the probability that at some point in the future allele k will drift to a frequency of 1? your answer should be a one decimal place answer.
The k allele's starting frequency is 0.2 0 or 20%. Consequently, there is a 20% chance that allele k's frequency changed to 1.
What effects does genetic drift have on allele frequencies?Summary. Genetic drift differs from natural selection in that it is independent of an allele's favorable or unfavorable consequences. Instead, as random subsets of individuals (and their gametes) are sampled to create the following generation, drift alters allele frequencies entirely by chance.
What does it mean for allele frequencies to change within a population?Allele frequencies in a population are a reflection of genetic diversity. Allele frequencies that fluctuate over time may be a sign of genetic drift or a population that has undergone new mutations.
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What makes radiation dangerous to cells?
A. It is uncontrollable and very warm.
B. It has very high energy waves and can break up DNA.
C. It encourages the building of more cells and overloads the body with new cells.
D. It cools cells down to a temprature where cells cannot reproduce.
Answer:
The answer would have to be B because it can cause damage to the DNA
Which uses of soil are discussed in the video? check all that apply. as a habitat for smokey (the) bear as a way to clean and store air as a place for plants and crops to grow as a material to clean and smooth skin as a building material for homes and buildings as a way to prohibit public access to forests
The discussion of soil's functions includes growing environments for plants and commodities, skin-cleansing and smoothing agents, and construction supplies for houses and other structures.
Successful agriculture depends on healthy soil, which is where we get the nutrients needed to grow crops. Plants like tomatoes that we consume get nutrients from the earth. Animals eat food, which includes nutrients. In the end, good soil is beneficial to us.
Mud frequently includes vitamins, minerals, and trace components that the body can readily absorb. Mud also aids in lowering the appearance of aging, boosting circulation, constricting big pores, removing blackheads, and clearing acne.
The number of different particle sizes in raw soil that is acceptable for earth building should be adequate to protect the material from problems including excessive shrinkage, bulging, cracking, & bond failure. Since clay holds the bigger particles together, soil clay content plays a significant role in earth building.
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Answer:
3, 4, and 5.
Explanation:
a dominant mutation in gene d can cause disease symptoms. gene d encodes an enzyme. the activity of the enzyme in homozygous normal individuals is 100%. the activity of the enzyme in heterozygotes is 25%. this observation is consistent with
The mutation mentioned here is a dominant negative.
Define mutation.
A mutation is a change in our DNA sequence that can be brought on by environmental factors like UV light and cigarette smoke or mistakes made when the DNA is copied.
When a mutant receptor prevents the function of the wild-type (WT) version of the receptor, the condition is known as a dominant-negative (DN) mutation.
A DN mutation generally results in a mutant polypeptide whose activity is reduced in comparison to the co-expressed wild-type protein. Dominant-negative mutations are known as antimorphs, indicating that they have the opposite impact of the gene from which they were produced, according to an early genetic study.
Oncogenes are examples of DN mutations that arise spontaneously. When only one copy of the gene is functioning, haploinsufficiency is frequently used to compare negative dominance . Since it directly affects the phenotypic diversity in this situation, the expression level of this gene is significant. Trisomy 21, which is brought on by errors in the genes producing transcription factors and other key proteins, is a classic example of a condition brought on by haploinsufficiency.
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a group of cels is assayed for dna content immediately following mitosis and is found to have an average of 8 picograms of dna per nucleus. how many picgorams wouldbe found at the end of s and hte end of g2
The cell cycle is split into the- G1 section additionally referred to as the increase section, the S -section additionally referred to as as synthesis section, the G2 section needed would be 24 picograms.
As given withinside the question, the DNA content material right away after mitosis is 12 picograms of DNA in keeping with nucleus.
DNA synthesis takes place withinside the S -section. The G1 section undergoes the increase of the mobileular and additionally prepares for S-section. Thus, at some stage in the G1 section because the DNA replication does now no longer take area the awareness of DNA withinside the cells stays the equal that is 12 picograms.
