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Why were tubes 1 and 2 included in the experiment? Tubes 1 and 2 are the control group to which other tubes can be compared - VCE - SSCE Biology - Question 5 - 2005 - Paper 1

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Why were tubes 1 and 2 included in the experiment? Tubes 1 and 2 are the control group to which other tubes can be compared. The diagram shows that the fungus grew... show full transcript

Worked Solution & Example Answer:Why were tubes 1 and 2 included in the experiment? Tubes 1 and 2 are the control group to which other tubes can be compared - VCE - SSCE Biology - Question 5 - 2005 - Paper 1

Step 1

Why were tubes 1 and 2 included in the experiment?

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Answer

Tubes 1 and 2 serve as control groups in the experiment. Control groups are essential for establishing a baseline to which experimental results can be compared. In this case, they help determine whether the abnormal fungus can grow in minimal media without any added amino acids.

Step 2

What sequences of nucleotides in DNA code for the amino acid histidine?

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Answer

Histidine can be coded by the following nucleotide sequences in DNA: the RNA codons for histidine are CAU and CAC, which correspond to the DNA sequences GTA and GTG.

Step 3

Which of the following DNA sequences could lead to the production of an uninterrupted chain of amino acids in the abnormal fungus?

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Answer

The DNA sequence that could lead to an uninterrupted chain of amino acids is:

sequence 3 TAATGACCCCGTG

This sequence does not have the DNA triplet for histidine (GTA or GTG), unlike sequences 1 and 2, which might lead to interruptions during translation.

Step 4

Explain why you made this selection in c.ii.

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Answer

I selected sequence 3 because it does not contain the triplet that codes for histidine. Sequences 1 and 2 include codons that could potentially lead to premature termination of the polypeptide chain, disrupting the production of the desired amino acids.

Step 5

What difference would it have made to the model of DNA had they used the results of laboratory 1 only?

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Answer

Using only the results from laboratory 1, which lacks crucial information obtained from laboratories 2 and 3, would have led to an incomplete understanding of the structure of DNA. The absence of diverse data would restrict the development of a comprehensive model, possibly overlooking significant characteristics of DNA.

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