Phagocytosis is the ingestion and destruction of particle matter by the amoeba
There are all sorts of ways to reconstruct the history of life on Earth. Pinning down when specific events occurred is often tricky, though. For this, biologists depend mainly on dating the rocks in which fossils are found, and by looking at the “molecular clocks” in the DNA of living organisms.
There are problems with each of these methods. The fossil record is like a movie with most of the frames cut out. Because it is so incomplete, it can be difficult to establish exactly when particular evolutionary changes happened.
Modern genetics allows scientists to measure how different species are from each other at a molecular level, and thus to estimate how much time has passed since a single lineage split into different species. Confounding factors rack up for species that are very distantly related, making the earlier dates more uncertain.
These difficulties mean that the dates in the timeline should be taken as approximate. As a general rule, they become more uncertain the further back along the geological timescale we look. Dates that are very uncertain are marked with a question mark.
If a linear piece of DNA has three sites for a particular restriction enzyme, it will be cut into 4 fragments. If the DNA is circular, the number of obtained fragments will be N for N recognition sequences for the specified restriction enzymes however if the DNA is linear, the number of obtained fragments will be (N+1).
A bacterial protein called the restriction enzyme cleaves DNA at specific locations. The recognition sequences, or short and distinct nucleotide sequences, are recognized by restriction enzymes in DNA. When a DNA sequence is recognized by the restriction enzyme, it hydrolyzes the bond between neighboring nucleotides and cleaves the DNA molecule.
The restriction enzymes guard against bacteriophages on the living bacteria. They identify the bacteriophage and cleave at its restriction sites, destroying its DNA.
The use of restriction enzymes in genetic engineering is crucial. In order to introduce foreign DNA for gene-editing purposes, restriction enzymes cut DNA at a specified location, which makes them a crucial tool.
To learn more about restriction enzyme, recognition sequences and bacteriophages here
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