The G2 section is the section that takes place after S-section. As the DNA receives replicated the awareness of the DNA receives doubled.
Thus, the awareness of DNA withinside the cells on the G2 section could be 24 picograms.
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a. moves water and solutes from the renal tubules into the peritubular capillaries b. is called secretion c. is called reabsorption d. occurs as water and solutes move from the glomerulus to the glomerular capsule.
The first step of urine production occurs as water and solutes move from the glomerulus to the glomerular capsule.
What is Urine Production?
Unwanted compounds are filtered out of the blood by the kidneys, which then eliminate them through urine. Glial filtration, reabsorption, and secretion are the three primary processes that lead to the generation of urine.
The glomerular capsule, also known as Bowman's capsule, surrounds the glomerulus, a network of capillaries. A filtration membrane in the capsule allows water and other solutes to pass from the capillaries into the bloodstream as it passes through the glomerulus.
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evolutionary development of a head and brain containing neural and sensory organs is a process called
Cephalization is the process through which the head and brain, which contain neurological and sensory organs, evolve.
What is Cephalization?The mouth, sense organs, and nerve ganglia get concentrated in the front of an animal over many generations, creating a head area. This is known as cephalization. This is connected to mobility and bilateral symmetry, resulting in a distinct head end for the animal. As a result, three different animal groups—arthropods, cephalopod molluscs, and vertebrates—developed very complex brains.
What is bilateria?The majority of animal phyla belong to the big group known as the Bilateria, which is distinguished by cephalization. These are able to move by contracting their muscles, and their body plans feature a front end that is the first part of the body to be stimulated as the animal moves forward. As a result, many of the body's sense organs, including those that can detect light, chemicals, and gravity, have developed in the front end. Additionally, a group of nerve cells that can process the data from these sense organs frequently exists. In some phyla, this group of nerve cells forms a brain, whereas in others, it forms one or more ganglia.
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A genetic trait might be caused by incomplete dominance if:
A. a gray cat and a black cat produce black kittens.
B. two black cats produce white kittens.
C. a white cat and a black cat produce gray kittens.
D. two white cats produce gray kittens.
the sequence of the coding strand of a dna molecule (that is, the dna strand that contains the codons specifying the protein sequence) is 5'-cggatgctta-3'. what is the sequence of the rna made from this dna?
Transcription of an RNA strand with the sequence "AUUGCGCGAA" from a DNA strand with the sequence "TAACGCCTT" As a result, C is the correct answer.
Transcription is the process by which mRNA is created from DNA in the nucleus of a cell. The nucleus contains all of the enzymes and nucleotides required for the production of mRNA. The messenger RNA (mRNA) is transcribed from DNA The mRNA sequence generated in a cell from DNA is complementary to the leading strand of DNA, with only the thymine residues replaced by uracil residues. Adenine base couples with uracil residues, and thymine base pairs with adenine residues. Cytosine bases couple with guanine bases and vice versa.
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What amino acid sequence is encoded in the partial DNA segment?
Question 2 options:
Serine- Threonine-Tyrosine
Serine-Serine-Tyrosine
Serine-Threonine-Methionine
Serine-Alanine-Methionine
In DNA sequence 3’ T C A T G C A T G 5’ mRNA sequence is 5' A G U A C G U A C 3' and amino acid codes (genetic codon) serine, threonine, and tyrosine.
What is a genetic codon?The genetic codon is the triplet of the mRNA sequence which codes an amino acid sequence in polypepetide chain.
DNA sequence is transcribe into mRNA by the process of transcription and mRNA is translate into amino acid squence by translation.
Therefore, 3’ T C A T G C A T G 5’ encoded amino acid sequence is serine, threonine, and tyrosine.
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Ligase catalyzes a reaction between the 5'-phosphate and the 3'-hydroxyl at the ends of DNA molecules. The enzyme calf intestinal phosphatase catalyzes the removal of the 5'-phosphate from DNA molecules.
