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                                                                            02107020/CAPE/SPEC/KMS 2017
                                                        BIOLOGY
                                                  UNIT 1 – PAPER 02
                                                 KEY AND MARK SCHEME

             Question 2 Specific Objectives: 2.6, 4.1, 4.2, 4.4, 5.4, 5.4

             (a)  (i)      D → C → A → B – 1 mark                                           [1 mark]

                   (ii)  Labelling of Stage B
                           Labels should show
                           -  cell plate (center)
                           -  cell wall (outer)
                           -  chromosomes

                           1 mark each                                                      [3 marks]

                   (iii)  Crossing over can occur at Stage D (prophase)                     [1 mark]

                           Crossing over and variation

                        -  Homologous chromosomes pair and wind around each other.
                        -  Where  two  chromatids  touch  each  other,  the  DNA  breaks  and
                            sections are exchanged between non-sister chromatids. This is
                            called crossing over.
                        -  Crossing over results in chromosomes that are part maternal in
                            origin and part paternal
                        -  This gives different combinations of alleles of different genes
                            - variation.

                           1 mark each = 4 marks
                                                                                            [5 marks]

             (b)  R-DNA process

                    1.     Isolation of genes: DNA is removed from a host source. (The
                           insulin gene (INS) coding for insulin production is extracted
                           from a sample of human DNA).

                    2.     Enzyme restriction: circular plasmid DNA from a bacterium is
                           “cut” via an endonuclease enzyme that breaks the DNA phosphate
                           backbone making it linear.

                    3.     Ligation: the “pasting together” of (different source) fragments
                           of DNA forming the recombinant DNA molecule… using the ligase
                           enzyme, the human insulin gene is then combined with the linear
                           plasmid DNA and is re-circularized.
                    4.     Uptake of plasmid: uptake of DNA by an organism (bacterium)...
                           the new recombinant DNA is taken-up by other bacteria to
                           facilitate replication of the plasmid.
                    5.     Cloning: the subsequent growth (ideal conditions) allows for
                           high production of multiple copies of the new plasmid (R-DNA
                           molecule) and production of the gene product ... insulin.

                           1 mark each = 5 marks
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