chapter 3 p6 Flashcards

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1
Q

gene.

A

A section of DNA that contains the complete sequence of codons to code for an entire protein

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2
Q

Transcription: p1

A

In a eukaryotic cell, DNA is contained within a double membrane called the nuclear envelope that encloses the nucleus.
This protects the DNA from being damaged in the cytoplasm.
Protein synthesis occurs in the cytoplasm at ribosomes, but a chromosomal DNA molecule is too large to leave the nucleus to supply the coding information needed to determine the protein’s amino acid sequence.
To get around this problem, the base sequences of genes have to be copied and transported to the site of protein synthesis, a ribosome.
This process is called transcription and produces shorter molecules of RNA.
Although transcription results in a different polynucleotide, it has many similarities with DNA replication.

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3
Q

Transcription: p2

A

The section of DNA that contains the gene unwinds and unzips under the control of a DNA helicase, beginning at a start codon.
This involves the breaking of hydrogen bonds between the bases.
Only one of the two strands of DNA contains the code for the protein to be synthesised.
This is the sense strand and it runs from 5’ to 3’.
The other strand (3’ to 5’) is a complementary copy of the sense strand and does not code for a protein.
This is the antisense strand and it acts as the template strand during transcription, so that the complementary RNA strand formed carries the same base sequence as the sense strand.
Free RNA nucleotides will base pair with complementary bases exposed on the antisense strand when the DNA unzips.

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4
Q

Transcription: p3

A

the thymine base in RNA nucleotides is replaced with the base uracil (U).
So RNA uracil binds to adenine on the DNA template strand.
Phosphodiester bonds are formed between the RNA nucleotides by the enzyme RNA polymerase.
Transcription stops at the end of the gene and the completed short strand of RNA is called messenger (m)RNA.
It has the same base sequence as the sequence of bases making up the gene on the DNA, except that it has uracil in place of thymine.
The mRNA then detaches from the DNA template and leaves the nucleus through a nuclear pore. The DNA double helix reforms.
This mRNA molecule then travels to a ribosome in the cell cytoplasm for the next step in protein synthesis.

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5
Q

Translation:

A

In eukaryotic cells, ribosomes are made up of two subunits, one large and one small.
These subunits are composed of almost equal amounts of protein and a form of RNA known as ribosomal (r)RNA.
rRNA is important in maintaining the structural stability of the protein synthesis sequence and plays a biochemical role in catalysing the reaction.
After leaving the nucleus, the mRNA binds to a specific site on the small subunit of a ribosome.
The ribosome holds mRNA in position while it is decoded, or translated, into a sequence of amino acids.
This process is called translation.

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6
Q

tRNA

A

Transfer (t)RNA is another form of RNA, which is necessary for the translation of the mRNA.
It is composed of a strand of RNA folded in such a way that three bases, called the anticodon, are at one end of the molecule (Figure 3).
This anticodon will bind to a complementary codon on mRNA following the normal base pairing rules.
The tRNA molecules carry an amino acid corresponding to that codon (Figure 4).
When the tRNA anticodons bind to complementary codons along the mRNA, the amino acids are brought together in the correct sequence to form the primary structure of the protein coded for by the mRNA.
This cannot happen all at once - Instead amino acids are added one at a time and the polypeptide chain (protein) grows as this happens.
Ribosomes act as the binding site for mRNA and tRNA and catalyse the assembly of the protein.

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7
Q

Summary of translation: P1

A

The mRNA binds to the small subunit of the ribosome at its start codon (AUG).
A tRNA with the complementary anticodon (UAC) binds to the mRNA start codon. This tRNA carries the amino acid methionine.
Another tRNA with the anticodon UGC and carrying the corresponding amino acid, threonine, then binds to the next codon on the mRNA (ACG).
A maximum of two tRNAs can be bound at the same time.

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8
Q

Summary of translation: P2

A

The first amino acid, methionine, is transferred to the amino acid (threonine) on the second tRNA by the formation of a peptide bond.
This is catalysed by the enzyme peptidyl transferase, which is an rRNA component of the ribosome.
The ribosome then moves along the mRNA, releasing the first tRNA. The second tRNA becomes the first.