What would be the consequence of treating the vector, before ligation, with calf intestinal phosphatase?
A) It would prevent the ends of the plasmids from being ligated.
B) It would prevent the plasmid's DNA from reversing polarity during ligation.
C) It would reverse the polarity of plasmids' DNA
D) It would ligate the ends of the plasmids.
A) It would prevent the ends of the plasmids from being ligated.
Ligases would avoid ligating the ends of the plasmids. The right response is option (A).
Ligases are enzymes that can catalyze the reaction of combining two big molecules by creating a new chemical bond, typically with concurrent hydrolysis of a minor chemical group on one of the bulky molecules or simply linking of two chemicals. The Ligase enzyme's role is to catalyze the removal of phosphate groups from the 5' ends of DNA strands by dephosphorylation. It specifically works to prevent the re-ligation of plasmid DNA that has been linearized using this technique so that additional DNA fragments cannot be ligated into the vector. In cloning, it is especially useful.
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what are the two mechanism by which lymph vessel keep lymph moving the right ddirection towards the cardiovascular system
The mechanism by which lymph vessel keep lymph moving the right ddirection towards the cardiovascular system is (intrinsic pump).
These vessels perform very just like your veins do: They paintings very low pressure, have a chain of valves in them to hold the fluid transferring in a single direction rest, about 1/three of lymph delivery withinside the human decrease extremities outcomes from compression through skeletal muscle contractions (extrinsic pump) and 2/three to energetic pumping (intrinsic pump) of the accumulating vessel network.
Most of the lymphatic vessels have valves like the ones in veins to hold the lymph, that may clot, flowing withinside the one direction (closer to the heart). Lymphatic vessels drain fluid known as lymph from tissues at some point of the frame and go back the fluid to the venous device via accumulating ducts.
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3. using a schematic depiction of the red blood cell cytoskeleton showing the major components, name and describe the all the protein structures and their functions (spectrin, actin, etc.). describe how these proteins are important to maintain the rbc deformability and flexibility in check. make sure to include a picture or a drawing pointing to each specific structure.
The major proteins found in the cytoskeleton of RBCs are as follows:
(A) Ankyrin complex - The ankyrin complex serves as an anchor for the cytoskeleton of red blood cells (RBCs) to the cell membrane. This complex, which is predominantly made up of band 3, protein 4.2, and ankyrin, is formed during the development of RBCs.
Nine band-3-associated complexes' cryo-electron microscopy structures show that protein 4.2 stabilizes the cytoplasmic region of the band 3 dimer. The superhelix-shaped ankyrin, which connects two band 3 dimers in the ankyrin complex, binds to protein 4.2 via ankyrin repeats (ARs) 6–13 and to a different band 3 dimer via ARs 17–20.
(B) Spectrin -The big, cytoskeletal protein known as spectrin has a modular structure made up of and subunits. Spectrin generally comprises 106 consecutive amino acid sequence motifs known as "spectrin repeats.
The integrity and structure of the cell membrane as well as the shape of a cell depend on the presence of spectrin. Additionally, it supports several cell processes include cell adhesion, cell spreading, and the cell cycle. Human disorders include cancer, type 5 spinocerebellar ataxia, hereditary hemolytic anemia, and others are caused by spectrin mutations.
(C) Junctional complex - These are the origins of the junction between the RBC and the outside environment, and from this location, cations and anion exchange that are needed for the cell's regular day-to-day operations may be obtained.
(D) F-actin A thin, membrane-bound F-actin network called the F-actin cortex controls cell shape. The F-actin cortex also creates tension and remodels the cellular periphery via myosin-II contractility.
(E) Tubulin-There are three different types of tubulin. -
(i) Sedimentable tubulin: Sed-tub, a form of tubulin found in the sedimentable fraction ("Sed-tub") of human erythrocytes, is sensitive to the drugs taxol and nocodazole, which alter microtubule assembly and disassembly, and is arranged as a protein network rather than in the typical microtubule form.
