Q.What is double fertilization? Describe the process in brief. OR Define r-DNA technology. Give the basic steps in r-DNA technology and give any 'three' examples of the therapeutic products produced by r-DNA technology.
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Start your 14-day free trial to unlock the full solution →Double fertilization is syngamy (male gamete + egg gives the diploid zygote) plus triple fusion (male gamete + secondary nucleus gives the triploid primary endosperm nucleus); the OR alternative asks for recombinant-DNA technology and three of its therapeutic products.
Part (a)
Double fertilization is the complex fertilization mechanism of flowering plants, discovered by Nawaschin in liliaceous plants such as Lilium and Fritillaria. Both of the male gametes delivered by one pollen tube take part in fusion, which is why it is called double.
- Pollen tube growth and entry. A compatible pollen grain germinates on the stigma; its pollen tube grows through the stigma, style and ovary chamber and enters the ovule, usually through the micropyle (porogamy), guided by chemicals secreted by the synergids.
- Release of the male gametes. The tube penetrates one synergid, absorbs its watery contents, ruptures, and releases the two non-motile male gametes (siphonogamy).
- Syngamy (generative fertilization). One male gamete fuses with the haploid egg to form the diploid zygote, which develops into the embryo.
- Triple fusion (vegetative fertilization). The second male gamete fuses with the diploid secondary nucleus (itself formed from the two polar nuclei) to form the triploid primary endosperm nucleus, which develops into the nutritive endosperm.
Its significance: it is unique to angiosperms, it ensures a food store is laid down only after the egg is fertilized, it restores the diploid condition in the zygote, and it provides the endosperm that nourishes the embryo. The NCERT Class 12 Biology chapter that the Maharashtra syllabus follows describes double fertilization in the same terms.
Part (b)
Recombinant DNA (r-DNA) technology is the set of techniques by which DNA from two different sources, typically a gene of interest and a vector such as a plasmid, is joined into a single hybrid molecule that can be introduced into a host cell and expressed there.
- Isolate the desired gene (the DNA insert) and a suitable vector. …
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