Mechanism of PCR: At the start of PCR, all the requirements are mixed together in ‘eppendorf tube’ and the following operations are performed sequentially:
Step i: Denaturation
The reaction mixture is heated to a temperature (90–98o C) to separate two strands of desired DNA. This is called denaturation.
Step ii: Annealing
The mixture is allowed to cool (40–60o C) that permits pairing of the primer to the complementary sequences in DNA. This step is called annealing.
Step iii: Primer extension / Polymerization
The temperature (70–75o C) allows thermostable Taq DNA polymerase to use single-stranded DNA as template and adds nucleotides. This is called primer extension. It takes around two minutes duration.
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| Column A | Column B |
| (1) Nutritive tissue of embryo | (a) Perisperm |
| (2) Remnants of nucellus in seed | (b) Cotyledon |
| (3) Nutritive tissue of developing microspores | (c) Endosperm |
| (4) First photosynthetic organ of embryo | (d) Tapetum |
| (1) Column A (Asexual) | Column B (Examples) |
| (1) Spore formation | (a) Spirogyra |
| (2) Conidia formation | (b) Yeast |
| (3) Fragmentation | (c) Chlamydomonas |
| (4) Budding | (d) Penicillium |