(ii) Membrane tubulin - Tubulin interacts with the plasma membrane at several different levels, including as an integral membrane protein, an attachment via palmitoylation, surface binding, and microtubules linked to proteins in the membrane via linker proteins.
(iii) Cytosolic tubulin: A dynamic cytoskeletal structure conserved in all eukaryotic cells, the tubulin heterodimer polymerizes to produce microtubules. Microtubules have critical functions during cytokinesis and interphase in addition to their conserved function throughout cell division (mitosis and meiosis).
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Determine the product of each pair of percentages or fractions.
1. 25% x 25% =
4. ½ x ¾=
2.4 x 4 =
3.75% x 50% =
5.25% x 0% =
6. 50% x 50% =
Answer:
1. 0.0625
2.3 by 8
3.0.375
4.16
5.0
6.0.25
Everyone is exposed regularly to ionizing radiation found in the soil, water, and air and from cosmic rays. In fact, 80% of the ionizing radiation people are exposed to comes from naturally occurring sources. Ionizing radiation can cause double-strand breaks in the DNA. Often, the DNA breaks have missing nucleotides at the broken ends. What type of repair would likely be used, and what would be the result of repairing this type of damage?
A. Nonhomologous end joining would be used and would lead to properly repaired DNA.
B. Direct repair would be used to join the DNA, but errors would still remain.
C. Nonhomologous end joining would be used to join the DNA, but errors would still remain.
D. Direct repair would be used and would lead to properly repaired DNA.
C
The result of repairing this type of damage would be, C. Non-homologous end joining would be used to join the DNA, but errors would still remain.
The double-strand breaks are fixed utilizing, non-homologous end joining (NHEJ), without a homologous sequence.
After the double-strand break removes some nucleotides from the ends, DNA ligase IV ligates the two ends. First, Ku proteins bind to the ends and recruit DNA-PKcs, which then recruit Artemis (a nuclease), which will remove any single-stranded DNA in that region.
Non-homologous end joining would be used to join the DNA, but errors would still remain because NHEJ results in the deletion of a small number of nucleotides. As a result, this is an error-prone repair mechanism.
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Brett learned that his car is better protected from the weather when it has been recently washed and waxed. Which best describes the major group of macromolecules that is protecting his car and how it is performing this task?.
Brett discovered that his car is better protected from the elements when it has recently been washed and waxed. The lipid in the wax coating is the macromolecule that protects his car.
What are lipids?The lipid is a macromolecule composed of carbon and hydrogen that is hydrophobic in nature and does not come into contact with water.
Because the wax is a lipid, it does not like water, and when it is applied to the car, it is protected from water damage.
Brett discovered that when his car has recently been washed and waxed, it is better protected from the elements. The macromolecule that protects his car is the lipid in the wax coating.
Thus, this is the major group of macromolecules that is protecting his car and the way it is performing this task.
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You are a bio-researcher on the planet Tawniwani, and you have been given the task of identifying and classifying the native fauna. Use this dichotomous key to identify Tawniwanian creature t.
Dichotomous keys are used to identify and classify organisms into a taxonomic group according to their morphological traits. In the exposed example, individual T is a Narrowus trispottis.
What is a dichotomous key?
The dichotomous key is a classification system used to identify organisms according to different traits -usually morphological traits-.
This is a simple method since the key provides two options, and the researcher needs to choose one of them according to the organism's features. Once the researcher has chosen one of the options, the key leads to the following description.
The procedure is the same in each step until the name of the taxonomic group is provided.
In the exposed example, we need to identify the organism T (the last one). We know we need to follow 4 steps before reaching our individual's name. So,
1) Does it has a large or small head? It has a small head, so we need to move to step 2.
2) Does it has a narrow or round body? It has a narrow body, so we need to move to step 6.
6) Does it has curly or straigh antennae? It has curly antennae, so we need to move to step 11.
