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lara31 [8.8K]
3 years ago
11

N the origin of the eukaryotes, endosymbiosis in the origin of the eukaryotes, endosymbiosis most likely began with a heterotrop

hic endosymbiont entering the cell as undigested prey or as an internal parasite. most likely began with the endosymbiont entering the host cell through the endomembrane system. describes the engulfing of a photosynthetic bacterium that ultimately gave rise to mitochondria. is thought to explain the origin of the nucleus.
Biology
1 answer:
masya89 [10]3 years ago
8 0
These are the choices for this question:

<span>(1) Endosymbiosis most likely began with a heterotrophic endosymbiont entering the cell as undigested prey or as an internal parasite.
(2) Most likely began with the endosymbiont entering the host cell through the endomembrane system
(3) Describes the engulfing of a photosynthetic bacterium that ultimately gave rise to mitochondria.
(4) Is thought to explain the origin of the nucleus.

The correct answer is "e</span>ndosymbiosis most likely began with a heterotrophic endosymbiont entering the cell as undigested prey or as an internal parasite". Endosymbiosis is described to be the origin of eukaryotic cell by a cell engulfing two prokaryotic organisms, one capable of cellular respiration and one capable of photosynthesis. The endosymbiont did not enter the cell through the endomembrane system as lysosomal/peroxisomal enzymes may kill these organisms instantly. 

Choice (3) is wrong as the photosynthetic bacterium gave rise to the chloroplast, not the mitochondria.  
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In the family tree below, people with the recessive trait of attached earlobes are shaded gray
serious [3.7K]
<h2><u>Full Question:</u></h2>

In the family tree below, people with the recessive trait of attached earlobes are shaded gray.

What must be true about the person labeled "A"?

A. It is a male with at least one dominant allele.

B. It is a male with two dominant alleles.

C. It is a female with at least one dominant allele.

D. It is a female with two dominant alleles.

<h2><u>Answer:</u></h2>

Its a male with atleast one dominant allele.

Option A.

<h3><u>Explanation:</u></h3>

The gene for the attached earlobe is recessive while the gene for the free earlobes is dominant. In the phylogenetic tree, we can see that both the father and mother aren't having attached earlobes. So both of them are having atleast one dominant allele which makes them have free earlobe.

In the F1 offsprings, one of the female and a male is having free earlobes. So both of them have atleast one dominant allele. The 2nd female is having an attached earlobe. So both the recessive allele have come form one parent each. So both of them are heterozygous.

Thus, the male marked as A atleast have one dominant allele. He can be a homozygous dominant, but the probability is 25%.

8 0
3 years ago
Match each term with the appropriate definition replication the ability of data to be duplicated repetition the ability of a pro
Nina [5.8K]

Answer:

can you separate them? I can't really see what the question is.

5 0
3 years ago
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Discuss the events of meiosis, and compare and<br> contrasthow meiosis differs from mitosis.
Arisa [49]

Answer:

Meiosis It is one of the ways of cell reproduction. This process is performed in the cells in the sex cells. It is a process of cell division in which a diploid cell (2n) undergoes two successive divisions, with the ability to generate four haploid cells (n). This process is carried out in two nuclear and cytoplasmic divisions, called first and second meiotic division or simply meiosis I and meiosis II

Explanation:

Phases of Meiosis

Two successive cell divisions occur in meiosis, Meiosis I (Reduction) and Meiosis II (Division). Meiosis produces 4 haploid cells. Meiosis is also known as reduction division.

In Meiosis I, the level of ploidy is reduced from 2n to n while in Meiosis II the "set" of remaining chromosomes is divided into a process similar to mitosis (division). The biggest difference in the process occurs during Meiosis I.

- MEIOSIS I: Prophase I

During mating, a key event occurs in the matching of homologous chromosomes.

- Metaphase I

In Metaphase I the tetrads line the equator of the cell. The spindle fibers "stick" to the centromere of each homologous pair and subsequent events are similar to mitosis.

- Anaphase I

During Anaphase I the tetrads separate and the chromosomes are dragged to the opposite poles by the spindle fibers. The centromeres in Anaphase I remain intact.

- Telophase I

Telophase I is similar to mitosis, except that in the end each "cell" has only one group of replicated chromosomes. Depending on the species, the new nuclear membrane can be formed (or not). Some animals can divide their centrioles during this phase.

Telophase may be absent in some species. If there is, it is followed by an interface called interkinesis; Unlike the mitotic interface, there is no duplication of genetic material since each chromosome already has two chromatids. The other difference is that these sister chromatids are no longer genetically identical, due to the cross-linking phenomenon.

- MEIOSIS II: Profase II

During Prophase II, the nuclear membrane (if formed during Telophase I) dissolves, and the spindle fibers appear, as in the prophase of mitosis. Actually, Meiosis II is very similar to mitosis.

- Metaphase II

Metaphase II is similar to that of mitosis, with chromosomes in the equatorial plane and spindle fibers sticking to the opposite faces of the centromere in the kinetochore region.

- Anaphase II

During Anaphase II, the centromere divides and the then chromatids, now chromosomes, are secreted to the opposite poles of the cell.

- Telophase II

Telophase II is identical to Telophase of mitosis. Cytokinesis separates the cells.

Comparison of Mitosis and Meiosis :

- Mitosis maintains the level of ploidy while meiosis reduces it.

- Meiosis can be considered as a phase of chromosome number reduction followed by a slightly different mitosis.

- Meiosis only occurs in relatively few cells of a multicellular organism, while mitosis is more common.

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3 years ago
Describe how an allosteric regulator can regulate enzyme activity.
Rainbow [258]

Answer:

Explanation:

An allosteric enzyme is one in which the activity of the enzyme can be controlled by the biniding of a molecule to the "allosteric site". This really just means somewhere other than the active site. Thus allosteric control of an enzyme can be classed in two ways. A positive allosteric modification is the binding of a molecule to the enzyme which increase the rate of reaction. Sort of like catalysing the catalysing effect of an enzyme. Obviously the opposite is true of negative allosteric modification. A good example for this is the activity of phosphofructokinase, which is promoted by a high AMP concentration, and inhibited by a high ATP concentration. This should make sense if you think about the action of a kinase etc.

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6 0
3 years ago
Which type of solution causes crenation or shrinkage of submerged red blood cells?
Nitella [24]

If a cell is placed in a hypertonic solution, water will leave the cell, and the cell will shrink.

Crenation is a phenomenon which occurs when cells of animal origin are exposed to a hypertonic solution, meaning that the solution which bathes the cells has a high concentration of solutes. In crenation, the cells shrink and their shapes become distorted, often with a ruffled or scalloped edge.

When a red blood cell is placed in a hypertonic solution, it shrinks as water is drawn out of the cell and into the surrounding solution. If the same blood cell placed in a hypotonic solution, the blood cell grows in size. Blood cells in isotonic solutions do not shrink or swell.

To learn more about Crenation , here

brainly.com/question/3365317

#SPJ4

3 0
1 year ago
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