Stages 3-5 are repeated, with another amino acid added to the chain each time.

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9
Q

Post transaltion

A

The process keeps repeating until the ribosome reaches the end of the mRNA at a stop codon and the polypeptide is released.
As the amino acids are joined together forming the primary structure of the protein, they fold into secondary and tertiary structures.
This folding and the bonds that are formed are determined by the sequence of amino acids in the primary structure.
The protein may undergo further modifications at the Golgi apparatus before it is fully functional and ready to carry out the specific role for which it has been synthesised.
Many ribosomes can follow on the mRNA behind the first, so that multiple identical polypeptides can be synthesised simultaneously (Figure 6).

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10
Q

Universal energy currency:

A

Muscle contraction, cell division, the transmission of nerve impulses, and even memory formation are just some of the many biological processes that require energy.
Energy comes in many forms, such as heat, light, and the energy in chemical bonds.
Energy has to be supplied in the right form and quantity to the processes that require it.

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11
Q

Cells require energy for three main types of activity:

A

synthesis - for example of large molecules such as proteins
transport - for example pumping molecules or ions across cell membranes by active transport
movement - for example protein fibres in muscle cells that cause muscle contraction.

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12
Q

ATP structure

A

Inside cells, molecules of adenosine triphosphate (ATP) are able to supply this energy in such a way that it can be used.
An ATP molecule is composed of a nitrogenous base, a pentose sugar and three phosphate groups, as shown in Figure 1 - it is a nucleotide.
the structure of ATP is very similar to that of the nucleotides involved in the structure of DNA and RNA
However, in ATP the base is always adenine and there are three phosphate groups instead of one. The sugar in ATP is ribose, as in RNA nucleotides.
ATP is used for energy transfer in all cells of all living things. Hence it is known as the universal energy currency.

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13
Q

ATP structure diagram

A
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14
Q
A
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15
Q

How ATP releases energy p1

A

Energy is needed to break bonds and is released when bonds are formed.
A small amount of energy is needed to break the relatively weak bond holding the last phosphate group in ATP.
However, a large amount of energy is then released when the liberated phosphate undergoes other reactions involving bond formation.
Overall a lot more energy is released than used, approximately 30.6 kJ mol-‘.
As water is involved in the removal of the phosphate group this is another example of a hydrolysis reaction.

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16
Q

How ATP releases energy p2

A

The hydrolysis of ATP does not happen in isolation but in association with energy-requiring reactions.
The reactions are said to be ‘coupled’ as they happen simultaneously.
ATP is hydrolysed into adenosine diphosphate (ADP) and a phosphate ion, releasing energy.

17
Q

How ATP releases energy p3

A

The instability of the phosphate bonds in ATP, however, means that it is not a good long-term energy store.
Fats and carbohydrates are much better for this.
The energy released in the breakdown of these molecules (a process called cellular respiration) is used to create ATP.
This occurs by reattaching a phosphate group to an ADP molecule. The process is called phosphorylation.
As water is removed in this process, the reaction is another example of a condensation reaction.
Due to the instability of ATP, cells do not store large amounts of it.
However, ATP is rapidly reformed by the phosphorylation of ADP (Figure 4).
This interconversion of ATP and ADP is happening constantly in all living cells, meaning cells do not need a large store of ATP.
ATP is therefore a good immediate energy store.

18
Q

Properties of ATP:
The structure and properties of ATP mean that it is ideally suited to carry out its function in energy transfer.

A summary of these properties:

A
  • Small - moves easily into, out of and within cells.
  • Water soluble - energy-requiring processes happen in aqueous environments
  • Contains bonds between phosphates with intermediate energy: large enough to be useful for cellular reactions but not so large that energy is wasted as heat.
  • Releases energy in small quantities - quantities are suitable to most cellular needs, so that energy is not wasted as heat.
  • Easily regenerated - can be recharged with energy.