11) Does it has narrow or round eyes? It seems like it has narrow eyes, so it might be Narrowus trispottis.
According to this dichotomous key, the T individual is a Narrowus trispottis.
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please describe one unsolved biological or biomedical problem that you find interesting and explain why
Because these problems are related to health and very fascinating to solve. The problems I mentioned in explanation are very real and need to solve these problem as soon as possible. According to me, these are very helpful if solved.
List of biological unsolved problems
I go over a few of the main awards given for success in the biological sciences. I'll list some of the most important scientific advances made over the past 50 years since the topics are related to unresolved biological mysteries. The Council for the Advancement of Science Writing (CASW) has compiled a list of fifty significant discoveries made between 1960 and 2010.
The ability of a cell to translate genetic code, recombinant DNA,
the eradication of smallpox,
the discovery of HIV,
and human embryonic stem cells, including IPS (Induced Pluripotent Stem Cells), which enables human skin cells to be reprogrammed into stem cells with embryonic characteristics, are just a few examples.
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Photosynthesis !! And animal represent?
what does the left and side and right side mean ? The top and bottom in words of summary? And the evidence to support the meaning thanks:) !
Answer: Left side means that the plant autotrophs from the sunlight which means it get food. On the right side it means that the chloroplast in the plant cell is making photosynthesis. Down side means that the animal cellular respiration is that the animal cell is breaking down the food and making it into energy which sends it to the ATP which is the powerhouse of the cell.
Explanation:
Which type of noncovalent interaction supports the double helix of dna and produces the base pairings a–t and g–c?.
Hydrogen bonding noncovalent interaction supports the double helix of DNA and produces the base pairings A-T and G-C.
The two different types of nucleic acids are as follows:
Deoxyribonucleic acid (DNA)
Ribonucleic acid (RNA)
Both RNA and DNA molecules couple their bases. Adenine, uracil, guanine, and cytosine are the bases found in RNA molecules while guanine, adenine, cytosine, and thymine are found in DNA molecules.
A is always linked with T in a DNA molecule, while G is always coupled with C, and base T is changed to base U in RNA. There is a weak hydrogen connection that can be easily broken between a base pair and the double helix of the DNA molecule.
The complete question is:
Which type of noncovalent interaction supports the double helix of DNA and produces the base pairings A-T and G-C?
a. ion-dipole interactions
b. dipole-dipole forces
c. ion-ion interactions
d. London dispersion forces
e. hydrogen bonding
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with age, the spine stiffens as a result of shrinkage of the intervertebral disc spaces, and the vertebrae become brittle. this increases the risk of
With age, the spine stiffens as a result of shrinkage of the intervertebral disc spaces, and the vertebrae become brittle. This increases the risk of Compression fractures.
What is compression fracture?
When one or more vertebrae are under too much stress, they might collapse and result in a spine compression fracture. Serious spinal compression fractures might impair your quality of life with painful or incapacitating symptoms.
With rest, the use of a brace, and painkillers, the majority of compression fractures resulting from injuries heal in 8 to 10 weeks. However, if surgery was performed, recuperation might take significantly longer.
Therefore, age causes the intervertebral disc gaps to contract, which stiffens the spine and makes the vertebrae more fragile. Compression fractures are now more likely as a result of this.
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at the end of tca cycle, glucose is converted to the final product, co2, and all the energy are released in the form of atp/gtp.
The end products of the TCA (tricarboxylic acid) cycle include 6 NADH, 2 ATP and 2FADH2.
The tricarboxylic acid (TCA) cycle, also known as the Krebs cycle or the citric acid cycle, is a series of eight-step processes, where the acetyl group of acetyl-CoA is oxidized to form two molecules of CO2 and in the process an ATP is produced. High energy reduced compounds, NADH and FADH2 are also produced. Two molecules of acetyl-CoA are produced from each molecule of glucose, so two rounds of the Krebs cycle are required, resulting in four CO2, six NADH, two FADH2 and two ATP. The tricarboxylic acid cycle (TCA cycle) is the second stage of cellular respiration, the three-step process by which living cells break down organic fuel molecules in the presence of oxygen to grow and divide the energy obtained after harvesting. This metabolic process occurs in most plants, animals, fungi and many bacteria. The TCA cycle takes place in the matrix of intracellular structures called mitochondria.
