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Nesterboy [21]
2 years ago
13

A scientist finds a new life form and determines that it performs photosynthesis. Which of the 6 kingdoms could it belong to? Se

lect the list that contains all the possible kingdoms. A. Eubacteria, Archaebacteria, Protista, and Plantae B. Eubacteria, Archaebacteria, Protista, and Fungi C. Protista and Fungi D. Eubacteria, Archaebacteria, Fungi, and Plantae
Biology
2 answers:
charle [14.2K]2 years ago
6 0
"<span>Eubacteria, Archaebacteria, Protista, and Plantae " is the one list among the following choices given that </span><span>contains all the possible kingdoms. The correct option among all the options that are given in the question is the first option or option "A". I hope that this answer has actually come to your help.</span>
Wewaii [24]2 years ago
3 0

The answer is A: Eubacteria, Archaebacteria, Protista, and Plantae

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We have a layout .. and our information that we conduct during our lab goes unerneath our "Materials and Methods" or the "Results"..
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3 years ago
What determines the function of a protein​
Sauron [17]

Answer:

The sequence of amino acids. - The three-dimensional shape of the folded protein. - If the coding sequence has a mutation that leads to a change in the amino acid sequence, the protein may have a different three-dimensional shape, reducing its activity.

Explanation:

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2 years ago
From a chemical view, how is an amino acid is being recognized by its specific aminoacyl tRNA synthetase?
hammer [34]

During translation, rRNA and tRNA read mRNA in 5´ to 3´ direction. According to the codons being readen, tRNA transfers the correct amino acids to build the polypeptide chain. A codon is a short sequence of three nucleotides that store the genetic information for the aminoacids´ assembly.

Each tRNA has two important sites. One of them that couples with the codon of the mRNA molecule, named anticodon. The other site couples with an amino acid through the action of the aminoacyl-tRNA synthase enzyme. The whole complex, amino acid + enzyme + tRNA is named aminoacyl-tRNA.        

Each tRNA is recognized by a specific aminoacyl-tRNA synthase enzyme. The enzyme is also capable of recognizing a specific amino acid. Let us say, for instance, that <em>tRNA is specific for phenylalanine.</em> The molecule is attached to the <em>enzyme that is specific for that tRNA(Phe)</em>. Then, when the enzyme and tRNA(Phe) are together, they get to <em>find phenylalanine</em>. The <em>enzyme links the aminoacid to the RNA</em>. Once the whole complex is formed, the <em>tRNA gets to pair its anticodon with the mRNA codon</em>. This is,

  1. Recognition of enzyme and the specific tRNA(aa) ⇒ aa being aminoacid
  2. Recognition of enzyme and the specific aminoacid
  3. Linkage of the aminoacid to RNA by the enzyme action
  4. Pairing of tRNA anticodon to mRNA codon.

Considering that there are twenty amino acids available, there are also twenty complexes of aminoacyl-tRNA, one for each amino acid. Each of the mRNA codons represents one of the 20 amino acids used to build the protein. Each amino acid can be codified by more than one codon. Of the total 64 codons, 61 codify amino acids, and one is a start codon. The left three codons are stopping translation points.

tRNA decodes genetic information from the nucleotidic sequence in the mRNA molecule and allows amino acids to align composing the new protein.  

Once the new peptidic link joins, placing together the new amino acid to the growing peptidic chain, the binding between the amino acid and the tRNA molecule breaks. The tRNA is now free to join another amino acid and repeat the cycle.

In conclusion, a specific aminoacyl-tRNA synthase enzyme recognizes a tRNA, which is also specific for a certain amino acid. When together, the enzyme recognizes the amino acid and links it to the RNA. The whole complex is known as aminoacyl-tRNA. Once the tRNA is joined to its amino acid, it gets to pair a codon of mRNA to add that amino acid to the new synthesizing protein.

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mario62 [17]
<span>A substance that is made of atoms of more than one type bound together is called a <span><u>compound</u>.
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4 0
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Compare and contrast Prophase and Telophase. what is different about DNA of the chromosomes in these phases. ( Max 5 Sentences )
shepuryov [24]

Answer:

The C. elegans embryo is a powerful model system for studying the mechanics of metazoan cell division. Its primary advantage is that the architecture of the syncytial gonad makes it possible to use RNAi to generate oocytes whose cytoplasm is reproducibly (typically >95%) depleted of targeted essential gene products via a process that does not depend exclusively on intrinsic protein turnover. The depleted oocytes can then be analyzed as they attempt their first mitotic division following fertilization. Here we outline the characteristics that contribute to the usefulness of the C. elegans embryo for cell division studies. We provide a timeline for the first embryonic mitosis and highlight some of its key features. We also summarize some of the recent discoveries made using this system, particularly in the areas of nuclear envelope assembly/ dissassembly, centrosome dynamics, formation of the mitotic spindle, kinetochore assembly, chromosome segregation, and cytokinesis.

1. The C. elegans embryo as a system to study cell division

The C. elegans embryo is a powerful model system for studying the mechanics of metazoan cell division. Its primary advantage is that the syncytial gonad makes it possible to use RNA interference (RNAi) to generate oocytes whose cytoplasm is reproducibly (>95%) depleted of targeted essential gene products. Introduction of dsRNA rapidly catalyzes the destruction of the corresponding mRNA in many different systems. However, depletion of pre-existing protein is generally a slow process that depends on the half-life of the targeted protein. In contrast, in the C. elegans gonad, the protein present when the dsRNA is introduced is depleted by the continual packaging of maternal cytoplasm into oocytes (Figure 1). Since depletion relies on the rate of embryo production instead of protein half-life, the kinetics tend to be similar for different targets. By 36-48 hours after introduction of the dsRNA, newly formed oocytes are typically >95% depleted of the target protein.

Explanation:

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