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be able to convert raw experiences into localized brain activations. can many seemingly different experiences be induced by altered activity in a single (but perhaps large) brain region?
Different activities can induce many experiences in a single large brain region.
For example, when we run. We need to move our legs and arms, and coordinate both of them simultaneously. Not only that but eyes also needed to synchronize all of the movement in our body and environment. All of that systems were using part of the human brain named the Cerebellum.
Cerebellum will help our brain and body coordinate and regulate. This is just one example out of many movements and regulations that needed single large brain regions to function.
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this information will be used for the next four questions. wheat kernel color is an additive trait controlled by two genes, gene a and gene b. the a1 and b1 alleles add 1 unit of color to the kernels. the a2 and b2 alleles add 0 units of color to the kernels. what is the best description of the a2 and b2 alleles?
This is the case of complete dominance.
What is complete dominance?
When one allele, or "version," of a gene completely obscures another, complete dominance occurs. Being "dominant" over the trait which is not expressed refers to the trait that is expressed. The majority of organisms are diploid, which means that each gene is received twice, once from each parent. An organism may possess a gene that has undergone a harmful mutation and be able to function since it possesses a healthy copy of the gene due to the protective effect of having two copies of each gene. Due to the fact that most organisms, including you, have two copies of each gene, scientists use the terms "dominant" and "recessive" genes to describe which one manifests as a specific characteristic.
In this the a1 and b1 act as a dominant allele , which add to the color and a2 and b2 are recessive one , which are completely masked by the other one . So it adds 0 unit to color .
Hence , a2 and b2 acts as recessive allele .
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which is more resistant to fatigue, cardiac or skeletal muscle? what is the anatomical basis for this difference and why is it important?
Cardiac muscle cells contain many mitochondria that provide the necessary energy for the cell in the form of adenosine triphosphate (ATP), making them highly resistant to fatigue.
Because cardiac muscle has more mitochondria than skeletal muscle, it is resistant to fatigue. It is up to 35 percent mitochondria, compared to just 1-2 percent in skeletal muscle. Mitochondria are necessary for the generation of ATP, which supplies cells with energy. The rapid, involuntary contraction and relaxation of the heart muscle are vital to pumping blood throughout the cardiovascular system. To achieve this, the structure of the heart muscle has distinct characteristics that allow it to contract in a coordinated manner and resist fatigue. This is mainly because the heart is made of cardiac muscle, which consists of special cells called cardiomyocytes. Unlike other muscle cells in the body, cardiomyocytes are highly resistant to fatigue.
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according to eysenck’s theory, the ascending reticulocortical activating system (aras) is located in what part of the brain?
The ascending reticulocortical activating system (aras) is located within the hypothalamus and brainstem.
What is eysenck's theory?
According to Eysenck's theory of personality, extroverts' cortical arousal at rest is lower compared to that of introverts. Scholars have thus hypothesized that extroverts should benefit from background music in cognitive tasks, whereas introverts' performance should decline with music in the background.
What is the function of the ARAS?
The ascending reticular activating system (ARAS), also known as the extrathoracic control modulatory system or simply the reticular activating system (RAS), is a set of connected nuclei in the brains of vertebrates that is responsible for regulating wakefulness and sleep-wake transitions.
What happens if the RAS is damaged?
Damage to the RAS causes unconsciousness, resulting in not being awake or aware. Along the length of the brainstem, there are midline raphe nuclei and two lateral types of nuclei: the medial group of nuclei and the small group of nuclei.
Thus, ARAS is located within the hypothalamus and brainstem.
To know more about the ARAS:
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